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Speedy, H. E., Kinnersley, B., Chubb, D., Broderick, P., Law, P. J., Litchfield, K., Jayne, S., Dyer, M. J. S., 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, 128 (19). pp. 2319-2326. ISSN 0006-4971

Went, M., Sud, A., Speedy, H., Sunter, N. J., Forsti, A., Law, P. J., Johnson, D. C., Mirabella, F., Holroyd, A., Li, N., Orlando, G., Weinhold, N., van Duin, M., Chen, B. W., 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., Jockel, K. H., Nickel, J., Nothen, M. M., da Silva, M. I., Thomsen, H., Walker, B. A., Broyl, A., Davies, F. E., Hansson, M., Goldschmidt, H., Dyer, M. J. S., 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 JOURNAL, 9. ISSN 2044-5385

E

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. Nature Communications, 6. ISSN 2041-1723

Sud, A., Thomsen, H., Orlando, G., Forsti, A., Law, P. J., Broderick, P., Cooke, R., Hariri, F., Pastinen, T., Easton, D. F., Pharoah, P. D. P., Dunning, A. M., Peto, J., Canzian, F., Eeles, R., Kote-Jarai, Z., Muir, K., Pashayan, N., Campa, D., Hoffmann, P., Nothen, M. M., Jockel, K. H., von Strandmann, E. P., Swerdlow, A. J., Engert, A., Orr, N., Hemminki, K., Houlston, R. S., Consortium, Practical (2018) Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma. BLOOD, 132 (19). pp. 2040-2052. ISSN 0006-4971

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., Nothen, M. M., Heilmann-Heimbach, S., Jockel, K. H., Easton, D. F., Pharaoh, P. D. P., Dunning, A. M., Peto, J., Canzian, F., Swerdlow, A., Eeles, R. A., Kote-Jarai, Z., Muir, K., Pashayan, N., Greaves, M., Zimmerman, M., Bartram, C. R., Schrappe, M., Stanulla, M., Hemminki, K., Houlston, R. S., Consortium, Practical (2018) Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia. NATURE COMMUNICATIONS, 9. ISSN 2041-1723

H

Ostrom, Q. T., Kinnersley, B., Armstrong, G., Rice, T., Chen, Y. W., 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. M., Yeager, M., Houlston, R. S., Jenkins, R. B., Wrensch, M. R., Melin, B., Bondy, M. L., Barnholtz-Sloan, J. S., GliomaScan, Consortium (2018) Age-specific genome-wide association study in glioblastoma identifies increased proportion of 'lower grade glioma'-like features associated with younger age. INTERNATIONAL JOURNAL OF CANCER, 143 (10). pp. 2359-2366. ISSN 0020-7136

Sud, A., Hemminki, K., Houlston, R. S. (2017) Candidate gene association studies and risk of Hodgkin lymphoma: a systematic review and meta-analysis. HEMATOLOGICAL ONCOLOGY, 35 (1). pp. 34-50. ISSN 0278-0232

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, 17. ISSN 1471-2407

He, Y. Z., Timofeeva, M., Farrington, S. M., Vaughan-Shaw, P., Svinti, V., Walker, M., Zgaga, L., Meng, X. R., Li, X., Spiliopoulou, A., Jiang, X., Hypponen, E., Kraft, P., Kiel, D. P., 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., Consortium, Sunlight (2018) Exploring causality in the association between circulating 25-hydroxyvitamin D and colorectal cancer risk: a large Mendelian randomisation study. BMC MEDICINE, 16. ISSN 1741-7015

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, 132 (9). pp. 973-976. ISSN 0006-4971

Liu, H. L., Liu, Z. S., Wang, Y. R., Stinchcombe, T. E., Owzar, K., Han, Y. H., Hung, R. J., Brhane, Y., McLaughlin, J., Brennan, P., Bickeboller, H., Rosenberger, A., Houlston, R. S., Caporaso, N., Landi, M. T., Bruske, I., Risch, A., Wu, X. F., Ye, Y. Q., Christiani, D. C., Amos, C. I., Wei, Q. Y., Team, Tricl Res (2017) Functional variants in DCAF4 associated with lung cancer risk in European populations. CARCINOGENESIS, 38 (5). pp. 541-551. ISSN 0143-3334

