(Q50303685)

2 March 2018

title

No evidence that common genetic risk variation is shared between schizophrenia and autism. (English)

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2 March 2018

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Louise Gallagher

4

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2 March 2018

Michael Gill

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2 March 2018

Herman van Engeland

7

object named as

Herman van Engeland

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2 March 2018

Eske M Derks

3

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René S. Kahn

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object named as

René S Kahn

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2 March 2018

Roel Ophoff

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object named as

Roel A Ophoff

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2 March 2018

author name string

Jacob A S Vorstman

1

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2 March 2018

Maretha V de Jonge

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2 March 2018

Autism Genome Project, the International Schizophrenia Consortium

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2 March 2018

publication date

28 November 2012

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2 March 2018

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

number of pages

6

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based on heuristic

inferred from page(s)

published in

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2 March 2018

volume

162B

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issue

1

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2 March 2018

page(s)

55-60

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2 March 2018

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

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Individual common variants exert weak effects on the risk for autism spectrum disorders

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Evidence for polygenic susceptibility to multiple sclerosis--the shape of things to come

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Genomewide association studies: history, rationale, and prospects for psychiatric disorders

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

The Kraepelinian dichotomy - going, going... but still not gone

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Psychosis and autism as diametrical disorders of the social brain

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Parental psychiatric disorders associated with autism spectrum disorders in the offspring

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Do common variants play a role in risk for autism? Evidence and theoretical musings

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

A family history study of Asperger syndrome

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Phenotypic variability and genetic susceptibility to genomic disorders

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Rare chromosomal deletions and duplications increase risk of schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Autistic disorder and schizophrenia: diagnostic overlaps.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Risk factors for autism: perinatal factors, parental psychiatric history, and socioeconomic status

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Genomic analysis of mental illness: a changing landscape

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Copy-number variants in neurodevelopmental disorders: promises and challenges

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Psychiatric disorders in adults diagnosed as children with atypical autism. A case control study.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Psychiatric disorders in individuals diagnosed with infantile autism as children: a case control study.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

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

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

PLINK: a tool set for whole-genome association and population-based linkage analyses

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

A family-based study of common polygenic variation and risk of schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Concepts of autism: a review of research

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Childhood schizophrenia reconsidered

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

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

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

The benefit of directly comparing autism and schizophrenia for revealing mechanisms of social cognitive impairment.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

dbSNP: the NCBI database of genetic variation

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Psychosis, affective disorders and anxiety in autistic spectrum disorder: prevalence and nosological considerations

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Bipolar disorder, schizophrenia, and other psychotic disorders in adults with childhood onset AD/HD and/or autism spectrum disorders

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Large recurrent microdeletions associated with schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Family history of schizophrenia and bipolar disorder as risk factors for autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Comorbid association of autism and schizophrenia.

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1002%2FAJMG.B.32121

Common SNPs explain a large proportion of the heritability for human height

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.B.32121

21 January 2018

Identifiers

DOI

10.1002/AJMG.B.32121

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2 March 2018

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2 March 2018