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Familial KCNQ2 mutation: a psychiatric perspective.
Iftimovici A, Charmet A, Desnous B, Ory A, Delorme R, Coutton C, Devillard F, Milh M, Maruani A. Iftimovici A, et al. Among authors: maruani a. Psychiatr Genet. 2024 Feb 1;34(1):24-27. doi: 10.1097/YPG.0000000000000360. Epub 2023 Dec 13. Psychiatr Genet. 2024. PMID: 38108335 Free PMC article.
Heterozygous FA2H mutations in autism spectrum disorders.
Scheid I, Maruani A, Huguet G, Leblond CS, Nygren G, Anckarsäter H, Beggiato A, Rastam M, Amsellem F, Gillberg IC, Elmaleh M, Leboyer M, Gillberg C, Betancur C, Coleman M, Hama H, Cook EH, Bourgeron T, Delorme R. Scheid I, et al. Among authors: maruani a. BMC Med Genet. 2013 Dec 3;14:124. doi: 10.1186/1471-2350-14-124. BMC Med Genet. 2013. PMID: 24299421 Free PMC article.
Postural Control and Emotion in Children with Autism Spectrum Disorders.
Gouleme N, Scheid I, Peyre H, Seassau M, Maruani A, Clarke J, Delorme R, Bucci MP. Gouleme N, et al. Among authors: maruani a. Transl Neurosci. 2017 Nov 15;8:158-166. doi: 10.1515/tnsci-2017-0022. eCollection 2017. Transl Neurosci. 2017. PMID: 29177103 Free PMC article.
Increased risk of ADHD in families with ASD.
Septier M, Peyre H, Amsellem F, Beggiato A, Maruani A, Poumeyreau M, Amestoy A, Scheid I, Gaman A, Bolognani F, Honey G, Bouquet C, Ly-Le Moal M, Bouvard M, Leboyer M, Bourgeron T, Delorme R. Septier M, et al. Among authors: maruani a. Eur Child Adolesc Psychiatry. 2019 Feb;28(2):281-288. doi: 10.1007/s00787-018-1206-0. Epub 2018 Sep 28. Eur Child Adolesc Psychiatry. 2019. PMID: 30267210
331 results