The molecular genetics of autism (Q34108364)

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Language	Label	Description	Also known as
English	The molecular genetics of autism	scientific article

Statements

instance of

scholarly article

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stated in

Europe PubMed Central

PubMed publication ID

11122951

retrieved

31 July 2017

review article

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stated in

Europe PubMed Central

title

The molecular genetics of autism (English)

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stated in

Europe PubMed Central

PubMed publication ID

11122951

retrieved

31 July 2017

main subject

autism

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author name string

Wassink TH

series ordinal

1

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stated in

Europe PubMed Central

PubMed publication ID

11122951

retrieved

31 July 2017

Piven J

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11122951

retrieved

31 July 2017

language of work or name

English

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publication date

1 April 2000

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Europe PubMed Central

PubMed publication ID

11122951

retrieved

31 July 2017

published in

Current Psychiatry Reports

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stated in

Europe PubMed Central

PubMed publication ID

11122951

retrieved

31 July 2017

volume

2

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stated in

Europe PubMed Central

PubMed publication ID

11122951

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31 July 2017

issue

2

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stated in

Europe PubMed Central

PubMed publication ID

11122951

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31 July 2017

page(s)

170-175

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stated in

Europe PubMed Central

PubMed publication ID

11122951

retrieved

31 July 2017

cites work

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

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New developments in the neurobiology of the tuberous sclerosis complex

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The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities

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12 December 2020

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Female with autistic disorder and monosomy X (Turner syndrome): parent-of-origin effect of the X chromosome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

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Inherited Interstitial Duplications of Proximal 15q: Genotype-Phenotype Correlations

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

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The epidemiology of autism: a review.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

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Infantile autism and associated autosomal chromosome abnormalities: a register-based study and a literature survey

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

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Cognitive Deficits in Parents from Multiple‐incidence Autism Families

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PubMed

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12 December 2020

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Comprehensive mutation analysis of TSC1 and TSC2-and phenotypic correlations in 150 families with tuberous sclerosis.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

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Autism and tuberous sclerosis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Personality and language characteristics in parents from multiple-incidence autism families

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

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Physical mapping of the serotonin 5-HT(7) receptor gene (HTR7) to chromosome 10 and pseudogene (HTR7P) to chromosome 12, and testing of linkage disequilibrium between HTR7 and autistic disorder

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

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Genetics of autism: overview and new directions

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

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Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

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An MRI study of the basal ganglia in autism

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

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Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

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Mutation screening of the UBE3A/E6-AP gene in autistic disorder

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

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Heterogeneity and the genetics of autism

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic studies of autistic disorder and chromosome 7

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

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inferred from PubMed ID database lookup

Infantile autism: a genetic study of 21 twin pairs

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

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Masquerading repeats: paralogous pitfalls of the human genome

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

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Executive function in parents of children with autism.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

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Autism and tuberous sclerosis complex: prevalence and clinical features

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

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Chromosomes in autism and related pervasive developmental disorders: a cytogenetic study

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An autosomal genomic screen for autism. Collaborative linkage study of autism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Xp deletions associated with autism in three females

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal disorders and autism

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A case-control family history study of autism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biology of the fragile X mental retardation protein, an RNA-binding protein

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genomic screen of autism: evidence for a multilocus etiology

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal abnormalities in a series of children with autistic disorder

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of the cytosolic tuberin-hamartin complex. Tuberin is a cytosolic chaperone for hamartin

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association study of the NF1 gene and autistic disorder

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autism: not an extremely rare disorder

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A large polymorphic repeat in the pericentromeric region of human chromosome 15q contains three partial gene duplications

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic studies in autistic disorder and chromosome 15.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11122951

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S11920-000-0063-X

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11122951

retrieved

31 July 2017

Dimensions Publication ID

1026889400

0 references

PubMed publication ID

11122951

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11122951

retrieved

31 July 2017

 

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