Marie Gomot

Summary

Country: France

Publications

  1. ncbi request reprint Cortical auditory processing and communication in children with autism: electrophysiological/behavioral relations
    Nicole 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
  2. ncbi request reprint Left temporal impairment of auditory information processing in prematurely born 9-year-old children: an electrophysiological study
    Marie 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
  3. doi request reprint Brain hyper-reactivity to auditory novel targets in children with high-functioning autism
    Marie Gomot
    INSERM U930, Centre de Pédopsychiatrie, CHU Bretonneau, Tours Cedex 9, France
    Brain 131:2479-88. 2008
  4. ncbi request reprint Hypersensitivity to acoustic change in children with autism: electrophysiological evidence of left frontal cortex dysfunctioning
    Marie Gomot
    INSERM U316, Child Psychiatry Unit, CHU Bretonneau, Tours, France
    Psychophysiology 39:577-84. 2002
  5. ncbi request reprint TM4SF2 gene involvement reconsidered in an XLMR family after neuropsychological assessment
    Marie Gomot
    Service de Genetique, INSERM 4316 CHU Bretonneau, Tours, France
    Am J Med Genet 112:400-4. 2002
  6. ncbi request reprint MECP2 gene mutations in non-syndromic X-linked mental retardation: phenotype-genotype correlation
    Marie Gomot
    Service de Genetique, CHU Bretomeau, INSERM U316, 2 boulevard Tonnelle, 37044 Tours Cedex, France
    Am J Med Genet A 123:129-39. 2003
  7. ncbi request reprint Change detection in children with autism: an auditory event-related fMRI study
    Marie Gomot
    Autism Research Centre, Department of Psychiatry, University of Cambridge, UK
    Neuroimage 29:475-84. 2006
  8. doi request reprint Electrophysiological correlates of automatic visual change detection in school-age children
    Helen Clery
    UMR_S Imagerie et Cerveau, INSERM U930, Universite Francois Rabelais de Tours, CHRU de Tours, France
    Neuropsychologia 50:979-87. 2012
  9. pmc X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family
    Frederic Laumonnier
    INSERM U619 Génétique de l Autisme et de la Déficience Mentale, CHU Bretonneau, Tours, France
    Am J Hum Genet 74:552-7. 2004
  10. doi request reprint Candidate electrophysiological endophenotypes of hyper-reactivity to change in autism
    Marie 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

Collaborators

Detail Information

Publications19

  1. ncbi request reprint Cortical auditory processing and communication in children with autism: electrophysiological/behavioral relations
    Nicole 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
    ....
  2. ncbi request reprint Left temporal impairment of auditory information processing in prematurely born 9-year-old children: an electrophysiological study
    Marie 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
    ....
  3. doi request reprint Brain hyper-reactivity to auditory novel targets in children with high-functioning autism
    Marie 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'...
  4. ncbi request reprint Hypersensitivity to acoustic change in children with autism: electrophysiological evidence of left frontal cortex dysfunctioning
    Marie 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...
  5. ncbi request reprint TM4SF2 gene involvement reconsidered in an XLMR family after neuropsychological assessment
    Marie Gomot
    Service de Genetique, INSERM 4316 CHU Bretonneau, Tours, France
    Am J Med Genet 112:400-4. 2002
    ....
  6. ncbi request reprint MECP2 gene mutations in non-syndromic X-linked mental retardation: phenotype-genotype correlation
    Marie 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...
  7. ncbi request reprint Change detection in children with autism: an auditory event-related fMRI study
    Marie 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'...
  8. doi request reprint Electrophysiological correlates of automatic visual change detection in school-age children
    Helen 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...
  9. pmc X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family
    Frederic Laumonnier
    INSERM U619 Génétique de l Autisme et de la Déficience Mentale, CHU Bretonneau, Tours, France
    Am J Hum Genet 74:552-7. 2004
    ....
  10. doi request reprint Candidate electrophysiological endophenotypes of hyper-reactivity to change in autism
    Marie 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...
  11. doi request reprint My voice or yours? An electrophysiological study
    Jérôme 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...
  12. doi request reprint Topography of syllable change-detection electrophysiological indices in children and adults with reading disabilities
    Caroline 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...
  13. doi request reprint Atypical visual change processing in children with autism: an electrophysiological study
    Helen Clery
    UMR 930 Imagerie et Cerveau, INSERM, Universite Francois Rabelais de Tours, CHRU de Tours, France
    Psychophysiology 50:240-52. 2013
    ..This study is thus consistent with the hypothesis of the existence of "general" atypical change detection processing in children with ASD that might contribute to their intolerance of change...
  14. doi request reprint 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...
  15. doi request reprint Validation of the repetitive and restricted behaviour scale in autism spectrum disorders
    Yannig 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...
  16. doi request reprint A challenging, unpredictable world for people with autism spectrum disorder
    Marie Gomot
    UMR S Imaging and Brain, INSERM U930, Universite Francois Rabelais de Tours, France
    Int J Psychophysiol 83:240-7. 2012
    ....
  17. ncbi request reprint FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation
    Ilaria 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...
  18. ncbi request reprint Specific clinical and brain MRI features in mentally retarded patients with mutations in the Oligophrenin-1 gene
    Vincent 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...
  19. ncbi request reprint ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation
    Thierry 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...