Genotypic and phenotypic analysis of familial male breast cancer shows under representation of the HER2 and basal subtypes in BRCA-associated carcinomas

بواسطة Deb, Siddhartha, Jene, Nicholas, investigators, kConFab, Fox, Stephen B
منشور في 2012

Large genomic rearrangements of both BRCA2 and BRCA1 are a feature of the inherited breast/ovarian cancer phenotype in selected families

بواسطة Woodward, A, Davis, T, Silva, A, kConFab, I, Kirk, J, Leary, J
منشور في 2005

Use of DNA–Damaging Agents and RNA Pooling to Assess Expression Profiles Associated with BRCA1 and BRCA2 Mutation Status in Familial Breast Cancer Patients

بواسطة Walker, Logan C., Thompson, Bryony A., Waddell, Nic, Investigators, kConFab, Grimmond, Sean M., Spurdle, Amanda B.
منشور في 2010

Bayes Analysis Provides Evidence of Pathogenicity for the BRCA1 c.135-1G>T (IVS3-1) and BRCA2 c.7977-1G>C (IVS17-1) Variants Displaying In Vitro Splicing Results of Equivocal Clini...

بواسطة Spurdle, Amanda B., Lakhani, Sunil R., Da Silva, Leonard M., Balleine, Rosemary L., Investigators, kConFab, Goldgar, David E.
منشور في 2010

BRCA2 carriers with male breast cancer show elevated tumour methylation

بواسطة Deb, Siddhartha, Gorringe, Kylie L., Pang, Jia-Min B., Byrne, David J., Takano, Elena A., Investigators, kConFab, Dobrovic, Alexander, Fox, Stephen B.
الحاوية / القاعدة BMC Cancer (2017)

Analysis of RAD51D in Ovarian Cancer Patients and Families with a History of Ovarian or Breast Cancer

بواسطة Thompson, Ella R., Rowley, Simone M., Sawyer, Sarah, kConFab, Eccles, Diana M., Trainer, Alison H., Mitchell, Gillian, James, Paul A., Campbell, Ian G.
منشور في 2013

Quantifying BRCA1 and BRCA2 mRNA Isoform Expression Levels in Single Cells

بواسطة Lattimore, Vanessa L., Pearson, John F., Morley-Bunker, Arthur E., Investigators, kConFab, Spurdle, Amanda B., Robinson, Bridget A., Currie, Margaret J., Walker, Logan C.
الحاوية / القاعدة Int J Mol Sci (2019)

Prostate screening uptake in Australian BRCA1 and BRCA2 carriers

بواسطة McKinley, Joanne M, Weideman, Prue C, Jenkins, Mark A, Friedlander, Michael L, Hopper, John L, McLachlan, Sue-Anne, Lindeman, Geoffrey J, Investigators, kConFab, Phillips, Kelly-Anne
منشور في 2007

BRCA1 and BRCA2 Missense Variants of High and Low Clinical Significance Influence Lymphoblastoid Cell Line Post-Irradiation Gene Expression

بواسطة Waddell, Nic, Ten Haaf, Anette, Marsh, Anna, Johnson, Julie, Walker, Logan C., Investigators, kConFab, Gongora, Milena, Brown, Melissa, Grover, Piyush, Girolami, Mark, Grimmond, Sean, Chenevix-Trench, Georgia, Spurdle, Amanda B.
منشور في 2008

Panel sequencing of 264 candidate susceptibility genes and segregation analysis in a cohort of non-BRCA1, non-BRCA2 breast cancer families

بواسطة Li, Jun, Li, Hongyan, Makunin, Igor, Investigators, kConFab, Thompson, Bryony A., Tao, Kayoko, Young, Erin L., Lopez, Jacqueline, Camp, Nicola J., Tavtigian, Sean V., John, Esther M., Andrulis, Irene L., Khanna, Kum Kum, Goldgar, David, Chenevix-Trench, Georgia
الحاوية / القاعدة Breast Cancer Res Treat (2017)

Motivators of Inappropriate Ovarian Cancer Screening: A Survey of Women and Their Clinicians

بواسطة Macdonald, Courtney, Mazza, Danielle, Hickey, Martha, Hunter, Morgan, Keogh, Louise A, Investigators, kConFab, Jones, Sandra C, Saunders, Christobel, Nesci, Stephanie, Milne, Roger L, McLachlan, Sue-Anne, Hopper, John L, Friedlander, Michael L, Emery, Jon, Phillips, Kelly-Anne
الحاوية / القاعدة JNCI Cancer Spectr (2020)

Identification of BRCA1 missense substitutions that confer partial functional activity: potential moderate risk variants?

