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

Arnon Adler

University Health Network

ORCID: 0000-0001-8142-4013

Also affiliated with Toronto General Hospital

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 6%percentile
0.292Author 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.

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

Papers

Driven by 5 papers — median percentile 44. Top paper: “Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy”.

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

An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome

Circulation(2020)10.1161/circulationaha.119.043132
N/A
0DataRank · unranked
402 citations

Valeria Novelli, Ahmad S. Amin, Emanuela Abiusi, Melanie Care, Eline A. Nannenberg +14 more

Identification, clinical manifestation and structural mechanisms of mutations in AMPK associated cardiac glycogen storage disease

EBioMedicine(2020)10.1016/j.ebiom.2020.102723
N/A
0DataRank · unranked
33 citations

Dong Hu, Liwen Liu, Daniel Barr, Yang Liu, Norma Balderrábano-Saucedo +15 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