Autism: recent molecular genetic advances.

No abstract is available for this paper.

• Publication year

  2000

• Venue

  Human Molecular Genetics

• Publication date

  2000-04-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1093/HMG/9.6.861PMID 10767308
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Genetic studies in autistic disorder and chromosome 15

  2000cited by this paper
• Genome-Wide Scan for Autism Susceptibility Genes

  1999influential reference
• Phenotype–genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patients

  1999cited by this paper
• Association study of the NF1 gene and autistic disorder.

  1999cited by this paper
• Replication of linkage studies of complex traits: an examination of variation in location estimates.

  1999cited by this paper
• The epidemiology of autism: a review

  1999cited by this paper
• Genetics and child psychiatry: II Empirical research findings.

  1999cited by this paper
• Mutation screening of the UBE3A/E6-AP gene in autistic disorder

  1999cited by this paper
• 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.

  1999cited by this paper
• Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study.

  1999cited by this paper
• A genomic screen of autism: evidence for a multilocus etiology.

  1999cited by this paper
• GABA and epileptogenesis: comparing gabrb3 gene-deficient mice with Angelman syndrome in man.

  1999cited by this paper
• Fragile sites-cytogenetic similarity with molecular diversity.

  1999cited by this paper
• Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13

  1999cited by this paper
• Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism.

  1999cited by this paper
• An autosomal genomic screen for autism. Collaborative linkage study of autism.

  1999cited by this paper
• Genetics of Angelman syndrome.

  1999cited by this paper
• An autosomal genomic screen for autism.

  1999influential reference
• Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).

  1999cited by this paper
• Genetic studies of autistic disorder and chromosome 7.

  1999influential reference
• Possible association between childhood absence epilepsy and the gene encoding GABRB3.

  1999cited by this paper
• 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.

  1999cited by this paper
• 5-HTTLPR variants not associated with autistic spectrum disorders

  1999cited by this paper
• Angelman syndrome: Correlations between epilepsy phenotypes and genotypes

  1998cited by this paper
• How Commonly Are Known Medical Conditions Associated with Autism?

  1998cited by this paper
• A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International Molecular Genetic Study of Autism Consortium.

  1998cited by this paper
• Fluoxetine in Treatment of Adolescent Patients with Autism: A Longitudinal Open Trial

  1998cited by this paper
• Autism: The Phenotype in Relatives

  1998cited by this paper
• Autism and Tuberous Sclerosis

  1998cited by this paper
• Autism and maternally derived aberrations of chromosome 15q.

  1998cited by this paper
• Autism: The Point of View from Fragile X Studies

  1998cited by this paper
• Mice Lacking the β3 Subunit of the GABAA Receptor Have the Epilepsy Phenotype and Many of the Behavioral Characteristics of Angelman Syndrome

  1998cited by this paper
• Autistic symptoms among children and young adults with isodicentric chromosome 15.

  1998cited by this paper
• Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers.

  1998cited by this paper
• Chromosomal Disorders and Autism

  1998cited by this paper
• Interstitial duplications of chromosome region 15q11q13: clinical and molecular characterization.

  1998cited by this paper
• Evidence of linkage between the serotonin transporter and autistic disorder

  1997cited by this paper
• Lack of association between juvenile myoclonic epilepsy and GABRA5 and GABRB3 genes.

  1997cited by this paper
• Autism or atypical autism in maternally but not paternally derived proximal 15q duplication.

  1997cited by this paper
• Clomipramine in Adults with Pervasive Developmental Disorders: A Prospective Open-Label Investigation

  1997cited by this paper
• Serotonin transporter (5-HTT) gene variants associated with autism?

  1997influential reference
• Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation.

  1996cited by this paper
• Male-to-male transmission in extended pedigrees with multiple cases of autism.

  1996influential reference
• AUTISM AND MEDICAL DISORDERS: A REVIEW OF THE LITERATURE

  1996cited by this paper
• Serotonin and autism: biochemical and molecular biology features.

