BRCA1 and BRCA2 as ovarian cancer susceptibility genes

HM Sowter, A Ashworth - Carcinogenesis, 2005 - academic.oup.com
Individuals carrying germline mutations in one allele of the BRCA1 or BRCA2 genes are at
significantly increased risk of developing cancer. Although the increased risk of breast …

Founder BRCA1 and BRCA2 mutations in French Canadian ovarian cancer cases unselected for family history

PN Tonin, AM Mes‐Masson, SA Narod… - Clinical …, 1999 - Wiley Online Library
The breast cancer susceptibility genes, BRCA1 and BRCA2, differ in their contribution to
ovarian cancer. Recently, founder mutations in each of these genes were identified in …

BRCA1 expression in a large series of sporadic ovarian carcinomas: a Gynecologic Oncology Group study

M Thrall, HH Gallion, R Kryscio, M Kapali… - International Journal of …, 2006 - ijgc.bmj.com
BRCA1 is a tumor suppressor gene that, when mutated, is associated with the development
of hereditary ovarian cancer. A role for BRCA1 in the pathoetiology of sporadic ovarian …

Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study.

SL Neuhausen, S Mazoyer, L Friedman… - American journal of …, 1996 - ncbi.nlm.nih.gov
Several BRCA1 mutations have now been found to occur in geographically diverse breast
and ovarian cancer families. To investigate mutation origin and mutation-specific …

Prevalence and clinical correlations of BRCA1/BRCA2 unclassified variant carriers among unselected primary ovarian cancer cases–preliminary report

EJ Majdak, GH De Bock, I Brozek, M Perkowska… - European Journal of …, 2005 - Elsevier
The objective of this study was to determine the prevalence of BRCA1 and BRCA2 gene
mutations in unselected ovarian cancer patients, and to analyse clinical and pathological …

Ovarian Cancer Risk in Ashkenazi Jewish Carriers of BRCA1 and BRCA2 Mutations

JM Satagopan, J Boyd, ND Kauff, M Robson… - Clinical Cancer …, 2002 - AACR
Purpose: Several studies to date have reported ovarian cancer risk due to inherited BRCA1
and BRCA2 mutations using familial data or population-based series of probands. Familial …

[HTML][HTML] Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study

SL Neuhausen, AK Godwin, R Gershoni-Baruch… - The American Journal of …, 1998 - cell.com
Several BRCA2 mutations are found to occur in geographically diverse breast and ovarian
cancer families. To investigate both mutation origin and mutation-specific phenotypes due to …

Mutation Analysis of the BRCA1 Gene in Ovarian Cancers

H Takahashi, K Behbakht, PE McGovern, HC Chiu… - Cancer research, 1995 - AACR
Germline mutations of the BRCA1 tumor suppressor gene on chromosome 17q are involved
in a significant fraction of hereditary breast and ovarian cancers. Allelic deletions that …

BRCA1 sequence variations in 160 individuals referred to a breast/ovarian family cancer clinic. Institut Curie Breast Cancer Group.

D Stoppa-Lyonnet, P Laurent-Puig… - American journal of …, 1997 - ncbi.nlm.nih.gov
An account of familial aggregation in breast/ovarian cancer has become possible with the
identification of BRCA1 germ-line mutations. We evaluated, for 249 individuals registered …

Pathology of Ovarian Cancers in BRCA1 and BRCA2 Carriers

SR Lakhani, S Manek, F Penault-Llorca… - Clinical Cancer …, 2004 - AACR
Purpose: Germline mutations in the BRCA1 and BRCA2 genes confer increased
susceptibility to ovarian cancer. There is evidence that tumors in carriers may exhibit a …