International audienceCDK12 variants were investigated as a genetic susceptibility to ovarian cancer in a series of 416 unrelated and consecutive patients with ovarian carcinoma and who carry neither germline BRCA1 nor BRCA2 pathogenic variant. The presence of CDK12 variants was searched in germline DNA by massive parallel sequencing on pooled DNAs. The lack of detection of deleterious variants and the observed proportion of missense variants in the series of ovarian carcinoma patients as compared with all human populations strongly suggests that CDK12 is not an ovarian cancer predisposing gene
At least 10% of all ovarian cancers are estimated to have a hereditary background. Hereditary breast...
Background: Few studies have attempted to characterise genomic changes occurring in hereditary epith...
BACKGROUND: Histology restricted genetic predisposition testing of ovarian carcinoma patients is a t...
International audienceCDK12 variants were investigated as a genetic susceptibility to ovarian cancer...
SummaryTo establish the contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cance...
BACKGROUND: Germline mutations in BRCA1 and BRCA2 are responsible for 5%-10% of epithelial ovarian c...
OBJECTIVES: Mutations in the BRCA1 and BRCA2 genes predispose women to ovarian and/or breast cancer....
Constitutional loss-of-function pathogenic variants in the tumor suppressor genes BRCA1 and BRCA2 ar...
Several lines of epidemiological study have suggested the presence of a genetic factor for carcinoge...
Clinical criteria for genetic testing of genes other than BRCA1/2 in epithelial ovarian cancer (EOC)...
Background Identification of families at risk for ovarian cancer offers the opportunity to consider ...
Identification of families at risk for ovarian cancer offers the opportunity to consider prophylacti...
A population-based series of 649 unselected incident cases of ovarian cancer diagnosed in Ontario, C...
Background: Histology restricted genetic predisposition testing of ovarian carcinoma patients is a t...
The objective of this study was to determine the prevalence of BRCA1 and BRCA2 gene mutations in uns...
At least 10% of all ovarian cancers are estimated to have a hereditary background. Hereditary breast...
Background: Few studies have attempted to characterise genomic changes occurring in hereditary epith...
BACKGROUND: Histology restricted genetic predisposition testing of ovarian carcinoma patients is a t...
International audienceCDK12 variants were investigated as a genetic susceptibility to ovarian cancer...
SummaryTo establish the contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cance...
BACKGROUND: Germline mutations in BRCA1 and BRCA2 are responsible for 5%-10% of epithelial ovarian c...
OBJECTIVES: Mutations in the BRCA1 and BRCA2 genes predispose women to ovarian and/or breast cancer....
Constitutional loss-of-function pathogenic variants in the tumor suppressor genes BRCA1 and BRCA2 ar...
Several lines of epidemiological study have suggested the presence of a genetic factor for carcinoge...
Clinical criteria for genetic testing of genes other than BRCA1/2 in epithelial ovarian cancer (EOC)...
Background Identification of families at risk for ovarian cancer offers the opportunity to consider ...
Identification of families at risk for ovarian cancer offers the opportunity to consider prophylacti...
A population-based series of 649 unselected incident cases of ovarian cancer diagnosed in Ontario, C...
Background: Histology restricted genetic predisposition testing of ovarian carcinoma patients is a t...
The objective of this study was to determine the prevalence of BRCA1 and BRCA2 gene mutations in uns...
At least 10% of all ovarian cancers are estimated to have a hereditary background. Hereditary breast...
Background: Few studies have attempted to characterise genomic changes occurring in hereditary epith...
BACKGROUND: Histology restricted genetic predisposition testing of ovarian carcinoma patients is a t...