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

Chris F. Inglehearn

University of Leeds

ORCID: 0000-0002-5143-2562

Also affiliated with St James's University Hospital

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 4%percentile
0.763Author DataRank

Indexed papers

5in 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 5 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.

RetiGene, a comprehensive gene atlas for inherited retinal diseases

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.08.017
Top 34%
0.580DataRank
Top 34%28 citations

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

Papers

Driven by 10 papers — median percentile 50. Top paper: “A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus”.

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
2.0DataRank · unranked
95 citations

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

An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes

Nature Cell Biology(2015)10.1038/ncb3201
N/A
0.831DataRank · unranked
253 citations

Gabrielle Wheway, Miriam Schmidts, Dorus A. Mans, Katarzyna Szymanska, Thanh-Minh T. Nguyen +71 more

RetiGene, a comprehensive gene atlas for inherited retinal diseases

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.08.017
Top 34%
0.580DataRank
Top 34%28 citations

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

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
0.269DataRank · unranked
5 citations

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

ACP4 Variants in Hypoplastic Amelogenesis Imperfecta

Calcified Tissue International(2026)10.1007/s00223-026-01512-y
N/A
0.104DataRank · unranked
1 citations

Cheuk Wang Au, Ummey Hany, Alice L. Rigby, Anesha Chauhan, Catriona Brown +8 more

ACP4 Variants In Hypoplastic Amelogenesis Imperfecta

10.21203/rs.3.rs-8797936/v1
N/A
0.104DataRank · unranked
1 citations

Cheuk Wang Au, Ummey Hany, Alice L. Rigby, Anesha Chauhan, Catriona Brown +8 more

Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability

Journal of Medical Genetics(2024)10.1136/jmg-2023-109728
N/A
0DataRank · unranked
5 citations

Virginie Laugel-Haushalter, Ummey Hany, Sunayna Best, Rachel L. Taylor, James A. Poulter +13 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