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., Forsti, 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 REPORTS, 20 (11). pp. 2556-2564. ISSN 2211-1247

Studd, J. B., Vijayakrishnan, J., Yang, M. J., Migliorini, G., Paulsson, K., Houlston, R. S. (2017) Genetic and regulatory mechanism of susceptibility to high-hyperdiploid acute lymphoblastic leukaemia at 10p21.2. Nature Communications, 8. ISSN 2041-1723

Studd, J. B., Yang, M. J., Li, Z. H., Vijayakrishnan, J., Lu, Y., Yeoh, A. E. J., 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, 33 (1). pp. 1-14. ISSN 0887-6924

Feng, Y., Wang, Y. R., Liu, H. L., Liu, Z. S., Mills, C., Han, Y. H., 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., Ye, Y. Q., Wu, X. F., Christiani, D. C., Amos, C. I., Wei, Q. Y. (2017) Genetic variants of PTPN2 are associated with lung cancer risk: a re-analysis of eight GWASs in the TRICL-ILCCO consortium. Scientific Reports, 7. ISSN 2045-2322

Kinnersley, B., Houlston, R. S., Bondy, M. L. (2018) Genome-Wide Association Studies in Glioma. CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 27 (4). pp. 418-428. ISSN 1055-9965

Claus, E. B., Cornish, A. J., Broderick, P., Schildkraut, J. M., Dobbins, S. E., Holroyd, A., Calvocoressi, L., Lu, L. G., Hansen, H. M., Smirnov, I., Walsh, K. M., Schramm, J., Hoffmann, P., Nothen, M. M., Jockel, K. H., 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-ONCOLOGY, 20 (11). pp. 1485-1493. ISSN 1522-8517

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. W., Zheng, T. Z., 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. M., Caporaso, N. E., Morton, L. M., Severson, R. K., Riboli, E., Vineis, P., Vermeulen, R. C. H., 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. S., Catovsky, D., Campo, E., Cerhan, J. R., Allan, J. M., Rothman, N., Houlston, R., Slager, S. L. (2017) Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia. Nature Communications, 8. ISSN 2041-1723

Sud, A., Kinnersley, B., Houlston, R. S. (2017) Genome-wide association studies of cancer: current insights and future perspectives. NATURE REVIEWS CANCER, 17 (11). pp. 692-704. ISSN 1474-175X

Meziane, I., Huhn, S., da Silva, M. I., Weinhold, N., Campo, C., Nickel, J., Hoffmann, P., Nothen, M. M., Jockel, K. H., Landi, S., Mitchell, J. S., Johnson, D., Jauch, A., Morgan, G. J., Houlston, R., Goldschmidt, H., Milani, P., Merlini, G., Rowcieno, D., Hawkins, P., Hegenbart, U., Palladini, G., Wechalekar, A., Forsti, A., Schonland, S. O., Hemminki, K. (2017) Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts. HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 102 (10). E411-E414. ISSN 0390-6078

da Silva, M. L., Forsti, A., Weinhold, N., Meziane, I., Campo, C., Huhn, S., Nickel, J., Hoffmann, P., Nothen, M. M., Jockel, K. H., 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., Schonland, S. O., Hemminki, K. (2017) Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts: comparison with myeloma. LEUKEMIA, 31 (8). pp. 1735-1742. ISSN 0887-6924

Berntsson, S. G., Merrell, R. T., Amirian, E. S., Armstrong, G. N., Lachance, D., Smits, A., Zhou, R. K., 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. JOURNAL OF NEUROLOGY, 265 (6). pp. 1432-1442. ISSN 0340-5354

Macauda, A., Calvetti, D., Maccari, G., Hemminki, K., Forsti, 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., Dudzinski, M., Jurczyszyn, A., Druzd-Sitek, A., Kruszewski, M., Subocz, E., Petrini, M., Iskierka-Jazdzewska, E., Razny, M., Szombath, G., Marques, H., Zawirska, D., Chraniuk, D., Halka, J., Jacobsen, S. E. H., Mazur, G., Sanz, R. G., Dumontet, C., Moreno, V., Stepien, A., Beider, K., Pelosini, M., Reis, R. M., Krawczyk-Kulis, M., Rymko, M., Avet-Loiseau, H., Lesueur, F., Grzasko, 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. INTERNATIONAL JOURNAL OF CANCER, 140 (3). pp. 526-534. ISSN 0020-7136

