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Fernandez-Rozadilla, C. Timofeeva, M. Chen, Z. Law, P. Thomas, M. Schmit, S. Díez-Obrero, V. Hsu, L. Fernandez-Tajes, J. Palles, C. Sherwood, K. Briggs, S. Svinti, V. Donnelly, K. Farrington, S. Blackmur, J. Vaughan-Shaw, P. Shu, X.-. Long, J. Cai, Q. Guo, X. Lu, Y. Broderick, P. Studd, J. Huyghe, J. Harrison, T. Conti, D. Dampier, C. Devall, M. Schumacher, F. Melas, M. Rennert, G. Obón-Santacana, M. Martín-Sánchez, V. Moratalla-Navarro, F. Oh, J.H. Kim, J. Jee, S.H. Jung, K.J. Kweon, S.-. Shin, M.-. Shin, A. Ahn, Y.-. Kim, D.-. Oze, I. Wen, W. Matsuo, K. Matsuda, K. Tanikawa, C. Ren, Z. Gao, Y.-. Jia, W.-. Hopper, J. Jenkins, M. Win, A.K. Pai, R. Figueiredo, J. Haile, R. Gallinger, S. Woods, M. Newcomb, P. Duggan, D. Cheadle, J. Kaplan, R. Maughan, T. Kerr, R. Kerr, D. Kirac, I. Böhm, J. Mecklin, L.-. Jousilahti, P. Knekt, P. Aaltonen, L. Rissanen, H. Pukkala, E. Eriksson, J. Cajuso, T. Hänninen, U. Kondelin, J. Palin, K. Tanskanen, T. Renkonen-Sinisalo, L. Zanke, B. Männistö, S. Albanes, D. Weinstein, S. Ruiz-Narvaez, E. Palmer, J. Buchanan, D. Platz, E. Visvanathan, K. Ulrich, C. Siegel, E. Brezina, S. Gsur, A. Campbell, P. Chang-Claude, J. Hoffmeister, M. Brenner, H. Slattery, M. Potter, J. Tsilidis, K. Schulze, M. Gunter, M. Murphy, N. Castells, A. Castellví-Bel, S. Moreira, L. Arndt, V. Shcherbina, A. Stern, M. Pardamean, B. Bishop, T. Giles, G. Southey, M. Idos, G. McDonnell, K. Abu-Ful, Z. Greenson, J. Shulman, K. Lejbkowicz, F. Offit, K. Su, Y.-. Steinfelder, R. Keku, T. van Guelpen, B. Hudson, T. Hampel, H. Pearlman, R. Berndt, S. Hayes, R. Martinez, M.E. Thomas, S. Corley, D. Pharoah, P. Larsson, S. Yen, Y. Lenz, H.-. White, E. Li, L. Doheny, K. Pugh, E. Shelford, T. Chan, A. Cruz-Correa, M. Lindblom, A. Hunter, D. Joshi, A. Schafmayer, C. Scacheri, P. Kundaje, A. Nickerson, D. Schoen, R. Hampe, J. Stadler, Z. Vodicka, P. Vodickova, L. Vymetalkova, V. Papadopoulos, N. Edlund, C. Gauderman, W. Thomas, D. Shibata, D. Toland, A. Markowitz, S. Kim, A. Chanock, S. van Duijnhoven, F. Feskens, E. Sakoda, L. Gago-Dominguez, M. Wolk, A. Naccarati, A. Pardini, B. FitzGerald, L. Lee, S.C. Ogino, S. Bien, S. Kooperberg, C. Li, C. Lin, Y. Prentice, R. Qu, C. Bézieau, S. Tangen, C. Mardis, E. Yamaji, T. Sawada, N. Iwasaki, M. Haiman, C. Le Marchand, L. Wu, A. Qu, C. McNeil, C. Coetzee, G. Hayward, C. Deary, I. Harris, S. Theodoratou, E. Reid, S. Walker, M. Ooi, L.Y. Moreno, V. Casey, G. Gruber, S. Tomlinson, I. Zheng, W. Dunlop, M. Houlston, R. Peters, U. (2023). Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries. Nat genet, Vol.55 (1), pp. 89-99.  show abstract

Li, W. Zhou, X. Yuan, S. Wang, L. Yu, L. Sun, J. Chen, J. Xiao, Q. Wan, Z. Zheng, J.-. Zhang, C.-. Larsson, S.C. Farrington, S.M. Law, P. Houlston, R.S. Tomlinson, I. Ding, K.-. Dunlop, M.G. Theodoratou, E. Li, X. (2023). Exploring the Complex Relationship between Gut Microbiota and Risk of Colorectal Neoplasia Using Bidirectional Mendelian Randomization Analysis. Cancer epidemiol biomarkers prev, Vol.32 (6), pp. 809-817.  show abstract

Thomas, M. Su, Y.-. Rosenthal, E.A. Sakoda, L.C. Schmit, S.L. Timofeeva, M.N. Chen, Z. Fernandez-Rozadilla, C. Law, P.J. Murphy, N. Carreras-Torres, R. Diez-Obrero, V. van Duijnhoven, F.J. Jiang, S. Shin, A. Wolk, A. Phipps, A.I. Burnett-Hartman, A. Gsur, A. Chan, A.T. Zauber, A.G. Wu, A.H. Lindblom, A. Um, C.Y. Tangen, C.M. Gignoux, C. Newton, C. Haiman, C.A. Qu, C. Bishop, D.T. Buchanan, D.D. Crosslin, D.R. Conti, D.V. Kim, D.-. Hauser, E. White, E. Siegel, E. Schumacher, F.R. Rennert, G. Giles, G.G. Hampel, H. Brenner, H. Oze, I. Oh, J.H. Lee, J.K. Schneider, J.L. Chang-Claude, J. Kim, J. Huyghe, J.R. Zheng, J. Hampe, J. Greenson, J. Hopper, J.L. Palmer, J.R. Visvanathan, K. Matsuo, K. Matsuda, K. Jung, K.J. Li, L. Le Marchand, L. Vodickova, L. Bujanda, L. Gunter, M.J. Matejcic, M. Jenkins, M.A. Slattery, M.L. D'Amato, M. Wang, M. Hoffmeister, M. Woods, M.O. Kim, M. Song, M. Iwasaki, M. Du, M. Udaltsova, N. Sawada, N. Vodicka, P. Campbell, P.T. Newcomb, P.A. Cai, Q. Pearlman, R. Pai, R.K. Schoen, R.E. Steinfelder, R.S. Haile, R.W. Vandenputtelaar, R. Prentice, R.L. Küry, S. Castellví-Bel, S. Tsugane, S. Berndt, S.I. Lee, S.C. Brezina, S. Weinstein, S.J. Chanock, S.J. Jee, S.H. Kweon, S.-. Vadaparampil, S. Harrison, T.A. Yamaji, T. Keku, T.O. Vymetalkova, V. Arndt, V. Jia, W.-. Shu, X.-. Lin, Y. Ahn, Y.-. Stadler, Z.K. Van Guelpen, B. Ulrich, C.M. Platz, E.A. Potter, J.D. Li, C.I. Meester, R. Moreno, V. Figueiredo, J.C. Casey, G. Lansdorp Vogelaar, I. Dunlop, M.G. Gruber, S.B. Hayes, R.B. Pharoah, P.D. Houlston, R.S. Jarvik, G.P. Tomlinson, I.P. Zheng, W. Corley, D.A. Peters, U. Hsu, L. (2023). Combining Asian and European genome-wide association studies of colorectal cancer improves risk prediction across racial and ethnic populations. Nat commun, Vol.14 (1), p. 6147.  show abstract

Hill, W. Lim, E.L. Weeden, C.E. Lee, C. Augustine, M. Chen, K. Kuan, F.-. Marongiu, F. Evans, E.J. Moore, D.A. Rodrigues, F.S. Pich, O. Bakker, B. Cha, H. Myers, R. van Maldegem, F. Boumelha, J. Veeriah, S. Rowan, A. Naceur-Lombardelli, C. Karasaki, T. Sivakumar, M. De, S. Caswell, D.R. Nagano, A. Black, J.R. Martínez-Ruiz, C. Ryu, M.H. Huff, R.D. Li, S. Favé, M.-. Magness, A. Suárez-Bonnet, A. Priestnall, S.L. Lüchtenborg, M. Lavelle, K. Pethick, J. Hardy, S. McRonald, F.E. Lin, M.-. Troccoli, C.I. Ghosh, M. Miller, Y.E. Merrick, D.T. Keith, R.L. Al Bakir, M. Bailey, C. Hill, M.S. Saal, L.H. Chen, Y. George, A.M. Abbosh, C. Kanu, N. Lee, S.-. McGranahan, N. Berg, C.D. Sasieni, P. Houlston, R. Turnbull, C. Lam, S. Awadalla, P. Grönroos, E. Downward, J. Jacks, T. Carlsten, C. Malanchi, I. Hackshaw, A. Litchfield, K. TRACERx Consortium, DeGregori, J. Jamal-Hanjani, M. Swanton, C. (2023). Lung adenocarcinoma promotion by air pollutants. Nature, Vol.616 (7955), pp. 159-167.  show abstract

Wills, C. Watts, K. Maughan, T.S. Fisher, D. Al-Tassan, N.A. Houlston, R.S. Escott-Price, V. Cheadle, J.P. (2023). Germline variation in RASAL2 may predict survival in patients with RAS-activated colorectal cancer. Genes chromosomes cancer, Vol.62 (6), pp. 332-341.  show abstract

Huntley, C. Torr, B. Sud, A. Rowlands, C.F. Way, R. Snape, K. Hanson, H. Swanton, C. Broggio, J. Lucassen, A. McCartney, M. Houlston, R.S. Hingorani, A.D. Jones, M.E. Turnbull, C. (2023). Utility of polygenic risk scores in UK cancer screening: a modelling analysis. Lancet oncol, Vol.24 (6), pp. 658-668.  show abstract

Panopoulou, A. Cairns, D.A. Holroyd, A. Nichols, I. Cray, N. Pawlyn, C. Cook, G. Drayson, M. Boyd, K. Davies, F.E. Jenner, M. Morgan, G.J. Owen, R. Houlston, R. Jackson, G. Kaiser, M.F. (2023). Optimizing the value of lenalidomide maintenance by extended genetic profiling: an analysis of 556 patients in the Myeloma XI trial. Blood, Vol.141 (14), pp. 1666-1674.  show abstract

Lindström, S. Wang, L. Feng, H. Majumdar, A. Huo, S. Macdonald, J. Harrison, T. Turman, C. Chen, H. Mancuso, N. Bammler, T. Breast Cancer Association Consortium (BCAC), Gallinger, S. Gruber, S.B. Gunter, M.J. Le Marchand, L. Moreno, V. Offit, K. Colorectal Transdisciplinary Study (CORECT), Colon Cancer Family Registry Study (CCFR), Genetics And Epidemiology Of Colorectal Cancer Consortium (GECCO), De Vivo, I. O'Mara, T.A. Spurdle, A.B. Tomlinson, I. Endometrial Cancer Association Consortium (ECAC), Fitzgerald, R. Gharahkhani, P. Gockel, I. Jankowski, J. Macgregor, S. Schumacher, J. Barnholtz-Sloan, J. Bondy, M.L. Houlston, R.S. Jenkins, R.B. Melin, B. Wrensch, M. Brennan, P. Christiani, D.C. Johansson, M. Mckay, J. Aldrich, M.C. Amos, C.I. Landi, M.T. Tardon, A. International Lung Cancer Consortium (ILCCO), Bishop, D.T. Demenais, F. Goldstein, A.M. Iles, M.M. Kanetsky, P.A. Law, M.H. Ovarian Cancer Association Consortium (OCAC), Amundadottir, L.T. Stolzenberg-Solomon, R. Wolpin, B.M. Pancreatic Cancer Cohort Consortium (Panscan), Klein, A. Petersen, G. Risch, H. Pancreatic Cancer Case-Control Consortium (Panc4), The PRACTICAL Consortium, Chanock, S.J. Purdue, M.P. Scelo, G. Pharoah, P. Kar, S. Hung, R.J. Pasaniuc, B. Kraft, P. (2023). Genome-wide analyses characterize shared heritability among cancers and identify novel cancer susceptibility regions. J natl cancer inst, Vol.115 (6), pp. 712-732.  show abstract

Morra, A. Schreurs, M.A. Andrulis, I.L. Anton-Culver, H. Augustinsson, A. Beckmann, M.W. Behrens, S. Bojesen, S.E. Bolla, M.K. Brauch, H. Broeks, A. Buys, S.S. Camp, N.J. Castelao, J.E. Cessna, M.H. Chang-Claude, J. Chung, W.K. NBCS Collaborators, Colonna, S.V. Couch, F.J. Cox, A. Cross, S.S. Czene, K. Daly, M.B. Dennis, J. Devilee, P. Dörk, T. Dunning, A.M. Dwek, M. Easton, D.F. Eccles, D.M. Eriksson, M. Evans, D.G. Fasching, P.A. Fehm, T.N. Figueroa, J.D. Flyger, H. Gabrielson, M. Gago-Dominguez, M. García-Closas, M. García-Sáenz, J.A. Genkinger, J. Grassmann, F. Gündert, M. Hahnen, E. Haiman, C.A. Hamann, U. Harrington, P.A. Hartikainen, J.M. Hoppe, R. Hopper, J.L. Houlston, R.S. Howell, A. ABCTB Investigators, kConFab Investigators, Jakubowska, A. Janni, W. Jernström, H. John, E.M. Johnson, N. Jones, M.E. Kristensen, V.N. Kurian, A.W. Lambrechts, D. Le Marchand, L. Lindblom, A. Lubiński, J. Lux, M.P. Mannermaa, A. Mavroudis, D. Mulligan, A.M. Muranen, T.A. Nevanlinna, H. Nevelsteen, I. Neven, P. Newman, W.G. Obi, N. Offit, K. Olshan, A.F. Park-Simon, T.-. Patel, A.V. Peterlongo, P. Phillips, K.-. Plaseska-Karanfilska, D. Polley, E.C. Presneau, N. Pylkäs, K. Rack, B. Radice, P. Rashid, M.U. Rhenius, V. Robson, M. Romero, A. Saloustros, E. Sawyer, E.J. Schmutzler, R.K. Schuetze, S. Scott, C. Shah, M. Smichkoska, S. Southey, M.C. Tapper, W.J. Teras, L.R. Tollenaar, R.A. Tomczyk, K. Tomlinson, I. Troester, M.A. Vachon, C.M. van Veen, E.M. Wang, Q. Wendt, C. Wildiers, H. Winqvist, R. Ziogas, A. Hall, P. Pharoah, P.D. Adank, M.A. Hollestelle, A. Schmidt, M.K. Hooning, M.J. (2023). Association of the CHEK2 c 1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival. Cancer med, Vol.12 (15), pp. 16142-16162.  show abstract

Middha, P. Wang, X. Behrens, S. Bolla, M.K. Wang, Q. Dennis, J. Michailidou, K. Ahearn, T.U. Andrulis, I.L. Anton-Culver, H. Arndt, V. Aronson, K.J. Auer, P.L. Augustinsson, A. Baert, T. Freeman, L.E. Becher, H. Beckmann, M.W. Benitez, J. Bojesen, S.E. Brauch, H. Brenner, H. Brooks-Wilson, A. Campa, D. Canzian, F. Carracedo, A. Castelao, J.E. Chanock, S.J. Chenevix-Trench, G. CTS Consortium, Cordina-Duverger, E. Couch, F.J. Cox, A. Cross, S.S. Czene, K. Dossus, L. Dugué, P.-. Eliassen, A.H. Eriksson, M. Evans, D.G. Fasching, P.A. Figueroa, J.D. Fletcher, O. Flyger, H. Gabrielson, M. Gago-Dominguez, M. Giles, G.G. González-Neira, A. Grassmann, F. Grundy, A. Guénel, P. Haiman, C.A. Håkansson, N. Hall, P. Hamann, U. Hankinson, S.E. Harkness, E.F. Holleczek, B. Hoppe, R. Hopper, J.L. Houlston, R.S. Howell, A. Hunter, D.J. Ingvar, C. ABCTB Investigators, kConFab Investigators, Isaksson, K. Jernström, H. John, E.M. Jones, M.E. Kaaks, R. Keeman, R. Kitahara, C.M. Ko, Y.-. Koutros, S. Kurian, A.W. Lacey, J.V. Lambrechts, D. Larson, N.L. Larsson, S. Le Marchand, L. Lejbkowicz, F. Li, S. Linet, M. Lissowska, J. Martinez, M.E. Maurer, T. Mulligan, A.M. Mulot, C. Murphy, R.A. Newman, W.G. Nielsen, S.F. Nordestgaard, B.G. Norman, A. O'Brien, K.M. Olson, J.E. Patel, A.V. Prentice, R. Rees-Punia, E. Rennert, G. Rhenius, V. Ruddy, K.J. Sandler, D.P. Scott, C.G. Shah, M. Shu, X.-. Smeets, A. Southey, M.C. Stone, J. Tamimi, R.M. Taylor, J.A. Teras, L.R. Tomczyk, K. Troester, M.A. Truong, T. Vachon, C.M. Wang, S.S. Weinberg, C.R. Wildiers, H. Willett, W. Winham, S.J. Wolk, A. Yang, X.R. Zamora, M.P. Zheng, W. Ziogas, A. Dunning, A.M. Pharoah, P.D. García-Closas, M. Schmidt, M.K. Kraft, P. Milne, R.L. Lindström, S. Easton, D.F. Chang-Claude, J. (2023). A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry. Breast cancer res, Vol.25 (1), p. 93.  show abstract

Kaiser, M.F. Hall, A. Walker, K. Sherborne, A. De Tute, R.M. Newnham, N. Roberts, S. Ingleson, E. Bowles, K. Garg, M. Lokare, A. Messiou, C. Houlston, R.S. Jackson, G. Cook, G. Pratt, G. Owen, R.G. Drayson, M.T. Brown, S.R. Jenner, M.W. (2023). Daratumumab, Cyclophosphamide, Bortezomib, Lenalidomide, and Dexamethasone as Induction and Extended Consolidation Improves Outcome in Ultra-High-Risk Multiple Myeloma. J clin oncol, Vol.41 (23), pp. 3945-3955.  show abstract

Zhou, X. Xiao, Q. Jiang, F. Sun, J. Wang, L. Yu, L. Zhou, Y. Zhao, J. Zhang, H. Yuan, S. Timofeeva, M. Spiliopoulou, A. Mesa-Eguiagaray, I. Farrington, S.M. Law, P.J. Houlston, R.S. Ding, K. Dunlop, M.G. Theodoratou, E. Li, X. (2023). Dissecting the pathogenic effects of smoking and its hallmarks in blood DNA methylation on colorectal cancer risk. Br j cancer, Vol.129 (8), pp. 1306-1313.  show abstract

Timmins, I.R. Jones, M.E. O'Brien, K.M. Adami, H.-. Aune, D. Baglietto, L. Bertrand, K.A. Brantley, K.D. Chen, Y. Clague DeHart, J. Clendenen, T.V. Dossus, L. Eliassen, A.H. Fletcher, O. Fournier, A. Håkansson, N. Hankinson, S.E. Houlston, R.S. Joshu, C.E. Kirsh, V.A. Kitahara, C.M. Koh, W.-. Linet, M.S. Park, H.L. Lynch, B.M. May, A.M. Mellemkjær, L. Milne, R.L. Palmer, J.R. Ricceri, F. Rohan, T.E. Ruddy, K.J. Sánchez, M.-. Shu, X.-. Smith-Byrne, K. Steindorf, K. Sund, M. Vachon, C.M. Vatten, L.J. Visvanathan, K. Weiderpass, E. Willett, W.C. Wolk, A. Yuan, J.-. Zheng, W. Nichols, H.B. Sandler, D.P. Swerdlow, A.J. Schoemaker, M.J. (2023). International Pooled Analysis of Leisure-Time Physical Activity and Premenopausal Breast Cancer in Women From 19 Cohorts. J clin oncol, , p. JCO2301101.  show abstract

Junk, S.V. Schaeffeler, E. Zimmermann, M. Möricke, A. Beier, R. Schütte, P. Fedders, B. Alten, J. Hinze, L. Klein, N. Kulozik, A. Muckenthaler, M.U. Koehler, R. Borkhardt, A. Vijayakrishnan, J. Ellinghaus, D. Forster, M. Franke, A. Wintering, A. Kratz, C.P. Schrappe, M. Schwab, M. Houlston, R.S. Cario, G. Stanulla, M. (2023). Chemotherapy-related hyperbilirubinemia in pediatric acute lymphoblastic leukemia: a genome-wide association study from the AIEOP-BFM ALL study group. J exp clin cancer res, Vol.42 (1), p. 21.  show abstract

Mueller, S.H. Lai, A.G. Valkovskaya, M. Michailidou, K. Bolla, M.K. Wang, Q. Dennis, J. Lush, M. Abu-Ful, Z. Ahearn, T.U. Andrulis, I.L. Anton-Culver, H. Antonenkova, N.N. Arndt, V. Aronson, K.J. Augustinsson, A. Baert, T. Freeman, L.E. Beckmann, M.W. Behrens, S. Benitez, J. Bermisheva, M. Blomqvist, C. Bogdanova, N.V. Bojesen, S.E. Bonanni, B. Brenner, H. Brucker, S.Y. Buys, S.S. Castelao, J.E. Chan, T.L. Chang-Claude, J. Chanock, S.J. Choi, J.-. Chung, W.K. NBCS Collaborators, Colonna, S.V. CTS Consortium, Cornelissen, S. Couch, F.J. Czene, K. Daly, M.B. Devilee, P. Dörk, T. Dossus, L. Dwek, M. Eccles, D.M. Ekici, A.B. Eliassen, A.H. Engel, C. Evans, D.G. Fasching, P.A. Fletcher, O. Flyger, H. Gago-Dominguez, M. Gao, Y.-. García-Closas, M. García-Sáenz, J.A. Genkinger, J. Gentry-Maharaj, A. Grassmann, F. Guénel, P. Gündert, M. Haeberle, L. Hahnen, E. Haiman, C.A. Håkansson, N. Hall, P. Harkness, E.F. Harrington, P.A. Hartikainen, J.M. Hartman, M. Hein, A. Ho, W.-. Hooning, M.J. Hoppe, R. Hopper, J.L. Houlston, R.S. Howell, A. Hunter, D.J. Huo, D. ABCTB Investigators, Ito, H. Iwasaki, M. Jakubowska, A. Janni, W. John, E.M. Jones, M.E. Jung, A. Kaaks, R. Kang, D. Khusnutdinova, E.K. Kim, S.-. Kitahara, C.M. Koutros, S. Kraft, P. Kristensen, V.N. Kubelka-Sabit, K. Kurian, A.W. Kwong, A. Lacey, J.V. Lambrechts, D. Le Marchand, L. Li, J. Linet, M. Lo, W.-. Long, J. Lophatananon, A. Mannermaa, A. Manoochehri, M. Margolin, S. Matsuo, K. Mavroudis, D. Menon, U. Muir, K. Murphy, R.A. Nevanlinna, H. Newman, W.G. Niederacher, D. O'Brien, K.M. Obi, N. Offit, K. Olopade, O.I. Olshan, A.F. Olsson, H. Park, S.K. Patel, A.V. Patel, A. Perou, C.M. Peto, J. Pharoah, P.D. Plaseska-Karanfilska, D. Presneau, N. Rack, B. Radice, P. Ramachandran, D. Rashid, M.U. Rennert, G. Romero, A. Ruddy, K.J. Ruebner, M. Saloustros, E. Sandler, D.P. Sawyer, E.J. Schmidt, M.K. Schmutzler, R.K. Schneider, M.O. Scott, C. Shah, M. Sharma, P. Shen, C.-. Shu, X.-. Simard, J. Surowy, H. Tamimi, R.M. Tapper, W.J. Taylor, J.A. Teo, S.H. Teras, L.R. Toland, A.E. Tollenaar, R.A. Torres, D. Torres-Mejía, G. Troester, M.A. Truong, T. Vachon, C.M. Vijai, J. Weinberg, C.R. Wendt, C. Winqvist, R. Wolk, A. Wu, A.H. Yamaji, T. Yang, X.R. Yu, J.-. Zheng, W. Ziogas, A. Ziv, E. Dunning, A.M. Easton, D.F. Hemingway, H. Hamann, U. Kuchenbaecker, K.B. (2023). Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry. Genome med, Vol.15 (1), p. 7.  show abstract

