Stacey Donnelly
0000-0001-5732-3300
Publication & Citation Trends
Publications
0 total
Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation Database
Cited by 2
Semantic Scholar
Author Correction: A genomic mutational constraint map using variation in 76,156 human genomes OA
Cited by 23
Semantic Scholar
A genomic mutational constraint map using variation in 76,156 human genomes
Cited by 1,020
Semantic Scholar
A genome-wide mutational constraint map quantified from variation in 76,156 human genomes OA
Cited by 250
Semantic Scholar
Author Correction: Evaluating drug targets through human loss-of-function genetic variation OA
Cited by 0
Semantic Scholar
Author Correction: Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals OA
Cited by 0
Semantic Scholar
Author Correction: The effect of LRRK2 loss-of-function variants in humans OA
Cited by 0
Semantic Scholar
Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans OA
Cited by 83
Semantic Scholar
Research Topics
Genomics and Rare Diseases
(22)
Genomic variations and chromosomal abnormalities
(6)
Genomics and Phylogenetic Studies
(5)
Genetic Associations and Epidemiology
(5)
Genomics and Chromatin Dynamics
(3)
Affiliations
Broad Institute
Texas A&M University – San Antonio
University of Dundee
Massachusetts Institute of Technology