Went, M., Sud, A., Forsti, A., Halvarsson, B. M., Weinhold, N., Kimber, S., van Duin, M., Thorleifsson, G., Holroydl, A., Johnson, D. C., Li, N., Orlando, G., Law, P. J., Ali, M., Chen, B. W., 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., Jockel, K. H., Johnsson, E., Kristinsson, S. Y., Mellqvist, U. H., 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., Nothen, M. M., Rafnar, T., Ross, F. M., Filho, M. I. D., Thomsen, H., Turesson, I., Vangsted, A., Andersen, N. F., Waage, A., Walker, B. A., Wihlborg, A. K., Broyl, A., Davies, F. E., Thorsteinsdottir, U., Langer, C., Hansson, M., Goldschmidt, H., Kaiser, M., Sonneveld, P., Stefansson, K., Morgans, G. J., Hemminki, K., Nilsson, B., Houlston, R. S., Consortium, Practical (2018) Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma. NATURE COMMUNICATIONS, 9. ISSN 2041-1723

Ji, X. M., Bosse, Y., Landi, M. T., Gui, J., Xiao, X. J., Qian, D., Joubert, P., Lamontagne, M., Li, Y. F., Gorlov, I., de Biasi, M., Han, Y. H., Gorlova, O., Hung, R. J., Wu, X. F., McKay, J., Zong, X. C., Carreras-Torres, R., Christiani, D. C., Caporaso, N., Johansson, M., Liu, G., Bojesen, S. E., Le Marchand, L., Albanes, D., Bickeboller, 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. B., Hong, Y. C., Yuan, J. M., Bertazzi, P. A., Pesatori, A. C., Ye, Y. Q., Diao, N., Su, L., Zhang, R. Y., Brhane, Y., Leighl, N., Johansen, J. S., Mellemgaard, A., Saliba, W., Haiman, C., Wilkens, L., Fernandez-Somoano, A., Fernandez-Tardon, G., van der Heijden, Ehfm, Kim, J. H., Dai, J. C., Hu, Z. B., Davies, M. P. A., Marcus, M. W., Brunnstrom, 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., Bruske, I., Manz, J., Muley, T., Risch, A., Rosenberger, A., Grankvist, K., Johansson, M., Shepherd, F., Tsao, M. S., 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. P., Gao, Y. T., 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. Y., Byun, J., Kamal, A., Zhu, D. K., Tyndale, R. F., Wei, W. Q., Chanock, S., Brennan, P., Amos, C. I. (2018) Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk. NATURE COMMUNICATIONS, 9. ISSN 2041-1723

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., Nothen, M. M., Jockel, K. H., 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. BRITISH JOURNAL OF CANCER, 118 (7). pp. 1020-1027. ISSN 0007-0920

Gu, F. Y., Zhang, H., Hyland, P. L., Berndt, S., Gapstur, S. M., Wheeler, W., Amos, C. I., Bezieau, S., Bickeboller, 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. H., Risch, A., Rossing, M. A., Wichmann, H. E., Shi, J. X., Schernhammer, E., Yu, K., Landi, M. T., Caporaso, N. E., Consortium, Ellipse (2017) Inherited variation in circadian rhythm genes and risks of prostate cancer and three other cancer sites in combined cancer consortia. INTERNATIONAL JOURNAL OF CANCER, 141 (9). pp. 1794-1802. ISSN 0020-7136

Jarvis, D., Mitchell, J. S., Law, P. J., Palin, K., Tuupanen, S., Gylfe, A., Hanninen, U. A., Cajuso, T., Tanskanen, T., Kondelin, J., Kaasinen, E., Sarin, A. P., Kaprio, J., Eriksson, J. G., Rissanen, H., Knekt, P., Pukkala, E., Jousilahti, P., Salomaa, V., Ripatti, S., Palotie, A., Jarvinen, H., Renkonen-Sinisalo, L., Lepisto, A., Bohm, J., Mecklin, J. P., 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. BRITISH JOURNAL OF CANCER, 115 (2). pp. 266-272. ISSN 0007-0920

