(Q37847947)

24 August 2017

1 reference

title

Autism spectrum disorders--a genetics review (English)

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24 August 2017

main subject

autism spectrum disorder

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autism

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author name string

Judith H Miles

series ordinal

1

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24 August 2017

language of work or name

English

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publication date

1 April 2011

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24 August 2017

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24 August 2017

volume

13

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24 August 2017

issue

4

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24 August 2017

page(s)

278-294

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Autism. The search for susceptibility genes.

24 August 2017

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Pervasive developmental disorders in Montreal, Quebec, Canada: prevalence and links with immunizations

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Vaccines and the changing epidemiology of autism

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Time trends in reported diagnoses of childhood neuropsychiatric disorders: a Danish cohort study.

21 January 2018

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The rise in autism and the role of age at diagnosis

21 January 2018

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Regression in Autistic Spectrum Disorders

21 January 2018

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Regression and word loss in autistic spectrum disorders.

21 January 2018

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Autism in Infancy and Early Childhood

21 January 2018

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Validation of the phenomenon of autistic regression using home videotapes.

21 January 2018

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Trajectory of development in adolescents and adults with autism

21 January 2018

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Adult outcome for children with autism

21 January 2018

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Autism and developmental receptive language disorder--a follow-up comparison in early adult life. II: Social, behavioural, and psychiatric outcomes.

21 January 2018

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Twenty-year outcome for individuals with autism and average or near-average cognitive abilities.

21 January 2018

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The long-term course of autistic disorders: update on follow-up studies

21 January 2018

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Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

21 January 2018

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Autism diagnostic observation schedule: a standardized observation of communicative and social behavior

21 January 2018

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Three Diagnostic Approaches to Asperger Syndrome: Implications for Research

21 January 2018

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A screening questionnaire for Asperger syndrome and other high-functioning autism spectrum disorders in school age children.

21 January 2018

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The Asperger Syndrome (and high-functioning autism) Diagnostic Interview (ASDI): a preliminary study of a new structured clinical interview.

21 January 2018

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The CAST (Childhood Asperger Syndrome Test): preliminary development of a UK screen for mainstream primary-school-age children

21 January 2018

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Personality traits of the relatives of autistic probands.

21 January 2018

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The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions

21 January 2018

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The Modified Checklist for Autism in Toddlers: an initial study investigating the early detection of autism and pervasive developmental disorders.

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Identification and Evaluation of Children With Autism Spectrum Disorders

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Intensive behavioral treatment at school for 4- to 7-year-old children with autism. A 1-year comparison controlled study

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Evidence-based comprehensive treatments for early autism

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Absence of seizures despite high prevalence of epileptiform EEG abnormalities in children with autism monitored in a tertiary care center.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

The Role of Epilepsy and Epileptiform EEGs in Autism Spectrum Disorders

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autism and epilepsy: a retrospective follow-up study

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

An examination of movement kinematics in young people with high-functioning autism and Asperger's disorder: further evidence for a motor planning deficit

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Evaluation, Diagnosis, and Treatment of Gastrointestinal Disorders in Individuals With ASDs: A Consensus Report

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Catatonia in autism: implications across the life span

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

The genetic basis of complex traits: rare variants or "common gene, common disease"?

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Common genetic variants on 5p14.1 associate with autism spectrum disorders

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

A genome-wide association study of autism reveals a common novel risk locus at 5p14.1

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

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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https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Structural variation of chromosomes in autism spectrum disorder

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Multiple forms of atypical rearrangements generating supernumerary derivative chromosome 15

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Relationship between clinical and genetic features in "inverted duplicated chromosome 15" patients

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autism and 15q11-q13 disorders: behavioral, genetic, and pathophysiological issues

21 January 2018

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https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Comorbidity of autistic spectrum disorders in children with Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Imprinting, the X-chromosome, and the male brain: explaining sex differences in the liability to autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Strong association of de novo copy number mutations with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Recurrent 16p11.2 microdeletions in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Association between microdeletion and microduplication at 16p11.2 and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Clinical genetic testing for patients with autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

A 15q13.3 microdeletion segregating with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

The role of copy number variation in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Phenotypic variability and genetic susceptibility to genomic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

De novo rates and selection of large copy number variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Microduplications of 16p11.2 are associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplications

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autistic spectrum disorder and the fragile X premutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

The emerging fragile X premutation phenotype: evidence from the domain of social cognition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Molecular and cognitive predictors of the continuum of autistic behaviours in fragile X

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

An fMRI study of the prefrontal activity during the performance of a working memory task in premutation carriers of the fragile X mental retardation 1 gene with and without fragile X-associated tremor/ataxia syndrome (FXTAS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autism profiles of males with fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Long CGG-repeat tracts are toxic to human cells: implications for carriers of Fragile X premutation alleles

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

The spectrum and evolution of phenotypic findings in PTEN mutation positive cases of Bannayan-Riley-Ruvalcaba syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

De novo germline PTEN mutation in a man with Lhermitte-Duclos disease which arose on the paternal chromosome and was transmitted to his child with polydactyly and Wormian bones

