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

Mathieu Quinodoz

University of Leicester

ORCID: 0000-0002-9841-4433

Also affiliated with University of Basel, University Hospital of Basel, Department of Biomedicine Basel, Genomics (United Kingdom), Institute of Molecular and Clinical Ophthalmology Basel

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

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.

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 9 papers — median percentile 50. Top paper: “RetiGene, a comprehensive gene atlas for inherited retinal diseases”.

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

Topography of Slowed Dark Adaptation in Pseudoxanthoma Elasticum: PROPXE Study Report 1

Investigative Ophthalmology & Visual Science(2025)10.1167/iovs.66.2.17
N/A
0.292DataRank · unranked
6 citations

Georg Ansari, Stephan Michels, Chantal Dysli, Sandra Liakopoulos, Jana Burghaus-Zhang +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

Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration

Genetics in Medicine(2024)10.1016/j.gim.2024.101106
N/A
0DataRank · unranked
14 citations

Kim Rodenburg, Tamar Hayman, Giacomo Calzetti, Karolina Kamińska, Mathieu Quinodoz +20 more

Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

Genetics in Medicine(2021)10.1038/s41436-021-01232-8
N/A
0DataRank · unranked
49 citations

Rebecca C. Spillmann, Harley T. Kurata, Shawn M. Lamothe, Jasmine Maghera, Rami Abou Jamra +92 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

Substitution of a single non-coding nucleotide upstream of TMEM216 causes non-syndromic retinitis pigmentosa and is associated with reduced TMEM216 expression

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.07.020
N/A
0DataRank · unranked
7 citations

Pooja Biswas, Anne-Marie Berry, Riccardo Sangermano, Mukhtar Ullah, Siying Lin +40 more

Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative

PLoS Genetics(2022)10.1371/journal.pgen.1010367
N/A
0DataRank · unranked
67 citations

Gundula Povysil, Jack A. Kosmicki, Elizabeth T. Cirulli, Theodore G. Drivas, Simone Furini +95 more

Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative

medRxiv(2022)10.1101/2022.03.28.22273040
N/A
0DataRank · unranked
7 citations

Gundula Povysil, Jack A. Kosmicki, Elizabeth T. Cirulli, Theodore G. Drivas, Simone Furini +95 more