Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 44 Records) |
Query Trace: Sleep and COMT[original query] |
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Genetic polymorphisms of DAT1 and COMT differentially associate with actigraphy-derived sleep-wake cycles in young adults. Chronobiology international 2014 Jun 31 (5): 705-14. Valomon Amandine, Holst Sebastian C, Bachmann Valérie, Viola Antoine U, Schmidt Christina, Zürcher Jurian, Berger Wolfgang, Cajochen Christian, Landolt Hans-Pet |
Catechol-O-methyltransferase, dopamine, and sleep-wake regulation. Sleep medicine reviews 2015 Aug 22 47-53. Dauvilliers Yves, Tafti Mehdi, Landolt Hans Pet |
Differences in planning performance, a neurocognitive endophenotype, are associated with a functional variant in PER3 gene. Chronobiology international 2015 Jun 32 (5): 591-5. González-Giraldo Yeimy, González-Reyes Rodrigo E, Mueller Shane T, Piper Brian J, Adan Ana, Forero Diego |
Genetic variation in catechol-O-methyltransferase modifies effects of clonidine treatment in chronic fatigue syndrome. The pharmacogenomics journal 2016 Jul . Hall K T, Kossowsky J, Oberlander T F, Kaptchuk T J, Saul J P, Wyller V B, Fagermoen E, Sulheim D, Gjerstad J, Winger A, Mukamal K |
Time to wake up: No impact of COMT Val158Met gene variation on circadian preferences, arousal regulation and sleep. Chronobiology international 2016 May 1-13. Jawinski Philippe, Tegelkamp Sophie, Sander Christian, Häntzsch Madlen, Huang Jue, Mauche Nicole, Scholz Markus, Spada Janek, Ulke Christine, Burkhardt Ralph, Reif Andreas, Hegerl Ulrich, Hensch Tilm |
Sleep duration, depression, and oxytocinergic genotype influence prepulse inhibition of the startle reflex in postpartum women. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2016 Apr 26 (4): 767-76. Comasco Erika, Gulinello Maria, Hellgren Charlotte, Skalkidou Alkistis, Sylven Sara, Sundström-Poromaa Ing |
Val158Met polymorphism in the COMT gene is associated with hypersomnia and mental health-related quality of life in a Colombian sample. Neuroscience letters 2017 Feb 644 43-47. Jiménez Karen M, Pereira-Morales Angela J, Forero Diego |
Variations in COMT and NTRK2 Influence Symptom Burden in Women Undergoing Breast Cancer Treatment. Biological research for nursing 2017 Jan 1099800417692877. Young Erin E, Kelly Debra Lynch, Shim Insop, Baumbauer Kyle M, Starkweather Angela, Lyon Debra |
Catechol-O-methyltransferase (COMT) genotype affects cognitive control during total sleep deprivation. Cortex; a journal devoted to the study of the nervous system and behavior 2017 Nov 99 179-186. Satterfield Brieann C, Hinson John M, Whitney Paul, Schmidt Michelle A, Wisor Jonathan P, Van Dongen Hans P |
Time-on-Task Effect During Sleep Deprivation in Healthy Young Adults Is Modulated by Dopamine Transporter Genotype. Sleep 2017 Oct . Satterfield Brieann C, Wisor Jonathan P, Schmidt Michelle A, Van Dongen Hans P |
Opioid-related genetic polymorphisms do not influence postoperative opioid requirement: A prospective observational study. European journal of anaesthesiology 2018 Feb . Aubrun Frédéric, Zahr Noël, Langeron Olivier, Boccheciampe Nicolas, Cozic Nathalie, Belin Lisa, Hulot Jean-Sebastien, Khiami Frederic, Riou Bru |
Effects of COMT genotype and tolcapone on lapses of sustained attention after sleep deprivation in healthy young men. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2018 Feb . Valomon Amandine, Holst Sebastian C, Borrello Alessandro, Weigend Susanne, Müller Thomas, Berger Wolfgang, Sommerauer Michael, Baumann Christian R, Landolt Hans-Pet |
Fast sleep spindle density is associated with rs4680 (Val108/158Met) genotype of catechol-O-methyltransferase (COMT). Sleep 2018 Jan . Schilling Claudia, Gappa Lena, Schredl Michael, Streit Fabian, Treutlein Jens, Frank Josef, Deuschle Michael, Meyer-Lindenberg Andreas, Rietschel Marcella, Witt Stephanie |
Sleep disturbance and neurocognitive outcomes in older patients with breast cancer: Interaction with genotype. Cancer 2019 Sep . Carroll Judith E, Small Brent J, Tometich Danielle B, Zhai Wanting, Zhou Xingtao, Luta George, Ahles Tim A, Saykin Andrew J, Nudelman Kelly N H, Clapp Jonathan D, Jim Heather S, Jacobsen Paul B, Hurria Arti, Graham Deena, McDonald Brenna C, Denduluri Neelima, Extermann Martine, Isaacs Claudine, Dilawari Asma A, Root James, Stern Robert A, Mandelblatt Jeanne S, |
Functional dyspepsia susceptibility is associated with TGFB1 gene polymorphisms (RS4803455, RS1800469) in H pylori-negative Chinese population. Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 2019 Aug e13681. Cheung Cynthia K Y, Lan Lin Lin, Chan Yawen, Yuen Kay, Cheong Pui Kuan, Fang Fanny, Wu Justin C |
