Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 431 Records) |
| Query Trace: Schizophrenia and COMT[original query] |
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| Early-Onset Schizophrenia: A Special Phenotype of the Disease Characterized by Increased MTHFR Polymorphisms and Aggravating Symptoms. Neuropsychiatric disease and treatment 2021 8 17 2511-2525. Wan Lin, Wei Ji |
| Cannabis, Schizophrenia Risk and Genetics: A Case Report of a Patient With Homozygous Valine Catechol-O-Methyltransferase Polymorphism. Cureus 2021 7 13 (6): e15740. Grechuk Katelyn, Azizi Heela, Sharma Vatsala, Khan Tasmia, Jolayemi Ayode |
| The Associations between COMT and MAO-B Genetic Variants with Negative Symptoms in Patients with Schizophrenia. Current issues in molecular biology 2021 Jul 43 (2): 618-636. Madzarac Zoran, Tudor Lucija, Sagud Marina, Nedic Erjavec Gordana, Mihaljevic Peles Alma, Pivac Ne |
| Interacting Roles of COMT and GAD1 Genes in Patients with Treatment-Resistant Schizophrenia: a Genetic Association Study of Schizophrenia Patients and Healthy Controls. Journal of molecular neuroscience : MN 2021 Jun . Kogure Masanobu, Kanahara Nobuhisa, Miyazawa Atsuhiro, Oishi Kengo, Nakata Yusuke, Oda Yasunori, Iyo Masao |
| 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 |
| Role of COMT V158M Polymorphism in the Development of Dystonia after Administration of Antipsychotic Drugs. Brain sciences 2021 10 11 (10): . Nicotera Antonio Gennaro, Di Rosa Gabriella, Turriziani Laura, Costanzo Maria Cristina, Stracuzzi Emanuela, Vitello Girolamo Aurelio, Rando Rosanna Galati, Musumeci Antonino, Vinci Mirella, Musumeci Sebastiano Antonino, Calì Frances |
| Variants in COMT, CYP3A5, CYP2B6, and ABCG2 Alter Quetiapine Pharmacokinetics. Pharmaceutics 2021 Sep 13 (10): . Zubiaur Pablo, Fernández-Campos Paula, Navares-Gómez Marcos, Soria-Chacartegui Paula, Villapalos-García Gonzalo, Román Manuel, Mejía-Abril Gina, Ochoa Dolores, Abad-Santos Francis |
| Toxoplasma gondii Seropositivity Interacts with Catechol-O-methyltransferase Val105/158Met Variation Increasing the Risk of Schizophrenia. Genes 2022 6 13 (6): . Rovira Paula, Gutiérrez Blanca, Sorlózano-Puerto Antonio, Gutiérrez-Fernández José, Molina Esther, Rivera Margarita, Martínez-Leal Rafael, Ibanez-Casas Inmaculada, Martín-Laguna María Victoria, Rosa Araceli, Torres-González Francisco, Cervilla Jorge |
| The effects of catechol-O-methyltransferase single nucleotide polymorphisms on positive and negative symptoms of schizophrenia: A systematic review and meta-analysis. PsyCh journal 2022 May . Misir Emre, Ozbek Mutlu Muhammed, Halac Eren, Turan Serkan, Alkas Gokce Elif, Ciray Remzi Ogulcan, Ermis Cagat |
| Association of Variants in COMT, RASSF1 and GPM6A with the Risk of Paranoid Schizophrenia Patients in Prof HB Saanin Psychiatric Hospital, West Sumatra, Indonesia. The Malaysian journal of medical sciences : MJMS 2022 Apr 29 (2): 31-42. Yunaini Luluk, Khairat Edwi |
