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

Roddy Walsh

St George's, University of London

ORCID: 0000-0001-5092-8825

Also affiliated with Genomics England

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 4%percentile
0.762Author 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.

ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel: Reappraisal of Genes associated with Hypertrophic Cardiomyopathy

medRxiv(2024)10.1101/2024.07.29.24311195
Top 40%
0.470DataRank
Top 40%11 citations

Amber Waddell, Babken Asatryan, Emma Owens, Courtney L Thaxton, Mhy-Lanie Adduru +25 more

Papers

Driven by 15 papers — median percentile 52. Top paper: “Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect”.

Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect

Nature Genetics(2021)10.1038/s41588-020-00762-2
N/A
7.0DataRank · unranked
297 citations

Catherine Francis, Xiao Yun Xu, Alexa M.C. Vermeer, Andrew R. Harper, Roy Huurman +65 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
1.0DataRank · unranked
56 citations

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

Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies

Nature Cardiovascular Research(2023)10.1038/s44161-023-00346-3
N/A
0.863DataRank · unranked
34 citations

Sean J. Jurgens, Francesco Mazzarotto, Mona Allouba, James P. Pirruccello, Yasmine Aguib +6 more

Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

Nature Genetics(2022)10.1038/s41588-021-01007-6
N/A
0.747DataRank · unranked
144 citations

Rafik Tadros, Charlotte Glinge, David Y. Chiang, Mariam Jouni, Floriane Simonet +95 more

Rare coding variant analysis for human diseases across biobanks and ancestries

Nature Genetics(2024)10.1038/s41588-024-01894-5
N/A
0.614DataRank · unranked
59 citations

Xin Wang, Seung Hoan Choi, Lu‐Chen Weng, Satoshi Koyama, James P. Pirruccello +20 more

Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience

Nature Genetics(2024)10.1038/s41588-024-01975-5
N/A
0.601DataRank · unranked
54 citations

Joel Rämö, Daria R. Kramarenko, Leonoor F. J. M. Wijdeveld, Jan Haas, Mark Chaffin +55 more

ClinGen Hereditary Cardiovascular Disease Gene Curation Expert Panel: Reappraisal of Genes associated with Hypertrophic Cardiomyopathy

medRxiv(2024)10.1101/2024.07.29.24311195
Top 40%
0.470DataRank
Top 40%11 citations

Amber Waddell, Babken Asatryan, Emma Owens, Courtney L Thaxton, Mhy-Lanie Adduru +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

Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions

medRxiv(2023)10.1101/2023.04.03.23287612
Top 56%
0.292DataRank
Top 56%6 citations

Angharad M. Roberts, Pantazis I. Theotokis, Roddy Walsh, Philip J. Ostrowski, Matthew Edwards +30 more

Automated patch clamp data improve variant classification and penetrance stratification for SCN5A –Brugada syndrome

European Heart Journal(2025)10.1093/eurheartj/ehaf874
N/A
0DataRank · unranked
4 citations

G. Joanne, Jessa L. Aldridge, Joseph F. Solus, Genevieve R Harvey, Paige H Roberson +8 more

An Evidence-based Assessment of Genes in Dilated Cardiomyopathy

medRxiv(2020)10.1101/2020.12.10.20247197
N/A
0DataRank · unranked
41 citations

Laiken Peterson, Tomohiko Ai, Babken Asatryan, Lucas Bronicki, Emily Brown +29 more

Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death

European Heart Journal(2021)10.1093/eurheartj/ehab687
N/A
0DataRank · unranked
145 citations

Arnon Adler, Ahmad S. Amin, Emanuela Abiusi, Melanie Care, Hennie Bikker +15 more

Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot

Genetics in Medicine(2021)10.1038/s41436-021-01212-y
N/A
0DataRank · unranked
17 citations

Najim Lahrouchi, Fernanda M. Bosada, Gregor Dombrowsky, Simon G. Williams, Robert Lesurf +49 more

Genes Associated With Hypertrophic Cardiomyopathy

Journal of the American College of Cardiology(2025)10.1016/j.jacc.2024.12.010
N/A
0DataRank · unranked
52 citations

Amber Waddell, Babken Asatryan, Emma Owens, Courtney L Thaxton, Mhy-Lanie Adduru +25 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