Vinicius Tragante

Also affiliated with Mahindra and Mahindra Limited (India), Netherlands Heart Institute, Amgen (Germany)

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 3%percentile

1.4Author 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

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

Papers

Driven by 20 papers — median percentile 85. Top paper: “Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals”.

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

Nature Genetics(2020)10.1038/s41588-020-00713-x

N/A

3.7DataRank · unranked

242 citations

Elena V. Feofanova, Najim Lahrouchi, Ioanna Ntalla, Savita Karthikeyan, James P. Cook +94 more

52 Genetic Loci Influencing Myocardial Mass

Journal of the American College of Cardiology(2016)10.1016/j.jacc.2016.07.729

N/A

2.4DataRank · unranked

135 citations

Jessica van Setten, Niek Verweij, Georg Vogler, Matthew T. Maurano, Xinchen Wang +172 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

Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study

UNC Libraries(2020)10.17615/n5vd-xm37

N/A

0.477DataRank · unranked

23 citations

Björn O. Eriksen, Ivana Išgum, Annette Peters, Christopher D. O’Donnell, Christa Meisinger +67 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

Loss-of-function variants in ITSN1 confer high risk of Parkinson’s disease

npj Parkinson s Disease(2024)10.1038/s41531-024-00752-9

N/A

0.385DataRank · unranked

12 citations

Vinicius Tragante, Garðar Sveinbjörnsson, Hannes Helgason, Árni Sturluson, Anna Bjornsdottir +18 more

Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization

Wellcome Open Research(2023)10.12688/wellcomeopenres.18754.1

N/A

0.357DataRank · unranked

7 citations

Natasha Hui Jin Ng, Juan Fernandez, Rebecca S. Fine, Eleanor Wheeler, Jennifer Wessel +95 more

Associations of Polymorphisms in the Peroxisome Proliferator-Activated Receptor Gamma Coactivator-1 Alpha Gene With Subsequent Coronary Heart Disease: An Individual-Level Meta-Analysis

Frontiers in Physiology(2022)10.3389/fphys.2022.909870

N/A

0DataRank · unranked

2 citations

Vinicius Tragante, Buamina Maitusong, Bruna Gigante, Sharon Cresci, Federica Laguzzi +52 more

Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura

Nature Genetics(2023)10.1038/s41588-023-01538-0

N/A

0DataRank · unranked

56 citations

Mona Ameri Chalmer, Lilja Stefánsdóttir, Ástrós Skúladóttir, Guðmundur Einarsson, Margrét B. Andrésdóttir +88 more

Polygenic risk scores associate with blood pressure traits across the lifespan

European Journal of Preventive Cardiology(2023)10.1093/eurjpc/zwad365

N/A

0DataRank · unranked

18 citations

Emma Ingeström, Michail Spitieris, Vinicius Tragante, Kaitlin H Wade, Laurent F. Thomas +8 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

Mendelian randomization of blood lipids for coronary heart disease

Utrecht University Repository (Utrecht University)(2020)10.17615/vm5z-r604

N/A

0DataRank · unranked

0 citations

Reecha Sofat, Sonia Shah, Suthesh Sivapalaratnam, Daniel I. Swerdlow, Jon White +27 more

Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentration

UNC Libraries(2020)10.17615/wr3c-2b58

N/A

0DataRank · unranked

0 citations

Brendan J. Keating, Fotios Drenos, Vinicius Tragante, Folkert W. Asselbergs, Matthew B. Lanktree +12 more

Polygenic Interactions With Environmental Exposures in Blood Pressure Regulation: The HUNT Study

Journal of the American Heart Association(2024)10.1161/jaha.123.034612

N/A

0DataRank · unranked

8 citations

Emma M. L. Ingeström, Michail Spitieris, Vinicius Tragante, Laurent F. Thomas, Ingelin Steinsland +7 more

Rare variant associations with birth weight identify genes involved in adipose tissue regulation, placental function and insulin-like growth factor signalling

medRxiv(2024)10.1101/2024.04.03.24305248

N/A

0DataRank · unranked

1 citations

Brandon E. M. Lim, Lena R Kaisinger, Valgerður Steinthórsdóttir, Luke N Sharp, Kashyap A. Patel +17 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

Genetically determined NLRP3 inflammasome activation associates with systemic inflammation and cardiovascular mortality

European Heart Journal(2021)10.1093/eurheartj/ehab107

N/A

0DataRank · unranked

93 citations

Marcus E. Kleber, Winfried März, Shichao Pang, Stephen Zewinger, Sarah Triem +63 more

Rare variant associations with birth weight identify genes involved in adipose tissue regulation, placental function and insulin-like growth factor signalling

Nature Communications(2025)10.1038/s41467-024-55761-2

N/A

0DataRank · unranked

6 citations

Brandon E. M. Lim, Lena R Kaisinger, Valgerður Steinthórsdóttir, Luke N Sharp, Kashyap A. Patel +17 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

GWASHub: An Automated Cloud-Based Platform for Genome-Wide Association Study Meta-Analysis

medRxiv(2025)10.1101/2025.10.21.25338463

N/A

0DataRank · unranked

0 citations

Drew Hite, Patrick Smadbeck, Quy Hoang, Dongkeun Jang, Vinicius Tragante +7 more

Vinicius Tragante

Indexed papers

Top data-sharing exemplar

Papers