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

The prevalence of PTEN mutations in a clinical pediatric cohort with autism spectrum disorders, developmental delay, and macrocephaly.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Haploinsufficiency for Pten and Serotonin transporter cooperatively influences brain size and social behavior

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

21 January 2018

The genetics of autism

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Association between the neurofibromatosis-1 (NF1) locus and autism in the Japanese population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

MeCP2 dysfunction in Rett syndrome and related disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

The diagnosis of autism in a female: could it be Rett syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

The methyl-CpG-binding protein MeCP2 and neurological disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autism and tuberous sclerosis complex: prevalence and clinical features

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

The psychopathologies of children and adolescents with tuberous sclerosis complex (TSC): a postal survey of UK families

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Neuroepileptic correlates of autistic symptomatology in tuberous sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Characterization of autism in young children with tuberous sclerosis complex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

CACNA1H mutations in autism spectrum disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Association of common variants in the Joubert syndrome gene (AHI1) with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autism and autistic behavior in Joubert syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Advances in autism research.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: no association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Mitochondrial dysfunction in autism spectrum disorders: a population-based study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Mitochondrial disease in autism spectrum disorder patients: a cohort analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Mitochondrial DNA abnormalities and autistic spectrum disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Nuclear and mitochondrial genome defects in autisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autism and mitochondrial disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autism and phenylketonuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Inborn errors of the purine nucleotide cycle: adenylosuccinase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autism and adenylosuccinase deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Screening of male patients with autism spectrum disorder for creatine transporter deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Behavior phenotype in the RSH/Smith-Lemli-Opitz syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Abnormalities of cholesterol metabolism in autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autism and Metabolic Diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Behavioural characteristics and autistic features in individuals with Cohen Syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Cole-Hughes macrocephaly syndrome and associated autistic manifestations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Behavioural phenotype of Cornelia de Lange syndrome: case-control study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Microarray based comparative genomic hybridization testing in deletion bearing patients with Angelman syndrome: genotype-phenotype correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Evaluation of autism traits in Angelman syndrome: a resource to unfold autism genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Socio-communicative deficits in young children with Williams syndrome: performance on the Autism Diagnostic Observation Schedule.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Association of Duchenne muscular dystrophy with autism spectrum disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autistic spectrum disorders in Möbius sequence: a comprehensive study of 25 individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Mobius sequence--a Swedish multidiscipline study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autism spectrum disorders in children and adolescents with Moebius sequence.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Linking autism, regression and Landau-Kleffner syndrome: integrative role of nerve growth factor.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autism spectrum disorders following in utero exposure to antiepileptic drugs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Matched follow-up study of 5 8-year-old ICSI singletons: child behaviour, parenting stress and child (health-related) quality of life.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

beta2-adrenergic receptor activation and genetic polymorphisms in autism: data from dizygotic twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

MMR vaccine and autism: an update of the scientific evidence

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Continuing increases in autism reported to California's developmental services system: mercury in retrograde

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

RETRACTED: Ileal-lymphoid-nodular hyperplasia, non-specific colitis, and pervasive developmental disorder in children

21 January 2018

2 references

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

21 January 2018

Methodology data of "A qualitative and quantitative citation analysis toward retracted articles: a case of study"

MMR vaccination and autism

3 August 2024

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

A statement by Dr Simon Murch. Allegations concerning our 1998 study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Measles outbreaks in a population with declining vaccine uptake.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Genetics of autistic disorders: review and clinical implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Genetics. Insights into the pathogenesis of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autism genetics: strategies, challenges, and opportunities

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Identifying autism loci and genes by tracing recent shared ancestry

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

The genetics of autism spectrum disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Recent advances in the genetics of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Neuroligins and neurexins link synaptic function to cognitive disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Contribution of SHANK3 mutations to autism spectrum disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Pervasive Developmental Disorders in Preschool Children

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Variable expression of the autism broader phenotype: findings from extended pedigrees.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autistic traits in the general population: a twin study

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Endophenotype approach to developmental psychopathology: implications for autism research

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autism spectrum disorders: developmental disconnection syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autism: highly heritable but not inherited

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Paternal age increases the risk for autism in an Iranian population sample

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Risk factors for autism: perinatal factors, parental psychiatric history, and socioeconomic status

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

A unified genetic theory for sporadic and inherited autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Genetic structure of reciprocal social behavior

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autism, affective and other psychiatric disorders: patterns of familial aggregation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Autism families with a high incidence of alcoholism

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

A family study of autism: cognitive patterns and levels in parents and siblings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Childhood autism: an investigation of aetiological factors in twenty-five cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Correlation of family history with specific autistic subgroups: Asperger's syndrome and bipolar affective disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

A case-control family history study of autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Effects of familial risk factors and place of birth on the risk of autism: a nationwide register-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Diagnosis of autism spectrum disorders in the first 3 years of life

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

Parents' perceptions of autism spectrum disorder etiology and recurrence risk and effects of their perceptions on family planning: Recommendations for genetic counselors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181FF67BA

10.1097/GIM.0B013E3181FF67BA

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

24 August 2017

1053227650

0 references

1 reference