(Q33691446)

28 July 2017

title

Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function (English)

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28 July 2017

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5

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28 July 2017

8

Mark J Daly

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28 July 2017

6

Pamela Sklar

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28 July 2017

Soumya Raychaudhuri

1

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28 July 2017

Joshua M Korn

2

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28 July 2017

Steven A McCarroll

3

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28 July 2017

International Schizophrenia Consortium

4

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28 July 2017

Shaun Purcell

7

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28 July 2017

publication date

9 September 2010

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28 July 2017

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28 July 2017

volume

6

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28 July 2017

issue

9

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28 July 2017

page(s)

e1001097

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Creative Commons Attribution 4.0 International

28 July 2017

copyright license

start time

9 September 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Copy number variations in East-Asian population and their evolutionary and functional implications

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Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

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Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci

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

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14 July 2018

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Variable locus length in the human genome leads to ascertainment bias in functional inference for non-coding elements.

14 July 2018

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Singleton deletions throughout the genome increase risk of bipolar disorder

14 July 2018

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Disruption of the neurexin 1 gene is associated with schizophrenia

14 July 2018

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A robust statistical method for case-control association testing with copy number variation

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Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

14 July 2018

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Large recurrent microdeletions associated with schizophrenia

14 July 2018

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Rare chromosomal deletions and duplications increase risk of schizophrenia

14 July 2018

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Strong association of de novo copy number mutations with sporadic schizophrenia

14 July 2018

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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

14 July 2018

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Structural variation of chromosomes in autism spectrum disorder

14 July 2018

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

14 July 2018

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14 July 2018

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14 July 2018

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14 July 2018

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Strong association of de novo copy number mutations with autism

14 July 2018

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Global variation in copy number in the human genome

14 July 2018

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14 July 2018

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14 July 2018

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PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes

14 July 2018

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14 July 2018

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A computational analysis of whole-genome expression data reveals chromosomal domains of gene expression

14 July 2018

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14 July 2018

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14 July 2018

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Gene expression analyses reveal molecular relationships among 20 regions of the human CNS.

14 July 2018

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Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001097

Integrated detection and population-genetic analysis of SNPs and copy number variation

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1001097

10.1371/JOURNAL.PGEN.1001097

21 January 2018

Identifiers

DOI

1 reference

28 July 2017

1 reference

28 July 2017

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