Publication & Citation Trends
Publications
0 total
Comparison of variant callers using 60 532 multi-ancestry whole genome sequences
Cited by 0
Semantic Scholar
Erratum for Yuan et al., “Case-control and genomic epidemiology characterization of SARS-CoV-2 breakthrough infections during Delta-to-Omicron transition”
Cited by 0
Semantic Scholar
Case-control and genomic epidemiology characterization of SARS-CoV-2 breakthrough infections during the Delta-to-Omicron transition
Cited by 0
Semantic Scholar
A rare genetic variant confers resistance to neurodegeneration across multiple neurological disorders by augmenting selective autophagy.
Cited by 4
Semantic Scholar
Complex genetic variation in nearly complete human genomes
Cited by 28
Semantic Scholar
Structural Variants Associated with Sporadic Alzheimer's Disease Pathologies and Segregates in Caribbean Hispanics and Non‐Hispanic White Families
Cited by 0
Semantic Scholar
Author Correction: Complex genetic variation in nearly complete human genomes
Cited by 2
Semantic Scholar
FAVOR 2.0: A reengineered functional annotation of variants online resource for interpreting genomic variation
Cited by 2
Semantic Scholar
Research Topics
Genomics and Phylogenetic Studies
(55)
Genomics and Rare Diseases
(36)
Chromosomal and Genetic Variations
(32)
Genomic variations and chromosomal abnormalities
(31)
Cancer Genomics and Diagnostics
(29)
Affiliations
Broad Institute
Seattle Pacific University
University of Southern California
Uppsala University
Brigham and Women's Hospital