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

Filip Van den Broeck

Ghent University Hospital

ORCID: 0009-0006-3330-6497

Also affiliated with Ghent University

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 100%percentile
0Author DataRank

Indexed papers

1in 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 1 indexed paper 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 →

Papers

Driven by 5 papers. Top paper: “Bi-allelic variants in three genes encoding distinct subunits of the vesicular AP-5 complex cause hereditary macular dystrophy”.

Bi-allelic variants in three genes encoding distinct subunits of the vesicular AP-5 complex cause hereditary macular dystrophy

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.02.015
N/A
0.208DataRank · unranked
3 citations

Francesca Cancellieri, Mathieu Quinodoz, Abigail R. Moye, Miriam Bauwens, Siying Lin +51 more

RPE65 variant p.(E519K) causes a novel dominant adult-onset maculopathy in 83 affected individuals

Research Square(2025)10.21203/rs.3.rs-5849564/v2
N/A
0.104DataRank · unranked
1 citations

Filip Van den Broeck, Quinten Mahieu, Eline Geens, Mattias Van Heetvelde, Marieke De Bruyne +32 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

RPE65 Variant p.(E519K) Causes a Novel Dominant Adult-Onset Maculopathy in 83 Affected Individuals

Investigative Ophthalmology & Visual Science(2025)10.1167/iovs.66.12.53
N/A
0DataRank · unranked
2 citations

Filip Van den Broeck, Quinten Mahieu, Eline Geens, Mattias Van Heetvelde, Marieke De Bruyne +32 more

Bi-allelic loss-of-function variants in POC5 cause a syndromic retinal, endocrine, and neuromuscular ciliopathy

Genetics in Medicine(2025)10.1016/j.gim.2025.101513
N/A
0DataRank · unranked
1 citations

Ingrid M. Jazet, Suzanne Yzer, Jeroen Pas, Serwet Demirdas, Elisabeth F. C. van Rossum +39 more