Circadian gene variants influence sleep and the sleep electroencephalogram in humans

References

• Achermann P, Dijk DJ, Brunner DP, Borbély AA. (1993). A model of human sleep homeostasis based on EEG slow-wave activity: Quantitative comparison of data and simulations. Brain Res Bull. 31:97–113.
   PubMed Web of Science ®Google Scholar
• Aeschbach D, Cajochen C, Landolt H-P, Borbély AA. (1996). Homeostatic sleep regulation in habitual short sleepers and long sleepers. Am J Physiol. 270:R41–R53.
   PubMed Web of Science ®Google Scholar
• Agnew HW, Jr., Webb WB, Williams RL. (1966). The first night effect: An EEG study of sleep. Psychophysiol. 2:263–266.
   PubMedGoogle Scholar
• Allebrandt KV, Teder-Laving M, Akyol M, et al. (2010). CLOCK gene variants associate with sleep duration in two independent populations. Biol Psychiatry. 67: 1040–1047.
   PubMed Web of Science ®Google Scholar
• Ambrosius U, Lietzenmaier S, Wehrle R, et al. (2008). Heritability of sleep electroencephalogram. Biol Psychiatry. 64:344–348.
   PubMed Web of Science ®Google Scholar
• Armitage R. (1995). The distribution of EEG frequencies in REM and NREM sleep stages in healthy young adults. Sleep. 18:334–341.
   PubMed Web of Science ®Google Scholar
• Bachmann V, Klein C, Bodenmann S, et al. (2012). The BDNF Val66Met polymorphism modulates sleep intensity: EEG frequency- and state-specificity. Sleep. 35:335–344.
   PubMed Web of Science ®Google Scholar
• Barrett JC, Fry B, Maller J, Daly MJ. (2005). Haploview: Analysis and visualization of LD and haplotype maps. Bioinformatics. 21:263–265.
   PubMed Web of Science ®Google Scholar
• Berlowitz DJ, Spong J, Gordon I, et al. (2012). Relationships between objective sleep indices and symptoms in a community sample of people with tetraplegia. Arch Phys Med Rehabil. 93: 1246–1252.
   PubMed Web of Science ®Google Scholar
• Bodenmann S, Hohoff C, Freitag C, et al. (2012). Polymorphisms of ADORA2A modulate psychomotor vigilance and the effects of caffeine on neurobehavioural performance and sleep EEG after sleep deprivation. Br J Pharmacol. 165: 1904–1913.
   PubMed Web of Science ®Google Scholar
• Bodenmann S, Landolt HP. (2010). Effects of modafinil on the sleep EEG depend on Val158Met genotype of COMT. Sleep. 33: 1027–1035.
   PubMed Web of Science ®Google Scholar
• Bollen KA, Curran PJ. (2005). Latent growth curve models: A structural equation perspective. Hoboken, NJ: Wiley.
   Google Scholar
• Borbély AA. (1982). A two process model of sleep regulation. Hum Neurobiol. 1:195–204.
   PubMedGoogle Scholar
• Carpen JD, Archer SN, Skene DJ, et al. (2005). A single-nucleotide polymorphism in the 5’-untranslated region of the hPER2 gene is associated with diurnal preference. J Sleep Res. 14:293–297.
   PubMed Web of Science ®Google Scholar
• Curie T, Mongrain V, Dorsaz S, et al. (2013). Homeostatic and circadian contribution to EEG and molecular state variables of sleep regulation. Sleep. 36:311–323.
   PubMed Web of Science ®Google Scholar
• Czeisler CA, Weitzman ED, Moore-Ede MC, et al. (1980). Human sleep: Its duration and organization depend on its circadian phase. Science. 210: 1264–1267.
   PubMed Web of Science ®Google Scholar
• Dijk DJ, Beersma DGM, Bloem G. (1989). Sex differences in the sleep EEG of young adults: Visual scoring and spectral analysis. Sleep. 12:500–507.
   PubMed Web of Science ®Google Scholar
• Dupuis J, Langenberg C, Prokopenko I, et al. (2010). New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat Genet. 42:105–116.
   PubMed Web of Science ®Google Scholar
• Ehlers CL, Kupfer DJ. (1997). Slow-wave sleep:Do young adult men and women age differently? J Sleep Res. 6:211–215.
   PubMed Web of Science ®Google Scholar
• Guindalini C, Mazzotti DR, Castro LS, et al. (2014). Brain-derived neurotrophic factor gene polymorphism predicts interindividual variation in the sleep electroencephalogram. Journal of neuroscience research. 92: 1018–1023.
   PubMed Web of Science ®Google Scholar
• Han B, Eskin E. (2011). Random-effects model aimed at discovering associations in meta-analysis of genome-wide association studies. Am J Hum Genet. 88:586–598.
