Human Genome Epidemiology Literature Finder
Records 1 - 23 (of 23 Records) |
Query Trace: Syndrome and MAOA[original query] |
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Evidence for a genetic association between monoamine oxidase A and restless legs syndrome. Neurology 2002 Jul 59 (2): 215-9. Desautels A, Turecki G, Montplaisir J, Brisebois K, Sequeira A, Adam B, Rouleau G |
Analysis of monoamine oxidase A (MAOA) promoter polymorphism in Finnish male alcoholics. Psychiatry research 2002 Mar 109 (2): 113-9. Saito Takuya, Lachman Herbert M, Diaz Libna, Hallikainen Tero, Kauhanen Jussi, Salonen Jukka T, Ryynänen Olli-Pekka, Karvonen Matti K, Syvälahti Erkka, Pohjalainen Tiina, Hietala Jarmo, Tiihonen Ja |
The association of DNA sequence variation at the MAOA genetic locus with quantitative behavioural traits in normal males. Human genetics 2006 Nov 120 (4): 447-59. Rosenberg Shai, Templeton Alan R, Feigin Paul D, Lancet Doron, Beckmann Jacques S, Selig Sara, Hamer Dean H, Skorecki Ka |
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 |
Brief report: aggression and stereotypic behavior in males with fragile X syndrome--moderating secondary genes in a "single gene" disorder. Journal of autism and developmental disorders 2008 Jan 38 (1): 184-9. Hessl David, Tassone Flora, Cordeiro Lisa, Koldewyn Kami, McCormick Carolyn, Green Cherie, Wegelin Jacob, Yuhas Jennifer, Hagerman Randi |
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 |
Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesis. Neurogenetics 2009 Feb 10 (1): 65-72. Filonzi Laura, Magnani Cinzia, Lavezzi Anna Maria, Rindi Guido, Parmigiani Stefano, Bevilacqua Giulio, Matturri Luigi, Marzano Francesco Nonn |
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 |
Prolactin levels in olanzapine treatment correlate with positive symptoms of schizophrenia: results from an open-label, flexible-dose study. Primary care companion to the Journal of clinical psychiatry 2009 11 (1): 16-20. Chen Yi-Lung, Cheng Ting-Sheng, Lung For-W |
Association study between antipsychotic-induced restless legs syndrome and polymorphisms of monoamine oxidase genes in schizophrenia. Human psychopharmacology 2010 Jul 25 (5): 397-403. Kang Seung-Gul, Park Young-Min, Choi Jung-Eun, Lim Se-Won, Lee Heon-Jeong, Lee Seung-Hwan, Kim Yong-Ku, Kim Seung-Hyun, Cho Sung Nam, Kim Le |
Serotonin transporter role in identifying similarities between SIDS and idiopathic ALTE. Pediatrics 2012 Jul 130 (1): e138-44. Filonzi Laura, Magnani Cinzia, Nosetti Luana, Nespoli Luigi, Borghi Camilla, Vaghi Marina, Nonnis Marzano Frances |
[Searching for Tourette's syndrome gene. Part 2. Patient's genome variability]. Post?py higieny i medycyny do?wiadczalnej (Online) 2012 66 (0): 89-95. Kowalska Anna, Midro Alina T, Janik Piotr, Gogol Anna, S?u?ewski Wojciech, Rajewski Andrz |
Association between a functional polymorphism in the MAOA gene and sudden infant death syndrome. Pediatrics 2012 Mar 129 (3): e756-61. Klintschar Michael, Heimbold Christi |
Sudden infant death syndrome (SIDS) and polymorphisms in Monoamine oxidase A gene (MAOA): a revisit. International journal of legal medicine 2014 Jan 128 (1): 43-9. Groß Maximilian, Bajanowski Thomas, Vennemann Mechtild, Poetsch Micae |
Genetic associations with intimate partner violence in a sample of hazardous drinking men in batterer intervention programs. Violence against women 2014 Apr 20 (4): 385-400. Stuart Gregory L, McGeary John E, Shorey Ryan C, Knopik Valerie S, Beaucage Kayla, Temple Jeff |
Testing for association of the monoamine oxidase A promoter polymorphism with brain structure volumes in both autism and the fragile X syndrome. Journal of neurodevelopmental disorders 2014 6 (1): 6. Wassink Thomas H, Hazlett Heather C, Davis Lea K, Reiss Allan L, Piven Jose |
Family-based association study between monoamine oxidase A (MAOA) gene promoter VNTR polymorphism and Tourette's syndrome in Chinese Han population. Neurocase 2015 Feb 21 (1): 106-8. Liu Shiguo, Wang Xueqin, Xu Longqiang, Zheng Lanlan, Ge Yinlin, Ma |
Platelet monoamine oxidase type B, MAOB intron 13 and MAOA-uVNTR polymorphism and symptoms of post-traumatic stress disorder. Stress (Amsterdam, Netherlands) 2016 Apr 1-12. Svob Strac Dubravka, Kovacic Petrovic Zrnka, Nikolac Perkovic Matea, Umolac Danica, Nedic Erjavec Gordana, Pivac Ne |
Molecular biomarkers predictive of sertraline treatment response in young children with fragile X syndrome. Brain & development 2017 Feb . AlOlaby Reem Rafik, Sweha Stefan R, Silva Marisol, Durbin-Johnson Blythe, Yrigollen Carolyn M, Pretto Dalyir, Hagerman Randi J, Tassone Flo |
Moderator Effects of Life Stress on the Association between MAOA-uVNTR, Depression, and Burnout. Neuropsychobiology 2019 Apr 1-9. Plieger Thomas, Melchers Martin, Felten Andrea, Lieser Thomas, Meermann Rolf, Reuter Mart |
Genetic modifiers in rare disorders: the case of fragile X syndrome. European journal of human genetics : EJHG 2020 8 29 (1): 173-183. Crawford Hayley, Scerif Gaia, Wilde Lucy, Beggs Andrew, Stockton Joanne, Sandhu Pria, Shelley Lauren, Oliver Chris, McCleery Jose |
Association between monoamine oxidase A promoter polymorphism and the risk of sudden infant death syndrome: a meta-analysis. International journal of legal medicine 2021 Feb . Zhou Qiaoxia, Gong Daoyin, Zhang Yu, Huang Feij |
Fibromyalgia: A Review of Related Polymorphisms and Clinical Relevance. Anais da Academia Brasileira de Ciencias 2021 11 93 (suppl 4): e20210618. Janssen Luísa P, Medeiros Liciane F, Souza Andressa DE, Silva Juliana |
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- Page last updated:Mar 25, 2024
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