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

Jean Muller

Inserm

ORCID: 0000-0002-7682-559X

Also affiliated with Hôpitaux Universitaires de Strasbourg, Génétique Médicale & Génomique Fonctionelle, Université de Strasbourg

Biochemistry, 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 2%percentile
1.8Author 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 Data Use Ontology to streamline responsible access to human biomedical datasets

Cell Genomics(2021)10.1016/j.xgen.2021.100028
Top 12%
1.8DataRank
Top 12%64 citations

Moran N. Cabili, Giselle Kerry, Tiffany Boughtwood, Adrian Thorogood, Pinar Alper +52 more

Papers

Driven by 5 papers — median percentile 88. Top paper: “Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy”.

Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy

Nature Genetics(2020)10.1038/s41588-020-0707-1
N/A
2.0DataRank · unranked
35 citations

Onuralp Söylemez, Aysegül Ozanturk, Niki Mourtzi, Sebastian Akle, Irwin Jungreis +16 more

The Data Use Ontology to streamline responsible access to human biomedical datasets

Cell Genomics(2021)10.1016/j.xgen.2021.100028
Top 12%
1.8DataRank
Top 12%64 citations

Moran N. Cabili, Giselle Kerry, Tiffany Boughtwood, Adrian Thorogood, Pinar Alper +52 more

Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy

bioRxiv (Cold Spring Harbor Laboratory)(2018)10.1101/362707
N/A
0.403DataRank · unranked
4 citations

Onuralp Söylemez, Aysegül Ozanturk, Sebastian Akle, Irwin Jungreis, Jean Muller +16 more

A BBS1 SVA F retrotransposon insertion is a frequent cause of Bardet‐Biedl syndrome

Clinical Genetics(2020)10.1111/cge.13878
N/A
0DataRank · unranked
26 citations

Samuel Nicaise, Manuela Antin, Anne‐Sophie Leuvrey, Elsa Nourisson, Carmen C. Leitch +22 more

SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice

Nature Communications(2022)10.1038/s41467-022-31566-z
N/A
0DataRank · unranked
39 citations

Kyung Ah Han, Dongwook Kim, Gyubin Jang, Somayeh Bakhtiari, Dongseok Lim +35 more