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[Autism, genetics and synaptic function alterations].
Perche O, Laumonnier F, Baala L, Ardourel MY, Menuet A, Robin V, Mortaud S, Montécot-Dubourg C, Richard O, Pichon J, Briault S. Perche O, et al. Pathol Biol (Paris). 2010 Oct;58(5):381-6. doi: 10.1016/j.patbio.2009.12.005. Epub 2010 Feb 23. Pathol Biol (Paris). 2010. PMID: 20181440 Review. French.
FG syndrome: the FGS2 locus revisited.
Perche O, Laudier B, Menuet A, Odent S, Laumonnier F, Briault S. Perche O, et al. Am J Med Genet A. 2012 Jun;158A(6):1489-92. doi: 10.1002/ajmg.a.35322. Epub 2012 Apr 23. Am J Med Genet A. 2012. PMID: 22528511 No abstract available.
Dysregulation of FOXG1 pathway in a 14q12 microdeletion case.
Perche O, Haddad G, Menuet A, Callier P, Marcos M, Briault S, Laudier B. Perche O, et al. Am J Med Genet A. 2013 Dec;161A(12):3072-7. doi: 10.1002/ajmg.a.36170. Epub 2013 Aug 16. Am J Med Genet A. 2013. PMID: 23956198
Visual sensorial impairments in neurodevelopmental disorders: evidence for a retinal phenotype in Fragile X Syndrome.
Rossignol R, Ranchon-Cole I, Pâris A, Herzine A, Perche A, Laurenceau D, Bertrand P, Cercy C, Pichon J, Mortaud S, Briault S, Menuet A, Perche O. Rossignol R, et al. Among authors: perche a, perche o. PLoS One. 2014 Aug 25;9(8):e105996. doi: 10.1371/journal.pone.0105996. eCollection 2014. PLoS One. 2014. PMID: 25153086 Free PMC article.
Pre- and postnatal exposure to low dose glufosinate ammonium induces autism-like phenotypes in mice.
Laugeray A, Herzine A, Perche O, Hébert B, Aguillon-Naury M, Richard O, Menuet A, Mazaud-Guittot S, Lesné L, Briault S, Jegou B, Pichon J, Montécot-Dubourg C, Mortaud S. Laugeray A, et al. Among authors: perche o. Front Behav Neurosci. 2014 Nov 20;8:390. doi: 10.3389/fnbeh.2014.00390. eCollection 2014. Front Behav Neurosci. 2014. PMID: 25477793 Free PMC article.
42 results