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The Influence of 5-HTTLPR, BDNF Rs6265 and COMT Rs4680 Polymorphisms on Impulsivity in Bipolar Disorder: The Role of Gender. Genes 2022 3 13 (3): . Boscutti Andrea, Pigoni Alessandro, Delvecchio Giuseppe, Lazzaretti Matteo, Mandolini Gian Mario, Girardi Paolo, Ferro Adele, Sala Michela, Abbiati Vera, Cappucciati Marco, Bellani Marcella, Perlini Cinzia, Rossetti Maria Gloria, Balestrieri Matteo, Damante Giuseppe, Bonivento Carolina, Rossi Roberta, Finos Livio, Serretti Alessandro, Brambilla Paolo, The Gecobip Grou |
Psychological and genetic risk factors associated with suicidal behavior in Korean patients with mood disorders. Journal of affective disorders 2018 Apr 235 489-498. Choi Hee-Yeon, Kim Ga Eun, Kong Kyoung Ae, Lee Yu Jin, Lim Weon-Jeong, Park So-Hyun, Ha Su Hee, Kim Soo |
Neuroplasticity, Neurotransmission and Brain-Related Genes in Major Depression and Bipolar Disorder: Focus on Treatment Outcomes in an Asiatic Sample. Advances in therapy 2018 10 35 (10): 1656-1670. Calabrò Marco, Mandelli Laura, Crisafulli Concetta, Lee Soo-Jung, Jun Tae-Youn, Wang Sheng-Min, Patkar Ashwin A, Masand Prakash S, Benedetti Francesco, Han Changsu, Pae Chi-Un, Serretti Alessand |
Glucocorticoid Receptors, Brain-Derived Neurotrophic Factor, Serotonin and Dopamine Neurotransmission are Associated with Interferon-Induced Depression. The international journal of neuropsychopharmacology 2016 Apr 19 (4): . Udina M, Navinés R, Egmond E, Oriolo G, Langohr K, Gimenez D, Valdés M, Gómez-Gil E, Grande I, Gratacós M, Kapczinski F, Artigas F, Vieta E, Solà R, Martín-Santos |
Disorder-specific genetic factors in obsessive-compulsive disorder: A comprehensive meta-analysis. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Nov . Taylor Stev |
Association of the COMT synonymous polymorphism Leu136Leu and missense variant Val158Met with mood disorders. Journal of affective disorders 2015 May 177 108-13. Pandolfo G, Gugliandolo A, Gangemi C, Arrigo R, Currò M, La Ciura G, Muscatello M R A, Bruno A, Zoccali R, Caccamo |
Direct, indirect and pleiotropic effects of candidate genes on internalizing disorder psychopathology. Psychological medicine 2015 Feb 1-10. Hettema J M, Chen X, Sun C, Brown T |
Impact of COMT genotype on serotonin-1A receptor binding investigated with PET. Brain structure & function 2014 Nov 219 (6): 2017-28. Baldinger Pia, Hahn Andreas, Mitterhauser Markus, Kranz Georg S, Friedl Marion, Wadsak Wolfgang, Kraus Christoph, Ungersböck Johanna, Hartmann Annette, Giegling Ina, Rujescu Dan, Kasper Siegfried, Lanzenberger Rupe |
Additive gene-environment effects on hippocampal structure in healthy humans. The Journal of neuroscience : the official journal of the Society for Neuroscience 2014 Jul 34 (30): 9917-26. Rabl Ulrich, Meyer Bernhard M, Diers Kersten, Bartova Lucie, Berger Andreas, Mandorfer Dominik, Popovic Ana, Scharinger Christian, Huemer Julia, Kalcher Klaudius, Pail Gerald, Haslacher Helmuth, Perkmann Thomas, Windischberger Christian, Brocke Burkhard, Sitte Harald H, Pollak Daniela D, Dreher Jean-Claude, Kasper Siegfried, Praschak-Rieder Nicole, Moser Ewald, Esterbauer Harald, Pezawas Luk |
Effect of COMT Val158Met polymorphism on personality traits and educational attainment in a longitudinal population representative study. European psychiatry : the journal of the Association of European Psychiatrists 2013 Oct 28 (8): 492-8. Lehto K, Akkermann K, Parik J, Veidebaum T, Harro |
