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

Médéric Jeanne

Université de Tours

ORCID: 0000-0003-1136-8890

Also affiliated with Boston Children's Hospital, Harvard University, Inserm, Centre Hospitalier Universitaire de Tours, Laboratoire National de Référence, Boston Children's Museum

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 100%percentile
0Author DataRank

Indexed papers

0in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 5 papers. Top paper: “Biallelic variants in the non-coding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes”.

Biallelic variants in the non-coding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes

medRxiv(2025)10.1101/2025.08.13.25333306
N/A
0.269DataRank · unranked
5 citations

Alexander J. M. Blakes, Yuyang Chen, Joachim De Jonghe, Javeria Raza Alvi, Florence Amblard +69 more

Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism

Annals of Clinical and Translational Neurology(2024)10.1002/acn3.51963
N/A
0.208DataRank · unranked
3 citations

Güney Bademci, Stephan Züchner, Médéric Jeanne, Nicholas A. Borja, Danique Beijer +8 more

Missense variants in DPYSL5 associated with neurodevelopmental disorders and brain malformations cause impaired neuronal maturation in vitro

Molecular Psychiatry(2025)10.1038/s41380-025-03364-8
N/A
0.104DataRank · unranked
1 citations

Solène Remizé, Liberty François‐Moutal, Dévina C. Ung, Audrey Dangoumau, Sylviane Marouillat +24 more

SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidance

Human Molecular Genetics(2022)10.1093/hmg/ddac114
N/A
0DataRank · unranked
17 citations

Martina Schaettin, Médéric Jeanne, Veranika Panasenkava, Anne‐Sophie Denommé‐Pichon, Boris Keren +43 more

Rare disease diagnosis using knowledge guided retrieval augmentation for ChatGPT

Journal of Biomedical Informatics(2024)10.1016/j.jbi.2024.104702
N/A
0DataRank · unranked
38 citations

Wendy K. Chung, Médéric Jeanne, Gongbo Zhang, Chunhua Weng, Charlotte Zelin