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

Petra Liskova

Charles University

ORCID: 0000-0001-7834-8486

Also affiliated with General University Hospital in Prague

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 3%percentile
1.7Author 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.

Axenfeld-Rieger syndrome: more than meets the eye

Journal of Medical Genetics(2022)10.1136/jmg-2022-108646
Top 12%
1.7DataRank
Top 12%81 citations

Mohit Maheshwari, Jenina Capasso, Hüban Atilla, Lubica Dudakova, Samuel Thompson +22 more

Papers

Driven by 11 papers — median percentile 88. Top paper: “Axenfeld-Rieger syndrome: more than meets the eye”.

Axenfeld-Rieger syndrome: more than meets the eye

Journal of Medical Genetics(2022)10.1136/jmg-2022-108646
Top 12%
1.7DataRank
Top 12%81 citations

Mohit Maheshwari, Jenina Capasso, Hüban Atilla, Lubica Dudakova, Samuel Thompson +22 more

Rare disease gene association discovery in the 100,000 GenomesProject

Nature(2025)10.1038/s41586-025-08623-w
N/A
0.515DataRank · unranked
18 citations

Letizia Vestito, Emma Magavern, Julius O.B. Jacobsen, Gavin Arno, Elijah R. Behr +56 more

The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosis

Experimental Eye Research(2019)10.1016/j.exer.2019.03.002
N/A
0.373DataRank · unranked
11 citations

Cerys J. Evans, Nikolas Pontikos, Nathaniel J. Hafford-Tear, Frantisek Malinka, Pavlina Skalicka +12 more

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa

Nature Genetics(2026)10.1038/s41588-025-02451-4
N/A
0.370DataRank · unranked
8 citations

Kim Rodenburg, Zuzana Cvackova, Karolina Kaminska, Suzanne E. de Bruijn, Ana Belén Iglesias-Romero +212 more

Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia

Human Mutation(2022)10.1002/humu.24371
N/A
0DataRank · unranked
20 citations

Britta Baumann, Peggy Reuter, Sten Andréasson, Isabelle Audo, Carmen Ayuso +46 more

Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritability

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100237
N/A
0DataRank · unranked
13 citations

Mubeen Khan, Rebekkah J. Hitti‐Malin, Ketan Mishra, Laura Whelan, Stéphanie S. Cornelis +14 more

Lisch Epithelial Corneal Dystrophy Is Caused by Heterozygous Loss-of-Function Variants in MCOLN1

American Journal of Ophthalmology(2023)10.1016/j.ajo.2023.10.011
N/A
0DataRank · unranked
8 citations

Jessica X. Chong, Doug D. Chung, Walter Lisch, Carol L. Karp, Erling Dreisler +16 more

Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data

medRxiv(2023)10.1101/2023.12.20.23300294
N/A
0DataRank · unranked
3 citations

Letizia Vestito, Emma Magavern, Julius O.B. Jacobsen, Gavin Arno, Elijah R. Behr +56 more

Comprehensive phenotypic and functional analysis of dominant and recessiveFOXE3alleles in ocular developmental disorders

Human Molecular Genetics(2021)10.1093/hmg/ddab142
N/A
0DataRank · unranked
20 citations

Елена А. Сорокина, Lubica Dudakova, Jana Moravíková, Pavlína Skalická, František Malinka +12 more

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa

medRxiv(2025)10.1101/2025.01.06.24317169
N/A
0DataRank · unranked
15 citations

Kim Rodenburg, Zuzana Cvačková, Karolina Kamińska, Suzanne E. de Bruijn, Ana Belén Iglesias-Romero +95 more

A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus

Communications Biology(2021)10.1038/s42003-021-01784-0
N/A
0DataRank · unranked
94 citations

Petra Liskova, Yelena Bykhovskaya, Bennet J. McComish, Alice E. Davidson, Chris F. Inglehearn +57 more