(Q34851994)

4 August 2017

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title

Autism: in search of susceptibility genes (English)

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4 August 2017

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Janine A Lamb

1

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4 August 2017

Jeremy R Parr

series ordinal

2

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4 August 2017

Anthony J Bailey

series ordinal

3

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4 August 2017

Anthony P Monaco

series ordinal

4

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4 August 2017

publication date

1 January 2002

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4 August 2017

published in

NeuroMolecular Medicine

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4 August 2017

volume

2

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4 August 2017

issue

1

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4 August 2017

page(s)

11-28

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

4 August 2017

cites work

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12 December 2020

Obstetric complications in autism: consequences or causes of the condition?

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12 December 2020

Seizure disorders in autism

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12 December 2020

Association between idiopathic infantile macrocephaly and autism spectrum disorders

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12 December 2020

Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism

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12 December 2020

How commonly are known medical conditions associated with autism?

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12 December 2020

SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease

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12 December 2020

The epidemiology of autism: a review.

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12 December 2020

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

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12 December 2020

A forkhead-domain gene is mutated in a severe speech and language disorder

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12 December 2020

Autism in Angelman syndrome: a population-based study

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12 December 2020

Autism and medical disorders: a review of the literature.

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12 December 2020

Human PEG1/MEST, an imprinted gene on chromosome 7

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12 December 2020

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

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12 December 2020

No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients.

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12 December 2020

A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p.

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12 December 2020

Sertraline in adults with pervasive developmental disorders: a prospective open-label investigation

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12 December 2020

Autism and tuberous sclerosis

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12 December 2020

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

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12 December 2020

Linkage disequilibrium in humans: models and data

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12 December 2020

Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism

1 reference

12 December 2020

Neuropathology of infantile autism

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12 December 2020

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region

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12 December 2020

Autism: recent molecular genetic advances

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12 December 2020

The autism genetic resource exchange: a resource for the study of autism and related neuropsychiatric conditions

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12 December 2020

The extent of linkage disequilibrium in four populations with distinct demographic histories

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12 December 2020

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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12 December 2020

Genetics of autism: overview and new directions

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12 December 2020

Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q.

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12 December 2020

Clomipramine in adults with pervasive developmental disorders: a prospective open-label investigation

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12 December 2020

Replication of linkage studies of complex traits: an examination of variation in location estimates

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Mutation screening and transmission disequilibrium study of ATP10C in autism

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12 December 2020

FOXP2 is not a major susceptibility gene for autism or specific language impairment

1 reference

12 December 2020

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

1 reference

12 December 2020

Autism: the phenotype in relatives

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12 December 2020

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

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12 December 2020

Heterogeneity and the genetics of autism

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12 December 2020

Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28

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12 December 2020

Studies on 5-hydroxyindole metabolism in autistic and other mentally retarded children

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12 December 2020

Autistic symptoms among children and young adults with isodicentric chromosome 15

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12 December 2020

Technical note: are perinatal complications causes or consequences of autism?

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12 December 2020

Interstitial duplications of chromosome region 15q11q13: clinical and molecular characterization

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12 December 2020

Genetic studies of autistic disorder and chromosome 7

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12 December 2020

A genomewide scan identifies two novel loci involved in specific language impairment

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12 December 2020

Infantile autism: a genetic study of 21 twin pairs

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12 December 2020

Lack of association of the (AAAT)6 allele of the GXAlu tetranucleotide repeat in intron 27b of the NF1 gene with autism

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12 December 2020

Metabolic approaches to the treatment of autism spectrum disorders.

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12 December 2020

The pharmacotherapy of target symptoms associated with autistic disorder and other pervasive developmental disorders

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12 December 2020

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

1 reference

12 December 2020

Language regression in childhood

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12 December 2020

Autism--an evolving concept

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12 December 2020

Value of a clinical morphology examination in autism

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12 December 2020

Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families

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12 December 2020

Full-genome scans with autistic disorder: a review

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12 December 2020

Autism: the point of view from fragile X studies

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12 December 2020

Regression in pervasive developmental disorders: seizures and epileptiform electroencephalogram correlates

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12 December 2020

Genomic screen and follow-up analysis for autistic disorder

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12 December 2020

Positional cloning moves from perditional to traditional

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12 December 2020

A genomewide screen for autism susceptibility loci

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12 December 2020

Autism and known medical conditions: myth and substance

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12 December 2020

A broader phenotype of autism: the clinical spectrum in twins

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12 December 2020

The neurobiology and genetics of infantile autism

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12 December 2020

Recent progress in psychiatric genetics-some hope but no hype

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12 December 2020

Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes

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12 December 2020

Autism and maternally derived aberrations of chromosome 15q.

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12 December 2020

Behavioral phenotypic variation in autism multiplex families: evidence for a continuous severity gradient.

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12 December 2020

Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families

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12 December 2020

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

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12 December 2020

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

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12 December 2020

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

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12 December 2020

1 reference

12 December 2020

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

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12 December 2020

Decrease in reelin and glutamic acid decarboxylase67 (GAD67) expression in schizophrenia and bipolar disorder: a postmortem brain study

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12 December 2020

Discovery of allelic variants of HOXA1 and HOXB1: genetic susceptibility to autism spectrum disorders

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12 December 2020

Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families

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12 December 2020

Autism and genetics: high incidence of specific genetic syndromes in 21 autistic adolescents and adults living in two residential homes in Belgium

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12 December 2020

A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

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12 December 2020

Brief report: the association of neurofibromatosis type 1 and autism

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12 December 2020

Psychiatric genetics: search for phenotypes.