Rodriguez-Broadbent, H., Law, P. J., Sud, A., Palin, K., Tuupanen, S., Gylfe, A., Hanninen, U. A., Cajuso, T., Tanskanen, T., Kondelin, J., Kaasinen, E., Sarin, A. P., Ripatti, S., Eriksson, J. G., Rissanen, H., Knekt, P., Pukkala, E., Jousilahti, P., Salomaa, V., Palotie, A., Renkonen-Sinisalo, L., Lepisto, A., Bohm, J., Mecklin, J. P., 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. INTERNATIONAL JOURNAL OF CANCER, 140 (12). pp. 2701-2708. ISSN 0020-7136

Frampton, M., Houlston, R. S. (2017) Modeling the prevention of colorectal cancer from the combined impact of host and behavioral risk factors. GENETICS IN MEDICINE, 19 (3). pp. 314-321. ISSN 1098-3600

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, 130 (14). pp. 1639-1643. ISSN 0006-4971

Zuber, V., Marconett, C. N., Shi, J. X., Hua, X., Wheeler, W., Yang, C. C., Song, L., Dale, A. M., Laplana, M., Risch, A., Witoelar, A., Thompson, W. K., Schork, A. J., Bettella, F., Wang, Y. P., Djurovic, S., Zhou, B. Y., Borok, Z., van der Heijden, H. F. M., de Graaf, J., Swinkels, D., Aben, K. K., McKay, J., Hung, R. J., Bikeboller, H., Stevens, V. L., Albanes, D., Caporaso, N. E., Han, Y. H., Wei, Y. 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. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 108 (12). p. 4. ISSN 0027-8874

Tamm, R., Magi, R., Tremmel, R., Winter, S., Mihailov, E., Smid, A., Moricke, A., Klein, K., Schrappe, M., Stanulla, M., Houlston, R., Weinshilboum, R., Rascan, I. M., 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. CLINICAL PHARMACOLOGY & THERAPEUTICS, 101 (5). pp. 684-695. ISSN 0009-9236

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., CSG, Ncri Haemato-oncology (2018) Prediction of outcome in newly diagnosed myeloma: a meta-analysis of the molecular profiles of 1905 trial patients. LEUKEMIA, 32 (1). pp. 102-110. ISSN 0887-6924

May-Wilson, S., Sud, A., Law, P. J., Palin, K., Tuupanen, S., Gylfe, A., Hanninen, U. A., Cajuso, T., Tanskanen, T., Kondelin, J., Kaasinen, E., Sarin, A. P., Eriksson, J. G., Rissanen, H., Knekt, P., Pukkala, E., Jousilahti, P., Salomaa, V., Ripatti, S., Palotie, A., Renkonen-Sinisalo, L., Lepisto, A., Bohm, J., Mecklin, J. P., 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. EUROPEAN JOURNAL OF CANCER, 84. pp. 228-238. ISSN 0959-8049

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. Nature Communications, 7. ISSN 2041-1723

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. JOURNAL OF CLINICAL ONCOLOGY, 35 (14). pp. 1584-1590. ISSN 0732-183X

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, 8 (22). pp. 36203-36210. ISSN 1949-2553

Ostrom, Q. T., Kinnersley, B., Wrensch, M. R., Eckel-Passow, J. E., Armstrong, G., Rice, T., Chen, Y. W., 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. M., Yeager, M., Houlston, R. S., Jenkins, R. B., Melin, B., Bondy, M. L., Barnholtz-Sloan, J. S., GliomaScan, Consortium (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. SCIENTIFIC REPORTS, 8. ISSN 2045-2322

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., Natl Canc Res Inst, Haematology (2018) Subclonal TP53 copy number is associated with prognosis in multiple myeloma. BLOOD, 132 (23). pp. 2465-2469. ISSN 0006-4971

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, 152 (1). pp. 75-77. ISSN 0016-5085

