Growing recognition of the role for rare missense substitutions in breast cancer susceptibility

Por Tavtigian, Sean V, Chenevix-Trench, Georgia
Publicado no Biomark Med (2014)

No germline mutations in the histone acetyltransferase gene EP300 in BRCA1 and BRCA2 negative families with breast cancer and gastric, pancreatic, or colorectal cancer

Por Campbell, Ian G, Choong, David, Chenevix-Trench, Georgia
Publicado em 2004

The application of nonsense-mediated mRNA decay inhibition to the identification of breast cancer susceptibility genes

Por Johnson, Julie K, Waddell, Nic, Chenevix-Trench, Georgia
Publicado em 2012

Are estrogen receptor-positive breast cancers in BRCA1 mutation carriers sporadic?

Por Lakhani, Sunil R, Khanna, Kum Kum, Chenevix-Trench, Georgia
Publicado em 2010

Variation in the RAD51 gene and familial breast cancer

Por Lose, Felicity, Lovelock, Paul, Chenevix-Trench, Georgia, Mann, Graham J, Pupo, Gulietta M, Spurdle, Amanda B
Publicado em 2006

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...

Por Chenevix-Trench, Georgia, Milne, Roger L, Antoniou, Antonis C, Couch, Fergus J, Easton, Douglas F, Goldgar, David E
Publicado em 2007

Evolutionary conservation analysis increases the colocalization of predicted exonic splicing enhancers in the BRCA1 gene with missense sequence changes and in-frame deletions, but...

Por Pettigrew, Christopher, Wayte, Nicola, Lovelock, Paul K, Tavtigian, Sean V, Chenevix-Trench, Georgia, Spurdle, Amanda B, Brown, Melissa A
Publicado em 2005

A fine-scale dissection of the DNA double-strand break repair machinery and its implications for breast cancer therapy

Por Liu, Chao, Srihari, Sriganesh, Cao, Kim-Anh Lê, Chenevix-Trench, Georgia, Simpson, Peter T., Ragan, Mark A., Khanna, Kum Kum
Publicado em 2014

No evidence for association of ataxia-telangiectasia mutated gene T2119C and C3161G amino acid substitution variants with risk of breast cancer

Por Spurdle, Amanda B, Hopper, John L, Chen, Xiaoqing, McCredie, Margaret RE, Giles, Graham G, Newman, Beth, Chenevix-Trench, Georgia, Khanna, KumKum
Publicado em 2002

Evidence of a genetic link between endometriosis and ovarian cancer

Por Lee, Alice W., Templeman, Claire, Stram, Douglas A., Beesley, Jonathan, Tyrer, Jonathan, Berchuck, Andrew, Pharoah, Paul P., Chenevix-Trench, Georgia, Pearce, Celeste Leigh
Publicado no Fertil Steril (2015)

High content screening application for cell-type specific behaviour in heterogeneous primary breast epithelial subpopulations

Por Johnston, Rebecca L., Wockner, Leesa, McCart Reed, Amy E., Wiegmans, Adrian, Chenevix-Trench, Georgia, Khanna, Kum Kum, Lakhani, Sunil R., Smart, Chanel E.
Publicado no Breast Cancer Res (2016)

Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: Linkage and loss of heterozygosity

Por 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
Publicado em 1993

BCoR-L1 variation and breast cancer

Por 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
Publicado em 2007

Correction: BCoR-L1 variation and breast cancer

Por 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
Publicado em 2008

A Common Cancer Risk-Associated Allele in the hTERT Locus Encodes a Dominant Negative Inhibitor of Telomerase

Por 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.
Publicado no PLoS Genet (2015)

The intronic G13964C variant in p53 is not a high-risk mutation in familial breast cancer in Australia

Por 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
Publicado em 2001

Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer

Por 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
Publicado em 2005

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

Por 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
Publicado em 2009

DNA Methylome of Familial Breast Cancer Identifies Distinct Profiles Defined by Mutation Status

Por Flanagan, James M., Cocciardi, Sibylle, Waddell, Nic, Johnstone, Cameron N., Marsh, Anna, Henderson, Stephen, Simpson, Peter, da Silva, Leonard, Khanna, Kumkum, Lakhani, Sunil, Boshoff, Chris, Chenevix-Trench, Georgia
Publicado em 2010

Association of Type and Location of BRCA1 and BRCA2 Mutations With Risk of Breast and Ovarian Cancer

Por Rebbeck, Timothy R., Mitra, Nandita, Wan, Fei, Sinilnikova, Olga M., Healey, Sue, McGuffog, Lesley, Mazoyer, Sylvie, Chenevix-Trench, Georgia, Easton, Douglas F., Antoniou, Antonis C., Nathanson, Katherine L.
Publicado no JAMA (2015)