HuGE Literature Finder
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| The Association between Circadian Clock Gene Polymorphisms and Metabolic Syndrome: A Systematic Review and Meta-Analysis. Biology 2021 Dec 11 (1): . Škrlec Ivana, Talapko Jasminka, Džijan Snježana, Cesar Vera, Lazi? Nikolina, Lepeduš Hrvo |
| Association Between CLOCK Gene Variants and Restless Legs Syndrome in Koreans. Psychiatry investigation 2021 Nov . Seo Jae Eun, Yeom Ji Won, Jeon Sehyun, Cho Chul-Hyun, Jeong Seunghwa, Lee Heon-Jeo |
| Effects of circadian clock genes and health-related behavior on metabolic syndrome in a Taiwanese population: Evidence from association and interaction analysis. PloS one 2017 12 (3): e0173861. Lin Eugene, Kuo Po-Hsiu, Liu Yu-Li, Yang Albert C, Kao Chung-Feng, Tsai Shih-J |
| CRY1, CRY2 and PRKCDBP genetic variants in metabolic syndrome. Hypertension research : official journal of the Japanese Society of Hypertension 2015 Mar 38 (3): 186-92. Kovanen Leena, Donner Kati, Kaunisto Mari, Partonen Ti |
| Association between restless legs syndrome and CLOCK and NPAS2 gene polymorphisms in schizophrenia. Chronobiology international 2014 Aug 31 (7): 838-44. Jung Jin-Sook, Lee Heon-Jeong, Cho Chul-Hyun, Kang Seung-Gul, Yoon Ho-Kyoung, Park Young-Min, Moon Joung-Ho, Yang Hee-Jung, Song Hyun-Mi, Kim Le |
| Beneficial effect of CLOCK gene polymorphism rs1801260 in combination with low-fat diet on insulin metabolism in the patients with metabolic syndrome. Chronobiology international 2014 Apr 31 (3): 401-8. Garcia-Rios Antonio, Gomez-Delgado Francisco Jesus, Garaulet Marta, Alcala-Diaz Juan Francisco, Delgado-Lista Francisco Javier, Marin Carmen, Rangel-Zuñiga Oriol Alberto, Rodriguez-Cantalejo Fernando, Gomez-Luna Purificacion, Ordovas Jose Maria, Perez-Jimenez Francisco, Lopez-Miranda Jose, Perez-Martinez Pab |
| [Molecular and genetic aspects of interactions of the circadian clock and the energy-producing substrate metabolism in mammals]. Genetika 2014 Feb 50 (2): 125-37. Podkolodnaia O |
| FMR1, circadian genes and depression: suggestive associations or false discovery? Journal of circadian rhythms 2013 11 (1): 3. Kripke Daniel F, Nievergelt Caroline M, Tranah Gregory J, Murray Sarah S, Rex Katharine M, Grizas Alexandra P, Hahn Elizabeth K, Lee Heon-Jeong, Kelsoe John R, Kline Lawrence |
| A Period 2 genetic variant interacts with plasma SFA to modify plasma lipid concentrations in adults with metabolic syndrome. The Journal of nutrition 2012 Jul 142 (7): 1213-8. Garcia-Rios Antonio, Perez-Martinez Pablo, Delgado-Lista Javier, Phillips Catherine M, Gjelstad Ingrid M F, Wright John W, Karlström Brita, Kiec-Wilk Beata, van Hees A M J, Helal Olfa, Polus Anna, Defoort Catherine, Riserus Ulf, Blaak Ellen E, Lovegrove Julie A, Drevon Christian A, Roche Helen M, Lopez-Miranda Jo |
| Tef polymorphism is associated with sleep disturbances in patients with Parkinson's disease. Sleep medicine 2012 Mar 13 (3): 297-300. Hua Ping, Liu Weiguo, Zhao Yanyan, Ding Haixia, Wang Li, Xiao Ho |
| Gene-gene interaction between serotonin transporter (SLC6A4) and CLOCK modulates the risk of metabolic syndrome in rotating shiftworkers. Chronobiology international 2010 Jul 27 (6): 1202-18. Sookoian Silvia, Gianotti Tomas Fernandez, Burgueño Adriana, Pirola Carlos Jo |
| Genotyping sleep disorders patients. Psychiatry investigation 2010 Mar 7 (1): 36-42. Kripke Daniel F, Shadan Farhad F, Dawson Arthur, Cronin John W, Jamil Shazia M, Grizas Alexandra P, Koziol James A, Kline Lawrence |
| CLOCK genetic variation and metabolic syndrome risk: modulation by monounsaturated fatty acids. The American journal of clinical nutrition 2009 Dec 90 (6): 1466-75. Garaulet Marta, Lee Yu-Chi, Shen Jian, Parnell Laurence D, Arnett Donna K, Tsai Michael Y, Lai Chao-Qiang, Ordovas Jose |
| NPAS2 and PER2 are linked to risk factors of the metabolic syndrome. Journal of circadian rhythms 2009 7 (1): 5. Englund Ani, Kovanen Leena, Saarikoski Sirkku T, Haukka Jari, Reunanen Antti, Aromaa Arpo, Lönnqvist Jouko, Partonen Ti |
| Casein kinase I epsilon (CKIvarepsilon) N408 allele is very rare in the Brazilian population and is not involved in susceptibility to circadian rhythm sleep disorders. Behavioural brain research 2008 Nov 193 (1): 156-7. Castro Rosa M R P S, Barbosa Ana A, Pedrazzoli Mario, Tufik Serg |