| Impact of COMT, PRODH and DISC1 Genetic Variants on Cognitive Performance of Patients with Schizophrenia. Archives of medical research 2022 4 53 (4): 388-398. Fricke-Galindo Ingrid, Pérez-Aldana Blanca E, Macías-Kauffer Luis R, González-Arredondo Susana, Dávila-Ortiz de Montellano David, Aviña-Cervantes Carlos L, López-López Marisol, Rodríguez-Agudelo Yaneth, Monroy-Jaramillo Nan |
| Catechol-O-methyltransferase (COMT) Val158Met Polymorphism and Prepulse Inhibition of the Change-related Cerebral Response. Psychiatry research. Neuroimaging 2022 4 323 111484. Motomura Eishi, Tanii Hisashi, Kawano Yasuhiro, Inui Koji, Okada Motohi |
| Dopamine DRD2 and DRD3 Polymorphisms Involvement in Nicotine Dependence in Patients with Treatment-Resistant Mental Disorders. Journal of personalized medicine 2022 4 12 (4): . Del Casale Antonio, Paolini Marco, Gentile Giovanna, Borro Marina, Zocchi Clarissa, Fiaschè Federica, Padovano Alessio, Zoppi Teodolinda, Modesti Martina Nicole, De Luca Ottavia, Pomes Leda Marina, Brugnoli Roberto, Ferracuti Stefano, Girardi Paolo, Pompili Maurizio, Simmaco Mauriz |
| Overlap between genetic variants associated with schizophrenia spectrum disorders and intelligence quotient: a systematic review. Journal of psychiatry & neuroscience : JPN 2022 11 47 (6): E393-E408. Murillo-García Nancy, Barrio-Martínez Sara, Setién-Suero Esther, Soler Jordi, Papiol Sergi, Fatjó-Vilas Mar, Ayesa-Arriola Ro |
| Gender divergent effect of COMT gene rs4680 polymorphism on the association between executive dysfunction and psychotic-like experiences. Behavioural brain research 2022 11 439 114215. Gong Jingbo, Zhang Tingting, Zhou Lihua, Mo Yanzi, Yu Feifei, Liu Min, Yang Luobin, Liu Jian |
| The inconsistent mediating effect of catechol O methyl transferase ValMet polymorphism on the sex difference of cognitive impairment in schizophrenia patients. Frontiers in psychiatry 2022 10 13 993859. Xu Hang, Zhou Yongjie, Xiu Meihong, Chen Dachun, Wang Weiwen, Wang Li, Zhang Xiangya |
| The Role of Dopaminergic Genes in Probabilistic Reinforcement Learning in Schizophrenia Spectrum Disorders. Brain sciences 2021 Dec 12 (1): . Frydecka Dorota, Misiak B?a?ej, Piotrowski Patryk, Bielawski Tomasz, Pawlak Edyta, K?osi?ska Ewa, Krefft Maja, Al Noaimy Kamila, Rymaszewska Joanna, Moustafa Ahmed A, Drapa?a Jaros? |
| [Association of gene polymorphisms DRD3 rs6280, COMT rs4680 and HTR2A rs7322347 with schizophrenia]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2022 122 (7): 115-120. Sofronov A G, Dobrovolskaya A E, Morozova A Yu, Gorina E A, Kolchev S A, Gvozdetckii A |
| Prognostic and immunomodulatory roles of schizophrenia-associated genes HTR2A, COMT, and PRODH in pan-cancer analysis and glioma survival prediction model. Frontiers in immunology 2023 8 14 1201252. Jing Shen, Qiang Wang, Fengquan Lu, Hua Xu, Peng Wang, Yu Fe |
| Genotypic and Haplotypic Association of Catechol-O-Methyltransferase rs4680 and rs4818 Gene Polymorphisms with Particular Clinical Symptoms in Schizophrenia. Genes 2023 7 14 (7): . Marina Sagud, Lucija Tudor, Gordana Nedic Erjavec, Matea Nikolac Perkovic, Suzana Uzun, Ninoslav Mimica, Zoran Madzarac, Maja Zivkovic, Oliver Kozumplik, Marcela Konjevod, Dubravka Svob Strac, Nela Piv |
| Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia. Molecular psychiatry 2023 3 . Lin Jhih-Rong, Zhao Yingjie, Jabalameli M Reza, Nguyen Nha, Mitra Joydeep, , Swillen Ann, Vorstman Jacob A S, Chow Eva W C, van den Bree Marianne, Emanuel Beverly S, Vermeesch Joris R, Owen Michael J, Williams Nigel M, Bassett Anne S, McDonald-McGinn Donna M, Gur Raquel E, Bearden Carrie E, Morrow Bernice E, Lachman Herbert M, Zhang Zhengdong |
| Associations between Catechol-O-methyltransferase (COMT) polymorphisms and cognitive impairments, psychiatric symptoms and tardive dyskinesia in schizophrenia. Brain research 2023 12 148740. Jinghui Chi, Yanyan Ma, Menglei Shi, Chenghao Lu, Qiaona Jiang, Yanzhe Li, Xiaofei Zhang, Xiaomei Shi, Shen Li, Lili Wa |
| Association of DRD2, DRD4 and COMT genes variants and their gene-gene interactions with antipsychotic treatment response in patients with schizophrenia. BMC psychiatry 2023 10 23 (1): 781. Narges Taheri, Rokhshid Pirboveiri, Mehdi Sayyah, Mahdi Bijanzadeh, Pegah Ghand |
| COMT and Neuregulin 1 Markers for Personalized Treatment of Schizophrenia Spectrum Disorders Treated with Risperidone Monotherapy. Biomolecules 2024 7 14 (7): . Mariana Bondrescu, Liana Dehelean, Simona Sorina Farcas, Ion Papava, Vlad Nicoras, Dana Violeta Mager, Anca Eliza Grecescu, Petre Adrian Podaru, Nicoleta Ioana Andrees |
| Family-based genome-wide association analysis of novelty seeking in a Korean schizophrenic population: A pilot study. Medicine 2024 6 103 (26): e38694. Ji Hye Kim, Byung Dae Lee, Je Min Park, Young Min Lee, Eunsoo Moon, Hwagyu Suh, Kyungwon Kim, Yoo Jun Kim, Hyun Ji Lee, Ha Young |
| Interaction between catechol-O-methyltransferase Val/Met polymorphism and cognitive reserve for negative symptoms in schizophrenia. World journal of psychiatry 2024 5 14 (5): 695-703. Wen-Peng Hou, Xiang-Qin Qin, Wei-Wei Hou, Yun-Yi Han, Qi-Jing Bo, Fang Dong, Fu-Chun Zhou, Xian-Bin Li, Chuan-Yue Wa |
| GENETIC VARIANTS IN ANTIPSYCHOTIC METABOLISM: POLYMORPHISM PROFILES IN KAZAKH COHORT WITH PARANOID SCHIZOPHRENIA. Georgian medical news 2024 12 (355): 99-103. K Kovaleva, Z Kachiyeva, A Abetova, N Raspopo |
| The moderating role of COMT gene rs4680 polymorphism between maladaptive metacognitive beliefs and negative symptoms in patients with schizophrenia. BMC psychiatry 2024 11 24 (1): 831. Feten Fekih-Romdhane, Georges Kerbage, Nagham Hachem, Michelle El Murr, Georges Haddad, Alexandre Andrade Loch, Rony Abou Khalil, Elissar El Hayek, Souheil Hall |
| Evaluation of the association COMT Val158Met variant and childhood trauma on aggression in Turkish SCZ patients. Nucleosides, nucleotides & nucleic acids 2024 1 1-11. P?nar Çetinay Ayd?n, Yusuf Ezel Y?ld?r?m, Ay?e Erol, Ayse Feyda Nursal, Ayça Öngel Atar, Yasemin Oyac?, Ye?im Ayar, Sati Ki?io?lu, Sacide Pehliv |
| Genetic variants in COMT and ESR1 genes shape treatment response to raloxifene in schizophrenia-spectrum disorders. Psychoneuroendocrinology 2025 1 172 107274. Bodyl A Brand, Anne Jetske Boer, Janna N de Boer, Kiymet Bozaoglu, Kim Morris, Susan Rossell, Iris E C Somm |
- Page last reviewed:Feb 1, 2024
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