Human Genome Epidemiology Literature Finder
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Records 1 - 17 (of 17 Records) |
| Query Trace: Syndrome and TPH2[original query] |
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| Polymorphisms in genes regulating the HPA axis associated with empirically delineated classes of unexplained chronic fatigue. Pharmacogenomics 2006 Apr 7 (3): 387-94. Smith Alicia K, White Peter D, Aslakson Eric, Vollmer-Conna Ute, Rajeevan Mangalathu |
| Combinations of single nucleotide polymorphisms in neuroendocrine effector and receptor genes predict chronic fatigue syndrome. Pharmacogenomics 2006 Apr 7 (3): 475-83. Goertzel Benjamin N, Pennachin Cassio, de Souza Coelho Lucio, Gurbaxani Brian, Maloney Elizabeth M, Jones James |
| Genetic evaluation of the serotonergic system in chronic fatigue syndrome. Psychoneuroendocrinology 2008 Feb 33 (2): 188-97. Smith Alicia K, Dimulescu Irina, Falkenberg Virginia R, Narasimhan Supraja, Heim Christine, Vernon Suzanne D, Rajeevan Mangalathu |
| Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the sudden infant death syndrome. Genomics 2008 Jun 91 (6): 485-91. Nonnis Marzano Francesco, Maldini Milena, Filonzi Laura, Lavezzi Anna Maria, Parmigiani Stefano, Magnani Cinzia, Bevilacqua Giulio, Matturri Lui |
| SERT Ileu425Val in autism, Asperger syndrome and obsessive-compulsive disorder. Psychiatric genetics 2008 Feb 18 (1): 31-9. Wendland Jens R, DeGuzman Theresa B, McMahon Francis, Rudnick Gary, Detera-Wadleigh Sevilla D, Murphy Dennis |
| Association study of serotonergic gene variants with antipsychotic-induced adverse reactions. Psychiatric genetics 2009 Dec 19 (6): 305-11. Al-Janabi Ismail, Arranz Maria J, Blakemore Alexandra I F, Saiz Pilar A, Susce Margaret T, Glaser Paul E A, Clark Daniel, de Leon Jo |
| Variations in tryptophan hydroxylase 2 linked to decreased serotonergic activity are associated with elevated risk for metabolic syndrome in depression. Molecular psychiatry 2010 Jul 15 (7): 736-47. Kloiber S, Kohli M A, Brueckl T, Ripke S, Ising M, Uhr M, Menke A, Unschuld P G, Horstmann S, Salyakina D, Muller-Myhsok B, Binder E B, Holsboer F, Lucae |
| Associations of tryptophan hydroxylase gene polymorphisms with irritable bowel syndrome. Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 2011 Mar 23 (3): 233-9, e116. Jun S, Kohen R, Cain K C, Jarrett M E, Heitkemper M |
| Association study of tryptophan hydroxylase-2 gene in schizophrenia and its clinical features in Chinese Han population. Journal of molecular neuroscience : MN 2011 Mar 43 (3): 406-11. Zhang Chen, Li Zezhi, Shao Yang, Xie Bin, Du Yasong, Fang Yiru, Yu Shunyi |
| TPH2 G/T polymorphism is associated with hyperphagia, IQ, and internalizing problems in Prader-Willi syndrome. Journal of child psychology and psychiatry, and allied disciplines 2011 May 52 (5): 580-7. Dykens Elisabeth M, Roof Elizabeth, Bittel Douglas, Butler Merlin |
| Influence of TPH2 variants on diagnosis and response to treatment in patients with major depression, bipolar disorder and schizophrenia. Psychiatry research 2011 Aug 189 (1): 26-32. Serretti Alessandro, Chiesa Alberto, Porcelli Stefano, Han Changsu, Patkar Ashwin A, Lee Soo-Jung, Park Moon Ho, Pae Chi- |
| Investigation of tryptophan hydroxylase 2 (TPH2) in schizophrenia and in the response to antipsychotics. Journal of psychiatric research 2012 Aug 46 (8): 1073-80. Schuhmacher Anna, Becker Tim, Rujescu Dan, Quednow Boris B, Lennertz Leonhard, Wagner Michael, Benninghoff Jens, Rietschel Marcella, Häfner Heinz, Franke Petra, Wölwer Wolfgang, Gaebel Wolfgang, Maier Wolfgang, Mössner Raina |
| TPH gene polymorphisms are associated with disease perception and quality of life in women with irritable bowel syndrome. Biological research for nursing 2014 Jan 16 (1): 95-104. Jun Sang-Eun, Kohen Ruth, Cain Kevin C, Jarrett Monica E, Heitkemper Margaret |
| Pilot study of Biomarkers for predicting effectiveness of ramosetron in diarrhea-predominant irritable bowel syndrome: expression of S100A10 and polymorphisms of TPH1. Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 2015 Jan 27 (1): 82-91. Shiotani A, Kusunoki H, Ishii M, Imamura H, Manabe N, Kamada T, Hata J, Merchant J L, Haruma |
| Investigation of previously implicated genetic variants in chronic tic disorders: a transmission disequilibrium test approach. European archives of psychiatry and clinical neuroscience 2017 May . Abdulkadir Mohamed, Londono Douglas, Gordon Derek, Fernandez Thomas V, Brown Lawrence W, Cheon Keun-Ah, Coffey Barbara J, Elzerman Lonneke, Fremer Carolin, Fründt Odette, Garcia-Delgar Blanca, Gilbert Donald L, Grice Dorothy E, Hedderly Tammy, Heyman Isobel, Hong Hyun Ju, Huyser Chaim, Ibanez-Gomez Laura, Jakubovski Ewgeni, Kim Young Key, Kim Young Shin, Koh Yun-Joo, Kook Sodahm, Kuperman Samuel, Leventhal Bennett, Ludolph Andrea G, Madruga-Garrido Marcos, Maras Athanasios, Mir Pablo, Morer Astrid, Müller-Vahl Kirsten, Münchau Alexander, Murphy Tara L, Plessen Kerstin J, Roessner Veit, Shin Eun-Young, Song Dong-Ho, Song Jungeun, Tübing Jennifer, van den Ban Els, Visscher Frank, Wanderer Sina, Woods Martin, Zinner Samuel H, King Robert A, Tischfield Jay A, Heiman Gary A, Hoekstra Pieter J, Dietrich Andr |
| Genetics of Aggression in Alzheimer's Disease (AD). Frontiers in aging neuroscience 2017 9 87. Lukiw Walter J, Rogaev Evgeny |
| Association of Fatigue With TPH2 Genetic Polymorphisms in Women With Irritable Bowel Syndrome. Biological research for nursing 2018 Oct 1099800418806055. Han Claire J, Jarrett Monica E, Cain Kevin C, Jun Sangeun, Heitkemper Margaret |
- Page last reviewed:Feb 1, 2023
- Page last updated:Jun 02, 2023
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