Pages that link to "Q24634378"
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The following pages link to Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes (Q24634378):
Displaying 40 items.
- schizophrenia (Q41112) (← links)
- bipolar disorder (Q131755) (← links)
- PTPRN2 (Q18030950) (← links)
- PHF8 (Q18036818) (← links)
- ERC2 (Q18037948) (← links)
- CACNA1B mutation is linked to unique myoclonus-dystonia syndrome (Q28249383) (← links)
- Major channels involved in neuropsychiatric disorders and therapeutic perspectives (Q28290639) (← links)
- Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 (Q29417143) (← links)
- Ion channels and schizophrenia: a gene set-based analytic approach to GWAS data for biological hypothesis testing (Q30457731) (← links)
- Advancing biomarker research: utilizing 'Big Data' approaches for the characterization and prevention of bipolar disorder (Q30713152) (← links)
- What is the impact of genome-wide supported risk variants for schizophrenia and bipolar disorder on brain structure and function? A systematic review (Q30928632) (← links)
- Practical Experience of the Application of a Weighted Burden Test to Whole Exome Sequence Data for Obesity and Schizophrenia (Q31006720) (← links)
- Comparative Linkage Meta-Analysis Reveals Regionally-Distinct, Disparate Genetic Architectures: Application to Bipolar Disorder and Schizophrenia (Q33895253) (← links)
- Mouse models of genetic effects on cognition: Relevance to schizophrenia (Q34183979) (← links)
- 17q24.2 microdeletions: a new syndromal entity with intellectual disability, truncal obesity, mood swings and hallucinations (Q35899350) (← links)
- Targeted pharmacogenetic analysis of antipsychotic response in the CATIE study (Q36456196) (← links)
- Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia (Q36486414) (← links)
- Evaluation of voltage-dependent calcium channel γ gene families identified several novel potential susceptible genes to schizophrenia (Q36824074) (← links)
- Mechanisms and Disease Associations of Haplotype-Dependent Allele-Specific DNA Methylation (Q36891490) (← links)
- A case-case study on sinonasal cancer prevention: effect from dust reduction in woodworking and risk of mastic/solvents in shoemaking (Q37118204) (← links)
- Involvement of PTPN5, the gene encoding the striatal-enriched protein tyrosine phosphatase, in schizophrenia and cognition (Q37140379) (← links)
- Replication of genome-wide association study (GWAS) susceptibility loci in a Latino bipolar disorder cohort. (Q37394229) (← links)
- Pharmacogenetics of second-generation antipsychotics (Q38217628) (← links)
- Mutational consequences of aberrant ion channels in neurological disorders (Q38239544) (← links)
- Patterned expression of ion channel genes in mouse dorsal raphe nucleus determined with the Allen Mouse Brain Atlas. (Q39216998) (← links)
- A rare schizophrenia risk variant of CACNA1I disrupts CaV3.3 channel activity (Q41497165) (← links)
- Tests of linkage and allelic association between markers in the 1p36 PRKCZ (protein kinase C zeta) gene region and bipolar affective disorder (Q43489312) (← links)
- Whole genome sequence association and ancestry-informed polygenic profile of EEG alpha in a Native American population. (Q46743684) (← links)
- LncRNA LINC00880 promotes cell proliferation, migration and invasion while inhibiting apoptosis by targeting CACNG5 through the MAPK signaling pathway in spinal cord ependymoma. (Q47320115) (← links)
- Genome-wide meta-analysis of copy number variations with alcohol dependence (Q47770528) (← links)
- A novel relationship for schizophrenia, bipolar and major depressive disorder Part 3: Evidence from chromosome 3 high density association screen (Q47782721) (← links)
- A genome-wide linkage scan of bipolar disorder in Latino families identifies susceptibility loci at 8q24 and 14q32. (Q48648177) (← links)
- Loss of function mutations in ATP2A2 and psychoses: A case report and literature survey (Q48799820) (← links)
- Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (Q57697186) (← links)
- Compositional epistasis detection using a few prototype disease models (Q64115133) (← links)
- Malignant Versus Benign Tumors of the Sinonasal Cavity: A Case-Control Study on Occupational Etiology (Q90617560) (← links)
- Personalized Epigenome Remodeling Under Biochemical and Psychological Changes During Long-Term Isolation Environment (Q92649576) (← links)
- A Peptide Link Between Human Cytomegalovirus Infection, Neuronal Migration, and Psychosis (Q95840809) (← links)
- Extreme enrichment of VNTR-associated polymorphicity in human subtelomeres: genes with most VNTRs are predominantly expressed in the brain (Q101165845) (← links)
- Association between DNA methylation and ADHD symptoms from birth to school age: a prospective meta-analysis (Q102053742) (← links)