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

Elise Héon

Hospital for Sick Children

ORCID: 0000-0003-4143-9311

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 3%percentile

1.5Author 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

The RUSH2A Study: Best-Corrected Visual Acuity, Full-Field Electroretinography Amplitudes, and Full-Field Stimulus Thresholds at Baseline

Translational Vision Science & Technology(2020)10.1167/tvst.9.11.9

Top 14%

1.5DataRank

Top 14%58 citations

Peiyao Cheng, Jacque L. Duncan, Allison R. Ayala, Maureen G. Maguire, Isabelle Audo +15 more

Papers

Driven by 16 papers — median percentile 86. Top paper: “The RUSH2A Study: Best-Corrected Visual Acuity, Full-Field Electroretinography Amplitudes, and Full-Field Stimulus Thresholds at Baseline”.

The RUSH2A Study: Best-Corrected Visual Acuity, Full-Field Electroretinography Amplitudes, and Full-Field Stimulus Thresholds at Baseline

Translational Vision Science & Technology(2020)10.1167/tvst.9.11.9

Top 14%

1.5DataRank

Top 14%58 citations

Peiyao Cheng, Jacque L. Duncan, Allison R. Ayala, Maureen G. Maguire, Isabelle Audo +15 more

Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy

Journal of Clinical Investigation(2021)10.1172/jci138267

N/A

0.756DataRank · unranked

153 citations

Natalia L. Sheremet, Claudia B. Catarino, Natalia A. Andreeva, Zahra Assouline, Piero Barboni +49 more

Tissue‐specific genotype–phenotype correlations among USH2A‐related disorders in the RUSH2A study

Human Mutation(2022)10.1002/humu.24365

N/A

0.477DataRank · unranked

23 citations

Wendi Liang, Jacque L. Duncan, Carmen C. Brewer, Isabelle Audo, Allison R. Ayala +14 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

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

0.312DataRank · unranked

7 citations

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

A large animal model of RDH5-associated retinopathy recapitulates important features of the human phenotype

Human Molecular Genetics(2021)10.1093/hmg/ddab316

N/A

0DataRank · unranked

18 citations

Anahita Daruwalla, Samantha R. De Silva, Paige A. Winkler, Kelian Sun, Nate Pasmanter +13 more

Deregulation of Neuro-Developmental Genes and Primary Cilium Cytoskeleton Anomalies in iPSC Retinal Sheets from Human Syndromic Ciliopathies

Stem Cell Reports(2020)10.1016/j.stemcr.2020.02.005

N/A

0DataRank · unranked

15 citations

Anthony Flamier, Roy Hanna, Elise Héon, Benjamin Freedman, Gilbert Bernier +1 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

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

Defective IFT57 underlies a novel cause of Bardet-Biedl syndrome

Human Molecular Genetics(2025)10.1093/hmg/ddaf058

N/A

0DataRank · unranked

2 citations

Qihong Zhang, Erika Tavares, Janice Min Li, Kashif Ahmed, Kit Green-Sanderson +8 more

CEP76 impairment at the centrosome-cilium interface contributes to a spectrum of ciliopathies

Science Advances(2025)10.1126/sciadv.adw3717

N/A

0DataRank · unranked

1 citations

Erika Tavares, Katherine Bishara, Ayşegül Ozantürk, Leila Qebibo, Stephan Frangakis +25 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

Variants in CFAP410 cause a range of retinal and skeletal phenotypes

npj Genomic Medicine(2025)10.1038/s41525-025-00489-1

N/A

0DataRank · unranked

0 citations

Amy E. Pohodich, David G. Birch, Kaylie Webb-Jones, Byron L. Lam, Emily H. Jung +44 more

Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease Severity

American Journal of Ophthalmology(2020)10.1016/j.ajo.2020.05.024

N/A

0DataRank · unranked

41 citations

Wendi Liang, Maureen G. Maguire, Isabelle Audo, Allison R. Ayala, David G. Birch +16 more

Treatments for inherited retinal degenerations are coming to Canada: brief update on a new standard of care for inherited retinal degenerations

Canadian Journal of Ophthalmology(2020)10.1016/j.jcjo.2020.10.019

N/A

0DataRank · unranked

4 citations

Robert K. Koenekoop, Elise Héon