Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 325 Records) |
Query Trace: SLC6A3[original query] |
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Epigenetic moderators of naltrexone efficacy in reducing heavy drinking in Alcohol Use Disorder: a randomized trial. The pharmacogenomics journal 2021 Aug . Schacht Joseph P, Hoffman Michaela, Chen Brian H, Anton Raymond |
Genetic Markers as Risk Factors for the Development of Impulsive-Compulsive Behaviors in Patients with Parkinson's Disease Receiving Dopaminergic Therapy. Journal of personalized medicine 2021 12 11 (12): . Fedosova Anna, Titova Nataliya, Kokaeva Zarema, Shipilova Natalia, Katunina Elena, Klimov Euge |
The role of the SLC6A3 3' UTR VNTR in nicotine effects on cognitive, affective, and motor function. Psychopharmacology 2021 Dec . Schröder Rebekka, Reuter Martin, Faßbender Kaja, Plieger Thomas, Poulsen Jessie, Lui Simon S Y, Chan Raymond C K, Ettinger Ulri |
VNTR polymorphism in the SLC6A3 gene does not influence dopamine transporter availability measured by [18F]FE-PE2I PET or [123I]FP-Cit SPECT. Nuclear medicine communications 2021 12 43 (3): 247-255. Jakobson Mo Susanna, Axelsson Jan, Stiernman Lars J, Larsson Anne, Af Bjerkén Sara, Bäckström David, Kellgren Therese Gabrielsson, Varrone Andrea, Riklund Katri |
Background sensitivity to chemotherapy-induced nausea and vomiting and response to antiemetics in paediatric patients: a genetic association study. Pharmacogenetics and genomics 2021 Nov . Eliasen Astrid, Kornholt Jonatan, Mathiasen René, Wadt Karin, Stoltze Ulrik, Brok Jesper, Rechnitzer Catherine, Schmiegelow Kjeld, Dalhoff K |
Corrigendum: The 10-Repeat 3'-UTR VNTR Polymorphism in the SLC6A3 Gene May Confer Protection Against Parkinson's Disease: A Meta-Analysis. Frontiers in genetics 2021 11 12 789112. Zeng Qiaoli, Ning Fan, Gu Shanshan, Zeng Qiaodi, Chen Riling, Peng Liuquan, Zou Dehua, Ma Guoda, Wang Yaj |
A common polymorphism in the dopamine transporter gene predicts working memory performance and in vivo dopamine integrity in aging. NeuroImage 2021 11 245 118707. Karalija Nina, Köhncke Ylva, Düzel Sandra, Bertram Lars, Papenberg Goran, Demuth Ilja, Lill Christina M, Johansson Jarkko, Riklund Katrine, Lövdén Martin, Bäckman Lars, Nyberg Lars, Lindenberger Ulman, Brandmaier Andreas |
Functional SLC6A3 polymorphisms differentially affect autism spectrum disorder severity: a study on Indian subjects. Metabolic brain disease 2021 11 37 (2): 397-410. Saha Sharmistha, Chatterjee Mahasweta, Shom Sayanti, Sinha Swagata, Mukhopadhyay Kanch |
SLC gene mutations and pediatric neurological disorders: diverse clinical phenotypes in a Saudi Arabian population. Human genetics 2021 11 141 (1): 81-99. Mir Ali, Almudhry Montaha, Alghamdi Fouad, Albaradie Raidah, Ibrahim Mona, Aldurayhim Fatimah, Alhedaithy Abdullah, Alamr Mushari, Bawazir Maryam, Mohammad Sahar, Abdelhay Salma, Bashir Shahid, Housawi Yous |
The dopamine transporter gene SLC6A3: multidisease risks. Molecular psychiatry 2021 10 27 (2): 1031-1046. Reith Maarten E A, Kortagere Sandhya, Wiers Corinde E, Sun Hui, Kurian Manju A, Galli Aurelio, Volkow Nora D, Lin Zhiche |
The 10-Repeat 3'-UTR VNTR Polymorphism in the SLC6A3 Gene May Confer Protection Against Parkinson's Disease: A Meta-analysis. Frontiers in genetics 2021 12 757601. Zeng Qiaoli, Ning Fan, Gu Shanshan, Zeng Qiaodi, Chen Riling, Peng Liuquan, Zou Dehua, Ma Guoda, Wang Yaj |
ANKK1 and TH gene variants in combination with paternal maltreatment increase susceptibility to both cognitive and attentive impulsivity. Frontiers in psychiatry 2022 8 13 868804. Palumbo Sara, Mariotti Veronica, Vellucci Stefano, Antonelli Klizia, Anderson Nathaniel, Harenski Carla, Pietrini Pietro, Kiehl Kent A, Pellegrini Silv |
Interaction between manganese and SLC6A3 genetic polymorphisms in relation to dyslexia. Neurotoxicology 2022 09 92 102-109. Zhu Kaiheng, Liu Qi, Xie Xinyan, Jiang Qi, Feng Yanan, Xiao Pei, Wu Xiaoqian, Zhu Bing, Song Ranr |
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 |
Specific dopaminergic genetic variants influence impulsivity, cognitive deficit, and disease severity of Indian ADHD probands. Molecular biology reports 2022 May . Maitra Subhamita, Chatterjee Mahasweta, Roychowdhury Anirban, Panda Chinmay Kumar, Sinha Swagata, Mukhopadhyay Kanch |
