(Q84797519)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21855394%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

title

Genetics of autism spectrum disorders (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21855394%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

main subject

autism spectrum disorder

1 reference

0 references

1

Daniel H Geschwind

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21855394%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

publication date

18 August 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21855394%20AND%20SRC:MED&resulttype=core&format=json

Trends in Cognitive Sciences

11 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21855394%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

volume

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21855394%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

issue

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21855394%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

page(s)

409-416

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21855394%20AND%20SRC:MED&resulttype=core&format=json

Autistic traits in the general population: a twin study

11 February 2020

cites work

1 reference

12 December 2020

Microduplications of 16p11.2 are associated with schizophrenia

1 reference

12 December 2020

CNTNAP2 variants affect early language development in the general population

1 reference

12 December 2020

Large recurrent microdeletions associated with schizophrenia

1 reference

12 December 2020

Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2

1 reference

12 December 2020

Neuroscience in the era of functional genomics and systems biology

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12 December 2020

Etiological heterogeneity in autism spectrum disorders: More than 100 genetic and genomic disorders and still counting

1 reference

12 December 2020

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

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12 December 2020

Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

1 reference

12 December 2020

Strong association of de novo copy number mutations with autism

1 reference

12 December 2020

Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patients

1 reference

12 December 2020

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size

1 reference

12 December 2020

Penetrance for copy number variants associated with schizophrenia

1 reference

12 December 2020

Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2

1 reference

12 December 2020

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

1 reference

12 December 2020

Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder

1 reference

12 December 2020

A common genetic variant in the neurexin superfamily member CNTNAP2 is associated with increased risk for selective mutism and social anxiety-related traits

1 reference

12 December 2020

Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism

1 reference

12 December 2020

Developmental trajectories in siblings of children with autism: cognition and language from 4 months to 7 years

1 reference

12 December 2020

Clinical assessment of autism in high-risk 18-month-olds

1 reference

12 December 2020

Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia

1 reference

12 December 2020

CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder

1 reference

12 December 2020

Neurocognitive and behavioral outcomes of younger siblings of children with autism spectrum disorder at age five.

1 reference

12 December 2020

Why the frontal cortex in autism might be talking only to itself: local over-connectivity but long-distance disconnection

1 reference

12 December 2020

Infantile autism: a genetic study of 21 twin pairs

1 reference

12 December 2020

The Genetics of Child Psychiatric Disorders: Focus on Autism and Tourette Syndrome

1 reference

12 December 2020

Structural variation of chromosomes in autism spectrum disorder

1 reference

12 December 2020

Rare De Novo and Transmitted Copy-Number Variation in Autistic Spectrum Disorders

1 reference

12 December 2020

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

1 reference

12 December 2020

Cilia in the nervous system: linking cilia function and neurodevelopmental disorders

1 reference

12 December 2020

Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome

1 reference

12 December 2020

Autism: many genes, common pathways?

1 reference

12 December 2020

Next-generation association studies for complex traits

1 reference

12 December 2020

A functional genetic link between distinct developmental language disorders

1 reference

12 December 2020

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample

1 reference

12 December 2020

Advances in autism genetics: on the threshold of a new neurobiology

1 reference

12 December 2020

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

1 reference

12 December 2020

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

1 reference

12 December 2020

Intergenerational transmission of subthreshold autistic traits in the general population

1 reference

12 December 2020

Pragmatic Language and School Related Linguistic Abilities in Siblings of Children with Autism

1 reference

12 December 2020

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies

1 reference

12 December 2020

Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?

1 reference

12 December 2020

Neuropsychological profile of autism and the broad autism phenotype

1 reference

12 December 2020

Defining the cognitive phenotype of autism.

1 reference

12 December 2020

Autism as a disorder of neural information processing: directions for research and targets for therapy

1 reference

12 December 2020

Disrupted neural synchronization in toddlers with autism

1 reference

12 December 2020

Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.

1 reference

12 December 2020

Teetering towards chaos and complexity

1 reference

12 December 2020

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

1 reference

12 December 2020

Autism spectrum disorders: developmental disconnection syndromes

1 reference

12 December 2020

Common genetic variants on 5p14.1 associate with autism spectrum disorders

1 reference

12 December 2020

Genetic advances in autism: heterogeneity and convergence on shared pathways

1 reference

12 December 2020

Genetic influences and infantile autism

1 reference

12 December 2020

Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome

1 reference

12 December 2020

A twin study of autism symptoms in Sweden

1 reference

12 December 2020

Genetic heterogeneity between the three components of the autism spectrum: a twin study

1 reference

12 December 2020

Traits contributing to the autistic spectrum

1 reference

12 December 2020

A case-control family history study of autism

1 reference

12 December 2020

Mechanisms of neurocognitive dysfunction and therapeutic considerations in tuberous sclerosis complex

1 reference

12 December 2020

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

1 reference

12 December 2020

Autism: highly heritable but not inherited

1 reference

12 December 2020

Self-referenced processing, neurodevelopment and joint attention in autism

1 reference

12 December 2020

A genome-wide scan for common alleles affecting risk for autism

1 reference

12 December 2020

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes

1 reference

12 December 2020

Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses

1 reference

12 December 2020

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

1 reference

12 December 2020

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism

1 reference

12 December 2020

Copy-number variations associated with neuropsychiatric conditions

1 reference

12 December 2020

Protein interactome reveals converging molecular pathways among autism disorders

1 reference

12 December 2020

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

1 reference

12 December 2020

Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2

1 reference

12 December 2020

The erosion of phenotypic specificity in psychiatric genetics: emerging lessons from CNTNAP2

1 reference

12 December 2020

Autism and abnormal development of brain connectivity.

1 reference

12 December 2020

Characteristics and concordance of autism spectrum disorders among 277 twin pairs

1 reference

12 December 2020

Familial aggregation of quantitative autistic traits in multiplex versus simplex autism

1 reference

12 December 2020

The Quantitative Nature of Autistic Social Impairment

1 reference

12 December 2020

Recurrent 16p11.2 microdeletions in autism

1 reference

12 December 2020

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

1 reference

12 December 2020

Association between microdeletion and microduplication at 16p11.2 and autism

1 reference

12 December 2020

The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms

1 reference

12 December 2020

Functional impact of global rare copy number variation in autism spectrum disorders

1 reference

12 December 2020

10.1016/J.TICS.2011.07.003

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21855394%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21855394%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

PubMed publication ID

21855394

1 reference