(Q34447169)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385368%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

title

Schizophrenia genetics: emerging themes for a complex disorder (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385368%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

0 references

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385368%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

Katherine E. Tansey

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385368%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

author name string

D H Kavanagh

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385368%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

M J Owen

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385368%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

language of work or name

English

0 references

publication date

11 November 2014

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385368%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385368%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

volume

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385368%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

page(s)

72-76

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385368%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385368%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/mp.2014.148

22 February 2020

exact match

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

Genome-wide association study of schizophrenia in a Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

Genetic architectures of psychiatric disorders: the emerging picture and its implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

21 January 2018

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GCTA: a tool for genome-wide complex trait analysis

21 January 2018

1 reference

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Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.

21 January 2018

1 reference

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CNVs: harbingers of a rare variant revolution in psychiatric genetics

21 January 2018

1 reference

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Strong association of de novo copy number mutations with sporadic schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

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

21 January 2018

1 reference

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Analysis of copy number variations at 15 schizophrenia-associated loci.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

Copy number variation in schizophrenia in Sweden

21 January 2018

1 reference

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Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

A copy number variation morbidity map of developmental delay

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

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.2014.148

Phenotypic variability and genetic susceptibility to genomic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

The penetrance of copy number variations for schizophrenia and developmental delay.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

Biological insights from 108 schizophrenia-associated genetic loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

Validating therapeutic targets through human genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

An integrated encyclopedia of DNA elements in the human genome

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2014.148

Is there a flame in the brain in psychosis?

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2014.148

De novo mutations in schizophrenia implicate synaptic networks

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

A polygenic burden of rare disruptive mutations in schizophrenia

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2014.148

De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

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.2014.148

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.2014.148

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.2014.148

De Novo Gene Disruptions in Children on the Autistic Spectrum

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2014.148

Diagnostic exome sequencing in persons with severe intellectual disability

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2014.148

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2014.148

A comprehensive assessment of parental age and psychiatric disorders

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2014.148

De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

The Research Domain Criteria: moving the goalposts to change the game.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

Progress in the genetics of polygenic brain disorders: significant new challenges for neurobiology

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2014.148

ZFN, TALEN, and CRISPR/Cas-based methods for genome engineering

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2014.148

CRISPR/Cas9 for genome editing: progress, implications and challenges.

21 January 2018

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https://api.crossref.org/works/10.1038%2FMP.2014.148

The challenges and promise of neuroimaging in psychiatry

21 January 2018

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

21 January 2018

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12 December 2020

Increased exonic de novo mutation rate in individuals with schizophrenia

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12 December 2020

Common variants conferring risk of schizophrenia

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12 December 2020

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

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12 December 2020

Linking the SWI/SNF complex to prostate cancer.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2014.148

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/MP.2014.148

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25385368%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

1 reference