Orlando, G., Law, P. J., Palin, K., Tuupanen, S., Gylfe, A., Hanninen, U. A., Cajuso, T., Tanskanen, T., Kondelin, J., Kaasinen, E., Sarin, A. P., Kaprio, J., Eriksson, J. G., Rissanen, H., Knekt, P., Pukkala, E., Jousilahti, P., Salomaa, V., Ripatti, S., Palotie, A., Jarvinen, H., Renkonen-Sinisalo, L., Lepisto, A., Bohm, J., Mecklin, J. P., 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. HUMAN MOLECULAR GENETICS, 25 (11). pp. 2349-2359. ISSN 0964-6906

Amirian, E. S., Zhou, R. K., 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 EPIDEMIOLOGY BIOMARKERS & PREVENTION, 25 (2). pp. 282-290. ISSN 1055-9965

Ware, J. J., Aveyard, P., Broderick, P., Houlston, R. S., Eisen, T., Munafo, 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 and Alcohol Dependence, 151. pp. 236-240. ISSN 0376-8716

Freitag, D. F., Butterworth, A. S., Willeit, P., Howson, J. M. M., Burgess, S., Kaptoge, S., Young, R., Ho, W. K., Wood, A. M., Sweeting, M., Spackman, S., Staley, J. R., Ramond, A., Harshfield, E., Nielsen, S. F., Grande, P., Lange, L. A., Bown, M. J., Jones, G. T., Scott, R. A., Bevan, S., Porcu, E., Thorleifsson, G., Zeng, L. Y., Kessler, T., Nikpay, M., Do, R., Zhang, W. H., Hopewell, J. C., Kleber, M., Delgado, G. E., Nelson, C. P., Goel, A., Bis, J. C., Dehghan, A., Ligthart, S., Smith, A. V., Qu, L. M., van 't Hof, F. N. G., de Bakker, P. I. W., Baas, A. F., van Rij, A., Tromp, G., Kuivaniemi, H., Ritchie, M. D., Verma, S. S., Crawford, D. C., Malinowski, J., de Andrade, M., Kullo, I. J., Peissig, P. L., McCarty, C. A., Bottinger, E. P., Gottesman, O., Crosslin, D. R., Carrell, D. S., Rasmussen-Torvik, L. J., Pacheco, J. A., Huang, J., Timpson, N. J., Kettunen, J., Ala-Korpela, M., Mitchell, G. F., Parsa, A., Wilkinson, I. B., Gorski, M., Li, Y., Franceschini, N., Keller, M. F., Ganesh, S. K., Langefeld, C. D., Bruijn, L., Brown, M. A., Evans, D. M., Baltic, S., Ferreira, M. A., Baurecht, H., Weidinger, S., Franke, A., Lubitz, S. A., Muller-Nurasyid, M., Felix, J. F., Smith, N. L., Sudman, M., Thompson, S. D., Zeggini, E., Panoutsopoulou, K., Nalls, M. A., Singleton, A., Polychronakos, C., Bradfield, J. P., Hakonarson, H., Easton, D. F., Thompson, D., Tomlinson, I. P., Dunlop, M., Hemminki, K., Morgan, G., Eisen, T., Goldschmidt, H., Allan, J. M., Henrion, M., Whiffin, N., Wang, Y. F., Chubb, D., Houlston, R. S., Iles, M. M., Bishop, D. T., Law, M. H., Hayward, N. K., Luo, Y., Nejentsev, S., Barbalic, M., Crossman, D., Sanna, S., Soranzo, N., Markus, H. S., Wareham, N. J., Rader, D. J., Reilly, M., Assimes, T., Harris, T. B., Hofman, A., Franco, O. H., Gudnason, V., Tracy, R., Psaty, B. M., Farrall, M., Watkins, H., Hall, A. S., Samani, N. J., Marz, W., Clarke, R., Collins, R., Kooner, J. S., Chambers, J. C., Kathiresan, S., McPherson, R., Erdmann, J., Kastrati, A., Schunkert, H., Stefansson, K., Thorsteinsdottir, U., Walston, J. D., Tybjaerg-Hansen, A., Alam, D. S., Majumder, A. A., Di Angelantonio, E., Chowdhury, R., Nordestgaard, B. G., Saleheen, D., Thompson, S. G., Danesh, J., Interleukin 1 Genetics, Consortium, European Prospective Invest, Canc, Aneurysm, Consortium, Elect Med, Records, Genomics, Netwo, Consortium, Uk K., European Prospective Invest, Canc, Consortium, Metastroke, Chronic Kidney Dis Genetics, Consor, Cohorts, Heart, Aging Res, Genomic, Australo-Anglo-Amer, Spondyloarthri, Australian Asthma Genetics, Consort, Atrial Fribrillation Genetics, Cons, Cohorts, Heart, Aging Res, Genomic, Consortium Juvenile Arthritis, Gene, Arthritis Res, U. K. Osteoarthritis Ge, Int Parkinson's Dis, Consortium, Breast Canc Assoc, Consortium, Melanoma Genetics, Consortium, Cohorts, Heart, Aging Res, Genomic, Myocardial Infarction Genetics, Con (2015) Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis. Lancet Diabetes & Endocrinology, 3 (4). pp. 243-253. ISSN 2213-8587

