Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios
about
Association of RGS4 variants with schizotypy and cognitive endophenotypes at the population levelThe genetics of bipolar disorder: genome ‘hot regions,’ genes, new potential candidates and future directionsThe genetics of bipolar disorderRGS4 polymorphisms associated with variability of cognitive performance in a family-based schizophrenia sampleFine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophreniaIdentification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brainA genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorderEssential 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 miceA blood based 12-miRNA signature of Alzheimer disease patientsA network of dopaminergic gene variations implicated as risk factors for schizophreniaWhole-genome association study of bipolar disorderDeletion of glutamate delta-1 receptor in mouse leads to aberrant emotional and social behaviorsMetabotropic glutamate receptor 3 is associated with heroin dependence but not depression or schizophrenia in a Chinese populationGenetic 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 genesA 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 behaviorsEthnic 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 disorderAssociation 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 disorderProbing 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 sampleDISC1 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 geneAssociation between the DAOA/G72 gene and bipolar disorder and meta-analyses in bipolar disorder and schizophrenia.
P2860
Q21203802-DA32CCC6-E731-4117-88DA-E0A2A03579F4Q22251105-225B3E5A-9A9E-40A5-8209-D5A97EDF9B2BQ22251249-E510DC2D-4C77-4E14-8E73-F805555EB172Q24622263-22A8BEFB-F4A1-4964-ABE1-16396DF62897Q24643955-46CA69C2-A40F-4431-83F0-BA577F0212E9Q24648621-2FAF78F1-E255-4785-AC8A-AEBD788DE99CQ24655759-B0B5F15C-A1A7-4D0D-A5CE-AB3435DEBAC2Q27305133-4767B228-0C58-4C41-B998-A4B3E5F9F514Q27314818-A2F2D394-71F2-4E3B-A9F5-84C22AA7E1C9Q27499741-E858AE4D-2DB4-4594-90A5-F009511E5542Q28259093-C75D850E-E04F-4FB4-A75E-5D62F6297246Q28271419-245DCBB8-B60B-4D81-BF2F-DD78D432731CQ28512821-5197282D-6573-433F-86FD-D00E650DE6A8Q28539376-1060F452-7174-41E2-8C7F-B285EF7866BAQ30367047-E798A99F-C875-45B7-B053-FF80E1F14DCAQ30416883-79A68FFF-63E4-4920-9AD9-2988542E79F8Q30439012-9E3AD7BE-C572-4F34-B715-8868CCC7FA20Q30441533-F307158F-2256-46D0-BCAC-379E54D2403FQ30450376-0F7BF357-2736-4448-AB4B-9C41BD8827B9Q30466238-EE9D6DE6-E600-411E-9F6B-BB52CDE3C952Q30468815-EA9BCC69-B222-41BC-89A0-CEAB88DB0DC9Q30475974-0A9DED14-CEA2-4A64-B56C-BA6B47FD29C5Q30479407-716637D1-5945-4BD9-B53C-CA64DF88B79AQ30488182-901CDAD2-8F1B-4EFD-B290-6A3FE91102C8Q30495175-59377BC9-74C4-41B9-A138-F853F084CCEFQ30511829-0E9CF61E-A93C-4296-AFAA-D871881AFBF8Q30846554-7A5ADF52-CC49-4B4C-84C4-EBFAF7156DE1Q33288672-5C91A740-6668-40D2-AF8B-8B6593C02648Q33295367-093D69FB-3BAA-48C2-9738-F7861F6EBFF4Q33319041-AC2D929C-E6D5-49B3-B619-A5BCDD1DDC30Q33611796-4E6AB911-8FDE-464B-86AE-2489D5E94A2EQ33634654-EA1BC25D-A73E-4B99-BFEE-23F9888E2D10Q33717601-7140FE85-EAA0-4918-9C1A-6C7D0D937CECQ33749231-8328560A-C012-4DB8-8941-BBD4DA22F941Q33758362-5594DAD7-1713-4DBF-BAEA-E0572D8CD640Q33782489-71E7D8B3-06A2-49D5-9811-908D60F3794FQ33809001-F56DA3EE-503E-41CF-BE8B-00B71CA14FA2Q33813559-594DB931-D278-4E8E-B046-914C4AF66415Q33818087-0AC5E2E4-0E9A-43DF-B20F-F2C71FB901C1Q33857039-755B3FC4-7A95-477F-BF0F-2E8C146937A5
P2860
Bipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent trios
description
2005 nî lūn-bûn
@nan
2005 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Bipolar I disorder and schizop ...... enazi Jewish case-parent trios
@ast
Bipolar I disorder and schizop ...... enazi Jewish case-parent trios
@en
Bipolar I disorder and schizop ...... enazi Jewish case-parent trios
@nl
type
label
Bipolar I disorder and schizop ...... enazi Jewish case-parent trios
@ast
Bipolar I disorder and schizop ...... enazi Jewish case-parent trios
@en
Bipolar I disorder and schizop ...... enazi Jewish case-parent trios
@nl
prefLabel
Bipolar I disorder and schizop ...... enazi Jewish case-parent trios
@ast
Bipolar I disorder and schizop ...... enazi Jewish case-parent trios
@en
Bipolar I disorder and schizop ...... enazi Jewish case-parent trios
@nl
P2093
P2860
P3181
P356
P1476
Bipolar I disorder and schizop ...... enazi Jewish case-parent trios
@en
P2093
Ann E Pulver
David Valle
Dimitrios Avramopoulos
Gary Steel
Gerald Nestadt
Kristin K Nicodemus
Kung-Yee Liang
M Daniele Fallin
Paula S Wolyniec
Richard L Huganir
P2860
P304
P3181
P356
10.1086/497703
P407
P577
2005-12-01T00:00:00Z