et al.RAD51D mutations have been recently identified in breast (BC) and ovarian cancer (OC) families. Although an etiological role in OC appears to be present, the association of RAD51D mutations and BC risk is more unclear. We aimed to determine the prevalence of germline RAD51D mutations in Spanish BC/OC families negative for BRCA1/BRCA2 mutations. We analyzed 842 index patients: 491 from BC/OC families, 171 BC families, 51 OC families and 129 patients without family history but with early-onset BC or OC or metachronous BC and OC. Mutation detection was performed with high-resolution melting, denaturing high-performance liquid chromatography or Sanger sequencing. Three mutations were found in four families with BC and OC cases (0.82%). Tw...
Whereas RAD51C mutations increase the relative risk for ovarian cancer (OC) to 5.88 (95% confidence ...
Several studies have reported that mutations in genes involved in maintenance of genome integrity ma...
In this study, we aim to gain insight in the germline mutation spectrum of ATM, BARD1, BRIP1, ERCC4,...
RAD51D mutations have been recently identified in breast (BC) and ovarian cancer (OC) families. Alth...
Background:Recent data show that mutations in RAD51D have an aetiological role in ovarian carcinoma,...
Mutations in RAD51D have been associated with an increased risk of hereditary ovarian cancer and alt...
BACKGROUND: Recent data show that mutations in RAD51D have an aetiological role in ovarian carcinoma...
Despite extensive analysis of the BRCA1 and BRCA2 genes, germline mutations are detected in < 20% of...
Recent studies have conferred that the RAD51C and RAD51D genes, which code for the essential protein...
International audienceBACKGROUND: Most currently known breast cancer predisposition genes play a rol...
There is strong evidence that overtly inactivating mutations in RAD51C predispose to hereditary brea...
Recently, RAD51C mutations were identified in families with breast and ovarian cancer(1). This obser...
A homozygous mutation in the RAD51C gene was recently found to cause Fanconi anemia-like disorder. F...
Background: In the last fifteen years, familiar ovarian carcinoma has been related to BRCA 1 and 2 m...
BRCA1 and BRCA2 are the most well-known breast cancer susceptibility genes. Additional genes involve...
Whereas RAD51C mutations increase the relative risk for ovarian cancer (OC) to 5.88 (95% confidence ...
Several studies have reported that mutations in genes involved in maintenance of genome integrity ma...
In this study, we aim to gain insight in the germline mutation spectrum of ATM, BARD1, BRIP1, ERCC4,...
RAD51D mutations have been recently identified in breast (BC) and ovarian cancer (OC) families. Alth...
Background:Recent data show that mutations in RAD51D have an aetiological role in ovarian carcinoma,...
Mutations in RAD51D have been associated with an increased risk of hereditary ovarian cancer and alt...
BACKGROUND: Recent data show that mutations in RAD51D have an aetiological role in ovarian carcinoma...
Despite extensive analysis of the BRCA1 and BRCA2 genes, germline mutations are detected in < 20% of...
Recent studies have conferred that the RAD51C and RAD51D genes, which code for the essential protein...
International audienceBACKGROUND: Most currently known breast cancer predisposition genes play a rol...
There is strong evidence that overtly inactivating mutations in RAD51C predispose to hereditary brea...
Recently, RAD51C mutations were identified in families with breast and ovarian cancer(1). This obser...
A homozygous mutation in the RAD51C gene was recently found to cause Fanconi anemia-like disorder. F...
Background: In the last fifteen years, familiar ovarian carcinoma has been related to BRCA 1 and 2 m...
BRCA1 and BRCA2 are the most well-known breast cancer susceptibility genes. Additional genes involve...
Whereas RAD51C mutations increase the relative risk for ovarian cancer (OC) to 5.88 (95% confidence ...
Several studies have reported that mutations in genes involved in maintenance of genome integrity ma...
In this study, we aim to gain insight in the germline mutation spectrum of ATM, BARD1, BRIP1, ERCC4,...