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

Frédéric Frénois

Université de Lille

ORCID: 0000-0002-1405-0629

Also affiliated with Centre Hospitalier Universitaire de Lille

MedicineBiochemistry, 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 3 papers. Top paper: “Missense variants affecting the actin-binding domains of PLS3 cause X-linked congenital diaphragmatic hernia and body wall defects”.

Missense variants affecting the actin-binding domains of PLS3 cause X-linked congenital diaphragmatic hernia and body wall defects

medRxiv(2021)10.1101/2021.07.07.21259278
N/A
0DataRank · unranked
2 citations

Mauro Longoni, Julie Wells, Richard S. Maser, Matthew J. Dysart, Hannah T. M. Contreras +33 more

PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.09.002
N/A
0DataRank · unranked
8 citations

Mauro Longoni, Julie Wells, Richard S. Maser, Eric L. Bogenschutz, Matthew J. Dysart +34 more

Functional characterization vs in silico prediction for TBX5 missense and splice variants in Holt-Oram syndrome

Genetics in Medicine(2024)10.1016/j.gim.2024.101267
N/A
0DataRank · unranked
1 citations

A.‐S. Jourdain, Frédéric Frénois, Emilie Ait‐Yahya, Mike Bamshad, Anne Dieux +10 more