Oral contraceptive use and ovarian cancer risk among carriers of BRCA1 or BRCA2 mutations von Whittemore, A S, Balise, R R, Pharoah, P D P, DiCioccio, R A, Oakley-Girvan, I, Ramus, S J, Daly, M, Usinowicz, M B, Garlinghouse-Jones, K, Ponder, B A J, Buys, S, Senie, R, Andrulis, I, John, E, Hopper, J L, Piver, M S

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Multifactorial Analysis of Differences Between Sporadic Breast Cancers and Cancers Involving BRCA1 and BRCA2 Mutations von Lakhani, Sunil R., Jacquemier, Jocelyne, Sloane, John P., Gusterson, Barry A., Anderson, Thomas J., van de Vijver, Marc J., Farid, Linda M., Venter, Deon, Antoniou, Antonios, Storfer-Isser, Amy, Smyth, Elizabeth, Steel, C. Michael, Haites, Neva, Scott, Rodney J., Goldgar, David, Neuhausen, Susan, Daly, Peter A., Ormiston, Wilma, McManus, Ross, Scherneck, Siegfried, Ponder, Bruce A. J., Ford, Debbie, Peto, Julian, Stoppa-Lyonnet, Dominique, Bignon, Yves-Jean, Struewing, Jeffery P., Spurr, Nigel K., Bishop, D. Timothy, Klijn, J. G. M., Devilee, Peter, Cornelisse, Cees J., Lasset, Christine, Lenoir, Gilbert, Barkardottir, Rosa Bjork, Egilsson, Valgardur, Hamann, Ute, Chang-Claude, Jenny, Sobol, Hagay, Weber, Barbara, Stratton, Michael R., Easton, Douglas F.

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Germline Homozygous Mutations at Codon 804 in the RET Protooncogene in Medullary Thyroid Carcinoma/Multiple Endocrine Neoplasia Type 2A Patients von Lesueur, F., Cebrian, A., Cranston, A., Leyland, J., Faid, T. M., Clements, M. R., Robledo, M., Whittaker, J., Ponder, B. A. J.

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UHRF1 is a novel molecular marker for diagnosis and the prognosis of bladder cancer von Unoki, M, Kelly, J D, Neal, D E, Ponder, B A J, Nakamura, Y, Hamamoto, R

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HapMap-based study of the 17q21 ERBB2 amplicon in susceptibility to breast cancer von Benusiglio, P R, Pharoah, P D, Smith, P L, Lesueur, F, Conroy, D, Luben, R N, Dew, G, Jordan, C, Dunning, A, Easton, D F, Ponder, B A J

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Interactions between genes involved in the antioxidant defence system and breast cancer risk von Oestergaard, M Z, Tyrer, J, Cebrian, A, Shah, M, Dunning, A M, Ponder, B A J, Easton, D F, Pharoah, P D P

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Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developm... von UPADHYAYA, M, RUGGIERI, M, KRAWCZAK, M, COOPER, D. N, MAYNARD, J, OSBORN, M, HARTOG, C, MUDD, S, PENTTINEN, M, CORDEIRO, I, PONDER, M, PONDER, B. A. J

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Guidelines for diagnosis and therapy of MEN type 1 and type 2 von Brandi, M L, Gagel, R F, Angeli, A, Bilezikian, J P, Beck-Peccoz, P, Bordi, C, Conte-Devolx, B, Falchetti, A, Gheri, R G, Libroia, A, Lips, C J, Lombardi, G, Mannelli, M, Pacini, F, Ponder, B A, Raue, F, Skogseid, B, Tamburrano, G, Thakker, R V, Thompson, N W, Tomassetti, P, Tonelli, F, Wells, Jr, S A, Marx, S J

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Common BRCA1 Variants and Susceptibility to Breast and Ovarian Cancer in the General Population von Dunning, Alison M., Chiano, Mathias, Smith, Neil R., Dearden, Joanna, Gore, Martin, Oakes, Suzy, Wilson, Charles, Stratton, Michael, Peto, Julian, Easton, Doug, Clayton, David, Ponder, Bruce A. J.

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Mutations truncating the EP300 acetylase in human cancers von Caldas, Carlos, Gayther, Simon A, Batley, Sarah J, Linger, Lori, Bannister, Andy, Thorpe, Karen, Chin, Suet-Feung, Daigo, Yataro, Russell, Paul, Wilson, Annie, Sowter, Heidi M, Delhanty, Joy D.A, Ponder, Bruce A.J, Kouzarides, Tony

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A Systematic Review Of Genetic Polymorphisms and Breast Cancer Risk von DUNNING, A. M, HEALEY, C. S, PHAROAH, P. D. P, TEARE, M. D, PONDER, B. A. J, EASTON, D. F

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No association between a polymorphism in the steroid metabolism gene CYP17 and risk of breast cancer von Dunning, AM, Healey, CS, Pharoah, PD, Foster, NA, Lipscombe, JM, Redman, KL, Easton, DF, Day, NE, Ponder, BAJ

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Familial gastric cancer: overview and guidelines for management von Caldas, Carlos, Carneiro, Fatima, Lynch, Henry T, Yokota, Jun, Wiesner, Georgia L, Powell, Steven M, Lewis, Frank R, Huntsman, David G, Pharoah, Paul D P, Jankowski, Janusz A, MacLeod, Patrick, Vogelsang, Holger, Keller, Gisela, Park, Ken G M, Richards, Frances M, Maher, Eamonn R, Gayther, Simon A, Oliveira, Carla, Grehan, Nicola, Wight, Derek, Seruca, Raquel, Roviello, Franco, Ponder, Bruce A J, Jackson, Charles E

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Paternal origin of new mutations in Von Recklinghausen neurofibromatosis von Jadayel, D, Fain, P, Upadhyaya, M, Ponder, M. A, Huson, S. M, Carey, J, Fryer, A, Mathew, C. G. P, Barker, D. F, Ponder, B. A. J

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Clonal Origin of Epithelial Ovarian Carcinoma: Analysis by Loss of Heterozygosity, p53 Mutation, and X-Chromosome Inactivation von Jacobs, I. J., Kohler, M. F., Wiseman, R. W., Marks, J. R., Whitaker, R., Kerns, B. A. J., Humphrey, P., Berchuck, A., Ponder, B. A. J., Bast, R. C.

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A clonal marker induced by mutation in mouse intestinal epithelium von Winton, D. J, Blount, M. A, Ponder, B. A. J

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Family history and the risk of breast cancer: A systematic review and meta‐analysis von Pharoah, Paul D.P., Day, Nicholas E., Duffy, Stephen, Easton, Douglas F., Ponder, Bruce A.J.

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Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene von Gayther, Simon A, Mangion, Jonathon, Russell, Paul, Seal, Sheila, Barfoot, Rita, Ponder, Bruce A.J, Stratton, Michael R, Easton, Douglas

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Mutation testing in melanoma families: INK4A, CDK4 and INK4D von Bishop, J A Newton, Harland, M, Bennett, D C, Bataille, V, Goldstein, A M, Tucker, M A, Ponder, B A J, Cuzick, J, Selby, P, Bishop, D T

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Identification of germ-line E-cadherin mutations in gastric cancer families of European origin von GAYTHER, S. A, GORRINGE, K. L, MACLEOD, P, POWELL, S. M, JACKSON, C. E, PONDER, B. A. J, CALDAS, C, RAMUS, S. J, HUNTSMAN, D, ROVIELLO, F, GREHAN, N, MACHADO, J. C, PINTO, E, SERUCA, R, HALLING, K

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