Strong evidence that GNB1L is associated with schizophrenia (Q34713665)

4 August 2017

Strong evidence that GNB1L is associated with schizophrenia (English)

1 reference

4 August 2017

0 references

12

1 reference

4 August 2017

15

1 reference

4 August 2017

Dirk Goossens

9

0 references

Kieran Murphy

Kieran C Murphy

14

0 references

Beate St Pourcain

Beate Glaser

2

0 references

Jurgen Del Favero

Jurgen Del Favero

8

0 references

Ina Giegling

11

Ina Giegling

1 reference

4 August 2017

10

Dan Rujescu

1 reference

4 August 2017

Hywel Williams

4

0 references

Valentina Escott-Price

6

Valentina Moskvina

1 reference

4 August 2017

13

Nicholas Craddock

1 reference

4 August 2017

Nigel M Williams

1

1 reference

4 August 2017

Nadine Norton

3

1 reference

4 August 2017

Timothy Pierce

5

1 reference

4 August 2017

Stephen Monks

7

1 reference

4 August 2017

Michael J Owen

16

1 reference

4 August 2017

13 November 2007

1 reference

4 August 2017

Human Molecular Genetics

1 reference

4 August 2017

17

1 reference

4 August 2017

4

1 reference

4 August 2017

555-566

1 reference

Heritability estimates for psychotic disorders: the Maudsley twin psychosis series

4 August 2017

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

A polygenic theory of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Chromosomal microdeletions: dissecting del22q11 syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Chromosome 22 deletion syndrome and schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

High rates of schizophrenia in adults with velo-cardio-facial syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

A survey of the 22q11 microdeletion in a large cohort of schizophrenia patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

A highly significant association between a COMT haplotype and schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

The ZDHHC8 gene did not associate with bipolar disorder or schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Evidence for association between novel polymorphisms in the PRODH gene and schizophrenia in a Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

ZDHHC8 as a candidate gene for schizophrenia: analysis of a putative functional intronic marker in case-control and family-based association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Is COMT a susceptibility gene for schizophrenia?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Association between PRODH and schizophrenia is not confirmed

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Failure to find association between PRODH deletion and schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Lack of association of the COMT (Val158/108 Met) gene and schizophrenia: a meta-analysis of case-control studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

A comprehensive analysis of 22q11 gene expression in the developing and adult brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Isolation and characterization of a novel gene containing WD40 repeats from the region deleted in velo-cardio-facial/DiGeorge syndrome on chromosome 22q11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

GNB1L, a gene deleted in the critical region for DiGeorge syndrome on 22q11, encodes a G-protein beta-subunit-like polypeptide

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Role of TBX1 in human del22q11.2 syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Human studies of prepulse inhibition of startle: normal subjects, patient groups, and pharmacological studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Mutations in TBX1 genocopy the 22q11.2 deletion and duplication syndromes: a new susceptibility factor for mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

PLINK: a tool set for whole-genome association and population-based linkage analyses

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

A haplotype map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Dosage balance in gene regulation: biological implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Best estimate of lifetime psychiatric diagnosis: a methodological study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

SCAN. Schedules for Clinical Assessment in Neuropsychiatry

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

A polydiagnostic application of operational criteria in studies of psychotic illness. Development and reliability of the OPCRIT system

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

A systematic genomewide linkage study in 353 sib pairs with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

The Bipolar Affective Disorder Dimension Scale (BADDS)--a dimensional scale for rating lifetime psychopathology in bipolar spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Comparison of direct interview and family history diagnoses of alcohol dependence.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Mutation analysis of TBX1 in non-deleted patients with features of DGS/VCFS or isolated cardiovascular defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Genomewide Linkage Scan in Schizoaffective Disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Association studies in psychiatric genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Design of Case-controls Studies with Unscreened Controls

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

Comparative sequencing of the proneurotensin gene and association studies in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDM330

21 January 2018

Identifiers

DOI

10.1093/HMG/DDM330

1 reference

4 August 2017

1 reference