The emerging spectrum of allelic variation in schizophrenia: current evidence and strategies for the identification and functional characterization of common and rare variants.
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Gsx1 expression defines neurons required for prepulse inhibition.S-SCAM, a rare copy number variation gene, induces schizophrenia-related endophenotypes in transgenic mouse model.Pre-pulse inhibition and antisaccade performance indicate impaired attention modulation of cognitive inhibition in 22q11.2 deletion syndrome (22q11DS).Recent challenges to the psychiatric diagnostic nosology: a focus on the genetics and genomics of neurodevelopmental disorders.Reduced CHRNA7 expression in C3H mice is associated with increases in hippocampal parvalbumin and glutamate decarboxylase-67 (GAD67) as well as altered levels of GABA(A) receptor subunits.DSM-IV "criterion A" schizophrenia symptoms across ethnically different populations: evidence for differing psychotic symptom content or structural organization?Excess of homozygosity in the major histocompatibility complex in schizophrenia.Replication of association between schizophrenia and chromosome 6p21-6p22.1 polymorphisms in Chinese Han populationNeurodevelopment, GABA system dysfunction, and schizophreniaAltered gene expression in schizophrenia: findings from transcriptional signatures in fibroblasts and blood.Random or stochastic monoallelic expressed genes are enriched for neurodevelopmental disorder candidate genes.Evidence for Association of Cell Adhesion Molecules Pathway and NLGN1 Polymorphisms with Schizophrenia in Chinese Han Population.Genetic Evaluation of Schizophrenia Using the Illumina HumanExome ChipAn integrated analysis tool for analyzing hybridization intensities and genotypes using new-generation population-optimized human arrays.Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders.Implications of genetic findings for understanding schizophrenia.Expression profiling of mouse subplate reveals a dynamic gene network and disease association with autism and schizophreniaAutism risk across generations: a population-based study of advancing grandpaternal and paternal age.Will brain cells derived from induced pluripotent stem cells or directly converted from somatic cells (iNs) be useful for schizophrenia research?KCNH2-3.1 expression impairs cognition and alters neuronal function in a model of molecular pathology associated with schizophrenia.Decanalization mediating gene-environment interactions in schizophrenia and other psychiatric disorders with neurodevelopmental etiology.Dopaminergic gene polymorphisms and cognitive function in a north Indian schizophrenia cohort.Investigation of single-nucleotide variants in MBD5 associated with autism spectrum disorders and schizophrenia phenotypes.Sex differences in the genetic risk for schizophrenia: history of the evidence for sex-specific and sex-dependent effects.The role of prefrontal catecholamines in attention and working memory.The onset and offset of psychosis--and what happens in between--a commentary on ‘Reappraising the long-term course and outcome of psychotic disorders: the AESOP-10 Study’ by Morgan et al. (2014).What causes aberrant salience in schizophrenia? A role for impaired short-term habituation and the GRIA1 (GluA1) AMPA receptor subunit.Recent genetic findings in schizophrenia and their therapeutic relevanceGenetic studies of schizophrenia: an update.Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders.The Human MSI2 Gene is Associated with Schizophrenia in the Chinese Han Population.Risk alleles of genes with monoallelic expression are enriched in gain-of-function variants and depleted in loss-of-function variants for neurodevelopmental disorders.Investigation of the role of TCF4 rare sequence variants in schizophrenia.Increased rare duplication burden genomewide in patients with treatment-resistant schizophrenia.Clinical and parental age characteristics of rare copy number variant burden in patients with schizophrenia.The John Cade Fellowship: Modifiable risk factors for serious mental illness.
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The emerging spectrum of allelic variation in schizophrenia: current evidence and strategies for the identification and functional characterization of common and rare variants.
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
The emerging spectrum of allel ...... n of common and rare variants.
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type
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The emerging spectrum of allel ...... n of common and rare variants.
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prefLabel
The emerging spectrum of allel ...... n of common and rare variants.
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P2860
P356
P1433
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The emerging spectrum of allel ...... n of common and rare variants.
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P2860
P2888
P356
10.1038/MP.2012.34
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2012-05-01T00:00:00Z
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P6179
1030917392