Section of Epidemiology and Biostatistics

2011 Publications

Yokoyama, S., Woods, S. L., Boyle, G. M., Aoude, L. G., Macgregor, S., Zismann, V., Gartside, M., Cust, A. E., Haq, R., Harland, M., Taylor, J. C., Duffy, D. L., Holohan, K., Dutton-Regester, K., Palmer, J. M., Bonazzi, V., Stark, M. S., Symmons, J., Law, M. H., Schmidt, C., Lanagan, C., O'Connor, L., Holland, E. A., Schmid, H., Maskiell, J. A., Jetann, J., Ferguson, M., Jenkins, M. A., Kefford, R. F., Giles, G. G., Armstrong, B. K., Aitken, J. F., Hopper, J. L., Whiteman, D. C., Pharoah, P. D., Easton, D. F., Dunning, A. M., Newton-Bishop, J. A., Montgomery, G. W., Martin, N. G., Mann, G. J., Bishop, D. T., Tsao, H., Trent, J. M., Fisher, D. E., Hayward, N. K., and Brown, K. M. A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma. Nature, 2011.

Winney, B., Boumertit, A., Day, T., Davison, D., Echeta, C., Evseeva, I., Hutnik, K., Leslie, S., Nicodemus, K., Royrvik, E. C., Tonks, S., Yang, X., Cheshire, J., Longley, P., Mateos, P., Groom, A., Relton, C., Bishop, D. T., Black, K., Northwood, E., Parkinson, L., Frayling, T. M., Steele, A., Sampson, J. R., King, T., Dixon, R., Middleton, D., Jennings, B., Bowden, R., Donnelly, P., and Bodmer, W. People of the British Isles: preliminary analysis of genotypes and surnames in a UK-control population. European journal of human genetics : EJHG, 2011.

van der Ploeg, A. P., van Akkooi, A. C., Rutkowski, P., Nowecki, Z. I., Michej, W., Mitra, A., Newton-Bishop, J. A., Cook, M., van der Ploeg, I. M., Nieweg, O. E., van den Hout, M. F., van Leeuwen, P. A., Voit, C. A., Cataldo, F., Testori, A., Robert, C., Hoekstra, H. J., Verhoef, C., Spatz, A., and Eggermont, A. M. Prognosis in patients with sentinel node-positive melanoma is accurately defined by the combined rotterdam tumor load and dewar topography criteria. Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 29: 2206-14, 2011.

Suppa, M., Elliott, F., Mikeljevic, J. S., Mukasa, Y., Chan, M., Leake, S., Karpavicius, B., Haynes, S., Bakker, E., Peris, K., Barrett, J. H., Bishop, D. T., and Newton Bishop, J. A. The determinants of periorbital skin ageing in participants of a melanoma case-control study in the U.K. The British journal of dermatology, 165: 1011-21, 2011.

Storr, S. J., Safuan, S., Mitra, A., Elliott, F., Walker, C., Vasko, M. J., Ho, B., Cook, M., Mohammed, R. A., Patel, P. M., Ellis, I. O., Newton-Bishop, J. A., and Martin, S. G. Objective assessment of blood and lymphatic vessel invasion and association with macrophage infiltration in cutaneous melanoma. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2011.

Schmidt, H. M., Ha, D. M., Taylor, E. F., Kovach, Z., Goh, K. L., Fock, K. M., Barrett, J. H., Forman, D., and Mitchell, H. Variation in human genetic polymorphisms, their association with H pylori acquisition and gastric cancer in a multi-ethnic country. Journal of gastroenterology and hepatology, 2011.

Richman, S. D., Barrett, J. H., and Seymour, M. T. Failure to validate toxicity and outcome biomarkers from the FFCD 2000-05 trial in the MRC CR08 FOCUS trial. Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 29: e354-5; author reply e356-7, 2011.

Rafnar, T., Vermeulen, S. H., Sulem, P., Thorleifsson, G., Aben, K. K., Witjes, J. A., Grotenhuis, A. J., Verhaegh, G. W., Hulsbergen-van de Kaa, C. A., Besenbacher, S., Gudbjartsson, D., Stacey, S. N., Gudmundsson, J., Johannsdottir, H., Bjarnason, H., Zanon, C., Helgadottir, H., Jonasson, J. G., Tryggvadottir, L., Jonsson, E., Geirsson, G., Nikulasson, S., Petursdottir, V., Bishop, D. T., Chung-Sak, S., Choudhury, A., Elliott, F., Barrett, J. H., Knowles, M. A., de Verdier, P. J., Ryk, C., Lindblom, A., Rudnai, P., Gurzau, E., Koppova, K., Vineis, P., Polidoro, S., Guarrera, S., Sacerdote, C., Panadero, A., Sanz-Velez, J. I., Sanchez, M., Valdivia, G., Garcia-Prats, M. D., Hengstler, J. G., Selinski, S., Gerullis, H., Ovsiannikov, D., Khezri, A., Aminsharifi, A., Malekzadeh, M., van den Berg, L. H., Ophoff, R. A., Veldink, J. H., Zeegers, M. P., Kellen, E., Fostinelli, J., Andreoli, D., Arici, C., Porru, S., Buntinx, F., Ghaderi, A., Golka, K., Mayordomo, J. I., Matullo, G., Kumar, R., Steineck, G., Kiltie, A. E., Kong, A., Thorsteinsdottir, U., Stefansson, K., and Kiemeney, L. A. European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene. Human molecular genetics, 2011.

Qiao, B., Scott, G. B., Elliott, F., Vaslin, L., Bentley, J., Hall, J., Bishop, D. T., Knowles, M. A., and Kiltie, A. E. Functional assays to determine the significance of two common XPC 3'UTR variants found in bladder cancer patients. BMC medical genetics, 12: 84, 2011.

Qiao, B., Ansari, A. H., Scott, G. B., Sak, S. C., Chambers, P. A., Elliott, F., Teo, M. T., Bentley, J., Churchman, M., Hall, J., Taylor, C. F., Bishop, D. T., Knowles, M. A., and Kiltie, A. E. In vitro functional effects of XPC gene rare variants from bladder cancer patients. Carcinogenesis, 2011.

Olsen, C. M., Zens, M. S., Green, A. C., Stukel, T. A., Holman, C. D., Mack, T., Elwood, J. M., Holly, E. A., Sacerdote, C., Gallagher, R., Swerdlow, A. J., Armstrong, B. K., Rosso, S., Kirkpatrick, C., Zanetti, R., Bishop, J. N., Bataille, V., Chang, Y. M., Mackie, R., Osterlind, A., Berwick, M., Karagas, M. R., and Whiteman, D. C. Biologic markers of sun exposure and melanoma risk in women: pooled case-control analysis. International journal of cancer. Journal international du cancer, 129: 713-23, 2011.

