(Q35145888)

6 August 2017

1 reference

title

Genetics and genomics of behavioral and psychiatric disorders (English)

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6 August 2017

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2

James R Lupski

1 reference

6 August 2017

Ken Inoue

1

1 reference

6 August 2017

1 June 2003

1 reference

Current Opinion in Genetics & Development

6 August 2017

1 reference

6 August 2017

13

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6 August 2017

303-309

1 reference

6 August 2017

3

1 reference

Genetics. Rethinking behavior genetics

6 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Linkage analysis in psychiatric disorders: the emerging picture

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Genetics of austim: complex aetiology for a heterogeneous disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Association studies of bipolar disorder.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Molecular linkage studies of bipolar disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Psychiatric disorders and mutations at the Wolfram syndrome locus

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Aggressive behavior and altered amounts of brain serotonin and norepinephrine in mice lacking MAOA

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Role of genotype in the cycle of violence in maltreated children

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Evidence for positive selection and population structure at the human MAO-A gene

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

A forkhead-domain gene is mutated in a severe speech and language disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

FOXP2 is not a major susceptibility gene for autism or specific language impairment

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Evaluation of FOXP2 as an autism susceptibility gene

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Molecular evolution of FOXP2, a gene involved in speech and language

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Serotonin transporter genetic variation and the response of the human amygdala

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Genetic perspectives on the serotonin transporter

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

The BDNF val66met polymorphism affects activity-dependent secretion of BDNF and human memory and hippocampal function

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Linkage and linkage disequilibrium mapping of ERP and EEG phenotypes

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Familial transmission of risk factors in the first-degree relatives of schizophrenic people

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Genetics of event-related brain potentials in response to a semantic priming paradigm in families with a history of alcoholism

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Association of promoter variants in the alpha7 nicotinic acetylcholine receptor subunit gene with an inhibitory deficit found in schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Endophenotypes in bipolar disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Molecular mechanisms for genomic disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Genome architecture, rearrangements and genomic disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Schizophrenia and velo-cardio-facial syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Prefrontal neurons and the genetics of schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

A highly significant association between a COMT haplotype and schizophrenia.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Genetic variation in the 22q11 locus and susceptibility to schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Deletion of 150 kb in the minimal DiGeorge/velocardiofacial syndrome critical region in mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Molecular genetics and animal models in autistic disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Association between a GABRB3 polymorphism and autism.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Genetic basis of anxiety-like behaviour: a critical review

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

A Polymorphic Genomic Duplication on Human Chromosome 15 Is a Susceptibility Factor for Panic and Phobic Disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Failure to find DUP25 in patients with anxiety disorders, in control individuals, or in previously reported positive control cell lines.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Mouse models for psychiatric disorders.

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Mouse genetic models for prepulse inhibition: an early review

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Targeted gene mutation approaches to the study of anxiety-like behavior in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Genetic animal models: focus on schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Neuregulin 1 and susceptibility to schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Association of neuregulin 1 with schizophrenia confirmed in a Scottish population

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Mice with reduced NMDA receptor expression display behaviors related to schizophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

QTL analysis and genomewide mutagenesis in mice: complementary genetic approaches to the dissection of complex traits

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Complex-trait genetics: emergence of multivariate strategies

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Using mouse models to dissect the genetics of obesity

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Capitalizing on large-scale mouse mutagenesis screens

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

The other, forgotten genome: mitochondrial DNA and mental disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0959-437X%2803%2900057-1

7 January 2021

10.1016/S0959-437X(03)00057-1

Identifiers

DOI

1 reference

release_as3ahstg4vbmjaxoazgupvrxvu

6 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/as3ahstg4vbmjaxoazgupvrxvu

24 November 2022

mapped directly with Wikidata item

PubMed ID

12787794

1 reference

PubMed ID

12787794