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Paper Details

The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the population.
Hum Mol Genet
99
2014
BRCA1, BRCA1 mutation, BRCA2, BRCA2 mutation, Barcoded fragment libraries, EOC, MLH1, MSH2, MSH2 mutation, MSH6, PMS2, coding sequence, germline DNA, invasive epithelial ovarian cancer, mismatch repair, mismatch repair gene, mismatch repair genes, ovarian cancer, susceptibility genes, women
Author NameAffiliation
Honglin SongUniversity of Cambridge
Mine S CicekMayo Clinic
Susan J RamusKeck School of Medicine, USC/Norris Comprehensive Cancer Center, University of Southern California
Susan J RamusKeck School of Medicine, USC/Norris Comprehensive Cancer Center, University of Southern California
Brooke L FridleyUniversity of Kansas Medical Center
Jonathan TyrerUniversity of Cambridge
Jennifer AlsopUniversity of Cambridge
Mercedes Jimenez-LinanAddenbrooke's Hospital
Simon A GaytherKeck School of Medicine, USC/Norris Comprehensive Cancer Center, University of Southern California
Ellen L GoodeMayo Clinic
Paul D P PharoahUniversity of Cambridge
Paul D P PharoahUniversity of Cambridge
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