Nsengimana, J., and Barrett, J. H. Analysis of genetic interactions involving maternal and offspring genotypes at different loci: power simulation and application to testicular cancer. Genetic Epidemiology, Submitted, 2011.

Newton-Bishop, J. A., Chang, Y. M., Elliott, F., Chan, M., Leake, S., Karpavicius, B., Haynes, S., Fitzgibbon, E., Kukalizch, K., Randerson-Moor, J., Elder, D. E., Bishop, D. T., and Barrett, J. H. Relationship between sun exposure and melanoma risk for tumours in different body sites in a large case-control study in a temperate climate. Eur J Cancer, 2011.

Macgregor, S., Montgomery, G. W., Liu, J. Z., Zhao, Z. Z., Henders, A. K., Stark, M., Schmid, H., Holland, E. A., Duffy, D. L., Zhang, M., Painter, J. N., Nyholt, D. R., Maskiell, J. A., Jetann, J., Ferguson, M., Cust, A. E., Jenkins, M. A., Whiteman, D. C., Olsson, H., Puig, S., Bianchi-Scarra, G., Hansson, J., Demenais, F., Landi, M. T., Debniak, T., Mackie, R., Azizi, E., Bressac-de Paillerets, B., Goldstein, A. M., Kanetsky, P. A., Gruis, N. A., Elder, D. E., Newton-Bishop, J. A., Bishop, D. T., Iles, M. M., Helsing, P., Amos, C. I., Wei, Q., Wang, L. E., Lee, J. E., Qureshi, A. A., Kefford, R. F., Giles, G. G., Armstrong, B. K., Aitken, J. F., Han, J., Hopper, J. L., Trent, J. M., Brown, K. M., Martin, N. G., Mann, G. J., and Hayward, N. K. Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3. Nature genetics, 2011.

Lang, J. M., Shennan, M., Njauw, J. C., Luo, S., Bishop, J. N., Harland, M., Hayward, N. K., Tucker, M. A., Goldstein, A. M., Landi, M. T., Puig, S., Gruis, N. A., Bergman, W., Bianchi-Scarra, G., Ghiorzo, P., Hogg, D., and Tsao, H. A flexible multiplex bead-based assay for detecting germline CDKN2A and CDK4 variants in melanoma-prone kindreds. J Invest Dermatol, 131: 480-6, 2011.

Konig, R. I., and Nsengimana, J. Multiple testing in high-throughput sequence data: experiences from group 8 of the genetic analysis workship 17. Genetic Epidemiology, In press, 2011.

Iles, M. M. Genome-wide association studies. Methods Mol Biol, 713: 89-103, 2011.

Field, S., and Newton-Bishop, J. A. Melanoma and vitamin D, 1878-0261 (Electronic) 1574-7891 (Linking), 2011.

Elliott, F., Suppa, M., Chan, M., Leake, S., Karpavicius, B., Haynes, S., Barrett, J. H., Bishop, D. T., and Newton-Bishop, J. A. Relationship between sunbed use and melanoma risk in a large case-control study in the United Kingdom. International journal of cancer. Journal international du cancer, 2011.

Davies, J. R., Chang, Y. M., Snowden, H., Chan, M., Leake, S., Karpavicius, B., Haynes, S., Kukalizch, K., Randerson-Moor, J., Elliott, F., Barth, J., Kanetsky, P. A., Harland, M., Bishop, D. T., Barrett, J. H., and Newton-Bishop, J. A. The determinants of serum vitamin D levels in participants in a melanoma case-control study living in a temperate climate. Cancer causes & control : CCC, 22: 1471-82, 2011.

Cust, A. E., Harland, M., Makalic, E., Schmidt, D., Dowty, J. G., Aitken, J. F., Agha-Hamilton, C., Armstrong, B. K., Barrett, J. H., Chan, M., Chang, Y. M., Gascoyne, J., Giles, G. G., Holland, E. A., Kefford, R. F., Kukalizch, K., Lowery, J., Randerson-Moor, J. A., Schmid, H., Taylor, C. F., Whitaker, L., Hopper, J. L., Newton-Bishop, J. A., Mann, G. J., Bishop, D. T., and Jenkins, M. A. Melanoma risk for CDKN2A mutation carriers who are relatives of population-based case carriers in Australia and the UK. J Med Genet, 2011.

Coulthard, L. R., Taylor, J. C., Eyre, S., Robinson, J. I., Wilson, A. G., Isaacs, J. D., Hyrich, K., Emery, P., Barton, A., Barrett, J. H., Morgan, A. W., and McDermott, M. F. Genetic variants within the MAP kinase signalling network and anti-TNF treatment response in rheumatoid arthritis patients. Ann Rheum Dis, 70: 98-103, 2011.

Cairns, D. A. Statistical issues in quality control of proteomic analyses: Good experimental design and planning. Proteomics, 2011.

Burn, J., Bishop, D. T., Chapman, P. D., Elliott, F., Bertario, L., Dunlop, M. G., Eccles, D., Ellis, A., Evans, D. G., Fodde, R., Maher, E. R., Moslein, G., Vasen, H. F., Coaker, J., Phillips, R. K., Bulow, S., and Mathers, J. C. A Randomized Placebo-Controlled Prevention Trial of Aspirin and/or Resistant Starch in Young People with Familial Adenomatous Polyposis. Cancer prevention research, 4: 655-665, 2011.

Barrett, J. H., and Nsengimana, J. Two-stage analyses of sequence variants in assoication with quantitative traits. BMC Proceedings, In Press, 2011.

Barrett, J. H., Iles, M. M., Harland, M., Taylor, J. C., Aitken, J. F., Andresen, P. A., Akslen, L. A., Armstrong, B. K., Avril, M. F., Azizi, E., Bakker, B., Bergman, W., Bianchi-Scarra, G., Bressac-de Paillerets, B., Calista, D., Cannon-Albright, L. A., Corda, E., Cust, A. E., Debniak, T., Duffy, D., Dunning, A. M., Easton, D. F., Friedman, E., Galan, P., Ghiorzo, P., Giles, G. G., Hansson, J., Hocevar, M., Hoiom, V., Hopper, J. L., Ingvar, C., Janssen, B., Jenkins, M. A., Jonsson, G., Kefford, R. F., Landi, G., Landi, M. T., Lang, J., Lubinski, J., Mackie, R., Malvehy, J., Martin, N. G., Molven, A., Montgomery, G. W., van Nieuwpoort, F. A., Novakovic, S., Olsson, H., Pastorino, L., Puig, S., Puig-Butille, J. A., Randerson-Moor, J., Snowden, H., Tuominen, R., Van Belle, P., van der Stoep, N., Whiteman, D. C., Zelenika, D., Han, J., Fang, S., Lee, J. E., Wei, Q., Lathrop, G. M., Gillanders, E. M., Brown, K. M., Goldstein, A. M., Kanetsky, P. A., Mann, G. J., Macgregor, S., Elder, D. E., Amos, C. I., Hayward, N. K., Gruis, N. A., Demenais, F., Bishop, J. A., and Bishop, D. T. Genome-wide association study identifies three new melanoma susceptibility loci. Nature genetics, 2011.