Shi, J. Shiraishi, K. Choi, J. Matsuo, K. Chen, T.-. Dai, J. Hung, R.J. Chen, K. Shu, X.-. Kim, Y.T. Landi, M.T. Lin, D. Zheng, W. Yin, Z. Zhou, B. Song, B. Wang, J. Seow, W.J. Song, L. Chang, I.-. Hu, W. Chien, L.-. Cai, Q. Hong, Y.-. Kim, H.N. Wu, Y.-. Wong, M.P. Richardson, B.D. Funderburk, K.M. Li, S. Zhang, T. Breeze, C. Wang, Z. Blechter, B. Bassig, B.A. Kim, J.H. Albanes, D. Wong, J.Y. Shin, M.-. Chung, L.P. Yang, Y. An, S.-. Zheng, H. Yatabe, Y. Zhang, X.-. Kim, Y.-. Caporaso, N.E. Chang, J. Ho, J.C. Kubo, M. Daigo, Y. Song, M. Momozawa, Y. Kamatani, Y. Kobayashi, M. Okubo, K. Honda, T. Hosgood, D.H. Kunitoh, H. Patel, H. Watanabe, S.-. Miyagi, Y. Nakayama, H. Matsumoto, S. Horinouchi, H. Tsuboi, M. Hamamoto, R. Goto, K. Ohe, Y. Takahashi, A. Goto, A. Minamiya, Y. Hara, M. Nishida, Y. Takeuchi, K. Wakai, K. Matsuda, K. Murakami, Y. Shimizu, K. Suzuki, H. Saito, M. Ohtaki, Y. Tanaka, K. Wu, T. Wei, F. Dai, H. Machiela, M.J. Su, J. Kim, Y.H. Oh, I.-. Lee, V.H. Chang, G.-. Tsai, Y.-. Chen, K.-. Huang, M.-. Su, W.-. Chen, Y.-. Seow, A. Park, J.Y. Kweon, S.-. Chen, K.-. Gao, Y.-. Qian, B. Wu, C. Lu, D. Liu, J. Schwartz, A.G. Houlston, R. Spitz, M.R. Gorlov, I.P. Wu, X. Yang, P. Lam, S. Tardon, A. Chen, C. Bojesen, S.E. Johansson, M. Risch, A. Bickeböller, H. Ji, B.-. Wichmann, H.-. Christiani, D.C. Rennert, G. Arnold, S. Brennan, P. McKay, J. Field, J.K. Shete, S.S. Le Marchand, L. Liu, G. Andrew, A. Kiemeney, L.A. Zienolddiny-Narui, S. Grankvist, K. Johansson, M. Cox, A. Taylor, F. Yuan, J.-. Lazarus, P. Schabath, M.B. Aldrich, M.C. Jeon, H.-. Jiang, S.S. Sung, J.S. Chen, C.-. Hsiao, C.-. Jung, Y.J. Guo, H. Hu, Z. Burdett, L. Yeager, M. Hutchinson, A. Hicks, B. Liu, J. Zhu, B. Berndt, S.I. Wu, W. Wang, J. Li, Y. Choi, J.E. Park, K.H. Sung, S.W. Liu, L. Kang, C.H. Wang, W.-. Xu, J. Guan, P. Tan, W. Yu, C.-. Yang, G. Sihoe, A.D. Chen, Y. Choi, Y.Y. Kim, J.S. Yoon, H.-. Park, I.K. Xu, P. He, Q. Wang, C.-. Hung, H.-. Vermeulen, R.C. Cheng, I. Wu, J. Lim, W.-. Tsai, F.-. Chan, J.K. Li, J. Chen, H. Lin, H.-. Jin, L. Liu, J. Sawada, N. Yamaji, T. Wyatt, K. Li, S.A. Ma, H. Zhu, M. Wang, Z. Cheng, S. Li, X. Ren, Y. Chao, A. Iwasaki, M. Zhu, J. Jiang, G. Fei, K. Wu, G. Chen, C.-. Chen, C.-. Yang, P.-. Yu, J. Stevens, V.L. Fraumeni, J.F. Chatterjee, N. Gorlova, O.Y. Hsiung, C.A. Amos, C.I. Shen, H. Chanock, S.J. Rothman, N. Kohno, T. Lan, Q. (2023). Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population. Nat commun, Vol.14 (1), p. 3043.  show abstract

Sud, A. Horton, R.H. Hingorani, A.D. Tzoulaki, I. Turnbull, C. Houlston, R.S. Lucassen, A. (2023). Realistic expectations are key to realising the benefits of polygenic scores. Bmj, Vol.380, p. e073149.  show abstract

Saunders, C.N. Kinnersley, B. Culliford, R. Cornish, A.J. Law, P.J. Houlston, R.S. (2022). Relationship between genetically determined telomere length and glioma risk. Neuro oncol, Vol.24 (2), pp. 171-181.  show abstract

Zhou, X. Wang, L. Xiao, J. Sun, J. Yu, L. Zhang, H. Meng, X. Yuan, S. Timofeeva, M. Law, P.J. Houlston, R.S. Ding, K. Dunlop, M.G. Theodoratou, E. Li, X. (2022). Alcohol consumption, DNA methylation and colorectal cancer risk: Results from pooled cohort studies and Mendelian randomization analysis. Int j cancer, Vol.151 (1), pp. 83-94.  show abstract

Reijns, M.A. Parry, D.A. Williams, T.C. Nadeu, F. Hindshaw, R.L. Rios Szwed, D.O. Nicholson, M.D. Carroll, P. Boyle, S. Royo, R. Cornish, A.J. Xiang, H. Ridout, K. Genomics England Research Consortium, Colorectal Cancer Domain UK 100,000 Genomes Project, Schuh, A. Aden, K. Palles, C. Campo, E. Stankovic, T. Taylor, M.S. Jackson, A.P. (2022). Signatures of TOP1 transcription-associated mutagenesis in cancer and germline. Nature, Vol.602 (7898), pp. 623-631.  show abstract

Zhang, X. Li, X. He, Y. Law, P.J. Farrington, S.M. Campbell, H. Tomlinson, I.P. Houlston, R.S. Dunlop, M.G. Timofeeva, M. Theodoratou, E. (2022). Phenome-wide association study (PheWAS) of colorectal cancer risk SNP effects on health outcomes in UK Biobank. Br j cancer, Vol.126 (5), pp. 822-830.  show abstract

Palles, C. West, H.D. Chew, E. Galavotti, S. Flensburg, C. Grolleman, J.E. Jansen, E.A. Curley, H. Chegwidden, L. Arbe-Barnes, E.H. Lander, N. Truscott, R. Pagan, J. Bajel, A. Sherwood, K. Martin, L. Thomas, H. Georgiou, D. Fostira, F. Goldberg, Y. Adams, D.J. van der Biezen, S.A. Christie, M. Clendenning, M. Thomas, L.E. Deltas, C. Dimovski, A.J. Dymerska, D. Lubinski, J. Mahmood, K. van der Post, R.S. Sanders, M. Weitz, J. Taylor, J.C. Turnbull, C. Vreede, L. van Wezel, T. Whalley, C. Arnedo-Pac, C. Caravagna, G. Cross, W. Chubb, D. Frangou, A. Gruber, A.J. Kinnersley, B. Noyvert, B. Church, D. Graham, T. Houlston, R. Lopez-Bigas, N. Sottoriva, A. Wedge, D. Genomics England Research Consortium, CORGI Consortium, WGS500 Consortium, Jenkins, M.A. Kuiper, R.P. Roberts, A.W. Cheadle, J.P. Ligtenberg, M.J. Hoogerbrugge, N. Koelzer, V.H. Rivas, A.D. Winship, I.M. Ponte, C.R. Buchanan, D.D. Power, D.G. Green, A. Tomlinson, I.P. Sampson, J.R. Majewski, I.J. de Voer, R.M. (2022). Germline MBD4 deficiency causes a multi-tumor predisposition syndrome. Am j hum genet, Vol.109 (5), pp. 953-960.  show abstract

Briggs, S.E. Law, P. East, J.E. Wordsworth, S. Dunlop, M. Houlston, R. Hippisley-Cox, J. Tomlinson, I. (2022). Integrating genome-wide polygenic risk scores and non-genetic risk to predict colorectal cancer diagnosis using UK Biobank data: population based cohort study. Bmj, Vol.379, p. e071707.  show abstract

Ajore, R. Niroula, A. Pertesi, M. Cafaro, C. Thodberg, M. Went, M. Bao, E.L. Duran-Lozano, L. Lopez de Lapuente Portilla, A. Olafsdottir, T. Ugidos-Damboriena, N. Magnusson, O. Samur, M. Lareau, C.A. Halldorsson, G.H. Thorleifsson, G. Norddahl, G.L. Gunnarsdottir, K. Försti, A. Goldschmidt, H. Hemminki, K. van Rhee, F. Kimber, S. Sperling, A.S. Kaiser, M. Anderson, K. Jonsdottir, I. Munshi, N. Rafnar, T. Waage, A. Weinhold, N. Thorsteinsdottir, U. Sankaran, V.G. Stefansson, K. Houlston, R. Nilsson, B. (2022). Functional dissection of inherited non-coding variation influencing multiple myeloma risk. Nat commun, Vol.13 (1), p. 151.  show abstract

Robbe, P. Ridout, K.E. Vavoulis, D.V. Dréau, H. Kinnersley, B. Denny, N. Chubb, D. Appleby, N. Cutts, A. Cornish, A.J. Lopez-Pascua, L. Clifford, R. Burns, A. Stamatopoulos, B. Cabes, M. Alsolami, R. Antoniou, P. Oates, M. Cavalieri, D. Genomics England Research Consortium, CLL pilot consortium, Gibson, J. Prabhu, A.V. Schwessinger, R. Jennings, D. James, T. Maheswari, U. Duran-Ferrer, M. Carninci, P. Knight, S.J. Månsson, R. Hughes, J. Davies, J. Ross, M. Bentley, D. Strefford, J.C. Devereux, S. Pettitt, A.R. Hillmen, P. Caulfield, M.J. Houlston, R.S. Martín-Subero, J.I. Schuh, A. (2022). Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features. Nat genet, Vol.54 (11), pp. 1675-1689.  show abstract

Loveday, C. Garrett, A. Law, P. Hanks, S. Poyastro-Pearson, E. Adlard, J.W. Barwell, J. Berg, J. Brady, A.F. Brewer, C. Chapman, C. Cook, J. Davidson, R. Donaldson, A. Douglas, F. Greenhalgh, L. Henderson, A. Izatt, L. Kumar, A. Lalloo, F. Miedzybrodzka, Z. Morrison, P.J. Paterson, J. Porteous, M. Rogers, M.T. Walker, L. Breast and Ovarian Cancer Susceptibility Collaboration, Eccles, D. Evans, D.G. Snape, K. Hanson, H. Houlston, R.S. Turnbull, C. (2022). Analysis of rare disruptive germline mutations in 2135 enriched BRCA-negative breast cancers excludes additional high-impact susceptibility genes. Ann oncol, Vol.33 (12), pp. 1318-1327.  show abstract

Clay-Gilmour, A. Chattopadhyay, S. Hildebrandt, M.A. Thomsen, H. Weinhold, N. Vodicka, P. Vodickova, L. Hoffmann, P. Nöthen, M.M. Jöckel, K.-. Schmidt, B. Langer, C. Hajek, R. Hallmans, G. Pettersson-Kymmer, U. Ohlsson, C. Späth, F. Houlston, R. Goldschmidt, H. Manasanch, E.E. Norman, A. Kumar, S. Rajkumar, S.V. Slager, S. Försti, A. Vachon, C.M. Hemminki, K. (2022). Genome-wide meta-analysis of monoclonal gammopathy of undetermined significance (MGUS) identifies risk loci impacting IRF-6. Blood cancer j, Vol.12 (4), p. 60.

He, Y. Zhang, X. Timofeeva, M. Farrington, S.M. Li, X. Xu, W. Campbell, H. Houlston, R.S. Tomlinson, I.P. Theodoratou, E. Dunlop, M.G. (2022). Bidirectional Mendelian randomisation analysis of the relationship between circulating vitamin D concentration and colorectal cancer risk. Int j cancer, Vol.150 (2), pp. 303-307.  show abstract

Watts, K. Wills, C. Madi, A. Palles, C. Maughan, T.S. Kaplan, R. Al-Tassan, N.A. Kerr, R. Kerr, D.J. Houlston, R.S. Escott-Price, V. Cheadle, J.P. (2022). Genetic variation in ST6GAL1 is a determinant of capecitabine and oxaliplatin induced hand-foot syndrome. Int j cancer, Vol.151 (6), pp. 957-966.  show abstract

Andreou, A. Yngvadottir, B. Bassaganyas, L. Clark, G. Martin, E. Whitworth, J. Cornish, A.J. Genomics England Research Consortium, Houlston, R.S. Rich, P. Egan, C. Hodgson, S.V. Warren, A.Y. Snape, K. Maher, E.R. (2022). Elongin C (ELOC/TCEB1)-associated von Hippel-Lindau disease. Hum mol genet, Vol.31 (16), pp. 2728-2737.  show abstract

Yngvadottir, B. Andreou, A. Bassaganyas, L. Larionov, A. Cornish, A.J. Chubb, D. Saunders, C.N. Smith, P.S. Zhang, H. Cole, Y. Research Consortium, G.E. Larkin, J. Browning, L. Turajlic, S. Litchfield, K. Houlston, R.S. Maher, E.R. (2022). Frequency of pathogenic germline variants in cancer susceptibility genes in 1336 renal cell carcinoma cases. Hum mol genet, Vol.31 (17), pp. 3001-3011.  show abstract

Martin, S. Tyrrell, J. Thomas, E.L. Bown, M.J. Wood, A.R. Beaumont, R.N. Tsoi, L.C. Stuart, P.E. Elder, J.T. Law, P. Houlston, R. Kabrhel, C. Papadimitriou, N. Gunter, M.J. Bull, C.J. Bell, J.A. Vincent, E.E. Sattar, N. Dunlop, M.G. Tomlinson, I.P. Lindström, S. INVENT consortium, Bell, J.D. Frayling, T.M. Yaghootkar, H. (2022). Disease consequences of higher adiposity uncoupled from its adverse metabolic effects using Mendelian randomisation. Elife, Vol.11.  show abstract

Went, M. Hoang, P.H. Law, P.J. Kaiser, M.F. Houlston, R.S. (2022). Exploiting gene dependency to inform drug development for multiple myeloma. Sci rep, Vol.12 (1), p. 12696.  show abstract

Vickers, A.J. Sud, A. Bernstein, J. Houlston, R. (2022). Polygenic risk scores to stratify cancer screening should predict mortality not incidence. Npj precis oncol, Vol.6 (1), p. 32.  show abstract

Yang, W. Liu, H. Zhang, R. Freedman, J.A. Han, Y. Hung, R.J. Brhane, Y. McLaughlin, J. Brennan, P. Bickeboeller, H. Rosenberger, A. Houlston, R.S. Caporaso, N.E. Landi, M.T. Brueske, I. Risch, A. Christiani, D.C. Amos, C.I. Chen, X. Patierno, S.R. Wei, Q. (2022). Deciphering associations between three RNA splicing-related genetic variants and lung cancer risk. Npj precis oncol, Vol.6 (1), p. 48.  show abstract

Saunders, C.N. Cornish, A.J. Kinnersley, B. Law, P.J. Houlston, R.S. Collaborators, (2021). Searching for causal relationships of glioma: a phenome-wide Mendelian randomisation study. Br j cancer, Vol.124 (2), pp. 447-454.  show abstract

Weinhold, N. Salwender, H.J. Cairns, D.A. Raab, M.S. Waldron, G. Blau, I.W. Bertsch, U. Hielscher, T. Morgan, G.J. Jauch, A. Davies, F.E. Hänel, M. Cook, G. Scheid, C. Houlston, R. Goldschmidt, H. Jackson, G. Kaiser, M.F. (2021). Chromosome 1q21 abnormalities refine outcome prediction in patients with multiple myeloma - a meta-analysis of 2,596 trial patients. Haematologica, Vol.106 (10), pp. 2754-2758.

Watts, K. Wills, C. Madi, A. Palles, C. Maughan, T.S. Kaplan, R. Al-Tassan, N.A. Kerr, R. Kerr, D. Gray, V. West, H. Houlston, R.S. Escott-Price, V. Cheadle, J.P. (2021). Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Int j cancer, Vol.149 (9), pp. 1713-1722.  show abstract

Ostrom, Q.T. Edelson, J. Byun, J. Han, Y. Kinnersley, B. Melin, B. Houlston, R.S. Monje, M. GLIOGENE Consortium, Walsh, K.M. Amos, C.I. Bondy, M.L. (2021). Partitioned glioma heritability shows subtype-specific enrichment in immune cells. Neuro oncol, Vol.23 (8), pp. 1304-1314.  show abstract

Lesseur, C. Ferreiro-Iglesias, A. McKay, J.D. Bossé, Y. Johansson, M. Gaborieau, V. Landi, M.T. Christiani, D.C. Caporaso, N.C. Bojesen, S.E. Amos, C.I. Shete, S. Liu, G. Rennert, G. Albanes, D. Aldrich, M.C. Tardon, A. Chen, C. Triantafillos, L. Field, J.K. Teare, M.D. Kiemeney, L.A. Diergaarde, B. Ferris, R.L. Zienolddiny, S. Lam, S. Olshan, A.F. Weissler, M.C. Lacko, M. Risch, A. Bickeböller, H. Ness, A.R. Thomas, S. Le Marchand, L. Schabath, M.B. Wünsch-Filho, V. Tajara, E.H. Andrew, A.S. Clifford, G.M. Lazarus, P. Grankvist, K. Johansson, M. Arnold, S. Melander, O. Brunnström, H. Boccia, S. Cadoni, G. Timens, W. Obeidat, M. Xiao, X. Houlston, R.S. Hung, R.J. Brennan, P. (2021). Genome-wide association meta-analysis identifies pleiotropic risk loci for aerodigestive squamous cell cancers. Plos genet, Vol.17 (3), p. e1009254.  show abstract

Zhang, X. Theodoratou, E. Li, X. Farrington, S.M. Law, P.J. Broderick, P. Walker, M. Klimentidis, Y.C. Rees, J.M. Houlston, R.S. Tomlinson, I.P. Burgess, S. Campbell, H. Dunlop, M.G. Timofeeva, M. (2021). Genetically predicted physical activity levels are associated with lower colorectal cancer risk: a Mendelian randomisation study. Br j cancer, Vol.124 (7), pp. 1330-1338.  show abstract

Culliford, R. Cornish, A.J. Law, P.J. Farrington, S.M. Palin, K. Jenkins, M.A. Casey, G. Hoffmeister, M. Brenner, H. Chang-Claude, J. Kirac, I. Maughan, T. Brezina, S. Gsur, A. Cheadle, J.P. Aaltonen, L.A. Dunlop, M.G. Houlston, R.S. (2021). Lack of an association between gallstone disease and bilirubin levels with risk of colorectal cancer: a Mendelian randomisation analysis. Br j cancer, Vol.124 (6), pp. 1169-1174.  show abstract

Maguire, S. Perraki, E. Tomczyk, K. Jones, M.E. Fletcher, O. Pugh, M. Winter, T. Thompson, K. Cooke, R. kConFab Consortium, Trainer, A. James, P. Bojesen, S. Flyger, H. Nevanlinna, H. Mattson, J. Friedman, E. Laitman, Y. Palli, D. Masala, G. Zanna, I. Ottini, L. Silvestri, V. Hollestelle, A. Hooning, M.J. Novaković, S. Krajc, M. Gago-Dominguez, M. Castelao, J.E. Olsson, H. Hedenfalk, I. Saloustros, E. Georgoulias, V. Easton, D.F. Pharoah, P. Dunning, A.M. Bishop, D.T. Neuhausen, S.L. Steele, L. Ashworth, A. Garcia Closas, M. Houlston, R. Swerdlow, A. Orr, N. (2021). Common Susceptibility Loci for Male Breast Cancer. J natl cancer inst, Vol.113 (4), pp. 453-461.  show abstract

Loveday, C. Sud, A. Jones, M.E. Broggio, J. Scott, S. Gronthound, F. Torr, B. Garrett, A. Nicol, D.L. Jhanji, S. Boyce, S.A. Williams, M. Barry, C. Riboli, E. Kipps, E. McFerran, E. Muller, D.C. Lyratzopoulos, G. Lawler, M. Abulafi, M. Houlston, R.S. Turnbull, C. (2021). Prioritisation by FIT to mitigate the impact of delays in the 2-week wait colorectal cancer referral pathway during the COVID-19 pandemic: a UK modelling study. Gut, Vol.70 (6), pp. 1053-1060.  show abstract

Croft, J. Ellis, S. Sherborne, A.L. Sharp, K. Price, A. Jenner, M.W. Drayson, M.T. Owen, R.G. Chown, S. Lindsay, J. Karunanithi, K. Hunter, H. Gregory, W.M. Davies, F.E. Morgan, G.J. Cook, G. Atanesyan, L. Savola, S. Cairns, D.A. Jackson, G. Houlston, R.S. Kaiser, M.F. (2021). Copy number evolution and its relationship with patient outcome-an analysis of 178 matched presentation-relapse tumor pairs from the Myeloma XI trial. Leukemia, Vol.35 (7), pp. 2043-2053.  show abstract

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Studd, J.B. Cornish, A.J. Hoang, P.H. Law, P. Kinnersley, B. Houlston, R. (2021). Cancer drivers and clonal dynamics in acute lymphoblastic leukaemia subtypes. Blood cancer j, Vol.11 (11), p. 177.  show abstract

Sud, A. Law, P.J. Houlston, R.S. (2021). The clinical utility of polygenic risk scores for chronic lymphocytic leukemia. Leukemia, Vol.35 (12), pp. 3608-3610.

Wills, C. He, Y. Summers, M.G. Lin, Y. Phipps, A.I. Watts, K. Law, P.J. Al-Tassan, N.A. Maughan, T.S. Kaplan, R. Houlston, R.S. Peters, U. Newcomb, P.A. Chan, A.T. Buchanan, D.D. Gallinger, S. Marchand, L.L. Pai, R.K. Shi, Q. Alberts, S.R. Gray, V. West, H.D. Escott-Price, V. Dunlop, M.G. Cheadle, J.P. (2021). A genome-wide search for determinants of survival in 1926 patients with advanced colorectal cancer with follow-up in over 22,000 patients. Eur j cancer, Vol.159, pp. 247-258.  show abstract

Saunders, C.N. Chattopadhyay, S. Huhn, S. Weinhold, N. Hoffmann, P. Nöthen, M.M. Jöckel, K.-. Schmidt, B. Landi, S. Goldschmidt, H. Milani, P. Merlini, G. Rowcieno, D. Hawkins, P. Hegenbart, U. Palladini, G. Wechalekar, A. Schönland, S.O. Försti, A. Houlston, R. Hemminki, K. (2021). Search for AL amyloidosis risk factors using Mendelian randomization. Blood adv, Vol.5 (13), pp. 2725-2731.  show abstract

Hemminki, K. Försti, A. Houlston, R. Sud, A. (2021). Epidemiology, genetics and treatment of multiple myeloma and precursor diseases. Int j cancer, Vol.149 (12), pp. 1980-1996.  show abstract

Duran-Lozano, L. Thorleifsson, G. Lopez de Lapuente Portilla, A. Niroula, A. Went, M. Thodberg, M. Pertesi, M. Ajore, R. Cafaro, C. Olason, P.I. Stefansdottir, L. Bragi Walters, G. Halldorsson, G.H. Turesson, I. Kaiser, M.F. Weinhold, N. Abildgaard, N. Andersen, N.F. Mellqvist, U.-. Waage, A. Juul-Vangsted, A. Thorsteinsdottir, U. Hansson, M. Houlston, R. Rafnar, T. Stefansson, K. Nilsson, B. (2021). Germline variants at SOHLH2 influence multiple myeloma risk. Blood cancer j, Vol.11 (4), p. 76.  show abstract

Bartram, T. Schütte, P. Möricke, A. Houlston, R.S. Ellinghaus, E. Zimmermann, M. Bergmann, A. Löscher, B.-. Klein, N. Hinze, L. Junk, S.V. Forster, M. Bartram, C.R. Köhler, R. Franke, A. Schrappe, M. Kratz, C.P. Cario, G. Stanulla, M. (2021). Genetic Variation in ABCC4 and CFTR and Acute Pancreatitis during Treatment of Pediatric Acute Lymphoblastic Leukemia. J clin med, Vol.10 (21).  show abstract

Sud, A. Turnbull, C. Houlston, R. (2021). Will polygenic risk scores for cancer ever be clinically useful?. Npj precis oncol, Vol.5 (1), p. 40.

Lin, W.-. Fordham, S.E. Sunter, N. Elstob, C. Rahman, T. Willmore, E. Shepherd, C. Strathdee, G. Mainou-Fowler, T. Piddock, R. Mearns, H. Barrow, T. Houlston, R.S. Marr, H. Wallis, J. Summerfield, G. Marshall, S. Pettitt, A. Pepper, C. Fegan, C. Forconi, F. Dyer, M.J. Jayne, S. Sellors, A. Schuh, A. Robbe, P. Oscier, D. Bailey, J. Rais, S. Bentley, A. Cawkwell, L. Evans, P. Hillmen, P. Pratt, G. Allsup, D.J. Allan, J.M. (2021). Genome-wide association study identifies risk loci for progressive chronic lymphocytic leukemia. Nat commun, Vol.12 (1), p. 665.  show abstract

Lin, W.-. Fordham, S.E. Hungate, E. Sunter, N.J. Elstob, C. Xu, Y. Park, C. Quante, A. Strauch, K. Gieger, C. Skol, A. Rahman, T. Sucheston-Campbell, L. Wang, J. Hahn, T. Clay-Gilmour, A.I. Jones, G.L. Marr, H.J. Jackson, G.H. Menne, T. Collin, M. Ivey, A. Hills, R.K. Burnett, A.K. Russell, N.H. Fitzgibbon, J. Larson, R.A. Le Beau, M.M. Stock, W. Heidenreich, O. Alharbi, A. Allsup, D.J. Houlston, R.S. Norden, J. Dickinson, A.M. Douglas, E. Lendrem, C. Daly, A.K. Palm, L. Piechocki, K. Jeffries, S. Bornhäuser, M. Röllig, C. Altmann, H. Ruhnke, L. Kunadt, D. Wagenführ, L. Cordell, H.J. Darlay, R. Andersen, M.K. Fontana, M.C. Martinelli, G. Marconi, G. Sanz, M.A. Cervera, J. Gómez-Seguí, I. Cluzeau, T. Moreilhon, C. Raynaud, S. Sill, H. Voso, M.T. Lo-Coco, F. Dombret, H. Cheok, M. Preudhomme, C. Gale, R.E. Linch, D. Gaal-Wesinger, J. Masszi, A. Nowak, D. Hofmann, W.-. Gilkes, A. Porkka, K. Milosevic Feenstra, J.D. Kralovics, R. Grimwade, D. Meggendorfer, M. Haferlach, T. Krizsán, S. Bödör, C. Stölzel, F. Onel, K. Allan, J.M. (2021). Genome-wide association study identifies susceptibility loci for acute myeloid leukemia. Nat commun, Vol.12 (1), p. 6233.  show abstract

Ostrom, Q.T. Egan, K.M. Nabors, L.B. Gerke, T. Thompson, R.C. Olson, J.J. LaRocca, R. Chowdhary, S. Eckel-Passow, J.E. Armstrong, G. Wiencke, J.K. Bernstein, J.L. Claus, E.B. Il'yasova, D. Johansen, C. Lachance, D.H. Lai, R.K. Merrell, R.T. Olson, S.H. Sadetzki, S. Schildkraut, J.M. Shete, S. Houlston, R.S. Jenkins, R.B. Wrensch, M.R. Melin, B. Amos, C.I. Huse, J.T. Barnholtz-Sloan, J.S. Bondy, M.L. (2020). Glioma risk associated with extent of estimated European genetic ancestry in African Americans and Hispanics. Int j cancer, Vol.146 (3), pp. 739-748.  show abstract

Cornish, A.J. Law, P.J. Timofeeva, M. Palin, K. Farrington, S.M. Palles, C. Jenkins, M.A. Casey, G. Brenner, H. Chang-Claude, J. Hoffmeister, M. Kirac, I. Maughan, T. Brezina, S. Gsur, A. Cheadle, J.P. Aaltonen, L.A. Tomlinson, I. Dunlop, M.G. Houlston, R.S. (2020). Modifiable pathways for colorectal cancer: a mendelian randomisation analysis. Lancet gastroenterol hepatol, Vol.5 (1), pp. 55-62.  show abstract

Summers, M.G. Maughan, T.S. Kaplan, R. Law, P.J. Houlston, R.S. Escott-Price, V. Cheadle, J.P. (2020). Comprehensive analysis of colorectal cancer-risk loci and survival outcome: A prognostic role for CDH1 variants. Eur j cancer, Vol.124, pp. 56-63.  show abstract

Hoang, P.H. Cornish, A.J. Chubb, D. Jackson, G. Kaiser, M. Houlston, R.S. (2020). Impact of mitochondrial DNA mutations in multiple myeloma. Blood cancer j, Vol.10 (5), p. 46.

