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The role of candidate genes in unraveling the genetics of autism
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title
The role of candidate genes in unraveling the genetics of autism
(English)
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author name string
Christopher J. Stodgell
series ordinal
1
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Jennifer L. Ingram
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2
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Susan L. Hyman
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3
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publication date
2000
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published in
International Review of Research in Mental Retardation
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page(s)
57-81
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cites work
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A case-control family history study of autism
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No association of a tyrosine hydroxylase gene tetranucleotide repeat polymorphism in autism, Tourette syndrome, or ADHD.
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Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers
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Increased frequency of the extended or ancestral haplotype B44-SC30-DR4 in autism.
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Expression patterns of the homeo box-containing genes En-1 and En-2 and the proto-oncogene int-1 diverge during mouse development.
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Expression of the homeo box-containing gene En-2 delineates a specific region of the developing mouse brain
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Effects of fluoxetine treatment in young children with idiopathic autism.
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Bipolar affective disorders linked to DNA markers on chromosome 11
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Fluoxetine in treatment of adolescent patients with autism: a longitudinal open trial
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Autism: the point of view from fragile X studies
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Genes for Prader Willi syndrome/Angelman syndrome and fragile X syndrome are homologous, with genetic imprinting and unstable trinucleotide repeats causing mental retardation, autism and aggression.
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Localisation of a gene implicated in a severe speech and language disorder
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Finding specific genes that cause autism: a combination of approaches will be needed to maximize power.
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EVIDENCE THAT THE GENE FOR TUBEROUS SCLEROSIS IS ON CHROMOSOME 9
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Urinary homovanillic acid levels of autistic children.
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Autism and pervasive developmental disorders
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Chromosomal disorders and autism.
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Autistic behaviour in Moebius syndrome
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Regionalized organizing activity of the neural tube revealed by the regulation of lmx1 in the otic vesicle.
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Investigation of whole blood and urine monoamines in autism
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Autism and genetics: clinical approach and association study with two markers of HRAS gene.
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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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Prospects for gene therapy in cystic fibrosis
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Subtle Cerebellar Phenotype in Mice Homozygous for a Targeted Deletion of the En-2 Homeobox
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Molecular therapy for genetic muscle diseases--status 1999.
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Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish
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Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients.
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Serotonin transporter (5-HTT) gene variants associated with autism?
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7 January 2021
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Genes involved in hereditary ataxias.
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7 January 2021
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Genetic dissection of complex traits
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Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results
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A broader phenotype of autism: the clinical spectrum in twins
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Autism diagnostic observation schedule: a standardized observation of communicative and social behavior
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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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Molecular genetic investigations of autism.
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Trinucleotide repeat expansion and neuropsychiatric disease
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cDNA cloning of a human homologue of the Caenorhabditis elegans cell fate-determining gene mab-21: expression, chromosomal localization and analysis of a highly polymorphic (CAG)n trinucleotide repeat
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Monoamines (serotonin and catecholamines) and their derivatives in infantile autism: age-related changes and drug effects
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A double-blind, placebo-controlled study of risperidone in adults with autistic disorder and other pervasive developmental disorders
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Homeobox genes and axial patterning
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Autism in fetal alcohol syndrome: a report of six cases.
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Association study with two markers of a human homeogene in infantile autism
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The D4 dopamine receptor gene maps on 11p proximal to HRAS
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Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study
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Psychiatric Disorders in the Parents of Autistic Individuals
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7 January 2021
based on heuristic
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Int-2 influences the development of the nodose ganglion
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Lower Purkinje cell counts in the cerebella of four autistic subjects: initial findings of the UCLA-NSAC Autopsy Research Report.
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Embryological origin for autism: developmental anomalies of the cranial nerve motor nuclei
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Genes with triplet repeats: candidate mediators of neuropsychiatric disorders
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7 January 2021
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Regulation of a Purkinje cell-specific promoter by homeodomain proteins: repression by engrailed-2 vs. synergistic activation by Hoxa5 and Hoxb7.
1 reference
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7 January 2021
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Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity
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7 January 2021
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Genetic counseling in autism and pervasive developmental disorders.
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7 January 2021
based on heuristic
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Hyperserotoninemia and serotonin receptor antibodies in children with autism but not mental retardation.
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7 January 2021
based on heuristic
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Autism and tuberous sclerosis
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7 January 2021
based on heuristic
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Autism and genetics. A decade of research
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7 January 2021
based on heuristic
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Autism and tuberous sclerosis
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3
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7 January 2021
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Possible prevention of neural-tube defects by periconceptional vitamin supplementation
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Cross-sensitization between footshock stress and apomorphine on self-injurious behavior and neostriatal catecholamines in a rat model of Lesch-Nyhan syndrome.
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Autism in thalidomide embryopathy: a population study.
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Genetics of autism: overview and new directions
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7 January 2021
based on heuristic
inferred from DOI database lookup
Incidence of minor physical anomaly in autism
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7 January 2021
based on heuristic
inferred from DOI database lookup
Possible association of the extended MHC haplotype B44-SC30-DR4 with autism.
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
A male with fetal valproate syndrome and autism.
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7 January 2021
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Social language use in parents of autistic individuals
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based on heuristic
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10.1016/S0074-7750(00)80006-3
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