Barrett, J. H. Coronary artery disease: an example case study. Methods Mol Biol, 713: 215-25, 2011.

Amos, C. I., Wang, L. E., Lee, J. E., Gershenwald, J. E., Chen, W. V., Fang, S., Kosoy, R., Zhang, M., Qureshi, A. A., Vattathil, S., Schacherer, C. W., Gardner, J. M., Wang, Y., Bishop, D. T., Barrett, J. H., Macgregor, S., Hayward, N. K., Martin, N. G., Duffy, D. L., Mann, G. J., Cust, A., Hopper, J., Brown, K. M., Grimm, E. A., Xu, Y., Han, Y., Jing, K., McHugh, C., Laurie, C. C., Doheny, K. F., Pugh, E. W., Seldin, M. F., Han, J., and Wei, Q. Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. Human molecular genetics, 2011.

2010 Publications

Zauber, N. P., Denehy, T. R., Taylor, R. R., Ongcapin, E. H., Marotta, S. P., Sabbath-Solitare, M., Kulkarni, R., Pradhan, T. S., Hermelin, D., and Bishop, D. T. Microsatellite instability and DNA methylation of endometrial tumors and clinical features in young women compared with older women. International journal of gynecological cancer : official journal of the International Gynecological Cancer Society, 20: 1549-56, 2010.

Turnbull, C., Rapley, E. A., Seal, S., Pernet, D., Renwick, A., Hughes, D., Ricketts, M., Linger, R., Nsengimana, J., Deloukas, P., Huddart, R. A., Bishop, D. T., Easton, D. F., Stratton, M. R., and Rahman, N. Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer. Nature genetics, 42: 604-7, 2010.

Santibanez Koref, M., Wilson, V., Cartwright, N., Cunnington, M. S., Mathers, J. C., Bishop, D. T., Curtis, A., Dunlop, M. G., and Burn, J. MLH1 Differential allelic expression in mutation carriers and controls. Ann Hum Genet, 74: 479-88, 2010.

Rothman, N., Garcia-Closas, M., Chatterjee, N., Malats, N., Wu, X., Figueroa, J. D., Real, F. X., Van Den Berg, D., Matullo, G., Baris, D., Thun, M., Kiemeney, L. A., Vineis, P., De Vivo, I., Albanes, D., Purdue, M. P., Rafnar, T., Hildebrandt, M. A., Kiltie, A. E., Cussenot, O., Golka, K., Kumar, R., Taylor, J. A., Mayordomo, J. I., Jacobs, K. B., Kogevinas, M., Hutchinson, A., Wang, Z., Fu, Y. P., Prokunina-Olsson, L., Burdett, L., Yeager, M., Wheeler, W., Tardon, A., Serra, C., Carrato, A., Garcia-Closas, R., Lloreta, J., Johnson, A., Schwenn, M., Karagas, M. R., Schned, A., Andriole, G., Jr., Grubb, R., 3rd, Black, A., Jacobs, E. J., Diver, W. R., Gapstur, S. M., Weinstein, S. J., Virtamo, J., Cortessis, V. K., Gago-Dominguez, M., Pike, M. C., Stern, M. C., Yuan, J. M., Hunter, D. J., McGrath, M., Dinney, C. P., Czerniak, B., Chen, M., Yang, H., Vermeulen, S. H., Aben, K. K., Witjes, J. A., Makkinje, R. R., Sulem, P., Besenbacher, S., Stefansson, K., Riboli, E., Brennan, P., Panico, S., Navarro, C., Allen, N. E., Bueno-de-Mesquita, H. B., Trichopoulos, D., Caporaso, N., Landi, M. T., Canzian, F., Ljungberg, B., Tjonneland, A., Clavel-Chapelon, F., Bishop, D. T., Teo, M. T., Knowles, M. A., Guarrera, S., Polidoro, S., Ricceri, F., Sacerdote, C., Allione, A., Cancel-Tassin, G., Selinski, S., Hengstler, J. G., Dietrich, H., Fletcher, T., Rudnai, P., Gurzau, E., Koppova, K., Bolick, S. C., Godfrey, A., Xu, Z., et al. A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. Nat Genet, 42: 978-84, 2010.

Newton-Bishop, J. A., Chang, Y. M., Iles, M. M., Taylor, J. C., Bakker, B., Chan, M., Leake, S., Karpavicius, B., Haynes, S., Fitzgibbon, E., Elliott, F., Kanetsky, P. A., Harland, M., Barrett, J. H., and Bishop, D. T. Melanocytic nevi, nevus genes, and melanoma risk in a large case-control study in the United Kingdom. Cancer Epidemiol Biomarkers Prev, 19: 2043-54, 2010.

Newton-Bishop, J., and Gruis, N. Melanoma susceptibility genes. Melanoma Res, 20: 161-2, 2010.

Marsden, J. R., Newton-Bishop, J. A., Burrows, L., Cook, M., Corrie, P. G., Cox, N. H., Gore, M. E., Lorigan, P., MacKie, R., Nathan, P., Peach, H., Powell, B., and Walker, C. Revised U.K. guidelines for the management of cutaneous melanoma 2010. Br J Dermatol, 163: 238-56, 2010.

Marsden, J. R., Newton-Bishop, J. A., Burrows, L., Cook, M., Corrie, P. G., Cox, N. H., Gore, M. E., Lorigan, P., Mackie, R., Nathan, P., Peach, H., Powell, B., and Walker, C. Revised UK guidelines for the management of cutaneous melanoma 2010. J Plast Reconstr Aesthet Surg, 63: 1401-19, 2010.

Mai, P. L., Friedlander, M., Tucker, K., Phillips, K. A., Hogg, D., Jewett, M. A., Lohynska, R., Daugaard, G., Richard, S., Bonaiti-Pellie, C., Heidenreich, A., Albers, P., Bodrogi, I., Geczi, L., Olah, E., Daly, P. A., Guilford, P., Fossa, S. D., Heimdal, K., Liubchenko, L., Tjulandin, S. A., Stoll, H., Weber, W., Easton, D. F., Dudakia, D., Huddart, R., Stratton, M. R., Einhorn, L., Korde, L., Nathanson, K. L., Bishop, D. T., Rapley, E. A., and Greene, M. H. The International Testicular Cancer Linkage Consortium: a clinicopathologic descriptive analysis of 461 familial malignant testicular germ cell tumor kindred. Urol Oncol, 28: 492-9, 2010.