  1996influential reference
• Studies of the c-Harvey-Ras gene in psychiatric disorders.

  1996cited by this paper
• Autism in Angelman syndrome: a population-based study.

  1996cited by this paper
• Autism and genetics: clinical approach and association study with two markers of HRAS gene.

  1995cited by this paper
• Autism as a strongly genetic disorder: evidence from a British twin study

  1995cited by this paper
• Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.

  1995cited by this paper
• Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism.

  1995cited by this paper
• A case-control family history study of autism.

  1994cited by this paper
• Autism and known medical conditions: myth and substance.

  1994cited by this paper
• Inv dup(15) supernumerary marker chromosomes.

  1994cited by this paper
• Case Study: Autism Associated with Marker Chromosome

  1991cited by this paper
• Platelet serotonin, a possible marker for familial autism

  1991cited by this paper
• Autism associated with marker chromosome.

  1991cited by this paper
• Autism and tuberous sclerosis

  1991cited by this paper
• The UCLA-University of Utah epidemiologic survey of autism: the etiologic role of rare diseases.

  1990cited by this paper
• A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden.

  1989cited by this paper
• Autism and genetics. A decade of research.

  1988cited by this paper
• Handbook of Autism and Pervasive Developmental Disorders

  1987cited by this paper
• Whole blood serotonin in autistic and normal subjects.

  1987cited by this paper
• Catalogue of Unbalanced Chromosome Aberrations in Man

  1985cited by this paper
• Infantile autism: a genetic study of 21 twin pairs.

  1977cited by this paper
• Autistic children: infancy to adulthood.

  1970cited by this paper
• A Five- to Fifteen-Year Follow-up Study of Infantile Psychosis

  1969cited by this paper
• Autistic disturbances of affective contact.

  1968cited by this paper
• The inheritance of liability to certain diseases, estimated from the incidence among relatives

  1965cited by this paper
• Studies on 5-hydroxyindole metabolism in autistic and other mentally retarded children.

  1961cited by this paper

• Investigating the Effect of Capric Acid on Antibiotic‐Induced Autism‐Like Behavior in Rodents

  2024cites this paper
• The emerging role of α7nAChRs/caspase-3/Nrf-2 signaling pathway in citicoline improved autistic behavior induced by thimerosal in mice.

  2024cites this paper
• Cholesterol metabolism pathway in autism spectrum disorder: From animal models to clinical observations.

  2023cites this paper
• Downregulation of the GABAA receptor β2 subunit in a rat model of autism

  2023cites this paper
• Estratégias para o transtorno do espectro autista: interação social e intervenções terapêuticas

  2021cites this paper
• The effect of sodium channels on neurological/neuronal disorders: A systematic review

  2021cites this paper
• The Novel Potential Therapeutic Utility of Montelukast in Alleviating Autistic Behavior Induced by Early Postnatal Administration of Thimerosal in Mice

  2020cites this paper
• Novel potential of metformin on valproic acid‐induced autism spectrum disorder in rats: involvement of antioxidant defence system

  2020cites this paper
• DigitalCommons@USU DigitalCommons@USU

  2020cites this paper
• Steroid Metabolites Support Evidence of Autism as a Spectrum

  2019cites this paper
• Interested in publishing with us ? Contact book

  2018cites this paper
• Polymorphisms of Shank 3 gene in Chinese Han Children with Autism Spectrum Disorders ( ASD ) : A case-control study

  2018cites this paper
• Neural Dynamics of Autistic Repetitive Behaviors and Fragile X Syndrome: Basal Ganglia Movement Gating and mGluR-Modulated Adaptively Timed Learning

  2018cites this paper
• Single nucleotide polymorphism association studies of ABCA13 and ABHD11 genes and the bioinformatics analysis of the autism candidate genes localized on chromosome 7

  2016cites this paper
• If genetic variation could talk: What genomic data may teach us about the importance of gene expression regulation in the genetics of autism.

