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

Rajeeva Musunuri

New York Genome Center

ORCID: 0000-0001-5671-1766
Biochemistry, Genetics and Molecular BiologyNeuroscience

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
13.7Author DataRank

Indexed papers

4in 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 4 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.

High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios

Cell(2022)10.1016/j.cell.2022.08.004
Top 3%
6.3DataRank
Top 3%1056 citations

Uday S. Evani, Xuefang Zhao, Anna O. Basile, Haley Abel, Allison A. Regier +37 more

Papers

Driven by 10 papers — median percentile 92. Top paper: “High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios”.

High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios

Cell(2022)10.1016/j.cell.2022.08.004
Top 3%
6.3DataRank
Top 3%1056 citations

Uday S. Evani, Xuefang Zhao, Anna O. Basile, Haley Abel, Allison A. Regier +37 more

High coverage whole genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.02.06.430068
Top 4%
5.5DataRank
Top 4%260 citations

Uday S. Evani, Xuefang Zhao, Anna O. Basile, Haley Abel, Allison A. Regier +16 more

High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation

Genome Research(2024)10.1101/gr.279273.124
Top 13%
1.7DataRank
Top 13%78 citations

Sophia B Gibson, Nikhita Damaraju, Miranda Pg Zalusky, Kendra Hoekzema, David Twesigomwe +42 more

A strategy for building and using a human reference pangenome

F1000Research(2021)10.12688/f1000research.19630.2
N/A
0.533DataRank · unranked
10 citations

Giuseppe Narzisi, Valérie Schneider, Peter A. Audano, Evan Biederstedt, Lon Blauvelt +35 more

Somatic variant analysis of linked-reads sequencing data with Lancet

Bioinformatics(2020)10.1093/bioinformatics/btaa888
N/A
0.269DataRank · unranked
5 citations

Kanika Arora, André Corvelo, Minita Shah, Jennifer Shelton, Michael C. Zody +2 more

Comprehensive benchmarking of somatic single-nucleotide variant and indel detection at ultra-low allele fractions using short- and long-read data

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.10.13.681545
Top 70%
0.165DataRank
Top 70%2 citations

Dominika Maziec, Julia Markowski, Stephanie Georges, Nancy L. Parmalee, Michele Berselli +41 more

Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism

Human Genomics(2021)10.1186/s40246-021-00342-3
N/A
0DataRank · unranked
35 citations

Tristan J. Hayeck, Zhang Cheng, Sumantra Chatterjee, Brandon J. Mannion, Marta Byrska-Bishop +30 more

Somatic variant analysis of linked-reads sequencing data with Lancet

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.04.158063
N/A
0DataRank · unranked
0 citations

Kanika Arora, André Corvelo, Minita Shah, Jennifer Shelton, Michael C. Zody +2 more

Osteocalcin of maternal and embryonic origins synergize to establish homeostasis in offspring

EMBO Reports(2024)10.1038/s44319-023-00031-3
N/A
0DataRank · unranked
9 citations

Isabella Canal Delgado, Haiyang Yang, Alisson Clemenceau, André Corvelo, Giuseppe Narzisi +12 more

De Novo Mutation in an Enhancer of EBF3 in simplex autism

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.08.28.270751
N/A
0DataRank · unranked
2 citations

Tristan J. Hayeck, Brandon J. Mannion, Sumantra Chatterjee, Marta Byrska-Bishop, Rajeeva Musunuri +16 more