Current developments in the genetics of autism: from phenome to genome (Q24646514)

Journal of Neuropathology & Experimental Neurology

Europe PubMed Central

title

Current developments in the genetics of autism: from phenome to genome (English)

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4

Joseph Piven

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Patrick F. Sullivan

series ordinal

2

object named as

Patrick F Sullivan

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author name string

Molly Losh

series ordinal

1

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Dimitri Trembath

series ordinal

3

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language of work or name

English

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publication date

September 2008

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published in

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volume

67

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issue

9

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page(s)

829-37

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cites work

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Initial sequencing and analysis of the human genome

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27 September 2017

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Autism in tuberous sclerosis

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27 September 2017

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

27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.

30 May 2018

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Personality traits of the relatives of autistic probands.

30 May 2018

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Autism and tuberous sclerosis complex: prevalence and clinical features

30 May 2018

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30 May 2018

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

30 May 2018

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30 May 2018

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

30 May 2018

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Genetics of autism: characteristics of affected and unaffected children from 37 multiplex families.

30 May 2018

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The incidence of cognitive disabilities in the siblings of autistic children.

30 May 2018

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A family history study of neuropsychiatric disorders in the adult siblings of autistic individuals.

30 May 2018

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Autistic children and their first-degree relatives: relationships between serotonin and norepinephrine levels and intelligence.

30 May 2018

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30 May 2018

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Parents of Children with Asperger Syndrome: What is the Cognitive Phenotype?

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A quantitative trait locus analysis of social responsiveness in multiplex autism families

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28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Increasing knowledge of PTEN germline mutations: Two additional patients with autism and macrocephaly.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Social-cognition and the broad autism phenotype: identifying genetically meaningful phenotypes.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

The development of young siblings of children with autism from 4 to 54 months

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Visual Fixation Patterns during Reciprocal Social Interaction Distinguish a Subgroup of 6-Month-Old Infants At-Risk for Autism from Comparison Infants

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Early social and emotional communication in the infant siblings of children with autism spectrum disorders: an examination of the broad phenotype.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Communicative competence in parents of children with autism and parents of children with specific language impairment.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Association analysis of the NrCAM gene in autism and in subsets of families with severe obsessive-compulsive or self-stimulatory behaviors

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Gaze-fixation, brain activation, and amygdala volume in unaffected siblings of individuals with autism.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Cerebellar lesions in tuberous sclerosis complex: neurobehavioral and neuroimaging correlates

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Reelin gene polymorphisms in the Indian population: a possible paternal 5'UTR-CGG-repeat-allele effect on autism.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Evidence for multiple loci from a genome scan of autism kindreds.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Quantitative assessment of autism symptom-related traits in probands and parents: Broader Phenotype Autism Symptom Scale

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Development in infants with autism spectrum disorders: a prospective study.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

The development of siblings of children with autism at 4 and 14 months: social engagement, communication, and cognition.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Autistic social impairment in the siblings of children with pervasive developmental disorders.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Characteristics of the broader phenotype in autism: a study of siblings using the children's communication checklist-2.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Quantitative trait locus analysis of nonverbal communication in autism spectrum disorder.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Brief report: early social communication behaviors in the younger siblings of children with autism

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Evidence for linkage on 21q and 7q in a subset of autism characterized by developmental regression.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Quantitative genome scan and Ordered-Subsets Analysis of autism endophenotypes support language QTLs.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Serotonin transporter intron 2 polymorphism associated with rigid-compulsive behaviors in Dutch individuals with pervasive developmental disorder

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Mind-reading difficulties in the siblings of people with Asperger's syndrome: evidence for a genetic influence in the abnormal development of a specific cognitive domain.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

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.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

[Genetics of autism: from genome scans to candidate genes].

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Serotonin transporter gene promoter variants do not explain the hyperserotoninemia in autistic children

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Transmission disequilibrium mapping at the serotonin transporter gene (SLC6A4) region in autistic disorder

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Genomic screen and follow-up analysis for autistic disorder.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Autism in tuberous sclerosis complex is related to both cortical and subcortical dysfunction

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

The reelin pathway modulates the structure and function of retinal synaptic circuitry

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Evidence for an association with the serotonin transporter promoter region polymorphism and autism

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Exploring the cognitive phenotype of autism: weak "central coherence" in parents and siblings of children with autism: II. Real-life skills and preferences.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

The familial aggregation of the lesser variant in biological and nonbiological relatives of PDD probands: a family history study.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Predictors of cognitive test patterns in autism families.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Autism in tuberous sclerosis: evoked potential evidence for a deficit in auditory sensory processing.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

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.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Autism: the phenotype in relatives.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Genetics of autism: overview and new directions

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Cognitive deficits in parents from multiple-incidence autism families

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

A family study of autism: cognitive patterns and levels in parents and siblings.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2649757

Bannayan–Riley–Ruvalcaba syndrome with reactive nodular lymphoid hyperplasia and autism and a PTEN mutation

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18716561

12 December 2020

inferred from PubMed ID database lookup

Estimate of prevalence of proximal 15q duplication syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18716561

12 December 2020

inferred from PubMed ID database lookup

Incorporating language phenotypes strengthens evidence of linkage to autism.

1 reference

Crossref

https://api.crossref.org/works/10.1097%2FNEN.0B013E318184482D

7 January 2021

inferred from DOI database lookup

The Familial Aggregation of the Lesser Variant in Biological and Nonbiological Relatives of PDD Probands: a Family History Study

1 reference

Crossref

https://api.crossref.org/works/10.1097%2FNEN.0B013E318184482D

7 January 2021