(Q50313353)

2 March 2018

title

Association of DISC1 with autism and Asperger syndrome. (English)

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2 March 2018

Leena Helena Kilpinen-Barrett

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1

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2 March 2018

William Hennah

3

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2 March 2018

Teppo Varilo

5

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2 March 2018

author name string

Ylisaukko-Oja T

2

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2 March 2018

Palo OM

4

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2 March 2018

Vanhala R

6

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2 March 2018

Nieminen-von Wendt T

7

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2 March 2018

von Wendt L

8

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2 March 2018

Paunio T

9

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2 March 2018

Peltonen L

10

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2 March 2018

language of work or name

English

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publication date

19 June 2007

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2 March 2018

published in

Molecular Psychiatry

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2 March 2018

volume

13

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2 March 2018

issue

2

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2 March 2018

page(s)

187-196

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2 March 2018

https://scigraph.springernature.com/pub.10.1038/sj.mp.4002031

exact match

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cites work

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Replication of 1q42 linkage in Finnish schizophrenia pedigrees

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A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophrenia.

21 January 2018

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Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects

21 January 2018

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Variation in DISC1 affects hippocampal structure and function and increases risk for schizophrenia

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Association of DISC1/TRAX haplotypes with schizophrenia, reduced prefrontal gray matter, and impaired short- and long-term memory

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Disrupted in schizophrenia 1 (DISC1): association with schizophrenia, schizoaffective disorder, and bipolar disorder

21 January 2018

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Association between the TRAX/DISC locus and both bipolar disorder and schizophrenia in the Scottish population

21 January 2018

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Genetic association between schizophrenia and the DISC1 gene in the Scottish population.

21 January 2018

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A frameshift mutation in Disrupted in Schizophrenia 1 in an American family with schizophrenia and schizoaffective disorder

21 January 2018

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Impact of the DISC1 Ser704Cys polymorphism on risk for major depression, brain morphology and ERK signaling.

21 January 2018

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Association between genotype at an exonic SNP in DISC1 and normal cognitive aging.

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DISC1 and neurocognitive function in schizophrenia.

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Genomic structure and localisation within a linkage hotspot of Disrupted In Schizophrenia 1, a gene disrupted by a translocation segregating with schizophrenia.

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

21 January 2018

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DISC1 (Disrupted in Schizophrenia-1) is expressed in limbic regions of the primate brain.

21 January 2018

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Disrupted in Schizophrenia 1 and Nudel form a neurodevelopmentally regulated protein complex: implications for schizophrenia and other major neurological disorders

21 January 2018

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Yeast two-hybrid screens implicate DISC1 in brain development and function

21 January 2018

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Disrupted-In-Schizophrenia 1, a candidate gene for schizophrenia, participates in neurite outgrowth

21 January 2018

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DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL: regulation and loss of interaction with mutation

21 January 2018

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DISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signaling

21 January 2018

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21 January 2018

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21 January 2018

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A screening questionnaire for Asperger syndrome and other high-functioning autism spectrum disorders in school age children.

21 January 2018

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Asperger Syndrome?Some Epidemiological Considerations: A Research Note

21 January 2018

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The Asperger Syndrome (and high-functioning autism) Diagnostic Interview (ASDI): a preliminary study of a new structured clinical interview.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002031

Genome-wide scan for loci of Asperger syndrome

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002031

Independent replication and initial fine mapping of 3p21-24 in Asperger syndrome.

21 January 2018

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A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27

21 January 2018

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Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland

21 January 2018

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Use of population isolates for mapping complex traits

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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21 January 2018

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Evidence that a DISC1 frame-shift deletion associated with psychosis in a single family may not be a pathogenic mutation.

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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21 January 2018

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Ten-year follow-up of adolescent-onset anorexia nervosa: personality disorders

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002031

Children with schizophrenia spectrum and depressive disorders: a comparative study of premorbid adjustment, onset pattern and severity of impairment.

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002031

Correlation of family history with specific autistic subgroups: Asperger's syndrome and bipolar affective disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002031

A family history study of Asperger syndrome

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002031

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002031

Genes and schizophrenia: beyond schizophrenia: the role of DISC1 in major mental illness

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002031

Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002031

Identification of a novel neuroligin in humans which binds to PSD-95 and has a widespread expression

21 January 2018

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A novel multiple PDZ domain-containing molecule interacting with N-methyl-D-aspartate receptors and neuronal cell adhesion proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002031

Binding of neuroligins to PSD-95

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002031

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002031

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002031

Autism as a strongly genetic disorder: evidence from a British twin study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002031

7 January 2021

The epidemiology of Asperger syndrome. A total population study

1 reference

https://api.crossref.org/works/10.1038%2FSJ.MP.4002031

7 January 2021

Pre-morbid adjustment and personality in psychosis. Effects of sex and diagnosis

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002031

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Genetics. Two genes link two distinct psychoses

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Localization of postsynaptic density-93 to dendritic microtubules and interaction with microtubule-associated protein 1A

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Identification of a novel neuroligin in humans which binds to PSD-95 and has a widespread expression

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https://api.crossref.org/works/10.1038%2FSJ.MP.4002031

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Identifiers

DOI

10.1038/SJ.MP.4002031

1 reference

2 March 2018

1 reference

2 March 2018