| scholarly article | Q13442814 |
| P50 | author | Kenneth Kendler | Q6390313 |
| Dermot Walsh | Q113000839 | ||
| Po-Hsiu Kuo | Q38640970 | ||
| P2093 | author name string | F Anthony O'Neill | |
| Brandon Wormley | |||
| Zhongming Zhao | |||
| Brien Riley | |||
| Brion S Maher | |||
| Ayman H Fanous | |||
| Jingchun Sun | |||
| P2860 | cites work | Identification of a high-risk haplotype for the dystrobrevin binding protein 1 (DTNBP1) gene in the Irish study of high-density schizophrenia families | Q44894348 |
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| Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression. | Q53621277 | ||
| Comprehensive analysis of tagging sequence variants inDTNBP1shows no association with schizophrenia or with its composite neurocognitive endophenotypes | Q57253666 | ||
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| Identifying potential risk haplotypes for schizophrenia at the DTNBP1 locus in Han Chinese and Scottish populations | Q57403348 | ||
| The role of DTNBP1, NRG1, and AKT1 in the genetics of schizophrenia in Finland | Q57664212 | ||
| No evidence for association of the dysbindin gene [DTNBP1] with schizophrenia in an Irish population-based study | Q57699671 | ||
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| The Longue Durée of genetic ancestry: multiple genetic marker systems and Celtic origins on the Atlantic facade of Europe | Q24533759 | ||
| Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia | Q24612644 | ||
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| The structure of haplotype blocks in the human genome | Q27860500 | ||
| Haploview: analysis and visualization of LD and haplotype maps | Q27860955 | ||
| The genetic legacy of Paleolithic Homo sapiens sapiens in extant Europeans: a Y chromosome perspective | Q28143588 | ||
| Positive association of schizophrenia to JARID2 gene | Q28263150 | ||
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| Evidence of novel neuronal functions of dysbindin, a susceptibility gene for schizophrenia | Q28568230 | ||
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| Y-chromosome variation and Irish origins. | Q33896538 | ||
| The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the disease | Q33905352 | ||
| Association of the DTNBP1 locus with schizophrenia in a U.S. population | Q33910454 | ||
| Identification in 2 independent samples of a novel schizophrenia risk haplotype of the dystrobrevin binding protein gene (DTNBP1). | Q33977237 | ||
| Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria | Q33977974 | ||
| The PIP5K2A and RGS4 genes are differentially associated with deficit and non-deficit schizophrenia | Q34616234 | ||
| Contrasting linkage-disequilibrium patterns between cases and controls as a novel association-mapping method | Q34658015 | ||
| No gene is an island: the flip-flop phenomenon | Q35677798 | ||
| How repeatable are associations between polymorphisms in achaete-scute and bristle number variation in Drosophila? | Q35757698 | ||
| Predictors of schizophrenia--a review | Q36157733 | ||
| Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia | Q36168189 | ||
| Association of schizophrenia with DTNBP1 but not with DAO, DAOA, NRG1 and RGS4 nor their genetic interaction | Q40227028 | ||
| Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families | Q40722387 | ||
| The genetics of schizophrenia: a current, genetic-epidemiologic perspective | Q40821125 | ||
| The family history method using diagnostic criteria. Reliability and validity | Q44578310 | ||
| Association study of dysbindin gene with clinical and outcome measures in a representative cohort of Italian schizophrenic patients | Q44804253 | ||
| FP-TDI SNP scoring by manual and statistical procedures: a study of error rates and types | Q44892987 | ||
| P433 | issue | 2-3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | schizophrenia | Q41112 |
| P304 | page(s) | 245-253 | |
| P577 | publication date | 2009-10-02 | |
| P1433 | published in | Schizophrenia Research | Q7431607 |
| P1476 | title | The dystrobrevin binding protein 1 (DTNBP1) gene is associated with schizophrenia in the Irish Case Control Study of Schizophrenia (ICCSS) sample | |
| P478 | volume | 115 |
| Q28587869 | Ablation of Mrds1/Ofcc1 induces hyper-γ-glutamyl transpeptidasemia without abnormal head development and schizophrenia-relevant behaviors in mice |
| Q34543151 | Application of systems biology approach identifies and validates GRB2 as a risk gene for schizophrenia in the Irish Case Control Study of Schizophrenia (ICCSS) sample |
| Q34901624 | Association study of 167 candidate genes for schizophrenia selected by a multi-domain evidence-based prioritization algorithm and neurodevelopmental hypothesis |
| Q28244133 | Autoimmune diseases, gastrointestinal disorders and the microbiome in schizophrenia: more than a gut feeling |
| Q49050983 | Dysbindin gene (DTNBP1) in major depressive disorder (MDD) patients: lack of association with clinical phenotypes |
| Q50546206 | Dysbindin-1 gene contributes differentially to early- and adult-onset forms of functional psychosis |
| Q51739855 | Dysbindin-1 modifies signaling and cellular localization of recombinant, human D₃ and D₂ receptors. |
| Q36854707 | Effects of sex and DTNBP1 (dysbindin) null gene mutation on the developmental GluN2B-GluN2A switch in the mouse cortex and hippocampus |
| Q33691275 | GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia |
| Q28067507 | Gene × Environment Interactions in Schizophrenia: Evidence from Genetic Mouse Models |
| Q36882737 | Increased dysbindin-1B isoform expression in schizophrenia and its propensity in aggresome formation |
| Q38064198 | Losing your inhibition: linking cortical GABAergic interneurons to schizophrenia |
| Q34423863 | Neuroplasticity signaling pathways linked to the pathophysiology of schizophrenia |
| Q33809001 | No association of dysbindin with symptom factors of schizophrenia in an Irish case-control sample |
| Q24301877 | Nucleocytoplasmic Shuttling of Dysbindin-1, a Schizophrenia-related Protein, Regulates Synapsin I Expression |
| Q46359768 | Recognition deficits in mice carrying mutations of genes encoding BLOC-1 subunits pallidin or dysbindin. |
| Q33627540 | Schizophrenia gene networks and pathways and their applications for novel candidate gene selection |
| Q47308325 | Single point mutation on the gene encoding dysbindin results in recognition deficits. |
| Q33842202 | Synaptic dysbindin-1 reductions in schizophrenia occur in an isoform-specific manner indicating their subsynaptic location |
| Q36817544 | Variants in the 15q25 gene cluster are associated with risk for schizophrenia and bipolar disorder |
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