(Q36496092)

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Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.

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scholarly article

1 reference

Europe PubMed Central

14 August 2017

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC. (English)

1 reference

Europe PubMed Central

14 August 2017

genome-wide association study

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corrigendum / erratum

Erratum: Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC

1 reference

10.1038/MP.2012.89

12 July 2019

http://api.crossref.org/works?select=update-to&filter=doi:10.1038/MP.2012.89

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Europe PubMed Central

14 August 2017

Michael C O'Donovan

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Katherine Gordon-Smith

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K Gordon-Smith

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Detelina Grozeva

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D Grozeva

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A Corvin

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P Holmans

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E Green

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Europe PubMed Central

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Wellcome Trust Case Control Consortium 2

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Wellcome Trust Case Control Consortium 2

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Europe PubMed Central

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Kenneth Kendler

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K S Kendler

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Europe PubMed Central

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G. Bragi Walters

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J T R Walters

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Europe PubMed Central

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Derek W. Morris

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D Morris

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B Riley

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N Craddock

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author name string

M L Hamshere

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Europe PubMed Central

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A L Richards

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L Forty

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L Jones

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F A O'Neill

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P Sklar

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S Purcell

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Europe PubMed Central

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J Kranz

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Europe PubMed Central

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Schizophrenia Psychiatric Genome-wide Association Study Consortium

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Wellcome Trust Case Control Consortium+

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Europe PubMed Central

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M J Owen

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I Jones

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Europe PubMed Central

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R Smith

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language of work or name

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publication date

22 May 2012

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Molecular Psychiatry

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Europe PubMed Central

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708-712

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Europe PubMed Central

14 August 2017

https://scigraph.springernature.com/pub.10.1038/mp.2012.67

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Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia

1 reference

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30 September 2017

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724864

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Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

1 reference

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30 September 2017

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

1 reference

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30 September 2017

Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724864

30 September 2017

Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724864

30 September 2017

A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724864

30 September 2017

Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders

1 reference

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30 September 2017

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724864

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724864

30 September 2017

Common variants conferring risk of schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724864

30 September 2017

Nephronophthisis: disease mechanisms of a ciliopathy

1 reference

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30 September 2017

Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724864

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724864

30 September 2017

Identification of loci associated with schizophrenia by genome-wide association and follow-up

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724864

30 September 2017

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724864

30 September 2017

The surprisingly rich contours of schizophrenia epidemiology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724864

30 September 2017

Evaluation of diagnostic procedures in Swedish patients with schizophrenia and related psychoses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724864

30 September 2017

Reliability of clinical ICD-10 schizophrenia diagnoses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724864

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724864

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724864

30 September 2017

The neuropathology of schizophrenia. A critical review of the data and their interpretation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724864

30 September 2017

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe.

1 reference

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21 September 2018

Initial diagnosis and treatment in first-episode psychosis: can an operationalized diagnostic classification system enhance treating clinicians' diagnosis and the treatment chosen?

1 reference

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Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4724864

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Genome-wide association study identifies five new schizophrenia loci

1 reference

https://api.crossref.org/works/10.1038%2FMP.2012.67

21 January 2018

Identifiers

10.1038/MP.2012.67

1 reference

Europe PubMed Central

14 August 2017

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1 reference

Europe PubMed Central

14 August 2017

1 reference

Europe PubMed Central

14 August 2017

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