بواسطة Lovelock, Paul K, Spurdle, Amanda B, Mok, Myth TS, Farrugia, Daniel J, Lakhani, Sunil R, Healey, Sue, Arnold, Stephen, Buchanan, Daniel, Investigators, kConFab, Couch, Fergus J, Henderson, Beric R, Goldgar, David E, Tavtigian, Sean V, Chenevix-Trench, Georgia, Brown, Melissa A
منشور في 2007

Classification of BRCA1 missense variants of unknown clinical significance

بواسطة Phelan, C, Dapic, V, Tice, B, Favis, R, Kwan, E, Barany, F, Manoukian, S, Radice, P, van der Luijt, R B, van Nesselrooij, B P M, Chenevix-Trench, G, kConFab, Caldes, T, de La Hoya, M, Lindquist, S, Tavtigian, S, Goldgar, D, Borg, A, Narod, S, Monteiro, A
منشور في 2005

Comprehensive Assessment of BARD1 Messenger Ribonucleic Acid Splicing With Implications for Variant Classification

بواسطة Walker, Logan C., Lattimore, Vanessa Lilian, Kvist, Anders, Kleiblova, Petra, Zemankova, Petra, de Jong, Lucy, Wiggins, George A. R., Hakkaart, Christopher, Cree, Simone L., Behar, Raquel, Houdayer, Claude, Investigators, kConFab, Parsons, Michael T., Kennedy, Martin A., Spurdle, Amanda B., de la Hoya, Miguel
الحاوية / القاعدة Front Genet (2019)

VTRNA2-1: Genetic Variation, Heritable Methylation and Disease Association

بواسطة Dugué, Pierre-Antoine, Yu, Chenglong, McKay, Timothy, Wong, Ee Ming, Joo, Jihoon Eric, Tsimiklis, Helen, Hammet, Fleur, Mahmoodi, Maryam, Theys, Derrick, , kConFab, Hopper, John L., Giles, Graham G., Milne, Roger L., Steen, Jason A., Dowty, James G., Nguyen-Dumont, Tu, Southey, Melissa C.
الحاوية / القاعدة Int J Mol Sci (2021)

Exome sequencing identifies rare deleterious mutations in DNA repair genes FANCC and BLM as potential breast cancer susceptibility alleles.

بواسطة Ella R Thompson, Maria A Doyle, Georgina L Ryland, Simone M Rowley, David Y H Choong, Richard W Tothill, Heather Thorne, kConFab, Daniel R Barnes, Jason Li, Jason Ellul, Gayle K Philip, Yoland C Antill, Paul A James, Alison H Trainer, Gillian Mitchell, Ian G Campbell
منشور في 2012-09-01

Pathogenicity of the BRCA1 missense variant M1775K is determined by the disruption of the BRCT phosphopeptide-binding pocket: a multi-modal approach

بواسطة Tischkowitz, Marc, Hamel, Nancy, Carvalho, Marcelo A, Birrane, Gabriel, Soni, Aditi, van Beers, Erik H, Joosse, Simon A, Wong, Nora, Novak, David, Quenneville, Louise A, Grist, Scott A, kConFab, Nederlof, Petra M, Goldgar, David E, Tavtigian, Sean V, Monteiro, Alvaro N, Ladias, John AA, Foulkes, William D
منشور في 2008

Genetic, functional, and histopathological evaluation of two C‐terminal BRCA1 missense variants

بواسطة Lovelock, P K, Healey, S, Au, W, Sum, E Y M, Tesoriero, A, Wong, E M, Hinson, S, Brinkworth, R, Bekessy, A, Diez, O, Izatt, L, Solomon, E, Jenkins, M, Renard, H, Hopper, J, Waring, P, Investigators, kConFab, Tavtigian, S V, Goldgar, D, Lindeman, G J, Visvader, J E, Couch, F J, Henderson, B R, Southey, M, Chenevix‐Trench, G, Spurdle, A B, Brown, M A
منشور في 2006

Benign breast disease increases breast cancer risk independent of underlying familial risk profile: Findings from a Prospective Family Study Cohort

بواسطة Zeinomar, Nur, Phillips, Kelly-Anne, Daly, Mary B., Milne, Roger L., Dite, Gillian S., MacInnis, Robert J., Liao, Yuyan, Kehm, Rebecca D., Knight, Julia A., Southey, Melissa C., Chung, Wendy K., Giles, Graham G., McLachlan, Sue-Anne, Friedlander, Michael L., Weideman, Prue C., Glendon, Gord, Nesci, Stephanie, Investigators, kConFab, Andrulis, Irene L., Buys, Saundra S., John, Esther M., Hopper, John L., Terry, Mary Beth
الحاوية / القاعدة Int J Cancer (2019)

Modification of Ovarian Cancer Risk by BRCA1/2 Interacting Genes in a Multicenter Cohort of BRCA1/2 Mutation Carriers

بواسطة Rebbeck, Timothy R., Mitra, Nandita, Domchek, Susan M., Wan, Fei, Chuai, Shannon, Friebel, Tara M., Panossian, Saarene, Spurdle, Amanda, Chenevix-Trench, Georgia, kConFab, Singer, Christian F., Pfeiler, Georg, Neuhausen, Susan L., Lynch, Henry T., Garber, Judy E., Weitzel, Jeffrey N., Isaacs, Claudine, Couch, Fergus, Narod, Steven A., Rubinstein, Wendy S., Tomlinson, Gail E., Ganz, Patricia A., Olopade, Olufunmilayo I., Tung, Nadine, Blum, Joanne L., Greenberg, Roger, Nathanson, Katherine L., Daly, Mary B.
منشور في 2009