P.3.b.009 Association study of STAT6 polymorphism with schizophrenia and periodic psychosis
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Objective Recent molecular and genetic investigations have suggested that the current
nosology for major psychiatric disorders, based on the" two-entities-principal" is not accurate …

Objective Tardive dyskinesia (TD) is a human hyperkinetic movement disorder as a result of
potentially irreversible long-term chronic first-generation antipsychotic medications …

Objectives: ST8SIA2 (ST8 alpha-N-acetyl-neuraminide alpha-2, 8-sialyltransferase 2 gene)
is located at 15q26, a susceptibility locus for schizophrenia. Some previous research had …

Background Schizophrenia (SCZ) is a common and severe mental disorder. The
involvement of genetic factors in the disease is well known. In the present paper, we …

A whole genome association study was performed in a phase 3 clinical trial conducted to
evaluate a novel antipsychotic, iloperidone, administered to treat patients with …

Dear Editor, Genome-wide association studies (GWAS) provide evidence for a potentially
large polygenic component in schizophrenia risk (Purcell et al. 2009), and meta-analyses of …

Background Schizophrenia is a severe highly heritable mental disorder. The clinical
heterogeneity of schizophrenia is expressed in the difference in the leading symptoms and …

Schizophrenia, with incidence of 1% worldwide, is a common mental disorder.
Phosphoinositide-3-kinases (PI3Ks) are a family of enzymes involved in cellular functions …

Abstract Serotonin (5-hydroxytryptamine (5-HT)) transporter (SLC6A4) is known to influence
mood, emotion, cognition and efficacy of antidepressants, particularly that of selective …