Cyril Goizet

Centre National de la Recherche Scientifique

ORCID: 0000-0002-1913-889X

Also affiliated with Université de Bordeaux, École Pratique des Hautes Études, Centre Hospitalier Universitaire de Bordeaux, Hôpital Pellegrin, Génétique Médicale & Génomique Fonctionelle

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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 3 papers. Top paper: “Heterozygous Variants in KDM4B Lead to Global Developmental Delay and Neuroanatomical Defects”.

Heterozygous Variants in KDM4B Lead to Global Developmental Delay and Neuroanatomical Defects

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.11.001

N/A

0DataRank · unranked

30 citations

Antonio Vitobello, Stephan C. Collins, Valerie E. Vancollie, Christopher J. Lelliott, Lance H. Rodan +25 more

CAG repeat mosaicism is gene specific in spinocerebellar ataxias

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.03.015

N/A

0DataRank · unranked

26 citations

François‐Xavier Lejeune, Isabelle David, Susana Boluda, Giulia Coarelli, Sabrina Leclère-Turbant +14 more

From spastic paraplegia to infantile neurodegenerative disorder: Expanding the phenotypic spectrum associated with biallelic SPAST variants

European Journal of Neurology(2024)10.1111/ene.70025

N/A

0DataRank · unranked

6 citations

Chloé Angelini, Claire Bar, Wahiba Amer El Khedoud, Christine Barnérias, Razika Boulariah‐Hadjou +15 more