  2016cites this paper
• Common Genetic Variants Found in HLA and KIR Immune Genes in Autism Spectrum Disorder

  2016cites this paper
• Genetic Approaches-Investigating Psychiatry

  2015cites this paper
• The Population Level Impacts of Differential Fertility Behavior of Parents of Children with Autism

  2015cites this paper
• Changes in plasticity across the lifespan: cause of disease and target for intervention.

  2013cites this paper
• Autism as a disorder of deficiency of brain-derived neurotrophic factor and altered metabolism of polyunsaturated fatty acids.

  2013cites this paper
• Use of Transcranial Magnetic Stimulation in Autism Spectrum Disorders

  2013cites this paper
• Excitotoxicity in the Pathogenesis of Autism

  2012cites this paper
• Immunological Aetiology of Major Psychiatric Disorders

  2012cites this paper
• Analysis of Serotonin Transporter Gene (5HTT) Variants Association in Children with Autistic Disorder

  2012cites this paper
• Glutathione pathway gene variation and risk of autism spectrum disorders

  2011cites this paper
• CYTOGENETICS OF AUTISM

  2011cites this paper
• A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

  2011cites this paper
• Autism Spectrum Disorders: The Role of Genetics in Diagnosis and Treatment

  2011cites this paper
• HERAPY FOR A UTISTIC S PECTRUM D ISORDERS : R EVIEW AND C ASE R EPORT

  2011cites this paper
• The Genetic Basis of Phenotypic Diversity: Autism as an Extreme Tail of a Complex Dimensional Trait

  2011cites this paper
• MAOA, DBH, and SLC6A4 variants in CHARGE: a case–control study of autism spectrum disorders

  2011cites this paper
• International Encyclopedia of Rehabilitation

  2010cites this paper
• Autism from a Biometric Perspective

  2010cites this paper
• Cholinergic Component of Autism Spectrum Disorder

  2010cites this paper
• Association and gene–gene interaction of SLC6A4 and ITGB3 in autism

  2010cites this paper
• Social demographic change and autism

  2010cites this paper
• The Timing and Specificity of Prenatal Immune Risk Factors for Autism Modeled in the Mouse and Relevance to Schizophrenia

  2010cites this paper
• Influence of the 5-HTTLPR polymorphism and environmental risk factors in a Brazilian sample of patients with autism spectrum disorders.

  2009cites this paper
• Bio-electrographic method in detecting heterogeneity and unique features in autism

  2009cites this paper
• Increased activities of Na+/K+-ATPase and Ca2+/Mg2+-ATPase in the frontal cortex and cerebellum of autistic individuals.

  2009cites this paper
• Decreased serum Ou/Zn sOD in children with Autism

  2009cites this paper
• Autism, the Integrations of ‘Difference’ and the Origins of Modern Human Behaviour

  2009cites this paper
• The effects of applied verbal behaviour approach “AVB” in teaching children with autism

  2009cites this paper
• Abnormalities in Membrane Lipids, Membrane-Associated Proteins, and Signal Transduction in Autism

  2009cites this paper
• Influência de fatores genéticos e ambientais nos transtornos do espectro autista

  2009cites this paper
• Immunologic and neurodevelopmental susceptibilities of autism.

  2008cites this paper
• Intersubjectivity, affective neuroscience, and the neurobiology of autistic spectrum disorders: a systematic review.

  2008cites this paper
• Pre‐school teachers' knowledge, attitudes and practices on childhood developmental and behavioural disorders in Singapore

  2008cites this paper
• The neuropsychological endophenotype of specific language impairments and autism spectrum disorders: Category or continuum?

  2008cites this paper
• Autism

  2007cites this paper
• Computerized lifelong mentoring support using robot for autistic individuals.

  2007cites this paper
• Endophenotype Approach to Developmental Psychopathology: Implications for Autism Research

  2007cites this paper
• Autismo, cromosoma 15 y la hipótesis de disfunción GABAérgica. Revisión.

