Fragile X syndrome and autism at the intersection of genetic and neural networks (Q36603922)

15 August 2017

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title

Fragile X syndrome and autism at the intersection of genetic and neural networks (English)

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15 August 2017

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15 August 2017

Matthew K Belmonte

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language of work or name

English

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publication date

1 October 2006

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1221-1225

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https://scigraph.springernature.com/pub.10.1038/nn1765

15 August 2017

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cites work

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Absence of expression of the FMR-1 gene in fragile X syndrome

21 January 2018

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Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation

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Autism: the point of view from fragile X studies

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An MRI study of the basal ganglia in autism.

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Striatal volume on magnetic resonance imaging and repetitive behaviors in autism.

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Neurodevelopmental effects of the FMR-1 full mutation in humans.

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Brain anatomy, gender and IQ in children and adolescents with fragile X syndrome

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Correlates across the structural, functional, and molecular phenotypes of fragile X syndrome

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The mGluR theory of fragile X mental retardation

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Enhanced and diminished visuo-spatial information processing in autism depends on stimulus complexity

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Differential impact of the FMR1 gene on visual processing in fragile X syndrome

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Abnormal global processing along the dorsal visual pathway in autism: a possible mechanism for weak visuospatial coherence?

21 January 2018

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Tuberous sclerosis: a GAP at the crossroads of multiple signaling pathways

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Aberrant regulation of ras proteins in malignant tumour cells from type 1 neurofibromatosis patients

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Mechanism for the learning deficits in a mouse model of neurofibromatosis type 1

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Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations

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Pten regulates neuronal arborization and social interaction in mice

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Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

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Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?

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Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

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X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

21 January 2018

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Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients

21 January 2018

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Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands

21 January 2018

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NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population

21 January 2018

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Analysis of four neuroligin genes as candidates for autism.

21 January 2018

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Absence of coding mutations in the X-linked genes neuroligin 3 and neuroligin 4 in individuals with autism from the IMGSAC collection

21 January 2018

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The Arg451Cys-neuroligin-3 mutation associated with autism reveals a defect in protein processing

21 January 2018

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Control of excitatory and inhibitory synapse formation by neuroligins

21 January 2018

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The fragile X mental retardation protein is required for type-I metabotropic glutamate receptor-dependent translation of PSD-95

21 January 2018

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Model of autism: increased ratio of excitation/inhibition in key neural systems

21 January 2018

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Autism and the serotonin transporter: the long and short of it

21 January 2018

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Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors

21 January 2018

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Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder

21 January 2018

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Searching for ways out of the autism maze: genetic, epigenetic and environmental clues

21 January 2018

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Obsessive-compulsive behaviors in parents of multiplex autism families.

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21 January 2018

Identifiers

DOI

10.1038/NN1765

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15 August 2017

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PubMed ID

17001341