相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Targeted Resequencing of 30 Genes Improves the Detection of Deleterious Mutations in South Indian Women with Breast and/or Ovarian Cancers
Thangarajan Rajkumar et al.
Asian Pacific Journal of Cancer Prevention (2015)
Global Cancer Statistics, 2012
Lindsey A. Torre et al.
CA-A CANCER JOURNAL FOR CLINICIANS (2015)
Hereditary predisposition to ovarian cancer, looking beyond BRCA1/BRCA2
Lindsey E. Minion et al.
GYNECOLOGIC ONCOLOGY (2015)
A Systematic Comparison of Traditional and Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Genes in More Than 1000 Patients
Stephen E. Lincoln et al.
JOURNAL OF MOLECULAR DIAGNOSTICS (2015)
Global surveillance of cancer survival 1995-2009: analysis of individual data for 25 676 887 patients from 279 population-based registries in 67 countries (CONCORD-2)
Claudia Allemani et al.
LANCET (2015)
Frequency of Mutations in Individuals With Breast Cancer Referred for BRCA1 and BRCA2 Testing Using Next-Generation Sequencing With a 25-Gene Panel
Nadine Tung et al.
CANCER (2015)
Improved molecular diagnosis by the detection of exonic deletions with target gene capture and deep sequencing
Yanming Feng et al.
GENETICS IN MEDICINE (2015)
Cancer incidence and mortality worldwide: Sources, methods and major patterns in GLOBOCAN 2012
Jacques Ferlay et al.
INTERNATIONAL JOURNAL OF CANCER (2015)
Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes
Laurent Castera et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2014)
Clinical Evaluation of a Multiple-Gene Sequencing Panel for Hereditary Cancer Risk Assessment
Allison W. Kurian et al.
JOURNAL OF CLINICAL ONCOLOGY (2014)
Distribution of BRCA1 and BRCA2 Mutations in Asian Patients with Breast Cancer
Haeyoung Kim et al.
JOURNAL OF BREAST CANCER (2013)
Noninvasive detection of cancer-associated genome-wide hypomethylation and copy number aberrations by plasma DNA bisulfite sequencing
K. C. Allen Chan et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)
A Comprehensive Focus on Global Spectrum of BRCA1 and BRCA2 Mutations in Breast Cancer
Fatemeh Karami et al.
BIOMED RESEARCH INTERNATIONAL (2013)
Screening of 185DelAG, 1014DelGT and 3889DelAG BRCA1 Mutations in Breast Cancer Patients from North-East India
Jagadish Hansa et al.
ASIAN PACIFIC JOURNAL OF CANCER PREVENTION (2012)
Global Patterns of Cancer Incidence and Mortality Rates and Trends
Ahmedin Jemal et al.
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION (2010)
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene
Alfons Meindl et al.
NATURE GENETICS (2010)
BRCA1 and BRCA2 germline mutation analysis among Indian women from south India: identification of four novel mutations and high-frequency occurrence of 185delAG mutation
Kannan Vaidyanathan et al.
JOURNAL OF BIOSCIENCES (2009)
ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007
C. Sue Richards et al.
GENETICS IN MEDICINE (2008)
Nijmegen BREAKAGE SYNDROME mutations and risk of breast cancer
Natalia Bogdanova et al.
INTERNATIONAL JOURNAL OF CANCER (2008)
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
Nazneen Rahman et al.
NATURE GENETICS (2007)
Contribution of germline BRCA1 and BRCA2 sequence alterations to breast cancer in Northern India
Sunita Saxena et al.
BMC MEDICAL GENETICS (2006)
RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability
Katri Heikkinen et al.
CARCINOGENESIS (2006)
The variant E233G of the RAD51D gene could be a low-penetrance allele in high-risk breast cancer families without BRCA1/2 mutations
R Rodríguez-López et al.
INTERNATIONAL JOURNAL OF CANCER (2004)
Novel germline mutations in breast cancer susceptibility genes BRCA1, BRCA2 and p53 gene in breast cancer patients from India
S Hedau et al.
BREAST CANCER RESEARCH AND TREATMENT (2004)
D90A-SOD1 Mediated Amyotrophic Lateral Sclerosis: A Single Founder for All Cases With Evidence for a Cis-acting Disease Modifier in the Recessive Haplotype
Matthew J. Parton et al.
HUMAN MUTATION (2002)
Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations
H Meijers-Heijboer et al.
NATURE GENETICS (2002)
Germline BRCA1 mutation analysis in Indian breast/ovarian cancer families
BV Kumar et al.
CANCER BIOLOGY & THERAPY (2002)
BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function
SB Cantor et al.
CELL (2001)
ATM-heterozygous germline mutations contribute to breast cancer-susceptibility
A Broeks et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)
分享论文
