Association of DISC1 with autism and Asperger syndrome (Q50313353)

2 March 2018

title

Association of DISC1 with autism and Asperger syndrome (English)

1 reference

2 March 2018

Leena Helena Kilpinen-Barrett

0 references

0 references

1 reference

2 March 2018

William Hennah

1 reference

2 March 2018

Teppo Varilo

1 reference

2 March 2018

author name string

Ylisaukko-Oja T

1 reference

2 March 2018

Palo OM

1 reference

2 March 2018

Vanhala R

1 reference

2 March 2018

Nieminen-von Wendt T

1 reference

2 March 2018

von Wendt L

1 reference

2 March 2018

Paunio T

1 reference

2 March 2018

Peltonen L

1 reference

2 March 2018

language of work or name

English

0 references

publication date

19 June 2007

1 reference

2 March 2018

published in

Molecular Psychiatry

1 reference

2 March 2018

volume

1 reference

2 March 2018

issue

1 reference

2 March 2018

page(s)

187-196

1 reference

2 March 2018

Pervasive Developmental Disorders in Preschool Children

cites work

1 reference

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

The prevalence of autism spectrum disorders. Recent evidence and future challenges

21 January 2018

1 reference

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

Prevalence of autism in a US metropolitan area

21 January 2018

1 reference

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

Infantile autism: a genetic study of 21 twin pairs

21 January 2018

1 reference

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

A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden

21 January 2018

1 reference

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

Genetics of austim: complex aetiology for a heterogeneous disorder

21 January 2018

1 reference

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

The Epidemiology of Asperger Syndrome

21 January 2018

1 reference

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

Autism: towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives

21 January 2018

1 reference

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

Autism and Asperger syndrome: coexistence with other clinical disorders

21 January 2018

1 reference

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

Association within a family of a balanced autosomal translocation with major mental illness

21 January 2018

1 reference

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

Chromosome 1 loci in Finnish schizophrenia families

21 January 2018

1 reference

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

Replication of 1q42 linkage in Finnish schizophrenia pedigrees

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

DISC1 and neurocognitive function in schizophrenia.

21 January 2018

1 reference

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

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/10.1038%2FSJ.MP.4002031

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

1 reference

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

Disrupted-in-Schizophrenia-1 (DISC-1): mutant truncation prevents binding to NudE-like (NUDEL) and inhibits neurite outgrowth

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Autism: a window onto the development of the social and the analytic brain

21 January 2018

1 reference

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

Executive function deficits in autism spectrum disorders and attention-deficit/hyperactivity disorder: examining profiles across domains and ages

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Asperger Syndrome?Some Epidemiological Considerations: A Research Note

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Genome-wide scan for loci of Asperger syndrome

21 January 2018

1 reference

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

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Use of population isolates for mapping complex traits

21 January 2018

1 reference

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

A general method for isolation of high molecular weight DNA from eukaryotes

21 January 2018

1 reference

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

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

21 January 2018

1 reference

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

The family based association test method: strategies for studying general genotype--phenotype associations.

21 January 2018

1 reference

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

A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission

21 January 2018

1 reference

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

Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified

21 January 2018

1 reference

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

Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Contested boundaries of bipolar disorder and the limits of categorical diagnosis in psychiatry

21 January 2018

1 reference

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

Spatial working memory in Asperger's syndrome and in patients with focal frontal and temporal lobe lesions

21 January 2018

1 reference

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

Maturation of executive function in autism

21 January 2018

1 reference

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

A chart review of schizotypal personality disorders in children

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

1 reference

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

1 reference

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

1 reference

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

1 reference

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

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

1 reference

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

7 January 2021

Genetics. Two genes link two distinct psychoses

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

Identifiers

DOI

10.1038/SJ.MP.4002031

1 reference

2 March 2018

1 reference

2 March 2018