Torthaí cuardaigh - Chenevix–Trench, Georgia

Growing recognition of the role for rare missense substitutions in breast cancer susceptibility de réir Tavtigian, Sean V, Chenevix-Trench, Georgia

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The application of nonsense-mediated mRNA decay inhibition to the identification of breast cancer susceptibility genes de réir Johnson, Julie K, Waddell, Nic, Chenevix-Trench, Georgia

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No germline mutations in the histone acetyltransferase gene EP300 in BRCA1 and BRCA2 negative families with breast cancer and gastric, pancreatic, or colorectal cancer de réir Campbell, Ian G, Choong, David, Chenevix-Trench, Georgia

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Are estrogen receptor-positive breast cancers in BRCA1 mutation carriers sporadic? de réir Lakhani, Sunil R, Khanna, Kum Kum, Chenevix-Trench, Georgia

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The importance of using public data to validate reported associations de réir Chenevix-Trench, Georgia, Beesley, Jonathan, Pharoah, Paul D. P., Berchuck, Andrew

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SNPs in lncRNA Regions and Breast Cancer Risk de réir Suvanto, Maija, Beesley, Jonathan, Blomqvist, Carl, Chenevix-Trench, Georgia, Khan, Sofia, Nevanlinna, Heli

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Variation in the RAD51 gene and familial breast cancer de réir Lose, Felicity, Lovelock, Paul, Chenevix-Trench, Georgia, Mann, Graham J, Pupo, Gulietta M, Spurdle, Amanda B

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An international initiative to identify genetic modifiers of cancer risk in BRCA1 and BRCA2 mutation carriers: the Consortium of Investigators of Modifiers of BRCA1 and BRCA2 (CIMB... de réir Chenevix-Trench, Georgia, Milne, Roger L, Antoniou, Antonis C, Couch, Fergus J, Easton, Douglas F, Goldgar, David E

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Evolutionary conservation analysis increases the colocalization of predicted exonic splicing enhancers in the BRCA1 gene with missense sequence changes and in-frame deletions, but... de réir Pettigrew, Christopher, Wayte, Nicola, Lovelock, Paul K, Tavtigian, Sean V, Chenevix-Trench, Georgia, Spurdle, Amanda B, Brown, Melissa A

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A fine-scale dissection of the DNA double-strand break repair machinery and its implications for breast cancer therapy de réir Liu, Chao, Srihari, Sriganesh, Cao, Kim-Anh Lê, Chenevix-Trench, Georgia, Simpson, Peter T., Ragan, Mark A., Khanna, Kum Kum

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No evidence for association of ataxia-telangiectasia mutated gene T2119C and C3161G amino acid substitution variants with risk of breast cancer de réir Spurdle, Amanda B, Hopper, John L, Chen, Xiaoqing, McCredie, Margaret RE, Giles, Graham G, Newman, Beth, Chenevix-Trench, Georgia, Khanna, KumKum

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Evidence of a genetic link between endometriosis and ovarian cancer de réir Lee, Alice W., Templeman, Claire, Stram, Douglas A., Beesley, Jonathan, Tyrer, Jonathan, Berchuck, Andrew, Pharoah, Paul P., Chenevix-Trench, Georgia, Pearce, Celeste Leigh

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Is Schizophrenia a Risk Factor for Breast Cancer?—Evidence From Genetic Data de réir Byrne, Enda M, Ferreira, Manuel A R, Xue, Angli, Lindström, Sara, Jiang, Xia, Yang, Jian, Easton, Douglas F, Wray, Naomi R, Chenevix-Trench, Georgia

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Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: Linkage and loss of heterozygosity de réir Chenevix-Trench, Georgia, Wicking, Carol, Berkman, Jenny, Sharpe, Helen, Hockey, Athel, Haan, Eric, Oley, Christine, Ravine, David, Turner, Anne, Goldgar, David, Searle, Jeffrey, Wainwright, Brandon

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BCoR-L1 variation and breast cancer de réir Lose, Felicity, Arnold, Jeremy, Young, David B, Brown, Carolyn J, Mann, Graham J, Pupo, Gulietta M, Khanna, Kum Kum, Chenevix-Trench, Georgia, Spurdle, Amanda B

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Correction: BCoR-L1 variation and breast cancer de réir Lose, Felicity, Arnold, Jeremy, Young, David B, Brown, Carolyn J, Mann, Graham J, Pupo, Gulietta M, Khanna, Kum Kum, Chenevix-Trench, Georgia, Spurdle, Amanda B

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A Common Cancer Risk-Associated Allele in the hTERT Locus Encodes a Dominant Negative Inhibitor of Telomerase de réir Killedar, Anagha, Stutz, Michael D., Sobinoff, Alexander P., Tomlinson, Christopher G., Bryan, Tracy M., Beesley, Jonathan, Chenevix-Trench, Georgia, Reddel, Roger R., Pickett, Hilda A.

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Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer de réir Lewis, Aaron G, Flanagan, James, Marsh, Anna, Pupo, Gulietta M, Mann, Graham, Spurdle, Amanda B, Lindeman, Geoffrey J, Visvader, Jane E, Brown, Melissa A, Chenevix-Trench, Georgia

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Pooled analysis indicates that the GSTT1 deletion, GSTM1 deletion, and GSTP1 Ile105Val polymorphisms do not modify breast cancer risk in BRCA1 and BRCA2 mutation carriers de réir Spurdle, Amanda B., Fahey, Paul, Chen, Xiaoqing, McGuffog, Lesley, Easton, Douglas, Peock, Susan, Cook, Margaret, Simard, Jacques, Rebbeck, Tim R., Antoniou, Antonis C., Chenevix-Trench, Georgia

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The intronic G13964C variant in p53 is not a high-risk mutation in familial breast cancer in Australia de réir Marsh, Anna, Spurdle, Amanda B, Turner, Bruce C, Fereday, Sian, Thorne, Heather, Pupo, Gulietta M, Mann, Graham J, Hopper, John L, Sambrook, Joseph F, Chenevix-Trench, Georgia

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