Interaction of catechol O-methyltransferase and serotonin transporter genes modulates effective connectivity in a facial emotion-processing circuitry. Translational psychiatry 2012 Feb 2 . Surguladze SA, Radua J, El-Hage W, Gohier B, Sato JR, Kronhaus DM, Proitsi P, Powell J, Phillips ML |
COMT and age at onset in mood disorders: a replication and extension study. Neuroscience letters 2011 Jul 498 (3): 218-21. Massat Isabelle, Kocabas Neslihan Aygun, Crisafulli Concetta, Chiesa Alberto, Calati Raffaella, Linotte Sylvie, Kasper Siegfried, Fink Martin, Antonijevic Irina, Forray Carlos, Snyder Lenore, Bollen Joseph, Zohar Joseph, De Ronchi Diana, Souery Daniel, Serretti Alessandro, Mendlewicz Juli |
P2RX7 gene is associated consistently with mood disorders and predicts clinical outcome in three clinical cohorts. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011 Jun 156B (4): 435-47. Soronen Pia, Mantere Outi, Melartin Tarja, Suominen Kirsi, Vuorilehto Maria, Rytsälä Heikki, Arvilommi Petri, Holma Irina, Holma Mikael, Jylhä Pekka, Valtonen Hanna M, Haukka Jari, Isometsä Erkki, Paunio Tii |
Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients. Journal of psychiatric research 2010 Oct 44 (14): 971-8. Saus Ester, Brunet Anna, Armengol Lluís, Alonso Pino, Crespo José M, Fernández-Aranda Fernando, Guitart Miriam, Martín-Santos Rocío, Menchón José Manuel, Navinés Ricard, Soria Virginia, Torrens Marta, Urretavizcaya Mikel, Vallès Vicenç, Gratacòs Mònica, Estivill Xavi |
No association of COMT Val158Met polymorphism with suicidal behavior or CSF monoamine metabolites in mood disorders. Archives of suicide research : official journal of the International Academy for Suicide Research 2008 12 (4): 327-35. Zalsman Gil, Huang Yung-yu, Oquendo Maria A, Brent David A, Giner Lucas, Haghighi Fatemeh, Burke Ainsley K, Ellis Steven P, Currier Dianne, Mann J Jo |
Interaction between serotonin transporter gene, catechol-O-methyltransferase gene and stressful life events in mood disorders. The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2007 Aug 10 (4): 437-47. Mandelli Laura, Serretti Alessandro, Marino Elena, Pirovano Adele, Calati Raffaella, Colombo Cristi |
Catechol-O-methyltransferase gene variants in mood disorders in the Italian population. Psychiatric genetics 2006 Oct 16 (5): 181-2. Serretti Alessandro, Rotondo Alessandro, Lorenzi Cristina, Smeraldi Enrico, Cassano Gian Battis |
Association between COMT (Val158Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study. Molecular psychiatry 2005 Jun 10 (6): 598-605. Massat I, Souery D, Del-Favero J, Nothen M, Blackwood D, Muir W, Kaneva R, Serretti A, Lorenzi C, Rietschel M, Milanova V, Papadimitriou G N, Dikeos D, Van Broekhoven C, Mendlewicz |
BDNF and COMT polymorphisms: relation to memory phenotypes in young adults with childhood-onset mood disorder. Neuromolecular medicine 2004 5 (3): 181-92. Strauss J, Barr C L, George C J, Ryan C M, King N, Shaikh S, Kovacs M, Kennedy J |
Association study of MAO-A, COMT, 5-HT2A, DRD2, and DRD4 polymorphisms with illness time course in mood disorders. American journal of medical genetics 2002 May 114 (4): 380-90. Cusin Cristina, Serretti Alessandro, Lattuada Enrico, Lilli Roberta, Lorenzi Cristina, Smeraldi Enri |
Pharmacogenetics of lithium prophylaxis in mood disorders: analysis of COMT, MAO-A, and Gbeta3 variants. American journal of medical genetics 2002 May 114 (4): 370-9. Serretti Alessandro, Lorenzi Cristina, Lilli Roberta, Mandelli Laura, Pirovano Adele, Smeraldi Enri |
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