Concepedia
Statistics
Publications
8
Citations
768
H-Index
Active since
2012
Affiliations
Inserm(Current)
Université Paris Cité
Hôpital Necker-Enfants Malades
Délégation Paris 5
Sorbonne Paris Cité
Maéva Langouët is an author at Inserm specializing in life sciences, genetics, and molecular genetics.
Publications per year
2012–2022
De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy
Giulia Barcia, Matthew R. Fleming, Aline Deligniere et al. · Nature Genetics · 2012 · 528 citations · Full text
Life Sciences, Genetics, Neuroscience +14
Mutations in NONO lead to syndromic intellectual disability and inhibitory synaptic defects
Dennis Mircsof, Maéva Langouët, Marlène Rio et al. · Nature Neuroscience · 2015 · 94 citations
Life Sciences, Genetics, Molecular Genetics +16
Zinc finger protein 274 regulates imprinted expression of transcripts in Prader-Willi syndrome neurons
Maéva Langouët, Heather R. Glatt-Deeley, Michael Chung et al. · Human Molecular Genetics · 2017 · 42 citations · Full text
Life Sciences, Genetics, Neuroscience +17
An In Vivo EGF Receptor Localization Screen in C. elegans Identifies the Ezrin Homolog ERM-1 as a Temporal Regulator of Signaling
Andrea Haag, Peter L. Gutiérrez, Alessandra Bühler et al. · PLoS Genetics · 2014 · 36 citations · Full text
Life Sciences, Cell Biology, Molecular Biology +15
Mutation in <i>TTI2</i> Reveals a Role for Triple T Complex in Human Brain Development
Maéva Langouët, Abdelkrim Saadi, Guillaume Rieunier et al. · Human Mutation · 2013 · 25 citations
Life Sciences, Genetics, Molecular Genetics +17
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