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

Susanne Roosing

Radboud University Nijmegen

ORCID: 0000-0001-9038-0067

Also affiliated with University Medical Center, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences

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

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 →

Papers

Driven by 11 papers. Top paper: “An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes”.

An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes

Nature Cell Biology(2015)10.1038/ncb3201
N/A
0.831DataRank · unranked
253 citations

Gabrielle Wheway, Miriam Schmidts, Dorus A. Mans, Katarzyna Szymanska, Thanh-Minh T. Nguyen +71 more

Minigene-Based Splice Assays Reveal the Effect of Non-Canonical Splice Site Variants in USH2A

International Journal of Molecular Sciences(2022)10.3390/ijms232113343
N/A
0.577DataRank · unranked
9 citations

Jaap Oostrik, Marco Aben, Mariana Guimarães Ramos, Emma van Berkel, Monika Ołdak +5 more

Optical genome mapping and revisiting short-read genome sequencing data reveal previously overlooked structural variants disrupting retinal disease−associated genes

Genetics in Medicine(2023)10.1016/j.gim.2022.11.013
N/A
0.561DataRank · unranked
41 citations

Kim Rodenburg, Jordi Corominas, Tamar Ben-Yosef, Janine Reurink, Hannie Kremer +22 more

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

Genetics in Medicine(2024)10.1016/j.gim.2024.101106
N/A
0.416DataRank · unranked
15 citations

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

Expansion of the ABCA4-Associated Retinopathy Spectrum: Severe Variants Can be Associated With Early-Onset Severe Retinal Dystrophy

Investigative Ophthalmology & Visual Science(2025)10.1167/iovs.66.6.19
N/A
0.269DataRank · unranked
5 citations

Rebekkah J. Hitti‐Malin, Martin McKibbin, Suzanne E. de Bruijn, Erica G. M. Boonen, Andrea L. Vincent +10 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

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

Deciphering the largest disease-associated transcript isoforms in the human neural retina with advanced long-read sequencing approaches

Genome Research(2025)10.1101/gr.280060.124
N/A
0DataRank · unranked
1 citations

Tabea Riepe, Nick Zomer, Renee Salz, Michael Kwint, Jaap Oostrik +15 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

A RIPOR2 in-frame deletion is a frequent and highly penetrant cause of adult-onset hearing loss

Journal of Medical Genetics(2020)10.1136/jmedgenet-2020-106863
N/A
0DataRank · unranked
19 citations

Jeroen J. Smits, Chang Liu, Cris Lanting, Andy J. Beynon, Joëlle Blankevoort +12 more