The role of candidate genes in unraveling the genetics of autism (Q61853386)

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

A clinicopathological study of autism.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

A case-control family history study of autism

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Duplication of the 15q11-13 region in a patient with autism, epilepsy and ataxia.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Genetic anticipation. Expanding tandem repeats.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

No association of a tyrosine hydroxylase gene tetranucleotide repeat polymorphism in autism, Tourette syndrome, or ADHD.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

1 reference

7 January 2021

Evidence of linkage between the serotonin transporter and autistic disorder.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

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%2FS0074-7750%2800%2980006-3

7 January 2021

Expression patterns of the homeo box-containing genes En-1 and En-2 and the proto-oncogene int-1 diverge during mouse development.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Expression of the homeo box-containing gene En-2 delineates a specific region of the developing mouse brain

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Effects of fluoxetine treatment in young children with idiopathic autism.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Bipolar affective disorders linked to DNA markers on chromosome 11

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Autism is not associated with the fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Low medial prefrontal dopaminergic activity in autistic children.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Fluoxetine in treatment of adolescent patients with autism: a longitudinal open trial

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Autism: the point of view from fragile X studies

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

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.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Finding specific genes that cause autism: a combination of approaches will be needed to maximize power.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

EVIDENCE THAT THE GENE FOR TUBEROUS SCLEROSIS IS ON CHROMOSOME 9

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Urinary homovanillic acid levels of autistic children.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Autism and pervasive developmental disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Chromosomal disorders and autism.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Autistic behaviour in Moebius syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Regionalized organizing activity of the neural tube revealed by the regulation of lmx1 in the otic vesicle.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Investigation of whole blood and urine monoamines in autism

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

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%2FS0074-7750%2800%2980006-3

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%2FS0074-7750%2800%2980006-3

7 January 2021

Prospects for gene therapy in cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Subtle Cerebellar Phenotype in Mice Homozygous for a Targeted Deletion of the En-2 Homeobox

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Molecular therapy for genetic muscle diseases--status 1999.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Genes involved in hereditary ataxias.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Genetic dissection of complex traits

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

A broader phenotype of autism: the clinical spectrum in twins

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

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%2FS0074-7750%2800%2980006-3

7 January 2021

Molecular genetic investigations of autism.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Trinucleotide repeat expansion and neuropsychiatric disease

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Monoamines (serotonin and catecholamines) and their derivatives in infantile autism: age-related changes and drug effects

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

A double-blind, placebo-controlled study of risperidone in adults with autistic disorder and other pervasive developmental disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Homeobox genes and axial patterning

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Evidence of linkage of the inflammatory bowel disease susceptibility locus on chromosome 16 (IBD1) to ulcerative colitis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Autism in fetal alcohol syndrome: a report of six cases.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

The D4 dopamine receptor gene maps on 11p proximal to HRAS

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

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%2FS0074-7750%2800%2980006-3

7 January 2021

Psychiatric Disorders in the Parents of Autistic Individuals

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Int-2 influences the development of the nodose ganglion

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Lower Purkinje cell counts in the cerebella of four autistic subjects: initial findings of the UCLA-NSAC Autopsy Research Report.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Genes with triplet repeats: candidate mediators of neuropsychiatric disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Regulation of a Purkinje cell-specific promoter by homeodomain proteins: repression by engrailed-2 vs. synergistic activation by Hoxa5 and Hoxb7.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Genetic counseling in autism and pervasive developmental disorders.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Hyperserotoninemia and serotonin receptor antibodies in children with autism but not mental retardation.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Autism and tuberous sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Autism and genetics. A decade of research

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Autism and tuberous sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Possible prevention of neural-tube defects by periconceptional vitamin supplementation

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Cross-sensitization between footshock stress and apomorphine on self-injurious behavior and neostriatal catecholamines in a rat model of Lesch-Nyhan syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Autism in thalidomide embryopathy: a population study.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Altered segmental identity and abnormal migration of motor neurons in mice lacking Hoxb-1.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Genetics of autism: overview and new directions

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Incidence of minor physical anomaly in autism

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

A male with fetal valproate syndrome and autism.

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021

Social language use in parents of autistic individuals

1 reference

https://api.crossref.org/works/10.1016%2FS0074-7750%2800%2980006-3

7 January 2021