| Genetic variants of Clock transcription factor are associated with individual susceptibility to obesity. The American journal of clinical nutrition 2008 Jun 87 (6): 1606-15. Sookoian Silvia, Gemma Carolina, Gianotti Tomas Fernández, Burgueño Adriana, Castaño Gustavo, Pirola Carlos Jo |
| Association between polymorphisms in the Clock gene, obesity and the metabolic syndrome in man. International journal of obesity (2005) 2008 Apr 32 (4): 658-62. Scott E M, Carter A M, Grant P |
| Arylalkylamine N-acetyltransferase (AANAT) genotype as a personal trait in melatonin synthesis. Journal of toxicology and environmental health. Part A 2008 71 (13-14): 874-6. Blomeke Brunhilde, Golka Klaus, Griefahn Barbara, Roemer Hermann |
| Aryl hydrocarbon receptor nuclear translocator-like (BMAL1) is associated with susceptibility to hypertension and type 2 diabetes. Proceedings of the National Academy of Sciences of the United States of America 2007 Sep 104 (36): 14412-7. Woon Peng Y, Kaisaki Pamela J, Bragança José, Bihoreau Marie-Thérèse, Levy Jonathan C, Farrall Martin, Gauguier Dominiq |
| How do genes exert their role? Period 3 gene variants and possible influences on mood disorder phenotypes. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2007 Sep 17 (9): 587-94. Artioli Paola, Lorenzi Cristina, Pirovano Adele, Serretti Alessandro, Benedetti Francesco, Catalano Marco, Smeraldi Enri |
| Age-related change in the association between a polymorphism in the PER3 gene and preferred timing of sleep and waking activities. Journal of sleep research 2007 Mar 16 (1): 12-6. Jones Kay H S, Ellis Jason, von Schantz Malcolm, Skene Debra J, Dijk Derk-Jan, Archer Simon |
| Clock polymorphisms and circadian rhythms phenotypes in a sample of the Brazilian population. Chronobiology international 2007 24 (1): 1-8. Pedrazzoli Mario, Louzada Fernando Mazzili, Pereira Danyella Silva, Benedito-Silva Ana Amélia, Lopez Alberto Remesar, Martynhak Bruno Jacson, Korczak Anna Ligia, Koike Bruna Del Vechio, Barbosa Ana Alves, D'Almeida Vania, Tufik Serg |
| A silent polymorphism in the PER1 gene associates with extreme diurnal preference in humans. Journal of human genetics 2006 51 (12): 1122-5. Carpen Jayshan D, von Schantz Malcolm, Smits Marcel, Skene Debra J, Archer Simon |
| A missense variation in human casein kinase I epsilon gene that induces functional alteration and shows an inverse association with circadian rhythm sleep disorders. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2004 Oct 29 (10): 1901-9. Takano Atsuko, Uchiyama Makoto, Kajimura Naofumi, Mishima Kazuo, Inoue Yuichi, Kamei Yuichi, Kitajima Tsuyoshi, Shibui Kayo, Katoh Masaaki, Watanabe Tsuyoshi, Hashimotodani Yuki, Nakajima Toru, Ozeki Yuji, Hori Toru, Yamada Naoto, Toyoshima Ryoichi, Ozaki Norio, Okawa Masako, Nagai Katsuya, Takahashi Kiyohisa, Isojima Yasushi, Yamauchi Toshio, Ebisawa Takas |
| A length polymorphism in the circadian clock gene Per3 is linked to delayed sleep phase syndrome and extreme diurnal preference. Sleep 2003 Jun 26 (4): 413-5. Archer SN, Robilliard DL, Skene DJ, Smits M, Williams A, Arendt J, von Schantz M |
| The 3111 Clock gene polymorphism is not associated with sleep and circadian rhythmicity in phenotypically characterized human subjects. Journal of sleep research 2002 Dec 11 (4): 305-12. Robilliard Donna L, Archer Simon N, Arendt Josephine, Lockley Steven W, Hack Lisa M, English Judie, Leger Damien, Smits Marcel G, Williams Adrian, Skene Debra J, Von Schantz Malco |
| Mutation screening of the human Clock gene in circadian rhythm sleep disorders. Psychiatry research 2002 Mar 109 (2): 121-8. Iwase Toshio, Kajimura Naofumi, Uchiyama Makoto, Ebisawa Takashi, Yoshimura Kimio, Kamei Yuichi, Shibui Kayo, Kim Keiko, Kudo Yoshinao, Katoh Masaaki, Watanabe Tsuyoshi, Nakajima Toru, Ozeki Yuji, Sugishita Mariko, Hori Toru, Ikeda Masaaki, Toyoshima Ryoichi, Inoue Yuichi, Yamada Naoto, Mishima Kazuo, Nomura Masahiko, Ozaki Norio, Okawa Masako, Takahashi Kiyohisa, Yamauchi Tosh |
| Association of structural polymorphisms in the human period3 gene with delayed sleep phase syndrome. EMBO reports 2001 Apr 2 (4): 342-6. Ebisawa T, Uchiyama M, Kajimura N, Mishima K, Kamei Y, Katoh M, Watanabe T, Sekimoto M, Shibui K, Kim K, Kudo Y, Ozeki Y, Sugishita M, Toyoshima R, Inoue Y, Yamada N, Nagase T, Ozaki N, Ohara O, Ishida N, Okawa M, Takahashi K, Yamauchi T |
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- Page last updated:Jun 28, 2022
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