(Q33161703)

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A genome-wide association study of autism incorporating autism diagnostic interview-revised, autism diagnostic observation schedule, and social responsiveness scale

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scholarly article

1 reference

Europe PubMed Central

23 July 2017

A genome-wide association study of autism incorporating autism diagnostic interview-revised, autism diagnostic observation schedule, and social responsiveness scale (English)

1 reference

Europe PubMed Central

23 July 2017

genome-wide association study

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Hakon Hakonarson

3

object named as

Hakon Hakonarson

1 reference

Europe PubMed Central

23 July 2017

Joseph Glessner

2

object named as

Joseph T Glessner

2 references

ORCID Public Data File 2021

Europe PubMed Central

23 July 2017

author name string

John J Connolly

1

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Europe PubMed Central

23 July 2017

publication date

30 August 2012

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Europe PubMed Central

23 July 2017

Child Development

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Europe PubMed Central

23 July 2017

84

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Europe PubMed Central

23 July 2017

1

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Europe PubMed Central

23 July 2017

17-33

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Europe PubMed Central

23 July 2017

describes a project that uses

genome-wide association study

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based on heuristic

inferred from title

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Neuroanatomy of autism

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Synthetic associations are unlikely to account for many common disease genome-wide association signals

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: the Special Needs and Autism Project (SNAP)

1 reference

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21 January 2018

Distribution and activation of voltage-gated potassium channels in cell-attached and outside-out patches from large layer 5 cortical pyramidal neurons of the rat.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Properties of voltage-gated potassium currents in nucleated patches from large layer 5 cortical pyramidal neurons of the rat.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Impaired sadness recognition is linked to social interaction deficit in autism.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Amphiphysin II (SH3P9; BIN1), a member of the amphiphysin/Rvs family, is concentrated in the cortical cytomatrix of axon initial segments and nodes of ranvier in brain and around T tubules in skeletal muscle

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Identification of MeCP2 mutations in a series of females with autistic disorder

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Validation of a brief quantitative measure of autistic traits: comparison of the social responsiveness scale with the autism diagnostic interview-revised.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Rapid quantitative assessment of autistic social impairment by classroom teachers.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Copy-number variations associated with neuropsychiatric conditions

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Epilepsy in young adults with autism: a prospective population-based follow-up study of 120 individuals diagnosed in childhood.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Interrelationship between Autism Diagnostic Observation Schedule-Generic (ADOS-G), Autism Diagnostic Interview-Revised (ADI-R), and the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR) classification in children and adolescents with

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Rare variants create synthetic genome-wide associations

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Developmental changes of autistic symptoms.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Epidemiology of Pervasive Developmental Disorders

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Systematic association mapping identifies NELL1 as a novel IBD disease gene

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Autism: a world changing too fast for a mis-wired brain?

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Common variants in polygenic schizophrenia.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Strong synaptic transmission impact by copy number variations in schizophrenia

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Standardizing ADOS scores for a measure of severity in autism spectrum disorders

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

The Autism Diagnostic Observation Schedule: revised algorithms for improved diagnostic validity.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Using the Autism Diagnostic Interview-Revised and the Autism Diagnostic Observation Schedule with young children with developmental delay: evaluating diagnostic validity.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Genome-wide significance for dense SNP and resequencing data

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Gene expression profiling differentiates autism case-controls and phenotypic variants of autism spectrum disorders: evidence for circadian rhythm dysfunction in severe autism.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Novel clustering of items from the Autism Diagnostic Interview-Revised to define phenotypes within autism spectrum disorders.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

A haplotype map of the human genome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Gene structures and expression profiles of three human KCND (Kv4) potassium channels mediating A-type currents I(TO) and I(SA)

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Cognitive profiles and social-communicative functioning in children with autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Family-based association study between NOS-I and -IIA polymorphisms and autism spectrum disorders in Korean trios.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Kv4 potassium channel subunits control action potential repolarization and frequency-dependent broadening in rat hippocampal CA1 pyramidal neurones

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Skin conductance responses to another person's gaze in children with autism.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Changes in the developmental trajectories of striatum in autism.

1 reference

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21 January 2018

Effects of familial risk factors and place of birth on the risk of autism: a nationwide register-based study

1 reference

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21 January 2018

Emotional regulation, or: how I learned to stop worrying and love the nucleus accumbens

1 reference

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21 January 2018

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Finding the missing heritability of complex diseases

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Structural variation of chromosomes in autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Contribution of SHANK3 mutations to autism spectrum disorder

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Stability of the autism diagnostic interview-revised from pre-school to elementary school age in children with autism spectrum disorders.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Enhanced Perceptual Functioning in Autism: An Update, and Eight Principles of Autistic Perception

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

The genetics of autism

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Underconnected, but how? A survey of functional connectivity MRI studies in autism spectrum disorders

1 reference

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21 January 2018

The Epidemiology of Autism Spectrum Disorders *

1 reference

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21 January 2018

Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals

1 reference

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21 January 2018

Improved diagnostic validity of the ADOS revised algorithms: a replication study in an independent sample

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Epilepsy and EEG paroxysmal abnormalities in autism spectrum disorders.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Principal components analysis corrects for stratification in genome-wide association studies

1 reference

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21 January 2018

The future of genetic studies of complex human diseases

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Combining information from multiple sources in the diagnosis of autism spectrum disorders.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Rethinking the nature of genetic vulnerability to autistic spectrum disorders

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

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Stability and change among high-functioning children with pervasive developmental disorders: a 2-year outcome study

1 reference

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21 January 2018

Response to Mitchell and Porteus

1 reference

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21 January 2018

Biological, clinical and population relevance of 95 loci for blood lipids

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21 January 2018

Human NELL-1 expressed in unilateral coronal synostosis

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Abnormal electrodermal reactivity to novel visual stimuli in autistic children

1 reference

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21 January 2018

Differentiating between autism spectrum disorders and other developmental disabilities in children who failed a screening instrument for ASD.

1 reference

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21 January 2018

Endophenotype approach to developmental psychopathology: implications for autism research.

1 reference

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21 January 2018

CREB regulation of nucleus accumbens excitability mediates social isolation-induced behavioral deficits

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Analysing biological pathways in genome-wide association studies

1 reference

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21 January 2018

Interpretation of association signals and identification of causal variants from genome-wide association studies

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

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

1 reference

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21 January 2018

Molecular genetics of microvascular disease in diabetic retinopathy

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21 January 2018

Dscam and Sidekick proteins direct lamina-specific synaptic connections in vertebrate retina.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

A genomewide screen of 345 families for autism-susceptibility loci

1 reference

https://api.crossref.org/works/10.1111%2FJ.1467-8624.2012.01838.X

21 January 2018

Overexpression of Nell-1, a craniosynostosis-associated gene, induces apoptosis in osteoblasts during craniofacial development

1 reference

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21 January 2018

Craniosynostosis in transgenic mice overexpressing Nell-1

1 reference

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21 January 2018

Identifiers

10.1111/J.1467-8624.2012.01838.X

1 reference

Europe PubMed Central

23 July 2017

1 reference

Europe PubMed Central

23 July 2017

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