(Q22242872)

PubMed

28 March 2023

N. M. Williams

series ordinal

2

author given names

Nigel M

author last names

Williams

1 reference

PubMed

28 March 2023

M. J. Owen

series ordinal

3

author given names

Michael J

author last names

Owen

1 reference

PubMed

Searching for schizophrenia genes

28 March 2023

language of work or name

English

0 references

publication date

2 September 2003

0 references

published in

Human Molecular Genetics

0 references

volume

12

0 references

issue

suppl 2

0 references

page(s)

R125-R133

0 references

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Is there really a split in schizophrenia? The genetic evidence

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Large upward bias in estimation of locus-specific effects from genomewide scans

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Genome scan meta-analysis of schizophrenia and bipolar disorder, part I: Methods and power analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

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%2FDDG302

Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Identification of a high-risk haplotype for the dystrobrevin binding protein 1 (DTNBP1) gene in the Irish study of high-density schizophrenia families

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Dysbindin, a novel coiled-coil-containing protein that interacts with the dystrobrevins in muscle and brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Different dystrophin-like complexes are expressed in neurons and glia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Neuregulin 1 and susceptibility to schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Association of neuregulin 1 with schizophrenia confirmed in a Scottish population

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Support for genetic variation in neuregulin 1 and susceptibility to schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Glial growth factor/neuregulin inhibits Schwann cell myelination and induces demyelination

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Cell death in the Schwann cell lineage and its regulation by neuregulin

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

GGF/neuregulin is a neuronal signal that promotes the proliferation and survival and inhibits the differentiation of oligodendrocyte progenitors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

White matter changes in schizophrenia: evidence for myelin-related dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

The glial growth factors deficiency and synaptic destabilization hypothesis of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Genome-wide expression analysis reveals dysregulation of myelination-related genes in chronic schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

D-Amino acid oxidase: new findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

d -serine and serine racemase are present in the vertebrate retina and contribute to the physiological activation of NMDA receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Chromosomal abnormalities and schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Genetics of schizophrenia and the new millennium: progress and pitfalls

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Chromosomal abnormalities and mental illness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

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/10.1093%2FHMG%2FDDG302

A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Identification of polymorphisms within Disrupted in Schizophrenia 1 and Disrupted in Schizophrenia 2, and an investigation of their association with schizophrenia and bipolar affective disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

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%2FDDG302

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Candidate-gene association studies of schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Association between schizophrenia and homozygosity at the dopamine D3 receptor gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Positive association between a DNA sequence variant in the serotonin 2A receptor gene and schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Association between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Association and linkage analyses of RGS4 polymorphisms in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Analysis of complex brain disorders with gene expression microarrays: schizophrenia as a disease of the synapse

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Disease-specific changes in regulator of G-protein signaling 4 (RGS4) expression in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Soluble and particulate forms of rat catechol-O-methyltransferase distinguished by gel electrophoresis and immune fixation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Genomic organization of the human catechol O-methyltransferase gene and its expression from two distinct promoters

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Kinetics of human soluble and membrane-bound catechol O-methyltransferase: a revised mechanism and description of the thermolabile variant of the enzyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Association analysis of a functional catechol-o-methyltransferase gene polymorphism in schizophrenic patients in Taiwan

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

A functional polymorphism in the COMT gene and performance on a test of prefrontal cognition

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

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%2FDDG302

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

A family-based association study of T1945C polymorphism in the proline dehydrogenase gene and schizophrenia in the Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Genes for schizophrenia? Recent findings and their pathophysiological implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Genomewide multipoint linkage analysis of seven extended Palauan pedigrees with schizophrenia, by a Markov-chain Monte Carlo method

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Suggestive evidence for a schizophrenia susceptibility locus on chromosome 6q and a confirmation in an independent series of pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

NIMH Genetics Initiative Millenium Schizophrenia Consortium: linkage analysis of African-American pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

No evidence for association of the dysbindin gene [DTNBP1] with schizophrenia in an Irish population-based study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

Genome-wide scan for linkage to schizophrenia in a Spanish-origin cohort from Costa Rica

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

7 January 2021

Late‐Onset psychosis in the velo‐cardio‐facial syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

7 January 2021

Additional support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6 and 8

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

7 January 2021

Genome scan of European-American schizophrenia pedigrees: Results of the NIMH genetics initiative and millennium consortium

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

7 January 2021

Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

7 January 2021

Cis-acting variation in the expression of a high proportion of genes in human brain

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

7 January 2021

Association study of a functional catechol-O-methyltransferase gene polymorphism in Japanese schizophrenics

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

7 January 2021

Schizophrenia spectrum disorders: an autosomal-wide scan in multiplex pedigrees

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

7 January 2021

An international two–stage genome–wide search for schizophrenia susceptibility genes

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

7 January 2021

Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

7 January 2021

A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

7 January 2021

Support for the MnlI polymorphism of SNAP25; a Korean ADHD case-control study

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

7 January 2021

Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

7 January 2021

Preferential transmission of the high activity allele of COMT in schizophrenia

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

7 January 2021

Catechol-O-methyltransferase polymorphisms and schizophrenia: a transmission disequilibrium study in multiply affected families

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

7 January 2021

Characterization of membrane-bound and soluble catechol-O-methyltransferase from human frontal cortex

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

7 January 2021

No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDG302

7 January 2021

Identifiers

DOI

10.1093/HMG/DDG302

1 reference

Consolidated OpenCitations Corpus – April 2017

release_d62qecth4vf7poggxoliibbczi

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/d62qecth4vf7poggxoliibbczi

24 November 2022

mapped directly with Wikidata item

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017