Schizophrenia genetics: putting all the pieces together (Q37997954)

26 August 2017

0 references

Schizophrenia genetics: putting all the pieces together (English)

1 reference

26 August 2017

0 references

3

Guy A Rouleau

0 references

Patrick A Dion

series ordinal

2

object named as

Patrick A Dion

1 reference

26 August 2017

1

Simon L Girard

1 reference

26 August 2017

language of work or name

1 reference

1 June 2012

1 reference

Current Neurology and Neuroscience Reports

26 August 2017

published in

1 reference

26 August 2017

volume

12

1 reference

26 August 2017

issue

3

1 reference

26 August 2017

page(s)

261-266

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

26 August 2017

1 reference

A Danish Twin Study of Schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Schizophrenia in the National Academy of Sciences-National Research Council Twin Registry: a 16-year update.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Twin concordance for DSM-III-R schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

The genetic epidemiology of schizophrenia in a Finnish twin cohort. A population-based modeling study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Heritability estimates for psychotic disorders: the Maudsley twin psychosis series

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Linkage studies of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Neuregulin 1 and susceptibility to schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Disrupted-in-Schizophrenia-1 expression is regulated by beta-site amyloid precursor protein cleaving enzyme-1-neuregulin cascade

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Disruption of two novel genes by a translocation co-segregating with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Understanding the role of DISC1 in psychiatric disease and during normal development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Case-control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

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/10.1007%2FS11910-012-0266-7

A genome-wide association study in 574 schizophrenia trios using DNA pooling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Genomewide association for schizophrenia in the CATIE study: results of stage 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Replication of association between schizophrenia and ZNF804A in the Irish Case-Control Study of Schizophrenia sample

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Genome-wide association study identifies a susceptibility locus for schizophrenia in Han Chinese at 11p11.2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Genome-wide association study identifies five new schizophrenia loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Epigenetic silencing of miR-137 is an early event in colorectal carcinogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

miR-137 targets Cdc42 expression, induces cell cycle G1 arrest and inhibits invasion in colorectal cancer cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

miR-124 and miR-137 inhibit proliferation of glioblastoma multiforme cells and induce differentiation of brain tumor stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

miRNA 34a, 100, and 137 modulate differentiation of mouse embryonic stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Strong association of de novo copy number mutations with sporadic schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Rare chromosomal deletions and duplications increase risk of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Large recurrent microdeletions associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Microdeletions of 3q29 confer high risk for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Microduplications of 16p11.2 are associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

High frequencies of de novo CNVs in bipolar disorder and schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

De novo truncating mutation in Kinesin 17 associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Direct measure of the de novo mutation rate in autism and schizophrenia cohorts

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Exome sequencing supports a de novo mutational paradigm for schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

A de novo paradigm for mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Support for involvement of neuregulin 1 in schizophrenia pathophysiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-012-0266-7

Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

21 January 2018

1 reference

12 December 2020

Increased exonic de novo mutation rate in individuals with schizophrenia

1 reference

12 December 2020

Expanding the range of ZNF804A variants conferring risk of psychosis

1 reference

12 December 2020

The potential role of major histocompatibility complex class I in schizophrenia

1 reference

12 December 2020

Sequential strategy to identify a susceptibility gene for schizophrenia: report of potential linkage on chromosome 22q12-q13.1: Part 1

1 reference

12 December 2020

Common variants conferring risk of schizophrenia

1 reference

12 December 2020

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

1 reference

12 December 2020

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

1 reference

12 December 2020

Knockdown of the psychosis susceptibility gene ZNF804A alters expression of genes involved in cell adhesion.

1 reference

12 December 2020

10.1007/S11910-012-0266-7

Identifiers

DOI

1 reference

26 August 2017

1 reference