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OBSTETRICS AND GYNECOLOGY (2014)
Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer families
D. J. Osher et al.
BRITISH JOURNAL OF CANCER (2012)
Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)
Nasim Mavaddat et al.
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION (2012)
Analysis of RAD51C Germline Mutations in High-Risk Breast and Ovarian Cancer Families and Ovarian Cancer Patients
Ella R. Thompson et al.
HUMAN MUTATION (2012)
Association Between BRCA1 and BRCA2 Mutations and Survival in Women With Invasive Epithelial Ovarian Cancer
Kelly L. Bolton et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2012)
Online Tool to Guide Decisions for BRCA1/2 Mutation Carriers
Allison W. Kurian et al.
JOURNAL OF CLINICAL ONCOLOGY (2012)
Identification of Individuals at Risk for Lynch Syndrome Using Targeted Evaluations and Genetic Testing: National Society of Genetic Counselors and the Collaborative Group of the Americas on Inherited Colorectal Cancer Joint Practice Guideline
Scott M. Weissman et al.
JOURNAL OF GENETIC COUNSELING (2012)
Olaparib Maintenance Therapy in Platinum-Sensitive Relapsed Ovarian Cancer
Jonathan Ledermann et al.
NEW ENGLAND JOURNAL OF MEDICINE (2012)
BRCA1 and BRCA2: different roles in a common pathway of genome protection
Rohini Roy et al.
NATURE REVIEWS CANCER (2012)
Further evidence for the contribution of the RAD51C gene in hereditary breast and ovarian cancer susceptibility
Mikko Vuorela et al.
BREAST CANCER RESEARCH AND TREATMENT (2011)
RAD51C is a susceptibility gene for ovarian cancer
Liisa M. Pelttari et al.
HUMAN MOLECULAR GENETICS (2011)
Genetic Counseling Considerations in the Evaluation of Families for Lynch Syndrome-A Review
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JOURNAL OF GENETIC COUNSELING (2011)
Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers
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JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE (2011)
Olaparib in patients with recurrent high-grade serous or poorly differentiated ovarian carcinoma or triple-negative breast cancer: a phase 2, multicentre, open-label, non-randomised study
Karen A. Gelmon et al.
LANCET ONCOLOGY (2011)
Germline mutations in RAD51D confer susceptibility to ovarian cancer
Chey Loveday et al.
NATURE GENETICS (2011)
Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing
Tom Walsh et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
High Cancer Risk in Peutz-Jeghers Syndrome: A Systematic Review and Surveillance Recommendations
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AMERICAN JOURNAL OF GASTROENTEROLOGY (2010)
The Leu33Pro polymorphism in the ITGB3 gene does not modify BRCA1/2-associated breast or ovarian cancer risks: results from a multicenter study among 15,542 BRCA1 and BRCA2 mutation carriers
Anna Jakubowska et al.
BREAST CANCER RESEARCH AND TREATMENT (2010)
Occult ovarian cancers identified at risk-reducing salpingo-oophorectomy in a prospective cohort of BRCA1/2 mutation carriers
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BREAST CANCER RESEARCH AND TREATMENT (2010)
Oral contraceptive use and breast or ovarian cancer risk in BRCA1/2 carriers: A meta-analysis
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EUROPEAN JOURNAL OF CANCER (2010)
Peutz-Jeghers syndrome: a systematic review and recommendations for management
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GUT (2010)
SGO White Paper on Ovarian Cancer: Etiology, Screening and Surveillance
John O. Schorge et al.
GYNECOLOGIC ONCOLOGY (2010)
Truncating mutations in Peutz-Jeghers syndrome are associated with more polyps, surgical interventions and cancers
Heidi Salloch et al.
INTERNATIONAL JOURNAL OF COLORECTAL DISEASE (2010)
Association of Risk-Reducing Surgery in BRCA1 or BRCA2 Mutation Carriers With Cancer Risk and Mortality
Susan M. Domchek et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2010)
Poly(ADP)-Ribose Polymerase Inhibition: Frequent Durable Responses in BRCA Carrier Ovarian Cancer Correlating With Platinum-Free Interval
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JOURNAL OF CLINICAL ONCOLOGY (2010)
Oral poly(ADP-ribose) polymerase inhibitor olaparib in patients with BRCA1 or BRCA2 mutations and recurrent ovarian cancer: a proof-of-concept trial
M. William Audeh et al.
LANCET (2010)
Mutation of the RAD51C gene in a Fanconi anemia-like disorder
Fiona Vaz et al.
