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

Jennefer N. Carter

Stanford Health Care

ORCID: 0000-0003-0830-3535

Also affiliated with Stanford University

Biochemistry, Genetics and Molecular Biology

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

1in 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 1 indexed paper 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 8 papers. Top paper: “Biomni: A General-Purpose Biomedical AI Agent”.

Biomni: A General-Purpose Biomedical AI Agent

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.05.30.656746

N/A

0.700DataRank · unranked

105 citations

Serena Zhang, Hanchen Wang, Yuanhao Qu, Yingzhou Lu, Yusuf Roohani +18 more

The current landscape of clinical exome and genome reanalysis in the U.S.

Journal of Genetic Counseling(2025)10.1002/jgc4.1968

N/A

0.208DataRank · unranked

3 citations

Jennefer N. Carter, Matthew T. Wheeler, Chloe Reuter, Michelle Frees

Researcher views on returning results from multi-omics data to research participants: insights from The Molecular Transducers of Physical Activity Consortium (MoTrPAC) Study

BMC Medical Ethics(2025)10.1186/s12910-025-01174-9

N/A

0.208DataRank · unranked

3 citations

Caroline Stanclift, Chloe Reuter, Jennefer N. Carter, Kathleen Murphy, Maléne E. Lindholm +2 more

EditABLE: A Simple Web Application for Designing Genome Editing Experiments

Research Square(2024)10.21203/rs.3.rs-4775705/v1

N/A

0.104DataRank · unranked

1 citations

David Wu, Najani Shanee Johnson, Vivek Charu, Jennefer N. Carter, Shuchi Anand +3 more

RAPSN ‐Associated Congenital Myasthenic Syndrome due to Biallelic Single Nucleotide Variants at the Same Position

Case Reports in Genetics(2025)10.1155/crig/1882021

N/A

0DataRank · unranked

0 citations

Jennefer N. Carter, Elijah Kravets, Matthew T. Wheeler, Jonathan A. Bernstein, Ricardo A. Maselli +3 more

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder

medRxiv(2025)10.1101/2025.03.31.25324695

N/A

0DataRank · unranked

2 citations

Stephan Drukewitz, Sukhleen Kour, Anuradha Venkatakrishnan Chimata, Deepa Rajan, Senta Schönnagel +54 more

An optimized variant prioritization process for rare disease diagnostics: recommendations for Exomiser and Genomiser

medRxiv(2025)10.1101/2025.04.18.25326061

N/A

0DataRank · unranked

2 citations

Shruti Marwaha, Alistair Ward, Shilpa N. Kobren, Jennefer N. Carter, Undiagnosed Diseases Network +3 more

An optimized variant prioritization process for rare disease diagnostics: recommendations for Exomiser and Genomiser

Genome Medicine(2025)10.1186/s13073-025-01546-1

N/A

0DataRank · unranked

8 citations

Shruti Marwaha, Alistair Ward, Shilpa N. Kobren, Jennefer N. Carter, Undiagnosed Diseases Network +94 more