Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1. (Q34593858)

3 August 2017

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

1 reference

3 August 2017

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9

1 reference

3 August 2017

3

Tero Hiekkalinna

1 reference

Leena Helena Kilpinen-Barrett

3 August 2017

10

Tiina Paunio

0 references

Helena Kilpinen

5

0 references

William Hennah

William Hennah

1

0 references

Leena Peltonen-Palotie

13

Leena Peltonen

1 reference

3 August 2017

8

Kaisa Silander

1 reference

PubMed ID

17185386

Annamari Tuulio-Henriksson

3 August 2017

7

Annamari Tuulio-Henriksson

1 reference

3 August 2017

12

Jouko Lönnqvist

1 reference

3 August 2017

4

Outi M Palo

1 reference

3 August 2017

6

Jesper Ekelund

1 reference

3 August 2017

Liisa Tomppo

2

1 reference

PubMed ID

17185386

3 August 2017

Joseph D Terwilliger

11

1 reference

3 August 2017

21 December 2006

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3 August 2017

10

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published in

Human Molecular Genetics

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3 August 2017

16

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3 August 2017

5

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3 August 2017

453-462

1 reference

The genetic epidemiology of schizophrenia in a Finnish twin cohort. A population-based modeling study

3 August 2017

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

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%2FDDL462

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

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/10.1093%2FHMG%2FDDL462

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/10.1093%2FHMG%2FDDL462

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

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/10.1093%2FHMG%2FDDL462

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/10.1093%2FHMG%2FDDL462

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

DISC1 and neurocognitive function in schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

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/10.1093%2FHMG%2FDDL462

Heritability and number of quantitative trait loci of neurocognitive functions in families with schizophrenia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

Familial loading associates with impairment in visual span among healthy siblings of schizophrenia patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

A schizophrenia-associated mutation of DISC1 perturbs cerebral cortex development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

Chromosome 1 loci in Finnish schizophrenia families

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

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%2FDDL462

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%2FDDL462

Replication of 1q42 linkage in Finnish schizophrenia pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

Partial trisomy chromosome 5 cosegregating with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

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/10.1093%2FHMG%2FDDL462

Evidence of susceptibility loci on 4q32 and 16p12 for bipolar disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

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%2FDDL462

Neuregulin 1 and susceptibility to schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

Positive associations of polymorphisms in the metabotropic glutamate receptor type 3 gene (GRM3) with schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

A decrease of reelin expression as a putative vulnerability factor in schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

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/10.1093%2FHMG%2FDDL462

Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

A general test of association for quantitative traits in nuclear families

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

A haplotype map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

LIS1 and dynein motor function in neuronal migration and development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

Targeted mutagenesis of Lis1 disrupts cortical development and LIS1 homodimerization

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

Mitotic spindle regulation by Nde1 controls cerebral cortical size

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

Left hippocampal volume as a vulnerability indicator for schizophrenia: a magnetic resonance imaging morphometric study of nonpsychotic first-degree relatives.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

Cortex mapping reveals regionally specific patterns of genetic and disease-specific gray-matter deficits in twins discordant for schizophrenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

The cyclic AMP system and Drosophila learning.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

Clinical phenotype of schizophrenia in a Finnish isolate.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

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%2FDDL462

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%2FDDL462

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%2FDDL462

Localization of a susceptibility locus for schizophrenia on chromosome 5

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL462

21 January 2018

Identifiers

DOI

10.1093/HMG/DDL462

1 reference

3 August 2017

1 reference

PubMed ID

17185386