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

Frans P. M. Cremers

Radboud University Nijmegen

ORCID: 0000-0002-4954-5592

Also affiliated with University Medical Center, Radboud University Medical Center, Maastricht University

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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 6%percentile
0.183Author 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 →

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.

RetiGene, a comprehensive gene atlas for inherited retinal diseases (IRDs)

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.06.08.653722
Top 66%
0.183DataRank
Top 66%2 citations

Elifnaz Çelik, Dhryata Kamdar, Francesca Cancellieri, Karolina Kamińska, Mukhtar Ullah +26 more

Papers

Driven by 10 papers — median percentile 34. Top paper: “Minigene-Based Splice Assays Reveal the Effect of Non-Canonical Splice Site Variants in USH2A”.

Minigene-Based Splice Assays Reveal the Effect of Non-Canonical Splice Site Variants in USH2A

International Journal of Molecular Sciences(2022)10.3390/ijms232113343
N/A
0.577DataRank · unranked
9 citations

Jaap Oostrik, Marco Aben, Mariana Guimarães Ramos, Emma van Berkel, Monika Ołdak +5 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

RetiGene, a comprehensive gene atlas for inherited retinal diseases (IRDs)

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.06.08.653722
Top 66%
0.183DataRank
Top 66%2 citations

Elifnaz Çelik, Dhryata Kamdar, Francesca Cancellieri, Karolina Kamińska, Mukhtar Ullah +26 more

ABCA4c.859-25A>G, a Frequent Palestinian Founder Mutation Affecting the Intron 7 Branchpoint, Is Associated With Early-Onset Stargardt Disease

Investigative Ophthalmology & Visual Science(2022)10.1167/iovs.63.4.20
N/A
0DataRank · unranked
7 citations

Manar Salameh, Mubeen Khan, Elise Héon, Ketan Mishra, Rebekkah J. Hitti‐Malin +12 more

Compendium of Clinical Variant Classification for 2,246 Unique ABCA4 Variants to Clarify Variant Pathogenicity in Stargardt Disease Using a Modified ACMG/AMP Framework

Human Mutation(2023)10.1155/2023/6815504
N/A
0DataRank · unranked
20 citations

Miriam Bauwens, Lonneke Haer‐Wigman, Marieke De Bruyne, Madhulatha Pantrangi, Elfride De Baere +4 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

Expansion of the ABCA4-Associated Retinopathy Spectrum: Severe Variants Can be Associated With Early-Onset Severe Retinal Dystrophy

Investigative Ophthalmology & Visual Science(2025)10.1167/iovs.66.6.19
N/A
0DataRank · unranked
4 citations

Rebekkah J. Hitti‐Malin, Martin McKibbin, Suzanne E. de Bruijn, Erica G. M. Boonen, Andrea L. Vincent +10 more

Deciphering the largest disease-associated transcript isoforms in the human neural retina with advanced long-read sequencing approaches

Genome Research(2025)10.1101/gr.280060.124
N/A
0DataRank · unranked
1 citations

Tabea Riepe, Nick Zomer, Renee Salz, Michael Kwint, Jaap Oostrik +15 more

Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations

Progress in Retinal and Eye Research(2020)10.1016/j.preteyeres.2020.100861
N/A
0DataRank · unranked
313 citations

Winston Lee, Rob W.J. Collin, Rando Allikmets, Frans P. M. Cremers

A RIPOR2 in-frame deletion is a frequent and highly penetrant cause of adult-onset hearing loss

Journal of Medical Genetics(2020)10.1136/jmedgenet-2020-106863
N/A
0DataRank · unranked
19 citations

Jeroen J. Smits, Chang Liu, Cris Lanting, Andy J. Beynon, Joëlle Blankevoort +12 more