Kadyan, A., Aralikatti, A., Shah, S., Jewell, R., Paul, L., Darling, J., Wood, M., Gooi, J., Morrell, A. J., Newton Bishop, J. A., and Marr, J. E. Laryngo-onycho-cutaneous syndrome. Ophthalmology, 117: 1056-1056 e2, 2010.

Jewell, R., Conway, C., Mitra, A., Randerson-Moor, J., Lobo, S., Nsengimana, J., Harland, M., Marples, M., Edward, S., Cook, M., Powell, B., Boon, A., de Kort, F., Parker, K. A., Cree, I. A., Barrett, J. H., Knowles, M. A., Bishop, D. T., and Newton-Bishop, J. Patterns of expression of DNA repair genes and relapse from melanoma. Clin Cancer Res, 16: 5211-21, 2010.

Garbe, C., Peris, K., Hauschild, A., Saiag, P., Middleton, M., Spatz, A., Grob, J. J., Malvehy, J., Newton-Bishop, J., Stratigos, A., Pehamberger, H., and Eggermont, A. Diagnosis and treatment of melanoma: European consensus-based interdisciplinary guideline. Eur J Cancer, 46: 270-83, 2010.

Duffy, D. L., Iles, M. M., Glass, D., Zhu, G., Barrett, J. H., Hoiom, V., Zhao, Z. Z., Sturm, R. A., Soranzo, N., Hammond, C., Kvaskoff, M., Whiteman, D. C., Mangino, M., Hansson, J., Newton-Bishop, J. A., Bataille, V., Hayward, N. K., Martin, N. G., Bishop, D. T., Spector, T. D., and Montgomery, G. W. IRF4 variants have age-specific effects on nevus count and predispose to melanoma. American journal of human genetics, 87: 6-16, 2010.

Demenais, F., Mohamdi, H., Chaudru, V., Goldstein, A. M., Newton Bishop, J. A., Bishop, D. T., Kanetsky, P. A., Hayward, N. K., Gillanders, E., Elder, D. E., Avril, M. F., Azizi, E., van Belle, P., Bergman, W., Bianchi-Scarra, G., Bressac-de Paillerets, B., Calista, D., Carrera, C., Hansson, J., Harland, M., Hogg, D., Hoiom, V., Holland, E. A., Ingvar, C., Landi, M. T., Lang, J. M., Mackie, R. M., Mann, G. J., Ming, M. E., Njauw, C. J., Olsson, H., Palmer, J., Pastorino, L., Puig, S., Randerson-Moor, J., Stark, M., Tsao, H., Tucker, M. A., van der Velden, P., Yang, X. R., and Gruis, N. Association of MC1R variants and host phenotypes with melanoma risk in CDKN2A mutation carriers: a GenoMEL study. J Natl Cancer Inst, 102: 1568-83, 2010.

Coulthard, L. R., Taylor, J. C., Eyre, S., Robinson, J. I., Wilson, A. G., Isaacs, J. D., Hyrich, K., Emery, P., Barton, A., Barrett, J. H., Morgan, A. W., and McDermott, M. F. Genetic variants within the MAP kinase signalling network and anti-TNF treatment response in rheumatoid arthritis patients. Ann Rheum Dis, 70: 98-103, 2010.

Conway, C., Beswick, S., Elliott, F., Chang, Y. M., Randerson-Moor, J., Harland, M., Affleck, P., Marsden, J., Sanders, D. S., Boon, A., Knowles, M. A., Bishop, D. T., and Newton-Bishop, J. A. Deletion at chromosome arm 9p in relation to BRAF/NRAS mutations and prognostic significance for primary melanoma. Genes, chromosomes & cancer, 49: 425-38, 2010.

Choudhury, A., Nelson, L. D., Teo, M. T., Chilka, S., Bhattarai, S., Johnston, C. F., Elliott, F., Lowery, J., Taylor, C. F., Churchman, M., Bentley, J., Knowles, M. A., Harnden, P., Bristow, R. G., Bishop, D. T., and Kiltie, A. E. MRE11 expression is predictive of cause-specific survival following radical radiotherapy for muscle-invasive bladder cancer. Cancer Res, 70: 7017-26, 2010.

Brown, B. D., Nsengimana, J., Barrett, J. H., Lawrence, R. A., Steiner, L., Cheng, S., Bishop, D. T., Samani, N. J., Ball, S. G., Balmforth, A. J., and Hall, A. S. An evaluation of inflammatory gene polymorphisms in sibships discordant for premature coronary artery disease: the GRACE-IMMUNE study. BMC Med, 8: 5, 2010.

Branstrom, R., Kasparian, N. A., Chang, Y. M., Affleck, P., Tibben, A., Aspinwall, L. G., Azizi, E., Baron-Epel, O., Battistuzzi, L., Bergman, W., Bruno, W., Chan, M., Cuellar, F., Debniak, T., Pjanova, D., Ertmanski, S., Figl, A., Gonzalez, M., Hayward, N. K., Hocevar, M., Kanetsky, P. A., Leachman, S. A., Heisele, O., Palmer, J., Peric, B., Puig, S., Schadendorf, D., Gruis, N. A., Newton-Bishop, J., and Brandberg, Y. Predictors of sun protection behaviors and severe sunburn in an international online study. Cancer Epidemiol Biomarkers Prev, 19: 2199-210, 2010.

Bennett, C. E., Nsengimana, J., Bostock, J. A., Cymbalista, C., Futers, T. S., Knight, B. L., McCormack, L. J., Prasad, U. K., Riches, K., Rolton, D., Scarrott, T., Barrett, J. H., and Carter, A. M. CCAAT/enhancer binding protein alpha, beta and delta gene variants: associations with obesity related phenotypes in the Leeds Family Study. Diab Vasc Dis Res, 7: 195-203, 2010.

2009 Publications

Zauber, N. P., Marotta, S. P., Berman, E., Grann, A., Rao, M., Komati, N., Ribiero, K., and Bishop, D. T. Molecular genetic changes associated with colorectal carcinogenesis are not prognostic for tumor regression following preoperative chemoradiation of rectal carcinoma. Int J Radiat Oncol Biol Phys, 74: 472-6, 2009.

