Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 100 Records) |
Query Trace: GCH1[original query] |
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Genetic variants of GCH1 associate with chronic and acute crisis pain in African Americans with sickle cell disease. Experimental hematology 2018 Jul . Sadhu Nilanjana, Jhun Ellie H, Yao Yingwei, He Ying, Molokie Robert E, Wilkie Diana J, Wang Zaijie J |
Molecular genetics of tetrahydrobiopterin deficiency in Chinese patients. Journal of pediatric endocrinology & metabolism : JPEM 2018 7 31 (8): 911-916. Li Nana, Yu Ping, Rao Bin, Deng Ying, Guo Yixiong, Huang Yushan, Ding Lijie, Zhu Jun, Yang Huanming, Wang Jian, Guo Jian, Chen Fang, Liu Zh |
Common and rare GCH1 variants are associated with Parkinson's disease. Neurobiology of aging 2018 Sep . Rudakou Uladzislau, Ouled Amar Bencheikh Bouchra, Ruskey Jennifer A, Krohn Lynne, Laurent Sandra B, Spiegelman Dan, Liong Christopher, Fahn Stanley, Waters Cheryl, Monchi Oury, Fon Edward A, Dauvilliers Yves, Alcalay Roy N, Dupré Nicolas, Gan-Or Z |
Association of rs3783641 single-nucleotide polymorphism in GTP cyclohydrolase 1 gene with post-herpetic neuralgia. The Journal of dermatology 2019 Sep . Zheng Na-Na, Zhang Ruo-Chen, Yang Xiao-Xiao, Zhong Lian-She |
Genetic polymorphisms and prediction of chronic post-surgical pain after hysterectomy-a subgroup analysis of a multicenter cohort study. Acta anaesthesiologica Scandinavica 2019 Jun . Hoofwijk Daisy M N, van Reij Roel R I, Rutten Bart P F, Kenis Gunter, Theunissen Maurice, Joosten Elbert A, Buhre Wolfgang F, van den Hoogen Nynke |
Systematic Review and Meta-Analysis of Genetic Risk of Developing Chronic Postsurgical Pain. The journal of pain 2019 5 21 (1-2): 2-24. Chidambaran Vidya, Gang Yang, Pilipenko Valentina, Ashton Maria, Ding Li |
GCH1 haplotypes and cardiovascular risk in HIV. AIDS (London, England) 2019 May . Slaven James E, Haas David W, Liu Ziyue, Stein James H, Brown Todd T, Gupta Samir |
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and ?-synuclein mechanisms.
Movement disorders : official journal of the Movement Disorder Society 2019 Jun 34 (6): 866-875. Blauwendraat Cornelis, Heilbron Karl, Vallerga Costanza L, Bandres-Ciga Sara, von Coelln Rainer, Pihlstrøm Lasse, Simón-Sánchez Javier, Schulte Claudia, Sharma Manu, Krohn Lynne, Siitonen Ari, Iwaki Hirotaka, Leonard Hampton, Noyce Alastair J, Tan Manuela, Gibbs J Raphael, Hernandez Dena G, Scholz Sonja W, Jankovic Joseph, Shulman Lisa M, Lesage Suzanne, Corvol Jean-Christophe, Brice Alexis, van Hilten Jacobus J, Marinus Johan, , Eerola-Rautio Johanna, Tienari Pentti, Majamaa Kari, Toft Mathias, Grosset Donald G, Gasser Thomas, Heutink Peter, Shulman Joshua M, Wood Nicolas, Hardy John, Morris Huw R, Hinds David A, Gratten Jacob, Visscher Peter M, Gan-Or Ziv, Nalls Mike A, Singleton Andrew B, |
