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

Henrik Kjærulf Jensen

Aarhus University

ORCID: 0000-0003-1802-4302

Also affiliated with Aarhus University Hospital, Central Denmark Region, ERN GUARD-Heart

Medicine

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 3%percentile
1.3Author 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.

Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry

European Heart Journal(2023)10.1093/eurheartj/ehad418
Top 15%
1.3DataRank
Top 15%61 citations

Carla Spazzolini, Mette Nyegaard, Michael T. Overgaard, Maria‐Christina Kotta, Federica Dagradi +50 more

Papers

Driven by 9 papers — median percentile 85. Top paper: “Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry”.

Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry

European Heart Journal(2023)10.1093/eurheartj/ehad418
Top 15%
1.3DataRank
Top 15%61 citations

Carla Spazzolini, Mette Nyegaard, Michael T. Overgaard, Maria‐Christina Kotta, Federica Dagradi +50 more

Human RyR2 (Ryanodine Receptor 2) Loss-of-Function Mutations

Circulation Arrhythmia and Electrophysiology(2021)10.1161/circep.121.010013
N/A
0DataRank · unranked
38 citations

Jinhong Wei, Wenting Guo, Bo Sun, John Paul Estillore, Ruiwu Wang +10 more

Genetic Variant Score and Arrhythmogenic Right Ventricular Cardiomyopathy Phenotype in Plakophilin-2 Mutation Carriers

Cardiology(2021)10.1159/000519231
N/A
0DataRank · unranked
4 citations

Pyotr G. Platonov, Kristina H. Haugaa, Wojciech Zaręba, Henrik Kjærulf Jensen, Henning Bundgaard +11 more

Arrhythmic risk prediction in arrhythmogenic right ventricular cardiomyopathy: external validation of the arrhythmogenic right ventricular cardiomyopathy risk calculator

European Heart Journal(2022)10.1093/eurheartj/ehac289
N/A
0DataRank · unranked
77 citations

Laurens P. Bosman, Alessio Gasperetti, Andrea Mazzanti, Jean‐Baptiste Gourraud, Brianna Davies +36 more

Bidirectional Association Between Atrial Fibrillation and Myocardial Infarction, and Relation to Mortality in the Framingham Heart Study

Journal of the American Heart Association(2024)10.1161/jaha.123.032226
N/A
0DataRank · unranked
19 citations

Emelia J. Benjamin, Ludovic Trinquart, Honghuang Lin, Christina C. Dahm, Morten Krogh Christiansen +4 more

Implantable cardioverter defibrillator use in arrhythmogenic right ventricular cardiomyopathy in North America and Europe

European Heart Journal(2024)10.1093/eurheartj/ehad799
N/A
0DataRank · unranked
22 citations

Corrado De Marco, Alessio Gasperetti, Laurens P. Bosman, Jean‐Baptiste Gourraud, Alessandro Trancuccio +52 more

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy

medRxiv(2024)10.1101/2024.07.04.24309755
N/A
0DataRank · unranked
0 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +65 more

Cardiac ryanodine receptor calcium release deficiency syndrome

Science Translational Medicine(2021)10.1126/scitranslmed.aba7287
N/A
0DataRank · unranked
120 citations

Jinjing Yao, Mingke Ni, Jinhong Wei, Xiaowei Zhong, Wenting Guo +26 more

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.04.016
N/A
0DataRank · unranked
2 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +66 more