   PubMed Web of Science ®Google Scholar
• Hanlon EC, Van Cauter E. (2011). Quantification of sleep behavior and of its impact on the cross-talk between the brain and peripheral metabolism. Proceedings of the National Academy of Sciences of the United States of America. 108 Suppl 3:15609–15616.
   PubMed Web of Science ®Google Scholar
• He Y, Jones CR, Fujiki N, et al. (2009). The transcriptional repressor DEC2 regulates sleep length in mammals. Science. 325:866–870.
   PubMed Web of Science ®Google Scholar
• Ionita-Laza I, Lee S, Makarov V, et al. (2013). Sequence kernel association tests for the combined effect of rare and common variants. Am J Hum Genet. 92:841–853.
   PubMed Web of Science ®Google Scholar
• Landolt HP, Dijk D. (2010). Genetic basis of sleep in healthy humans. In MH Kryger, Roth T, WC Dement (Eds). Principles and Practice of Sleep Medicine. St. Louis, MO: Elsevier Saunders, pp. 175–183.
   Google Scholar
• Lane JM, Chang AM, Consortium C, et al. (2015). Impact of common variation at diabetes trait loci MTNR1B and CRY2 on sleep, circadian and melatonin physiology. Sleep. 38:A5–6.
   Google Scholar
• Lennox WG, Gibbs EL, Gibbs FA. (1945). The brain-wave pattern, an hereditary trait. The Journal of Heredity. 36:233–243.
   Web of Science ®Google Scholar
• Linkowski P. (1999). EEG sleep patterns in twins. J Sleep Res. 8 Suppl 1:11–13.
   PubMed Web of Science ®Google Scholar
• Lyssenko V, Nagorny CL, Erdos MR, et al. (2008). Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion. Nat Genet. 41:82–88.
   PubMed Web of Science ®Google Scholar
• Mignot E, Young T, Lin L, Finn L. (1999). Nocturnal sleep and daytime sleepiness in normal subjects with HLA-DQB1*0602. Sleep. 22:347–352.
   PubMed Web of Science ®Google Scholar
• Nedeltcheva AV, Scheer FA. (2014). Metabolic effects of sleep disruption, links to obesity and diabetes. Curr Opin Endocrinol Diabetes Obesity. 21:293–298.
   PubMed Web of Science ®Google Scholar
• Pandi-Perumal SR, Trakht I, et al. (2008). Physiological effects of melatonin: Role of melatonin receptors and signal transduction pathways. Prog Neurobiol. 85:335–353.
   PubMed Web of Science ®Google Scholar
• Prokopenko I, Langenberg C, Florez JC,et al. (2008). Variants in MTNR1B influence fasting glucose levels. Nat Genet. 41:77–81.
   PubMed Web of Science ®Google Scholar
• Purcell S, Neale B, Todd-Brown K, et al. (2007). PLINK: A tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet. 81:559–575.
   PubMed Web of Science ®Google Scholar
• Rechtschaffen A, Kales A. (1968). A manual of standardized terminology, techniques and scoring system for sleep stages of human Subjects. Washington, D.C.: US Government Printing Office.
   Google Scholar
• Retey JV, Adam M, Honegger E, et al. (2005). A functional genetic variation of adenosine deaminase affects the duration and intensity of deep sleep in humans. PNAS. 102:15676–15681.
   PubMed Web of Science ®Google Scholar
• Scheer FA, Zeitzer JM, Ayas NT, et al. (2006). Reduced sleep efficiency in cervical spinal cord injury; association with abolished night time melatonin secretion. Spinal Cord. 44:78–81.
   PubMed Web of Science ®Google Scholar
• Spiegel K, Knutson K, Leproult R, et al. (2005). Sleep loss: A novel risk factor for insulin resistance and Type 2 diabetes. J Appl Physiol. 99: 2008–2019.
   PubMed Web of Science ®Google Scholar
• Toh KL, Jones CR, He Y, et al. (2001). An h Per2 phosphorylation site mutation in familial advanced sleep-phase syndrome. Science. 291: 1040–1043.
   PubMed Web of Science ®Google Scholar
• van Beijsterveldt CE, van Baal GC. (2002). Twin and family studies of the human electroencephalogram: A review and a meta-analysis. Biol Psychol. 61:111–138.
   PubMed Web of Science ®Google Scholar
• Viola AU, Archer SN, James LM, et al. (2007). PER3 polymorphism predicts sleep structure and waking performance. Curr Biol. 17:1–6.
   PubMed Web of Science ®Google Scholar
• Ward LD, Kellis M. (2012). HaploReg: A resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants. Nucleic Acids Res. 40:D930–934.
   PubMed Web of Science ®Google Scholar