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Scheinfeldt, Laura B.; Gharani, Neda; Kasper, Rachel S.; Schmidlen, Tara J.; Gordon, Erynn S.; Jarvis, Joseph P.; Delaney, Susan; Kronenthal, Courtney J.; Gerry, Norman P.; Christman, Michael F.

Using the Coriell Personalized Medicine Collaborative Data to conduct a genome‐wide association study of sleep duration

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  • Medientyp: E-Artikel
  • Titel: Using the Coriell Personalized Medicine Collaborative Data to conduct a genome‐wide association study of sleep duration
  • Beteiligte: Scheinfeldt, Laura B.; Gharani, Neda; Kasper, Rachel S.; Schmidlen, Tara J.; Gordon, Erynn S.; Jarvis, Joseph P.; Delaney, Susan; Kronenthal, Courtney J.; Gerry, Norman P.; Christman, Michael F.
  • Erschienen: Wiley, 2015
  • Erschienen in: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
  • Sprache: Englisch
  • DOI: 10.1002/ajmg.b.32362
  • ISSN: 1552-4841; 1552-485X
  • Schlagwörter: Cellular and Molecular Neuroscience ; Psychiatry and Mental health ; Genetics (clinical)
  • Entstehung:
  • Anmerkungen:
  • Beschreibung: <jats:sec><jats:label /><jats:p>Sleep is critical to health and functionality, and several studies have investigated the inherited component of insomnia and other sleep disorders using genome‐wide association studies (GWAS). However, genome‐wide studies focused on sleep duration are less common. Here, we used data from participants in the Coriell Personalized Medicine Collaborative (CPMC) (n = 4,401) to examine putative associations between self‐reported sleep duration, demographic and lifestyle variables, and genome‐wide single nucleotide polymorphism (SNP) data to better understand genetic contributions to variation in sleep duration. We employed stepwise ordered logistic regression to select our model and retained the following predictive variables: age, gender, weight, physical activity, physical activity at work, smoking status, alcohol consumption, ethnicity, and ancestry (as measured by principal components analysis) in our association testing. Several of our strongest candidate genes were previously identified in GWAS related to sleep duration (<jats:italic>TSHZ2, ABCC9, FBXO15</jats:italic>) and narcolepsy (<jats:italic>NFATC2</jats:italic>, <jats:italic>SALL4</jats:italic>). In addition, we have identified novel candidate genes for involvement in sleep duration including <jats:italic>SORCS1</jats:italic> and <jats:italic>ELOVL2</jats:italic>. Our results demonstrate that the self‐reported data collected through the CPMC are robust, and our genome‐wide association analysis has identified novel candidate genes involved in sleep duration. More generally, this study contributes to a better understanding of the complexity of human sleep. © 2015 The Authors. <jats:italic>American Journal of Medical Genetics Part B: Neuropsychiatric Genetics</jats:italic> Published by Wiley Periodicals, Inc.</jats:p></jats:sec>