Association between dopamine transporter gene (DAT1/SLC6A3) variants and infertility in the Turkish females. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2022 May 1-4. Avsar Orcun, Derinoz Nesibe, Yilmaz Filiz, Yilmaz Musa, Gorkem Um |
A Genetic Assessment of Dopamine Agonist-Induced Impulse Control Disorder in Patients with Prolactinoma. The Journal of clinical endocrinology and metabolism 2022 Dec . Sahin Serdar, Sudutan Tugce, Kavla Yasin, Durcan Emre, Özogul Yeliz Yagiz, Poyraz Burc Cagri, Sayitoglu Muge, Ozkaya Hande Mefkure, Kadioglu Pin |
Correlations of psychological distress with plasma cytokine levels and gene mutations in acral and non-acral melanoma. Frontiers in psychiatry 2022 11 13 1024206. Kim Hong Euy, Shim Hyun Jung, Jung Chaeyong, Shin Il Seon, Kim Jae-Min, Yun Sook Ju |
Study of changes in rs2283265 polymorphisms in dopamine receptor D2 and rs27072 in dopamine transporter gene (SLC6A3) in patients with attention-deficit hyperactivity disorder. Iranian journal of child neurology 2022 16 (3): 121-132. Safavi Parvin, Soleimani Farsani Hossein, Farrokhi Effat, Malekpour Tehrani Afsaneh, Khoshdel Nika, Khoshdel Abolfa |
Correlation research of susceptibility single nucleotide polymorphisms and the severity of clinical symptoms in attention deficit hyperactivity disorder. Frontiers in psychiatry 2022 10 13 1003542. Xu Yunyu, Lin Shuangxiang, Tao Jiejie, Liu Xinmiao, Zhou Ronghui, Chen Shuangli, Vyas Punit, Yang Chuang, Chen Bicheng, Qian Andan, Wang Meih |
SLC6A3 gene polymorphisms are associated with striatal dopamine transporter changes after glucose loading. Synapse (New York, N.Y.) 2022 Feb 76 (1-2): e22223. Pak Kyoungjune, Seo Seongho, Kim Keunyoung, Lee Myung Jun, Kim In J |
Polymorphisms of the dopamine metabolic and signaling pathways are associated with susceptibility to motor levodopa-induced complications (MLIC) in Parkinson's disease: a systematic review and meta-analysis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 Jan . Soraya Gita Vita, Ulhaq Zulvikar Syambani, Shodry Syifaus, A'raaf Sirojan Kusuma Muhammad, Herawangsa Sarah, Sativa Maharani Oryza, Gustaf Aridin, Faridwazdi Dzakky Avecienna Nur, Florentia Shinta Wulandari, Raisa Neila, Bintang Andi Kurnia, Akbar Muhamm |
The 3'UTR VNTR SLC6A3 Genetic Variant and Major Depressive Disorder: A Systematic Review. Biomedicines 2023 8 11 (8): . Bruna Rodrigues Gontijo, Isabella Possatti, Caroline Ferreira Fratelli, Alexandre Sampaio Rodrigues Pereira, Larissa Sousa Silva Bonasser, Calliandra Maria de Souza Silva, Izabel Cristina Rodrigues da Sil |
Gene Interaction of Dopaminergic Synaptic Pathway Genes in Attention-Deficit Hyperactivity Disorder: a Case-Control Study in Chinese Children. Molecular neurobiology 2023 8 . Lin Zhong, Hongyao He, Jing Zhang, Xiaoyan Gao, Feifei Yin, Pengxiang Zuo, Ranran So |
Neurotransmitter Gene Polymorphisms Are Associated with Symptom Clusters in Patients Undergoing Radiation Therapy. Seminars in oncology nursing 2023 7 151461. Carolyn Harris, Kord M Kober, Steven M Paul, Bruce A Cooper, Joosun Shin, Kate Oppegaard, Lisa Morse, Alejandra Calvo-Schimmel, Yvette Conley, Jon D Levine, Christine Miaskows |
Nexus between genome-wide copy number variations and autism spectrum disorder in Northeast Han Chinese population. BMC psychiatry 2023 2 23 (1): 96. Qiu Shuang, Qiu Yingjia, Li Yong, Zhu Xiaojuan, Liu Yunkai, Qiao Yichun, Cheng Yi, Liu Yaw |
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 |
Potential impact of cuproptosis-related genes on tumor immunity in esophageal carcinoma. Aging 2023 12 15 (24): 15535-15556. Pengfei Guo, Zemiao Niu, Dengfeng Zhang, Fangchao Zhao, Jing Li, Tianxing Lu, Xuebo Qin, Shiquan Liu, Zhirong Li, Yishuai Li, Shujun |
DAT1 and BDNF polymorphisms interact to predict A? and tau pathology. Neurobiology of aging 2023 11 133 115-124. Claire J Ciampa, Thomas M Morin, Alice Murphy, Renaud La Joie, Susan M Landau, Anne S Berry, |
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 |
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- Page last updated:Apr 22, 2024
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