Cancer: Breast

Prevalence of BRCA1/BRCA2 pathogenic variation in Chinese Han population
Hui Dong, Khyati Chandratre, Yue Qin, Jing Zhang, Xiaoqing Tian, Ce Rong, Ning Wang, Maoni Guo, Guoping Zhao, San Ming Wang

Journal of Medical Genetics Aug 2021, 58 (8) 565-569; DOI: 10.1136/jmedgenet-2020-106970
Co-occurrence of germline BRCA1 and CDH1 pathogenic variants
Marie-Charlotte Villy, Emmanuelle Mouret-Fourme, Lisa Golmard, Véronique Becette, Nasrine Callet, Gilles Marx, Chrystelle Colas, Dominique Lamarque, Etienne Rouleau, Dominique Stoppa-Lyonnet

Journal of Medical Genetics Jun 2021, 58 (6) 357-361; DOI: 10.1136/jmedgenet-2020-106972
Variants of uncertain clinical significance in hereditary breast and ovarian cancer genes: best practices in functional analysis for clinical annotation
Alvaro N Monteiro, Peter Bouwman, Arne N Kousholt, Diana M Eccles, Gael A Millot, Jean-Yves Masson, Marjanka K Schmidt, Shyam K Sharan, Ralph Scully, Lisa Wiesmüller, Fergus Couch, Maaike P G Vreeswijk

Journal of Medical Genetics Aug 2020, 57 (8) 509-518; DOI: 10.1136/jmedgenet-2019-106368
Germline BRCA1 and BRCA2 testing for breast cancer survivors
Jennifer Wiggins, Anne McLoughlin, Angela George, Alistair Ring, Zoe Kemp

Journal of Medical Genetics Aug 2020, 57 (8) 528-530; DOI: 10.1136/jmedgenet-2019-106420
Evaluation of the relative effectiveness of the 2017 updated Manchester scoring system for predicting BRCA1/2 mutations in a Southeast Asian country
Winston Chew, Rajesh Babu Moorakonda, Eliza Courtney, Hazel Soh, Shao Tzu Li, Yanni Chen, Tarryn Shaw, John Carson Allen, Dafydd Gareth R Evans, Joanne Ngeow

Journal of Medical Genetics May 2018, 55 (5) 344-350; DOI: 10.1136/jmedgenet-2017-105073
Consensus for genes to be included on cancer panel tests offered by UK genetics services: guidelines of the UK Cancer Genetics Group
Amy Taylor, Angela F Brady, Ian M Frayling, Helen Hanson, Marc Tischkowitz, Clare Turnbull, Lucy Side

Journal of Medical Genetics Jun 2018, 55 (6) 372-377; DOI: 10.1136/jmedgenet-2017-105188
CDH1 germline mutations and the hereditary diffuse gastric and lobular breast cancer syndrome: a multicentre study
Patrick R Benusiglio, David Malka, Etienne Rouleau, Antoine De Pauw, Bruno Buecher, Catherine Noguès, Emmanuelle Fourme, Chrystelle Colas, Florence Coulet, Mathilde Warcoin, Sophie Grandjouan, Alain Sezeur, Pierre Laurent-Puig, Diane Molière, Camille Tlemsani, Marina Di Maria, Veronique Byrde, Suzette Delaloge, Martine Blayau, Olivier Caron

Journal of Medical Genetics Jul 2013, 50 (7) 486-489; DOI: 10.1136/jmedgenet-2012-101472
Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-BRCA1/2 breast cancer families
Inge M M Lakeman, Florentine S Hilbers, Mar Rodríguez-Girondo, Andrew Lee, Maaike P G Vreeswijk, Antoinette Hollestelle, Caroline Seynaeve, Hanne Meijers-Heijboer, Jan C Oosterwijk, Nicoline Hoogerbrugge, Edith Olah, Hans F A Vasen, Christi J van Asperen, Peter Devilee

Journal of Medical Genetics Sep 2019, 56 (9) 581-589; DOI: 10.1136/jmedgenet-2019-106072
A germline deletion of 9p21.3 presenting as familial melanoma, astrocytoma and breast cancer: clinical and genetic counselling challenges
Jaime Vengoechea, Christine Tallo

Journal of Medical Genetics Oct 2017, 54 (10) 682-684; DOI: 10.1136/jmedgenet-2017-104690
Rare, protein-truncating variants in ATM, CHEK2 and PALB2, but not XRCC2, are associated with increased breast cancer risks
Brennan Decker, Jamie Allen, Craig Luccarini, Karen A Pooley, Mitul Shah, Manjeet K Bolla, Qin Wang, Shahana Ahmed, Caroline Baynes, Don M Conroy, Judith Brown, Robert Luben, Elaine A Ostrander, Paul DP Pharoah, Alison M Dunning, Douglas F Easton

Journal of Medical Genetics Nov 2017, 54 (11) 732-741; DOI: 10.1136/jmedgenet-2017-104588

Main menu

Cancer: Breast

Pages

Log in using your username and password

Main menu

Log in using your username and password

You are here

Cancer: Breast

Pages