GCH1 (rs841) polymorphism in the nitric oxide-forming pathway has protective effects on obstructive sleep apnea. Scientific reports 2019 Dec 9 (1): 18664. Sheikhi Kouhsar Samaneh, Bigdeli Mohammadreza, Shakiba Yadollah, Sadeghniiat Khos |
GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control study. Translational neurodegeneration 2020 Aug 9 (1): 31. Pan Hong-Xu, Zhao Yu-Wen, Mei Jun-Pu, Fang Zheng-Huan, Wang Yige, Zhou Xun, Zhou Yang-Jie, Zhang Rui, Zhang Kai-Lin, Jiang Li, Zeng Qian, He Yan, Wang Zheng, Liu Zhen-Hua, Xu Qian, Sun Qi-Ying, Yang Yang, Hu Ya-Cen, Chen Ya-Se, Du Juan, Lei Li-Fang, Zhang Hai-Nan, Wang Chun-Yu, Yan Xin-Xiang, Shen Lu, Jiang Hong, Tan Jie-Qiong, Li Jin-Chen, Tang Bei-Sha, Guo Ji-Fe |
Association of TOR1A and GCH1 Polymorphisms with Isolated Dystonia in India. Journal of molecular neuroscience : MN 2020 Jul . Giri Subhajit, Ghosh Arunibha, Roy Shubhrajit, Sankhla Charulata Savant, Das Shyamal Kumar, Ray Kunal, Ray Jhar |
[Clinical and genetic analysis of a case with infantile Parkinsonism with motor delay due to tyrosine hydroxylase deficiency]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 3 37 (4): 455-458. Chen Chongfen, Kong Jinghui, Ge Lili, Liu Lei, Song Yins |
Clinical and Genetic Heterogeneity in a Cohort of Chinese Children With Dopa-Responsive Dystonia. Frontiers in pediatrics 2020 3 8 83. Chen Yan, Bao Xinhua, Wen Yongxin, Wang Jiaping, Zhang Qingping, Yan Jiay |
Targeted sequencing of Parkinson's disease loci genes highlights SYT11, FGF20 and other associations. Brain : a journal of neurology 2020 Dec . Rudakou Uladzislau, Yu Eric, Krohn Lynne, Ruskey Jennifer A, Asayesh Farnaz, Dauvilliers Yves, Spiegelman Dan, Greenbaum Lior, Fahn Stanley, Waters Cheryl H, Dupré Nicolas, Rouleau Guy A, Hassin-Baer Sharon, Fon Edward A, Alcalay Roy N, Gan-Or Z |
Comprehensive Analysis of Familial Parkinsonism Genes in Rapid-Eye-Movement Sleep Behavior Disorder. Movement disorders : official journal of the Movement Disorder Society 2020 10 36 (1): 235-240. Mufti Kheireddin, Rudakou Uladzislau, Yu Eric, Krohn Lynne, Ruskey Jennifer A, Asayesh Farnaz, Laurent Sandra B, Spiegelman Dan, Arnulf Isabelle, Hu Michele T M, Montplaisir Jacques Y, Gagnon Jean-François, Desautels Alex, Dauvilliers Yves, Gigli Gian Luigi, Valente Mariarosaria, Janes Francesco, Högl Birgit, Stefani Ambra, Holzknecht Evi, Šonka Karel, Kemlink David, Oertel Wolfgang, Janzen Annette, Plazzi Giuseppe, Antelmi Elena, Figorilli Michela, Puligheddu Monica, Mollenhauer Brit, Trenkwalder Claudia, Sixel-Döring Friederike, Cochen De Cock Valérie, Monaca Christelle Charley, Heidbreder Anna, Ferini-Strambi Luigi, Dijkstra Femke, Viaene Mineke, Abril Beatriz, Boeve Bradley F, Postuma Ronald B, Rouleau Guy A, Gan-Or Z |
A preliminary exome sequence in three patients with tardive dystonia. Psychiatric genetics 2019 Dec . Kanahara Nobuhisa, Nakata Yusuke, Iyo Masao |