Clinical and Clinical-Pharmacogenetic Models for Prediction of the Most Common Psychiatric Complications Due to Dopaminergic Treatment in Parkinson's Disease. The international journal of neuropsychopharmacology 2020 7 23 (8): 496-504. Redenšek Sara, Jenko Bizjan Barbara, Trošt Maja, Dolžan Vi |
Genetic basis of sleep bruxism and sleep apnea-response to a medical puzzle. Scientific reports 2020 May 10 (1): 7497. Wieckiewicz Mieszko, Bogunia-Kubik Katarzyna, Mazur Grzegorz, Danel Dariusz, Smardz Joanna, Wojakowska Anna, Poreba Rafal, Dratwa Marta, Chaszczewska-Markowska Monika, Winocur Efraim, Emodi-Perlman Alona, Martynowicz Hele |
The association between sleep-wake ratio and overnight picture recognition is moderated by BDNF genotype. Neurobiology of learning and memory 2020 Nov 107353. Halonen Risto, Kuula Liisa, Lahti Jari, Räikkönen Katri, Pesonen Anu-Katrii |
Clinical and genetic factors associated with anxiety and depression in breast cancer patients: a cross-sectional study. BMC cancer 2021 Jul 21 (1): 872. Hajj Aline, Hachem Roula, Khoury Rita, Hallit Souheil, ElJEBBAWI Bashar, Nasr Fady, El Karak Fadi, Chahine Georges, Kattan Joseph, Rabbaa Khabbaz Lyd |
Clinical and Genetic Factors Associated With the Breast Cancer-Related Sleep Disorders: The "CAGE-Sleep" Study-A Cross-Sectional Study. Journal of pain and symptom management 2021 2 62 (3): e46-e55. Hajj Aline, Hachem Roula, Khoury Rita, Nehme Tamara, Hallit Souheil, Nasr Fady, Karak Fady El, Chahine Georges, Kattan Joseph, Khabbaz Lydia Rabb |
Genetics and Cognitive Vulnerability to Sleep Deprivation in Healthy Subjects: Interaction of ADORA2A, TNF-? and COMT Polymorphisms. Life (Basel, Switzerland) 2021 Oct 11 (10): . Erblang Mégane, Drogou Catherine, Gomez-Merino Danielle, Rabat Arnaud, Guillard Mathias, Beers Pascal Van, Quiquempoix Michael, Boland Anne, Deleuze Jean François, Olaso Robert, Derbois Céline, Prost Maxime, Dorey Rodolphe, Léger Damien, Thomas Claire, Chennaoui Mounir, Sauvet Fabi |
Evaluation of the Association of COMT Rs4680 Polymorphism with Swimmers' Competitive Performance. Genes 2021 10 12 (10): . Zmijewski Piotr, Leo?ska-Duniec Agata, Stu?a Aleksander, Sawczuk Mar |
Clinical and genetic factors associated with self-reported cognitive deficits in women with breast cancer: the "CAGE-Cog" study. BMC cancer 2022 Sep 22 (1): 996. Hajj Aline, Khoury Rita, Hachem Roula, Awad Aya, Hallit Souheil, Sacre Hala, Nasr Fady, Karak Fadi El, Chahine Georges, Kattan Joseph, Khabbaz Lydia Rabb |
Are Pain Polymorphisms Associated with the Risk and Phenotype of Post-COVID Pain in Previously Hospitalized COVID-19 Survivors? Genes 2022 Jul 13 (8): . Fernández-de-Las-Peñas César, Giordano Rocco, Díaz-Gil Gema, Gil-Crujera Antonio, Gómez-Sánchez Stella M, Ambite-Quesada Silvia, Arendt-Nielsen La |
The association between overnight recognition accuracy and slow oscillation-spindle coupling is moderated by BDNF Val66Met. Behavioural brain research 2022 4 428 113889. Halonen Risto, Kuula Liisa, Lahti Jari, Räikkönen Katri, Pesonen Anu-Katrii |
The Associations of Single Nucleotide Polymorphisms with Risk and Symptoms of Irritable Bowel Syndrome. Journal of personalized medicine 2022 Jan 12 (2): . Zhao Tingting, Zhang Yiming, Lee Joochul, Starkweather Angela R, Young Erin E, Cong Xiaom |
Effects of acute caffeine intake on Insulin-like Growth Factor-1 responses to total sleep deprivation: interactions with COMT polymorphism, a randomized, cross over study. Lifestyle genomics 2023 6 . Catherine Drogou, Fabien Sauvet, Mégane Erblang, Damien Leger, Claire Thomas, Mounir Chennaoui, Danielle Gomez-Meri |
The polymorphism Val158Met in the COMT gene: disrupted dopamine system in fibromyalgia patients? Pain 2024 6 . Maria Carla Gerra, Cristina Dallabona, Matteo Manfredini, Rocco Giordano, Camilla Capriotti, Alberto González-Villar, Yolanda Triñanes, Lars Arendt-Nielsen, Maria Teresa Carrillo-de-la-Pe |
Association of OPRM1 rs1799971, HTR1B rs6296 and COMT rs4680 polymorphisms with clinical phenotype among women with fibromyalgia. Scientific reports 2024 5 14 (1): 11273. César Fernández-de-Las-Peñas, Silvia Ambite-Quesada, Luis M Fernández-Méndez, Carmen Jiménez-Antona, Cristina Gómez-Calero, Ricardo Pocinho, Juan Antonio Valera-Calero, Margarita Cigarán-Méndez, Lars Arendt-Niels |
Clinical prediction of opioid use disorder in chronic pain patients: a cohort-retrospective study with a pharmacogenetic approach. Minerva anestesiologica 2024 4 . Mónica Escorial, Javier Muriel, Laura Agulló, Thomas Zandonai, César Margarit, Domingo Morales, Ana M Pei |
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