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Ingrid Melle

Researcher at Oslo University Hospital

Publications -  592
Citations -  51862

Ingrid Melle is an academic researcher from Oslo University Hospital. The author has contributed to research in topics: Schizophrenia & Bipolar disorder. The author has an hindex of 82, co-authored 530 publications receiving 42391 citations. Previous affiliations of Ingrid Melle include University of Oslo & University of Bergen.

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Biological insights from 108 schizophrenia-associated genetic loci

Stephan Ripke, +354 more
- 24 Jul 2014 - 
TL;DR: Associations at DRD2 and several genes involved in glutamatergic neurotransmission highlight molecules of known and potential therapeutic relevance to schizophrenia, and are consistent with leading pathophysiological hypotheses.
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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

S. Hong Lee, +405 more
- 01 Sep 2013 - 
TL;DR: Empirical evidence of shared genetic etiology for psychiatric disorders can inform nosology and encourages the investigation of common pathophysiologies for related disorders.
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Large recurrent microdeletions associated with schizophrenia

Hreinn Stefansson, +81 more
- 11 Sep 2008 - 
TL;DR: In a genome-wide search for CNVs associating with schizophrenia, a population-based sample was used to identify de novo CNVs by analysing 9,878 transmissions from parents to offspring and three deletions significantly associate with schizophrenia and related psychoses in the combined sample.
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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.