Disney-Hogg, L. Kinnersley, B. Houlston, R. (2020). Algorithmic considerations when analysing capture Hi-C data. Wellcome open research, Vol.5, p. 289.  show abstract  full text

Bossé, Y. Li, Z. Xia, J. Manem, V. Carreras-Torres, R. Gabriel, A. Gaudreault, N. Albanes, D. Aldrich, M.C. Andrew, A. Arnold, S. Bickeböller, H. Bojesen, S.E. Brennan, P. Brunnstrom, H. Caporaso, N. Chen, C. Christiani, D.C. Field, J.K. Goodman, G. Grankvist, K. Houlston, R. Johansson, M. Johansson, M. Kiemeney, L.A. Lam, S. Landi, M.T. Lazarus, P. Le Marchand, L. Liu, G. Melander, O. Rennert, G. Risch, A. Rosenberg, S.M. Schabath, M.B. Shete, S. Song, Z. Stevens, V.L. Tardon, A. Wichmann, H.-. Woll, P. Zienolddiny, S. Obeidat, M. Timens, W. Hung, R.J. Joubert, P. Amos, C.I. McKay, J.D. (2020). Transcriptome-wide association study reveals candidate causal genes for lung cancer. Int j cancer, Vol.146 (7), pp. 1862-1878.  show abstract

Zhang, Y.D. Hurson, A.N. Zhang, H. Choudhury, P.P. Easton, D.F. Milne, R.L. Simard, J. Hall, P. Michailidou, K. Dennis, J. Schmidt, M.K. Chang-Claude, J. Gharahkhani, P. Whiteman, D. Campbell, P.T. Hoffmeister, M. Jenkins, M. Peters, U. Hsu, L. Gruber, S.B. Casey, G. Schmit, S.L. O'Mara, T.A. Spurdle, A.B. Thompson, D.J. Tomlinson, I. De Vivo, I. Landi, M.T. Law, M.H. Iles, M.M. Demenais, F. Kumar, R. MacGregor, S. Bishop, D.T. Ward, S.V. Bondy, M.L. Houlston, R. Wiencke, J.K. Melin, B. Barnholtz-Sloan, J. Kinnersley, B. Wrensch, M.R. Amos, C.I. Hung, R.J. Brennan, P. McKay, J. Caporaso, N.E. Berndt, S.I. Birmann, B.M. Camp, N.J. Kraft, P. Rothman, N. Slager, S.L. Berchuck, A. Pharoah, P.D. Sellers, T.A. Gayther, S.A. Pearce, C.L. Goode, E.L. Schildkraut, J.M. Moysich, K.B. Amundadottir, L.T. Jacobs, E.J. Klein, A.P. Petersen, G.M. Risch, H.A. Stolzenberg-Solomon, R.Z. Wolpin, B.M. Li, D. Eeles, R.A. Haiman, C.A. Kote-Jarai, Z. Schumacher, F.R. Al Olama, A.A. Purdue, M.P. Scelo, G. Dalgaard, M.D. Greene, M.H. Grotmol, T. Kanetsky, P.A. McGlynn, K.A. Nathanson, K.L. Turnbull, C. Wiklund, F. Breast Cancer Association Consortium (BCAC), Barrett’s and Esophageal Adenocarcinoma Consortium (BEACON), Colon Cancer Family Registry (CCFR), Transdisciplinary Studies of Genetic Variation in Colorectal Cancer (CORECT), Endometrial Cancer Association Consortium (ECAC), Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO), Melanoma Genetics Consortium (GenoMEL), Glioma International Case-Control Study (GICC), International Lung Cancer Consortium (ILCCO), Integrative Analysis of Lung Cancer Etiology and Risk (INTEGRAL) Consortium, International Consortium of Investigators Working on Non-Hodgkin’s Lymphoma Epidemiologic Studies (InterLymph), Ovarian Cancer Association Consortium (OCAC), Oral Cancer GWAS, Pancreatic Cancer Case-Control Consortium (PanC4), Pancreatic Cancer Cohort Consortium (PanScan), Prostate Cancer Association Group to Investigate Cancer Associated Alterations in the Genome (PRACTICAL), Renal Cancer GWAS, Testicular Cancer Consortium (TECAC), Chanock, S.J. Chatterjee, N. Garcia-Closas, M. (2020). Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers. Nat commun, Vol.11 (1), p. 3353.  show abstract

Pertesi, M. Went, M. Hansson, M. Hemminki, K. Houlston, R.S. Nilsson, B. (2020). Genetic predisposition for multiple myeloma. Leukemia, Vol.34 (3), pp. 697-708.  show abstract

Loveday, C. Litchfield, K. Proszek, P.Z. Cornish, A.J. Santo, F. Levy, M. Macintyre, G. Holryod, A. Broderick, P. Dudakia, D. Benton, B. Bakir, M.A. Hiley, C. Grist, E. Swanton, C. Huddart, R. Powles, T. Chowdhury, S. Shipley, J. O'Connor, S. Brenton, J.D. Reid, A. de Castro, D.G. Houlston, R.S. Turnbull, C. (2020). Genomic landscape of platinum resistant and sensitive testicular cancers. Nat commun, Vol.11 (1), p. 2189.  show abstract

Peto, J. Carpenter, J. Smith, G.D. Duffy, S. Houlston, R. Hunter, D.J. McPherson, K. Pearce, N. Romer, P. Sasieni, P. Turnbull, C. (2020). Weekly COVID-19 testing with household quarantine and contact tracing is feasible and would probably end the epidemic. R soc open sci, Vol.7 (6), p. 200915.  show abstract

Sud, A. Jones, M.E. Broggio, J. Loveday, C. Torr, B. Garrett, A. Nicol, D.L. Jhanji, S. Boyce, S.A. Gronthoud, F. Ward, P. Handy, J.M. Yousaf, N. Larkin, J. Suh, Y.-. Scott, S. Pharoah, P.D. Swanton, C. Abbosh, C. Williams, M. Lyratzopoulos, G. Houlston, R. Turnbull, C. (2020). Collateral damage: the impact on outcomes from cancer surgery of the COVID-19 pandemic. Ann oncol, Vol.31 (8), pp. 1065-1074.  show abstract

Semmes, E.C. Vijayakrishnan, J. Zhang, C. Hurst, J.H. Houlston, R.S. Walsh, K.M. (2020). Leveraging Genome and Phenome-Wide Association Studies to Investigate Genetic Risk of Acute Lymphoblastic Leukemia. Cancer epidemiol biomarkers prev, Vol.29 (8), pp. 1606-1614.  show abstract

Sud, A. Torr, B. Jones, M.E. Broggio, J. Scott, S. Loveday, C. Garrett, A. Gronthoud, F. Nicol, D.L. Jhanji, S. Boyce, S.A. Williams, M. Riboli, E. Muller, D.C. Kipps, E. Larkin, J. Navani, N. Swanton, C. Lyratzopoulos, G. McFerran, E. Lawler, M. Houlston, R. Turnbull, C. (2020). Effect of delays in the 2-week-wait cancer referral pathway during the COVID-19 pandemic on cancer survival in the UK: a modelling study. Lancet oncol, Vol.21 (8), pp. 1035-1044.  show abstract

Purdue, M.P. Song, L. Scélo, G. Houlston, R.S. Wu, X. Sakoda, L.C. Thai, K. Graff, R.E. Rothman, N. Brennan, P. Chanock, S.J. Yu, K. (2020). Pathway Analysis of Renal Cell Carcinoma Genome-Wide Association Studies Identifies Novel Associations. Cancer epidemiol biomarkers prev, Vol.29 (10), pp. 2065-2069.  show abstract

Hoang, P.H. Cornish, A.J. Sherborne, A.L. Chubb, D. Kimber, S. Jackson, G. Morgan, G.J. Cook, G. Kinnersley, B. Kaiser, M. Houlston, R.S. (2020). An enhanced genetic model of relapsed IGH-translocated multiple myeloma evolutionary dynamics. Blood cancer journal, Vol.10 (10).  show abstract

Ji, X. Mukherjee, S. Landi, M.T. Bosse, Y. Joubert, P. Zhu, D. Gorlov, I. Xiao, X. Han, Y. Gorlova, O. Hung, R.J. Brhane, Y. Carreras-Torres, R. Christiani, D.C. Caporaso, N. Johansson, M. Liu, G. Bojesen, S.E. Le Marchand, L. Albanes, D. Bickeböller, H. Aldrich, M.C. Bush, W.S. Tardon, A. Rennert, G. Chen, C. Byun, J. Dragnev, K.H. Field, J.K. Kiemeney, L.F. Lazarus, P. Zienolddiny, S. Lam, S. Schabath, M.B. Andrew, A.S. Bertazzi, P.A. Pesatori, A.C. Diao, N. Su, L. Song, L. Zhang, R. Leighl, N. Johansen, J.S. Mellemgaard, A. Saliba, W. Haiman, C. Wilkens, L. Fernandez-Somoano, A. Fernandez-Tardon, G. Heijden, E.H. Kim, J.H. Davies, M.P. Marcus, M.W. Brunnström, H. Manjer, J. Melander, O. Muller, D.C. Overvad, K. Trichopoulou, A. Tumino, R. Goodman, G.E. Cox, A. Taylor, F. Woll, P. Wichmann, E. Muley, T. Risch, A. Rosenberger, A. Grankvist, K. Johansson, M. Shepherd, F. Tsao, M.-. Arnold, S.M. Haura, E.B. Bolca, C. Holcatova, I. Janout, V. Kontic, M. Lissowska, J. Mukeria, A. Ognjanovic, S. Orlowski, T.M. Scelo, G. Swiatkowska, B. Zaridze, D. Bakke, P. Skaug, V. Butler, L.M. Offit, K. Srinivasan, P. Bandlamudi, C. Hellmann, M.D. Solit, D.B. Robson, M.E. Rudin, C.M. Stadler, Z.K. Taylor, B.S. Berger, M.F. Houlston, R. McLaughlin, J. Stevens, V. Nickle, D.C. Obeidat, M. Timens, W. Artigas, M.S. Shete, S. Brenner, H. Chanock, S. Brennan, P. McKay, J.D. Amos, C.I. (2020). Protein-altering germline mutations implicate novel genes related to lung cancer development. Nat commun, Vol.11 (1), p. 2220.  show abstract

Shah, V. Sherborne, A.L. Johnson, D.C. Ellis, S. Price, A. Chowdhury, F. Kendall, J. Jenner, M.W. Drayson, M.T. Owen, R.G. Gregory, W.M. Morgan, G.J. Davies, F.E. Cook, G. Cairns, D.A. Houlston, R.S. Jackson, G. Kaiser, M.F. on behalf of NCRI Haematology Clinical Studies Group, (2020). Predicting ultrahigh risk multiple myeloma by molecular profiling: an analysis of newly diagnosed transplant eligible myeloma XI trial patients. Leukemia, Vol.34 (11), pp. 3091-3096.

Yang, X. Song, H. Leslie, G. Engel, C. Hahnen, E. Auber, B. Horváth, J. Kast, K. Niederacher, D. Turnbull, C. Houlston, R. Hanson, H. Loveday, C. Dolinsky, J.S. LaDuca, H. Ramus, S.J. Menon, U. Rosenthal, A.N. Jacobs, I. Gayther, S.A. Dicks, E. Nevanlinna, H. Aittomäki, K. Pelttari, L.M. Ehrencrona, H. Borg, Å. Kvist, A. Rivera, B. Hansen, T.V. Djursby, M. Lee, A. Dennis, J. Bowtell, D.D. Traficante, N. Diez, O. Balmaña, J. Gruber, S.B. Chenevix-Trench, G. Investigators, K. Jensen, A. Kjær, S.K. Høgdall, E. Castéra, L. Garber, J. Janavicius, R. Osorio, A. Golmard, L. Vega, A. Couch, F.J. Robson, M. Gronwald, J. Domchek, S.M. Culver, J.O. de la Hoya, M. Easton, D.F. Foulkes, W.D. Tischkowitz, M. Meindl, A. Schmutzler, R.K. Pharoah, P.D. Antoniou, A.C. (2020). Ovarian and Breast Cancer Risks Associated With Pathogenic Variants in RAD51C and RAD51D. J natl cancer inst, Vol.112 (12), pp. 1242-1250.  show abstract

Chattopadhyay, S. Zheng, G. Sud, A. Sundquist, K. Sundquist, J. Försti, A. Houlston, R. Hemminki, A. Hemminki, K. (2020). Second primary cancers in non-Hodgkin lymphoma: Family history and survival. Int j cancer, Vol.146 (4), pp. 970-976.  show abstract

Li, X. Timofeeva, M. Spiliopoulou, A. McKeigue, P. He, Y. Zhang, X. Svinti, V. Campbell, H. Houlston, R.S. Tomlinson, I.P. Farrington, S.M. Dunlop, M.G. Theodoratou, E. (2020). Prediction of colorectal cancer risk based on profiling with common genetic variants. Int j cancer, Vol.147 (12), pp. 3431-3437.  show abstract

Saunders, C.N. Cornish, A.J. Kinnersley, B. Law, P.J. Claus, E.B. Il'yasova, D. Schildkraut, J. Barnholtz-Sloan, J.S. Olson, S.H. Bernstein, J.L. Lai, R.K. Chanock, S. Rajaraman, P. Johansen, C. Jenkins, R.B. Melin, B.S. Wrensch, M.R. Sanson, M. Bondy, M.L. Houlston, R.S. (2020). Lack of association between modifiable exposures and glioma risk: a Mendelian randomization analysis. Neuro oncol, Vol.22 (2), pp. 207-215.  show abstract

Went, M. Cornish, A.J. Law, P.J. Kinnersley, B. van Duin, M. Weinhold, N. Försti, A. Hansson, M. Sonneveld, P. Goldschmidt, H. Morgan, G.J. Hemminki, K. Nilsson, B. Kaiser, M. Houlston, R.S. (2020). Search for multiple myeloma risk factors using Mendelian randomization. Blood adv, Vol.4 (10), pp. 2172-2179.  show abstract

Disney-Hogg, L. Kinnersley, B. Houlston, R. (2020). Algorithmic considerations when analysing capture Hi-C data. Wellcome open res, Vol.5, p. 289.  show abstract

Disney-Hogg, L. Kinnersley, B. Houlston, R. (2020). Algorithmic considerations when analysing capture Hi-C data. , .  show abstract

Johansson, M. Carreras-Torres, R. Scelo, G. Purdue, M.P. Mariosa, D. Muller, D.C. Timpson, N.J. Haycock, P.C. Brown, K.M. Wang, Z. Ye, Y. Hofmann, J.N. Foll, M. Gaborieau, V. Machiela, M.J. Colli, L.M. Li, P. Garnier, J.-. Blanche, H. Boland, A. Burdette, L. Prokhortchouk, E. Skryabin, K.G. Yeager, M. Radojevic-Skodric, S. Ognjanovic, S. Foretova, L. Holcatova, I. Janout, V. Mates, D. Mukeriya, A. Rascu, S. Zaridze, D. Bencko, V. Cybulski, C. Fabianova, E. Jinga, V. Lissowska, J. Lubinski, J. Navratilova, M. Rudnai, P. Benhamou, S. Cancel-Tassin, G. Cussenot, O. Weiderpass, E. Ljungberg, B. Tumkur Sitaram, R. Häggström, C. Bruinsma, F. Jordan, S.J. Severi, G. Winship, I. Hveem, K. Vatten, L.J. Fletcher, T. Larsson, S.C. Wolk, A. Banks, R.E. Selby, P.J. Easton, D.F. Andreotti, G. Beane Freeman, L.E. Koutros, S. Männistö, S. Weinstein, S. Clark, P.E. Edwards, T.L. Lipworth, L. Gapstur, S.M. Stevens, V.L. Carol, H. Freedman, M.L. Pomerantz, M.M. Cho, E. Wilson, K.M. Gaziano, J.M. Sesso, H.D. Freedman, N.D. Parker, A.S. Eckel-Passow, J.E. Huang, W.-. Kahnoski, R.J. Lane, B.R. Noyes, S.L. Petillo, D. Teh, B.T. Peters, U. White, E. Anderson, G.L. Johnson, L. Luo, J. Buring, J. Lee, I.-. Chow, W.-. Moore, L.E. Eisen, T. Henrion, M. Larkin, J. Barman, P. Leibovich, B.C. Choueiri, T.K. Lathrop, G.M. Deleuze, J.-. Gunter, M. McKay, J.D. Wu, X. Houlston, R.S. Chanock, S.J. Relton, C. Richards, J.B. Martin, R.M. Davey Smith, G. Brennan, P. (2019). The influence of obesity-related factors in the etiology of renal cell carcinoma-A mendelian randomization study. Plos med, Vol.16 (1), p. e1002724.  show abstract

Studd, J.B. Yang, M. Li, Z. Vijayakrishnan, J. Lu, Y. Yeoh, A.E. Paulsson, K. Houlston, R.S. (2019). Genetic predisposition to B-cell acute lymphoblastic leukemia at 14q11 2 is mediated by a CEBPE promoter polymorphism. Leukemia, Vol.33 (1), pp. 1-14.  show abstract

Law, P.J. Houlston, R.S. (2019). Genetic predisposition to chronic lymphocytic leukemia. Hemasphere, Vol.3, pp. 37-3.

Ostrom, Q.T. Coleman, W. Huang, W. Rubin, J.B. Lathia, J.D. Berens, M.E. Speyer, G. Liao, P. Wrensch, M.R. Eckel-Passow, J.E. Armstrong, G. Rice, T. Wiencke, J.K. McCoy, L.S. Hansen, H.M. Amos, C.I. Bernstein, J.L. Claus, E.B. Houlston, R.S. Il'yasova, D. Jenkins, R.B. Johansen, C. Lachance, D.H. Lai, R.K. Merrell, R.T. Olson, S.H. Sadetzki, S. Schildkraut, J.M. Shete, S. Andersson, U. Rajaraman, P. Chanock, S.J. Linet, M.S. Wang, Z. Yeager, M. GliomaScan consortium, Melin, B. Bondy, M.L. Barnholtz-Sloan, J.S. (2019). Sex-specific gene and pathway modeling of inherited glioma risk. Neuro oncol, Vol.21 (1), pp. 71-82.  show abstract

Gray, V. Briggs, S. Palles, C. Jaeger, E. Iveson, T. Kerr, R. Saunders, M.P. Paul, J. Harkin, A. McQueen, J. Summers, M.G. Johnstone, E. Wang, H. Gatcombe, L. Maughan, T.S. Kaplan, R. Escott-Price, V. Al-Tassan, N.A. Meyer, B.F. Wakil, S.M. Houlston, R.S. Cheadle, J.P. Tomlinson, I. Church, D.N. (2019). Pattern Recognition Receptor Polymorphisms as Predictors of Oxaliplatin Benefit in Colorectal Cancer. J natl cancer inst, Vol.111 (8), pp. 828-836.  show abstract

Gunter, M.J. Alhomoud, S. Arnold, M. Brenner, H. Burn, J. Casey, G. Chan, A.T. Cross, A.J. Giovannucci, E. Hoover, R. Houlston, R. Jenkins, M. Laurent-Puig, P. Peters, U. Ransohoff, D. Riboli, E. Sinha, R. Stadler, Z.K. Brennan, P. Chanock, S.J. (2019). Meeting report from the joint IARC-NCI international cancer seminar series: a focus on colorectal cancer. Ann oncol, Vol.30 (4), pp. 510-519.  show abstract

Amirian, E.S. Ostrom, Q.T. Armstrong, G.N. Lai, R.K. Gu, X. Jacobs, D.I. Jalali, A. Claus, E.B. Barnholtz-Sloan, J.S. Il'yasova, D. Schildkraut, J.M. Ali-Osman, F. Sadetzki, S. Jenkins, R.B. Lachance, D.H. Olson, S.H. Bernstein, J.L. Merrell, R.T. Wrensch, M.R. Johansen, C. Houlston, R.S. Scheurer, M.E. Shete, S. Amos, C.I. Melin, B. Bondy, M.L. (2019). Aspirin, NSAIDs, and Glioma Risk: Original Data from the Glioma International Case-Control Study and a Meta-analysis. Cancer epidemiol biomarkers prev, Vol.28 (3), pp. 555-562.  show abstract

Zheng, G. Chattopadhyay, S. Sud, A. Sundquist, K. Sundquist, J. Försti, A. Houlston, R. Hemminki, A. Hemminki, K. (2019). Second primary cancers in patients with acute lymphoblastic, chronic lymphocytic and hairy cell leukaemia. Br j haematol, Vol.185 (2), pp. 232-239.  show abstract

Labreche, K. Daniau, M. Sud, A. Law, P.J. Royer-Perron, L. Holroyd, A. Broderick, P. Went, M. Benazra, M. Ahle, G. Soubeyran, P. Taillandier, L. Chinot, O.L. Casasnovas, O. Bay, J.-. Jardin, F. Oberic, L. Fabbro, M. Damaj, G. Brion, A. Mokhtari, K. Philippe, C. Sanson, M. Houillier, C. Soussain, C. Hoang-Xuan, K. Houlston, R.S. Alentorn, A. LOC Network, (2019). A genome-wide association study identifies susceptibility loci for primary central nervous system lymphoma at 6p25 3 and 3p22 1: a LOC Network study. Neuro oncol, Vol.21 (8), pp. 1039-1048.  show abstract

Zhu, Y. Wei, Y. Zhang, R. Dong, X. Shen, S. Zhao, Y. Bai, J. Albanes, D. Caporaso, N.E. Landi, M.T. Zhu, B. Chanock, S.J. Gu, F. Lam, S. Tsao, M.-. Shepherd, F.A. Tardon, A. Fernández-Somoano, A. Fernandez-Tardon, G. Chen, C. Barnett, M.J. Doherty, J. Bojesen, S.E. Johansson, M. Brennan, P. McKay, J.D. Carreras-Torres, R. Muley, T. Risch, A. Wichmann, H.-. Bickeboeller, H. Rosenberger, A. Rennert, G. Saliba, W. Arnold, S.M. Field, J.K. Davies, M.P. Marcus, M.W. Wu, X. Ye, Y. Le Marchand, L. Wilkens, L.R. Melander, O. Manjer, J. Brunnström, H. Hung, R.J. Liu, G. Brhane, Y. Kachuri, L. Andrew, A.S. Duell, E.J. Kiemeney, L.A. van der Heijden, E.H. Haugen, A. Zienolddiny, S. Skaug, V. Grankvist, K. Johansson, M. Woll, P.J. Cox, A. Taylor, F. Teare, D.M. Lazarus, P. Schabath, M.B. Aldrich, M.C. Houlston, R.S. McLaughlin, J. Stevens, V.L. Shen, H. Hu, Z. Dai, J. Amos, C.I. Han, Y. Zhu, D. Goodman, G.E. Chen, F. Christiani, D.C. (2019). Elevated Platelet Count Appears to Be Causally Associated with Increased Risk of Lung Cancer: A Mendelian Randomization Analysis. Cancer epidemiol biomarkers prev, Vol.28 (5), pp. 935-942.  show abstract

Hoang, P.H. Cornish, A.J. Dobbins, S.E. Kaiser, M. Houlston, R.S. (2019). Mutational processes contributing to the development of multiple myeloma. Blood cancer j, Vol.9 (8), p. 60.  show abstract

Went, M. Sud, A. Li, N. Johnson, D.C. Mitchell, J.S. Kaiser, M. Houlston, R.S. (2019). Regions of homozygosity as risk factors for multiple myeloma. Ann hum genet, Vol.83 (4), pp. 231-238.  show abstract

Loveday, C. Sud, A. Litchfield, K. Levy, M. Holroyd, A. Broderick, P. Kote-Jarai, Z. Dunning, A.M. Muir, K. Peto, J. Eeles, R. Easton, D.F. Dudakia, D. Orr, N. Pashayan, N. UK Testicular Cancer Collaboration, PRACTICAL Consortium, Reid, A. Huddart, R.A. Houlston, R.S. Turnbull, C. (2019). Runs of homozygosity and testicular cancer risk. Andrology, Vol.7 (4), pp. 555-564.  show abstract

