Publication & Citation Trends
Publications
32 total
Rare coding variants in CHRNB3 associate with reduced daily cigarette smoking across ancestries
Cited by 0
Semantic Scholar
Population-scale repeat expansions elucidate disease risk and brain atrophy
Cited by 0
Semantic Scholar
Genomic Ascertainment of CHEK2-Related Cancer Predisposition
Cited by 1
Semantic Scholar
Insights from the Biorepository and Integrative Genomics pediatric resource
Cited by 2
Semantic Scholar
The impact of common and rare genetic variants on bradyarrhythmia development OA
Cited by 10
Semantic Scholar
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
Cited by 18
Semantic Scholar
Exclusion-based exome sequencing in critically ill adults 18–40 years old has a 24% diagnostic rate and finds racial disparities in access to genetic testing
Cited by 2
Semantic Scholar
Research Topics
Genetic Associations and Epidemiology
(12)
Genomics and Rare Diseases
(8)
BRCA gene mutations in cancer
(6)
Blood Coagulation and Thrombosis Mechanisms
(4)
Cardiomyopathy and Myosin Studies
(3)
Affiliations
Regeneron (United States)
Kristianstad University
Geisinger Health System
Icahn School of Medicine at Mount Sinai