Inherited breast cancer predisposition in Asians: multigene panel testing outcomes from Singapore

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

(2015) Sue Richards et al.   GENETICS IN MEDICINE

Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk

(2015) Douglas F. Easton et al.   NEW ENGLAND JOURNAL OF MEDICINE

Predictive Factors for BRCA1 and BRCA2 Genetic Testing in an Asian Clinic-Based Population

(2015) Edward S. Y. Wong et al.   PLoS One

Evaluation and optimisation of indel detection workflows for ion torrent sequencing of the BRCA1 and BRCA2 genes

(2014) Zhen Yeo et al.   BMC GENOMICS

Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients

(2014) Holly LaDuca et al.   GENETICS IN MEDICINE

Clinical Evaluation of a Multiple-Gene Sequencing Panel for Hereditary Cancer Risk Assessment

(2014) Allison W. Kurian et al.   JOURNAL OF CLINICAL ONCOLOGY

Realizing the promise of cancer predisposition genes

(2014) Nazneen Rahman   NATURE

Breast-Cancer Risk in Families with Mutations in PALB2

(2014)   NEW ENGLAND JOURNAL OF MEDICINE

Breast-Cancer Risk in Families with Mutations in PALB2

(2014) Antonis C. Antoniou et al.   NEW ENGLAND JOURNAL OF MEDICINE

Germline Variation in Cancer-Susceptibility Genes in a Healthy, Ancestrally Diverse Cohort: Implications for Individual Genome Sequencing

(2014) Dale L. Bodian et al.   PLoS One

BRCA1 testing should be offered to individuals with triple-negative breast cancer diagnosed below 50 years

(2012) L Robertson et al.   BRITISH JOURNAL OF CANCER

Development of a Next-Generation Sequencing Method for BRCA Mutation Screening

(2012) Maurice Chan et al.   JOURNAL OF MOLECULAR DIAGNOSTICS

Comprehensive Analysis of Missense Variations in the BRCT Domain of BRCA1 by Structural and Functional Assays

(2010) Megan S. Lee et al.   CANCER RESEARCH

MutationTaster evaluates disease-causing potential of sequence alterations

(2010) Jana Marie Schwarz et al.   NATURE METHODS

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

(2010) K. Wang et al.   NUCLEIC ACIDS RESEARCH

BRCA1 and BRCA2 germline mutations in Korean ovarian cancer patients

(2009) Myong Cheol Lim et al.   JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

(2009) Prateek Kumar et al.   Nature Protocols

Germline BRCA1 mutations predispose to pancreatic adenocarcinoma

(2008) Wigdan Al-Sukhni et al.   HUMAN GENETICS

Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results

(2008) Sharon E. Plon et al.   HUMAN MUTATION