(Q33895132)

29 July 2017

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title

Genetic studies of autism: from the 1970s into the millennium (English)

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29 July 2017

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Rutter M

1

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29 July 2017

1 February 2000

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Journal of Abnormal Child Psychology

29 July 2017

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29 July 2017

28

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29 July 2017

3-14

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29 July 2017

1

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https://scigraph.springernature.com/pub.10.1023/a:1005113900068

29 July 2017

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cites work

Psychiatric family history and neurological disease in autistic spectrum disorders

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Obstetric complications in autism: consequences or causes of the condition?

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The TDT and other family-based tests for linkage disequilibrium and association

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Autism: beyond "theory of mind".

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Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism

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Social language use in parents of autistic individuals

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Integrating nature and nurture: implications of person-environment correlations and interactions for developmental psychopathology

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Gene chips and arrays revealed: a primer on their power and their uses

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Autism and tuberous sclerosis

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Personality characteristics of the parents of autistic individuals

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Basic concepts in the study of diseases with complex genetics

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A simple method for analyzing microsatellite allele image patterns generated from DNA pools and its application to allelic association studies

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Genomics and human disease--variations on variation

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Psychiatric genetics: research challenges and pathways forward

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Localisation of a gene implicated in a severe speech and language disorder

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Etiology of autism: genetic influences

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Autism: the phenotype in relatives.

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

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Infantile autism: a genetic study of 21 twin pairs

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Executive functions in young children with autism.

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A third source of developmental differences

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An advanced test of theory of mind: understanding of story characters' thoughts and feelings by able autistic, mentally handicapped, and normal children and adults.

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The genetics, if any, of infantile autism and childhood schizophrenia

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Executive function in parents of children with autism.

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

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

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Autism and known medical conditions: myth and substance

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A broader phenotype of autism: the clinical spectrum in twins

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Autism and maternally derived aberrations of chromosome 15q.

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12 December 2020

The incidence of cognitive disabilities in the siblings of autistic children.

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Autism or atypical autism in maternally but not paternally derived proximal 15q duplication

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Genetics, chance, and morphogenesis.

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Are there "autistic-like" features in congenitally blind children?

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Benefits and pitfalls encountered in psychiatric genetic association studies

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Prevalence of the fragile X anomaly amongst autistic twins and singletons.

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12 December 2020

Can standard measures identify subclinical markers of autism?

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12 December 2020

A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

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A family history study of neuropsychiatric disorders in the adult siblings of autistic individuals.

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Genetics and child psychiatry: II Empirical research findings

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Evidence by allelic association-dependent methods for a type 1 diabetes polygene (IDDM6) on chromosome 18q21.

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Follow-up report on autism in congenital rubella

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Autism, affective disorders, and social phobia

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Prenatal growth markers in schizophrenia: a monozygotic co-twin control study

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The future of genetic studies of complex human diseases

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Psychiatric Disorders in the Parents of Autistic Individuals

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Psychosocial adversity and child psychopathology

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Serotonin transporter (5-HTT) gene variants associated with autism?

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Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers

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Broader autism phenotype: evidence from a family history study of multiple-incidence autism families

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Single-gene influences on brain and behavior.

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Quantitative-trait locus for specific language and reading deficits on chromosome 6p

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Genetic influences and infantile autism

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Chromosome abnormalities in infantile autism and other childhood psychoses: a population study of 66 cases.

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Transmission of haplotypes of microsatellite markers rather than single marker alleles in the mapping of a putative type 1 diabetes susceptibility gene (IDDM6)

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A case-control family history study of autism

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12 December 2020

Population genetics--making sense out of sequence

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12 December 2020

Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium.

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12 December 2020

The Awkward Moments Test: a naturalistic measure of social understanding in autism.

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12 December 2020

Quasi-autistic patterns following severe early global privation. English and Romanian Adoptees (ERA) Study Team

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12 December 2020

An improved multipoint sib-pair analysis of quantitative traits

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12 December 2020

Autism diagnostic interview: a standardized investigator-based instrument.

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12 December 2020

Autism as a strongly genetic disorder: evidence from a British twin study

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12 December 2020

Spontaneous Narrative-Discourse Performance of Parents of Autistic Individuals

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12 December 2020

A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia

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12 December 2020

Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15

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12 December 2020

Gametic imprinting in mammals

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12 December 2020

Complete multipoint sib-pair analysis of qualitative and quantitative traits

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12 December 2020

A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium

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Transmission-disequilibrium tests for quantitative traits

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12 December 2020

The Emanuel Miller Memorial Lecture 1998. Autism: two-way interplay between research and clinical work.

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12 December 2020

Towards a cognitive phenotype for autism: increased prevalence of executive dysfunction and superior spatial span amongst siblings of children with autism

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12 December 2020

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

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12 December 2020

Molecular and cytogenetic investigations of the fragile X region including the Frax A and Frax E CGG trinucleotide repeat sequences in families multiplex for autism and related phenotypes.

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12 December 2020

Genetic animal models of alcohol and drug abuse

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12 December 2020

Association mapping of disease loci, by use of a pooled DNA genomic screen

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12 December 2020

Identifiers

DOI

10.1023/A:1005113900068

1 reference

PubMed ID

10772346

Dimensions Publication ID

29 July 2017

0 references

1 reference

PubMed ID

10772346