NATURE GENETICS (2010)
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene
Alfons Meindl et al.
NATURE GENETICS (2010)
PARP inhibition: PARP1 and beyond
Michele Rouleau et al.
NATURE REVIEWS CANCER (2010)
Modification of Ovarian Cancer Risk by BRCA1/2-interacting Genes in a Multicenter Cohort of BRCA1/2 Mutation Carriers
Timothy R. Rebbeck et al.
CANCER RESEARCH (2009)
EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome
Glenn E. Palomaki et al.
GENETICS IN MEDICINE (2009)
Meta-analysis of Risk Reduction Estimates Associated With Risk-Reducing Salpingo-oophorectomy in BRCA1 or BRCA2 Mutation Carriers
Timothy R. Rebbeck et al.
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE (2009)
Inhibition of Poly(ADP-Ribose) Polymerase in Tumors from BRCA Mutation Carriers.
Peter C. Fong et al.
NEW ENGLAND JOURNAL OF MEDICINE (2009)
Microsatellite instability and mismatch repair protein defects in ovarian epithelial neoplasms in patients 50 years of age and younger
Kristin C. Jensen et al.
AMERICAN JOURNAL OF SURGICAL PATHOLOGY (2008)
Effect of Reproductive Factors and Oral Contraceptives on Breast Cancer Risk in BRCA1/2 Mutation Carriers and Noncarriers: Results from a Population-Based Study
Eunjung Lee et al.
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION (2008)
Systematic Review and Meta-analysis of Ovarian Cancers: Estimation of Microsatellite-High Frequency and Characterization of Mismatch Repair Deficient Tumor Histology
Tuya Pal et al.
CLINICAL CANCER RESEARCH (2008)
Probability of BRCA1/2 mutation varies with ovarian histology:: results from screening 442 ovarian cancer families
D. G. R. Evans et al.
CLINICAL GENETICS (2008)
Colorectal cancer in HNPCC: cumulative lifetime incidence, survival and tumour distribution. A report of 121 families with proven mutations
E. Barrow et al.
CLINICAL GENETICS (2008)
The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome
Patrice Watson et al.
INTERNATIONAL JOURNAL OF CANCER (2008)
Risk-reducing salpingo-oophorectomy for the prevention of BRCA1- and BRCA2-associated breast and gynecologic cancer:: A multicenter, prospective study
Noah D. Kauff et al.
JOURNAL OF CLINICAL ONCOLOGY (2008)
Feasibility of Screening for Lynch Syndrome Among Patients With Colorectal Cancer
Heather Hampel et al.
JOURNAL OF CLINICAL ONCOLOGY (2008)
BRCAness Syndrome in Ovarian Cancer: A Case-Control Study Describing the Clinical Features and Outcome of Patients With Epithelial Ovarian Cancer Associated With BRCA1 and BRCA2 Mutations
David S. P. Tan et al.
JOURNAL OF CLINICAL ONCOLOGY (2008)
Effect of BRCA1/2 mutations on long-term survival of patients with invasive ovarian cancer: The national Israeli study of ovarian cancer
Angela Chetrit et al.
JOURNAL OF CLINICAL ONCOLOGY (2008)
Society of Gynecologic Oncologists education committee statement on risk assessment for inherited gynecologic cancer predispositions
Johnathan M. Lancaster et al.
GYNECOLOGIC ONCOLOGY (2007)
Molecular and clinical characteristics in 46 families affected with peutz-jeghers syndrome
Hamid Mehenni et al.
DIGESTIVE DISEASES AND SCIENCES (2007)
Ovarian cancer at young age:: the contribution of mismatch-repair defects in a population-based series of epithelial ovarian cancer before age 40
K. Domanska et al.
INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER (2007)
Meta-analysis of BRCA1 and BRCA2 penetrance
Sining Chen et al.
JOURNAL OF CLINICAL ONCOLOGY (2007)
BRCA1 and BRCA2 mutation carriers, oral contraceptive use, and breast cancer before age 50
Robert W. Haile et al.
