Arthur A.M. Wilde

Also affiliated with Academic Center for Dentistry Amsterdam, Amsterdam Neuroscience, ERN GUARD-Heart, Amsterdam University Medical Centers, Amsterdam University of Applied Sciences, University of Amsterdam

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 2%percentile

3.0Author DataRank

Indexed papers

3in 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 3 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 →

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

An International Multicenter Evaluation of Type 5 Long QT Syndrome

Circulation(2020)10.1161/circulationaha.119.043114

Top 15%

1.4DataRank

Top 15%60 citations

S. Yukiko Asaki, Andrea Mazzanti, J. Martijn Bos, Izabela Tuleta, Alison Muir +54 more

Papers

Driven by 26 papers — median percentile 85. Top paper: “An International Multicenter Evaluation of Type 5 Long QT Syndrome”.

An International Multicenter Evaluation of Type 5 Long QT Syndrome

Circulation(2020)10.1161/circulationaha.119.043114

Top 15%

1.4DataRank

Top 15%60 citations

S. Yukiko Asaki, Andrea Mazzanti, J. Martijn Bos, Izabela Tuleta, Alison Muir +54 more

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

Genetic testing in early-onset atrial fibrillation

European Heart Journal(2024)10.1093/eurheartj/ehae298

N/A

1.1DataRank · unranked

39 citations

Sean J. Jurgens, Joel Rämö, Ingrid E. Christophersen, Michiel Rienstra, Mina K. Chung +14 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

Machine learning of electrophysiological signals for the prediction of ventricular arrhythmias: systematic review and examination of heterogeneity between studies

EBioMedicine(2023)10.1016/j.ebiom.2023.104462

N/A

0.590DataRank · unranked

50 citations

Brototo Deb, Samuel Ruipérez-Campillo, Neil K. Bhatia, Paul Clopton, Arthur A.M. Wilde +4 more

Clinical characteristics and electrophysiologic properties of SCN5A variants in fever-induced Brugada syndrome

EBioMedicine(2022)10.1016/j.ebiom.2022.104388

N/A

0.385DataRank · unranked

12 citations

Héctor Barajas-Martínez, Giuseppe Ciconte, Cheng‐I Wu, Michelle M. Monasky, Hao Xia +16 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

Fractionated Epicardial Electrograms

JACC. Clinical electrophysiology(2021)10.1016/j.jacep.2020.12.009

N/A

0DataRank · unranked

6 citations

Henry H. Hsia, Pieter G. Postema, Arthur A.M. Wilde, Bence Patocskai, José M. Di Diego +3 more

Dynamic prediction of malignant ventricular arrhythmias using neural networks in patients with an implantable cardioverter-defibrillator

EBioMedicine(2023)10.1016/j.ebiom.2023.104937

N/A

0DataRank · unranked

30 citations

Samuel Ruipérez-Campillo, Laura Alvarez-Florez, Brototo Deb, Erik J. Bekkers, Cornelis P. Allaart +8 more

A Systematic Analysis of the Clinical Outcome Associated with Multiple Reclassified Desmosomal Gene Variants in Arrhythmogenic Right Ventricular Cardiomyopathy Patients

Journal of Cardiovascular Translational Research(2023)10.1007/s12265-023-10403-8

N/A

0DataRank · unranked

16 citations

Edgar T. Hoorntje, Wouter P. te Rijdt, Laurens P. Bosman, Petros Syrris, Alexandros Protonotarios +36 more

Clinical Management of Brugada Syndrome: Commentary From the Experts

Circulation Arrhythmia and Electrophysiology(2023)10.1161/circep.123.012072

N/A

0DataRank · unranked

13 citations

Lee L. Eckhardt, Elizabeth S. Kaufman, Elena Arbelo, Elijah R. Behr, Pedro Brugada +23 more

Effects of cohort, genotype, variant, and maternal β-blocker treatment on foetal heart rate predictors of inherited long QT syndrome

EP Europace(2023)10.1093/europace/euad319

N/A

0DataRank · unranked

12 citations

Annika Winbo, Sally‐Ann B. Clur, Susan P. Etheridge, Michael J. Ackerman, Hitoshi Horigome +14 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

0DataRank · unranked

12 citations

Sean Zheng, Christopher Grace, Paloma Jordà, Catherine Francis, Sean J. Jurgens +57 more

Clinical features and outcomes in carriers of pathogenic desmoplakin variants

European Heart Journal(2024)10.1093/eurheartj/ehae571

N/A

0DataRank · unranked

70 citations

Richard Carrick, Alexandros Protonotarios, Brittney Murray, Mikaël Laredo, Iris van der Schaaf +56 more

A novel tool for arrhythmic risk stratification in desmoplakin gene variant carriers

European Heart Journal(2024)10.1093/eurheartj/ehae409

N/A

0DataRank · unranked

60 citations

Alessio Gasperetti, Alexandros Protonotarios, Brittney Murray, Mikaël Laredo, Iris van der Schaaf +57 more

Long-Term Arrhythmic Follow-Up and Risk Stratification of Patients With Desmoplakin-Associated Arrhythmogenic Right Ventricular Cardiomyopathy

JACC Advances(2024)10.1016/j.jacadv.2024.100832

N/A

0DataRank · unranked

41 citations

Richard Carrick, Alexandros Protonotarios, Mikaël Laredo, Iris van der Schaaf, Petros Syrris +41 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

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

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

Life-threatening arrhythmias with autosomal recessive TECRL variants

EP Europace(2020)10.1093/europace/euaa376

N/A

0DataRank · unranked

31 citations

Elhadi H. Aburawi, Marie Chaix, Stephanie F. Chandler, Roger S. Y. Foo, AKM Monwarul Islam +13 more

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

0DataRank · unranked

296 citations

Catherine Francis, Xiao Yun Xu, Alexa M.C. Vermeer, Andrew R. Harper, Roy Huurman +65 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

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

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

A phenotype-enhanced variant classification framework to decrease the burden of missense variants of uncertain significance in type 1 long QT syndrome

Heart Rhythm(2021)10.1016/j.hrthm.2021.11.017

N/A

0DataRank · unranked

20 citations

Steven M. Dotzler, Christian Krijger, John R. Giudicessi, Dan Ye, Hennie Bikker +6 more

Arthur A.M. Wilde

Indexed papers

Top data-sharing exemplar

Papers