Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 333 Records) |
| Query Trace: Disease and COMT[original query] |
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| Impact of single nucleotide polymorphisms and cigarette smoking on cancer risk and survival of patients with head and neck squamous cell carcinoma. Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals 2022 Jul 1-12. Andersson Bengt-Åke, Nilsson Mats, Oliva Del |
| Polymorphism of neurodegeneration-related genes associated with Parkinson's disease risk. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 6 43 (9): 5301-5312. Li Jiaxin, Yi Minhan, Li Binbin, Yin Shujuan, Zhang Ying, Huang Zini, Shu Li, Zhang Yu |
| 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 |
| Experiences of ethnic discrimination and COMT rs4680 polymorphism are associated with depressive symptoms in Latinx adults at risk for cardiovascular disease. Heart & lung : the journal of critical care 2022 Apr 55 77-81. Key Kaitlin Voigts, Estus Steven, Lennie Terry A, Linares Ana Maria, Mudd-Martin G |
| 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 |
| The correlation between genetic factors and freezing of gait in patients with Parkinson's disease. Parkinsonism & related disorders 2022 4 98 7-12. Radojevi? Branislava, Dragaševi?-Miškovi? Nataša T, Marjanovi? Ana, Brankovi? Marija, Milovanovi? Andona, Petrovi? Igor, Svetel Marina, Jan?i? Ivan, Stanisavljevi? Dejana, Mili?evi? Ognjen, Savi? Miroslav M, Kosti? Vladimir |
| 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 |
| HUMAN STUDY COMT and DRD3 haplotype-associated pain intensity and acute care utilization in adult sickle cell disease. Experimental biology and medicine (Maywood, N.J.) 2022 3 247 (17): 1601-1608. Powell-Roach Keesha L, Yao Yingwei, Wallace Margaret R, Chamala Srikar, Cruz-Almeida Yenisel, Jhun Ellie, Molokie Robert E, Wang Zajie Jim, Wilkie Diana |
| UNRAVELING THE CLINICO-GENETIC ASSOCIATION OF CATECHOL-O-METHYLTRANSFERASE-RS4680 G>A GENE POLYMORPHISM IN WOMEN WITH FIBROMYALGIA SYNDROME. Wiadomosci lekarskie (Warsaw, Poland : 1960) 2022 12 75 (10): 2439-2444. Parvez Sidrah, Fatima Ghizal, Mahdi Farzana, Fedacko Jan, Hadi Najah |
| Estrogen-DNA Adducts and Breast Cancer Risk in Premenopausal Asian Women. Cancer prevention research (Philadelphia, Pa.) 2022 12 . Lin Ching-Hung, Zahid Muhammad, Kuo Wen-Hung, Hu Fu-Chang, Wang Ming-Yang, Chen I-Chun, Beseler Cheryl L, Mondal Bodhisattwa, Lu Yen-Shen, Rogan Eleanor G, Cheng Ann-L |
| Genetic variation in the dopamine system is associated with mixed-strategy decision-making in patients with Parkinson's disease. The European journal of neuroscience 2022 12 . Parr Ashley C, Riek Heidi C, Coe Brian C, Pari Giovanna, Masellis Mario, Marras Connie, Munoz Douglas |
| 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 |
| COMT rs4818 less common allele is associated with psychological and psychiatric worse indicators in a cohort of individuals born with cleft lip and palate. Orthodontics & craniofacial research 2022 10 . Vieira Alexandre Rezende, Barros Mariana S, Soares Maria Sueli Marques, Lacerda Rosa Helena Wanderl |
| Association of Catechol-O-Methyltransferase Gene rs4680 Polymorphism and Levodopa Induced Dyskinesia in Parkinson's Disease: A Meta-Analysis and Systematic Review. Journal of geriatric psychiatry and neurology 2022 May 8919887221103580. Dwivedi Archana, Dwivedi Nidhi, Kumar Anand, Singh Varun K, Pathak Abhishek, Chaurasia R N, Mishra V N, Mohanty Sujata, Joshi Deepi |
| The relation of ApoE and COMT gene-gene interactions to cognitive and motor function in community-dwelling older adults: a pilot study. Frontiers in aging neuroscience 2023 9 15 1206473. Kendra L Pizzonia, Julie A Suhr, Leatha A Clark, Brian C Cla |
| Relationship between gene-environment interaction and obsessive-compulsive disorder: A systematic review. Journal of psychiatric research 2023 6 164 281-290. Lina Wang, Yu Chen, Miao Wang, Chaoben Zhao, Dongdong Qi |
