Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios - Test2 - elhamkhani - TriplyDB

Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios

Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios

http://www.wikidata.org/entity/Q24538580

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Association of RGS4 variants with schizotypy and cognitive endophenotypes at the population level The genetics of bipolar disorder: genome ‘hot regions,’ genes, new potential candidates and future directions The genetics of bipolar disorder RGS4 polymorphisms associated with variability of cognitive performance in a family-based schizophrenia sample Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder Essential role of GluD1 in dendritic spine development and GluN2B to GluN2A NMDAR subunit switch in the cortex and hippocampus reveals ability of GluN2B inhibition in correcting hyperconnectivity.Brain-specific Crmp2 deletion leads to neuronal development deficits and behavioural impairments in mice A blood based 12-miRNA signature of Alzheimer disease patients A network of dopaminergic gene variations implicated as risk factors for schizophrenia Whole-genome association study of bipolar disorder Deletion of glutamate delta-1 receptor in mouse leads to aberrant emotional and social behaviors Metabotropic glutamate receptor 3 is associated with heroin dependence but not depression or schizophrenia in a Chinese population Genetic assessment of additional endophenotypes from the Consortium on the Genetics of Schizophrenia Family Study.Schizophrenia and Depression Co-Morbidity: What We have Learned from Animal Models.Genome-wide linkage analyses of 12 endophenotypes for schizophrenia from the Consortium on the Genetics of Schizophrenia.A genomewide search finds major susceptibility loci for nicotine dependence on chromosome 10 in African Americans.Analysis of 94 candidate genes and 12 endophenotypes for schizophrenia from the Consortium on the Genetics of Schizophrenia.The association of schizophrenia risk D-amino acid oxidase polymorphisms with sensorimotor gating, working memory and personality in healthy males.Genetic regulation of Nrxn1 [corrected] expression: an integrative cross-species analysis of schizophrenia candidate genes A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations.GABA(A) receptors and their associated proteins: implications in the etiology and treatment of schizophrenia and related disorders.Abnormal social behavior, hyperactivity, impaired remote spatial memory, and increased D1-mediated dopaminergic signaling in neuronal nitric oxide synthase knockout mice.Setdb1 histone methyltransferase regulates mood-related behaviors and expression of the NMDA receptor subunit NR2B.Convergent functional genomic studies of ω-3 fatty acids in stress reactivity, bipolar disorder and alcoholism.Early-life stress links 5-hydroxymethylcytosine to anxiety-related behaviors Ethnic stratification of the association of RGS4 variants with antipsychotic treatment response in schizophrenia.Dysfunctional and compensatory prefrontal cortical systems, genes and the pathogenesis of schizophrenia.Association of RGS2 and RGS5 variants with schizophrenia symptom severity.The neurobiology of D-amino acid oxidase and its involvement in schizophrenia.Family-based association study of Neuregulin 1 with psychotic bipolar disorder Association of obesity and treated hypertension and diabetes with cognitive ability in bipolar disorder and schizophrenia.NMDA receptor hypofunction induces dysfunctions of energy metabolism and semaphorin signaling in rats: a synaptic proteome study.Relationship of the Brief UCSD Performance-based Skills Assessment (UPSA-B) to multiple indicators of functioning in people with schizophrenia and bipolar disorder Probing the lithium-response pathway in hiPSCs implicates the phosphoregulatory set-point for a cytoskeletal modulator in bipolar pathogenesis.No association of dysbindin with symptom factors of schizophrenia in an Irish case-control sample DISC1 and Huntington's disease--overlapping pathways of vulnerability to neurological disorder?DTNBP1 (Dystrobrevin binding protein 1) and schizophrenia: association evidence in the 3' end of the gene Association between the DAOA/G72 gene and bipolar disorder and meta-analyses in bipolar disorder and schizophrenia.

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Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios

http://www.wikidata.org/entity/Q24538580

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Ann E Pulver

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David Valle

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Dimitrios Avramopoulos

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Gary Steel

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Gerald Nestadt

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Kristin K Nicodemus

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Kung-Yee Liang

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M Daniele Fallin

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Paula S Wolyniec

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Richard L Huganir

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P2860

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia

Calcineurin A alpha (PPP3CA), calcineurin A beta (PPP3CB) and calcineurin B (PPP3R1) are located on human chromosomes 4, 10q21-->q22 and 2p16-->p15 respectively

The DiGeorge syndrome minimal critical region contains a goosecoid-like (GSCL) homeobox gene that is expressed early in human development

Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene

UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome

Neuregulin-3 (NRG3): a novel neural tissue-enriched protein that binds and activates ErbB4

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series

Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia

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