Related references
Note: Only part of the references are listed.Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
Sarah E. Medland et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
MERIT40 controls BRCA1-Rap80 complex integrity and recruitment to DNA double-strand breaks
Genze Shao et al.
GENES & DEVELOPMENT (2009)
MERIT40 facilitates BRCA1 localization and DNA damage repair
Lin Feng et al.
GENES & DEVELOPMENT (2009)
NBA1, a new player in the Brca1 A complex, is required for DNA damage resistance and checkpoint control
Bin Wang et al.
GENES & DEVELOPMENT (2009)
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers
Antonis C. Antoniou et al.
HUMAN MOLECULAR GENETICS (2009)
Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers
Antonis C. Antoniou et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions
A. C. Antoniou et al.
BRITISH JOURNAL OF CANCER (2008)
Identification of Common Variants on the SHBG Gene Affecting Sex Hormone-Binding Globulin Levels and Breast Cancer Risk in Postmenopausal Women
Deborah J. Thompson et al.
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION (2008)
The average cumulative risks of breast and ovarian cancer for carriers of mutations in BRCA1 and BRCA2 attending genetic counseling units in Spain
Roger L. Milne et al.
CLINICAL CANCER RESEARCH (2008)
Variation of breast cancer risk among BRCA1/2 carriers
Colin B. Begg et al.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION (2008)
Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer
Simon N. Stacey et al.
NATURE GENETICS (2008)
A Genomic Background Based Method for Association Analysis in Related Individuals
Najaf Amin et al.
PLOS ONE (2007)
RAD51 135G→C modifies breast cancer risk among BRCA2 mutation carriers:: Results from a combined analysis of 19 studies
Antonis C. Antoniou et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer
Simon N. Stacey et al.
NATURE GENETICS (2007)
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
David J. Hunter et al.
NATURE GENETICS (2007)
Genome-wide association study identifies novel breast cancer susceptibility loci
Douglas F. Easton et al.
NATURE (2007)
GenABEL: an R library for genome-wide association analysis
Yurii S. Aulchenko et al.
BIOINFORMATICS (2007)
An R package for analysis of whole-genome association studies
David Clayton et al.
HUMAN HEREDITY (2007)
Overcoming the winner's curse:: Estimating penetrance parameters from case-control data
Sebastian Zollner et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
The 185delAG mutation (c.68_ 69delAG) in the BRCA1 gene triggers translation reinitiation at a downstream AUG codon
Monique Buisson et al.
HUMAN MUTATION (2006)
Familial clustering of site-specific cancer risks associated with BRCA1 and BRCA2 mutations in the Ashkenazi Jewish population
S Simchoni et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Prediction of BRCA1 status in patients with breast cancer using estrogen receptor and basal phenotype
SR Lakhani et al.
CLINICAL CANCER RESEARCH (2005)
A weighted cohort approach for analysing factors modifying disease risks in carriers of high-risk susceptibility genes
AC Antoniou et al.
GENETIC EPIDEMIOLOGY (2005)
Estimation of the inbreeding coefficient through use of genomic data
AL Leutenegger et al.
AMERICAN JOURNAL OF HUMAN GENETICS (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)
The nonsense-mediated mRNA decay pathway triggers degradation of most BRCA1 mRNAs bearing premature termination codons
L Perrin-Vidoz et al.
HUMAN MOLECULAR GENETICS (2002)
The pathology of familial breast cancer:: Predictive value of immunohistochemical markers estrogen receptor, progesterone receptor, HER-2, and p53 in patients with mutations in BRCA1 and BRCA2
SR Lakhani et al.
JOURNAL OF CLINICAL ONCOLOGY (2002)
A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes
HX Liu et al.
NATURE GENETICS (2001)
Share Paper
