Publication & Citation Trends
Publications
0 total
Mapping the causal chain from genetic risk variants to lipid dysmetabolism in Parkinsons disease
Cited by 2
Semantic Scholar
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
Cited by 18
Semantic Scholar
Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia
Cited by 0
Semantic Scholar
A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus
Cited by 21
Semantic Scholar
Author Correction: Comprehensive molecular characterization of mitochondrial genomes in human cancers OA
Cited by 1
Semantic Scholar
Author Correction: The landscape of viral associations in human cancers OA
Cited by 1
Semantic Scholar
Author Correction: Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer OA
Cited by 1
Semantic Scholar
Author Correction: The evolutionary history of 2,658 cancers OA
Cited by 5
Semantic Scholar
Research Topics
Genomics and Rare Diseases
(204)
Genomic variations and chromosomal abnormalities
(131)
Genomics and Phylogenetic Studies
(125)
Cancer Genomics and Diagnostics
(118)
Genetic Associations and Epidemiology
(98)
Affiliations
Boston College
University of California, Riverside
Broad Institute
Human Genome Sciences (United States)
California Institute of Technology