Vincent Michaud

Centre de Coopération Internationale en Recherche Agronomique pour le Développement

Also affiliated with Université de Bordeaux, Inserm, Université de Montpellier, Centre Hospitalier Universitaire de Bordeaux, Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement, Animal, Santé, Territoires, Risques et Ecosystèmes, Bordeaux Population Health, Institute of Molecular Genetics, Maladies Rares: Génétique et Métabolisme

Biochemistry, Genetics and Molecular BiologyAgricultural and Biological Sciences

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 4 papers. Top paper: “BLOC1S5 pathogenic variants cause a new type of Hermansky–Pudlak syndrome”.

BLOC1S5 pathogenic variants cause a new type of Hermansky–Pudlak syndrome

Genetics in Medicine(2020)10.1038/s41436-020-0867-5

N/A

0.670DataRank · unranked

86 citations

Linh Le, Angèle Tingaud‐Sequeira, Mathieu Fiore, Anne Bauters, Nguyen Van Duong Béatrice +14 more

KCNT2‐Related Disorders: Phenotypes, Functional, and Pharmacological Properties

Annals of Neurology(2023)10.1002/ana.26662

N/A

0.464DataRank · unranked

21 citations

Ilaria Mosca, Paolo Ambrosino, Deborah Puzo, Allan Bayat, Saskia B. Wortmann +21 more

Monoallelic intragenic POU3F2 variants lead to neurodevelopmental delay and hyperphagic obesity, confirming the gene’s candidacy in 6q16.1 deletions

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.04.010

N/A

0.430DataRank · unranked

9 citations

Wenjun Jin, Christin Findeisen, Irene Valenzuela, Laura A. Devlin, Jill R. Murrell +35 more

De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability

Journal of Medical Genetics(2021)10.1136/jmedgenet-2021-107751

N/A

0DataRank · unranked

30 citations

Margot A. Cousin, Nikita R. Dsouza, Thomas D. Challman, Karen E. Wain, Zöe Powis +67 more