Rare variants in neuronal excitability genes influence risk for bipolar disorder. - Wikidata - wikimedia - TriplyDB

Rare variants in neuronal excitability genes influence risk for bipolar disorder.

Rare variants in neuronal excitability genes influence risk for bipolar disorder.

http://www.wikidata.org/entity/Q35212607

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Toward a Deeper Understanding of the Genetics of Bipolar Disorder Molecular neurobiological clues to the pathogenesis of bipolar disorder Trio-based exome sequencing arrests de novo mutations in early-onset high myopia Exome sequencing for bipolar disorder points to roles of de novo loss-of-function and protein-altering mutations.Gene-wide Association Study Reveals RNF122 Ubiquitin Ligase as a Novel Susceptibility Gene for Attention Deficit Hyperactivity Disorder.An Efficient Stepwise Statistical Test to Identify Multiple Linked Human Genetic Variants Associated with Specific Phenotypic Traits.Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene.Addiction pharmacogenetics: a systematic review of the genetic variation of the dopaminergic system Calcium channel genes associated with bipolar disorder modulate lithium's amplification of circadian rhythms.Innovative approaches to bipolar disorder and its treatment A systematic review of calcium channel antagonists in bipolar disorder and some considerations for their future development.Neuropsychiatric genomics in precision medicine: diagnostics, gene discovery, and translation.Bipolar Disorder Associated microRNA, miR-1908-5p, Regulates the Expression of Genes Functioning in Neuronal Glutamatergic Synapses.Cav1.2 channels mediate persistent chronic stress-induced behavioral deficits that are associated with prefrontal cortex activation of the p25/Cdk5-glucocorticoid receptor pathway.Targeting voltage-gated calcium channels in neurological and psychiatric diseases.Effect of social interactions on hippocampal protein expression in animal dominant and submissive model of behavioral disorders.Personalized medicine: evidence of normativity in its quantitative definition of health.L-type Ca2+ channels in mood, cognition and addiction: integrating human and rodent studies with a focus on behavioural endophenotypes.Enrichment of deleterious variants of mitochondrial DNA polymerase gene (POLG1) in bipolar disorder.The genetic overlap between mood disorders and cardiometabolic diseases: a systematic review of genome wide and candidate gene studies.Positive Traits in the Bipolar Spectrum: The Space between Madness and Genius.From Gene to Behavior: L-Type Calcium Channel Mechanisms Underlying Neuropsychiatric Symptoms.Enrichment of SNPs in Functional Categories Reveals Genes Affecting Complex Traits.The Neuropsychiatric Disease-Associated Gene cacna1c Mediates Survival of Young Hippocampal Neurons Exome Sequencing of Familial Bipolar Disorder.Staging model raises fundamental questions about the nature of bipolar disorder.Enhancing VTA Cav1.3 L-type Ca2+ channel activity promotes cocaine and mood-related behaviors via overlapping AMPA receptor mechanisms in the nucleus accumbens.A Rare Variant in CACNA1D Segregates with 7 Bipolar I Disorder Cases in a Large Pedigree.Genetic disruption of ankyrin-G in adult mouse forebrain causes cortical synapse alteration and behavior reminiscent of bipolar disorder Deletion of psychiatric risk gene Cacna1c impairs hippocampal neurogenesis in cell-autonomous fashion.Unraveling the biology of bipolar disorder using induced pluripotent stem-derived neurons.De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.Progress in Genetic Studies of Tourette's Syndrome.Contribution of genes in the GABAergic pathway to bipolar disorder and its executive function deficit in the Chinese Han population.The Emerging Neurobiology of Bipolar Disorder.GABAA and GABAB receptor dysregulation in superior frontal cortex of subjects with schizophrenia and bipolar disorder.[Genetics of bipolar disorder].An examination of multiple classes of rare variants in extended families with bipolar disorder.Taking Systems Medicine to Heart.From the Psychiatrist's Couch to Induced Pluripotent Stem Cells: Bipolar Disease in a Dish.

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Rare variants in neuronal excitability genes influence risk for bipolar disorder.

http://www.wikidata.org/entity/Q35212607

description

2015 nî lūn-bûn

@nan

2015 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի փետրվարին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

@zh-hant

2015年論文

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2015年論文

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2015年論文

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2015年论文

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name

Rare variants in neuronal excitability genes influence risk for bipolar disorder.

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Rare variants in neuronal excitability genes influence risk for bipolar disorder.

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type

label

Rare variants in neuronal excitability genes influence risk for bipolar disorder.

@ast

Rare variants in neuronal excitability genes influence risk for bipolar disorder.

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prefLabel

Rare variants in neuronal excitability genes influence risk for bipolar disorder.

@ast

Rare variants in neuronal excitability genes influence risk for bipolar disorder.

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PNAS.1424958112

P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

Rare variants in neuronal excitability genes influence risk for bipolar disorder.

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P2093

Anna-Barbara Stittrich

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Bipolar Genome Study

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David Craig

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Denise E Mauldin

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Elliot S Gershon

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Jared C Roach

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John R Kelsoe

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Judith A Badner

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Katherine Rouleau

http://www.w3.org/2001/XMLSchema#string

Mary E Brunkow

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P2860

Analysis of genetic inheritance in a family quartet by whole-genome sequencing

Defining functional DNA elements in the human genome

The evolutionary history and tissue mapping of GPR123: specific CNS expression pattern predominantly in thalamic nuclei and regions containing large pyramidal cells

The accessible chromatin landscape of the human genome

Genome-wide association study of bipolar disorder in European American and African American individuals

Fast and accurate short read alignment with Burrows-Wheeler transform

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

Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene

Mutations in NOTCH1 cause Adams-Oliver syndrome

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

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3576-3581

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scholarly article

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10.1073/PNAS.1424958112

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11

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112

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Gustavo Glusman

Francis J. McMahon

Howard J Edenberg

John I. Nurnberger

Justin Ashworth

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2015-02-17T00:00:00Z

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273501126

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25730879

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bipolar disorder

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4371952

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