Molecular genetics and animal models in autistic disorder (Q34517515)

2 August 2017

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title

Molecular genetics and animal models in autistic disorder (English)

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2 August 2017

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Christian Andres

1

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2 August 2017

1 January 2002

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2 August 2017

Brain Research Bulletin

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2 August 2017

57

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2 August 2017

1

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2 August 2017

109-119

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Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons.

2 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Genetic studies of autistic disorder and chromosome 7

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Medial temporal lobe structures and autism: a review of clinical and experimental findings.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Brief report: medial temporal lobe and autism: a putative animal model in primates

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Genetic studies in autistic disorder and chromosome 15.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Screening for UBE3A gene mutations in a group of Angelman syndrome patients selected according to non-stringent clinical criteria.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Effects of early midline cerebellar lesion on cognitive and emotional functions in the rat.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

A look at linkage disequilibrium

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

A case-control family history study of autism

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Association of tuberous sclerosis of temporal lobes with autism and atypical autism

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Prader-Willi and Angelman syndromes: sister imprinted disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

An animal model of autism: behavioural studies in the GS guinea-pig.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Molecular genetic advances in tuberous sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Breakthroughs in molecular and cellular mechanisms underlying X-linked mental retardation

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Developmental defects of the ear, cranial nerves and hindbrain resulting from targeted disruption of the mouse homeobox gene Hox-1.6

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Genetic epidemiology of single-nucleotide polymorphisms.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Studies of the c-Harvey-Ras gene in psychiatric disorders.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Platelet serotonin studies in hyperserotonemic relatives of children with autistic disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

The serotonin system in autism

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Evidence of linkage between the serotonin transporter and autistic disorder.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Deficiency of the beta 3 subunit of the type A gamma-aminobutyric acid receptor causes cleft palate in mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Mildly impaired water maze performance in male Fmr1 knockout mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Increased frequency of the extended or ancestral haplotype B44-SC30-DR4 in autism.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Critical overview of current approaches to genetic mechanisms in schizophrenia research

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

GABA and epileptogenesis: comparing gabrb3 gene-deficient mice with Angelman syndrome in man.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Microdialysis administration of vasopressin into the septum improves social recognition in Brattleboro rats.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Autism: the point of view from fragile X studies

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Social amnesia in mice lacking the oxytocin gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Practice parameter: screening and diagnosis of autism: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Genetic influences and infantile autism

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Chromosome 7q: where autism meets language disorder?

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

The epidemiology of autism: a review.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Adenylosuccinate lyase (ADSL) and infantile autism: absence of previously reported point mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Chromosomal disorders and autism.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

A double-blind comparison of clomipramine, desipramine, and placebo in the treatment of autistic disorder.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Autism associated with the mitochondrial DNA G8363A transfer RNA(Lys) mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Oxytocin and autistic disorder: alterations in peptide forms

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Autism and the X chromosome. Multipoint sib-pair analysis.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Construction of a physical and transcript map flanking the imprinted MEST/PEG1 region at 7q32

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Possible association of c-Harvey-Ras-1 (HRAS-1) marker with autism.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Autism and genetics: clinical approach and association study with two markers of HRAS gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Serotonin and autism: biochemical and molecular biology features.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Scan statistics to scan markers for susceptibility genes

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Decreased binding of [11C]flumazenil in Angelman syndrome patients with GABA(A) receptor beta3 subunit deletions

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Discovery of allelic variants ofHOXA1 andHOXB1: Genetic susceptibility to autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Prenatal exposure of rats to valproic acid reproduces the cerebellar anomalies associated with autism

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Oxytocin, vasopressin, and autism: is there a connection?