Bartram, T., Burkhardt, B., Wossmann, 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-Munster Study Group. LEUKEMIA & LYMPHOMA, 56 (3). pp. 814-816. ISSN 1042-8194

Kinnersley, B., Chubb, D., Dobbins, S. E., Frampton, M., Buch, S., Timofeeva, M. N., Castellvi-Bel, S., Farrington, S. M., Forsti, A., Hampe, J., Hemminki, K., Hofstra, R. M. W., Northwood, E., Palles, C., Pinheiro, M., Ruiz-Ponte, C., Schafmayer, C., Teixeira, M. R., Westers, H., van Wezel, T., Bishop, D. T., Tomlinson, I., Dunlop, M. G., Houlston, R. S. (2016) Correspondence: SEMA4A variation and risk of colorectal cancer. Nature Communications, 7. ISSN 2041-1723

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. JOURNAL OF CLINICAL ONCOLOGY, 33 (5). pp. 426-432. ISSN 0732-183X

Johnson, D. C., Weinhold, N., Mitchell, J., Chen, B., Stephens, O. W., Forsti, 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, 30 (4). pp. 883-888. ISSN 0887-6924

Johnson, D. C., Weinhold, N., Mitchell, J. S., Chen, B. W., Kaiser, M., Begum, D. B., Hillengass, J., Bertsch, U., Gregory, W. A., Cairns, D., Jackson, G. H., Forsti, A., Nickel, J., Hoffmann, P., Noethen, 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. Nature Communications, 7. ISSN 2041-1723

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. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 107 (1). p. 4. ISSN 0027-8874

Amirian, E. S., Armstrong, G. N., Zhou, R. K., 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., Brannstrom, 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. AMERICAN JOURNAL OF EPIDEMIOLOGY, 183 (2). pp. 85-91. ISSN 0002-9262

Brenner, D. R., Amos, C. I., Brhane, Y., Timofeeva, M. N., Caporaso, N., Wang, Y. F., Christiani, D. C., Bickeboller, 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., Njolstad, I., Chen, C., Goodman, G., Lathrop, M., Vooder, T., Valk, K., Nelis, M., Metspalu, A., Broderick, P., Eisen, T., Wu, X. F., Zhang, D., Chen, W., Spitz, M. R., Wei, Y. 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. A., Marcus, M., McLaughlin, J., Orlow, I., Han, Y. H., Li, Y. F., Zong, X. C., Johansson, M., Liu, G., Tworoger, S. S., Le Marchand, L., Henderson, B. E., Wilkens, L. R., Dai, J. C., Shen, H. B., Houlston, R. S., Landi, M. T., Brennan, P., Hung, R. J., Investigators, Epic (2015) Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia. CARCINOGENESIS, 36 (11). pp. 1314-1326. ISSN 0143-3334

Frampton, M. J. E., 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. ANNALS OF ONCOLOGY, 27 (3). pp. 429-434. ISSN 0923-7534

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., Buchannan, 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. Scientific Reports, 5. ISSN 2045-2322