Hung, R.J. Spitz, M.R. Houlston, R.S. Schwartz, A.G. Field, J.K. Ying, J. Li, Y. Han, Y. Ji, X. Chen, W. Wu, X. Gorlov, I.P. Na, J. de Andrade, M. Liu, G. Brhane, Y. Diao, N. Wenzlaff, A. Davies, M.P. Liloglou, T. Timofeeva, M. Muley, T. Rennert, H. Saliba, W. Ryan, B.M. Bowman, E. Barros-Dios, J.-. Pérez-Ríos, M. Morgenstern, H. Zienolddiny, S. Skaug, V. Ugolini, D. Bonassi, S. van der Heijden, E.H. Tardon, A. Bojesen, S.E. Landi, M.T. Johansson, M. Bickeböller, H. Arnold, S. Le Marchand, L. Melander, O. Andrew, A. Grankvist, K. Caporaso, N. Teare, M.D. Schabath, M.B. Aldrich, M.C. Kiemeney, L.A. Wichmann, H.-. Lazarus, P. Mayordomo, J. Neri, M. Haugen, A. Zhang, Z.-. Ruano-Raviña, A. Brenner, H. Harris, C.C. Orlow, I. Rennert, G. Risch, A. Brennan, P. Christiani, D.C. Amos, C.I. Yang, P. Gorlova, O.Y. (2019). Lung Cancer Risk in Never-Smokers of European Descent is Associated With Genetic Variation in the 5p15 33 TERT-CLPTM1Ll Region. J thorac oncol, Vol.14 (8), pp. 1360-1369.  show abstract

Cornish, A.J. Hoang, P.H. Dobbins, S.E. Law, P.J. Chubb, D. Orlando, G. Houlston, R.S. (2019). Identification of recurrent noncoding mutations in B-cell lymphoma using capture Hi-C. Blood adv, Vol.3 (1), pp. 21-32.  show abstract

Speedy, H.E. Beekman, R. Chapaprieta, V. Orlando, G. Law, P.J. Martín-García, D. Gutiérrez-Abril, J. Catovsky, D. Beà, S. Clot, G. Puiggròs, M. Torrents, D. Puente, X.S. Allan, J.M. López-Otín, C. Campo, E. Houlston, R.S. Martín-Subero, J.I. (2019). Insight into genetic predisposition to chronic lymphocytic leukemia from integrative epigenomics. Nat commun, Vol.10 (1), p. 3615.  show abstract

Cornish, A.J. Tomlinson, I.P. Houlston, R.S. (2019). Mendelian randomisation: A powerful and inexpensive method for identifying and excluding non-genetic risk factors for colorectal cancer. Mol aspects med, Vol.69, pp. 41-47.  show abstract

Thompson, D.J. Genovese, G. Halvardson, J. Ulirsch, J.C. Wright, D.J. Terao, C. Davidsson, O.B. Day, F.R. Sulem, P. Jiang, Y. Danielsson, M. Davies, H. Dennis, J. Dunlop, M.G. Easton, D.F. Fisher, V.A. Zink, F. Houlston, R.S. Ingelsson, M. Kar, S. Kerrison, N.D. Kinnersley, B. Kristjansson, R.P. Law, P.J. Li, R. Loveday, C. Mattisson, J. McCarroll, S.A. Murakami, Y. Murray, A. Olszewski, P. Rychlicka-Buniowska, E. Scott, R.A. Thorsteinsdottir, U. Tomlinson, I. Moghadam, B.T. Turnbull, C. Wareham, N.J. Gudbjartsson, D.F. International Lung Cancer Consortium (INTEGRAL-ILCCO), Breast Cancer Association Consortium, Consortium of Investigators of Modifiers of BRCA1/2, Endometrial Cancer Association Consortium, Ovarian Cancer Association Consortium, Prostate Cancer Association Group to Investigate Cancer Associated Alterations in the Genome (PRACTICAL) Consortium, Kidney Cancer GWAS Meta-Analysis Project, eQTLGen Consortium, Biobank-based Integrative Omics Study (BIOS) Consortium, 23andMe Research Team, Kamatani, Y. Hoffmann, E.R. Jackson, S.P. Stefansson, K. Auton, A. Ong, K.K. Machiela, M.J. Loh, P.-. Dumanski, J.P. Chanock, S.J. Forsberg, L.A. Perry, J.R. (2019). Genetic predisposition to mosaic Y chromosome loss in blood. Nature, Vol.575 (7784), pp. 652-657.  show abstract

Ofoegbu, T.C. David, A. Kelley, L.A. Mezulis, S. Islam, S.A. Mersmann, S.F. Strömich, L. Vakser, I.A. Houlston, R.S. Sternberg, M.J. (2019). PhyreRisk: A Dynamic Web Application to Bridge Genomics, Proteomics and 3D Structural Data to Guide Interpretation of Human Genetic Variants. J mol biol, Vol.431 (13), pp. 2460-2466.  show abstract

Law, P.J. Timofeeva, M. Fernandez-Rozadilla, C. Broderick, P. Studd, J. Fernandez-Tajes, J. Farrington, S. Svinti, V. Palles, C. Orlando, G. Sud, A. Holroyd, A. Penegar, S. Theodoratou, E. Vaughan-Shaw, P. Campbell, H. Zgaga, L. Hayward, C. Campbell, A. Harris, S. Deary, I.J. Starr, J. Gatcombe, L. Pinna, M. Briggs, S. Martin, L. Jaeger, E. Sharma-Oates, A. East, J. Leedham, S. Arnold, R. Johnstone, E. Wang, H. Kerr, D. Kerr, R. Maughan, T. Kaplan, R. Al-Tassan, N. Palin, K. Hänninen, U.A. Cajuso, T. Tanskanen, T. Kondelin, J. Kaasinen, E. Sarin, A.-. Eriksson, J.G. Rissanen, H. Knekt, P. Pukkala, E. Jousilahti, P. Salomaa, V. Ripatti, S. Palotie, A. Renkonen-Sinisalo, L. Lepistö, A. Böhm, J. Mecklin, J.-. Buchanan, D.D. Win, A.-. Hopper, J. Jenkins, M.E. Lindor, N.M. Newcomb, P.A. Gallinger, S. Duggan, D. Casey, G. Hoffmann, P. Nöthen, M.M. Jöckel, K.-. Easton, D.F. Pharoah, P.D. Peto, J. Canzian, F. Swerdlow, A. Eeles, R.A. Kote-Jarai, Z. Muir, K. Pashayan, N. PRACTICAL consortium, Harkin, A. Allan, K. McQueen, J. Paul, J. Iveson, T. Saunders, M. Butterbach, K. Chang-Claude, J. Hoffmeister, M. Brenner, H. Kirac, I. Matošević, P. Hofer, P. Brezina, S. Gsur, A. Cheadle, J.P. Aaltonen, L.A. Tomlinson, I. Houlston, R.S. Dunlop, M.G. (2019). Association analyses identify 31 new risk loci for colorectal cancer susceptibility. Nat commun, Vol.10 (1), p. 2154.  show abstract

Atkins, I. Kinnersley, B. Ostrom, Q.T. Labreche, K. Il'yasova, D. Armstrong, G.N. Eckel-Passow, J.E. Schoemaker, M.J. Nöthen, M.M. Barnholtz-Sloan, J.S. Swerdlow, A.J. Simon, M. Rajaraman, P. Chanock, S.J. Shildkraut, J. Bernstein, J.L. Hoffmann, P. Jöckel, K.-. Lai, R.K. Claus, E.B. Olson, S.H. Johansen, C. Wrensch, M.R. Melin, B. Jenkins, R.B. Sanson, M. Bondy, M.L. Houlston, R.S. (2019). Transcriptome-Wide Association Study Identifies New Candidate Susceptibility Genes for Glioma. Cancer res, Vol.79 (8), pp. 2065-2071.  show abstract

Sud, A. Chattopadhyay, S. Thomsen, H. Sundquist, K. Sundquist, J. Houlston, R.S. Hemminki, K. (2019). Analysis of 153 115 patients with hematological malignancies refines the spectrum of familial risk. Blood, Vol.134 (12), pp. 960-969.  show abstract

Went, M. Kinnersley, B. Sud, A. Johnson, D.C. Weinhold, N. Försti, A. van Duin, M. Orlando, G. Mitchell, J.S. Kuiper, R. Walker, B.A. Gregory, W.M. Hoffmann, P. Jackson, G.H. Nöthen, M.M. da Silva Filho, M.I. Thomsen, H. Broyl, A. Davies, F.E. Thorsteinsdottir, U. Hansson, M. Kaiser, M. Sonneveld, P. Goldschmidt, H. Stefansson, K. Hemminki, K. Nilsson, B. Morgan, G.J. Houlston, R.S. (2019). Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes. Hum genomics, Vol.13 (1), p. 37.  show abstract

Takahashi, H. Cornish, A.J. Sud, A. Law, P.J. Disney-Hogg, L. Calvocoressi, L. Lu, L. Hansen, H.M. Smirnov, I. Walsh, K.M. Schramm, J. Hoffmann, P. Nöthen, M.M. Jöckel, K.-. Schildkraut, J.M. Simon, M. Bondy, M. Wrensch, M. Wiemels, J.L. Claus, E.B. Turnbull, C. Houlston, R.S. (2019). Mendelian randomization provides support for obesity as a risk factor for meningioma. Sci rep, Vol.9 (1), p. 309.  show abstract

Vijayakrishnan, J. Qian, M. Studd, J.B. Yang, W. Kinnersley, B. Law, P.J. Broderick, P. Raetz, E.A. Allan, J. Pui, C.-. Vora, A. Evans, W.E. Moorman, A. Yeoh, A. Yang, W. Li, C. Bartram, C.R. Mullighan, C.G. Zimmerman, M. Hunger, S.P. Schrappe, M. Relling, M.V. Stanulla, M. Loh, M.L. Houlston, R.S. Yang, J.J. (2019). Identification of four novel associations for B-cell acute lymphoblastic leukaemia risk. Nat commun, Vol.10 (1), p. 5348.  show abstract

Jiang, X. Finucane, H.K. Schumacher, F.R. Schmit, S.L. Tyrer, J.P. Han, Y. Michailidou, K. Lesseur, C. Kuchenbaecker, K.B. Dennis, J. Conti, D.V. Casey, G. Gaudet, M.M. Huyghe, J.R. Albanes, D. Aldrich, M.C. Andrew, A.S. Andrulis, I.L. Anton-Culver, H. Antoniou, A.C. Antonenkova, N.N. Arnold, S.M. Aronson, K.J. Arun, B.K. Bandera, E.V. Barkardottir, R.B. Barnes, D.R. Batra, J. Beckmann, M.W. Benitez, J. Benlloch, S. Berchuck, A. Berndt, S.I. Bickeböller, H. Bien, S.A. Blomqvist, C. Boccia, S. Bogdanova, N.V. Bojesen, S.E. Bolla, M.K. Brauch, H. Brenner, H. Brenton, J.D. Brook, M.N. Brunet, J. Brunnström, H. Buchanan, D.D. Burwinkel, B. Butzow, R. Cadoni, G. Caldés, T. Caligo, M.A. Campbell, I. Campbell, P.T. Cancel-Tassin, G. Cannon-Albright, L. Campa, D. Caporaso, N. Carvalho, A.L. Chan, A.T. Chang-Claude, J. Chanock, S.J. Chen, C. Christiani, D.C. Claes, K.B. Claessens, F. Clements, J. Collée, J.M. Correa, M.C. Couch, F.J. Cox, A. Cunningham, J.M. Cybulski, C. Czene, K. Daly, M.B. deFazio, A. Devilee, P. Diez, O. Gago-Dominguez, M. Donovan, J.L. Dörk, T. Duell, E.J. Dunning, A.M. Dwek, M. Eccles, D.M. Edlund, C.K. Edwards, D.R. Ellberg, C. Evans, D.G. Fasching, P.A. Ferris, R.L. Liloglou, T. Figueiredo, J.C. Fletcher, O. Fortner, R.T. Fostira, F. Franceschi, S. Friedman, E. Gallinger, S.J. Ganz, P.A. Garber, J. García-Sáenz, J.A. Gayther, S.A. Giles, G.G. Godwin, A.K. Goldberg, M.S. Goldgar, D.E. Goode, E.L. Goodman, M.T. Goodman, G. Grankvist, K. Greene, M.H. Gronberg, H. Gronwald, J. Guénel, P. Håkansson, N. Hall, P. Hamann, U. Hamdy, F.C. Hamilton, R.J. Hampe, J. Haugen, A. Heitz, F. Herrero, R. Hillemanns, P. Hoffmeister, M. Høgdall, E. Hong, Y.-. Hopper, J.L. Houlston, R. Hulick, P.J. Hunter, D.J. Huntsman, D.G. Idos, G. Imyanitov, E.N. Ingles, S.A. Isaacs, C. Jakubowska, A. James, P. Jenkins, M.A. Johansson, M. Johansson, M. John, E.M. Joshi, A.D. Kaneva, R. Karlan, B.Y. Kelemen, L.E. Kühl, T. Khaw, K.-. Khusnutdinova, E. Kibel, A.S. Kiemeney, L.A. Kim, J. Kjaer, S.K. Knight, J.A. Kogevinas, M. Kote-Jarai, Z. Koutros, S. Kristensen, V.N. Kupryjanczyk, J. Lacko, M. Lam, S. Lambrechts, D. Landi, M.T. Lazarus, P. Le, N.D. Lee, E. Lejbkowicz, F. Lenz, H.-. Leslie, G. Lessel, D. Lester, J. Levine, D.A. Li, L. Li, C.I. Lindblom, A. Lindor, N.M. Liu, G. Loupakis, F. Lubiński, J. Maehle, L. Maier, C. Mannermaa, A. Marchand, L.L. Margolin, S. May, T. McGuffog, L. Meindl, A. Middha, P. Miller, A. Milne, R.L. MacInnis, R.J. Modugno, F. Montagna, M. Moreno, V. Moysich, K.B. Mucci, L. Muir, K. Mulligan, A.M. Nathanson, K.L. Neal, D.E. Ness, A.R. Neuhausen, S.L. Nevanlinna, H. Newcomb, P.A. Newcomb, L.F. Nielsen, F.C. Nikitina-Zake, L. Nordestgaard, B.G. Nussbaum, R.L. Offit, K. Olah, E. Olama, A.A. Olopade, O.I. Olshan, A.F. Olsson, H. Osorio, A. Pandha, H. Park, J.Y. Pashayan, N. Parsons, M.T. Pejovic, T. Penney, K.L. Peters, W.H. Phelan, C.M. Phipps, A.I. Plaseska-Karanfilska, D. Pring, M. Prokofyeva, D. Radice, P. Stefansson, K. Ramus, S.J. Raskin, L. Rennert, G. Rennert, H.S. van Rensburg, E.J. Riggan, M.J. Risch, H.A. Risch, A. Roobol, M.J. Rosenstein, B.S. Rossing, M.A. De Ruyck, K. Saloustros, E. Sandler, D.P. Sawyer, E.J. Schabath, M.B. Schleutker, J. Schmidt, M.K. Setiawan, V.W. Shen, H. Siegel, E.M. Sieh, W. Singer, C.F. Slattery, M.L. Sorensen, K.D. Southey, M.C. Spurdle, A.B. Stanford, J.L. Stevens, V.L. Stintzing, S. Stone, J. Sundfeldt, K. Sutphen, R. Swerdlow, A.J. Tajara, E.H. Tangen, C.M. Tardon, A. Taylor, J.A. Teare, M.D. Teixeira, M.R. Terry, M.B. Terry, K.L. Thibodeau, S.N. Thomassen, M. Bjørge, L. Tischkowitz, M. Toland, A.E. Torres, D. Townsend, P.A. Travis, R.C. Tung, N. Tworoger, S.S. Ulrich, C.M. Usmani, N. Vachon, C.M. Van Nieuwenhuysen, E. Vega, A. Aguado-Barrera, M.E. Wang, Q. Webb, P.M. Weinberg, C.R. Weinstein, S. Weissler, M.C. Weitzel, J.N. West, C.M. White, E. Whittemore, A.S. Wichmann, H.-. Wiklund, F. Winqvist, R. Wolk, A. Woll, P. Woods, M. Wu, A.H. Wu, X. Yannoukakos, D. Zheng, W. Zienolddiny, S. Ziogas, A. Zorn, K.K. Lane, J.M. Saxena, R. Thomas, D. Hung, R.J. Diergaarde, B. McKay, J. Peters, U. Hsu, L. García-Closas, M. Eeles, R.A. Chenevix-Trench, G. Brennan, P.J. Haiman, C.A. Simard, J. Easton, D.F. Gruber, S.B. Pharoah, P.D. Price, A.L. Pasaniuc, B. Amos, C.I. Kraft, P. Lindström, S. (2019). Shared heritability and functional enrichment across six solid cancers. Nat commun, Vol.10 (1), p. 431.  show abstract

Zheng, G. Chattopadhyay, S. Sud, A. Sundquist, K. Sundquist, J. Försti, A. Houlston, R.S. Hemminki, A. Hemminki, K. (2019). Types of second primary cancers influence survival in chronic lymphocytic and hairy cell leukemia patients. Blood cancer j, Vol.9 (4), p. 40.

Schmidt, A.F. Holmes, M.V. Preiss, D. Swerdlow, D.I. Denaxas, S. Fatemifar, G. Faraway, R. Finan, C. Valentine, D. Fairhurst-Hunter, Z. Hartwig, F.P. Horta, B.L. Hypponen, E. Power, C. Moldovan, M. van Iperen, E. Hovingh, K. Demuth, I. Norman, K. Steinhagen-Thiessen, E. Demuth, J. Bertram, L. Lill, C.M. Coassin, S. Willeit, J. Kiechl, S. Willeit, K. Mason, D. Wright, J. Morris, R. Wanamethee, G. Whincup, P. Ben-Shlomo, Y. McLachlan, S. Price, J.F. Kivimaki, M. Welch, C. Sanchez-Galvez, A. Marques-Vidal, P. Nicolaides, A. Panayiotou, A.G. Onland-Moret, N.C. van der Schouw, Y.T. Matullo, G. Fiorito, G. Guarrera, S. Sacerdote, C. Wareham, N.J. Langenberg, C. Scott, R.A. Luan, J. Bobak, M. Malyutina, S. Pająk, A. Kubinova, R. Tamosiunas, A. Pikhart, H. Grarup, N. Pedersen, O. Hansen, T. Linneberg, A. Jess, T. Cooper, J. Humphries, S.E. Brilliant, M. Kitchner, T. Hakonarson, H. Carrell, D.S. McCarty, C.A. Lester, K.H. Larson, E.B. Crosslin, D.R. de Andrade, M. Roden, D.M. Denny, J.C. Carty, C. Hancock, S. Attia, J. Holliday, E. Scott, R. Schofield, P. O'Donnell, M. Yusuf, S. Chong, M. Pare, G. van der Harst, P. Said, M.A. Eppinga, R.N. Verweij, N. Snieder, H. Lifelines Cohort authors, Christen, T. Mook-Kanamori, D.O. ICBP Consortium, Gustafsson, S. Lind, L. Ingelsson, E. Pazoki, R. Franco, O. Hofman, A. Uitterlinden, A. Dehghan, A. Teumer, A. Baumeister, S. Dörr, M. Lerch, M.M. Völker, U. Völzke, H. Ward, J. Pell, J.P. Meade, T. Christophersen, I.E. Maitland-van der Zee, A.H. Baranova, E.V. Young, R. Ford, I. Campbell, A. Padmanabhan, S. Bots, M.L. Grobbee, D.E. Froguel, P. Thuillier, D. Roussel, R. Bonnefond, A. Cariou, B. Smart, M. Bao, Y. Kumari, M. Mahajan, A. Hopewell, J.C. Seshadri, S. METASTROKE Consortium of the ISGC, Dale, C. Costa, R.P. Ridker, P.M. Chasman, D.I. Reiner, A.P. Ritchie, M.D. Lange, L.A. Cornish, A.J. Dobbins, S.E. Hemminki, K. Kinnersley, B. Sanson, M. Labreche, K. Simon, M. Bondy, M. Law, P. Speedy, H. Allan, J. Li, N. Went, M. Weinhold, N. Morgan, G. Sonneveld, P. Nilsson, B. Goldschmidt, H. Sud, A. Engert, A. Hansson, M. Hemingway, H. Asselbergs, F.W. Patel, R.S. Keating, B.J. Sattar, N. Houlston, R. Casas, J.P. Hingorani, A.D. (2019). Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9. Bmc cardiovasc disord, Vol.19 (1), p. 240.  show abstract

Chattopadhyay, S. Thomsen, H. Yadav, P. da Silva Filho, M.I. Weinhold, N. Nöthen, M.M. Hoffman, P. Bertsch, U. Huhn, S. Morgan, G.J. Goldschmidt, H. Houlston, R. Hemminki, K. Försti, A. (2019). Genome-wide interaction and pathway-based identification of key regulators in multiple myeloma. Commun biol, Vol.2, p. 89.  show abstract

Shah, V. Sherborne, A.L. Walker, B.A. Johnson, D.C. Boyle, E.M. Ellis, S. Begum, D.B. Proszek, P.Z. Jones, J.R. Pawlyn, C. Savola, S. Jenner, M.W. Drayson, M.T. Owen, R.G. Houlston, R.S. Cairns, D.A. Gregory, W.M. Cook, G. Davies, F.E. Jackson, G.H. Morgan, G.J. Kaiser, M.F. (2018). Prediction of outcome in newly diagnosed myeloma: a meta-analysis of the molecular profiles of 1905 trial patients. Leukemia, Vol.32 (1), pp. 102-110.  show abstract

Tanskanen, T. van den Berg, L. Välimäki, N. Aavikko, M. Ness-Jensen, E. Hveem, K. Wettergren, Y. Bexe Lindskog, E. Tõnisson, N. Metspalu, A. Silander, K. Orlando, G. Law, P.J. Tuupanen, S. Gylfe, A.E. Hänninen, U.A. Cajuso, T. Kondelin, J. Sarin, A.-. Pukkala, E. Jousilahti, P. Salomaa, V. Ripatti, S. Palotie, A. Järvinen, H. Renkonen-Sinisalo, L. Lepistö, A. Böhm, J. Mecklin, J.-. Al-Tassan, N.A. Palles, C. Martin, L. Barclay, E. Tenesa, A. Farrington, S.M. Timofeeva, M.N. Meyer, B.F. Wakil, S.M. Campbell, H. Smith, C.G. Idziaszczyk, S. Maughan, T.S. Kaplan, R. Kerr, R. Kerr, D. Buchanan, D.D. Win, A.K. Hopper, J. Jenkins, M.A. Newcomb, P.A. Gallinger, S. Conti, D. Schumacher, F.R. Casey, G. Cheadle, J.P. Dunlop, M.G. Tomlinson, I.P. Houlston, R.S. Palin, K. Aaltonen, L.A. (2018). Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci. Int j cancer, Vol.142 (3), pp. 540-546.  show abstract

Lawler, M. Alsina, D. Adams, R.A. Anderson, A.S. Brown, G. Fearnhead, N.S. Fenwick, S.W. Halloran, S.P. Hochhauser, D. Hull, M.A. Koelzer, V.H. McNair, A.G. Monahan, K.J. Näthke, I. Norton, C. Novelli, M.R. Steele, R.J. Thomas, A.L. Wilde, L.M. Wilson, R.H. Tomlinson, I. Bowel Cancer UK Critical Research Gaps in Colorectal Cancer Initiative, (2018). Critical research gaps and recommendations to inform research prioritisation for more effective prevention and improved outcomes in colorectal cancer. Gut, Vol.67 (1), pp. 179-193.  show abstract

Feng, Y. Wang, Y. Liu, H. Liu, Z. Mills, C. Owzar, K. Xie, J. Han, Y. Qian, D.C. Hung Rj, R.J. Brhane, Y. McLaughlin, J. Brennan, P. Bickeböller, H. Rosenberger, A. Houlston, R.S. Caporaso, N. Landi, M.T. Brüske, I. Risch, A. Ye, Y. Wu, X. Christiani, D.C. Amos, C.I. Wei, Q. (2018). Novel genetic variants in the P38MAPK pathway gene ZAK and susceptibility to lung cancer. Mol carcinog, Vol.57 (2), pp. 216-224.  show abstract

Burns, A. Alsolami, R. Becq, J. Stamatopoulos, B. Timbs, A. Bruce, D. Robbe, P. Vavoulis, D. Clifford, R. Cabes, M. Dreau, H. Taylor, J. Knight, S.J. Mansson, R. Bentley, D. Beekman, R. Martín-Subero, J.I. Campo, E. Houlston, R.S. Ridout, K.E. Schuh, A. (2018). Whole-genome sequencing of chronic lymphocytic leukaemia reveals distinct differences in the mutational landscape between IgHVmut and IgHVunmut subgroups. Leukemia, Vol.32 (2), pp. 332-342.  show abstract

Kinnersley, B. Houlston, R.S. Bondy, M.L. (2018). Genome-Wide Association Studies in Glioma. Cancer epidemiol biomarkers prev, Vol.27 (4), pp. 418-428.  show abstract

Disney-Hogg, L. Sud, A. Law, P.J. Cornish, A.J. Kinnersley, B. Ostrom, Q.T. Labreche, K. Eckel-Passow, J.E. Armstrong, G.N. Claus, E.B. Il'yasova, D. Schildkraut, J. Barnholtz-Sloan, J.S. Olson, S.H. Bernstein, J.L. Lai, R.K. Swerdlow, A.J. Simon, M. Hoffmann, P. Nöthen, M.M. Jöckel, K.-. Chanock, S. Rajaraman, P. Johansen, C. Jenkins, R.B. Melin, B.S. Wrensch, M.R. Sanson, M. Bondy, M.L. Houlston, R.S. (2018). Influence of obesity-related risk factors in the aetiology of glioma. Br j cancer, Vol.118 (7), pp. 1020-1027.  show abstract