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

A single base substitution in the coding region for neurophysin II associated with familial central diabetes insipidus

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Xeroderma pigmentosum group C splice mutation associated with autism and hypoglycinemia

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Mutation screening of human 5-HT(2B)receptor gene in early-onset obsessive-compulsive disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Transgenic rescue from embryonic lethality and renal carcinogenesis in the Eker rat model by introduction of a wild-type Tsc2 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Transgenic mouse model for the fragile X syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Autism: recent molecular genetic advances

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

The TSC1 tumour suppressor hamartin regulates cell adhesion through ERM proteins and the GTPase Rho

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Organization of the human serotonin transporter gene

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Genetically driven variation in serotonin uptake: is there a link to affective spectrum, neurodevelopmental, and neurodegenerative disorders?

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

A novel non-ataxic guinea pig strain with cerebrocortical and cerebellar abnormalities.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Social interaction and sensorimotor gating abnormalities in mice lacking Dvl1

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contig.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Identifying autism susceptibility genes

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Towards a molecular understanding of Prader-Willi and Angelman syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Increased density of the platelet serotonin transporter in autism.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Mutation analysis in adenylosuccinate lyase deficiency: eight novel mutations in the re-evaluated full ADSL coding sequence

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

A double-blind, placebo-controlled study of fluvoxamine in adults with autistic disorder.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

A serotonin transporter gene intron 2 polymorphic region, correlated with affective disorders, has allele-dependent differential enhancer-like properties in the mouse embryo

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

A tetranucleotide polymorphic microsatellite, located in the first intron of the tyrosine hydroxylase gene, acts as a transcription regulatory element in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Plasma oxytocin levels in autistic children.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Tests and estimates of allelic association in complex inheritance

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Molecular manipulations as tools for enhancing our understanding of 5-HT neurotransmission

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Animal model for fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Statistical approaches to gene mapping

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Molecular genetic studies of schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Enhanced cardiomyocyte DNA synthesis during myocardial hypertrophy in mice expressing a modified TSC2 transgene

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

(Over)correction of FMR1 deficiency with YAC transgenics: behavioral and physical features

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Adenosine deaminase alleles and autistic disorder: case-control and family-based association studies

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Association study with two markers of a human homeogene in infantile autism

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

X chromosome and infantile autism.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Developmental brain injury associated with abnormal play behavior in neonatally Borna disease virus-infected Lewis rats: a model of autism

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Autistic symptoms among children and young adults with isodicentric chromosome 15

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

A genomic screen of autism: evidence for a multilocus etiology

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Searching for genetic determinants in the new millennium

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Embryological origin for autism: developmental anomalies of the cranial nerve motor nuclei

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Linking etiologies in humans and animal models: studies of autism

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Exclusion of linkage to the HLA region in ninety multiplex sibships with autism.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Association analysis between a Cys23ser substitution polymorphism of the human 5-HT2c receptor gene and neuronal hyperexcitability

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Autism and maternally derived aberrations of chromosome 15q.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Molecular cloning of hSLP-1, a novel human brain-specific member of the band 7/MEC-2 family similar to Caenorhabditis elegans UNC-24.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Autism and tuberous sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

A mutation in adenylosuccinate lyase associated with mental retardation and autistic features

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Autism in thalidomide embryopathy: a population study.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

1 reference

7 January 2021

Genetics of autism: overview and new directions

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Eating disorder and epilepsy in mice lacking 5-HT2c serotonin receptors

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Genetic clues to the biological basis of autism

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Pharmacogenetics and the serotonin system: initial studies and future directions.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Adequacy of single-locus approximations for linkage analyses of oligogenic traits

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Increased frequency of the null allele at the complement C4b locus in autism.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Possible association of the extended MHC haplotype B44-SC30-DR4 with autism.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Strong association of the third hypervariable region of HLA-DR beta 1 with autism.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

The molecular genetics of autism

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Evidence supporting WNT2 as an autism susceptibility gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

Early amygdala damage in the rat as a model for neurodevelopmental psychopathological disorders.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

A mouse model for Prader-Willi syndrome imprinting-centre mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

5-HTTLPR variants not associated with autistic spectrum disorders.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2801%2900642-6

7 January 2021

10.1016/S0361-9230(01)00642-6

Identifiers

DOI

1 reference

2 August 2017

1 reference

PubMed ID

11827743