(Q48149496)

9 February 2018

title

Neurodevelopmental and neuropsychiatric disorders represent an interconnected molecular system. (English)

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9 February 2018

author

Ziarih Hawi

3

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9 February 2018

Mark A. Bellgrove

5

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9 February 2018

Charles Claudianos

8

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9 February 2018

author name string

A S Cristino

1

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9 February 2018

S M Williams

2

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9 February 2018

J-Y An

4

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9 February 2018

C E Schwartz

6

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9 February 2018

L da F Costa

7

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9 February 2018

language of work or name

English

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publication date

26 February 2013

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9 February 2018

published in

Molecular Psychiatry

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9 February 2018

volume

19

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9 February 2018

issue

3

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9 February 2018

page(s)

294-301

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9 February 2018

https://scigraph.springernature.com/pub.10.1038/mp.2013.16

exact match

0 references

cites work

Genetic basis of autism: is there a way forward?

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Deep sequencing reveals 50 novel genes for recessive cognitive disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

The genetic basis of complex human behaviors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

AutDB: a gene reference resource for autism research

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Patterns and rates of exonic de novo mutations in autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Autism spectrum disorders--a genetics review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

21 January 2018

XLMR genes: update 2007.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Fragile X and X-linked intellectual disability: four decades of discovery

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Candidate gene studies of ADHD: a meta-analytic review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Genome-wide association studies in ADHD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

SZGR: a comprehensive schizophrenia gene resource

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Meta-analysis of 32 genome-wide linkage studies of schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

A multi-dimensional evidence-based candidate gene prioritization approach for complex diseases-schizophrenia as a case

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Candidate genes for schizophrenia: a survey of association studies and gene ranking

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Networks of neuronal genes affected by common and rare variants in autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Strong association of de novo copy number mutations with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Gene expression studies in autism: moving from the genome to the transcriptome and beyond

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Pathogenetic model for Tourette syndrome delineates overlap with related neurodevelopmental disorders including Autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Neuroligins and neurexins link synaptic function to cognitive disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Role of serotonin in the paradoxical calming effect of psychostimulants on hyperactivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Hyperlocomotion and indifference to cocaine and amphetamine in mice lacking the dopamine transporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Family-based genome-wide association scan of attention-deficit/hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Genome-wide association scan of attention deficit hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Case-control genome-wide association study of attention-deficit/hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Twin studies of schizophrenia: from bow-and-arrow concordances to star wars Mx and functional genomics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

The endophenotype concept in psychiatry: etymology and strategic intentions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

A genome-wide linkage and association scan reveals novel loci for autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Neurexin-1 and frontal lobe white matter: an overlapping intermediate phenotype for schizophrenia and autism spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

BioGRID: a general repository for interaction datasets

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Human Proteinpedia: a unified discovery resource for proteomics research

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Human Proteinpedia enables sharing of human protein data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Human Proteinpedia as a resource for clinical proteomics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Community structure in social and biological networks

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

TRANSFAC: an integrated system for gene expression regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

A new generation of JASPAR, the open-access repository for transcription factor binding site profiles

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

miRBase: integrating microRNA annotation and deep-sequencing data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Genome-wide association study identifies five new schizophrenia loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

De Novo Gene Disruptions in Children on the Autistic Spectrum

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Sporadic male patients with intellectual disability: contribution of X-chromosome copy number variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Rate of de novo mutations and the importance of father's age to disease risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

MicroRNAs: target recognition and regulatory functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

21 January 2018

Genomics of microRNA.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.16

Common variants on chromosome 6p22.1 are associated with schizophrenia

21 January 2018

1 reference

12 December 2020

Neurobiology of schizophrenia

1 reference

12 December 2020

Attention-deficit hyperactivity disorder: a category or a continuum? Genetic analysis of a large-scale twin study

1 reference

12 December 2020

Common variants conferring risk of schizophrenia

1 reference

12 December 2020

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

1 reference

12 December 2020

Identifiers

DOI

10.1038/MP.2013.16

1 reference

9 February 2018

Dimensions Publication ID

0 references

1 reference

9 February 2018