Takahashi, H. Cornish, A.J. Sud, A. Law, P.J. Kinnersley, B. Ostrom, Q.T. Labreche, K. Eckel-Passow, J.E. Armstrong, G.N. Claus, E.B. Il'yasova, D. Schildkraut, J. Barnholtz-Sloan, J.S. Olson, S.H. Bernstein, J.L. Lai, R.K. Schoemaker, M.J. Simon, M. Hoffmann, P. Nöthen, M.M. Jöckel, K.-. Chanock, S. Rajaraman, P. Johansen, C. Jenkins, R.B. Melin, B.S. Wrensch, M.R. Sanson, M. Bondy, M.L. Turnbull, C. Houlston, R.S. (2018). Mendelian randomisation study of the relationship between vitamin D and risk of glioma. Sci rep, Vol.8 (1), p. 2339.  show abstract

Labreche, K. Kinnersley, B. Berzero, G. Di Stefano, A.L. Rahimian, A. Detrait, I. Marie, Y. Grenier-Boley, B. Hoang-Xuan, K. Delattre, J.-. Idbaih, A. Houlston, R.S. Sanson, M. (2018). Diffuse gliomas classified by 1p/19q co-deletion, TERT promoter and IDH mutation status are associated with specific genetic risk loci. Acta neuropathol, Vol.135 (5), pp. 743-755.  show abstract

Berntsson, S.G. Merrell, R.T. Amirian, E.S. Armstrong, G.N. Lachance, D. Smits, A. Zhou, R. Jacobs, D.I. Wrensch, M.R. Olson, S.H. Il'yasova, D. Claus, E.B. Barnholtz-Sloan, J.S. Schildkraut, J. Sadetzki, S. Johansen, C. Houlston, R.S. Jenkins, R.B. Bernstein, J.L. Lai, R. Shete, S. Amos, C.I. Bondy, M.L. Melin, B.S. (2018). Glioma-related seizures in relation to histopathological subtypes: a report from the glioma international case-control study. J neurol, Vol.265 (6), pp. 1432-1442.  show abstract

Shah, V. Johnson, D.C. Sherborne, A.L. Ellis, S. Aldridge, F.M. Howard-Reeves, J. Begum, F. Price, A. Kendall, J. Chiecchio, L. Savola, S. Jenner, M.W. Drayson, M.T. Owen, R.G. Gregory, W.M. Morgan, G.J. Davies, F.E. Houlston, R.S. Cook, G. Cairns, D.A. Jackson, G. Kaiser, M.F. National Cancer Research Institute Haematology Clinical Studies Group, (2018). Subclonal TP53 copy number is associated with prognosis in multiple myeloma. Blood, Vol.132 (23), pp. 2465-2469.  show abstract

Li, Y. Xiao, X. Han, Y. Gorlova, O. Qian, D. Leighl, N. Johansen, J.S. Barnett, M. Chen, C. Goodman, G. Cox, A. Taylor, F. Woll, P. Wichmann, H.-. Manz, J. Muley, T. Risch, A. Rosenberger, A. Arnold, S.M. Haura, E.B. Bolca, C. Holcatova, I. Janout, V. Kontic, M. Lissowska, J. Mukeria, A. Ognjanovic, S. Orlowski, T.M. Scelo, G. Swiatkowska, B. Zaridze, D. Bakke, P. Skaug, V. Zienolddiny, S. Duell, E.J. Butler, L.M. Houlston, R. Soler Artigas, M. Grankvist, K. Johansson, M. Shepherd, F.A. Marcus, M.W. Brunnström, H. Manjer, J. Melander, O. Muller, D.C. Overvad, K. Trichopoulou, A. Tumino, R. Liu, G. Bojesen, S.E. Wu, X. Marchand, L.L. Albanes, D. Bickeböller, H. Aldrich, M.C. Bush, W.S. Tardon, A. Rennert, G. Teare, M.D. Field, J.K. Kiemeney, L.A. Lazarus, P. Haugen, A. Lam, S. Schabath, M.B. Andrew, A.S. Bertazzi, P.A. Pesatori, A.C. Christiani, D.C. Caporaso, N. Johansson, M. McKay, J.D. Brennan, P. Hung, R.J. Amos, C.I. (2018). Genome-wide interaction study of smoking behavior and non-small cell lung cancer risk in Caucasian population. Carcinogenesis, Vol.39 (3), pp. 336-346.  show abstract

Chattopadhyay, S. Zheng, G. Sud, A. Yu, H. Sundquist, K. Sundquist, J. Försti, A. Hemminki, A. Houlston, R. Hemminki, K. (2018). Risk of second primary cancer following myeloid neoplasia and risk of myeloid neoplasia as second primary cancer: a nationwide, observational follow up study in Sweden. Lancet haematol, Vol.5 (8), pp. e368-e377.  show abstract

Sud, A. Thomsen, H. Orlando, G. Försti, A. Law, P.J. Broderick, P. Cooke, R. Hariri, F. Pastinen, T. Easton, D.F. Pharoah, P.D. Dunning, A.M. Peto, J. Canzian, F. Eeles, R. Kote-Jarai, Z. Muir, K. Pashayan, N. Campa, D. PRACTICAL Consortium, Hoffmann, P. Nöthen, M.M. Jöckel, K.-. von Strandmann, E.P. Swerdlow, A.J. Engert, A. Orr, N. Hemminki, K. Houlston, R.S. (2018). Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma. Blood, Vol.132 (19), pp. 2040-2052.  show abstract

Vijayakrishnan, J. Studd, J. Broderick, P. Kinnersley, B. Holroyd, A. Law, P.J. Kumar, R. Allan, J.M. Harrison, C.J. Moorman, A.V. Vora, A. Roman, E. Rachakonda, S. Kinsey, S.E. Sheridan, E. Thompson, P.D. Irving, J.A. Koehler, R. Hoffmann, P. Nöthen, M.M. Heilmann-Heimbach, S. Jöckel, K.-. Easton, D.F. Pharaoh, P.D. Dunning, A.M. Peto, J. Canzian, F. Swerdlow, A. Eeles, R.A. Kote-Jarai, Z. Muir, K. Pashayan, N. PRACTICAL Consortium, Greaves, M. Zimmerman, M. Bartram, C.R. Schrappe, M. Stanulla, M. Hemminki, K. Houlston, R.S. (2018). Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia. Nat commun, Vol.9 (1), p. 1340.  show abstract

Claus, E.B. Cornish, A.J. Broderick, P. Schildkraut, J.M. Dobbins, S.E. Holroyd, A. Calvocoressi, L. Lu, L. Hansen, H.M. Smirnov, I. Walsh, K.M. Schramm, J. Hoffmann, P. Nöthen, M.M. Jöckel, K.-. Swerdlow, A. Larsen, S.B. Johansen, C. Simon, M. Bondy, M. Wrensch, M. Houlston, R.S. Wiemels, J.L. (2018). Genome-wide association analysis identifies a meningioma risk locus at 11p15 5. Neuro oncol, Vol.20 (11), pp. 1485-1493.  show abstract

Ostrom, Q.T. Kinnersley, B. Wrensch, M.R. Eckel-Passow, J.E. Armstrong, G. Rice, T. Chen, Y. Wiencke, J.K. McCoy, L.S. Hansen, H.M. Amos, C.I. Bernstein, J.L. Claus, E.B. Il'yasova, D. Johansen, C. Lachance, D.H. Lai, R.K. Merrell, R.T. Olson, S.H. Sadetzki, S. Schildkraut, J.M. Shete, S. Rubin, J.B. Lathia, J.D. Berens, M.E. Andersson, U. Rajaraman, P. Chanock, S.J. Linet, M.S. Wang, Z. Yeager, M. GliomaScan consortium, Houlston, R.S. Jenkins, R.B. Melin, B. Bondy, M.L. Barnholtz-Sloan, J.S. (2018). Sex-specific glioma genome-wide association study identifies new risk locus at 3p21 31 in females, and finds sex-differences in risk at 8q24 21. Sci rep, Vol.8 (1), p. 7352.  show abstract

Loveday, C. Law, P. Litchfield, K. Levy, M. Holroyd, A. Broderick, P. Kote-Jarai, Z. Dunning, A.M. Muir, K. Peto, J. Eeles, R. Easton, D.F. Dudakia, D. Orr, N. Pashayan, N. UK Testicular Cancer Collaboration, The PRACTICAL Consortium, Reid, A. Huddart, R.A. Houlston, R.S. Turnbull, C. (2018). Large-scale Analysis Demonstrates Familial Testicular Cancer to have Polygenic Aetiology. Eur urol, Vol.74 (3), pp. 248-252.  show abstract

Turnbull, C. Sud, A. Houlston, R.S. (2018). Cancer genetics, precision prevention and a call to action. Nat genet, Vol.50 (9), pp. 1212-1218.  show abstract

Orlando, G. Law, P.J. Cornish, A.J. Dobbins, S.E. Chubb, D. Broderick, P. Litchfield, K. Hariri, F. Pastinen, T. Osborne, C.S. Taipale, J. Houlston, R.S. (2018). Promoter capture Hi-C-based identification of recurrent noncoding mutations in colorectal cancer. Nat genet, Vol.50 (10), pp. 1375-1380.  show abstract

Hoang, P.H. Dobbins, S.E. Cornish, A.J. Chubb, D. Law, P.J. Kaiser, M. Houlston, R.S. (2018). Whole-genome sequencing of multiple myeloma reveals oncogenic pathways are targeted somatically through multiple mechanisms. Leukemia, Vol.32 (11), pp. 2459-2470.

Kinnersley, B. Sud, A. Coker, E.A. Tym, J.E. Di Micco, P. Al-Lazikani, B. Houlston, R.S. (2018). Leveraging Human Genetics to Guide Cancer Drug Development. Jco clin cancer inform, Vol.2, pp. 1-11.  show abstract

Went, M. Sud, A. Försti, A. Halvarsson, B.-. Weinhold, N. Kimber, S. van Duin, M. Thorleifsson, G. Holroyd, A. Johnson, D.C. Li, N. Orlando, G. Law, P.J. Ali, M. Chen, B. Mitchell, J.S. Gudbjartsson, D.F. Kuiper, R. Stephens, O.W. Bertsch, U. Broderick, P. Campo, C. Bandapalli, O.R. Einsele, H. Gregory, W.A. Gullberg, U. Hillengass, J. Hoffmann, P. Jackson, G.H. Jöckel, K.-. Johnsson, E. Kristinsson, S.Y. Mellqvist, U.-. Nahi, H. Easton, D. Pharoah, P. Dunning, A. Peto, J. Canzian, F. Swerdlow, A. Eeles, R.A. Kote-Jarai, Z. Muir, K. Pashayan, N. Nickel, J. Nöthen, M.M. Rafnar, T. Ross, F.M. da Silva Filho, M.I. Thomsen, H. Turesson, I. Vangsted, A. Andersen, N.F. Waage, A. Walker, B.A. Wihlborg, A.-. Broyl, A. Davies, F.E. Thorsteinsdottir, U. Langer, C. Hansson, M. Goldschmidt, H. Kaiser, M. Sonneveld, P. Stefansson, K. Morgan, G.J. Hemminki, K. Nilsson, B. Houlston, R.S. PRACTICAL consortium, (2018). Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma. Nat commun, Vol.9 (1), p. 3707.  show abstract

Ji, X. Bossé, Y. Landi, M.T. Gui, J. Xiao, X. Qian, D. Joubert, P. Lamontagne, M. Li, Y. Gorlov, I. de Biasi, M. Han, Y. Gorlova, O. Hung, R.J. Wu, X. McKay, J. Zong, X. Carreras-Torres, R. Christiani, D.C. Caporaso, N. Johansson, M. Liu, G. Bojesen, S.E. Le Marchand, L. Albanes, D. Bickeböller, H. Aldrich, M.C. Bush, W.S. Tardon, A. Rennert, G. Chen, C. Teare, M.D. Field, J.K. Kiemeney, L.A. Lazarus, P. Haugen, A. Lam, S. Schabath, M.B. Andrew, A.S. Shen, H. Hong, Y.-. Yuan, J.-. Bertazzi, P.A. Pesatori, A.C. Ye, Y. Diao, N. Su, L. Zhang, R. Brhane, Y. Leighl, N. Johansen, J.S. Mellemgaard, A. Saliba, W. Haiman, C. Wilkens, L. Fernandez-Somoano, A. Fernandez-Tardon, G. van der Heijden, E.H. Kim, J.H. Dai, J. Hu, Z. Davies, M.P. Marcus, M.W. Brunnström, H. Manjer, J. Melander, O. Muller, D.C. Overvad, K. Trichopoulou, A. Tumino, R. Doherty, J. Goodman, G.E. Cox, A. Taylor, F. Woll, P. Brüske, I. Manz, J. Muley, T. Risch, A. Rosenberger, A. Grankvist, K. Johansson, M. Shepherd, F. Tsao, M.-. Arnold, S.M. Haura, E.B. Bolca, C. Holcatova, I. Janout, V. Kontic, M. Lissowska, J. Mukeria, A. Ognjanovic, S. Orlowski, T.M. Scelo, G. Swiatkowska, B. Zaridze, D. Bakke, P. Skaug, V. Zienolddiny, S. Duell, E.J. Butler, L.M. Koh, W.-. Gao, Y.-. Houlston, R. McLaughlin, J. Stevens, V. Nickle, D.C. Obeidat, M. Timens, W. Zhu, B. Song, L. Artigas, M.S. Tobin, M.D. Wain, L.V. Gu, F. Byun, J. Kamal, A. Zhu, D. Tyndale, R.F. Wei, W.-. Chanock, S. Brennan, P. Amos, C.I. (2018). Identification of susceptibility pathways for the role of chromosome 15q25 1 in modifying lung cancer risk. Nat commun, Vol.9 (1), p. 3221.  show abstract

He, Y. Timofeeva, M. Farrington, S.M. Vaughan-Shaw, P. Svinti, V. Walker, M. Zgaga, L. Meng, X. Li, X. Spiliopoulou, A. Jiang, X. Hyppönen, E. Kraft, P. Kiel, D.P. SUNLIGHT consortium, Hayward, C. Campbell, A. Porteous, D. Vucic, K. Kirac, I. Filipovic, M. Harris, S.E. Deary, I.J. Houlston, R. Tomlinson, I.P. Campbell, H. Theodoratou, E. Dunlop, M.G. (2018). Exploring causality in the association between circulating 25-hydroxyvitamin D and colorectal cancer risk: a large Mendelian randomisation study. Bmc med, Vol.16 (1), p. 142.  show abstract

Chattopadhyay, S. Sud, A. Zheng, G. Yu, H. Sundquist, K. Sundquist, J. Försti, A. Houlston, R. Hemminki, A. Hemminki, K. (2018). Second primary cancers in non-Hodgkin lymphoma: Bidirectional analyses suggesting role for immune dysfunction. Int j cancer, Vol.143 (10), pp. 2449-2457.  show abstract

Ostrom, Q.T. Kinnersley, B. Armstrong, G. Rice, T. Chen, Y. Wiencke, J.K. McCoy, L.S. Hansen, H.M. Amos, C.I. Bernstein, J.L. Claus, E.B. Eckel-Passow, J.E. Il'yasova, D. Johansen, C. Lachance, D.H. Lai, R.K. Merrell, R.T. Olson, S.H. Sadetzki, S. Schildkraut, J.M. Shete, S. Rubin, J.B. Andersson, U. Rajaraman, P. Chanock, S.J. Linet, M.S. Wang, Z. Yeager, M. GliomaScan consortium, Houlston, R.S. Jenkins, R.B. Wrensch, M.R. Melin, B. Bondy, M.L. Barnholtz-Sloan, J.S. (2018). Age-specific genome-wide association study in glioblastoma identifies increased proportion of 'lower grade glioma'-like features associated with younger age. Int j cancer, Vol.143 (10), pp. 2359-2366.  show abstract

Disney-Hogg, L. Cornish, A.J. Sud, A. Law, P.J. Kinnersley, B. Jacobs, D.I. Ostrom, Q.T. Labreche, K. Eckel-Passow, J.E. Armstrong, G.N. Claus, E.B. Il'yasova, D. Schildkraut, J. Barnholtz-Sloan, J.S. Olson, S.H. Bernstein, J.L. Lai, R.K. Schoemaker, M.J. Simon, M. Hoffmann, P. Nöthen, M.M. Jöckel, K.-. Chanock, S. Rajaraman, P. Johansen, C. Jenkins, R.B. Melin, B.S. Wrensch, M.R. Sanson, M. Bondy, M.L. Houlston, R.S. (2018). Impact of atopy on risk of glioma: a Mendelian randomisation study. Bmc med, Vol.16 (1), p. 42.  show abstract

Stanulla, M. Dagdan, E. Zaliova, M. Möricke, A. Palmi, C. Cazzaniga, G. Eckert, C. Te Kronnie, G. Bourquin, J.-. Bornhauser, B. Koehler, R. Bartram, C.R. Ludwig, W.-. Bleckmann, K. Groeneveld-Krentz, S. Schewe, D. Junk, S.V. Hinze, L. Klein, N. Kratz, C.P. Biondi, A. Borkhardt, A. Kulozik, A. Muckenthaler, M.U. Basso, G. Valsecchi, M.G. Izraeli, S. Petersen, B.-. Franke, A. Dörge, P. Steinemann, D. Haas, O.A. Panzer-Grümayer, R. Cavé, H. Houlston, R.S. Cario, G. Schrappe, M. Zimmermann, M. TRANSCALL Consortium, International BFM Study Group, (2018). IKZF1plus Defines a New Minimal Residual Disease-Dependent Very-Poor Prognostic Profile in Pediatric B-Cell Precursor Acute Lymphoblastic Leukemia. J clin oncol, Vol.36 (12), pp. 1240-1249.  show abstract

Went, M. Sud, A. Speedy, H. Sunter, N.J. Försti, A. Law, P.J. Johnson, D.C. Mirabella, F. Holroyd, A. Li, N. Orlando, G. Weinhold, N. van Duin, M. Chen, B. Mitchell, J.S. Mansouri, L. Juliusson, G. Smedby, K.E. Jayne, S. Majid, A. Dearden, C. Allsup, D.J. Bailey, J.R. Pratt, G. Pepper, C. Fegan, C. Rosenquist, R. Kuiper, R. Stephens, O.W. Bertsch, U. Broderick, P. Einsele, H. Gregory, W.M. Hillengass, J. Hoffmann, P. Jackson, G.H. Jöckel, K.-. Nickel, J. Nöthen, M.M. da Silva Filho, M.I. Thomsen, H. Walker, B.A. Broyl, A. Davies, F.E. Hansson, M. Goldschmidt, H. Dyer, M.J. Kaiser, M. Sonneveld, P. Morgan, G.J. Hemminki, K. Nilsson, B. Catovsky, D. Allan, J.M. Houlston, R.S. (2018). Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology. Blood cancer j, Vol.9 (1), p. 1.  show abstract

Loveday, C. Litchfield, K. Levy, M. Holroyd, A. Broderick, P. Kote-Jarai, Z. Dunning, A.M. Muir, K. Peto, J. Eeles, R. Easton, D.F. Dudakia, D. Orr, N. Pashayan, N. Reid, A. Huddart, R.A. Houlston, R.S. Turnbull, C. (2018). Validation of loci at 2q14 2 and 15q21 3 as risk factors for testicular cancer. Oncotarget, Vol.9 (16), pp. 12630-12638.  show abstract

Sud, A. Chattopadhyay, S. Thomsen, H. Sundquist, K. Sundquist, J. Houlston, R.S. Hemminki, K. (2018). Familial risks of acute myeloid leukemia, myelodysplastic syndromes, and myeloproliferative neoplasms. Blood, Vol.132 (9), pp. 973-976.

Gu, F. Zhang, H. Hyland, P.L. Berndt, S. Gapstur, S.M. Wheeler, W. Ellipse Consortium, T. Amos, C.I. Bezieau, S. Bickeböller, H. Brenner, H. Brennan, P. Chang-Claude, J. Conti, D.V. Doherty, J.A. Gruber, S.B. Harrison, T.A. Hayes, R.B. Hoffmeister, M. Houlston, R.S. Hung, R.J. Jenkins, M.A. Kraft, P. Lawrenson, K. McKay, J. Markt, S. Mucci, L. Phelan, C.M. Qu, C. Risch, A. Rossing, M.A. Wichmann, H.-. Shi, J. Schernhammer, E. Yu, K. Landi, M.T. Caporaso, N.E. (2017). Inherited variation in circadian rhythm genes and risks of prostate cancer and three other cancer sites in combined cancer consortia. Int j cancer, Vol.141 (9), pp. 1794-1802.  show abstract

Sud, A. Thomsen, H. Law, P.J. Försti, A. Filho, M.I. Holroyd, A. Broderick, P. Orlando, G. Lenive, O. Wright, L. Cooke, R. Easton, D. Pharoah, P. Dunning, A. Peto, J. Canzian, F. Eeles, R. Kote-Jarai, Z. Muir, K. Pashayan, N. PRACTICAL consortium, Hoffmann, P. Nöthen, M.M. Jöckel, K.-. Strandmann, E.P. Lightfoot, T. Kane, E. Roman, E. Lake, A. Montgomery, D. Jarrett, R.F. Swerdlow, A.J. Engert, A. Orr, N. Hemminki, K. Houlston, R.S. (2017). Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility. Nat commun, Vol.8 (1), p. 1892.  show abstract

Broderick, P. Dobbins, S.E. Chubb, D. Kinnersley, B. Dunlop, M.G. Tomlinson, I. Houlston, R.S. (2017). Validation of Recently Proposed Colorectal Cancer Susceptibility Gene Variants in an Analysis of Families and Patients-a Systematic Review. Gastroenterology, Vol.152 (1), pp. 75-77.e4.  show abstract

Macauda, A. Calvetti, D. Maccari, G. Hemminki, K. Försti, A. Goldschmidt, H. Weinhold, N. Houlston, R. Andersen, V. Vogel, U. Buda, G. Varkonyi, J. Sureda, A. Martinez Lopez, J. Watek, M. Butrym, A. Sarasquete, M.E. Dudziński, M. Jurczyszyn, A. Druzd-Sitek, A. Kruszewski, M. Subocz, E. Petrini, M. Iskierka-Jażdżewska, E. Raźny, M. Szombath, G. Marques, H. Zawirska, D. Chraniuk, D. Halka, J. Hove Jacobsen, S.E. Mazur, G. García Sanz, R. Dumontet, C. Moreno, V. Stępień, A. Beider, K. Pelosini, M. Manuel Reis, R. Krawczyk-Kulis, M. Rymko, M. Avet-Loiseau, H. Lesueur, F. Grząśko, N. Ostrovsky, O. Jamroziak, K. Vangsted, A.J. Jerez, A. Tomczak, W. Zaucha, J.M. Kadar, K. Sainz, J. Nagler, A. Landi, S. Gemignani, F. Canzian, F. (2017). Identification of miRSNPs associated with the risk of multiple myeloma. Int j cancer, Vol.140 (3), pp. 526-534.  show abstract

Liu, H. Liu, Z. Wang, Y. Stinchcombe, T.E. Owzar, K. Han, Y. Hung, R.J. Brhane, Y. McLaughlin, J. Brennan, P. Bickeböller, H. Rosenberger, A. Houlston, R.S. Caporaso, N. Landi, M.T. Brüske, I. Risch, A. Wu, X. Ye, Y. Christiani, D.C. Amos, C.I. Wei, Q. Transdisciplinary Research in Cancer of the Lung (TRICL) Research Team, (2017). Functional variants in DCAF4 associated with lung cancer risk in European populations. Carcinogenesis, Vol.38 (5), pp. 541-551.  show abstract

Vijayakrishnan, J. Kumar, R. Henrion, M.Y. Moorman, A.V. Rachakonda, P.S. Hosen, I. da Silva Filho, M.I. Holroyd, A. Dobbins, S.E. Koehler, R. Thomsen, H. Irving, J.A. Allan, J.M. Lightfoot, T. Roman, E. Kinsey, S.E. Sheridan, E. Thompson, P.D. Hoffmann, P. Nöthen, M.M. Heilmann-Heimbach, S. Jöckel, K.H. Greaves, M. Harrison, C.J. Bartram, C.R. Schrappe, M. Stanulla, M. Hemminki, K. Houlston, R.S. (2017). A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26 13 and 12q23 1. Leukemia, Vol.31 (3), pp. 573-579.  show abstract

Sud, A. Hemminki, K. Houlston, R.S. (2017). Second cancer risk following Hodgkin lymphoma. Oncotarget, Vol.8 (45), pp. 78261-78262.

