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

Francesco Mazzarotto

Brescia University

ORCID: 0000-0002-6159-9980
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 100%percentile
0Author DataRank

Indexed papers

0in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 10 papers. Top paper: “Spatial and Functional Distribution of MYBPC3 Pathogenic Variants and Clinical Outcomes in Patients With Hypertrophic Cardiomyopathy”.

Spatial and Functional Distribution of MYBPC3 Pathogenic Variants and Clinical Outcomes in Patients With Hypertrophic Cardiomyopathy

Circulation Genomic and Precision Medicine(2020)10.1161/circgen.120.002929
N/A
0DataRank · unranked
100 citations

Andrea D. Thompson, Amelia A. Glazier, Neha Hafeez, Samat Kabani, Juliani Rodriguez +18 more

An Evidence-based Assessment of Genes in Dilated Cardiomyopathy

medRxiv(2020)10.1101/2020.12.10.20247197
N/A
0DataRank · unranked
41 citations

Laiken Peterson, Tomohiko Ai, Babken Asatryan, Lucas Bronicki, Emily Brown +29 more

Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretation

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.29.402974
N/A
0DataRank · unranked
0 citations

Adam Helms, Anamika Kannan, Jaime Yob, Neal K. Lakdawala, Samuel G. Wittekind +15 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

Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretation

Genetics in Medicine(2021)10.1038/s41436-021-01134-9
N/A
0DataRank · unranked
18 citations

Adam Helms, Anamika Kannan, Jaime Yob, Neal K. Lakdawala, Samuel G. Wittekind +14 more

Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies

Nature Cardiovascular Research(2023)10.1038/s44161-023-00346-3
N/A
0DataRank · unranked
34 citations

Sean J. Jurgens, Francesco Mazzarotto, Mona Allouba, James P. Pirruccello, Yasmine Aguib +6 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

Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

Nature Genetics(2025)10.1038/s41588-025-02087-4
N/A
0DataRank · unranked
55 citations

Sean L. Zheng, Christopher Grace, Paloma Jordà, Catherine Francis, Dominique M West +95 more

The complementary roles of rare variant burden scores and common variant polygenic risk scores in genetic risk polygenic risk scores in genetic risk prediction of complex disorders

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.09.15.676308
N/A
0DataRank · unranked
0 citations

Massimo Gennarelli, Graham K. Murray, Emanuele F. Osimo, Francesco Mazzarotto