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Stanley I. Shyn

Researcher at Kaiser Permanente

Publications -  24
Citations -  6805

Stanley I. Shyn is an academic researcher from Kaiser Permanente. The author has contributed to research in topics: Genome-wide association study & Major depressive disorder. The author has an hindex of 14, co-authored 22 publications receiving 5650 citations. Previous affiliations of Stanley I. Shyn include University of California, San Francisco & Group Health Cooperative.

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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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Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

Naomi R. Wray, +262 more
- 26 Apr 2018 - 
TL;DR: A genome-wide association meta-analysis of individuals with clinically assessed or self-reported depression identifies 44 independent and significant loci and finds important relationships of genetic risk for major depression with educational attainment, body mass, and schizophrenia.
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A mega-analysis of genome-wide association studies for major depressive disorder

Stephan Ripke, +115 more
- 01 Apr 2013 - 
TL;DR: This article conducted a genome-wide association studies (GWAS) mega-analysis for major depressive disorder (MDD) using more than 1.2 million autosomal and X chromosome single-nucleotide polymorphisms (SNPs) in 18,759 independent and unrelated subjects of recent European ancestry.
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Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Colm O'Dushlaine, +404 more
- 19 Jan 2015 - 
TL;DR: It is indicated that risk variants for psychiatric disorders aggregate in particular biological pathways and that these pathways are frequently shared between disorders.
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A genomewide association study of citalopram response in major depressive disorder.

TL;DR: Although the findings reported here do not meet a genomewide threshold for significance, the regions identified from this study provide targets for independent replication and novel pathways to investigate mechanisms of antidepressant response.