Studd, J.B. Vijayakrishnan, J. Yang, M. Migliorini, G. Paulsson, K. Houlston, R.S. (2017). Genetic and regulatory mechanism of susceptibility to high-hyperdiploid acute lymphoblastic leukaemia at 10p21 2. Nat commun, Vol.8, p. 14616.  show abstract

Frampton, M. Houlston, R.S. (2017). Modeling the prevention of colorectal cancer from the combined impact of host and behavioral risk factors. Genet med, Vol.19 (3), pp. 314-321.  show abstract

Sud, A. Hemminki, K. Houlston, R.S. (2017). Candidate gene association studies and risk of Hodgkin lymphoma: a systematic review and meta-analysis. Hematol oncol, Vol.35 (1), pp. 34-50.  show abstract

Zhou, F. Wang, Y. Liu, H. Ready, N. Han, Y. Hung, R.J. Brhane, Y. McLaughlin, J. Brennan, P. Bickeböller, H. Rosenberger, A. Houlston, R.S. Caporaso, N. Landi, M.T. Brüske, I. Risch, A. Ye, Y. Wu, X. Christiani, D.C. Goodman, G. Chen, C. Transdisciplinary Research in Cancer of the Lung (TRICL) Research Team, Amos, C.I. Wei, Q. (2017). Susceptibility loci of CNOT6 in the general mRNA degradation pathway and lung cancer risk-A re-analysis of eight GWASs. Mol carcinog, Vol.56 (4), pp. 1227-1238.  show abstract

Melin, B.S. Barnholtz-Sloan, J.S. Wrensch, M.R. Johansen, C. Il'yasova, D. Kinnersley, B. Ostrom, Q.T. Labreche, K. Chen, Y. Armstrong, G. Liu, Y. Eckel-Passow, J.E. Decker, P.A. Labussière, M. Idbaih, A. Hoang-Xuan, K. Di Stefano, A.-. Mokhtari, K. Delattre, J.-. Broderick, P. Galan, P. Gousias, K. Schramm, J. Schoemaker, M.J. Fleming, S.J. Herms, S. Heilmann, S. Nöthen, M.M. Wichmann, H.-. Schreiber, S. Swerdlow, A. Lathrop, M. Simon, M. Sanson, M. Andersson, U. Rajaraman, P. Chanock, S. Linet, M. Wang, Z. Yeager, M. GliomaScan Consortium, Wiencke, J.K. Hansen, H. McCoy, L. Rice, T. Kosel, M.L. Sicotte, H. Amos, C.I. Bernstein, J.L. Davis, F. Lachance, D. Lau, C. Merrell, R.T. Shildkraut, J. Ali-Osman, F. Sadetzki, S. Scheurer, M. Shete, S. Lai, R.K. Claus, E.B. Olson, S.H. Jenkins, R.B. Houlston, R.S. Bondy, M.L. (2017). Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. Nat genet, Vol.49 (5), pp. 789-794.  show abstract

Johnson, D.C. Lenive, O. Mitchell, J. Jackson, G. Owen, R. Drayson, M. Cook, G. Jones, J.R. Pawlyn, C. Davies, F.E. Walker, B.A. Wardell, C. Gregory, W.M. Cairns, D. Morgan, G.J. Houlston, R.S. Kaiser, M.F. (2017). Neutral tumor evolution in myeloma is associated with poor prognosis. Blood, Vol.130 (14), pp. 1639-1643.  show abstract

Tamm, R. Mägi, R. Tremmel, R. Winter, S. Mihailov, E. Smid, A. Möricke, A. Klein, K. Schrappe, M. Stanulla, M. Houlston, R. Weinshilboum, R. Mlinarič Raščan, I. Metspalu, A. Milani, L. Schwab, M. Schaeffeler, E. (2017). Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: A meta-analysis of three genome-wide association studies. Clin pharmacol ther, Vol.101 (5), pp. 684-695.  show abstract

Shah, V. Boyd, K.D. Houlston, R.S. Kaiser, M.F. (2017). Constitutional mutation in CDKN2A is associated with long term survivorship in multiple myeloma: a case report. Bmc cancer, Vol.17 (1), p. 718.  show abstract

Yin, J. Liu, H. Liu, Z. Owzar, K. Han, Y. Su, L. Wei, Y. Hung, R.J. Brhane, Y. McLaughlin, J. Brennan, P. Bickeboeller, H. Rosenberger, A. Houlston, R.S. Caporaso, N. Landi, M.T. Heinrich, J. Risch, A. Christiani, D.C. Amos, C.I. Wei, Q. (2017). Pathway-analysis of published genome-wide association studies of lung cancer: A potential role for the CYP4F3 locus. Mol carcinog, Vol.56 (6), pp. 1663-1672.  show abstract

Rasche, L. Angtuaco, E. McDonald, J.E. Buros, A. Stein, C. Pawlyn, C. Thanendrarajan, S. Schinke, C. Samant, R. Yaccoby, S. Walker, B.A. Epstein, J. Zangari, M. van Rhee, F. Meissner, T. Goldschmidt, H. Hemminki, K. Houlston, R. Barlogie, B. Davies, F.E. Morgan, G.J. Weinhold, N. (2017). Low expression of hexokinase-2 is associated with false-negative FDG-positron emission tomography in multiple myeloma. Blood, Vol.130 (1), pp. 30-34.  show abstract

Law, P.J. Berndt, S.I. Speedy, H.E. Camp, N.J. Sava, G.P. Skibola, C.F. Holroyd, A. Joseph, V. Sunter, N.J. Nieters, A. Bea, S. Monnereau, A. Martin-Garcia, D. Goldin, L.R. Clot, G. Teras, L.R. Quintela, I. Birmann, B.M. Jayne, S. Cozen, W. Majid, A. Smedby, K.E. Lan, Q. Dearden, C. Brooks-Wilson, A.R. Hall, A.G. Purdue, M.P. Mainou-Fowler, T. Vajdic, C.M. Jackson, G.H. Cocco, P. Marr, H. Zhang, Y. Zheng, T. Giles, G.G. Lawrence, C. Call, T.G. Liebow, M. Melbye, M. Glimelius, B. Mansouri, L. Glenn, M. Curtin, K. Diver, W.R. Link, B.K. Conde, L. Bracci, P.M. Holly, E.A. Jackson, R.D. Tinker, L.F. Benavente, Y. Boffetta, P. Brennan, P. Maynadie, M. McKay, J. Albanes, D. Weinstein, S. Wang, Z. Caporaso, N.E. Morton, L.M. Severson, R.K. Riboli, E. Vineis, P. Vermeulen, R.C. Southey, M.C. Milne, R.L. Clavel, J. Topka, S. Spinelli, J.J. Kraft, P. Ennas, M.G. Summerfield, G. Ferri, G.M. Harris, R.J. Miligi, L. Pettitt, A.R. North, K.E. Allsup, D.J. Fraumeni, J.F. Bailey, J.R. Offit, K. Pratt, G. Hjalgrim, H. Pepper, C. Chanock, S.J. Fegan, C. Rosenquist, R. de Sanjose, S. Carracedo, A. Dyer, M.J. Catovsky, D. Campo, E. Cerhan, J.R. Allan, J.M. Rothman, N. Houlston, R. Slager, S. (2017). Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia. Nat commun, Vol.8, p. 14175.  show abstract

Litchfield, K. Levy, M. Orlando, G. Loveday, C. Law, P.J. Migliorini, G. Holroyd, A. Broderick, P. Karlsson, R. Haugen, T.B. Kristiansen, W. Nsengimana, J. Fenwick, K. Assiotis, I. Kote-Jarai, Z. Dunning, A.M. Muir, K. Peto, J. Eeles, R. Easton, D.F. Dudakia, D. Orr, N. Pashayan, N. UK Testicular Cancer Collaboration, PRACTICAL Consortium, Bishop, D.T. Reid, A. Huddart, R.A. Shipley, J. Grotmol, T. Wiklund, F. Houlston, R.S. Turnbull, C. (2017). Identification of 19 new risk loci and potential regulatory mechanisms influencing susceptibility to testicular germ cell tumor. Nat genet, Vol.49 (7), pp. 1133-1140.  show abstract

McKay, J.D. Hung, R.J. Han, Y. Zong, X. Carreras-Torres, R. Christiani, D.C. Caporaso, N.E. Johansson, M. Xiao, X. Li, Y. Byun, J. Dunning, A. Pooley, K.A. Qian, D.C. Ji, X. Liu, G. Timofeeva, M.N. Bojesen, S.E. Wu, X. Le Marchand, L. Albanes, D. Bickeböller, H. Aldrich, M.C. Bush, W.S. Tardon, A. Rennert, G. Teare, M.D. Field, J.K. Kiemeney, L.A. Lazarus, P. Haugen, A. Lam, S. Schabath, M.B. Andrew, A.S. Shen, H. Hong, Y.-. Yuan, J.-. Bertazzi, P.A. Pesatori, A.C. Ye, Y. Diao, N. Su, L. Zhang, R. Brhane, Y. Leighl, N. Johansen, J.S. Mellemgaard, A. Saliba, W. Haiman, C.A. Wilkens, L.R. Fernandez-Somoano, A. Fernandez-Tardon, G. van der Heijden, H.F. Kim, J.H. Dai, J. Hu, Z. Davies, M.P. Marcus, M.W. Brunnström, H. Manjer, J. Melander, O. Muller, D.C. Overvad, K. Trichopoulou, A. Tumino, R. Doherty, J.A. Barnett, M.P. Chen, C. Goodman, G.E. Cox, A. Taylor, F. Woll, P. Brüske, I. Wichmann, H.-. Manz, J. Muley, T.R. Risch, A. Rosenberger, A. Grankvist, K. Johansson, M. Shepherd, F.A. Tsao, M.-. Arnold, S.M. Haura, E.B. Bolca, C. Holcatova, I. Janout, V. Kontic, M. Lissowska, J. Mukeria, A. Ognjanovic, S. Orlowski, T.M. Scelo, G. Swiatkowska, B. Zaridze, D. Bakke, P. Skaug, V. Zienolddiny, S. Duell, E.J. Butler, L.M. Koh, W.-. Gao, Y.-. Houlston, R.S. McLaughlin, J. Stevens, V.L. Joubert, P. Lamontagne, M. Nickle, D.C. Obeidat, M. Timens, W. Zhu, B. Song, L. Kachuri, L. Artigas, M.S. Tobin, M.D. Wain, L.V. SpiroMeta Consortium, Rafnar, T. Thorgeirsson, T.E. Reginsson, G.W. Stefansson, K. Hancock, D.B. Bierut, L.J. Spitz, M.R. Gaddis, N.C. Lutz, S.M. Gu, F. Johnson, E.O. Kamal, A. Pikielny, C. Zhu, D. Lindströem, S. Jiang, X. Tyndale, R.F. Chenevix-Trench, G. Beesley, J. Bossé, Y. Chanock, S. Brennan, P. Landi, M.T. Amos, C.I. (2017). Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. Nat genet, Vol.49 (7), pp. 1126-1132.  show abstract

da Silva Filho, M.I. Försti, A. Weinhold, N. Meziane, I. Campo, C. Huhn, S. Nickel, J. Hoffmann, P. Nöthen, M.M. Jöckel, K.-. Landi, S. Mitchell, J.S. Johnson, D. Morgan, G.J. Houlston, R. Goldschmidt, H. Jauch, A. Milani, P. Merlini, G. Rowcieno, D. Hawkins, P. Hegenbart, U. Palladini, G. Wechalekar, A. Schönland, S.O. Hemminki, K. (2017). Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts: comparison with myeloma. Leukemia, Vol.31 (8), pp. 1735-1742.  show abstract

Levy, M. Hall, D. Sud, A. Law, P. Litchfield, K. Dudakia, D. Haugen, T.B. Karlsson, R. Reid, A. Huddart, R.A. Grotmol, T. Wiklund, F. Houlston, R.S. Turnbull, C. (2017). Mendelian randomisation analysis provides no evidence for a relationship between adult height and testicular cancer risk. Andrology, Vol.5 (5), pp. 914-922.  show abstract

Scelo, G. Purdue, M.P. Brown, K.M. Johansson, M. Wang, Z. Eckel-Passow, J.E. Ye, Y. Hofmann, J.N. Choi, J. Foll, M. Gaborieau, V. Machiela, M.J. Colli, L.M. Li, P. Sampson, J.N. Abedi-Ardekani, B. Besse, C. Blanche, H. Boland, A. Burdette, L. Chabrier, A. Durand, G. Le Calvez-Kelm, F. Prokhortchouk, E. Robinot, N. Skryabin, K.G. Wozniak, M.B. Yeager, M. Basta-Jovanovic, G. Dzamic, Z. Foretova, L. Holcatova, I. Janout, V. Mates, D. Mukeriya, A. Rascu, S. Zaridze, D. Bencko, V. Cybulski, C. Fabianova, E. Jinga, V. Lissowska, J. Lubinski, J. Navratilova, M. Rudnai, P. Szeszenia-Dabrowska, N. Benhamou, S. Cancel-Tassin, G. Cussenot, O. Baglietto, L. Boeing, H. Khaw, K.-. Weiderpass, E. Ljungberg, B. Sitaram, R.T. Bruinsma, F. Jordan, S.J. Severi, G. Winship, I. Hveem, K. Vatten, L.J. Fletcher, T. Koppova, K. Larsson, S.C. Wolk, A. Banks, R.E. Selby, P.J. Easton, D.F. Pharoah, P. Andreotti, G. Freeman, L.E. Koutros, S. Albanes, D. Männistö, S. Weinstein, S. Clark, P.E. Edwards, T.L. Lipworth, L. Gapstur, S.M. Stevens, V.L. Carol, H. Freedman, M.L. Pomerantz, M.M. Cho, E. Kraft, P. Preston, M.A. Wilson, K.M. Michael Gaziano, J. Sesso, H.D. Black, A. Freedman, N.D. Huang, W.-. Anema, J.G. Kahnoski, R.J. Lane, B.R. Noyes, S.L. Petillo, D. Teh, B.T. Peters, U. White, E. Anderson, G.L. Johnson, L. Luo, J. Buring, J. Lee, I.-. Chow, W.-. Moore, L.E. Wood, C. Eisen, T. Henrion, M. Larkin, J. Barman, P. Leibovich, B.C. Choueiri, T.K. Mark Lathrop, G. Rothman, N. Deleuze, J.-. McKay, J.D. Parker, A.S. Wu, X. Houlston, R.S. Brennan, P. Chanock, S.J. (2017). Genome-wide association study identifies multiple risk loci for renal cell carcinoma. Nat commun, Vol.8, p. 15724.  show abstract

Sud, A. Thomsen, H. Sundquist, K. Houlston, R.S. Hemminki, K. (2017). Risk of Second Cancer in Hodgkin Lymphoma Survivors and Influence of Family History. J clin oncol, Vol.35 (14), pp. 1584-1590.  show abstract

May-Wilson, S. Sud, A. Law, P.J. Palin, K. Tuupanen, S. Gylfe, A. Hänninen, U.A. Cajuso, T. Tanskanen, T. Kondelin, J. Kaasinen, E. Sarin, A.-. Eriksson, J.G. Rissanen, H. Knekt, P. Pukkala, E. Jousilahti, P. Salomaa, V. Ripatti, S. Palotie, A. Renkonen-Sinisalo, L. Lepistö, A. Böhm, J. Mecklin, J.-. Al-Tassan, N.A. Palles, C. Farrington, S.M. Timofeeva, M.N. Meyer, B.F. Wakil, S.M. Campbell, H. Smith, C.G. Idziaszczyk, S. Maughan, T.S. Fisher, D. Kerr, R. Kerr, D. Passarelli, M.N. Figueiredo, J.C. Buchanan, D.D. Win, A.K. Hopper, J.L. Jenkins, M.A. Lindor, N.M. Newcomb, P.A. Gallinger, S. Conti, D. Schumacher, F. Casey, G. Aaltonen, L.A. Cheadle, J.P. Tomlinson, I.P. Dunlop, M.G. Houlston, R.S. (2017). Pro-inflammatory fatty acid profile and colorectal cancer risk: A Mendelian randomisation analysis. Eur j cancer, Vol.84, pp. 228-238.  show abstract

Machiela, M.J. Hofmann, J.N. Carreras-Torres, R. Brown, K.M. Johansson, M. Wang, Z. Foll, M. Li, P. Rothman, N. Savage, S.A. Gaborieau, V. McKay, J.D. Ye, Y. Henrion, M. Bruinsma, F. Jordan, S. Severi, G. Hveem, K. Vatten, L.J. Fletcher, T. Koppova, K. Larsson, S.C. Wolk, A. Banks, R.E. Selby, P.J. Easton, D.F. Pharoah, P. Andreotti, G. Freeman, L.E. Koutros, S. Albanes, D. Mannisto, S. Weinstein, S. Clark, P.E. Edwards, T.E. Lipworth, L. Gapstur, S.M. Stevens, V.L. Carol, H. Freedman, M.L. Pomerantz, M.M. Cho, E. Kraft, P. Preston, M.A. Wilson, K.M. Gaziano, J.M. Sesso, H.S. Black, A. Freedman, N.D. Huang, W.-. Anema, J.G. Kahnoski, R.J. Lane, B.R. Noyes, S.L. Petillo, D. Colli, L.M. Sampson, J.N. Besse, C. Blanche, H. Boland, A. Burdette, L. Prokhortchouk, E. Skryabin, K.G. Yeager, M. Mijuskovic, M. Ognjanovic, M. Foretova, L. Holcatova, I. Janout, V. Mates, D. Mukeriya, A. Rascu, S. Zaridze, D. Bencko, V. Cybulski, C. Fabianova, E. Jinga, V. Lissowska, J. Lubinski, J. Navratilova, M. Rudnai, P. Szeszenia-Dabrowska, N. Benhamou, S. Cancel-Tassin, G. Cussenot, O. Bueno-de-Mesquita, H.B. Canzian, F. Duell, E.J. Ljungberg, B. Sitaram, R.T. Peters, U. White, E. Anderson, G.L. Johnson, L. Luo, J. Buring, J. Lee, I.-. Chow, W.-. Moore, L.E. Wood, C. Eisen, T. Larkin, J. Choueiri, T.K. Lathrop, G.M. Teh, B.T. Deleuze, J.-. Wu, X. Houlston, R.S. Brennan, P. Chanock, S.J. Scelo, G. Purdue, M.P. (2017). Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma. Eur urol, Vol.72 (5), pp. 747-754.  show abstract

Sud, A. Kinnersley, B. Houlston, R.S. (2017). Genome-wide association studies of cancer: current insights and future perspectives. Nat rev cancer, Vol.17 (11), pp. 692-704.  show abstract

Feng, Y. Wang, Y. Liu, H. Liu, Z. Mills, C. Han, Y. Hung, R.J. Brhane, Y. McLaughlin, J. Brennan, P. Bickeboeller, H. Rosenberger, A. Houlston, R.S. Caporaso, N.E. Teresa Landi, M. Brueske, I. Risch, A. Ye, Y. Wu, X. Christiani, D.C. Amos, C.I. Wei, Q. (2017). Genetic variants of PTPN2 are associated with lung cancer risk: a re-analysis of eight GWASs in the TRICL-ILCCO consortium. Sci rep, Vol.7 (1), p. 825.  show abstract

Li, N. Johnson, D.C. Weinhold, N. Kimber, S. Dobbins, S.E. Mitchell, J.S. Kinnersley, B. Sud, A. Law, P.J. Orlando, G. Scales, M. Wardell, C.P. Försti, A. Hoang, P.H. Went, M. Holroyd, A. Hariri, F. Pastinen, T. Meissner, T. Goldschmidt, H. Hemminki, K. Morgan, G.J. Kaiser, M. Houlston, R.S. (2017). Genetic Predisposition to Multiple Myeloma at 5q15 Is Mediated by an ELL2 Enhancer Polymorphism. Cell rep, Vol.20 (11), pp. 2556-2564.  show abstract

Liu, N.Q. Ter Huurne, M. Nguyen, L.N. Peng, T. Wang, S.-. Studd, J.B. Joshi, O. Ongen, H. Bramsen, J.B. Yan, J. Andersen, C.L. Taipale, J. Dermitzakis, E.T. Houlston, R.S. Hubner, N.C. Stunnenberg, H.G. (2017). The non-coding variant rs1800734 enhances DCLK3 expression through long-range interaction and promotes colorectal cancer progression. Nat commun, Vol.8, p. 14418.  show abstract

Rodriguez-Broadbent, H. Law, P.J. Sud, A. Palin, K. Tuupanen, S. Gylfe, A. Hänninen, U.A. Cajuso, T. Tanskanen, T. Kondelin, J. Kaasinen, E. Sarin, A.-. Ripatti, S. Eriksson, J.G. Rissanen, H. Knekt, P. Pukkala, E. Jousilahti, P. Salomaa, V. Palotie, A. Renkonen-Sinisalo, L. Lepistö, A. Böhm, J. Mecklin, J.-. Al-Tassan, N.A. Palles, C. Martin, L. Barclay, E. Farrington, S.M. Timofeeva, M.N. Meyer, B.F. Wakil, S.M. Campbell, H. Smith, C.G. Idziaszczyk, S. Maughan, T.S. Kaplan, R. Kerr, R. Kerr, D. Passarelli, M.N. Figueiredo, J.C. Buchanan, D.D. Win, A.K. Hopper, J.L. Jenkins, M.A. Lindor, N.M. Newcomb, P.A. Gallinger, S. Conti, D. Schumacher, F. Casey, G. Aaltonen, L.A. Cheadle, J.P. Tomlinson, I.P. Dunlop, M.G. Houlston, R.S. (2017). Mendelian randomisation implicates hyperlipidaemia as a risk factor for colorectal cancer. Int j cancer, Vol.140 (12), pp. 2701-2708.  show abstract

Went, M. Sud, A. Law, P.J. Johnson, D.C. Weinhold, N. Försti, A. van Duin, M. Mitchell, J.S. Chen, B. Kuiper, R. Stephens, O.W. Bertsch, U. Campo, C. Einsele, H. Gregory, W.M. Henrion, M. Hillengass, J. Hoffmann, P. Jackson, G.H. Lenive, O. Nickel, J. Nöthen, M.M. da Silva Filho, M.I. Thomsen, H. Walker, B.A. Broyl, A. Davies, F.E. Langer, C. Hansson, M. Kaiser, M. Sonneveld, P. Goldschmidt, H. Hemminki, K. Nilsson, B. Morgan, G.J. Houlston, R.S. (2017). Assessing the effect of obesity-related traits on multiple myeloma using a Mendelian randomisation approach. Blood cancer j, Vol.7 (6), p. e573.

Pan, Y. Liu, H. Wang, Y. Kang, X. Liu, Z. Owzar, K. Han, Y. Su, L. Wei, Y. Hung, R.J. Brhane, Y. McLaughlin, J. Brennan, P. Bickeböller, H. Rosenberger, A. Houlston, R.S. Caporaso, N. Teresa Landi, M. Heinrich, J. Risch, A. Wu, X. Ye, Y. Christiani, D.C. Amos, C.I. Wei, Q. (2017). Associations between genetic variants in mRNA splicing-related genes and risk of lung cancer: a pathway-based analysis from published GWASs. Sci rep, Vol.7, p. 44634.  show abstract

Monahan, K.J. Alsina, D. Bach, S. Buchanan, J. Burn, J. Clark, S. Dawson, P. De Souza, B. Din, F.V. Dolwani, S. Dunlop, M.G. East, J. Evans, D.G. Fearnhead, N. Frayling, I.M. Glynne-Jones, R. Hill, J. Houlston, R. Hull, M. Lalloo, F. Latchford, A. Lishman, S. Quirke, P. Rees, C. Rutter, M. Sasieni, P. Senapati, A. Speake, D. Thomas, H. Tomlinson, I. (2017). Urgent improvements needed to diagnose and manage Lynch syndrome. Bmj, Vol.356, p. j1388.

