Functional Variation Mapping
Functional Variation Mapping is a methodological framework in population genomics that identifies and characterizes genomic variants with phenotypic or biochemical effects by integrating genetic variation data with functional genomic annotations to distinguish causal variants from neutral polymorphisms.
155
Publications
12.6K
Citations
1.4K
Authors
549
Institutions
Publications per year
2017–2026
54
Parents
155
Transcriptome and genome sequencing uncovers functional variation in humans
Tuuli Lappalainen, Michael Sammeth, Marc R. Friedländer et al. · Nature · 2013 · 2.2K citations · Full text
1–5 of 155
1.4K
5
h-index
3
h-index
3
h-index
3
h-index
3
h-index
1–5 of 1.4K
549

Broad Institute
Cambridge, United States
8 h-index
21 publications
7K citations
National Institutes of Health
Bethesda, United States
7 h-index
14 publications
808 citations
University of Oxford
Oxford, United Kingdom
7 h-index
30 publications
10.1K citations
University of Florida
Gainesville, United States
7 h-index
30 publications
1.1K citations
University of Washington
Seattle, United States
6 h-index
16 publications
1.8K citations

Centre for Human Genetics
Oxford, United Kingdom
6 h-index
13 publications
9.2K citations
University of Chicago
Chicago, United States
6 h-index
27 publications
2.6K citations

Washington University in St. Louis
St Louis, United States
6 h-index
35 publications
4.6K citations
1–8 of 549
6 publications · 202 citations
7
h-index
6 publications · 479 citations
6
h-index
6 publications · 861 citations
6
h-index
Repository · 4 publications · 160 citations
4
h-index
PNAS · 4 publications · 653 citations
4
h-index
1–5