The genetics of Autism Spectrum Disorders--a guide for clinicians (Q34034825)

30 July 2017

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title

The genetics of Autism Spectrum Disorders--a guide for clinicians (English)

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30 July 2017

autism spectrum disorder

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autism

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author name string

Karsten M Heil

series ordinal

1

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30 July 2017

Christian P Schaaf

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2

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30 July 2017

language of work or name

English

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publication date

1 January 2013

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Current Psychiatry Reports

30 July 2017

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30 July 2017

15

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30 July 2017

1

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30 July 2017

334

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https://scigraph.springernature.com/pub.10.1007/s11920-012-0334-3

30 July 2017

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Development and pilot evaluation of novel genetic educational materials designed for an underserved patient population

21 January 2018

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Identification of incestuous parental relationships by SNP-based DNA microarrays.

21 January 2018

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Ancient exaptation of a CORE-SINE retroposon into a highly conserved mammalian neuronal enhancer of the proopiomelanocortin gene

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Autism spectrum disorders--a genetics review

21 January 2018

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Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders

21 January 2018

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Strong association of de novo copy number mutations with autism

21 January 2018

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Structural variation of chromosomes in autism spectrum disorder

21 January 2018

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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

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Clinical genetic testing for patients with autism spectrum disorders

21 January 2018

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Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

21 January 2018

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Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

21 January 2018

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Autism: The importance of getting the dose right.

21 January 2018

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Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders

21 January 2018

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Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders

21 January 2018

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A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

21 January 2018

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Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders

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CNVs: harbingers of a rare variant revolution in psychiatric genetics

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Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses

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Functional impact of global rare copy number variation in autism spectrum disorders

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A synaptic trek to autism

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Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?

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High frequency of neurexin 1beta signal peptide structural variants in patients with autism

21 January 2018

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Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

21 January 2018

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Rare deletions at the neurexin 3 locus in autism spectrum disorder

21 January 2018

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

21 January 2018

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Analysis of four neuroligin genes as candidates for autism.

21 January 2018

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SHANK1 Deletions in Males with Autism Spectrum Disorder

21 January 2018

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Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation

21 January 2018

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Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

21 January 2018

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Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3

21 January 2018

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MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number

21 January 2018

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Reversal of neurological defects in a mouse model of Rett syndrome

21 January 2018

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Correction of fragile X syndrome in mice.

21 January 2018

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Identifying disease mutations in genomic medicine settings: current challenges and how to accelerate progress

21 January 2018

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Exome and whole-genome sequencing for gene discovery: the future is now!

21 January 2018

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Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

21 January 2018

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Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

21 January 2018

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Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions.

21 January 2018

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3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome

21 January 2018

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Duplication of GTF2I results in separation anxiety in mice and humans

21 January 2018

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Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

21 January 2018

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12 December 2020

Whole-genome and whole-exome sequencing in neurological diseases.

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12 December 2020

Family history of schizophrenia and bipolar disorder as risk factors for autism

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Traditional banding of chromosomes for cytogenetic analysis

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10.1007/S11920-012-0334-3

Identifiers

DOI

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Dimensions Publication ID

30 July 2017

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