A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes von ANTONIOU, A. C, PHAROAH, P. D. P, MCMULLAN, G, DAY, N. E, STRATTON, M. R, PETO, J, PONDER, B. J, EASTON, D. F

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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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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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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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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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A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes von Antoniou, A C, Pharoah, P D P, McMullan, G, Day, N E, Stratton, M R, Peto, J, Ponder, B J, Easton, D F

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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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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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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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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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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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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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Common Polymorphisms in Checkpoint Kinase 2 Are not Associated with Breast Cancer Risk von KUSCHEL, B, AURANEN, A, GREGORY, C. S, DAY, N. E, EASTON, D. F, PONDER, B. A. J, DUNNING, A. M, PHAROAH, Paul D. P

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Common germ-line polymorphism of C1QA and breast cancer survival von Azzato, E M, Lee, A J X, Teschendorff, A, Ponder, B A J, Pharoah, P, Caldas, C, Maia, A T

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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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Further evidence for an HLA-related recessive mutation in nasopharyngeal carcinoma among the Chinese von Hu, S P, Day, N E, Li, D R, Luben, R N, Cai, K L, Ou-Yang, T, Li, B, Lu, X Z, Ponder, B A J

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Tagging single-nucleotide polymorphisms in candidate oncogenes and susceptibility to ovarian cancer von Quaye, L, Song, H, Ramus, S J, Gentry-Maharaj, A, Høgdall, E, DiCioccio, R A, McGuire, V, Wu, A H, Van Den Berg, D J, Pike, M C, Wozniak, E, Doherty, J A, Rossing, M A, Ness, R B, Moysich, K B, Høgdall, C, Blaakaer, J, Easton, D F, Ponder, B A J, Jacobs, I J, Menon, U, Whittemore, A S, Krüger-Kjaer, S, Pearce, C L, Pharoah, P D P, Gayther, S A

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Mutation analysis of CBP and PCAF reveals rare inactivating mutations in cancer cell lines but not in primary tumours von Özdağ, H, Batley, S J, Försti, A, Iyer, N G, Daigo, Y, Boutell, J, Arends, M J, Ponder, B A J, Kouzarides, T, Caldas, C

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Comparison of prophylactic oophorectomy specimens from carriers and noncarriers of a BRCA1 or BRCA2 gene mutation von STRATTON, J. F, BUCKLEY, C. H, LOWE, D, PONDER, B. A. J

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MRI breast screening in high-risk women: cancer detection and survival analysis von Gareth, Evans D., Nisha, Kesavan, Yit, Lim, Soujanye, Gadde, Emma, Hurley, Massat, Nathalie J., Maxwell, Anthony J., Sarah, Ingham, Rosalind, Eeles, Leach, Martin O., Anthony, Howell, Stephen, Duffy

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