  2007cites this paper
• Characterization of an Autism-Associated Segmental Maternal Heterodisomy of the Chromosome 15q11–13 Region

  2007cites this paper
• Assessing autism-like behavior in mice: variations in social interactions among inbred strains.

  2007cites this paper
• The Intense World Syndrome – an Alternative Hypothesis for Autism

  2007cites this paper
• Influence of human histocompatibility antigens on susceptibility to and clinical expression of psychiatric diseases

  2006cites this paper
• Altered neocortical microcircuitry in the valproic acid rat model of autism

  2006cites this paper
• A heterogeneity-based genome search meta-analysis for autism-spectrum disorders

  2006cites this paper
• Neural dynamics of autistic behaviors: cognitive, emotional, and timing substrates.

  2006cites this paper
• The yield of subtelomeric FISH analysis in the evaluation of autistic spectrum disorders

  2006cites this paper
• Genetic Basis of Autism

  2006cites this paper
• Oxidative stress in autism.

  2006cites this paper
• Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine 152 Molecular Characterisation of Structural Chromosomal Abnormalities Associated with Congenital Disorders

  2006cites this paper
• Influência dos antígenos de histocompatibilidade humanos na susceptibilidade e expressão clínica de doenças psiquiátricas

  2006cites this paper
• Reduced MeCP2 Expression is Frequent in Autism Frontal Cortex and Correlates with Aberrant MECP2 Promoter Methylation

  2006cites this paper
• Injection of Neuroinflammatory Chemokine Alters Developmental Course of Social and Exploratory Behaviors of Neonatal Rats

  2006cites this paper
• Psychiatric Disorders: The Search for Genes

  2006cites this paper
• A Case of Partial Trisomy of Chromosome 8p Associated with Autism

  2006cites this paper
• Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression

  2005cites this paper
• The Autism Genome Project

  2005cites this paper
• Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs

  2005cites this paper
• Ceruloplasmin, superoxide dismutase and copper in autistic patients.

  2005cites this paper
• Gene expression in Autism

  2005cites this paper
• Immunological aetiology of major psychiatric disorders: evidence and therapeutic implications.

  2005cites this paper
• Genetic Influences and Autism

  2005cites this paper
• [Genetics of autism].

  2004cites this paper
• Genetics of autism Genética do autismo

  2004cites this paper
• Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders.

  2004cites this paper
• Variants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autism

  2004cites this paper
• A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A

  2004cites this paper
• The prenatal autistic imprinting hypothesis: developmental maladaptation to the environmental changes between womb and the social world.

  2004influential citation
• Autism and pervasive developmental disorders.

  2004cites this paper
• Alteration in amino-glycerophospholipids levels in the plasma of children with autism: a potential biochemical diagnostic marker.

  2004cites this paper
• Genetics of autism

  2004cites this paper
• Linkage analysis for autism in a subset families with obsessive–compulsive behaviors: Evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19

  2004cites this paper
• The genetics of autism.

  2004cites this paper
• Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder

  2004cites this paper
• Epidemiology and Possible Causes of Autism

  2003cites this paper
• Maternal neuronal antibodies associated with autism and a language disorder

  2003cites this paper
• Calcr, a brain-specific imprinted mouse calcitonin receptor gene in the imprinted cluster of the proximal region of chromosome 6

  2003cites this paper
• Postural Stability in Children with Autism Spectrum Disorder

  2003cites this paper
• Bioinformatic analysis of autism positional candidate genes using biological databases and computational gene network prediction

  2003cites this paper
• Evidence of brain overgrowth in the first year of life in autism.

  2003cites this paper
• Etiological, diagnostic and treatment conundrum

  2003cites this paper
• The neurobiology of autism: New pieces of the puzzle

  2003cites this paper
• Identifying neurocognitive phenotypes in autism.

  2003cites this paper
• A genomewide screen of 345 families for autism-susceptibility loci.

  2003cites this paper
• Sodium channels SCN1A, SCN2A and SCN3A in familial autism

  2003cites this paper
• The neurobiological context of autism

  2003cites this paper