Publication & Citation Trends
Publications
0 total
Africa-specific human genetic variation near CHD1L associates with HIV-1 load OA
Cited by 24
Semantic Scholar
Strong protective effect of the APOL1 p.N264K variant against G2-associated FSGS and kidney disease OA
Cited by 2
Semantic Scholar
Ancestry adjustment improves genome-wide estimates of regional intolerance. OA
Cited by 2
Semantic Scholar
Genetics in Chronic Kidney Disease: Conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference OA
Cited by 156
Semantic Scholar
Association of rare predicted loss-of-function variants of influenza-related type I IFN genes with critical COVID-19 pneumonia. Reply. OA
Cited by 5
Semantic Scholar
Using reported pathogenic variants to identify therapeutic opportunities for genetic diseases OA
Cited by 1
Semantic Scholar
Predicting the genetic ancestry of 2.6 million New York City patients using clinical data OA
Cited by 0
Semantic Scholar
Disease heritability inferred from familial relationships reported in medical records OA
Cited by 101
Semantic Scholar
Research Topics
Genomics and Rare Diseases
(131)
Genetic Associations and Epidemiology
(79)
Genomic variations and chromosomal abnormalities
(46)
Hepatitis C virus research
(41)
Genetics and Neurodevelopmental Disorders
(40)
Affiliations
AstraZeneca (United Kingdom)
Broad Institute
Intermountain Healthcare
Roche (Switzerland)
Boston Children's Hospital
External Profiles
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