Wu, X., Ye, Y., Kiemeney, L. A., Sulem, P., Rafnar, T., Matullo, G., Seminara, D., Yoshida, T., Saeki, N., Andrew, A. S., Dinney, C. P., Czerniak, B., Zhang, Z. F., Kiltie, A. E., Bishop, D. T., Vineis, P., Porru, S., Buntinx, F., Kellen, E., Zeegers, M. P., Kumar, R., Rudnai, P., Gurzau, E., Koppova, K., Mayordomo, J. I., Sanchez, M., Saez, B., Lindblom, A., de Verdier, P., Steineck, G., Mills, G. B., Schned, A., Guarrera, S., Polidoro, S., Chang, S. C., Lin, J., Chang, D. W., Hale, K. S., Majewski, T., Grossman, H. B., Thorlacius, S., Thorsteinsdottir, U., Aben, K. K., Witjes, J. A., Stefansson, K., Amos, C. I., Karagas, M. R., and Gu, J. Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer. Nat Genet, 41: 991-5, 2009.

Taioli, E., Garza, M. A., Ahn, Y. O., Bishop, D. T., Bost, J., Budai, B., Chen, K., Gemignani, F., Keku, T., Lima, C. S., Le Marchand, L., Matsuo, K., Moreno, V., Plaschke, J., Pufulete, M., Thomas, S. B., Toffoli, G., Wolf, C. R., Moore, C. G., and Little, J. Meta- and pooled analyses of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and colorectal cancer: a HuGE-GSEC review. Am J Epidemiol, 170: 1207-21, 2009.

Stern, M. C., Lin, J., Figueroa, J. D., Kelsey, K. T., Kiltie, A. E., Yuan, J. M., Matullo, G., Fletcher, T., Benhamou, S., Taylor, J. A., Placidi, D., Zhang, Z. F., Steineck, G., Rothman, N., Kogevinas, M., Silverman, D., Malats, N., Chanock, S., Wu, X., Karagas, M. R., Andrew, A. S., Nelson, H. H., Bishop, D. T., Sak, S. C., Choudhury, A., Barrett, J. H., Elliot, F., Corral, R., Joshi, A. D., Gago-Dominguez, M., Cortessis, V. K., Xiang, Y. B., Gao, Y. T., Vineis, P., Sacerdote, C., Guarrera, S., Polidoro, S., Allione, A., Gurzau, E., Koppova, K., Kumar, R., Rudnai, P., Porru, S., Carta, A., Campagna, M., Arici, C., Park, S. S., and Garcia-Closas, M. Polymorphisms in DNA repair genes, smoking, and bladder cancer risk: findings from the international consortium of bladder cancer. Cancer Res, 69: 6857-64, 2009.

Silva Idos, S., Higgins, C. D., Abramsky, T., Swanwick, M. A., Frazer, J., Whitaker, L. M., Blanshard, M. E., Bradshaw, J., Apps, J. M., Bishop, D. T., Newton-Bishop, J. A., and Swerdlow, A. J. Overseas sun exposure, nevus counts, and premature skin aging in young English women: a population-based survey. J Invest Dermatol, 129: 50-9, 2009.

Robinson, J. I., Barrett, J. H., Taylor, J. C., Naven, M., Corscadden, D., Barton, A., Wilson, A. G., Emery, P., Isaacs, J. D., and Morgan, A. W. Dissection of the FCGR3A association with RA: increased association in men and with autoantibody positive disease. Ann Rheum Dis, 69: 1054-7, 2009.

Richman, S. D., Seymour, M. T., Chambers, P., Elliott, F., Daly, C. L., Meade, A. M., Taylor, G., Barrett, J. H., and Quirke, P. KRAS and BRAF mutations in advanced colorectal cancer are associated with poor prognosis but do not preclude benefit from oxaliplatin or irinotecan: results from the MRC FOCUS trial. J Clin Oncol, 27: 5931-7, 2009.

Rice, A., Nsengimana, J., Simmons, I. G., Toomes, C., Hoole, J., Willoughby, C. E., Cassidy, F., Williams, G. A., George, N. D., Sheridan, E., Young, T. L., Hunter, T. I., Barrett, B. T., Elliott, D. B., Bishop, D. T., and Inglehearn, C. F. Replication of the recessive STBMS1 locus but with dominant inheritance. Invest Ophthalmol Vis Sci, 50: 3210-7, 2009.

Rapley, E. A., Turnbull, C., Al Olama, A. A., Dermitzakis, E. T., Linger, R., Huddart, R. A., Renwick, A., Hughes, D., Hines, S., Seal, S., Morrison, J., Nsengimana, J., Deloukas, P., Rahman, N., Bishop, D. T., Easton, D. F., and Stratton, M. R. A genome-wide association study of testicular germ cell tumor. Nat Genet, 41: 807-10, 2009.

Rafnar, T., Sulem, P., Stacey, S. N., Geller, F., Gudmundsson, J., Sigurdsson, A., Jakobsdottir, M., Helgadottir, H., Thorlacius, S., Aben, K. K., Blondal, T., Thorgeirsson, T. E., Thorleifsson, G., Kristjansson, K., Thorisdottir, K., Ragnarsson, R., Sigurgeirsson, B., Skuladottir, H., Gudbjartsson, T., Isaksson, H. J., Einarsson, G. V., Benediktsdottir, K. R., Agnarsson, B. A., Olafsson, K., Salvarsdottir, A., Bjarnason, H., Asgeirsdottir, M., Kristinsson, K. T., Matthiasdottir, S., Sveinsdottir, S. G., Polidoro, S., Hoiom, V., Botella-Estrada, R., Hemminki, K., Rudnai, P., Bishop, D. T., Campagna, M., Kellen, E., Zeegers, M. P., de Verdier, P., Ferrer, A., Isla, D., Vidal, M. J., Andres, R., Saez, B., Juberias, P., Banzo, J., Navarrete, S., Tres, A., Kan, D., Lindblom, A., Gurzau, E., Koppova, K., de Vegt, F., Schalken, J. A., van der Heijden, H. F., Smit, H. J., Termeer, R. A., Oosterwijk, E., van Hooij, O., Nagore, E., Porru, S., Steineck, G., Hansson, J., Buntinx, F., Catalona, W. J., Matullo, G., Vineis, P., Kiltie, A. E., Mayordomo, J. I., Kumar, R., Kiemeney, L. A., Frigge, M. L., Jonsson, T., Saemundsson, H., Barkardottir, R. B., Jonsson, E., Jonsson, S., Olafsson, J. H., Gulcher, J. R., Masson, G., Gudbjartsson, D. F., Kong, A., Thorsteinsdottir, U., and Stefansson, K. Sequence variants at the TERT-CLPTM1L locus associate with many cancer types. Nat Genet, 41: 221-7, 2009.

