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

Hannie Kremer

Radboud University Nijmegen

ORCID: 0000-0002-0841-8693

Also affiliated with Radboud University Medical Center

NeuroscienceBiochemistry, Genetics and Molecular Biology

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 5%percentile
0.428Author 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 →

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.

The natural history and genotype–phenotype correlations of TMPRSS3 hearing loss: an international, multi-center, cohort analysis

Human Genetics(2024)10.1007/s00439-024-02648-3
Top 43%
0.428DataRank
Top 43%7 citations

Cris Lanting, Molly Smeal, Susan H. Blanton, Derek M. Dykxhoorn, Pei-Ciao Tang +75 more

Papers

Driven by 7 papers — median percentile 57. Top paper: “Minigene-Based Splice Assays Reveal the Effect of Non-Canonical Splice Site Variants in USH2A”.

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

The natural history and genotype–phenotype correlations of TMPRSS3 hearing loss: an international, multi-center, cohort analysis

Human Genetics(2024)10.1007/s00439-024-02648-3
Top 43%
0.428DataRank
Top 43%7 citations

Cris Lanting, Molly Smeal, Susan H. Blanton, Derek M. Dykxhoorn, Pei-Ciao Tang +75 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

Affinity purification of in vivo assembled whirlin-associated protein complexes from the zebrafish retina

Journal of Proteomics(2022)10.1016/j.jprot.2022.104666
N/A
0DataRank · unranked
2 citations

Ralph Slijkerman, Lisette Hetterschijt, Theo Peters, Sanne Broekman, Aurélie Clément +7 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

Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss

medRxiv(2021)10.1101/2021.01.27.21250652
N/A
0DataRank · unranked
8 citations

Marina T. DiStefano, Andrea M. Oza, Madeline Y. Hughes, Emma H. Wilcox, Sarah E. Hemphill +18 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