Richard Redon

Centre National de la Recherche Scientifique

Also affiliated with Inserm, ERN GUARD-Heart, Institut du Thorax, Nantes Université, Core Laboratories (United States)

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 9 papers. Top paper: “Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients”.

Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients

Science Advances(2020)10.1126/sciadv.abc9207

N/A

0.691DataRank · unranked

99 citations

Dong Li, Samuel G. Cox, Dylan M. Marchione, Evan F. Joiner, Khadija Wilson +95 more

Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2021.12.011

N/A

0.483DataRank · unranked

24 citations

Frédéric Ebstein, Alice Mollé, Thomas Besnard, Ming-Kang Lee, Virginie Vignard +53 more

Rare pathogenic variants in WNK3 cause X-linked intellectual disability

Genetics in Medicine(2022)10.1016/j.gim.2022.05.009

N/A

0.416DataRank · unranked

15 citations

Jinwei Zhang, Thomas Besnard, Alfonso Caro‐Llopis, Xue Zeng, Stephanie M. Robert +75 more

Benchmark of computational methods to detect digenism in sequencing data

European Journal of Human Genetics(2025)10.1038/s41431-025-01834-9

N/A

0.165DataRank · unranked

2 citations

Donald F. Conrad, Anaı̈s Baudot, Elisabeth Tournier‐Lasserve, Principal investigators, Emmanuelle Génin +30 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

Targeting the Microtubule EB1-CLASP2 Complex Modulates Na V 1.5 at Intercalated Discs

Circulation Research(2021)10.1161/circresaha.120.318643

N/A

0DataRank · unranked

38 citations

Mariam Jouni, David Y. Chiang, Marta Pérez-Hernández, Svitlana Podliesna, Nuo Yu +21 more

TAD boundary deletion causes PITX2-related cardiac electrical and structural defects

Nature Communications(2024)10.1038/s41467-024-47739-x

N/A

0DataRank · unranked

24 citations

Hiroshige Murata, Fernanda M. Bosada, Uirá Souto Melo, Takanori Aizawa, Pierre Lindenbaum +39 more

Isolated prolapse of the posterior mitral valve leaflet: phenotypic refinement, heritability and genetic etiology

medRxiv(2024)10.1101/2024.10.16.24315096

N/A

0DataRank · unranked

0 citations

Damien Duval, Daniel Trujillano, Florence Kyndt, Antoine Jobbé‐Duval, Pierre Lindenbaum +34 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