A distinctive DNA methylation pattern in insufficient sleep

[1]  Max A. Little,et al.  GWAS in 446,118 European adults identifies 78 genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates , 2018, bioRxiv.

[2]  S. Horvath,et al.  An epigenome-wide association study meta-analysis of educational attainment , 2017, Molecular Psychiatry.

[3]  M. Trivedi,et al.  Short-term sleep deprivation leads to decreased systemic redox metabolites and altered epigenetic status , 2017, PloS one.

[4]  M. Walker,et al.  Sleep and Human Aging , 2017, Neuron.

[5]  T. Paunio,et al.  Common Genetic Variation Near Melatonin Receptor 1A Gene Linked to Job-Related Exhaustion in Shift Workers , 2017, Sleep.

[6]  P. Rautava,et al.  Gender differences in actual and preferred nocturnal sleep duration among Finnish employed population. , 2016, Maturitas.

[7]  H. Schiöth,et al.  One-night sleep deprivation induces changes in the DNA methylation and serum activity indices of stearoyl-CoA desaturase in young healthy men , 2016, Lipids in Health and Disease.

[8]  T. Lallukka,et al.  Prevalence of insomnia‐related symptoms continues to increase in the Finnish working‐age population , 2016, Journal of sleep research.

[9]  Andres Metspalu,et al.  Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci , 2016, PLoS genetics.

[10]  U. Hegerl,et al.  Genome‐wide association analysis of actigraphic sleep phenotypes in the LIFE Adult Study , 2016, Journal of sleep research.

[11]  T. Lehtimäki,et al.  Prolonged sleep restriction induces changes in pathways involved in cholesterol metabolism and inflammatory responses , 2016, Scientific Reports.

[12]  H. Schiöth,et al.  Acute Sleep Loss Induces Tissue-Specific Epigenetic and Transcriptional Alterations to Circadian Clock Genes in Men. , 2015, The Journal of clinical endocrinology and metabolism.

[13]  T. Porkka-Heiskanen,et al.  Spontaneous sleep–wake cycle and sleep deprivation differently induce Bdnf1, Bdnf4 and Bdnf9a DNA methylation and transcripts levels in the basal forebrain and frontal cortex in rats , 2015, Journal of sleep research.

[14]  Eric W. Danielson,et al.  S-SCAM, A Rare Copy Number Variation Gene, Induces Schizophrenia-Related Endophenotypes in Transgenic Mouse Model , 2015, The Journal of Neuroscience.

[15]  K. Makar,et al.  Nightshift work and genome-wide DNA methylation , 2015, Chronobiology international.

[16]  Tyson V. Sharp,et al.  The hypoxic tumor microenvironment: driving the tumorigenesis of non-small-cell lung cancer. , 2014, Future oncology.

[17]  Martin J. Aryee,et al.  Minfi: a flexible and comprehensive Bioconductor package for the analysis of Infinium DNA methylation microarrays , 2014, Bioinform..

[18]  M. Shago,et al.  Mosaic microdeletion of 17p11.2–p12 and duplication of 17q22–q24 in a girl with Smith–Magenis phenotype and peripheral neuropathy , 2014, American journal of medical genetics. Part A.

[19]  Ståle Pallesen,et al.  A 10-year trend of insomnia prevalence in the adult Norwegian population. , 2014, Sleep medicine.

[20]  C. Möller-Levet,et al.  Mistimed sleep disrupts circadian regulation of the human transcriptome , 2014, Proceedings of the National Academy of Sciences.

[21]  J. Carrier,et al.  The genome-wide landscape of DNA methylation and hydroxymethylation in response to sleep deprivation impacts on synaptic plasticity genes , 2014, Translational Psychiatry.

[22]  T. Porkka-Heiskanen,et al.  Sleep, its regulation and possible mechanisms of sleep disturbances , 2013, Acta physiologica.

[23]  S. Tufik,et al.  Changes in gene expression in the frontal cortex of rats with pilocarpine-induced status epilepticus after sleep deprivation , 2013, Epilepsy & Behavior.

[24]  S. Pallesen,et al.  Shift Work Disorder in a Random Population Sample – Prevalence and Comorbidities , 2013, PloS one.

[25]  C. Trempus,et al.  Accelerated elimination of ultraviolet-induced DNA damage through apoptosis in CDC25A-deficient skin. , 2012, Carcinogenesis.

