Concepedia

Camille Maillard

CM

9

Publications

300

Citations

9

H-Index

2016

Active since

Affiliations

Inserm(Current)

Institut des Maladies Génétiques Imagine

Sorbonne Paris Cité

Université Paris Cité

Délégation Paris 5

Camille Maillard is an author at Inserm specializing in medicine, genetics, and neurogenetics.

Top concepts

Publications per year

2016–2021

9

Publications

9

Delineating <i>FOXG1</i> syndrome

Nancy Végas, Mara Cavallin, Camille Maillard et al. · Neurology Genetics · 2018 · 75 citations · Full text

WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells

Mara Cavallin, Maria A. Rujano, Nathalie Bednarek et al. · Brain · 2017 · 58 citations · Full text

, , +24

Mutations in the Heterotopia Gene Eml1/EML1 Severely Disrupt the Formation of Primary Cilia

Ana Uzquiano, Carmen Cifuentes-Díaz, Ammar Jabali et al. · Cell Reports · 2019 · 46 citations · Full text

Recurrent KIF2A mutations are responsible for classic lissencephaly

Mara Cavallin, Emilia K. Bijlsma, Adrienne El Morjani et al. · Neurogenetics · 2016 · 27 citations

, , +5

Neuropathological Hallmarks of Brain Malformations in Extreme Phenotypes Related to DYNC1H1 Mutations

Annie Laquerrière, Camille Maillard, Mara Cavallin et al. · Journal of Neuropathology & Experimental Neurology · 2017 · 26 citations · Full text

, , +20

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