Pages that link to "Q28143069"
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The following pages link to Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22 (Q28143069):
Displaying 50 items.
- Increased expression in dorsolateral prefrontal cortex of CAPON in schizophrenia and bipolar disorder (Q21144717) (← links)
- Recent advances in the genetics of schizophrenia (Q22242872) (← links)
- Rare chromosomal deletions and duplications increase risk of schizophrenia (Q22337245) (← links)
- Genome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia (Q24532517) (← links)
- Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family. (Q24535773) (← links)
- Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23 (Q24536215) (← links)
- Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample (Q24540539) (← links)
- A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27 (Q24617215) (← links)
- Schizophrenia: more dopamine, more D2 receptors (Q24630726) (← links)
- The schizophrenia phenotype in 22q11 deletion syndrome (Q24633796) (← links)
- Connexin 50 gene on human chromosome 1q21 is associated with schizophrenia in matched case control and family-based studies (Q24648392) (← links)
- Large recurrent microdeletions associated with schizophrenia (Q24654741) (← links)
- Evidence for association of schizophrenia with genetic variation in the 8p21.3 gene, PPP3CC, encoding the calcineurin gamma subunit (Q24678549) (← links)
- Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata (Q24680203) (← links)
- The suppression of brain cold-stable microtubules in mice induces synaptic defects associated with neuroleptic-sensitive behavioral disorders (Q24682931) (← links)
- Genome scans and microarrays: converging on genes for schizophrenia? (Q24791617) (← links)
- The glial growth factors deficiency and synaptic destabilization hypothesis of schizophrenia (Q24798030) (← links)
- Disrupted-In-Schizophrenia 1, a candidate gene for schizophrenia, participates in neurite outgrowth (Q28188775) (← links)
- Genes for schizophrenia? Recent findings and their pathophysiological implications (Q28207952) (← links)
- Molecular genetic studies of schizophrenia (Q28242041) (← links)
- Genome-wide scan for loci of Asperger syndrome (Q28245439) (← links)
- Association study of the G-protein signaling 4 (RGS4) and proline dehydrogenase (PRODH) genes with schizophrenia: a meta-analysis (Q28247655) (← links)
- Evidence for linkage between regulatory enzymes in glycolysis and schizophrenia in a multiplex sample (Q28258455) (← links)
- A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42 (Q28271774) (← links)
- Regulator of G-protein signalling 4 expression is not altered in the prefrontal cortex in schizophrenia (Q28287000) (← links)
- The role of phospholipases A2 in schizophrenia (Q28305324) (← links)
- Injured astrocytes are repaired by Synaptotagmin XI-regulated lysosome exocytosis. (Q28508854) (← links)
- PLC-beta1 knockout mice as a model of disrupted cortical development and plasticity: behavioral endophenotypes and dysregulation of RGS4 gene expression (Q28509915) (← links)
- Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia (Q29614929) (← links)
- Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence (Q29618819) (← links)
- From genomics to proteomics: new directions in molecular neuropsychiatry. (Q30385730) (← links)
- Deletion of PLCB1 gene in schizophrenia-affected patients (Q30415884) (← links)
- Disruption of dopamine neuron activity pattern regulation through selective expression of a human KCNN3 mutation. (Q30425716) (← links)
- Ion channels and schizophrenia: a gene set-based analytic approach to GWAS data for biological hypothesis testing (Q30457731) (← links)
- Increasing Genotype-Phenotype Model Determinism: Application to Bivariate Reading/Language Traits and Epistatic Interactions in Language-Impaired Families (Q30470934) (← links)
- Genetics of schizophrenia: from animal models to clinical studies (Q30532039) (← links)
- Genetic heterogeneity in schizophrenia: stratification of genome scan data using co-segregating related phenotypes (Q30621093) (← links)
- Prefrontal neurons and the genetics of schizophrenia (Q30666934) (← links)
- Childhood-onset schizophrenia: research update (Q30671060) (← links)
- The natural product berberine is a human prolyl oligopeptidase inhibitor (Q33273395) (← links)
- Ethnic stratification of the association of RGS4 variants with antipsychotic treatment response in schizophrenia. (Q33288672) (← links)
- Gene expression assays (Q33293342) (← links)
- Association of RGS2 and RGS5 variants with schizophrenia symptom severity (Q33319041) (← links)
- Genomic structural variation in psychiatric disorders (Q33354553) (← links)
- Tailoring the definition of the clinical schizophrenia phenotype in linkage studies (Q33390317) (← links)
- Molecular and cellular basis of small--and intermediate-conductance, calcium-activated potassium channel function in the brain (Q33560844) (← links)
- Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls (Q33625398) (← links)
- Finding schizophrenia genes (Q33831956) (← links)
- Evidence for a role of the NOS1AP (CAPON) gene in schizophrenia and its clinical dimensions: an association study in a South American population isolate. (Q33846861) (← links)
- Comparative linkage meta-analysis reveals regionally-distinct, disparate genetic architectures: application to bipolar disorder and schizophrenia (Q33895253) (← links)