(Q33652520)

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708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits

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scholarly article

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Europe PubMed Central

28 July 2017

708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits (English)

1 reference

Europe PubMed Central

28 July 2017

Peter M. Visscher

24

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Europe PubMed Central

28 July 2017

W. Richard McCombie

26

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Europe PubMed Central

28 July 2017

Kamna Ramakrishnan

object named as

K Ramakrishnan

5

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Douglas Blackwood

25

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D H Blackwood

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28 July 2017

23

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I J Deary

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28 July 2017

author name string

P A Thomson

1

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Europe PubMed Central

28 July 2017

J S Parla

2

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Europe PubMed Central

28 July 2017

A F McRae

3

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Europe PubMed Central

28 July 2017

M Kramer

4

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Europe PubMed Central

28 July 2017

J Yao

6

1 reference

Europe PubMed Central

28 July 2017

D C Soares

7

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Europe PubMed Central

28 July 2017

S McCarthy

8

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Europe PubMed Central

28 July 2017

S W Morris

9

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Europe PubMed Central

28 July 2017

L Cardone

10

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Europe PubMed Central

28 July 2017

S Cass

11

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28 July 2017

E Ghiban

12

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Europe PubMed Central

28 July 2017

W Hennah

13

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Europe PubMed Central

28 July 2017

K L Evans

14

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Europe PubMed Central

28 July 2017

D Rebolini

15

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28 July 2017

J K Millar

16

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Europe PubMed Central

28 July 2017

S E Harris

17

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Europe PubMed Central

28 July 2017

J M Starr

18

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Europe PubMed Central

28 July 2017

D J MacIntyre

19

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Europe PubMed Central

28 July 2017

Generation Scotland

20

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Europe PubMed Central

28 July 2017

A M McIntosh

21

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Europe PubMed Central

28 July 2017

J D Watson

22

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28 July 2017

D J Porteous

27

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28 July 2017

language of work or name

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publication date

4 June 2013

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Europe PubMed Central

28 July 2017

Molecular Psychiatry

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28 July 2017

19

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28 July 2017

6

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Europe PubMed Central

28 July 2017

668-675

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Europe PubMed Central

28 July 2017

copyright license

Creative Commons Attribution 3.0 Unported

4 June 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

https://scigraph.springernature.com/pub.10.1038/mp.2013.68

0 references

An integrated encyclopedia of DNA elements in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Network-assisted investigation of combined causal signals from genome-wide association studies in schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Genetic architectures of psychiatric disorders: the emerging picture and its implications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Exome sequencing and the genetic basis of complex traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

A t(1;11) translocation linked to schizophrenia and affective disorders gives rise to aberrant chimeric DISC1 transcripts that encode structurally altered, deleterious mitochondrial proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

A mega-analysis of genome-wide association studies for major depressive disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Deep resequencing and association analysis of schizophrenia candidate genes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

The DISC1 promoter: characterization and regulation by FOXP2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

DISC1 variants 37W and 607F disrupt its nuclear targeting and regulatory role in ATF4-mediated transcription

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Genetic contributions to stability and change in intelligence from childhood to old age.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

DISC1: Structure, Function, and Therapeutic Potential for Major Mental Illness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Common DISC1 polymorphisms disrupt Wnt/GSK3β signaling and brain development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Linking neurodevelopmental and synaptic theories of mental illness through DISC1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Temporal dynamics and genetic control of transcription in the human prefrontal cortex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

DISC1 at 10: connecting psychiatric genetics and neuroscience

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Genome-wide association studies establish that human intelligence is highly heritable and polygenic

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Meta-analysis indicates that common variants at the DISC1 locus are not associated with schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

DISC1-binding proteins in neural development, signalling and schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

DISC1 in schizophrenia: genetic mouse models and human genomic imaging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Rethinking schizophrenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

A map of human genome variation from population-scale sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Identification of high risk DISC1 protein structural variants in patients with bipolar spectrum disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

The DISC1 Ser704Cys substitution affects centrosomal localization of its binding partner PCM1 in glia in human brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

A method and server for predicting damaging missense mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Insoluble DISC1-Boymaw fusion proteins generated by DISC1 translocation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Meta-analysis of 32 genome-wide linkage studies of schizophrenia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Disrupted in schizophrenia 1 regulates neuronal progenitor proliferation via modulation of GSK3beta/beta-catenin signaling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

The DISC1 pathway modulates expression of neurodevelopmental, synaptogenic and sensory perception genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

SNPnexus: a web database for functional annotation of newly discovered and public domain single nucleotide polymorphisms.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Convergent functional genomics of genome-wide association data for bipolar disorder: comprehensive identification of candidate genes, pathways and mechanisms.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Nuclear DISC1 regulates CRE-mediated gene transcription and sleep homeostasis in the fruit fly.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Mapping short DNA sequencing reads and calling variants using mapping quality scores

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Elucidating the relationship between DISC1, NDEL1 and NDE1 and the risk for schizophrenia: evidence of epistasis and competitive binding

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

The Lothian Birth Cohort 1936: a study to examine influences on cognitive ageing from age 11 to age 70 and beyond

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Isoform-selective susceptibility of DISC1/phosphodiesterase-4 complexes to dissociation by elevated intracellular cAMP levels.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

PLINK: a tool set for whole-genome association and population-based linkage analyses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

DISC1-NDEL1/NUDEL protein interaction, an essential component for neurite outgrowth, is modulated by genetic variations of DISC1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

PMUT: a web-based tool for the annotation of pathological mutations on proteins.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

PANTHER: a library of protein families and subfamilies indexed by function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Chromosomal location and genomic structure of the human translin-associated factor X gene (TRAX; TSNAX) revealed by intergenic splicing to DISC1, a gene disrupted by a translocation segregating with schizophrenia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Sequence and structure-based prediction of eukaryotic protein phosphorylation sites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Natural history of Diagnostic Interview Schedule/DSM-IV major depression. The Baltimore Epidemiologic Catchment Area follow-up

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Family history of depression in clinic and community samples

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031635

21 June 2018

Severe mental disorders in offspring with 2 psychiatrically ill parents.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.68

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.68

21 January 2018

A 1q42 deletion involving DISC1, DISC2, and TSNAX in an autism spectrum disorder.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.68

21 January 2018

Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.68

21 January 2018

DISC1 exon 11 rare variants found more commonly in schizoaffective spectrum cases than controls.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.68

21 January 2018

Genome-wide association study identifies five new schizophrenia loci

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.68

21 January 2018

The severity of mental disorders is linked to interaction among candidate genes.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.68

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.68

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.68

21 January 2018

Disrupted in Schizophrenia-1 regulates intracellular trafficking of mitochondria in neurons.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.68

21 January 2018

Association of DISC1 variants with age of onset in a population-based sample of recurrent major depression.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.68

21 January 2018

Using and understanding RepeatMasker.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.68

21 January 2018

Cognitive ability at age 11 and 70 years, information processing speed, and APOE variation: the Lothian Birth Cohort 1936 study.

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.68

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FMP.2013.68

21 January 2018

Recovery From Major Depression

1 reference

https://pubmed.ncbi.nlm.nih.gov/23732877

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The P-value illusion: how to improve (psychiatric) genetic studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/23732877

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/MP.2013.68

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

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