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Open Biology|September 22, 2020
Prader-Willi syndrome: reflections on seminal studies and future therapiesMichael S Chung, Maéva Langouët, Stormy J Chamberlain, et al.Human Mutation|August 20, 2013
Mutation in TTI2 reveals a role for triple T complex in human brain developmentMaéva Langouët, Abdelkrim Saadi, Guillaume Rieunier, et al.Human Molecular Genetics|December 12, 2017
Zinc finger protein 274 regulates imprinted expression of transcripts in Prader-Willi syndrome neuronsMaéva Langouët, Heather R Glatt-Deeley, Michael S Chung, et al.Molecular Genetics & Genomic Medicine|June 2, 2015
Contiguous mutation syndrome in the era of high-throughput sequencingMaéva Langouët, Karine Siquier-Pernet, Sylvia Sanquer, et al.Human Molecular Genetics|September 25, 2020
Specific ZNF274 binding interference at SNORD116 activates the maternal transcripts in Prader-Willi syndrome neuronsMaéva Langouët, Dea Gorka, Clarisse Orniacki, et al.Science Advances|September 7, 2022
Mutations in BCOR, a co-repressor of CRX/OTX2, are associated with early-onset retinal degenerationMaéva Langouët, Christine Jolicoeur, Awais Javed, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|November 12, 2025
CD33 epitope editing unlocks UM171-expanded cord blood grafts for AML immunotherapyBernhard Lehnertz, Maéva Langouët, Sophie Corneau, et al.Nature Neuroscience|November 17, 2015
Mutations in NONO lead to syndromic intellectual disability and inhibitory synaptic defectsDennis Mircsof, Maéva Langouët, Marlène Rio, et al.Pageof 1