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

Kerry Goetz

Topcon (Netherlands)

ORCID: 0000-0002-9821-7704
MedicineHealth Professions

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 2%percentile
2.6Author DataRank

Indexed papers

3in 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 3 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.

Genotype–phenotype associations in a large PRPH2‐related retinopathy cohort

Human Mutation(2020)10.1002/humu.24065
Top 13%
1.7DataRank
Top 13%41 citations

Kerry Goetz, Bin Guan, Ehsan Ullah, Delphine Blain, Wadih M. Zein +3 more

Papers

Driven by 16 papers — median percentile 74. Top paper: “Genotype–phenotype associations in a large PRPH2‐related retinopathy cohort”.

Genotype–phenotype associations in a large PRPH2‐related retinopathy cohort

Human Mutation(2020)10.1002/humu.24065
Top 13%
1.7DataRank
Top 13%41 citations

Kerry Goetz, Bin Guan, Ehsan Ullah, Delphine Blain, Wadih M. Zein +3 more

Advancing Toward a Common Data Model in Ophthalmology

Ophthalmology Science(2023)10.1016/j.xops.2023.100391
Top 26%
0.775DataRank
Top 26%23 citations

William Halfpenny, Michael V. Boland, Harold P. Lehmann, Michelle R. Hribar, Kerry Goetz +2 more

Systematic assessment of the contribution of structural variants to inherited retinal diseases

Human Molecular Genetics(2023)10.1093/hmg/ddad032
N/A
0.373DataRank · unranked
11 citations

Meng C. Wang, Xinye Qian, Yumei Li, Keqing Wang, Jongsu Choi +13 more

Barriers to Extracting and Harmonizing Glaucoma Testing Data: Gaps, Shortcomings, and the Pursuit of FAIRness

Ophthalmology Science(2024)10.1016/j.xops.2024.100621
N/A
0.241DataRank · unranked
4 citations

Shahin Hallaj, Michael V. Boland, Brian C. Stagg, Sophia Y. Wang, Benjamin Y. Xu +14 more

Genotype–Phenotype Spectrum of eyeGENE Patients With Familial Exudative Vitreoretinopathy: Novel Variants in Norrin/β-Catenin Signaling Pathway Genes

Investigative Ophthalmology & Visual Science(2025)10.1167/iovs.66.2.9
Top 67%
0.169DataRank
Top 67%2 citations

Melissa Reeves, Sairah Yousaf, Ehsan Ullah, Bin Guan, Kerry Goetz +3 more

The qMini assay identifies an overlooked class of splice variants

medRxiv(2023)10.1101/2023.11.02.23297963
N/A
0.104DataRank · unranked
1 citations

Chelsea Bender, Madhulatha Pantrangi, Nia Moore, Melissa Reeves, Amelia Naik +10 more

Artificial intelligence at the national eye institute

Current Opinion in Ophthalmology(2022)10.1097/icu.0000000000000889
N/A
0DataRank · unranked
2 citations

Emily Y. Chew, Michael F. Chiang, Michelle R. Hribar, James Gao, Kerry Goetz +1 more

Rare and common variants in ROM1 and PRPH2 genes trans-modify Stargardt/ABCA4 disease

PLoS Genetics(2022)10.1371/journal.pgen.1010129
N/A
0DataRank · unranked
16 citations

Winston Lee, Jun Wang, Kerry Goetz, Ehsan Ullah, Takayuki Nagasaki +9 more

Clinical, social, and policy factors in COVID-19 cases and deaths: methodological considerations for feature selection and modeling in county-level analyses

BMC Public Health(2022)10.1186/s12889-022-13168-y
N/A
0DataRank · unranked
36 citations

Ken Wilkens, Nicole G. Weiskopf, Nina Cesare, Sharmodeep Bhattacharyya, Naomi O. Riches +10 more

Systematic assessment of the contribution of structural variants to inherited retinal diseases

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.02.522522
N/A
0DataRank · unranked
5 citations

Meng C. Wang, Xinye Qian, Yumei Li, Keqing Wang, Jongsu Choi +13 more

Similar Risk of Kidney Failure among Patients with Blinding Diseases Who Receive Ranibizumab, Aflibercept, and Bevacizumab

Ophthalmology Retina(2024)10.1016/j.oret.2024.03.014
N/A
0DataRank · unranked
17 citations

Akihiko Nishimura, Mary G. Bowring, Erik Westlund, Diep Tran, Jia Hwei Ng +32 more

Identification of Deep-Intronic Splice Mutations in a Large Cohort of Patients With Inherited Retinal Diseases

Frontiers in Genetics(2021)10.3389/fgene.2021.647400
N/A
0DataRank · unranked
69 citations

Jun Wang, Meng C. Wang, Austin D. Igelman, Kaylie Webb-Jones, Yumei Li +7 more

Special Commentary: Cerebral/Cortical Visual Impairment Working Definition

Ophthalmology(2024)10.1016/j.ophtha.2024.09.017
N/A
0DataRank · unranked
48 citations

Lotfi B. Merabet, Mark Borchert, Arvind Chandna, Gena Heidary, Barry Kran +19 more

The OHDSI Network in Ophthalmology—The Promise of Observational Health Data

JAMA Ophthalmology(2025)10.1001/jamaophthalmol.2025.0399
N/A
0DataRank · unranked
4 citations

Cindy X. Cai, Kerry Goetz, George Hripcsak, Michelle R. Hribar

Ocular Health and National Data Standards: A Case for Including Visual Acuity in the United States Core Data for Interoperability (USCDI)

Ophthalmology Science(2022)10.1016/j.xops.2022.100210
N/A
0DataRank · unranked
14 citations

Amberlynn A. Reed, April Y. Maa, Michael V. Boland, Durga S. Borkar, Eric N. Brown +3 more

Mutation Screening in the miR-183/96/182 Cluster in Patients With Inherited Retinal Dystrophy

Frontiers in Cell and Developmental Biology(2020)10.3389/fcell.2020.619641
N/A
0DataRank · unranked
9 citations

Ardian Coku, Chithra Muraleedharan, Ali Harajli, Eric Mishulin, Chafic Dahabra +7 more