Law, P.J. Sud, A. Mitchell, J.S. Henrion, M. Orlando, G. Lenive, O. Broderick, P. Speedy, H.E. Johnson, D.C. Kaiser, M. Weinhold, N. Cooke, R. Sunter, N.J. Jackson, G.H. Summerfield, G. Harris, R.J. Pettitt, A.R. Allsup, D.J. Carmichael, J. Bailey, J.R. Pratt, G. Rahman, T. Pepper, C. Fegan, C. von Strandmann, E.P. Engert, A. Försti, A. Chen, B. Filho, M.I. Thomsen, H. Hoffmann, P. Noethen, M.M. Eisele, L. Jöckel, K.-. Allan, J.M. Swerdlow, A.J. Goldschmidt, H. Catovsky, D. Morgan, G.J. Hemminki, K. Houlston, R.S. (2017). Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci. Sci rep, Vol.7, p. 41071.  show abstract

Scales, M. Chubb, D. Dobbins, S.E. Johnson, D.C. Li, N. Sternberg, M.J. Weinhold, N. Stein, C. Jackson, G. Davies, F.E. Walker, B.A. Wardell, C.P. Houlston, R.S. Morgan, G.J. (2017). Search for rare protein altering variants influencing susceptibility to multiple myeloma. Oncotarget, Vol.8 (22), pp. 36203-36210.  show abstract

Fehringer, G. Kraft, P. Pharoah, P.D. Eeles, R.A. Chatterjee, N. Schumacher, F.R. Schildkraut, J.M. Lindström, S. Brennan, P. Bickeböller, H. Houlston, R.S. Landi, M.T. Caporaso, N. Risch, A. Amin Al Olama, A. Berndt, S.I. Giovannucci, E.L. Grönberg, H. Kote-Jarai, Z. Ma, J. Muir, K. Stampfer, M.J. Stevens, V.L. Wiklund, F. Willett, W.C. Goode, E.L. Permuth, J.B. Risch, H.A. Reid, B.M. Bezieau, S. Brenner, H. Chan, A.T. Chang-Claude, J. Hudson, T.J. Kocarnik, J.K. Newcomb, P.A. Schoen, R.E. Slattery, M.L. White, E. Adank, M.A. Ahsan, H. Aittomäki, K. Baglietto, L. Blomquist, C. Canzian, F. Czene, K. Dos-Santos-Silva, I. Eliassen, A.H. Figueroa, J.D. Flesch-Janys, D. Fletcher, O. Garcia-Closas, M. Gaudet, M.M. Johnson, N. Hall, P. Hazra, A. Hein, R. Hofman, A. Hopper, J.L. Irwanto, A. Johansson, M. Kaaks, R. Kibriya, M.G. Lichtner, P. Liu, J. Lund, E. Makalic, E. Meindl, A. Müller-Myhsok, B. Muranen, T.A. Nevanlinna, H. Peeters, P.H. Peto, J. Prentice, R.L. Rahman, N. Sanchez, M.J. Schmidt, D.F. Schmutzler, R.K. Southey, M.C. Tamimi, R. Travis, R.C. Turnbull, C. Uitterlinden, A.G. Wang, Z. Whittemore, A.S. Yang, X.R. Zheng, W. Buchanan, D.D. Casey, G. Conti, D.V. Edlund, C.K. Gallinger, S. Haile, R.W. Jenkins, M. Le Marchand, L. Li, L. Lindor, N.M. Schmit, S.L. Thibodeau, S.N. Woods, M.O. Rafnar, T. Gudmundsson, J. Stacey, S.N. Stefansson, K. Sulem, P. Chen, Y.A. Tyrer, J.P. Christiani, D.C. Wei, Y. Shen, H. Hu, Z. Shu, X.-. Shiraishi, K. Takahashi, A. Bossé, Y. Obeidat, M. Nickle, D. Timens, W. Freedman, M.L. Li, Q. Seminara, D. Chanock, S.J. Gong, J. Peters, U. Gruber, S.B. Amos, C.I. Sellers, T.A. Easton, D.F. Hunter, D.J. Haiman, C.A. Henderson, B.E. Hung, R.J. Ovarian Cancer Association Consortium (OCAC), PRACTICAL Consortium, Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON), Colorectal Transdisciplinary (CORECT) Study, African American Breast Cancer Consortium (AABC) and African Ancestry Prostate Cancer Consortium (AAPC), (2016). Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. Cancer res, Vol.76 (17), pp. 5103-5114.  show abstract

Mitchell, J.S. Li, N. Weinhold, N. Försti, A. Ali, M. van Duin, M. Thorleifsson, G. Johnson, D.C. Chen, B. Halvarsson, B.-. Gudbjartsson, D.F. Kuiper, R. Stephens, O.W. Bertsch, U. Broderick, P. Campo, C. Einsele, H. Gregory, W.A. Gullberg, U. Henrion, M. Hillengass, J. Hoffmann, P. Jackson, G.H. Johnsson, E. Jöud, M. Kristinsson, S.Y. Lenhoff, S. Lenive, O. Mellqvist, U.-. Migliorini, G. Nahi, H. Nelander, S. Nickel, J. Nöthen, M.M. Rafnar, T. Ross, F.M. da Silva Filho, M.I. Swaminathan, B. Thomsen, H. Turesson, I. Vangsted, A. Vogel, U. Waage, A. Walker, B.A. Wihlborg, A.-. Broyl, A. Davies, F.E. Thorsteinsdottir, U. Langer, C. Hansson, M. Kaiser, M. Sonneveld, P. Stefansson, K. Morgan, G.J. Goldschmidt, H. Hemminki, K. Nilsson, B. Houlston, R.S. (2016). Genome-wide association study identifies multiple susceptibility loci for multiple myeloma. Nat commun, Vol.7, p. 12050.  show abstract

Orlando, G. Law, P.J. Palin, K. Tuupanen, S. Gylfe, A. Hänninen, U.A. Cajuso, T. Tanskanen, T. Kondelin, J. Kaasinen, E. Sarin, A.-. Kaprio, J. Eriksson, J.G. Rissanen, H. Knekt, P. Pukkala, E. Jousilahti, P. Salomaa, V. Ripatti, S. Palotie, A. Järvinen, H. Renkonen-Sinisalo, L. Lepistö, A. Böhm, J. Mecklin, J.-. Al-Tassan, N.A. Palles, C. Martin, L. Barclay, E. Tenesa, A. Farrington, S. Timofeeva, M.N. Meyer, B.F. Wakil, S.M. Campbell, H. Smith, C.G. Idziaszczyk, S. Maughan, T.S. Kaplan, R. Kerr, R. Kerr, D. Buchanan, D.D. Win, A.K. Hopper, J. Jenkins, M. Lindor, N.M. Newcomb, P.A. Gallinger, S. Conti, D. Schumacher, F. Casey, G. Taipale, J. Cheadle, J.P. Dunlop, M.G. Tomlinson, I.P. Aaltonen, L.A. Houlston, R.S. (2016). Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease. Hum mol genet, Vol.25 (11), pp. 2349-2359.  show abstract

Patel, Y.M. Park, S.L. Han, Y. Wilkens, L.R. Bickeböller, H. Rosenberger, A. Caporaso, N. Landi, M.T. Brüske, I. Risch, A. Wei, Y. Christiani, D.C. Brennan, P. Houlston, R. McKay, J. McLaughlin, J. Hung, R. Murphy, S. Stram, D.O. Amos, C. Le Marchand, L. (2016). Novel Association of Genetic Markers Affecting CYP2A6 Activity and Lung Cancer Risk. Cancer res, Vol.76 (19), pp. 5768-5776.  show abstract

Amirian, E.S. Zhou, R. Wrensch, M.R. Olson, S.H. Scheurer, M.E. Il'yasova, D. Lachance, D. Armstrong, G.N. McCoy, L.S. Lau, C.C. Claus, E.B. Barnholtz-Sloan, J.S. Schildkraut, J. Ali-Osman, F. Sadetzki, S. Johansen, C. Houlston, R.S. Jenkins, R.B. Bernstein, J.L. Merrell, R.T. Davis, F.G. Lai, R. Shete, S. Amos, C.I. Melin, B.S. Bondy, M.L. (2016). Approaching a Scientific Consensus on the Association between Allergies and Glioma Risk: A Report from the Glioma International Case-Control Study. Cancer epidemiol biomarkers prev, Vol.25 (2), pp. 282-290.  show abstract

Frampton, M.J. Law, P. Litchfield, K. Morris, E.J. Kerr, D. Turnbull, C. Tomlinson, I.P. Houlston, R.S. (2016). Implications of polygenic risk for personalised colorectal cancer screening. Ann oncol, Vol.27 (3), pp. 429-434.  show abstract

Kang, X. Liu, H. Onaitis, M.W. Liu, Z. Owzar, K. Han, Y. Su, L. Wei, Y. Hung, R.J. Brhane, Y. McLaughlin, J. Brennan, P. Bickeböller, H. Rosenberger, A. Houlston, R.S. Caporaso, N. Landi, M.T. Heinrich, J. Risch, A. Wu, X. Ye, Y. Christiani, D.C. Amos, C.I. Wei, Q. Transdisciplinary Research in Cancer of the Lung (TRICL) Research Team, (2016). Polymorphisms of the centrosomal gene (FGFR1OP) and lung cancer risk: a meta-analysis of 14,463 cases and 44,188 controls. Carcinogenesis, Vol.37 (3), pp. 280-289.  show abstract

Johnson, D.C. Weinhold, N. Mitchell, J. Chen, B. Stephens, O.W. Försti, A. Nickel, J. Kaiser, M. Gregory, W.A. Cairns, D. Jackson, G.H. Hoffmann, P. Noethen, M.M. Hillengass, J. Bertsch, U. Barlogie, B. Davis, F.E. Hemminki, K. Goldschmidt, H. Houlston, R.S. Morgan, G.J. (2016). Genetic factors influencing the risk of multiple myeloma bone disease. Leukemia, Vol.30 (4), pp. 883-888.  show abstract

Kinnersley, B. Kamatani, Y. Labussière, M. Wang, Y. Galan, P. Mokhtari, K. Delattre, J.-. Gousias, K. Schramm, J. Schoemaker, M.J. Swerdlow, A. Fleming, S.J. Herms, S. Heilmann, S. Nöthen, M.M. Simon, M. Sanson, M. Lathrop, M. Houlston, R.S. (2016). Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis. Eur j hum genet, Vol.24 (5), pp. 717-724.  show abstract

Cheng, T.H. Thompson, D.J. O'Mara, T.A. Painter, J.N. Glubb, D.M. Flach, S. Lewis, A. French, J.D. Freeman-Mills, L. Church, D. Gorman, M. Martin, L. National Study of Endometrial Cancer Genetics Group (NSECG), Hodgson, S. Webb, P.M. Australian National Endometrial Cancer Study Group (ANECS), Attia, J. Holliday, E.G. McEvoy, M. Scott, R.J. Henders, A.K. Martin, N.G. Montgomery, G.W. Nyholt, D.R. Ahmed, S. Healey, C.S. Shah, M. Dennis, J. Fasching, P.A. Beckmann, M.W. Hein, A. Ekici, A.B. Hall, P. Czene, K. Darabi, H. Li, J. Dörk, T. Dürst, M. Hillemanns, P. Runnebaum, I. Amant, F. Schrauwen, S. Zhao, H. Lambrechts, D. Depreeuw, J. Dowdy, S.C. Goode, E.L. Fridley, B.L. Winham, S.J. Njølstad, T.S. Salvesen, H.B. Trovik, J. Werner, H.M. Ashton, K. Otton, G. Proietto, T. Liu, T. Mints, M. Tham, E. RENDOCAS, Consortium, C. Jun Li, M. Yip, S.H. Wang, J. Bolla, M.K. Michailidou, K. Wang, Q. Tyrer, J.P. Dunlop, M. Houlston, R. Palles, C. Hopper, J.L. AOCS Group, Peto, J. Swerdlow, A.J. Burwinkel, B. Brenner, H. Meindl, A. Brauch, H. Lindblom, A. Chang-Claude, J. Couch, F.J. Giles, G.G. Kristensen, V.N. Cox, A. Cunningham, J.M. Pharoah, P.D. Dunning, A.M. Edwards, S.L. Easton, D.F. Tomlinson, I. Spurdle, A.B. (2016). Five endometrial cancer risk loci identified through genome-wide association analysis. Nat genet, Vol.48 (6), pp. 667-674.  show abstract

Yuan, H. Liu, H. Liu, Z. Owzar, K. Han, Y. Su, L. Wei, Y. Hung, R.J. McLaughlin, J. Brhane, Y. Brennan, P. Bickeboeller, H. Rosenberger, A. Houlston, R.S. Caporaso, N. Landi, M.T. Heinrich, J. Risch, A. Christiani, D.C. Gümüş, Z.H. Klein, R.J. Amos, C.I. Wei, Q. (2016). A Novel Genetic Variant in Long Non-coding RNA Gene NEXN-AS1 is Associated with Risk of Lung Cancer. Sci rep, Vol.6, p. 34234.  show abstract

Johnson, D.C. Weinhold, N. Mitchell, J.S. Chen, B. Kaiser, M. Begum, D.B. Hillengass, J. Bertsch, U. Gregory, W.A. Cairns, D. Jackson, G.H. Försti, A. Nickel, J. Hoffmann, P. Nöethen, M.M. Stephens, O.W. Barlogie, B. Davis, F.E. Hemminki, K. Goldschmidt, H. Houlston, R.S. Morgan, G.J. (2016). Genome-wide association study identifies variation at 6q25 1 associated with survival in multiple myeloma. Nat commun, Vol.7, p. 10290.  show abstract

Speedy, H.E. Kinnersley, B. Chubb, D. Broderick, P. Law, P.J. Litchfield, K. Jayne, S. Dyer, M.J. Dearden, C. Follows, G.A. Catovsky, D. Houlston, R.S. (2016). Germ line mutations in shelterin complex genes are associated with familial chronic lymphocytic leukemia. Blood, Vol.128 (19), pp. 2319-2326.  show abstract

Kinnersley, B. Chubb, D. Dobbins, S.E. Frampton, M. Buch, S. Timofeeva, M.N. Castellví-Bel, S. Farrington, S.M. Forsti, A. Hampe, J. Hemminki, K. Hofstra, R.M. Northwood, E. Palles, C. Pinheiro, M. Ruiz-Ponte, C. Schafmayer, C. Teixeira, M.R. Westers, H. van Wezel, T. Timothy Bishop, D. Tomlinson, I. Dunlop, M.G. Houlston, R.S. (2016). Correspondence: SEMA4A variation and risk of colorectal cancer. Nat commun, Vol.7, p. 10611.

Zuber, V. Marconett, C.N. Shi, J. Hua, X. Wheeler, W. Yang, C. Song, L. Dale, A.M. Laplana, M. Risch, A. Witoelar, A. Thompson, W.K. Schork, A.J. Bettella, F. Wang, Y. Djurovic, S. Zhou, B. Borok, Z. van der Heijden, H.F. de Graaf, J. Swinkels, D. Aben, K.K. McKay, J. Hung, R.J. Bikeböller, H. Stevens, V.L. Albanes, D. Caporaso, N.E. Han, Y. Wei, Y. Panadero, M.A. Mayordomo, J.I. Christiani, D.C. Kiemeney, L. Andreassen, O.A. Houlston, R. Amos, C.I. Chatterjee, N. Laird-Offringa, I.A. Mills, I.G. Landi, M.T. (2016). Pleiotropic Analysis of Lung Cancer and Blood Triglycerides. J natl cancer inst, Vol.108 (12).  show abstract

Jarvis, D. Mitchell, J.S. Law, P.J. Palin, K. Tuupanen, S. Gylfe, A. Hänninen, U.A. Cajuso, T. Tanskanen, T. Kondelin, J. Kaasinen, E. Sarin, A.-. Kaprio, J. Eriksson, J.G. Rissanen, H. Knekt, P. Pukkala, E. Jousilahti, P. Salomaa, V. Ripatti, S. Palotie, A. Järvinen, H. Renkonen-Sinisalo, L. Lepistö, A. Böhm, J. Meklin, J.-. Al-Tassan, N.A. Palles, C. Martin, L. Barclay, E. Farrington, S.M. Timofeeva, M.N. Meyer, B.F. Wakil, S.M. Campbell, H. Smith, C.G. Idziaszczyk, S. Maughan, T.S. Kaplan, R. Kerr, R. Kerr, D. Buchanan, D.D. Win, A.K. Hopper, J.L. Jenkins, M.A. Lindor, N.M. Newcomb, P.A. Gallinger, S. Conti, D. Schumacher, F. Casey, G. Taipale, J. Aaltonen, L.A. Cheadle, J.P. Dunlop, M.G. Tomlinson, I.P. Houlston, R.S. (2016). Mendelian randomisation analysis strongly implicates adiposity with risk of developing colorectal cancer. Br j cancer, Vol.115 (2), pp. 266-272.  show abstract

Johnson, N. De Ieso, P. Migliorini, G. Orr, N. Broderick, P. Catovsky, D. Matakidou, A. Eisen, T. Goldsmith, C. Dudbridge, F. Peto, J. Dos-Santos-Silva, I. Ashworth, A. Ross, G. Houlston, R.S. Fletcher, O. (2016). Cytochrome P450 Allele CYP3A7*1C Associates with Adverse Outcomes in Chronic Lymphocytic Leukemia, Breast, and Lung Cancer. Cancer res, Vol.76 (6), pp. 1485-1493.  show abstract

Amirian, E.S. Armstrong, G.N. Zhou, R. Lau, C.C. Claus, E.B. Barnholtz-Sloan, J.S. Il'yasova, D. Schildkraut, J. Ali-Osman, F. Sadetzki, S. Johansen, C. Houlston, R.S. Jenkins, R.B. Lachance, D. Olson, S.H. Bernstein, J.L. Merrell, R.T. Wrensch, M.R. Davis, F.G. Lai, R. Shete, S. Amos, C.I. Scheurer, M.E. Aldape, K. Alafuzoff, I. Brännström, T. Broholm, H. Collins, P. Giannini, C. Rosenblum, M. Tihan, T. Melin, B.S. Bondy, M.L. (2016). The Glioma International Case-Control Study: A Report From the Genetic Epidemiology of Glioma International Consortium. Am j epidemiol, Vol.183 (2), pp. 85-91.  show abstract

Karami, S. Han, Y. Pande, M. Cheng, I. Rudd, J. Pierce, B.L. Nutter, E.L. Schumacher, F.R. Kote-Jarai, Z. Lindstrom, S. Witte, J.S. Fang, S. Han, J. Kraft, P. Hunter, D.J. Song, F. Hung, R.J. McKay, J. Gruber, S.B. Chanock, S.J. Risch, A. Shen, H. Haiman, C.A. Boardman, L. Ulrich, C.M. Casey, G. Peters, U. Amin Al Olama, A. Berchuck, A. Berndt, S.I. Bezieau, S. Brennan, P. Brenner, H. Brinton, L. Caporaso, N. Chan, A.T. Chang-Claude, J. Christiani, D.C. Cunningham, J.M. Easton, D. Eeles, R.A. Eisen, T. Gala, M. Gallinger, S.J. Gayther, S.A. Goode, E.L. Grönberg, H. Henderson, B.E. Houlston, R. Joshi, A.D. Küry, S. Landi, M.T. Le Marchand, L. Muir, K. Newcomb, P.A. Permuth-Wey, J. Pharoah, P. Phelan, C. Potter, J.D. Ramus, S.J. Risch, H. Schildkraut, J. Slattery, M.L. Song, H. Wentzensen, N. White, E. Wiklund, F. Zanke, B.W. Sellers, T.A. Zheng, W. Chatterjee, N. Amos, C.I. Doherty, J.A. GECCO and the GAME-ON Network: CORECT, DRIVE, ELLIPSE, FOCI, and TRICL, (2016). Telomere structure and maintenance gene variants and risk of five cancer types. Int j cancer, Vol.139 (12), pp. 2655-2670.  show abstract

Litchfield, K. Levy, M. Dudakia, D. Proszek, P. Shipley, C. Basten, S. Rapley, E. Bishop, D.T. Reid, A. Huddart, R. Broderick, P. Castro, D.G. O'Connor, S. Giles, R.H. Houlston, R.S. Turnbull, C. (2016). Rare disruptive mutations in ciliary function genes contribute to testicular cancer susceptibility. Nat commun, Vol.7, p. 13840.  show abstract

Chubb, D. Broderick, P. Dobbins, S.E. Frampton, M. Kinnersley, B. Penegar, S. Price, A. Ma, Y.P. Sherborne, A.L. Palles, C. Timofeeva, M.N. Bishop, D.T. Dunlop, M.G. Tomlinson, I. Houlston, R.S. (2016). Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer. Nat commun, Vol.7, p. 11883.  show abstract

Kandaswamy, R. Sava, G.P. Speedy, H.E. Beà, S. Martín-Subero, J.I. Studd, J.B. Migliorini, G. Law, P.J. Puente, X.S. Martín-García, D. Salaverria, I. Gutiérrez-Abril, J. López-Otín, C. Catovsky, D. Allan, J.M. Campo, E. Houlston, R.S. (2016). Genetic Predisposition to Chronic Lymphocytic Leukemia Is Mediated by a BMF Super-Enhancer Polymorphism. Cell rep, Vol.16 (8), pp. 2061-2067.  show abstract

Li, N. Johnson, D.C. Weinhold, N. Studd, J.B. Orlando, G. Mirabella, F. Mitchell, J.S. Meissner, T. Kaiser, M. Goldschmidt, H. Hemminki, K. Morgan, G.J. Houlston, R.S. (2016). Multiple myeloma risk variant at 7p15 3 creates an IRF4-binding site and interferes with CDCA7L expression. Nat commun, Vol.7, p. 13656.  show abstract

Dobbins, S.E. Broderick, P. Chubb, D. Kinnersley, B. Sherborne, A.L. Houlston, R.S. (2016). Undefined familial colorectal cancer and the role of pleiotropism in cancer susceptibility genes. Fam cancer, Vol.15 (4), pp. 593-599.  show abstract

Chubb, D. Broderick, P. Dobbins, S.E. Houlston, R.S. (2016). CanVar: A resource for sharing germline variation in cancer patients. F1000res, Vol.5, p. 2813.  show abstract

Ware, J.J. Aveyard, P. Broderick, P. Houlston, R.S. Eisen, T. Munafò, M.R. (2015). The association of rs1051730 genotype on adherence to and consumption of prescribed nicotine replacement therapy dose during a smoking cessation attempt. Drug alcohol depend, Vol.151, pp. 236-240.  show abstract

Kinnersley, B. Labussière, M. Holroyd, A. Di Stefano, A.-. Broderick, P. Vijayakrishnan, J. Mokhtari, K. Delattre, J.-. Gousias, K. Schramm, J. Schoemaker, M.J. Fleming, S.J. Herms, S. Heilmann, S. Schreiber, S. Wichmann, H.-. Nöthen, M.M. Swerdlow, A. Lathrop, M. Simon, M. Bondy, M. Sanson, M. Houlston, R.S. (2015). Genome-wide association study identifies multiple susceptibility loci for glioma. Nat commun, Vol.6, p. 8559.  show abstract

Cheng, T.H. Thompson, D. Painter, J. O'Mara, T. Gorman, M. Martin, L. Palles, C. Jones, A. Buchanan, D.D. Win, A.K. Hopper, J. Jenkins, M. Lindor, N.M. Newcomb, P.A. Gallinger, S. Conti, D. Schumacher, F. Casey, G. Giles, G.G. Pharoah, P. Peto, J. Cox, A. Swerdlow, A. Couch, F. Cunningham, J.M. Goode, E.L. Winham, S.J. Lambrechts, D. Fasching, P. Burwinkel, B. Brenner, H. Brauch, H. Chang-Claude, J. Salvesen, H.B. Kristensen, V. Darabi, H. Li, J. Liu, T. Lindblom, A. Hall, P. de Polanco, M.E. Sans, M. Carracedo, A. Castellvi-Bel, S. Rojas-Martinez, A. Aguiar Jnr, S. Teixeira, M.R. Dunning, A.M. Dennis, J. Otton, G. Proietto, T. Holliday, E. Attia, J. Ashton, K. Scott, R.J. McEvoy, M. Dowdy, S.C. Fridley, B.L. Werner, H.M. Trovik, J. Njolstad, T.S. Tham, E. Mints, M. Runnebaum, I. Hillemanns, P. Dörk, T. Amant, F. Schrauwen, S. Hein, A. Beckmann, M.W. Ekici, A. Czene, K. Meindl, A. Bolla, M.K. Michailidou, K. Tyrer, J.P. Wang, Q. Ahmed, S. Healey, C.S. Shah, M. Annibali, D. Depreeuw, J. Al-Tassan, N.A. Harris, R. Meyer, B.F. Whiffin, N. Hosking, F.J. Kinnersley, B. Farrington, S.M. Timofeeva, M. Tenesa, A. Campbell, H. Haile, R.W. Hodgson, S. Carvajal-Carmona, L. Cheadle, J.P. Easton, D. Dunlop, M. Houlston, R. Spurdle, A. Tomlinson, I. (2015). Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1. Sci rep, Vol.5, p. 17369.  show abstract

Galvan, A. Colombo, F. Frullanti, E. Dassano, A. Noci, S. Wang, Y. Eisen, T. Matakidou, A. Tomasello, L. Vezzalini, M. Sorio, C. Dugo, M. Ambrogi, F. Iacobucci, I. Martinelli, G. Incarbone, M. Alloisio, M. Nosotti, M. Tosi, D. Santambrogio, L. Pelosi, G. Pastorino, U. Houlston, R.S. Dragani, T.A. (2015). Germline polymorphisms and survival of lung adenocarcinoma patients: a genome-wide study in two European patient series. Int j cancer, Vol.136 (5), pp. E262-E271.  show abstract

Bainbridge, M.N. Armstrong, G.N. Gramatges, M.M. Bertuch, A.A. Jhangiani, S.N. Doddapaneni, H. Lewis, L. Tombrello, J. Tsavachidis, S. Liu, Y. Jalali, A. Plon, S.E. Lau, C.C. Parsons, D.W. Claus, E.B. Barnholtz-Sloan, J. Il'yasova, D. Schildkraut, J. Ali-Osman, F. Sadetzki, S. Johansen, C. Houlston, R.S. Jenkins, R.B. Lachance, D. Olson, S.H. Bernstein, J.L. Merrell, R.T. Wrensch, M.R. Walsh, K.M. Davis, F.G. Lai, R. Shete, S. Aldape, K. Amos, C.I. Thompson, P.A. Muzny, D.M. Gibbs, R.A. Melin, B.S. Bondy, M.L. Gliogene Consortium, (2015). Germline mutations in shelterin complex genes are associated with familial glioma. J natl cancer inst, Vol.107 (1), p. 384.  show abstract

Kinnersley, B. Mitchell, J.S. Gousias, K. Schramm, J. Idbaih, A. Labussière, M. Marie, Y. Rahimian, A. Wichmann, H.-. Schreiber, S. Hoang-Xuan, K. Delattre, J.-. Nöthen, M.M. Mokhtari, K. Lathrop, M. Bondy, M. Simon, M. Sanson, M. Houlston, R.S. (2015). Quantifying the heritability of glioma using genome-wide complex trait analysis. Sci rep, Vol.5, p. 17267.  show abstract

Bartram, T. Burkhardt, B. Wössmann, W. Seidemann, K. Zimmermann, M. Cario, G. Lisfeld, J. Ellinghaus, E. Franke, A. Houlston, R.S. Schrappe, M. Reiter, A. Stanulla, M. (2015). Childhood acute lymphoblastic leukemia-associated risk-loci IKZF1, ARID5B and CEBPE and risk of pediatric non-Hodgkin lymphoma: a report from the Berlin-Frankfurt-Münster Study Group. Leuk lymphoma, Vol.56 (3), pp. 814-816.

Weinhold, N. Meissner, T. Johnson, D.C. Seckinger, A. Moreaux, J. Försti, A. Chen, B. Nickel, J. Chubb, D. Rawstron, A.C. Doughty, C. Dahir, N.B. Begum, D.B. Young, K. Walker, B.A. Hoffmann, P. Nöthen, M.M. Davies, F.E. Klein, B. Goldschmidt, H. Morgan, G.J. Houlston, R.S. Hose, D. Hemminki, K. (2015). The 7p15 3 (rs4487645) association for multiple myeloma shows strong allele-specific regulation of the MYC-interacting gene CDCA7L in malignant plasma cells. Haematologica, Vol.100 (3), pp. e110-e113.

Sava, G.P. Speedy, H.E. Di Bernardo, M.C. Dyer, M.J. Holroyd, A. Sunter, N.J. Marr, H. Mansouri, L. Deaglio, S. Karabon, L. Frydecka, I. Jamroziak, K. Woszczyk, D. Juliusson, G. Smedby, K.E. Jayne, S. Majid, A. Wang, Y. Dearden, C. Hall, A.G. Mainou-Fowler, T. Jackson, G.H. Summerfield, G. Harris, R.J. Pettitt, A.R. Allsup, D.J. Bailey, J.R. Pratt, G. Pepper, C. Fegan, C. Rosenquist, R. Catovsky, D. Allan, J.M. Houlston, R.S. (2015). Common variation at 12q24 13 (OAS3) influences chronic lymphocytic leukemia risk. Leukemia, Vol.29 (3), pp. 748-751.

