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

Kate Thomson

University of Oxford

ORCID: 0000-0003-2807-3431

Also affiliated with Oxford University Hospitals NHS Trust

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 5%percentile
0.481Author 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.

Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM)

Journal of Molecular Diagnostics(2021)10.1016/j.jmoldx.2021.01.014
Top 40%
0.481DataRank
Top 40%8 citations

Alexander Ing, Christian Antolik, Christina Austin‐Tse, Linnea M. Baudhuin, Lucas Bronicki +25 more

Papers

Driven by 10 papers — median percentile 60. Top paper: “Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM)”.

Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM)

Journal of Molecular Diagnostics(2021)10.1016/j.jmoldx.2021.01.014
Top 40%
0.481DataRank
Top 40%8 citations

Alexander Ing, Christian Antolik, Christina Austin‐Tse, Linnea M. Baudhuin, Lucas Bronicki +25 more

Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

medRxiv(2023)10.1101/2023.01.28.23285147
N/A
0.436DataRank · unranked
12 citations

Sean Zheng, Christopher Grace, Paloma Jordà, Catherine Francis, Sean J. Jurgens +57 more

Multi-site validation of a functional assay to adjudicate SCN5A Brugada Syndrome-associated variants

medRxiv(2023)10.1101/2023.12.19.23299592
N/A
0.165DataRank · unranked
2 citations

Matthew J. O’Neill, Ebony Richardson, Kate Thomson, Jodie Ingles, Ayesha Muhammad +15 more

A calibrated functional patch-clamp assay to enhance clinical variant interpretation in KCNH2-related long QT syndrome

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.05.002
N/A
0DataRank · unranked
41 citations

Ebony Richardson, Jessica Farr, Adam P. Hill, Rizwan Ullah, Brett M. Kroncke +6 more

Multisite Validation of a Functional Assay to Adjudicate SCN5A Brugada Syndrome–Associated Variants

Circulation Genomic and Precision Medicine(2024)10.1161/circgen.124.004569
N/A
0DataRank · unranked
11 citations

Matthew J. O’Neill, Ebony Richardson, Kate Thomson, Jodie Ingles, Ayesha Muhammad +15 more

Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

Nature Genetics(2025)10.1038/s41588-025-02087-4
N/A
0DataRank · unranked
55 citations

Sean L. Zheng, Christopher Grace, Paloma Jordà, Catherine Francis, Dominique M West +95 more

An assessment of the role of vinculin loss of function variants in inherited cardiomyopathy

Human Mutation(2020)10.1002/humu.24061
N/A
0DataRank · unranked
19 citations

Naif A. M. Almontashiri, Leslie G. Biesecker, Natalie Berger, Wendy K. Chung, John Garcia +17 more

Titin-related familial dilated cardiomyopathy: factors associated with disease onset

European Heart Journal(2025)10.1093/eurheartj/ehaf380
N/A
0DataRank · unranked
9 citations

Robert A. Fletcher, Stacey Peters, Monique Ohanian, Magdalena Soka, Andrei Smolnikov +95 more

Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity

Nature Genetics(2021)10.1038/s41588-020-00764-0
N/A
0DataRank · unranked
344 citations

Anuj Goel, Christopher Grace, Kate Thomson, Steffen E. Petersen, Xiao Hua Xu +64 more

A calibrated functional patch clamp assay to enhance clinical variant interpretation in KCNH2 -related long QT syndrome

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.12.13.472492
N/A
0DataRank · unranked
0 citations

Ebony Richardson, Jessica Farr, Adam P. Hill, Rizwan Ullah, Brett M. Kroncke +6 more