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István Bitter

Researcher at Semmelweis University

Publications -  269
Citations -  12420

István Bitter is an academic researcher from Semmelweis University. The author has contributed to research in topics: Schizophrenia (object-oriented programming) & Olanzapine. The author has an hindex of 42, co-authored 254 publications receiving 10719 citations. Previous affiliations of István Bitter include Eli Lilly and Company & New York University.

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Genome-wide association study identifies five new schizophrenia loci

Stephan Ripke, +210 more
- 01 Oct 2011 - 
TL;DR: The authors examined the role of common genetic variation in schizophrenia in a genome-wide association study of substantial size: a stage 1 discovery sample of 21,856 individuals of European ancestry and a stage 2 replication sample of 29,839 independent subjects.
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Common variants conferring risk of schizophrenia

Hreinn Stefansson, +94 more
- 06 Aug 2009 - 
TL;DR: Findings implicating the MHC region are consistent with an immune component to schizophrenia risk, whereas the association with NRGN and TCF4 points to perturbation of pathways involved in brain development, memory and cognition.
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Prevalence and correlates of adult attention-deficit hyperactivity disorder: meta-analysis.

TL;DR: Prevalence of ADHD in adults declines with age in the general population and the unclear validity of DSM–IV diagnostic criteria for this condition can lead to reduced prevalence rates by underestimation of the prevalence of adult ADHD.
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Clozapine treatment for suicidality in schizophrenia: International Suicide Prevention Trial (InterSePT).

Herbert Y. Meltzer, +87 more
TL;DR: It is suggested that clozapine therapy significantly reduces suicidal behavior in patients with schizophrenia and schizoaffective disorder at high risk for suicide, and use of clozAPine in this population should lead to a significant reduction in suicidal behavior.
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Duloxetine in the acute and long-term treatment of major depressive disorder: a placebo- and paroxetine-controlled trial

TL;DR: These data support previous findings that duloxetine is safe, efficacious, and well tolerated in the acute treatment of major depressive disorder.