Adam E. Locke
0000-0001-6227-198X
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
Polygenic prediction of body mass index and obesity through the life course and across ancestries
Cited by 18
Semantic Scholar
Genomic Ascertainment of CHEK2-Related Cancer Predisposition
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
Germline Variants Influence Chronic Liver Disease Progression through Distinct Pathways
Cited by 0
Semantic Scholar
Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood
Cited by 3
Semantic Scholar
Research Topics
Genetic Associations and Epidemiology
(81)
Genomics and Rare Diseases
(23)
Nutrition, Genetics, and Disease
(18)
Liver Disease Diagnosis and Treatment
(15)
Metabolomics and Mass Spectrometry Studies
(14)
Affiliations
James S. McDonnell Foundation
MACOM (United States)
Centre for Human Genetics
University of Helsinki
Emory University