| Association of COMT Val158Met Polymorphism with Fibromyalgia in Khartoum State, Sudan. Pain research & management 2023 6 2023 7313578. Safaa Mamoun Abdelmageid, Faisal Mousa Alamir, Hassan Yousif Abdelrahman, Hind Mohamed Abusha |
| [Irritable bowel syndrome phenotypes: leading factors of genetics and epigenetics, mechanisms of formation]. Terapevticheskii arkhiv 2023 5 95 (2): 164-172. O V Gaus, M A Livz |
| Association of Catechol-O-Methyltransferase Gene Polymorphisms and Haplotypes in the Levodopa-Induced Adverse Events in Subjects with Parkinson's Disease. Indian journal of clinical biochemistry : IJCB 2023 4 38 (2): 262-274. Fatima Tasneem Sd, Fathima Syed Tazeem, Kandadai Rukmini Mridula, Borgohain Rupam, Sreenu Boddupally, Kutala Vijay Kum |
| 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 variants in levodopa metabolic pathway genes and levodopa-induced dyskinesia in Parkinson's disease. Neuroscience letters 2023 2 801 137140. Yan Jia-Hui, Ge Yi-Lun, Wang Pu-Zhi, Li Wen, Jin Hong, Zhang Jin-Ru, Chen Jing, Wang Fen, Li Dan, Mao Cheng-Jie, Li Kai, Liu Chun-Fe |
| Pharmacogenetics of anxiety and depression in Alzheimer's disease. Pharmacogenomics 2023 1 24 (1): 27-57. Cacabelos Ramón, Carril Juan C, Corzo Lola, Pego Rocío, Cacabelos Natalia, Alcaraz Margarita, Muñiz Adriana, Martínez-Iglesias Olaia, Naidoo Vinogr |
| Association of monoaminergic gene polymorphisms in chronic inflammatory pulmonary disease patients with successful smoking cessation. BMC pulmonary medicine 2024 8 24 (1): 411. Angela Mikaczo, Csaba Papp, Tamas Erdei, Aniko Posa, Gabor Zahuczky, Csaba Varga, Janos Szabo, Rudolf Gesztelyi, Maria Szilasi, Judit Zsu |
| Longitudinal study investigating the influence of COMT gene polymorphism on cortical thickness changes in Parkinson's disease over four years. Scientific reports 2024 4 14 (1): 9920. Amin Tajeri |
| Critical evaluation of the current landscape of pharmacogenomics in Parkinson's disease - What is missing? A systematic review. Parkinsonism & related disorders 2024 11 107206. Henry Mauricio Chaparro-Solano, Maria Rivera Paz, Saar Anis, Jennifer K Hockings, Avery Kundrick, Camila C Piccinin, Ekhlas Assaedi, Leila Saadatpour, Ignacio F Ma |
| Different risk and protective factors predict change of planning ability in middle versus older age. Scientific reports 2024 10 14 (1): 25275. Josef M Unterrainer, Julia Petersen, Peter Schmidt, Mareike Ernst, Markus A Wirtz, Anna C Reinwarth, Felix Wicke, Jasmin Ghaemi Kerahrodi, Matthias Michal, Thomas Münzel, Jochem König, Karl J Lackner, Norbert Pfeiffer, Oliver Tüscher, Peter R Galle, Manfred Beutel, Philipp S Wi |
| Identifying methamphetamine use predictors in HIV infection: Immune-dopaminergic signatures in peripheral leukocytes and the role of COMT genotype. Brain, behavior, & immunity - health 2024 10 42 100873. Liana V Basova, Tera Riley, Donald Franklin, Violaine Delorme-Walker, Wei Ling Lim, Igor Grant, Scott L Letendre, Jennifer E Iudicello, Mariana Cherner, Ronald J Ellis, Maria Cecilia Garibaldi Marcond |
| Association between the Val66Met (rs6265) polymorphism of the brain-derived neurotrophic factor (BDNF) gene, BDNF protein level in the blood and the risk of developing early?onset Parkinson's disease. Acta neurobiologiae experimentalis 2024 10 84 (3): 296-308. Iwona Przybylska, Jaros?aw Marusiak, Beata Toczy?owska, Adam St?pie?, Bogdan Brodacki, Józef Langfort, Ma?gorzata Chalimoni |
| Single Nucleotide Variants (SNVs) of the Mesocorticolimbic System Associated with Cardiovascular Diseases and Type 2 Diabetes: A Systematic Review. Genes 2024 1 15 (1): . Mohammed Merzah, Shewaye Natae, János Sándor, Szilvia Fiat |
| Catechol-O-methyltransferase gene (COMT) is associated with neurocognitive functioning in patients with sickle cell disease. Current research in translational medicine 2024 1 72 (2): 103433. Andrew M Heitzer, Sara R Rashkin, Ana Trpchevska, Jennifer N Longoria, Evadnie Rampersaud, Yunusa Olufadi, Winfred C Wang, Darcy Raches, Brian Potter, Martin H Steinberg, Allison A King, Guolian Kang, Clifford M Takemoto, Jane S Hanki |
- Page last reviewed:Feb 1, 2024
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