Olsen, C. M., Zens, M. S., Stukel, T. A., Sacerdote, C., Chang, Y. M., Armstrong, B. K., Bataille, V., Berwick, M., Elwood, J. M., Holly, E. A., Kirkpatrick, C., Mack, T., Bishop, J. N., Osterlind, A., Swerdlow, A. J., Zanetti, R., Green, A. C., Karagas, M. R., and Whiteman, D. C. Nevus density and melanoma risk in women: a pooled analysis to test the divergent pathway hypothesis. International journal of cancer. Journal international du cancer, 124: 937-44, 2009.

Newton-Bishop, J. A., Beswick, S., Randerson-Moor, J., Chang, Y. M., Affleck, P., Elliott, F., Chan, M., Leake, S., Karpavicius, B., Haynes, S., Kukalizch, K., Whitaker, L., Jackson, S., Gerry, E., Nolan, C., Bertram, C., Marsden, J., Elder, D. E., Barrett, J. H., and Bishop, D. T. Serum 25-hydroxyvitamin D3 levels are associated with breslow thickness at presentation and survival from melanoma. J Clin Oncol, 27: 5439-44, 2009.

Morgan, A. W., Thomson, W., Martin, S. G., Carter, A. M., Erlich, H. A., Barton, A., Hocking, L., Reid, D. M., Harrison, P., Wordsworth, P., Steer, S., Worthington, J., Emery, P., Wilson, A. G., and Barrett, J. H. Reevaluation of the interaction between HLA-DRB1 shared epitope alleles, PTPN22, and smoking in determining susceptibility to autoantibody-positive and autoantibody-negative rheumatoid arthritis in a large UK Caucasian population. Arthritis Rheum, 60: 2565-76, 2009.

Mai, P. L., Chen, B. E., Tucker, K., Friedlander, M., Phillips, K. A., Hogg, D., Jewett, M. A., Bodrogi, I., Geczi, L., Olah, E., Heimdal, K., Fossa, S. D., Nathanson, K. L., Korde, L., Easton, D. F., Dudakia, D., Huddart, R., Stratton, M. R., Bishop, D. T., Rapley, E. A., and Greene, M. H. Younger age-at-diagnosis for familial malignant testicular germ cell tumor. Fam Cancer, 8: 451-6, 2009.

Lens, M., Rosdahl, I., and Newton-Bishop, J. Cutaneous melanoma during pregnancy: is the controversy over? J Clin Oncol, 27: e11-2; author reply e13-4, 2009.

Leachman, S. A., Carucci, J., Kohlmann, W., Banks, K. C., Asgari, M. M., Bergman, W., Bianchi-Scarra, G., Brentnall, T., Bressac-de Paillerets, B., Bruno, W., Curiel-Lewandrowski, C., de Snoo, F. A., Debniak, T., Demierre, M. F., Elder, D., Goldstein, A. M., Grant-Kels, J., Halpern, A. C., Ingvar, C., Kefford, R. F., Lang, J., MacKie, R. M., Mann, G. J., Mueller, K., Newton-Bishop, J., Olsson, H., Petersen, G. M., Puig, S., Rigel, D., Swetter, S. M., Tucker, M. A., Yakobson, E., Zitelli, J. A., and Tsao, H. Selection criteria for genetic assessment of patients with familial melanoma. J Am Acad Dermatol, 61: 677 e1-14, 2009.

Falchi, M., Bataille, V., Hayward, N. K., Duffy, D. L., Bishop, J. A., Pastinen, T., Cervino, A., Zhao, Z. Z., Deloukas, P., Soranzo, N., Elder, D. E., Barrett, J. H., Martin, N. G., Bishop, D. T., Montgomery, G. W., and Spector, T. D. Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. Nat Genet, 41: 915-9, 2009.

Curtin, K., Lin, W. Y., George, R., Katory, M., Shorto, J., Cannon-Albright, L. A., Smith, G., Bishop, D. T., Cox, A., and Camp, N. J. Genetic variants in XRCC2: new insights into colorectal cancer tumorigenesis. Cancer Epidemiol Biomarkers Prev, 18: 2476-84, 2009.

Curtin, K., Lin, W. Y., George, R., Katory, M., Shorto, J., Cannon-Albright, L. A., Bishop, D. T., Cox, A., and Camp, N. J. Meta association of colorectal cancer confirms risk alleles at 8q24 and 18q21. Cancer Epidemiol Biomarkers Prev, 18: 616-21, 2009.

Curtin, K., Iles, M. M., and Camp, N. J. Identifying rarer genetic variants for common complex diseases: diseased versus neutral discovery panels. Ann Hum Genet, 73: 54-60, 2009.

Conway, C., Mitra, A., Jewell, R., Randerson-Moor, J., Lobo, S., Nsengimana, J., Edward, S., Sanders, D. S., Cook, M., Powell, B., Boon, A., Elliott, F., de Kort, F., Knowles, M. A., Bishop, D. T., and Newton-Bishop, J. Gene expression profiling of paraffin-embedded primary melanoma using the DASL assay identifies increased osteopontin expression as predictive of reduced relapse-free survival. Clinical cancer research : an official journal of the American Association for Cancer Research, 15: 6939-46, 2009.

Chang, Y. M., Newton-Bishop, J. A., Bishop, D. T., Armstrong, B. K., Bataille, V., Bergman, W., Berwick, M., Bracci, P. M., Elwood, J. M., Ernstoff, M. S., Green, A. C., Gruis, N. A., Holly, E. A., Ingvar, C., Kanetsky, P. A., Karagas, M. R., Le Marchand, L., Mackie, R. M., Olsson, H., Osterlind, A., Rebbeck, T. R., Reich, K., Sasieni, P., Siskind, V., Swerdlow, A. J., Titus-Ernstoff, L., Zens, M. S., Ziegler, A., and Barrett, J. H. A pooled analysis of melanocytic nevus phenotype and the risk of cutaneous melanoma at different latitudes. Int J Cancer, 124: 420-8, 2009.

Chang, Y. M., Barrett, J. H., Bishop, D. T., Armstrong, B. K., Bataille, V., Bergman, W., Berwick, M., Bracci, P. M., Elwood, J. M., Ernstoff, M. S., Gallagher, R. P., Green, A. C., Gruis, N. A., Holly, E. A., Ingvar, C., Kanetsky, P. A., Karagas, M. R., Lee, T. K., Le Marchand, L., Mackie, R. M., Olsson, H., Osterlind, A., Rebbeck, T. R., Sasieni, P., Siskind, V., Swerdlow, A. J., Titus-Ernstoff, L., Zens, M. S., and Newton-Bishop, J. A. Sun exposure and melanoma risk at different latitudes: a pooled analysis of 5700 cases and 7216 controls. Int J Epidemiol, 38: 814-30, 2009.

Cairns, D. A., Barrett, J. H., Billingham, L. J., Stanley, A. J., Xinarianos, G., Field, J. K., Johnson, P. J., Selby, P. J., and Banks, R. E. Sample size determination in clinical proteomic profiling experiments using mass spectrometry for class comparison. Proteomics, 9: 74-86, 2009.

