Related references
Note: Only part of the references are listed.Common variants at the CHEK2 gene locus and risk of epithelial ovarian cancer
Kate Lawrenson et al.
CARCINOGENESIS (2015)
Fanconi anemia: a model disease for studies on human genetics and advanced therapeutics
Massimo Bogliolo et al.
CURRENT OPINION IN GENETICS & DEVELOPMENT (2015)
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
Sue Richards et al.
GENETICS IN MEDICINE (2015)
The Fanconi Anemia Pathway Maintains Genome Stability by Coordinating Replication and Transcription
Rebekka A. Schwab et al.
MOLECULAR CELL (2015)
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
Karoline B. Kuchenbaecker et al.
NATURE GENETICS (2015)
Mutation Analysis of the RAD51C and RAD51D Genes in High-Risk Ovarian Cancer Patients and Families from the Czech Republic
Marketa Janatova et al.
PLOS ONE (2015)
BRCA1 regulates PIG3-mediated apoptosis in a p53-dependent manner
Wenwen Zhang et al.
ONCOTARGET (2015)
Reevaluation of the BRCA2 truncating allele c.9976A > T (p.Lys3326Ter) in a familial breast cancer context
Ella R. Thompson et al.
SCIENTIFIC REPORTS (2015)
Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas
Kathryn P. Pennington et al.
CLINICAL CANCER RESEARCH (2014)
Biallelic MUTYH mutations can mimic Lynch syndrome
Monika Morak et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2014)
Domain within the helicase subunit Mcm4 integrates multiple kinase signals to control DNA replication initiation and fork progression
Yi-Jun Sheu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
BRCA2 is epistatic to the RAD51 paralogs in response to DNA damage
Ryan B. Jensen et al.
DNA REPAIR (2013)
DNA polymerase POLQ and cellular defense against DNA damage
Matthew J. Yousefzadeh et al.
DNA REPAIR (2013)
GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer
Paul D. P. Pharoah et al.
NATURE GENETICS (2013)
Analysis of RAD51D in Ovarian Cancer Patients and Families with a History of Ovarian or Breast Cancer
Ella R. Thompson et al.
PLOS ONE (2013)
A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3
Pablo Cingolani et al.
FLY (2012)
Extracolonic Manifestations of Lynch Syndrome
Brian Bansidhar
Clinics in Colon and Rectal Surgery (2012)
Germline mutations in RAD51D confer susceptibility to ovarian cancer
Chey Loveday et al.
NATURE GENETICS (2011)
A framework for variation discovery and genotyping using next-generation DNA sequencing data
Mark A. DePristo 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)
Interplay between BRCA1 and RHAMM Regulates Epithelial Apicobasal Polarization and May Influence Risk of Breast Cancer
Christopher A. Maxwell et al.
PLOS BIOLOGY (2011)
Missense Variants in ATM in 26,101 Breast Cancer Cases and 29,842 Controls
Olivia Fletcher et al.
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION (2010)
Mouse Rad1 deletion enhances susceptibility for skin tumor development
Lu Han et al.
MOLECULAR CANCER (2010)
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene
Alfons Meindl et al.
NATURE GENETICS (2010)
The Sequence Alignment/Map format and SAMtools
Heng Li et al.
BIOINFORMATICS (2009)
Fast and accurate short read alignment with Burrows-Wheeler transform
Heng Li et al.
BIOINFORMATICS (2009)
Polk mutant mice have a spontaneous mutator phenotype
J. Nicole Kosarek Stancel et al.
DNA REPAIR (2009)
Fancm-deficient mice reveal unique features of Fanconi anemia complementation group M
Sietske T. Bakker et al.
HUMAN MOLECULAR GENETICS (2009)
Genetic variants of uncertain significance: Flies in the ointment
Susan Domchek et al.
JOURNAL OF CLINICAL ONCOLOGY (2008)
The frequency of Muir-Torre syndrome among lynch syndrome families
Christopher D. South et al.
JOURNAL OF THE NATIONAL CANCER INSTITUTE (2008)
Germline BRCA2 mutations and the risk of esophageal squamous cell carcinoma
M. R. Akbari et al.
ONCOGENE (2008)
Network modeling links breast cancer susceptibility and centrosome dysfunction
Miguel Angel Pujana et al.
NATURE GENETICS (2007)
Counting potentially functional variants in BRCA1, BRCA2 and ATM predicts breast cancer susceptibility
Nichola Johnson et al.
HUMAN MOLECULAR GENETICS (2007)
A recurrent mutation in PALB2 in Finnish cancer families
Hannele Erkko et al.
NATURE (2007)
A viable allele of Mcm4 causes chromosome instability and mammary adenocarcinomas in mice
Naoko Shima et al.
NATURE GENETICS (2007)
Variants in the GH-IGF axis confer susceptibility to lung cancer
Matthew F. Rudd et al.
GENOME RESEARCH (2006)
Absence of mouse REC8 cohesin promotes synapsis of sister chromatids in meiosis
HL Xu et al.
DEVELOPMENTAL CELL (2005)
Increased prevalence of the BRCA2 polymorphic stop codon K3326X among individuals with familial pancreatic cancer
ST Martin et al.
ONCOGENE (2005)
RAD52 Y415X truncation polymorphism and epithelial ovarian cancer risk in Australian women
L Kelemen et al.
CANCER LETTERS (2005)
RAD51 localization and activation following DNA damage
M Tarsounas et al.
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES (2004)
SIFT: predicting amino acid changes that affect protein function
PC Ng et al.
NUCLEIC ACIDS RESEARCH (2003)
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)
Initial sequencing and analysis of the human genome
ES Lander et al.
NATURE (2001)
dbSNP: the NCBI database of genetic variation
ST Sherry et al.
NUCLEIC ACIDS RESEARCH (2001)
ATM-heterozygous germline mutations contribute to breast cancer-susceptibility
A Broeks et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)