Interleukin 1 Genetics Consortium, (2015). Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis. Lancet diabetes endocrinol, Vol.3 (4), pp. 243-253.  show abstract

Jalali, A. Amirian, E.S. Bainbridge, M.N. Armstrong, G.N. Liu, Y. Tsavachidis, S. Jhangiani, S.N. Plon, S.E. Lau, C.C. Claus, E.B. Barnholtz-Sloan, J.S. Il'yasova, D. Schildkraut, J. Ali-Osman, F. Sadetzki, S. Johansen, C. Houlston, R.S. Jenkins, R.B. Lachance, D. Olson, S.H. Bernstein, J.L. Merrell, R.T. Wrensch, M.R. Davis, F.G. Lai, R. Shete, S. Aldape, K. Amos, C.I. Muzny, D.M. Gibbs, R.A. Melin, B.S. Bondy, M.L. (2015). Targeted sequencing in chromosome 17q linkage region identifies familial glioma candidates in the Gliogene Consortium. Sci rep, Vol.5, p. 8278.  show abstract

Litchfield, K. Thomsen, H. Mitchell, J.S. Sundquist, J. Houlston, R.S. Hemminki, K. Turnbull, C. (2015). Quantifying the heritability of testicular germ cell tumour using both population-based and genomic approaches. Sci rep, Vol.5, p. 13889.  show abstract

Chubb, D. Broderick, P. Frampton, M. Kinnersley, B. Sherborne, A. Penegar, S. Lloyd, A. Ma, Y.P. Dobbins, S.E. Houlston, R.S. (2015). Genetic diagnosis of high-penetrance susceptibility for colorectal cancer (CRC) is achievable for a high proportion of familial CRC by exome sequencing. J clin oncol, Vol.33 (5), pp. 426-432.  show abstract

Timofeeva, M.N. Kinnersley, B. Farrington, S.M. Whiffin, N. Palles, C. Svinti, V. Lloyd, A. Gorman, M. Ooi, L.-. Hosking, F. Barclay, E. Zgaga, L. Dobbins, S. Martin, L. Theodoratou, E. Broderick, P. Tenesa, A. Smillie, C. Grimes, G. Hayward, C. Campbell, A. Porteous, D. Deary, I.J. Harris, S.E. Northwood, E.L. Barrett, J.H. Smith, G. Wolf, R. Forman, D. Morreau, H. Ruano, D. Tops, C. Wijnen, J. Schrumpf, M. Boot, A. Vasen, H.F. Hes, F.J. van Wezel, T. Franke, A. Lieb, W. Schafmayer, C. Hampe, J. Buch, S. Propping, P. Hemminki, K. Försti, A. Westers, H. Hofstra, R. Pinheiro, M. Pinto, C. Teixeira, M. Ruiz-Ponte, C. Fernández-Rozadilla, C. Carracedo, A. Castells, A. Castellví-Bel, S. Campbell, H. Bishop, D.T. Tomlinson, I.P. Dunlop, M.G. Houlston, R.S. (2015). Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer. Sci rep, Vol.5, p. 16286.  show abstract

Hung, R.J. Ulrich, C.M. Goode, E.L. Brhane, Y. Muir, K. Chan, A.T. Marchand, L.L. Schildkraut, J. Witte, J.S. Eeles, R. Boffetta, P. Spitz, M.R. Poirier, J.G. Rider, D.N. Fridley, B.L. Chen, Z. Haiman, C. Schumacher, F. Easton, D.F. Landi, M.T. Brennan, P. Houlston, R. Christiani, D.C. Field, J.K. Bickeböller, H. Risch, A. Kote-Jarai, Z. Wiklund, F. Grönberg, H. Chanock, S. Berndt, S.I. Kraft, P. Lindström, S. Al Olama, A.A. Song, H. Phelan, C. Wentzensen, N. Peters, U. Slattery, M.L. GECCO, Sellers, T.A. FOCI, Casey, G. Gruber, S.B. CORECT, Hunter, D.J. DRIVE, Amos, C.I. Henderson, B. GAME-ON Network, (2015). Cross Cancer Genomic Investigation of Inflammation Pathway for Five Common Cancers: Lung, Ovary, Prostate, Breast, and Colorectal Cancer. J natl cancer inst, Vol.107 (11).  show abstract

Brenner, D.R. Amos, C.I. Brhane, Y. Timofeeva, M.N. Caporaso, N. Wang, Y. Christiani, D.C. Bickeböller, H. Yang, P. Albanes, D. Stevens, V.L. Gapstur, S. McKay, J. Boffetta, P. Zaridze, D. Szeszenia-Dabrowska, N. Lissowska, J. Rudnai, P. Fabianova, E. Mates, D. Bencko, V. Foretova, L. Janout, V. Krokan, H.E. Skorpen, F. Gabrielsen, M.E. Vatten, L. Njølstad, I. Chen, C. Goodman, G. Lathrop, M. Vooder, T. Välk, K. Nelis, M. Metspalu, A. Broderick, P. Eisen, T. Wu, X. Zhang, D. Chen, W. Spitz, M.R. Wei, Y. Su, L. Xie, D. She, J. Matsuo, K. Matsuda, F. Ito, H. Risch, A. Heinrich, J. Rosenberger, A. Muley, T. Dienemann, H. Field, J.K. Raji, O. Chen, Y. Gosney, J. Liloglou, T. Davies, M.P. Marcus, M. McLaughlin, J. Orlow, I. Han, Y. Li, Y. Zong, X. Johansson, M. EPIC Investigators, Liu, G. Tworoger, S.S. Le Marchand, L. Henderson, B.E. Wilkens, L.R. Dai, J. Shen, H. Houlston, R.S. Landi, M.T. Brennan, P. Hung, R.J. (2015). Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia. Carcinogenesis, Vol.36 (11), pp. 1314-1326.  show abstract

Wang, Y. Wei, Y. Gaborieau, V. Shi, J. Han, Y. Timofeeva, M.N. Su, L. Li, Y. Eisen, T. Amos, C.I. Landi, M.T. Christiani, D.C. McKay, J.D. Houlston, R.S. (2015). Deciphering associations for lung cancer risk through imputation and analysis of 12,316 cases and 16,831 controls. Eur j hum genet, Vol.23 (12), pp. 1723-1728.  show abstract

Labreche, K. Simeonova, I. Kamoun, A. Gleize, V. Chubb, D. Letouzé, E. Riazalhosseini, Y. Dobbins, S.E. Elarouci, N. Ducray, F. de Reyniès, A. Zelenika, D. Wardell, C.P. Frampton, M. Saulnier, O. Pastinen, T. Hallout, S. Figarella-Branger, D. Dehais, C. Idbaih, A. Mokhtari, K. Delattre, J.-. Huillard, E. Mark Lathrop, G. Sanson, M. Houlston, R.S. POLA Network, (2015). TCF12 is mutated in anaplastic oligodendroglioma. Nat commun, Vol.6, p. 7207.  show abstract

Vijayakrishnan, J. Henrion, M. Moorman, A.V. Fiege, B. Kumar, R. da Silva Filho, M.I. Holroyd, A. Koehler, R. Thomsen, H. Irving, J.A. Allan, J.M. Lightfoot, T. Roman, E. Kinsey, S.E. Sheridan, E. Thompson, P.D. Hoffmann, P. Nöthen, M.M. Mühleisen, T.W. Eisele, L. Bartram, C.R. Schrappe, M. Greaves, M. Hemminki, K. Harrison, C.J. Stanulla, M. Houlston, R.S. (2015). The 9p21 3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A. Sci rep, Vol.5, p. 15065.  show abstract

Zhang, C. Doherty, J.A. Burgess, S. Hung, R.J. Lindström, S. Kraft, P. Gong, J. Amos, C.I. Sellers, T.A. Monteiro, A.N. Chenevix-Trench, G. Bickeböller, H. Risch, A. Brennan, P. Mckay, J.D. Houlston, R.S. Landi, M.T. Timofeeva, M.N. Wang, Y. Heinrich, J. Kote-Jarai, Z. Eeles, R.A. Muir, K. Wiklund, F. Grönberg, H. Berndt, S.I. Chanock, S.J. Schumacher, F. Haiman, C.A. Henderson, B.E. Amin Al Olama, A. Andrulis, I.L. Hopper, J.L. Chang-Claude, J. John, E.M. Malone, K.E. Gammon, M.D. Ursin, G. Whittemore, A.S. Hunter, D.J. Gruber, S.B. Knight, J.A. Hou, L. Le Marchand, L. Newcomb, P.A. Hudson, T.J. Chan, A.T. Li, L. Woods, M.O. Ahsan, H. Pierce, B.L. GECCO and GAME-ON Network: CORECT, DRIVE, ELLIPSE, FOCI, and TRICL, (2015). Genetic determinants of telomere length and risk of common cancers: a Mendelian randomization study. Hum mol genet, Vol.24 (18), pp. 5356-5366.  show abstract

Litchfield, K. Mitchell, J.S. Shipley, J. Huddart, R. Rajpert-De Meyts, E. Skakkebæk, N.E. Houlston, R.S. Turnbull, C. (2015). Polygenic susceptibility to testicular cancer: implications for personalised health care. Br j cancer, Vol.113 (10), pp. 1512-1518.  show abstract

Jäger, R. Migliorini, G. Henrion, M. Kandaswamy, R. Speedy, H.E. Heindl, A. Whiffin, N. Carnicer, M.J. Broome, L. Dryden, N. Nagano, T. Schoenfelder, S. Enge, M. Yuan, Y. Taipale, J. Fraser, P. Fletcher, O. Houlston, R.S. (2015). Capture Hi-C identifies the chromatin interactome of colorectal cancer risk loci. Nat commun, Vol.6, p. 6178.  show abstract

Al-Tassan, N.A. Whiffin, N. Hosking, F.J. Palles, C. Farrington, S.M. Dobbins, S.E. Harris, R. Gorman, M. Tenesa, A. Meyer, B.F. Wakil, S.M. Kinnersley, B. Campbell, H. Martin, L. Smith, C.G. Idziaszczyk, S. Barclay, E. Maughan, T.S. Kaplan, R. Kerr, R. Kerr, D. Buchanan, D.D. Win, A.K. Hopper, J. Jenkins, M. Lindor, N.M. Newcomb, P.A. Gallinger, S. Conti, D. Schumacher, F. Casey, G. Dunlop, M.G. Tomlinson, I.P. Cheadle, J.P. Houlston, R.S. (2015). A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer. Sci rep, Vol.5, p. 10442.  show abstract

Litchfield, K. Summersgill, B. Yost, S. Sultana, R. Labreche, K. Dudakia, D. Renwick, A. Seal, S. Al-Saadi, R. Broderick, P. Turner, N.C. Houlston, R.S. Huddart, R. Shipley, J. Turnbull, C. (2015). Whole-exome sequencing reveals the mutational spectrum of testicular germ cell tumours. Nat commun, Vol.6, p. 5973.  show abstract

Sud, A. Cooke, R. Swerdlow, A.J. Houlston, R.S. (2015). Genome-wide homozygosity signature and risk of Hodgkin lymphoma. Sci rep, Vol.5, p. 14315.  show abstract

Mitchell, J.S. Johnson, D.C. Litchfield, K. Broderick, P. Weinhold, N. Davies, F.E. Gregory, W.A. Jackson, G.H. Kaiser, M. Morgan, G.J. Houlston, R.S. (2015). Implementation of genome-wide complex trait analysis to quantify the heritability in multiple myeloma. Sci rep, Vol.5, p. 12473.  show abstract

Litchfield, K. Holroyd, A. Lloyd, A. Broderick, P. Nsengimana, J. Eeles, R. Easton, D.F. Dudakia, D. Bishop, D.T. Reid, A. Huddart, R.A. Grotmol, T. Wiklund, F. Shipley, J. Houlston, R.S. Turnbull, C. (2015). Identification of four new susceptibility loci for testicular germ cell tumour. Nat commun, Vol.6, p. 8690.  show abstract

Li, W. Dobbins, S. Tomlinson, I. Houlston, R. Pal, D.K. Strug, L.J. (2015). Prioritizing rare variants with conditional likelihood ratios. Hum hered, Vol.79 (1), pp. 5-13.  show abstract

Morris, E.J. Penegar, S. Whiffin, N. Broderick, P. Bishop, D.T. Northwood, E. Quirke, P. Finan, P. Houlston, R.S. (2015). A retrospective observational study of the relationship between single nucleotide polymorphisms associated with the risk of developing colorectal cancer and survival. Plos one, Vol.10 (2), p. e0117816.  show abstract

Henrion, M.Y. Purdue, M.P. Scelo, G. Broderick, P. Frampton, M. Ritchie, A. Meade, A. Li, P. McKay, J. Johansson, M. Lathrop, M. Larkin, J. Rothman, N. Wang, Z. Chow, W.-. Stevens, V.L. Diver, W.R. Albanes, D. Virtamo, J. Brennan, P. Eisen, T. Chanock, S. Houlston, R.S. (2015). Common variation at 1q24 1 (ALDH9A1) is a potential risk factor for renal cancer. Plos one, Vol.10 (3), p. e0122589.  show abstract

Derkach, A. Chiang, T. Gong, J. Addis, L. Dobbins, S. Tomlinson, I. Houlston, R. Pal, D.K. Strug, L.J. (2014). Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statistic. Bioinformatics, Vol.30 (15), pp. 2179-2188.  show abstract

Sava, G.P. Speedy, H.E. Houlston, R.S. (2014). Candidate gene association studies and risk of chronic lymphocytic leukemia: a systematic review and meta-analysis. Leuk lymphoma, Vol.55 (1), pp. 160-167.  show abstract

Speedy, H.E. Di Bernardo, M.C. Sava, G.P. Dyer, M.J. Holroyd, A. Wang, Y. Sunter, N.J. Mansouri, L. Juliusson, G. Smedby, K.E. Roos, G. Jayne, S. Majid, A. Dearden, C. Hall, A.G. Mainou-Fowler, T. Jackson, G.H. Summerfield, G. Harris, R.J. Pettitt, A.R. Allsup, D.J. Bailey, J.R. Pratt, G. Pepper, C. Fegan, C. Rosenquist, R. Catovsky, D. Allan, J.M. Houlston, R.S. (2014). A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia. Nat genet, Vol.46 (1), pp. 56-60.  show abstract

Whiffin, N. Hosking, F.J. Farrington, S.M. Palles, C. Dobbins, S.E. Zgaga, L. Lloyd, A. Kinnersley, B. Gorman, M. Tenesa, A. Broderick, P. Wang, Y. Barclay, E. Hayward, C. Martin, L. Buchanan, D.D. Win, A.K. Hopper, J. Jenkins, M. Lindor, N.M. Newcomb, P.A. Gallinger, S. Conti, D. Schumacher, F. Casey, G. Liu, T. Swedish Low-Risk Colorectal Cancer Study Group, Campbell, H. Lindblom, A. Houlston, R.S. Tomlinson, I.P. Dunlop, M.G. (2014). Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis. Hum mol genet, Vol.23 (17), pp. 4729-4737.  show abstract

Morgan, G.J. Johnson, D.C. Weinhold, N. Goldschmidt, H. Landgren, O. Lynch, H.T. Hemminki, K. Houlston, R.S. (2014). Inherited genetic susceptibility to multiple myeloma. Leukemia, Vol.28 (3), pp. 518-524.  show abstract

Sawyer, E. Roylance, R. Petridis, C. Brook, M.N. Nowinski, S. Papouli, E. Fletcher, O. Pinder, S. Hanby, A. Kohut, K. Gorman, P. Caneppele, M. Peto, J. Dos Santos Silva, I. Johnson, N. Swann, R. Dwek, M. Perkins, K.-. Gillett, C. Houlston, R. Ross, G. De Ieso, P. Southey, M.C. Hopper, J.L. Provenzano, E. Apicella, C. Wesseling, J. Cornelissen, S. Keeman, R. Fasching, P.A. Jud, S.M. Ekici, A.B. Beckmann, M.W. Kerin, M.J. Marme, F. Schneeweiss, A. Sohn, C. Burwinkel, B. Guénel, P. Truong, T. Laurent-Puig, P. Kerbrat, P. Bojesen, S.E. Nordestgaard, B.G. Nielsen, S.F. Flyger, H. Milne, R.L. Perez, J.I. Menéndez, P. Benitez, J. Brenner, H. Dieffenbach, A.K. Arndt, V. Stegmaier, C. Meindl, A. Lichtner, P. Schmutzler, R.K. Lochmann, M. Brauch, H. Fischer, H.-. Ko, Y.-. GENICA Network, Nevanlinna, H. Muranen, T.A. Aittomäki, K. Blomqvist, C. Bogdanova, N.V. Dörk, T. Lindblom, A. Margolin, S. Mannermaa, A. Kataja, V. Kosma, V.-. Hartikainen, J.M. Chenevix-Trench, G. KConFab Investigators, Lambrechts, D. Weltens, C. Van Limbergen, E. Hatse, S. Chang-Claude, J. Rudolph, A. Seibold, P. Flesch-Janys, D. Radice, P. Peterlongo, P. Bonanni, B. Volorio, S. Giles, G.G. Severi, G. Baglietto, L. McLean, C.A. Haiman, C.A. Henderson, B.E. Schumacher, F. Le Marchand, L. Simard, J. Goldberg, M.S. Labrèche, F. Dumont, M. Kristensen, V. Winqvist, R. Pylkäs, K. Jukkola-Vuorinen, A. Kauppila, S. Andrulis, I.L. Knight, J.A. Glendon, G. Mulligan, A.M. Devillee, P. Tollenaar, R.A. Seynaeve, C.M. Kriege, M. Figueroa, J. Chanock, S.J. Sherman, M.E. Hooning, M.J. Hollestelle, A. van den Ouweland, A.M. van Deurzen, C.H. Li, J. Czene, K. Humphreys, K. Cox, A. Cross, S.S. Reed, M.W. Shah, M. Jakubowska, A. Lubinski, J. Jaworska-Bieniek, K. Durda, K. Swerdlow, A. Ashworth, A. Orr, N. Schoemaker, M. Couch, F.J. Hallberg, E. González-Neira, A. Pita, G. Alonso, M.R. Tessier, D.C. Vincent, D. Bacot, F. Bolla, M.K. Wang, Q. Dennis, J. Michailidou, K. Dunning, A.M. Hall, P. Easton, D. Pharoah, P. Schmidt, M.K. Tomlinson, I. Garcia-Closas, M. (2014). Genetic predisposition to in situ and invasive lobular carcinoma of the breast. Plos genet, Vol.10 (4), p. e1004285.  show abstract

Park, S.L. Fesinmeyer, M.D. Timofeeva, M. Caberto, C.P. Kocarnik, J.M. Han, Y. Love, S.-. Young, A. Dumitrescu, L. Lin, Y. Goodloe, R. Wilkens, L.R. Hindorff, L. Fowke, J.H. Carty, C. Buyske, S. Schumacher, F.R. Butler, A. Dilks, H. Deelman, E. Cote, M.L. Chen, W. Pande, M. Christiani, D.C. Field, J.K. Bickeboeller, H. Risch, A. Heinrich, J. Brennan, P. Wang, Y. Eisen, T. Houlston, R.S. Thun, M. Albanes, D. Caporaso, N. Peters, U. North, K.E. Heiss, G. Crawford, D.C. Bush, W.S. Haiman, C.A. Landi, M.T. Hung, R.J. Kooperberg, C. Amos, C.I. Le Marchand, L. Cheng, I. (2014). Pleiotropic Associations of Risk Variants Identified for Other Cancers With Lung Cancer Risk: The PAGE and TRICL Consortia. Jnci-journal of the national cancer institute, Vol.106 (4).

Ongen, H. Andersen, C.L. Bramsen, J.B. Oster, B. Rasmussen, M.H. Ferreira, P.G. Sandoval, J. Vidal, E. Whiffin, N. Planchon, A. Padioleau, I. Bielser, D. Romano, L. Tomlinson, I. Houlston, R.S. Esteller, M. Orntoft, T.F. Dermitzakis, E.T. (2014). Putative cis-regulatory drivers in colorectal cancer. Nature, Vol.512 (7512), pp. 87-90.  show abstract

Wang, Y. McKay, J.D. Rafnar, T. Wang, Z. Timofeeva, M.N. Broderick, P. Zong, X. Laplana, M. Wei, Y. Han, Y. Lloyd, A. Delahaye-Sourdeix, M. Chubb, D. Gaborieau, V. Wheeler, W. Chatterjee, N. Thorleifsson, G. Sulem, P. Liu, G. Kaaks, R. Henrion, M. Kinnersley, B. Vallée, M. LeCalvez-Kelm, F. Stevens, V.L. Gapstur, S.M. Chen, W.V. Zaridze, D. Szeszenia-Dabrowska, N. Lissowska, J. Rudnai, P. Fabianova, E. Mates, D. Bencko, V. Foretova, L. Janout, V. Krokan, H.E. Gabrielsen, M.E. Skorpen, F. Vatten, L. Njølstad, I. Chen, C. Goodman, G. Benhamou, S. Vooder, T. Välk, K. Nelis, M. Metspalu, A. Lener, M. Lubiński, J. Johansson, M. Vineis, P. Agudo, A. Clavel-Chapelon, F. Bueno-de-Mesquita, H.B. Trichopoulos, D. Khaw, K.-. Johansson, M. Weiderpass, E. Tjønneland, A. Riboli, E. Lathrop, M. Scelo, G. Albanes, D. Caporaso, N.E. Ye, Y. Gu, J. Wu, X. Spitz, M.R. Dienemann, H. Rosenberger, A. Su, L. Matakidou, A. Eisen, T. Stefansson, K. Risch, A. Chanock, S.J. Christiani, D.C. Hung, R.J. Brennan, P. Landi, M.T. Houlston, R.S. Amos, C.I. (2014). Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer. Nat genet, Vol.46 (7), pp. 736-741.  show abstract

Andersson, U. Wibom, C. Cederquist, K. Aradottir, S. Borg, A. Armstrong, G.N. Shete, S. Lau, C.C. Bainbridge, M.N. Claus, E.B. Barnholtz-Sloan, J. Lai, R. Il'yasova, D. Houlston, R.S. Schildkraut, J. Bernstein, J.L. Olson, S.H. Jenkins, R.B. Lachance, D.H. Wrensch, M. Davis, F.G. Merrell, R. Johansen, C. Sadetzki, S. Gliogene Consortium, Bondy, M.L. Melin, B.S. (2014). Germline rearrangements in families with strong family history of glioma and malignant melanoma, colon, and breast cancer. Neuro oncol, Vol.16 (10), pp. 1333-1340.  show abstract

Labussière, M. Di Stefano, A.L. Gleize, V. Boisselier, B. Giry, M. Mangesius, S. Bruno, A. Paterra, R. Marie, Y. Rahimian, A. Finocchiaro, G. Houlston, R.S. Hoang-Xuan, K. Idbaih, A. Delattre, J.-. Mokhtari, K. Sanson, M. (2014). TERT promoter mutations in gliomas, genetic associations and clinico-pathological correlations. Br j cancer, Vol.111 (10), pp. 2024-2032.  show abstract

Jaeger, R. Harutyunyan, A.S. Rumi, E. Pietra, D. Berg, T. Olcaydu, D. Houlston, R.S. Cazzola, M. Kralovics, R. (2014). Common germline variation at the TERT locus contributes to familial clustering of myeloproliferative neoplasms. American journal of hematology, Vol.89 (12), pp. 1107-1110.

Hemminki, K. Houlston, R.S. (2014). Special section editorial. International journal of cancer, Vol.135 (8), pp. 1755-1755.

Weinhold, N. Johnson, D.C. Rawstron, A.C. Foersti, A. Doughty, C. Vijayakrishnan, J. Broderick, P. Dahir, N.B. Begum, D.B. Hosking, F.J. Yong, K. Walker, B.A. Hoffmann, P. Muehleisen, T.W. Langer, C. Doerner, E. Joeckel, K.-. Eisele, L. Noethen, M.M. Hose, D. Davies, F.E. Goldschmidt, H. Morgan, G.J. Hemminki, K. Houlston, R.S. (2014). Inherited genetic susceptibility to monoclonal gammopathy of unknown significance. Blood, Vol.123 (16), pp. 2513-2517.

Lucassen, A. Houlston, R.S. (2014). The challenges of genome analysis in the health care setting. Genes (basel), Vol.5 (3), pp. 576-585.  show abstract

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Kinnersley, B. Buch, S. Castellví-Bel, S. Farrington, S.M. Forsti, A. Hampe, J. Hemminki, K. Hofstra, R.M. Northwood, E. Palles, C. Pinheiro, M. Ruiz-Ponte, C. Schafmayer, C. Teixeira, M.R. Westers, H. Wezel, T.V. Bishop, D.T. Tomlinson, I. Dunlop, M.G. Houlston, R.S. (2014). Re: Role of the Oxidative DNA Damage Repair Gene OGG1 in Colorectal Tumorigenesis. Journal of the national cancer institute, .

Di Bernardo, M.C. Broderick, P. Harris, S. Dyer, M.J. Matutes, E. Dearden, C. Catovsky, D. Houlston, R.S. (2013). Risk of developing chronic lymphocytic leukemia is influenced by HLA-A class I variation. Leukemia, Vol.27 (1), pp. 255-258.

Wang, J. Carvajal-Carmona, L.G. Chu, J.-. Zauber, A.G. APC Trial Collaborators, Kubo, M. Matsuda, K. Dunlop, M. Houlston, R.S. Sieber, O. Lipton, L. Gibbs, P. Martin, N.G. Montgomery, G.W. Young, J. Baird, P.N. Ratain, M.J. Nakamura, Y. Weiss, S.T. Tomlinson, I. Bertagnolli, M.M. (2013). Germline variants and advanced colorectal adenomas: adenoma prevention with celecoxib trial genome-wide association study. Clin cancer res, Vol.19 (23), pp. 6430-6437.  show abstract

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