Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population. (Q33997189)

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English	Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population.	scientific article

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Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population (English)

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Maarten J Van Den Bossche

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Kristel Van Steen

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Jurgen Del Favero

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Lars-Göran Nilsson

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Lars-Göran Nilsson

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Lotte N Moens

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Wim Glassee

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Sonia De Zutter

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An-Sofie Lenaerts

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Annelie Nordin

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Ignacio Medina Castello

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Karl-Fredrik Norrback

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11 August 2011

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0 references

Neurobiology and phenotypic expression in early onset schizophrenia

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Protein secondary structure appears to be robust under in silico evolution while protein disorder appears not to be.

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5 July 2018

DISC1 splice variants are upregulated in schizophrenia and associated with risk polymorphisms

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5 July 2018

Oligomer assembly of the C-terminal DISC1 domain (640-854) is controlled by self-association motifs and disease-associated polymorphism S704C

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The role of intrinsically unstructured proteins in neurodegenerative diseases

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5 July 2018

Discovery of rare variants via sequencing: implications for the design of complex trait association studies

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Quantification of rare allelic variants from pooled genomic DNA

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New findings from genetic association studies of schizophrenia

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Association of the SerCys DISC1 polymorphism with human hippocampal formation gray matter and function during memory encoding

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Recruitment of PCM1 to the centrosome by the cooperative action of DISC1 and BBS4: a candidate for psychiatric illnesses

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Intrinsically Disordered Proteins in Human Diseases: Introducing the D 2 Concept

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5 July 2018

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

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5 July 2018

No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric genetics

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5 July 2018

Specific developmental disruption of disrupted-in-schizophrenia-1 function results in schizophrenia-related phenotypes in mice

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5 July 2018

The DISC locus in psychiatric illness

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5 July 2018

Disrupted-In-Schizophrenia 1 regulates integration of newly generated neurons in the adult brain

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5 July 2018

Schizophrenia: a common disease caused by multiple rare alleles

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5 July 2018

DISC1 regulates the transport of the NUDEL/LIS1/14-3-3epsilon complex through kinesin-1

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5 July 2018

DISC1 regulates neurotrophin-induced axon elongation via interaction with Grb2

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5 July 2018

A "silent" polymorphism in the MDR1 gene changes substrate specificity

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5 July 2018

Disrupted in Schizophrenia 1 Interactome: evidence for the close connectivity of risk genes and a potential synaptic basis for schizophrenia

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Alternative splicing in concert with protein intrinsic disorder enables increased functional diversity in multicellular organisms

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

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Disrupted in schizophrenia 1: building brains and memories

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A schizophrenia-associated mutation of DISC1 perturbs cerebral cortex development

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

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5 July 2018

A functional link between Disrupted-In-Schizophrenia 1 and the eukaryotic translation initiation factor 3.

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5 July 2018

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

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5 July 2018

A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42

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5 July 2018

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5 July 2018

Disrupted in Schizophrenia 1 (DISC1) is a multicompartmentalized protein that predominantly localizes to mitochondria

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5 July 2018

DISC1 localizes to the centrosome by binding to kendrin

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5 July 2018

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

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5 July 2018

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

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5 July 2018

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

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5 July 2018

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

1 reference

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5 July 2018

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

1 reference

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5 July 2018

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

1 reference

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5 July 2018

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5 July 2018

Intrinsic disorder and protein function

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5 July 2018

Chromosome 1 loci in Finnish schizophrenia families

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5 July 2018

Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements

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5 July 2018

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5 July 2018

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

1 reference

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5 July 2018

Case-control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population.

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21 January 2018

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

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21 January 2018

Replication of 1q42 linkage in Finnish schizophrenia pedigrees.

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21 January 2018

DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorder.

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21 January 2018

Linkage of schizophrenia with chromosome 1q loci in Taiwanese families.

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21 January 2018

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

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21 January 2018

Case-control association study of Disrupted-in-Schizophrenia-1 (DISC1) gene and schizophrenia in the Chinese population.

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21 January 2018

Differential expression of disrupted-in-schizophrenia (DISC1) in bipolar disorder.

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21 January 2018

Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments.

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21 January 2018

Positive association of the Disrupted-in-Schizophrenia-1 gene (DISC1) with schizophrenia in the Chinese Han population.

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21 January 2018

Association between a disrupted-in-schizophrenia 1 (DISC1) single nucleotide polymorphism and schizophrenia in a combined Scandinavian case-control sample.

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21 January 2018

Association of DISC1 with autism and Asperger syndrome.

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21 January 2018

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

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21 January 2018

DISC1 and neurocognitive function in schizophrenia.

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21 January 2018

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

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21 January 2018

Expression of Disrupted-In-Schizophrenia-1, a schizophrenia-associated gene, is prominent in the mouse hippocampus throughout brain development.

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21 January 2018

Expression of DISC1 binding partners is reduced in schizophrenia and associated with DISC1 SNPs

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21 January 2018

Expression of disrupted in schizophrenia 1 (DISC1) protein in the adult and developing mouse brain indicates its role in neurodevelopment.

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21 January 2018

Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure.

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21 January 2018

Identification of high risk DISC1 structural variants with a 2% attributable risk for schizophrenia.

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21 January 2018

GAD1 (2q31.1), which encodes glutamic acid decarboxylase (GAD67), is associated with childhood-onset schizophrenia and cortical gray matter volume loss

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21 January 2018

Polymorphisms in the 13q33.2 gene G72/G30 are associated with childhood-onset schizophrenia and psychosis not otherwise specified.

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21 January 2018

Neuregulin 1 (8p12) and childhood-onset schizophrenia: susceptibility haplotypes for diagnosis and brain developmental trajectories.

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21 January 2018

Dysbindin (DTNBP1, 6p22.3) is associated with childhood-onset psychosis and endophenotypes measured by the Premorbid Adjustment Scale (PAS).

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023450

21 January 2018

The protein trinity--linking function and disorder.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023450

21 January 2018

DISC-1 Leu607Phe alleles differentially affect centrosomal PCM1 localization and neurotransmitter release.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023450

21 January 2018

Genomewide Linkage Scan in Schizoaffective Disorder

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023450

21 January 2018

The role of disorder in interaction networks: a structural analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3154939

29 October 2018

Betula: A Prospective Cohort Study on Memory, Health and Aging

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023450

21 January 2018

The betula prospective cohort study: Memory, health, and aging

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023450

21 January 2018

Genome scan of pedigrees multiply affected with bipolar disorder provides further support for the presence of a susceptibility locus on chromosome 12q23-q24, and suggests the presence of additional loci on 1p and 1q

2 references

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023450

21 January 2018

https://pubmed.ncbi.nlm.nih.gov/21853134

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurobiology of schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/21853134

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abundance of intrinsic disorder in protein associated with cardiovascular disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21853134

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Age at onset and causes of disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21853134

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0023450

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21853134%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

2011PLoSO...623450M

0 references

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21853134%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21853134%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

ResearchGate publication ID

0 references

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