(Q34713665)

4 August 2017

title

Strong evidence that GNB1L is associated with schizophrenia (English)

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4 August 2017

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4 August 2017

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4 August 2017

Dirk Goossens

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Kieran C Murphy

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Beate Glaser

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Jurgen Del Favero

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Ina Giegling

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4 August 2017

Dan Rujescu

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4 August 2017

Hywel Williams

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Valentina Escott-Price

object named as

Valentina Moskvina

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4 August 2017

Nicholas Craddock

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4 August 2017

Nigel M Williams

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4 August 2017

Nadine Norton

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4 August 2017

Timothy Pierce

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4 August 2017

Stephen Monks

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4 August 2017

Michael J Owen

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4 August 2017

publication date

13 November 2007

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4 August 2017

published in

Human Molecular Genetics

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4 August 2017

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4 August 2017

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4 August 2017

page(s)

555-566

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Heritability estimates for psychotic disorders: the Maudsley twin psychosis series

4 August 2017

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Chromosomal microdeletions: dissecting del22q11 syndrome

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Chromosome 22 deletion syndrome and schizophrenia

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

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

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

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

21 January 2018

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A highly significant association between a COMT haplotype and schizophrenia.

21 January 2018

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

21 January 2018

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

The ZDHHC8 gene did not associate with bipolar disorder or schizophrenia

21 January 2018

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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

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

21 January 2018

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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

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

21 January 2018

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Is COMT a susceptibility gene for schizophrenia?

21 January 2018

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Association between PRODH and schizophrenia is not confirmed

21 January 2018

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Failure to find association between PRODH deletion and schizophrenia

21 January 2018

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Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Isolation and Characterization of a Gene from the DiGeorge Chromosomal Region Homologous to the MouseTbx1Gene

21 January 2018

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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

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Role of TBX1 in human del22q11.2 syndrome

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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

21 January 2018

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A systematic genomewide linkage study in 353 sib pairs with schizophrenia

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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21 January 2018

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21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Genomewide Linkage Scan in Schizoaffective Disorder

21 January 2018

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

21 January 2018

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21 January 2018

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21 January 2018

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Comparative sequencing of the proneurotensin gene and association studies in schizophrenia

21 January 2018

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21 January 2018

Identifiers

DOI

10.1093/HMG/DDM330

1 reference

4 August 2017

1 reference