Kang, X. Z., Liu, H. L., Onaitis, M. W., Liu, Z. S., Owzar, K., Han, Y. H., Su, L., Wei, Y. Y., Hung, R. J., Brhane, Y., McLaughlin, J., Brennan, P., Bickeboller, H., Rosenberger, A., Houlston, R. S., Caporaso, N., Landi, M. T., Heinrich, J., Risch, A., Wu, X. F., Ye, Y. Q., Christiani, D. C., Amos, C. I., Wei, Q. Y., Transdisciplinary Res Canc, Lung (2016) Polymorphisms of the centrosomal gene (FGFR1OP) and lung cancer risk: a meta-analysis of 14 463 cases and 44 188 controls. CARCINOGENESIS, 37 (3). pp. 280-289. ISSN 0143-3334

Li, W. L., Dobbins, S., Tomlinson, I., Houlston, R., Pal, D. K., Strug, L. J. (2015) Prioritizing Rare Variants with Conditional Likelihood Ratios. HUMAN HEREDITY, 79 (1). pp. 5-13. ISSN 0001-5652

Kinnersley, B., Mitchell, J. S., Gousias, K., Schramm, J., Idbaih, A., Labussiere, M., Marie, Y., Rahimian, A., Wichmann, H. E., Schreiber, S., Khe, H. X., Delattre, J. Y., Nothen, 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. Scientific Reports, 5. ISSN 2045-2322

Timofeeva, M. N., Ben, Kinnersley, Farrington, S. M., Whiffin, N., Palles, C., Svinti, V., Lloyd, A., Gorman, M., Ooi, L. Y., 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. A., Hes, F. J., van Wezel, T., Franke, A., Lieb, W., Schafmayer, C., Hampe, J., Buch, S., Propping, P., Hemminki, K., Forsti, A., Westers, H., Hofstra, R., Pinheiro, M., Pinto, C., Teixeira, M., Ruiz-Ponte, C., Fernandez-Rozadilla, C., Carracedo, A., Castells, A., Castellvi-Bel, S., Campbell, H., Bishop, D. T., Tomlinson, I. P. M., Dunlop, M. G., Houlston, R. S. (2015) Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer. Scientific Reports, 5. ISSN 2045-2322

Morris, E. J. A., 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, 10 (2). ISSN 1932-6203

Labreche, K., Simeonova, I., Kamoun, A., Gleize, V., Chubb, D., Letouze, E., Riazalhosseini, Y., Dobbins, S. E., Elarouci, N., Ducray, F., de Reynies, 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. Y., Huillard, E., Lathrop, G. M., Sanson, M., Houlston, R. S., Network, Pola (2015) TCF12 is mutated in anaplastic oligodendroglioma. Nature Communications, 6. ISSN 2041-1723

Kandaswamy, R., Sava, G. P., Speedy, H. E., Bea, S., Martin-Subero, J. I., Studd, J. B., Migliorini, G., Law, P. J., Puente, X. S., Martin-Garcia, D., Salaverria, I., Gutierrez-Abril, J., Lopez-Otin, 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 Reports, 16 (8). pp. 2061-2067. ISSN 2211-1247

Sava, G. P., Speedy, H. E., Di Bernardo, M. C., Dyer, M. J. S., Holroyd, A., Sunter, N. J., Marr, H., Mansouri, L., Deaglios, 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, 29 (3). pp. 748-751. ISSN 0887-6924

Weinhold, N., Meissner, T., Johnson, D. C., Seckinger, A., Moreaux, J., Forsti, A., Chen, B. W., Nickel, J., Chubb, D., Rawstron, A. C., Doughty, C., Dahir, N. B., Begum, D. B., Young, K., Walker, B. A., Hoffmann, P., Nothen, 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-THE HEMATOLOGY JOURNAL, 100 (3). E110-E113. ISSN 0390-6078

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. Scientific Reports, 5. ISSN 2045-2322

Jager, 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. Nature Communications, 6. ISSN 2041-1723

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 RESEARCH, 76 (6). pp. 1485-1493. ISSN 0008-5472

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O

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Litchfield, K., Mitchell, J. S., Shipley, J., Huddart, R., Meyts, E. R. D., Skakkebaek, N. E., Houlston, R. S., Turnbull, C. (2015) Polygenic susceptibility to testicular cancer: implications for personalised health care. BRITISH JOURNAL OF CANCER, 113 (10). pp. 1512-1518. ISSN 0007-0920

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