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12 December 2020

Deletion of chromosome 2q37 and autism: a distinct subtype?

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12 December 2020

Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three U.S. populations: collaborative study on the genetics of asthma

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12 December 2020

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

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12 December 2020

Postmortem brain abnormalities of the glutamate neurotransmitter system in autism

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12 December 2020

Imprinting, the X-chromosome, and the male brain: explaining sex differences in the liability to autism

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12 December 2020

A clinicopathological study of autism

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12 December 2020

Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans

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12 December 2020

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

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12 December 2020

Multilocus linkage tests based on affected relative pairs.

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12 December 2020

Xp deletions associated with autism in three females

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12 December 2020

Evidence supporting WNT2 as an autism susceptibility gene.

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12 December 2020

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

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12 December 2020

Chromosome 7q: where autism meets language disorder?

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12 December 2020

Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples

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12 December 2020

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12 December 2020

Major factors influencing linkage disequilibrium by analysis of different chromosome regions in distinct populations: demography, chromosome recombination frequency and selection

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12 December 2020

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

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12 December 2020

Is there a basis for novel pharmacotherapy of autism?

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12 December 2020

Autism and measles, mumps, and rubella vaccine: no epidemiological evidence for a causal association

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12 December 2020

Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations

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12 December 2020

Pharmacogenetics and the practice of medicine

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12 December 2020

The serotonin system in autism

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12 December 2020

Subgroups in autism: are there behavioural phenotypes typical of underlying medical conditions?

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12 December 2020

Serotonin and autism: biochemical and molecular biology features

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12 December 2020

Autism: evidence of association with adenosine deaminase genetic polymorphism

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12 December 2020

Chromosomal disorders and autism

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12 December 2020

Autism and tuberous sclerosis

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12 December 2020

Autistic regression and disintegrative disorder: how important the role of epilepsy?

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12 December 2020

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

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12 December 2020

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

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12 December 2020

Three probands with autistic disorder and isodicentric chromosome 15.

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12 December 2020

Extent and distribution of linkage disequilibrium in three genomic regions

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12 December 2020

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

12 December 2020

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

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12 December 2020

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

1 reference

12 December 2020

Head circumference is an independent clinical finding associated with autism

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12 December 2020

A genomic screen of autism: evidence for a multilocus etiology

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12 December 2020

An extended family with a dominantly inherited speech disorder

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12 December 2020

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

1 reference

12 December 2020

Single nucleotide polymorphism and linkage disequilibrium within the TCR alpha/delta locus

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12 December 2020

The Sequence of the Human Genome

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12 December 2020

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

1 reference

12 December 2020

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

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12 December 2020

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

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12 December 2020

Evidence of linkage between the serotonin transporter and autistic disorder

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12 December 2020

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

1 reference

12 December 2020

RETRACTED: Ileal-lymphoid-nodular hyperplasia, non-specific colitis, and pervasive developmental disorder in children

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12 December 2020

gamma2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome

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12 December 2020

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

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12 December 2020

Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex

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12 December 2020

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

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12 December 2020

The syndrome of inv dup (15): clinical, electroencephalographic, and imaging findings

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12 December 2020

MMR vaccine--worries are not justified

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12 December 2020

A decrease of reelin expression as a putative vulnerability factor in schizophrenia

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12 December 2020

Dissection of behavior and psychiatric disorders using the mouse as a model

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12 December 2020

Dysregulation of Reelin and Bcl-2 proteins in autistic cerebellum

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12 December 2020

Association study of the NF1 gene and autistic disorder

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12 December 2020

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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12 December 2020

High-resolution haplotype structure in the human genome

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12 December 2020

Chromosomal abnormalities in a clinic sample of individuals with autistic disorder

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12 December 2020

Construction of a physical map of an autism susceptibility region in 7q32.3-q33.

1 reference

12 December 2020

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

12 December 2020

No evidence for measles, mumps, and rubella vaccine-associated inflammatory bowel disease or autism in a 14-year prospective study

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12 December 2020

Variable expression of the autism broader phenotype: findings from extended pedigrees

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12 December 2020

Autistic children: infancy to adulthood

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12 December 2020

No association between the WNT2 gene and autistic disorder

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12 December 2020

Autism: current theories regarding its pathogenesis and implications for rational pharmacotherapy

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12 December 2020

5-HTTLPR variants not associated with autistic spectrum disorders

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12 December 2020

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

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12 December 2020

Pervasive Developmental Disorders in Preschool Children

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12 December 2020

The genome-wide distribution of background linkage disequilibrium in a population isolate

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12 December 2020

A five- to fifteen-year follow-up study of infantile psychosis

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12 December 2020

Haplotype tagging for the identification of common disease genes

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12 December 2020

Initial sequencing and analysis of the human genome

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12 December 2020

Identifiers

DOI

10.1385/NMM:2:1:11

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Dimensions Publication ID

4 August 2017

1027510152

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Fatcat ID

release_t5qcpgwtcvfidekyajjjmu6jia

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/t5qcpgwtcvfidekyajjjmu6jia

24 November 2022

mapped directly with Wikidata item

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