A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression - Wikidata - awgldk - TriplyDB

A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression

A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression

http://www.wikidata.org/entity/Q35014891

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The genetics of substance dependence Single-neuron and genetic correlates of autistic behavior in macaque.A simple cell-based assay reveals that diverse neuropsychiatric risk genes converge on primary cilia Adjusting family relatedness in data-driven burden test of rare variants What is the impact of genome-wide supported risk variants for schizophrenia and bipolar disorder on brain structure and function? A systematic review.Hematopoietic stem cells exhibit a specific ABC transporter gene expression profile clearly distinct from other stem cells.Assessing the contribution family data can make to case-control studies of rare variants.A data-driven method for identifying rare variants with heterogeneous trait effects.Cohort profile: the Lothian Birth Cohorts of 1921 and 1936.Interferon-gamma-inducible kynurenines/pteridines inflammation cascade: implications for aging and aging-associated psychiatric and medical disorders.A closer look at siblings of patients with schizophrenia: the association of depression history and sex with cognitive phenotypes.ABCA8 stimulates sphingomyelin production in oligodendrocytes.Mitochondria, oligodendrocytes and inflammation in bipolar disorder: evidence from transcriptome studies points to intriguing parallels with multiple sclerosis Schizophrenia gene expression profile reverted to normal levels by antipsychotics Rare nonsynonymous variants in alpha-4 nicotinic acetylcholine receptor gene protect against nicotine dependence.A-Subclass ATP-Binding Cassette Proteins in Brain Lipid Homeostasis and Neurodegeneration.Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia.Resequencing and association analysis of the KALRN and EPHB1 genes and their contribution to schizophrenia susceptibility.Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive Disorder.Overlap between Parkinson disease and Alzheimer disease in ABCA7 functional variants.Association of CHRNA4 polymorphisms with smoking behavior in two populations.Advanced paternal age increases the risk of schizophrenia and obsessive-compulsive disorder in a Chinese Han population.Proteomic Analysis of the Peri-Infarct Area after Human Umbilical Cord Mesenchymal Stem Cell Transplantation in Experimental Stroke.Genomics and pharmacogenomics of schizophrenia.Early life stress paradigms in rodents: potential animal models of depression?Evolution of ABC transporters by gene duplication and their role in human disease.Function and regulation of ABCA1--membrane meso-domain organization and reorganization.Progress in defining the biological causes of schizophrenia.The emerging spectrum of allelic variation in schizophrenia: current evidence and strategies for the identification and functional characterization of common and rare variants.Genomic structural variation in affective, anxiety, and stress-related disorders.Cognitive endophenotypes in a family with bipolar disorder with a risk locus on chromosome 4.Transcriptional regulation of neurodevelopmental and metabolic pathways by NPAS3.Poisson Approximation-Based Score Test for Detecting Association of Rare Variants.Currently recognized genes for schizophrenia: High-resolution chromosome ideogram representation.Expression of the 49 human ATP binding cassette (ABC) genes in pluripotent embryonic stem cells and in early- and late-stage multipotent mesenchymal stem cells: possible role of ABC plasma membrane transporters in maintaining human stem cell pluripo A kainate receptor GluK4 deletion, protective against bipolar disorder, is associated with enhanced cognitive performance across diagnoses in the TwinsUK cohort.Therapeutic Response to Paroxetine in Major Depressive Disorder Predicted by DNA Methylation.Association between the variability of the ABCA13 gene and the risk of major depressive disorder and schizophrenia in the Han Chinese population.The effects of neurological disorder-related codon variations of ABCA13 on the function of the ABC protein.Identification of rare nonsynonymous variants in SYNE1/CPG2 in bipolar affective disorder.

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A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression

http://www.wikidata.org/entity/Q35014891

description

2009 nî lūn-bûn

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2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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A cytogenetic abnormality and ...... polar disorder, and depression

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Alison Condie

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Angela White

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Douglas H R Blackwood

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Margaret van Beck

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Mary P Malloy

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P2860

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

High Concordance of Bipolar I Disorder in a Nationwide Sample of Twins

The Heritability of Bipolar Affective Disorder and the Genetic Relationship to Unipolar Depression

Rare chromosomal deletions and duplications increase risk of schizophrenia

The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools

The Protein Data Bank

H662 is the linchpin of ATP hydrolysis in the nucleotide-binding domain of the ABC transporter HlyB

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

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

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

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Peter M. Visscher

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