Bishop, D. T., Demenais, F., Iles, M. M., Harland, M., Taylor, J. C., Corda, E., Randerson-Moor, J., Aitken, J. F., Avril, M. F., Azizi, E., Bakker, B., Bianchi-Scarra, G., Bressac-de Paillerets, B., Calista, D., Cannon-Albright, L. A., Chin, A. W. T., Debniak, T., Galore-Haskel, G., Ghiorzo, P., Gut, I., Hansson, J., Hocevar, M., Hoiom, V., Hopper, J. L., Ingvar, C., Kanetsky, P. A., Kefford, R. F., Landi, M. T., Lang, J., Lubinski, J., Mackie, R., Malvehy, J., Mann, G. J., Martin, N. G., Montgomery, G. W., van Nieuwpoort, F. A., Novakovic, S., Olsson, H., Puig, S., Weiss, M., van Workum, W., Zelenika, D., Brown, K. M., Goldstein, A. M., Gillanders, E. M., Boland, A., Galan, P., Elder, D. E., Gruis, N. A., Hayward, N. K., Lathrop, G. M., Barrett, J. H., and Bishop, J. A. Genome-wide association study identifies three loci associated with melanoma risk. Nat Genet, 41: 920-5, 2009.

Bapat, B., Lindor, N. M., Baron, J., Siegmund, K., Li, L., Zheng, Y., Haile, R., Gallinger, S., Jass, J. R., Young, J. P., Cotterchio, M., Jenkins, M., Grove, J., Casey, G., Thibodeau, S. N., Bishop, D. T., Hopper, J. L., Ahnen, D., Newcomb, P. A., Le Marchand, L., Potter, J. D., and Seminara, D. The association of tumor microsatellite instability phenotype with family history of colorectal cancer. Cancer Epidemiol Biomarkers Prev, 18: 967-75, 2009.

2008 Publications

Tomlinson, I. P., Webb, E., Carvajal-Carmona, L., Broderick, P., Howarth, K., Pittman, A. M., Spain, S., Lubbe, S., Walther, A., Sullivan, K., Jaeger, E., Fielding, S., Rowan, A., Vijayakrishnan, J., Domingo, E., Chandler, I., Kemp, Z., Qureshi, M., Farrington, S. M., Tenesa, A., Prendergast, J. G., Barnetson, R. A., Penegar, S., Barclay, E., Wood, W., Martin, L., Gorman, M., Thomas, H., Peto, J., Bishop, D. T., Gray, R., Maher, E. R., Lucassen, A., Kerr, D., Evans, D. G., Schafmayer, C., Buch, S., Volzke, H., Hampe, J., Schreiber, S., John, U., Koessler, T., Pharoah, P., van Wezel, T., Morreau, H., Wijnen, J. T., Hopper, J. L., Southey, M. C., Giles, G. G., Severi, G., Castellvi-Bel, S., Ruiz-Ponte, C., Carracedo, A., Castells, A., Forsti, A., Hemminki, K., Vodicka, P., Naccarati, A., Lipton, L., Ho, J. W., Cheng, K. K., Sham, P. C., Luk, J., Agundez, J. A., Ladero, J. M., de la Hoya, M., Caldes, T., Niittymaki, I., Tuupanen, S., Karhu, A., Aaltonen, L., Cazier, J. B., Campbell, H., Dunlop, M. G., and Houlston, R. S. A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. Nat Genet, 40: 623-30, 2008.

Strauss, R. M., and Newton Bishop, J. A. Spontaneous involution of congenital melanocytic nevi of the scalp. Journal of the American Academy of Dermatology, 58: 508-11, 2008.

Papaemmanuil, E., Carvajal-Carmona, L., Sellick, G. S., Kemp, Z., Webb, E., Spain, S., Sullivan, K., Barclay, E., Lubbe, S., Jaeger, E., Vijayakrishnan, J., Broderick, P., Gorman, M., Martin, L., Lucassen, A., Bishop, D. T., Evans, D. G., Maher, E. R., Steinke, V., Rahner, N., Schackert, H. K., Goecke, T. O., Holinski-Feder, E., Propping, P., Van Wezel, T., Wijnen, J., Cazier, J. B., Thomas, H., Houlston, R. S., and Tomlinson, I. Deciphering the genetics of hereditary non-syndromic colorectal cancer. Eur J Hum Genet, 16: 1477-86, 2008.

Morgan, A. W., Haroon-Rashid, L., Martin, S. G., Gooi, H. C., Worthington, J., Thomson, W., Barrett, J. H., and Emery, P. The shared epitope hypothesis in rheumatoid arthritis: evaluation of alternative classification criteria in a large UK Caucasian cohort. Arthritis Rheum, 58: 1275-83, 2008.

Mitchell, H., English, D. R., Elliott, F., Gengos, M., Barrett, J. H., Giles, G. G., and Forman, D. Immunoblotting using multiple antigens is essential to demonstrate the true risk of H. pylori infection for gastric cancer. Aliment Pharmacol Ther, 2008.

Linger, R., Dudakia, D., Huddart, R., Tucker, K., Friedlander, M., Phillips, K. A., Hogg, D., Jewett, M. A., Lohynska, R., Daugaard, G., Richard, S., Chompret, A., Stoppa-Lyonnet, D., Bonaiti-Pellie, C., Heidenreich, A., Albers, P., Olah, E., Geczi, L., Bodrogi, I., Daly, P. A., Guilford, P., Fossa, S. D., Heimdal, K., Tjulandin, S. A., Liubchenko, L., Stoll, H., Weber, W., Einhorn, L., McMaster, M., Korde, L., Greene, M. H., Nathanson, K. L., Cortessis, V., Easton, D. F., Bishop, D. T., Stratton, M. R., and Rapley, E. A. Analysis of the DND1 gene in men with sporadic and familial testicular germ cell tumors. Genes Chromosomes Cancer, 47: 247-52, 2008.

Liljegren, A., Barker, G., Elliott, F., Bertario, L., Bisgaard, M. L., Eccles, D., Evans, G., Macrae, F., Maher, E., Lindblom, A., Rotstein, S., Nilsson, B., Mecklin, J. P., Moslein, G., Jass, J., Fodde, R., Mathers, J., Burn, J., and Bishop, D. T. Prevalence of adenomas and hyperplastic polyps in mismatch repair mutation carriers among CAPP2 participants: report by the colorectal adenoma/carcinoma prevention programme 2. J Clin Oncol, 26: 3434-9, 2008.