[26]  S. Löwel,et al.  Deletion of the Presynaptic Scaffold CAST Reduces Active Zone Size in Rod Photoreceptors and Impairs Visual Processing , 2012, The Journal of Neuroscience.

[27]  W. Hahn,et al.  Nek4 Regulates Entry into Replicative Senescence and the Response to DNA Damage in Human Fibroblasts , 2012, Molecular and Cellular Biology.

[28]  Stephen R. Williams,et al.  Smith-Magenis syndrome results in disruption of CLOCK gene transcription and reveals an integral role for RAI1 in the maintenance of circadian rhythmicity. , 2012, American journal of human genetics.

[29]  A. Oshlack,et al.  SWAN: Subset-quantile Within Array Normalization for Illumina Infinium HumanMethylation450 BeadChips , 2012, Genome Biology.

[30]  Devin C. Koestler,et al.  DNA methylation arrays as surrogate measures of cell mixture distribution , 2012, BMC Bioinformatics.

[31]  S. Pallesen,et al.  Shift Work Disorder in Nurses – Assessment, Prevalence and Related Health Problems , 2012, PloS one.

[32]  T. Laatikainen,et al.  Self-reported sleep duration, all-cause mortality, cardiovascular mortality and morbidity in Finland. , 2011, Sleep medicine.

[33]  Markus Perola,et al.  An Immune Response Network Associated with Blood Lipid Levels , 2010, PLoS genetics.

[34]  L. Grover,et al.  Growth hormone rescues hippocampal synaptic function after sleep deprivation. , 2010, American journal of physiology. Regulatory, integrative and comparative physiology.

[35]  C. Wagner,et al.  Potassium restriction, high protein intake, and metabolic acidosis increase expression of the glutamine transporter SNAT3 (Slc38a3) in mouse kidney. , 2009, American journal of physiology. Renal physiology.

[36]  T. Åkerstedt,et al.  Shift work disorder among oil rig workers in the North Sea. , 2009, Sleep.

[37]  E. Hattori,et al.  Genetic and expression analyses reveal elevated expression of syntaxin 1A ( STX1A) in high functioning autism. , 2008, The international journal of neuropsychopharmacology.

[38]  P. Fletcher,et al.  Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1‐targeted mice , 2008, Genes, brain, and behavior.

[39]  Jianguo Li,et al.  Effect of deficiency in SREBP cleavage-activating protein on lipid metabolism during intermittent hypoxia. , 2007, Physiological genomics.

[40]  N. Nowak,et al.  17p11.2p12 triplication and del(17)q11.2q12 in a severely affected child with dup(17)p11.2p12 syndrome , 2007, Clinical genetics.

[41]  J. Lupski,et al.  Gender, genotype, and phenotype differences in Smith–Magenis syndrome: a meta‐analysis of 105 cases , 2007, Clinical genetics.

[42]  G. Tononi,et al.  Extensive and Divergent Effects of Sleep and Wakefulness on Brain Gene Expression , 2004, Neuron.

[43]  T. Åkerstedt,et al.  Shift work and disturbed sleep/wakefulness. , 2003, Sleep medicine reviews.

[44]  E. Guenther,et al.  Alterations in NMDA receptor expression during retinal degeneration in the RCS rat , 2001, Visual Neuroscience.

[45]  B Claustrat,et al.  Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome. , 2001, The Journal of pediatrics.

[46]  G. Tononi,et al.  Gene expression in the brain across the sleep–waking cycle 1 1 Published on the World Wide Web on 30 October 2000. , 2000, Brain Research.

[47]  T. Higashide,et al.  Characterization of the gene for HRG4 (UNC119), a novel photoreceptor synaptic protein homologous to unc-119. , 1999, Genomics.

[48]  T. Åkerstedt.  Shift work and disturbed sleep/wakefulness. , 1998, Occupational medicine.

[49]  C McCluggage,et al.  Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2) , 1996, American journal of medical genetics.

[50]  M Partinen,et al.  Genetic and environmental determination of human sleep. , 1983, Sleep.

[51]  L. Lannfelt,et al.  Acute sleep deprivation increases serum levels of neuron-specific enolase (NSE) and S100 calcium binding protein B (S-100B) in healthy young men. , 2014, Sleep.