Research Topics
Species | Marie GomotSummaryCountry: France Publications
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Detail Information
Publications
Cortical auditory processing and communication in children with autism: electrophysiological/behavioral relationsNicole Bruneau
Service Universitaire d Explorations Fonctionnelles, et de Neurophysiologie en Pédopsychiatrie, 2, Bd Tonnelle, 37 044, Tours, France
Int J Psychophysiol 51:17-25. 2003....- Left temporal impairment of auditory information processing in prematurely born 9-year-old children: an electrophysiological studyMarie Gomot
INSERM U619, Universite Francois Rabelais, CHRU de Tours, Service Universitaire d Explorations Fonctionnelles et Neurophysiologie en Pédopsychiatrie, Tours, France
Int J Psychophysiol 64:123-9. 2007.... - Hypersensitivity to acoustic change in children with autism: electrophysiological evidence of left frontal cortex dysfunctioningMarie Gomot
INSERM U316, Child Psychiatry Unit, CHU Bretonneau, Tours, France
Psychophysiology 39:577-84. 2002..The electrophysiological pattern reported here emphasized a left frontal cortex dysfunctioning that might also be implicated in cognitive and behavioral impairment characteristic, of this complex neurodevelopmental disorder... - TM4SF2 gene involvement reconsidered in an XLMR family after neuropsychological assessmentMarie Gomot
Service de Genetique, INSERM 4316 CHU Bretonneau, Tours, France
Am J Med Genet 112:400-4. 2002.... - MECP2 gene mutations in non-syndromic X-linked mental retardation: phenotype-genotype correlationMarie Gomot
Service de Genetique, CHU Bretomeau, INSERM U316, 2 boulevard Tonnelle, 37044 Tours Cedex, France
Am J Med Genet A 123:129-39. 2003..Regression of language skills was suspected in three patients. Phenotype-genotype correlation could thus be suspected and is discussed in these three families... 
Brain hyper-reactivity to auditory novel targets in children with high-functioning autismMarie Gomot
INSERM U930, Centre de Pédopsychiatrie, CHU Bretonneau, Tours Cedex 9, France
Brain 131:2479-88. 2008..This finding may shed light on the neurophysiological process underlying narrow interests and what clinically is called 'need for sameness'...- Change detection in children with autism: an auditory event-related fMRI studyMarie Gomot
Autism Research Centre, Department of Psychiatry, University of Cambridge, UK
Neuroimage 29:475-84. 2006..Abnormalities involved a cortical network known to have a role in attention switching and attentional resource distribution. These results throw light on the neurophysiological processes underlying autistic 'resistance to change'... - Electrophysiological correlates of automatic visual change detection in school-age childrenHelen Clery
UMR_S Imagerie et Cerveau, INSERM U930, Universite Francois Rabelais de Tours, CHRU de Tours, France
Neuropsychologia 50:979-87. 2012..The findings showed that the organization of the vMMN response is not mature in 11-year-old children and that a longer time is still necessary to process simple visual deviancy at this late stage of child development... 
X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin familyFrederic Laumonnier
INSERM U619 Génétique de l Autisme et de la Déficience Mentale, CHU Bretonneau, Tours, France
Am J Hum Genet 74:552-7. 2004....- Candidate electrophysiological endophenotypes of hyper-reactivity to change in autismMarie Gomot
UMRS Imagerie et Cerveau, INSERM U930, CNRS FRE 2448, Universite Francois Rabelais de Tours, CHRU, Tours, France
J Autism Dev Disord 41:705-14. 2011..The atypical neurophysiological mechanism of change perception identified might thus be associated with one of the hallmark behavioural manifestations of autism... - Topography of syllable change-detection electrophysiological indices in children and adults with reading disabilitiesCaroline Hommet
UMRS Imagerie et Cerveau, INSERM U930, CNRS FRE 2448, Universite Francois Rabelais de Tours, CHRU, Tours, France
Neuropsychologia 47:761-70. 2009..Developmental dyslexia (DD) is a frequent language-based learning disorder. The predominant etiological view postulates that reading problems originate from a phonological impairment... - Validation of the repetitive and restricted behaviour scale in autism spectrum disordersYannig Bourreau
UMRS Inserm U930, CNRS ERL3106, Universite Francois Rabelais de Tours, CHRU de Tours, Tours, France
Eur Child Adolesc Psychiatry 18:675-82. 2009..The RRB scale has good psychometric qualities and constitutes a real breakthrough towards a neurofunctional approach to autistic disorders. It should be valuable for research and treatment, and in clinical practice... - Could autism with mental retardation result from digenism and frequent de novo mutations?Claude Moraine
INSERM, U930, Tours, France
World J Biol Psychiatry 10:1030-6. 2009..Finally, we hypothesize that in those autistic subjects with mendelian MR, the XL-MR or AD-MR gene (G1) would pave the way for a second Mendelian factor (G2) responsible for autism symptoms... - My voice or yours? An electrophysiological studyJérôme Graux
UMR Inserm U930, CNRS ERL 3106, Universite Francois Rabelais de Tours, CHRU de Tours, Tours, France
Brain Topogr 26:72-82. 2013..This early response involved a left inferior frontal component, the activity of which lasted throughout the time course of the discriminative response, which included both MMN and P3a... - A challenging, unpredictable world for people with autism spectrum disorderMarie Gomot
UMR S Imaging and Brain, INSERM U930, Universite Francois Rabelais de Tours, France
Int J Psychophysiol 83:240-7. 2012.... - FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardationIlaria Meloni
Medical Genetics, Department of Molecular Biology, University of Siena, Italy
Nat Genet 30:436-40. 2002..FACL4 is the first gene shown to be involved in nonspecific mental retardation and fatty-acid metabolism... - Specific clinical and brain MRI features in mentally retarded patients with mutations in the Oligophrenin-1 geneVincent des Portes
Service de Pediatrie, HCL, Centre Hospitalier Lyon Sud, 69395 Pierre Bénite, France
Am J Med Genet A 124:364-71. 2004..In addition, OPHN-1 inactivation should be considered as a relevant model of developmental vermis disorganization, leading to a better understanding of the possible role of the cerebellum in MR... - ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardationThierry Bienvenu
Institut Cochin CHU Cochin Port Royal, 75014 Paris, France
Hum Mol Genet 11:981-91. 2002..The absence of detectable brain malformations in patients suggests that ARX may have an essential role, in mature neurons, required for the development of cognitive abilities...