🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Brett Collins

Child Health and Development Institute

ORCID: 0000-0003-3194-9756

Also affiliated with Icahn School of Medicine at Mount Sinai

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile
0Author DataRank

Indexed papers

2in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology
Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 2 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 7 papers. Top paper: “Rare coding variation provides insight into the genetic architecture and phenotypic context of autism”.

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

Nature Genetics(2022)10.1038/s41588-022-01104-0
N/A
0.969DataRank · unranked
638 citations

F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong +112 more

FGF1 and insulin control lipolysis by convergent pathways

Cell Metabolism(2022)10.1016/j.cmet.2021.12.004
N/A
0.709DataRank · unranked
112 citations

Sihao Liu, Emanuel Gasser, Jacqueline G. Alvarez, Christopher P. Moutos, Kyeongkyu Kim +17 more

Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations

Nature Genetics(2023)10.1038/s41588-023-01305-1
N/A
0.654DataRank · unranked
77 citations

Dara Meyer, Brian Fennessy, Claudia Feng, Esther Cheng, Jessica Johnson +95 more

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

10.1101/2021.12.20.21267194
N/A
0.538DataRank · unranked
35 citations

F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong +60 more

Large deletions perturb peripheral transcriptomic and metabolomic profiles in Phelan-McDermid syndrome

medRxiv(2022)10.1101/2022.07.06.22277334
N/A
0DataRank · unranked
0 citations

Xuanjia Fan, Tess Levy, Rebecca M. Pollak, Brett Collins, Aya Osman +10 more

Peer Providers and Linkage with Buprenorphine Care after Hospitalization: A Retrospective Cohort Study

Substance Abuse(2022)10.1080/08897077.2022.2095078
N/A
0DataRank · unranked
13 citations

Eric D. Denisiuk, Brett Collins, Dan Stephens, Kendra L. Blalock, Jared W. Klein +5 more

Large 22q13.3 deletions perturb peripheral transcriptomic and metabolomic profiles in Phelan-McDermid syndrome

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100145
N/A
0DataRank · unranked
7 citations

Xuanjia Fan, Tess Levy, Rebecca M. Pollak, Brett Collins, Aya Osman +17 more