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

Veronika Barešová

Charles University

ORCID: 0000-0001-8989-6090

Also affiliated with General University Hospital in Prague

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 100%percentile
0Author DataRank

Indexed papers

0in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 4 papers. Top paper: “Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing”.

Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing

Nature Genetics(2013)10.1038/ng.2543
N/A
0.862DataRank · unranked
313 citations

Andreas Gnirke, David B. Jaffe, Veronika Barešová, Nathalie Pochet, Brendan Blumenstiel +43 more

An international cohort study of autosomal dominant tubulointerstitial kidney disease due to mutations identifies distinct clinical subtypes

Kidney International(2020)10.1016/j.kint.2020.06.041
N/A
0DataRank · unranked
43 citations

Kendrah Kidd, Mohamad Zaidan, Petr Vyleťal, Veronika Barešová, Kateřina Hodaňová +51 more

Bi-allelic REN Mutations and Undetectable Plasma Renin Activity in a Patient With Progressive CKD

Kidney International Reports(2023)10.1016/j.ekir.2023.01.017
N/A
0DataRank · unranked
1 citations

Kendrah Kidd, Petr Vyleťal, Estela Nogueira, Lauren Martin, Katrice Howard +11 more

Long-Read Sequencing of the MUC1 VNTR: Genomic Variation, Mutational Landscape, and Its Impact on ADTKD Diagnosis and Progression

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.09.06.673538
N/A
0DataRank · unranked
3 citations

Anna Přistoupilová, Kendrah Kidd, Václav Janoušek, Martin Radina, Petr Vyleťal +38 more