Pathways-based analyses of whole-genome association study data in bipolar disorder reveal genes mediating ion channel activity and synaptic neurotransmission (Q33389202)

From Wikidata

Jump to navigation Jump to search

scientific article

Language	Label	Description	Also known as
English	Pathways-based analyses of whole-genome association study data in bipolar disorder reveal genes mediating ion channel activity and synaptic neurotransmission	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Pathways-based analyses of whole-genome association study data in bipolar disorder reveal genes mediating ion channel activity and synaptic neurotransmission (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

bipolar disorder

1 reference

based on heuristic

inferred from title

whole genome sequencing

1 reference

based on heuristic

inferred from title

3

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Kathleen D Askland

object named as

Kathleen Askland

1

0 references

3

object named as

Jason Moore

0 references

author name string

Cynthia Read

2

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Kathleen Askland

1

0 references

publication date

4 December 2008

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

125

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

63-79

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activity of Erythrocyte Na,K-ATPase in Manic Patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exploratory visual analysis of pharmacogenomic results.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Strong association of de novo copy number mutations with autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of voltage-gated ion channels in mammalian brain

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The neuron as a dynamic electrogenic machine: modulation of sodium-channel expression as a basis for functional plasticity in neurons

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contribution of Na+,K(+)-ATPase to focal epilepsy: a brief review.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The MAOA promoter polymorphism, disruptive behavior disorders, and early onset substance use disorder: gene-environment interaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Erythrocyte sodium pump activity in bipolar affective disorder and other psychiatric disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Towards understanding the schizophrenia code: an expanded convergent functional genomics approach

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular diversity of voltage-gated sodium channel alpha subunits expressed in neuronal and non-neuronal excitable cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RefSeq and LocusLink: NCBI gene-centered resources

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Candidate gene studies of bipolar disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Visual analysis of statistical results from microarray studies of human breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extending pathways based on gene lists using InterPro domain signatures

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of family-based association tests in chromosome regions selected by linkage-based confidence intervals

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Synaptic clefts are made to be crossed: neurotransmitter signaling in the central nervous system

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

GEFs: master regulators of G-protein activation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Calcium channel mutations and migraine

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in human monoamine-related neurotransmitter pathway genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A network of dopaminergic gene variations implicated as risk factors for schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathway-based approaches for analysis of genomewide association studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Toward a biaxial model of "bipolar" affective disorders: spectrum phenotypes as the products of neuroelectrical and neurochemical alterations

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparative immunohistochemical distribution of three small-conductance Ca2+-activated potassium channel subunits, SK1, SK2, and SK3 in mouse brain

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscarinic acetylcholine neurotransmission enhances the late-phase of long-term potentiation in the hippocampal-prefrontal cortex pathway of rats in vivo: a possible involvement of monoaminergic systems.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifying a series of candidate genes for mania and psychosis: a convergent functional genomics approach

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Convergent Functional Genomics of bipolar disorder: from animal model pharmacogenomics to human genetics and biomarkers.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The success of the genome-wide association approach: a brief story of a long struggle

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linked gene ontology categories are novel and differ from associated gene ontology categories for the bipolar disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The functional significance of neurotransmitter diversity

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Candidate genes, pathways and mechanisms for bipolar (manic-depressive) and related disorders: an expanded convergent functional genomics approach

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Schizophrenia: a common disease caused by multiple rare alleles

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bioinformatic analysis of human CNS-expressed ion channels as candidates for episodic nervous system disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A highly polymorphic poly-glutamine stretch in the potassium channel KCNN3 in migraine.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rare variants of the gene encoding the potassium chloride co-transporter 3 are associated with bipolar disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Toward a biaxial model of "bipolar" affective disorders: further exploration of genetic, molecular and cellular substrates.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HuGE Watch: tracking trends and patterns of published studies of genetic association and human genome epidemiology in near-real time

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure-functional diversity of human L-type Ca2+ channel: perspectives for new pharmacological targets

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Migraine as a complex disease: heterogeneity, comorbidity and genotype-phenotype interactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential expression of the small-conductance, calcium-activated potassium channel SK3 is critical for pacemaker control in dopaminergic midbrain neurons.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel ATP1A2 gene mutation in an Irish familial hemiplegic migraine kindred.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alcohol dependence and polymorphisms of serotonin-related genes: association studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phylogeny of ion channels: clues to structure and function

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of voltage-gated sodium channels in movement disorders and epilepsy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Whole-genome association study of bipolar disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sodium channels and their genes: dynamic expression in the normal nervous system, dysregulation in disease states(1).

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unzipping ion channels

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exploratory Visual Analysis of statistical results from microarray experiments comparing high and low grade glioma

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heritability estimates for psychotic disorders: the Maudsley twin psychosis series

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human small conductance calcium-regulated potassium channel gene (hSKCa3) contains two CAG repeats in exon 1, is on chromosome 1q21.3, and shows a possible association with schizophrenia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular pharmacology of non-L-type calcium channels.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for an allelic association between bipolar disorder and a Na+, K+ adenosine triphosphatase alpha subunit gene (ATP1A3).

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ion channel functional candidate genes in multigenic neuropsychiatric disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sodium channels SCN1A, SCN2A and SCN3A in familial autism

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of serotonergic and noradrenergic systems in the pathophysiology of depression and anxiety disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Commonality of functional annotation: a method for prioritization of candidate genes from genome-wide linkage studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

AnkyrinG. A new ankyrin gene with neural-specific isoforms localized at the axonal initial segment and node of Ranvier

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile spasms as an epileptic feature of DEND syndrome associated with an activating mutation in the potassium adenosine triphosphate (ATP) channel, Kir6.2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epigenetic alterations of the dopaminergic system in major psychiatric disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifying the biologically relevant gene categories based on gene expression and biological data: an example on prostate cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diverse functions and dynamic expression of neuronal sodium channels

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathway-based association analysis of genome-wide screening data suggest that genes associated with the gamma-aminobutyric acid receptor signaling pathway are involved in neuroleptic-induced, treatment-resistant tardive dyskinesia

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular evolution of voltage-sensitive ion channel genes: on the origins of electrical excitability

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ion channels and epilepsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

WholePathwayScope: a comprehensive pathway-based analysis tool for high-throughput data

1 reference

https://pubmed.ncbi.nlm.nih.gov/19052778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-008-0600-Y

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q33389202&oldid=2195313114"