Items where Division or Clinical Unit is:
ICR divisions > Molecular Pathology > Myeloma Group
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- ICR divisions (92)
- Molecular Pathology (92)
- Myeloma Group (92)
- Molecular Pathology (92)
- ICR divisions (92)
C
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
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Cytochrome P450 Allele CYP3A7*1C Associates with Adverse Outcomes in Chronic Lymphocytic Leukemia, Breast, and Lung Cancer.
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The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A.
Scientific Reports, 5.
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Vijayakrishnan, J., Kumar, R., Henrion, M. Y. R., Moorman, A. V., Rachakonda, P. S., Hosen, I., da Silva, 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., Nothen, M. M., Heilmann-Heimbach, S., Jockel, K. H., Greaves, M., Harrison, C. J., Bartram, C. R., Schrappe, M., Stanulla, M., Hemminki, K., Houlston, R. S.
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A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1.
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Genome-wide association study identifies multiple risk loci for renal cell carcinoma.
Nature Communications, 8.
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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.
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Multiple myeloma risk variant at 7p15.3 creates an IRF4-binding site and interferes with CDCA7L expression.
Nature Communications, 7.
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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., 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.
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Impact of atopy on risk of glioma: a Mendelian randomisation study.
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Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.
Scientific Reports, 5.
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Sud, A., Thomsen, H., Law, P. J., Forsti, A., da Silva, 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., Hoffmann, P., Nothen, M. M., Jockel, K. H., von 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., Consortium, Practical
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Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility.
NATURE COMMUNICATIONS, 8.
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Kinnersley, B., Kamatani, Y., Labussiere, M., Wang, Y. F., Galan, P., Mokhtari, K., Delattre, J. Y., Gousias, K., Schramm, J., Schoemaker, M. J., Swerdlow, A., Fleming, S. J., Herms, S., Heilmann, S., Nothen, M. M., Simon, M., Sanson, M., Lathrop, M., Houlston, R. S.
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Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis.
EUROPEAN JOURNAL OF HUMAN GENETICS, 24 (5).
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Identification of 19 new risk loci and potential regulatory mechanisms influencing susceptibility to testicular germ cell tumor.
NATURE GENETICS, 49 (7).
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Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma (vol 72, pg 747, 2017).
[Correction]
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Large-scale Analysis Demonstrates Familial Testicular Cancer to have Polygenic Aetiology.
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BRITISH JOURNAL OF CANCER, 113 (10).
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Genome-wide homozygosity signature and risk of Hodgkin lymphoma.
Scientific Reports, 5.
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Kinnersley, B., Labussiere, M., Holroyd, A., Di Stefano, A. L., Broderick, P., Vijayakrishnan, J., Mokhtari, K., Delattre, J. Y., Gousias, K., Schramm, J., Schoemaker, M. J., Fleming, S. J., Herms, S., Heilmann, S., Schreiber, S., Wichmann, H. E., Nothen, M. M., Swerdlow, A., Lathrop, M., Simon, M., Bondy, M., Sanson, M., Houlston, R. S.
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Genome-wide association study identifies multiple susceptibility loci for glioma.
Nature Communications, 6.
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Quantifying the heritability of testicular germ cell tumour using both population-based and genomic approaches.
Scientific Reports, 5.
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Rare disruptive mutations in ciliary function genes contribute to testicular cancer susceptibility.
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