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION (2006)
Salpingo-oophorectomy and the risk of ovarian, fallopian tube, and peritoneal cancers in women with a BRCA1 or BRCA2 mutation
Amy Finch et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2006)
LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome
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JOURNAL OF MEDICAL GENETICS (2006)
Characterization of BRCA1 and BRCA2 mutations in a large United States sample
SN Chen et al.
JOURNAL OF CLINICAL ONCOLOGY (2006)
Clinical and pathologic findings of prophylactic salpingo-oophorectomies in 159 BRCA1 and BRCA2 carriers
A Finch et al.
GYNECOLOGIC ONCOLOGY (2006)
BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases
T Pal et al.
CANCER (2005)
High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome
S Aretz et al.
HUMAN MUTATION (2005)
Breast cancer risk following bilateral oophorectorny in BRCA1 and BRCA2 mutation carriers:: An international case-control study
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JOURNAL OF CLINICAL ONCOLOGY (2005)
Genetic risk assessment and BRCA mutation testing for breast and ovarian cancer susceptibility:: Recommendation statement
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ANNALS OF INTERNAL MEDICINE (2005)
Screening for familial ovarian cancer: Failure of current protocols to detect ovarian cancer at an early stage according to the International Federation of Gynecology and Obstetrics System
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JOURNAL OF CLINICAL ONCOLOGY (2005)
Specific killing of BRCA2-deficient tumours with inhibitors of poly(ADP-ribose) polymerase
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NATURE (2005)
Risk-reducing salpingo-oophorectomy in BRCA mutation carriers: Role of serial sectioning in the detection of occult malignancy
CB Powell et al.
JOURNAL OF CLINICAL ONCOLOGY (2005)
The hamartomatous polyposis syndromes: A clinical and molecular review
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AMERICAN JOURNAL OF GASTROENTEROLOGY (2005)
Oral contraceptive use and risk of early-onset breast cancer in carriers and noncarriers of BRCA1 and BRCA2 mutations
RL Milne et al.
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION (2005)
Survival of patients with ovarian cancer due to a mismatch repair defect
TEM Crijnen et al.
FAMILIAL CANCER (2005)
Genotype-phenotype correlations in Peutz-Jeghers syndrome
CI Amos et al.
JOURNAL OF MEDICAL GENETICS (2004)
Pathology of ovarian cancers in BRCA1 and BRCA2 carriers
SR Lakhani et al.
CLINICAL CANCER RESEARCH (2004)
Mapping of a translocation breakpoint in a Peutz-Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STKII-negative PJS cases
N Hearle et al.
GENES CHROMOSOMES & CANCER (2004)
Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations:: Impact on counseling and surveillance
YMC Hendriks et al.
GASTROENTEROLOGY (2004)
Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history:: A combined analysis of 22 studies
A Antoniou et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
Improved survival in women with BRCA-associated ovarian carcinoma
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CANCER (2003)
Hereditary polyposis syndromes and hereditary non-polyposis colorectal cancer
BA Allen et al.
BEST PRACTICE & RESEARCH CLINICAL GASTROENTEROLOGY (2003)
Heritable colorectal cancer syndromes: recognition and preventive management
LA Boardman
GASTROENTEROLOGY CLINICS OF NORTH AMERICA (2002)
Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2:: Analysis of 10,000 individuals
TS Frank et al.
JOURNAL OF CLINICAL ONCOLOGY (2002)
The clinical features of ovarian cancer in hereditary nonpolyposis colorectal cancer
P Watson et al.
GYNECOLOGIC ONCOLOGY (2001)
Parity, oral contraceptives, and the risk of ovarian cancer among carriers and noncarriers of a BRCA1 or BRCA2 mutation
B Modan et al.
NEW ENGLAND JOURNAL OF MEDICINE (2001)
Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer
HA Risch et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Variation in cancer risks, by mutation position, in BRCA2 mutation carriers
D Thompson et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Very high risk of cancer in familial Peutz-Jeghers syndrome
FM Giardiello et al.
GASTROENTEROLOGY (2000)
Clinicopathologic features of BRCA-linked and sporadic ovarian cancer
J Boyd et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2000)
BRCA1 and BRCA2 mutation analysis of 208 Ashkenazi Jewish women with ovarian cancer
R Moslehi et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)
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