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

Angela E. Scheuerle

Southwestern Medical Center

ORCID: 0000-0002-9025-3276

Also affiliated with Southwestern Medical Center, The University of Texas Southwestern Medical Center

MedicineBiochemistry, 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 7%percentile
0.165Author 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.

Pathogenic XPO1 variants cause a dominant neurodevelopmental disorder

Genetics in Medicine(2025)10.1016/j.gim.2025.101555
Top 70%
0.165DataRank
Top 70%2 citations

Pavla Nedbalova, Miroslava Hančárová, Jan Prchal, Darina Prchalová, Markéta Vlčková +74 more

Papers

Driven by 5 papers — median percentile 30. Top paper: “Phenotypic and genotypic insights into concurrent tertiary trisomy for 9p and 18p”.

Phenotypic and genotypic insights into concurrent tertiary trisomy for 9p and 18p

Molecular Cytogenetics(2025)10.1186/s13039-025-00704-9
N/A
0.195DataRank · unranked
2 citations

Angela E. Scheuerle, Kathleen Wilson, Rolando García, Prasad Koduru, Carter A. Wright

Pathogenic XPO1 variants cause a dominant neurodevelopmental disorder

Genetics in Medicine(2025)10.1016/j.gim.2025.101555
Top 70%
0.165DataRank
Top 70%2 citations

Pavla Nedbalova, Miroslava Hančárová, Jan Prchal, Darina Prchalová, Markéta Vlčková +74 more

Overcoming presynaptic effects of VAMP2 mutations with 4‐aminopyridine treatment

Human Mutation(2020)10.1002/humu.24109
N/A
0DataRank · unranked
21 citations

Haiyan Li, Barış Alten, Magda Santos, Ruiji Jiang, Brianna M. Paul +15 more

Prune belly syndrome in surviving males can be caused by Hemizygous missense mutations in the X-linked Filamin A gene

BMC Medical Genetics(2020)10.1186/s12881-020-0973-x
N/A
0DataRank · unranked
31 citations

Thomas Jascur, Steven M. Harrison, Angelena Edwards, Luke Smith, Erin S. Choi +9 more

Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype–phenotype correlations and common mechanisms

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63247
N/A
0DataRank · unranked
41 citations

Justin Blair, Batsal Devkota, Sierra Fortunato, Dinah Clark, Audrey Lawrence +92 more