Jeffrey G. Reid
0000-0001-8645-4713
Publication & Citation Trends
Publications
0 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
Variant Classification Using Proteomics-Informed Large Language Models Increases Power of Rare Variant Association Studies and Enhances Target Discovery
Cited by 1
Semantic Scholar
Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes
Cited by 0
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
Thrombotic risk determined by ABO, F8, and VWF variants in a population-based cohort study
Cited by 2
Semantic Scholar
Research Topics
Genomics and Rare Diseases
(48)
Genetic Associations and Epidemiology
(47)
Cancer Genomics and Diagnostics
(17)
Genomic variations and chromosomal abnormalities
(14)
Genomics and Phylogenetic Studies
(12)
Affiliations
University of Siena
United States Nuclear Regulatory Commission
Centers for Disease Control and Prevention
MACOM (United States)
University Medical Center Groningen