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

Kevin E. Glinton

Baylor College of Medicine

ORCID: 0000-0003-1854-7875

Also affiliated with Texas Children's Hospital

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 7%percentile
0.165Author 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 →

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 8 papers — median percentile 30. Top paper: “Comparison of Untargeted Metabolomic Profiling vs Traditional Metabolic Screening to Identify Inborn Errors of Metabolism”.

Comparison of Untargeted Metabolomic Profiling vs Traditional Metabolic Screening to Identify Inborn Errors of Metabolism

JAMA Network Open(2021)10.1001/jamanetworkopen.2021.14155
N/A
0.648DataRank · unranked
74 citations

Jing Xiao, Charul Gijavanekar, Kirk L. Pappan, Kevin E. Glinton, Brian J. Shayota +5 more

Natural history of TANGO2 deficiency disorder: Baseline assessment of 73 patients

Genetics in Medicine(2022)10.1016/j.gim.2022.11.020
N/A
0.590DataRank · unranked
50 citations

Erica Julianne Lay, Claudia Soler‐Alfonso, Kevin E. Glinton, Kimberly Houck, Mustafa Tosur +29 more

De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.02.007
N/A
0.373DataRank · unranked
11 citations

Alice M. Tao, Shenzhao Lu, Mengqi Ma, Shabab B. Hannan, Rachel Slaugh +43 more

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

Monitoring the treatment of urea cycle disorders using phenylbutyrate metabolite analyses: Still many lessons to learn

Molecular Genetics and Metabolism(2023)10.1016/j.ymgme.2023.107699
N/A
0DataRank · unranked
5 citations

Charles G. Minard, Ning Liu, Qin Sun, Sarah H. Elsea, Lindsay C. Burrage +2 more

Untargeted Metabolomics of Slc13a5 Deficiency Reveal Critical Liver–Brain Axis for Lipid Homeostasis

Metabolites(2022)10.3390/metabo12040351
N/A
0DataRank · unranked
18 citations

Kevin E. Glinton, Xiqi Li, Ana Santos de Medeiros, Patrick J. Gillespie, John R. Seavitt +3 more

Integrated analysis of metabolomic profiling and exome data supplements sequence variant interpretation, classification, and diagnosis

Genetics in Medicine(2020)10.1038/s41436-020-0827-0
N/A
0DataRank · unranked
53 citations

Kevin E. Glinton, Ning Liu, Jing Xiao, Yaping Yang, V. Reid Sutton +2 more

Improving access to exome sequencing in a medically underserved population through the Texome Project

Genetics in Medicine(2024)10.1016/j.gim.2024.101102
N/A
0DataRank · unranked
3 citations

Ryan J. German, Seema R. Lalani, Chaya N. Murali, Carlos A. Bacino, Stephanie Baskin +31 more