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

Anna Raper

Pacific Northwest Diabetes Research Institute

ORCID: 0000-0003-0949-9963

Also affiliated with Children's Hospital of Philadelphia, Roslin Institute, RIKEN Center for Brain Science, University of Edinburgh

Immunology and MicrobiologyBiochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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 →

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.

Practice-Based Insights into Adult Genetics: High Diagnostic Yield, Demographic Determinants, and Patterns of Test Utilization across 10,000 Patient Encounters

medRxiv(2025)10.1101/2025.10.09.25337579
Top 100%
0DataRank
Top 100%0 citations

Yehuda Elkaim, Stephanie Asher, Anna Raper, Courtney Condit, Zoe Bogus +15 more

Papers

Driven by 10 papers — median percentile 0. Top paper: “Germline POT1 variants can predispose to myeloid and lymphoid neoplasms”.

Germline POT1 variants can predispose to myeloid and lymphoid neoplasms

Leukemia(2022)10.1038/s41375-021-01335-w
N/A
0.533DataRank · unranked
34 citations

David B. Lieberman, Adam R. Davis, Alison W. Loren, Ryan Hausler, Ashkan Bigdeli +12 more

A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associations

Nature Communications(2025)10.1038/s41467-025-57077-1
N/A
0.428DataRank · unranked
14 citations

Tomoki Nomakuchi, Elizabeth Chao, Carolyn Horton, Jill S. Dolinsky, Amal Yussuf +23 more

Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2322582121
N/A
0.292DataRank · unranked
6 citations

Oguz Kanca, Rishi V. Shridharan, Paul C. Marcogliese, Benjamin Steger, Marie Morimoto +92 more

Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

Genetics in Medicine(2024)10.1016/j.gim.2024.101174
N/A
0.241DataRank · unranked
4 citations

Kristhen N Atala, Yiming Zheng, Debdeep Dutta, Dorothy K. Grange, Wen‐Wen Lin +95 more

ELFN1 deficiency: The mechanistic basis and phenotypic spectrum of a neurodevelopmental disorder with epilepsy

Genetics in Medicine(2025)10.1016/j.gim.2025.101506
N/A
0.208DataRank · unranked
3 citations

Chu-Ting Chang, A. Declève, Gloria Brunori, W.H. Ludlam, Alden Huang +93 more

A stable NTN1 fluorescent reporter chicken reveals cell specific molecular signatures during optic fissure closure

Scientific Reports(2025)10.1038/s41598-025-94589-8
N/A
0DataRank · unranked
4 citations

Holly Hardy, Teresa Requena, Amy S. Findlay, Jason Ioannidis, Dominique Meunier +6 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

A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associations

medRxiv(2023)10.1101/2023.08.08.23293676
N/A
0DataRank · unranked
4 citations

Tomoki Nomakuchi, Elizabeth Chao, Carolyn Horton, Jill S. Dolinsky, Amal Yussuf +12 more

An Unusual Cause of Hexokinase 1 Deficiency—Case Report

eJHaem(2025)10.1002/jha2.70123
N/A
0DataRank · unranked
0 citations

Kelly Maurer, Tanaya Jadhav, Tejas Jammihal, Zhe Zhang, Helge Hartung +11 more

Practice-Based Insights into Adult Genetics: High Diagnostic Yield, Demographic Determinants, and Patterns of Test Utilization across 10,000 Patient Encounters

medRxiv(2025)10.1101/2025.10.09.25337579
Top 100%
0DataRank
Top 100%0 citations

Yehuda Elkaim, Stephanie Asher, Anna Raper, Courtney Condit, Zoe Bogus +15 more