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

Dror Sharon

Hebrew University of Jerusalem

ORCID: 0000-0002-1789-5811

Also affiliated with Hadassah Medical Center

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 11 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

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

KCNV2-associated retinopathy: genotype–phenotype correlations –KCNV2study group report 3

British Journal of Ophthalmology(2023)10.1136/bjo-2023-323640
N/A
0DataRank · unranked
5 citations

Michalis Georgiou, Anthony G. Robson, Kaoru Fujinami, Ajoy Vincent, Fadi Nasser +31 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

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

Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study

British Journal of Ophthalmology(2024)10.1136/bjo-2023-323747
N/A
0DataRank · unranked
7 citations

Elizabeth White, Alaa Tayyib, Lesley Everett, Ajoy Vincent, Elise Héon +52 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

Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy

Genetics in Medicine(2025)10.1016/j.gim.2025.101401
N/A
0DataRank · unranked
4 citations

Maayan Avraham, Sandeep Sarma Asodu, Abigail R. Moye, Riccardo Sangermano, Leah Rizel +19 more

Non-coding single-nucleotide and structural variants affecting the EYS putative promoter cause autosomal recessive retinitis pigmentosa

Genetics in Medicine(2025)10.1016/j.gim.2025.101427
N/A
0DataRank · unranked
3 citations

Shai Ovadia, Jaya Krishnan, Manon Bouckaert, Daan M. Panneman, Milton A. English +13 more

KCNV2-Associated Retinopathy: Detailed Retinal Phenotype and Structural Endpoints—KCNV2 Study Group Report 2

American Journal of Ophthalmology(2021)10.1016/j.ajo.2021.03.004
N/A
0DataRank · unranked
28 citations

Kaoru Fujinami, Ajoy Vincent, Fadi Nasser, Samer Khateb, Mauricio E. Vargas +32 more