The mutational constraint spectrum quantified from variation in 141,456 humans
2020 · Nature · 9,856 citations
https://doi.org/10.1038/s41586-020-2308-7
R
Ryan L. Collins
Broad Institute(US)
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Ryan L. Collins is an academic researcher from Broad Institute. The author has contributed to research in topics: Genomics and Rare Diseases & Genomic variations and chromosomal abnormalities & Genomics and Phylogenetic Studies. The author has an h-index of 49, co-authored 110 publications.
ORCID: 0000-0003-1268-9995Papers by this author
worksLarge-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
2020 · Cell · 2,318 citations
https://doi.org/10.1016/j.cell.2019.12.036
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders
2019 · Cell · 1,446 citations
https://doi.org/10.1016/j.cell.2019.11.020
A genomic mutational constraint map using variation in 76,156 human genomes
2023 · Nature · 1,193 citations
https://doi.org/10.1038/s41586-023-06045-0
A structural variation reference for medical and population genetics
2020 · Nature · 1,132 citations
https://doi.org/10.1038/s41586-020-2287-8
A structural variation reference for medical and population genetics
2020 · Nature · 1,132 citations
https://doi.org/10.1038/s41586-020-2287-8
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