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

Jonas Ghouse

University of Copenhagen

ORCID: 0000-0002-9634-5964

Also affiliated with Aarhus University, Aarhus University Hospital, Copenhagen University Hospital, Rigshospitalet

Biochemistry, Genetics and Molecular BiologyMedicine

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 2%percentile
3.7Author 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.

Genome-wide association study identifies 18 novel loci associated with left atrial volume and function

European Heart Journal(2021)10.1093/eurheartj/ehab466
Top 9%
2.3DataRank
Top 9%68 citations

Laura Andreasen, Jonas Ghouse, Litten Bertelsen, Henning Bundgaard, Stig Haunsø +3 more

Papers

Driven by 9 papers — median percentile 88. Top paper: “Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study”.

Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study

European Heart Journal(2023)10.1093/eurheartj/ehad142
N/A
2.9DataRank · unranked
113 citations

Christian Dina, Aeron Small, Christian M. Shaffer, Rebecca T. Levinson, Anna Helgadóttir +52 more

Genome-wide association study identifies 18 novel loci associated with left atrial volume and function

European Heart Journal(2021)10.1093/eurheartj/ehab466
Top 9%
2.3DataRank
Top 9%68 citations

Laura Andreasen, Jonas Ghouse, Litten Bertelsen, Henning Bundgaard, Stig Haunsø +3 more

Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis

Nature Genetics(2024)10.1038/s41588-024-01720-y
Top 15%
1.4DataRank
Top 15%63 citations

Garðar Sveinbjörnsson, Marijana Vujković, Anne-Sofie Seidelin, Helene Gellert‐Kristensen, Gustav Ahlberg +47 more

Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases

Nature Genetics(2025)10.1038/s41588-024-02072-3
N/A
0.821DataRank · unranked
50 citations

Ida Surakka, Morten S. Olesen, Garðar Sveinbjörnsson, Nicholas Marston, Seung Hoan Choi +95 more

Genome-wide meta-analysis identifies nine loci associated with higher risk of hepatocellular carcinoma development

JHEP Reports(2025)10.1016/j.jhepr.2025.101485
N/A
0.410DataRank · unranked
11 citations

Helene Gellert‐Kristensen, Colm J. O’Rourke, Anne-Sofie Seidelin, Gudmar Thorleifsson, Garðar Sveinbjörnsson +43 more

Germline Variants Influence Chronic Liver Disease Progression through Distinct Pathways

medRxiv(2025)10.1101/2025.09.16.25335186
N/A
0DataRank · unranked
1 citations

David E. Kaplan, Jonas Ghouse, Bao‐Li Loza, Joseph Brancale, Adam Lewis +68 more

Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci

European Heart Journal(2022)10.1093/eurheartj/ehac322
N/A
0DataRank · unranked
17 citations

Vinicius Tragante, Ayesha Muhammad, Gustav Ahlberg, Morten W. Skov, Dan M. Roden +22 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

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