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

Caroline Cusick

Broad Institute

ORCID: 0000-0002-2743-9545
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 1%percentile
6.7Author 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 →

Top data-sharing exemplar

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8
Top 3%
6.7DataRank
Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Papers

Driven by 11 papers — median percentile 97. Top paper: “Rare coding variants in ten genes confer substantial risk for schizophrenia”.

Rare coding variants in ten genes confer substantial risk for schizophrenia

Nature(2022)10.1038/s41586-022-04556-w
N/A
7.2DataRank · unranked
900 citations

Timothy Poterba, David Curtis, Huda Akil, Mariam Al Eissa, Jack D. Barchas +95 more

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8
Top 3%
6.7DataRank
Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Nature Communications(2023)10.1038/s41467-023-39539-6
N/A
1.2DataRank · unranked
56 citations

David Lewis‐Smith, Ryan L. Collins, Lisa‐Marie Niestroj, Shridhar Parthasarathy, Julie Xian +94 more

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.04.009
N/A
0.617DataRank · unranked
60 citations

Gundula Povysil, Ryan S. Dhindsa, Kate E. Stanley, Andrew S. Allen, Yen‐Chen Anne Feng +95 more

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

Nature Neuroscience(2024)10.1038/s41593-024-01747-8
N/A
0.612DataRank · unranked
58 citations

Siwei Chen, Bassel Abou‐Khalil, Zaid Afawi, Quratulain Zulfiqar Ali, Elisabetta Amadori +95 more

Principled distillation of UK Biobank phenotype data reveals underlying structure in human variation

Nature Human Behaviour(2024)10.1038/s41562-024-01909-5
N/A
0.564DataRank · unranked
18 citations

Rebecca Shafee, Robbee Wedow, Amanda Elliott, Duncan S. Palmer, John Compitello +14 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

Principled distillation of multidimensional UK Biobank data reveals insights into the correlated human phenome

medRxiv(2022)10.1101/2022.09.02.22279546
N/A
0.294DataRank · unranked
4 citations

Rebecca Shafee, Amanda Elliott, Duncan S. Palmer, John Compitello, Masahiro Kanai +14 more

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

Nature Genetics(2023)10.1038/s41588-023-01485-w
N/A
0DataRank · unranked
217 citations

Ciarán Campbell, Siwei Chen, Bassel Abou‐Khalil, Oluyomi M. Adesoji, Zaid Afawi +95 more

Pan-UK Biobank GWAS improves discovery, analysis of genetic architecture, and resolution into ancestry-enriched effects

medRxiv(2024)10.1101/2024.03.13.24303864
N/A
0DataRank · unranked
173 citations

Rahul Gupta, Masahiro Kanai, Wenhan Lu, Kristin Tsuo, Ying Wang +24 more

Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations

medRxiv(2025)10.1101/2024.12.27.24319460
N/A
0DataRank · unranked
3 citations

Seulgi Jung, F. Kyle Satterstrom, Jack Fu, Tess Levy, Laura G Sloofman +49 more