Vijai, Joseph

Selected publications

Prospective Evaluation of Germline Alterations in Patients With Exocrine Pancreatic Neoplasms. Journal of the National Cancer Institute. 2018 Academic Article GET IT
Times cited: 27
Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer. Nature Genetics. 2017 Academic Article GET IT
Times cited: 66
Clinical Evaluation of Cisplatin Sensitivity of Germline Polymorphisms in Neoadjuvant Chemotherapy for Urothelial Cancer. Clinical Genitourinary Cancer. 2016 Academic Article GET IT
Times cited: 2
A recurrent ERCC3 truncating mutation confers moderate risk for breast cancer. Cancer Discovery. 2016 Academic Article GET IT
Times cited: 15
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus. Nature Communications. 2016 Academic Article GET IT
Times cited: 24
Collaborative science in the next-generation sequencing era: A viewpoint on how to combine exome sequencing data across sites to identify novel disease susceptibility genes. Briefings in Bioinformatics. 2016 Academic Article GET IT
Times cited: 2
Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus. Breast Cancer Research. 2016 Academic Article GET IT
Times cited: 13
Evaluation of ACMG-Guideline-Based Variant Classification of Cancer Susceptibility and Non-Cancer-Associated Genes in Families Affected by Breast Cancer. American Journal of Human Genetics. 2016 Academic Article GET IT
Times cited: 45
No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer. Gynecologic Oncology. 2016 Review GET IT
Times cited: 8
Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes. Human Molecular Genetics. 2016 Academic Article GET IT
Times cited: 26
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170. Nature Genetics. 2016 Review GET IT
Times cited: 53
Genome sequencing of multiple primary tumors reveals a novel PALB2 variant. Journal of Clinical Oncology. 2016 Academic Article GET IT
Times cited: 3
Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia. Nature Communications. 2016 Review GET IT
Times cited: 41
Male breast cancer in BRCA1 and BRCA2 mutation carriers: Pathology data from the Consortium of Investigators of Modifiers of BRCA1/2. Breast Cancer Research. 2016 Academic Article GET IT
Times cited: 33
Analysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer types. Journal of the National Cancer Institute. 2016 Academic Article GET IT
Times cited: 68
Tissue-specific enrichment of lymphoma risk loci in regulatory elements. PLoS ONE. 2015 Academic Article GET IT
Times cited: 2
Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of european ancestry. Human Molecular Genetics. 2015 Review GET IT
Times cited: 20
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers. Breast Cancer Research. 2015 Academic Article GET IT
Times cited: 13
FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor. Human Molecular Genetics. 2015 Academic Article GET IT
Times cited: 43
Assessing associations between the AURKAHMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers. PLoS ONE. 2015 Academic Article GET IT
Times cited: 11
A genome-wide association study of marginal zone lymphoma shows association to the HLA region. Nature Communications. 2015 Academic Article GET IT
Times cited: 29
Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer. JAMA - Journal of the American Medical Association. 2015 Academic Article GET IT
Times cited: 178
Germline ETV6 Mutations Confer Susceptibility to Acute Lymphoblastic Leukemia and Thrombocytopenia. PLoS Genetics. 2015 Academic Article GET IT
Times cited: 72
Identification of six new susceptibility loci for invasive epithelial ovarian cancer. Nature Genetics. 2015 Review GET IT
Times cited: 133
Prediction of breast cancer risk based on profiling with common genetic variants. Journal of the National Cancer Institute. 2015 Academic Article GET IT
Times cited: 216
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers. Breast Cancer Research. 2014 Academic Article GET IT
Times cited: 25
Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma. Nature Genetics. 2014 Review GET IT
Times cited: 77
Genetic variation in DNA repair pathways and risk of non-Hodgkin's lymphoma. PLoS ONE. 2014 Academic Article GET IT
Times cited: 7
Cancer genomics and inherited risk. Journal of Clinical Oncology. 2014 Academic Article GET IT
Times cited: 69
DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers. PLoS Genetics. 2014 Academic Article GET IT
Times cited: 22
Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region. American Journal of Human Genetics. 2014 Academic Article GET IT
Times cited: 55
Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins. Nature Communications. 2014 Academic Article GET IT
Times cited: 72
Prevalence of HOXB13 mutation in a population of Ashkenazi Jewish men treated for prostate cancer. Familial Cancer. 2013 Academic Article GET IT
Times cited: 5
A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia. Nature Genetics. 2013 Academic Article GET IT
Times cited: 147
Assessment of SLX4 Mutations in Hereditary Breast Cancers. PLoS ONE. 2013 Academic Article GET IT
Times cited: 18
Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk. PLoS Genetics. 2013 Academic Article GET IT
Times cited: 169
Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk. PLoS Genetics. 2013 Academic Article GET IT
Times cited: 75
Susceptibility Loci Associated with Specific and Shared Subtypes of Lymphoid Malignancies. PLoS Genetics. 2013 Academic Article GET IT
Times cited: 33
Rare de novo germline copy-number variation in testicular cancer. American Journal of Human Genetics. 2012 Academic Article GET IT
Times cited: 14
Comparison of 6q25 breast cancer hits from Asian and European genome wide association studies in the Breast Cancer Association consortium (BCAC). PLoS ONE. 2012 Academic Article GET IT
Times cited: 44
A nonsynonymous polymorphism in IRS1 modifies risk of developing breast and ovarian cancers in BRCA1 and ovarian cancer in BRCA2 mutation carriers. Cancer Epidemiology Biomarkers and Prevention. 2012 Academic Article GET IT
Times cited: 13
Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers. Cancer Epidemiology Biomarkers and Prevention. 2012 Academic Article GET IT
Times cited: 34
Prevalence of BRCA1 and BRCA2 mutations in Ashkenazi Jewish families with breast and pancreatic cancer. Cancer. 2012 Academic Article GET IT
Times cited: 58
Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers. Human Genetics. 2011 Academic Article GET IT
Times cited: 12
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers. Journal of the National Cancer Institute. 2011 Academic Article GET IT
Times cited: 31
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population. Nature Genetics. 2010 Academic Article GET IT
Times cited: 234
Common genetic variants and modification of penetrance of BRCA2-associated breast cancer. PLoS Genetics. 2010 Academic Article GET IT
Times cited: 73
Genome-wide association studies of cancer predisposition. Hematology/Oncology Clinics of North America. 2010 Review GET IT
Times cited: 32
Susceptibility loci associated with prostate cancer progression and mortality. Clinical Cancer Research. 2010 Academic Article GET IT
Times cited: 59

VIVO Weill Cornell Medical College

Vijai, Joseph External Author

Publications

Selected publications