The Kraepelinian dichotomy - going, going... but still not gone - Wikidata - awgldk - TriplyDB

The Kraepelinian dichotomy - going, going... but still not gone

The Kraepelinian dichotomy - going, going... but still not gone

http://www.wikidata.org/entity/Q22241683

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Gene x environment interactions in schizophrenia and bipolar disorder: evidence from neuroimaging An MRI study of amygdala in schizophrenia and psychotic bipolar disorder Suicide in the Early Stage of Schizophrenia The prevalence of psychosis in epilepsy; a systematic review and meta-analysis Genetic determinants of depression: recent findings and future directions Single-neuron and genetic correlates of autistic behavior in macaque.Considerations on the ICD-11 classification of psychotic depression Genome-wide association analysis identifies 13 new risk loci for schizophrenia 50 years of hurdles and hope in anxiolytic drug discovery Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder Schizophrenia.Biomarkers of bipolar disorder: specific or shared with schizophrenia?Early Recognition of High Risk of Bipolar Disorder and Psychosis: An Overview of the ZInEP "Early Recognition" Study.Phenotype ontologies and cross-species analysis for translational research Psychological processes mediate the impact of familial risk, social circumstances and life events on mental health Neuropsychological and functional outcomes in recent-onset major depression, bipolar disorder and schizophrenia-spectrum disorders: a longitudinal cohort study.Analyzing gene expression data in mice with the Neuro Behavior Ontology.Replication and cross-phenotype study based upon schizophrenia GWASs data in the Japanese population: support for association of MHC region with psychosis.Mutations in the BLOC-1 subunits dysbindin and muted generate divergent and dosage-dependent phenotypes.Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice.Social neuroscience: bringing an end to the destructive and misguided "social" versus "biological" in psychiatry.Research Domain Criteria: cognitive systems, neural circuits, and dimensions of behavior.The 2nd Schizophrenia International Research Society Conference, 10-14 April 2010, Florence, Italy: summaries of oral sessions.Family history of schizophrenia and bipolar disorder as risk factors for autism.Increased prepulse inhibition and sensitization of the startle reflex in autistic children.Multimodal assessments of the hippocampal formation in schizophrenia and bipolar disorder: evidences from neurobehavioral measures and functional and structural MRI.Brain changes in early-onset bipolar and unipolar depressive disorders: a systematic review in children and adolescents.Schizophrenia genetics: emerging themes for a complex disorder.Research Domain Criteria: toward future psychiatric nosologies.De novo mutations in schizophrenia implicate synaptic networks CACNA1C risk variant and amygdala activity in bipolar disorder, schizophrenia and healthy controls Graph analysis of dream reports is especially informative about psychosis.Evidence-based guidelines for treating bipolar disorder: Revised third edition recommendations from the British Association for Psychopharmacology How are autism and schizotypy related? Evidence from a non-clinical population.Fractional anisotropy in individuals with schizophrenia and their nonpsychotic siblings.Genetic variants on 3q21 and in the Sp8 transcription factor gene (SP8) as susceptibility loci for psychotic disorders: a genetic association study.Functional genetic variants in the vesicular monoamine transporter 1 modulate emotion processing Memoir and the Diagnosis of Schizophrenia: Reflections on The Center Cannot Hold, Me, Myself, and Them, and the 'Crumbling Twin Pillars' of Kraepelinian Psychiatry Bipolar and Depressive Disorders in Diagnostic and Statistical Manual of Mental Disorders-5: Clinical Implications of Revisions from Diagnostic and Statistical Manual of Mental Disorders-IV.

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The Kraepelinian dichotomy - going, going... but still not gone

http://www.wikidata.org/entity/Q22241683

description

2010 nî lūn-bûn

@nan

2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի փետրվարին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年論文

@yue

2010年論文

@zh-hant

2010年論文

@zh-hk

2010年論文

@zh-mo

2010年論文

@zh-tw

2010年论文

@wuu

name

The Kraepelinian dichotomy - going, going... but still not gone

@ast

The Kraepelinian dichotomy - going, going... but still not gone

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The Kraepelinian dichotomy - going, going... but still not gone

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The Kraepelinian dichotomy - going, going... but still not gone

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type

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The Kraepelinian dichotomy - going, going... but still not gone

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The Kraepelinian dichotomy - going, going... but still not gone

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The Kraepelinian dichotomy - going, going... but still not gone

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The Kraepelinian dichotomy - going, going... but still not gone

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The Kraepelinian dichotomy - going, going... but still not gone

@ast

The Kraepelinian dichotomy - going, going... but still not gone

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The Kraepelinian dichotomy - going, going... but still not gone

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The Kraepelinian dichotomy - going, going... but still not gone

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P2860

Rare chromosomal deletions and duplications increase risk of schizophrenia

The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia

Microduplications of 16p11.2 are associated with schizophrenia

Rethinking psychosis: the disadvantages of a dichotomous classification now outweigh the advantages

Neurexin 1 (NRXN1) deletions in schizophrenia

Large recurrent microdeletions associated with schizophrenia

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

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

Association between microdeletion and microduplication at 16p11.2 and autism

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

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scholarly article

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