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

Christian Gilissen

Radboud University Nijmegen

ORCID: 0000-0003-1693-9699

Also affiliated with University Medical Center, Radboud University 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 2%percentile
2.1Author DataRank

Indexed papers

4in 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 4 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.

Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2203491119
Top 14%
1.5DataRank
Top 14%73 citations

Chang N. Kim, Trygve E. Bakken, Madelyn A. Gillentine, Barbara Henning, Yafei Mao +94 more

Papers

Driven by 18 papers — median percentile 77. Top paper: “Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders”.

Integrated gene analyses of de novo variants from 46,612 trios with autism and developmental disorders

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2203491119
Top 14%
1.5DataRank
Top 14%73 citations

Chang N. Kim, Trygve E. Bakken, Madelyn A. Gillentine, Barbara Henning, Yafei Mao +94 more

BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorder

Human Mutation(2020)10.1002/humu.23992
N/A
0.961DataRank · unranked
28 citations

Hui Guo, Evan E. Eichler, Jill A. Rosenfeld, Kaifang Pang, Zhandong Liu +20 more

A de novo paradigm for male infertility

Nature Communications(2022)10.1038/s41467-021-27132-8
N/A
0.691DataRank · unranked
99 citations

RM Smits, H E Smith, Francesco Mastrorosa, Giles Holt, Brendan J. Houston +59 more

Population sequencing data reveal a compendium of mutational processes in the human germ line

Science(2021)10.1126/science.aba7408
N/A
0.648DataRank · unranked
74 citations

Ruslan Soldatov, Evan M. Koch, Ryan J. McGinty, Jakob M. Goldmann, Ryan D. Hernandez +38 more

Mutations in the V‐ATPase Assembly Factor VMA21 Cause a Congenital Disorder of Glycosylation With Autophagic Liver Disease

Hepatology(2020)10.1002/hep.31218
N/A
0.596DataRank · unranked
52 citations

Laurie A. Graham, Angel Ashikov, Lars Elmann Larsen, Kimiyo Raymond, Sharita Timal +23 more

Integrated gene analyses of de novo mutations from 46,612 trios with autism and developmental disorders

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.09.15.460398
Top 33%
0.594DataRank
Top 33%13 citations

Chang H. Kim, Trygve E. Bakken, Madelyn A. Gillentine, Barbara Henning, Yafei Mao +4 more

CERT1 mutations perturb human development by disrupting sphingolipid homeostasis

Journal of Clinical Investigation(2023)10.1172/jci165019
N/A
0.568DataRank · unranked
43 citations

Museer A. Lone, Winston Lee, Laura Capolupo, Sylvia Ho, Adekemi M. Adeyemi +80 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

Lack of evidence for a role of PIWIL1 variants in human male infertility

Cell(2021)10.1016/j.cell.2021.03.001
N/A
0.434DataRank · unranked
17 citations

Ludmila Voložonoka, Corinna Friedrich, Sabine Kliesch, Liina Nagirnaja, Christian Gilissen +7 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

Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles

Genome Medicine(2024)10.1186/s13073-024-01339-y
N/A
0.292DataRank · unranked
6 citations

Jacqueline Chrast, Giovanna Ambrosini, Norine Voisin, Frédéric Schütz, Alfredo Brusco +49 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

Structural variation in 1,019 diverse humans based on long-read sequencing

Nature(2025)10.1038/s41586-025-09290-7
N/A
0DataRank · unranked
56 citations

Samarendra Pani, Jana Ebler, Carsten Hain, Vasiliki Tsapalou, Arda Soylev +27 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

Cochlear supporting cells require GAS2 for cytoskeletal architecture and hearing

Developmental Cell(2021)10.1016/j.devcel.2021.04.017
N/A
0DataRank · unranked
53 citations

Alex M Rohacek, Matthew A. Caporizzo, Amir Nankali, Jeroen J. Smits, Jaap Oostrik +13 more

A de novo paradigm for male infertility

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.02.27.433155
N/A
0DataRank · unranked
1 citations

RM Smits, H E Smith, FK Mastrorosa, GS Holt, BJ Houston +35 more

Impact of rare and common genetic variation in the Interleukin-1 pathway on human cytokine responses

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.14.949602
N/A
0DataRank · unranked
2 citations

Peer Arts, Giulio Cavalli, Martin Jaeger, Marloes Steehouwer, Maartje van de Vorst +9 more

Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles

medRxiv(2024)10.1101/2024.01.14.24301100
N/A
0DataRank · unranked
1 citations

Jacqueline Chrast, Giovanna Ambrosini, Norine Voisin, Frédéric Schütz, Alfredo Brusco +47 more