Lightfoot, T. J., Barrett, J. H., Bishop, T., Northwood, E. L., Smith, G., Wilkie, M. J., Steele, R. J., Carey, F. A., Key, T. J., Wolf, R., and Forman, D. Methylene tetrahydrofolate reductase genotype modifies the chemopreventive effect of folate in colorectal adenoma, but not colorectal cancer. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 17: 2421-30, 2008.

Law, G. R., Feltbower, R. G., Taylor, J. C., Parslow, R. C., Gilthorpe, M. S., Boyle, P., and McKinney, P. A. What do epidemiologists mean by 'population mixing'? Pediatr Blood Cancer, 51: 155-60, 2008.

Kiemeney, L. A., Thorlacius, S., Sulem, P., Geller, F., Aben, K. K., Stacey, S. N., Gudmundsson, J., Jakobsdottir, M., Bergthorsson, J. T., Sigurdsson, A., Blondal, T., Witjes, J. A., Vermeulen, S. H., Hulsbergen-van de Kaa, C. A., Swinkels, D. W., Ploeg, M., Cornel, E. B., Vergunst, H., Thorgeirsson, T. E., Gudbjartsson, D., Gudjonsson, S. A., Thorleifsson, G., Kristinsson, K. T., Mouy, M., Snorradottir, S., Placidi, D., Campagna, M., Arici, C., Koppova, K., Gurzau, E., Rudnai, P., Kellen, E., Polidoro, S., Guarrera, S., Sacerdote, C., Sanchez, M., Saez, B., Valdivia, G., Ryk, C., de Verdier, P., Lindblom, A., Golka, K., Bishop, D. T., Knowles, M. A., Nikulasson, S., Petursdottir, V., Jonsson, E., Geirsson, G., Kristjansson, B., Mayordomo, J. I., Steineck, G., Porru, S., Buntinx, F., Zeegers, M. P., Fletcher, T., Kumar, R., Matullo, G., Vineis, P., Kiltie, A. E., Gulcher, J. R., Thorsteinsdottir, U., Kong, A., Rafnar, T., and Stefansson, K. Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. Nat Genet, 40: 1307-12, 2008.

Iles, M. M. What can genome-wide association studies tell us about the genetics of common disease? PLoS Genet, 4: e33, 2008.

Iles, M. M. Quantification and correction of bias in tagging SNPs caused by insufficient sample size and marker density by means of haplotype-dropping. Genet Epidemiol, 32: 20-8, 2008.

Freedberg, D. E., Rigas, S. H., Russak, J., Gai, W., Kaplow, M., Osman, I., Turner, F., Randerson-Moor, J. A., Houghton, A., Busam, K., Timothy Bishop, D., Bastian, B. C., Newton-Bishop, J. A., and Polsky, D. Frequent p16-independent inactivation of p14ARF in human melanoma. Journal of the National Cancer Institute, 100: 784-95, 2008.

Downing, A., Yu, X. Q., Newton-Bishop, J., and Forman, D. Trends in prognostic factors and survival from cutaneous melanoma in Yorkshire, UK and New South Wales, Australia between 1993 and 2003. Int J Cancer, 123: 861-6, 2008.

de Snoo, F. A., Bishop, D. T., Bergman, W., van Leeuwen, I., van der Drift, C., van Nieuwpoort, F. A., Out-Luiting, C. J., Vasen, H. F., ter Huurne, J. A., Frants, R. R., Willemze, R., Breuning, M. H., and Gruis, N. A. Increased risk of cancer other than melanoma in CDKN2A founder mutation (p16-Leiden)-positive melanoma families. Clin Cancer Res, 14: 7151-7, 2008.

Choudhury, A., Elliott, F., Iles, M. M., Churchman, M., Bristow, R. G., Bishop, D. T., and Kiltie, A. E. Analysis of variants in DNA damage signalling genes in bladder cancer. BMC Med Genet, 9: 69, 2008.

Cairns, D. A., Thompson, D., Perkins, D. N., Stanley, A. J., Selby, P. J., and Banks, R. E. Proteomic profiling using mass spectrometry--does normalising by total ion current potentially mask some biological differences? Proteomics, 8: 21-7, 2008.

Burn, J., Bishop, D. T., Mecklin, J. P., Macrae, F., Moslein, G., Olschwang, S., Bisgaard, M. L., Ramesar, R., Eccles, D., Maher, E. R., Bertario, L., Jarvinen, H. J., Lindblom, A., Evans, D. G., Lubinski, J., Morrison, P. J., Ho, J. W., Vasen, H. F., Side, L., Thomas, H. J., Scott, R. J., Dunlop, M., Barker, G., Elliott, F., Jass, J. R., Fodde, R., Lynch, H. T., and Mathers, J. C. Effect of aspirin or resistant starch on colorectal neoplasia in the Lynch syndrome. N Engl J Med, 359: 2567-78, 2008.

Brown, K. M., Macgregor, S., Montgomery, G. W., Craig, D. W., Zhao, Z. Z., Iyadurai, K., Henders, A. K., Homer, N., Campbell, M. J., Stark, M., Thomas, S., Schmid, H., Holland, E. A., Gillanders, E. M., Duffy, D. L., Maskiell, J. A., Jetann, J., Ferguson, M., Stephan, D. A., Cust, A. E., Whiteman, D., Green, A., Olsson, H., Puig, S., Ghiorzo, P., Hansson, J., Demenais, F., Goldstein, A. M., Gruis, N. A., Elder, D. E., Bishop, J. N., Kefford, R. F., Giles, G. G., Armstrong, B. K., Aitken, J. F., Hopper, J. L., Martin, N. G., Trent, J. M., Mann, G. J., and Hayward, N. K. Common sequence variants on 20q11.22 confer melanoma susceptibility. Nat Genet, 40: 838-40, 2008.

Braun, M. S., Richman, S. D., Quirke, P., Daly, C., Adlard, J. W., Elliott, F., Barrett, J. H., Selby, P., Meade, A. M., Stephens, R. J., Parmar, M. K., and Seymour, M. T. Predictive biomarkers of chemotherapy efficacy in colorectal cancer: results from the UK MRC FOCUS trial. J Clin Oncol, 26: 2690-8, 2008.

Barrett, J. H., and Cairns, D. A. Application of the random forest classification method to peaks detected from mass spectrometric proteomic profiles of cancer patients and controls. Stat Appl Genet Mol Biol, 7: Article4, 2008.

  Allan, J. M., Shorto, J., Adlard, J., Bury, J., Coggins, R., George, R., Katory, M., Quirke, P., Richman, S., Scott, D., Scott, K., Seymour, M., Travis, L. B., Worrillow, L. J., Bishop, D. T., and Cox, A. MLH1 -93G>A promoter polymorphism and risk of mismatch repair deficient colorectal cancer. Int J Cancer, 123: 2456-9, 2008.