Clinical and Genetic Analysis of Costa Rican Patients With Parkinson's Disease. Frontiers in neurology 2021 8 12 656342. Torrealba-Acosta Gabriel, Yu Eric, Lobo-Prada Tanya, Ruíz-Martínez Javier, Gorostidi-Pagola Ana, Gan-Or Ziv, Carazo-Céspedes Kenneth, Trempe Jean-François, Mata Ignacio F, Fornaguera-Trías Jai |
Polymorphisms of Nav1.6 sodium channel, Brain-derived Neurotrophic Factor, Catechol-O-methyltransferase and Guanosine Triphosphate Cyclohydrolase 1 genes in trigeminal neuralgia. Clinical neurology and neurosurgery 2021 Aug 208 106880. Romero Jgaj, Costa Grazielle Mara Ferreira, Rocha Luiz Paulo Carvalho, Siqueira Srdt, Moreira Paula Rocha, Almeida-Leite Camila Mega |
Atremorine in Parkinson's disease: From dopaminergic neuroprotection to pharmacogenomics. Medicinal research reviews 2021 6 41 (5): 2841-2886. Cacabelos Ramón, Carrera Iván, Martínez Olaia, Alejo Ramón, Fernández-Novoa Lucía, Cacabelos Pablo, Corzo Lola, Rodríguez Susana, Alcaraz Margarita, Nebril Laura, Tellado Iván, Cacabelos Natalia, Pego Rocío, Naidoo Vinogran, Carril Juan |
Genetic landscape of Segawa disease in Spain. Long-term treatment outcomes. Parkinsonism & related disorders 2021 12 94 67-78. Fernández-Ramos Joaquín A, De la Torre-Aguilar María José, Quintáns Beatriz, Pérez-Navero Juan Luis, Beyer Katrin, López-Laso Eduardo, |
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 |
Frequency of Parkinson's Disease Genes and Role of PARK2 in Amyotrophic Lateral Sclerosis: An NGS Study. Genes 2022 Jul 13 (8): . Vacchiano Veria, Bartoletti-Stella Anna, Rizzo Giovanni, Avoni Patrizia, Parchi Piero, Salvi Fabrizio, Liguori Rocco, Capellari Sabi |
The mutation spectrum of Parkinson-disease-related genes in early-onset Parkinson's disease in ethnic Chinese. European journal of neurology 2022 Jul . Chen Yong-Ping, Yu Shi-Hui, Zhang Guo-Hui, Hou Yan-Bing, Gu Xiao-Jing, Ou Ru-Wei, Shen Ying, Song Wei, Chen Xue-Ping, Zhao Bi, Cao Bei, Zhang Ling-Yu, Sun Ming-Ming, Liu Fei-Fei, Wei Qian-Qian, Liu Kun-Cheng, Lin Jun-Yu, Yang Tian-Mi, Yang Jing, Wu Ying, Jiang Zheng, Liu Jiao, Cheng Yang-Fan, Xiao Yi, Su Wei-Ming, Feng Fei, Cai Ying-Ying, Li Shi-Rong, Hu Tao, Yuan Xiao-Qin, Zhou Qing-Qing, Shao Na, Ma Sha, Shang Hui-Fa |
Genome-Wide Polygenic Score Predicts Large Number of High Risk Individuals in Monogenic Undiagnosed Young Onset Parkinson's Disease Patients from India. Advanced biology 2022 Jul e2101326. Kukkle Prashanth Lingappa, Geetha Thenral S, Chaudhary Ruchi, Sathirapongsasuti Jarupon F, Goyal Vinay, Kandadai Rukmini Mridula, Kumar Hrishikesh, Borgohain Rupam, Mukherjee Adreesh, Oliver Merina, Sunil Meeta, Mootor Mohammed Faizal Eeman, Kapil Shruti, Mandloi Nitin, Wadia Pettarusp M, Yadav Ravi, Desai Soaham, Kumar Niraj, Biswas Atanu, Pal Pramod Kumar, Muthane Uday B, Das Shymal Kumar, Sakthivel Murugan Sakthivel M, Peterson Andrew S, Stawiski Eric W, Seshagiri Somasekar, Gupta Ravi, Ramprasad Vedam L, Prai Parkinson Research Alliance Of Ind |
Novel Immune-Related Ferroptosis Signature in Esophageal Cancer: An Informatics Exploration of Biological Processes Related to the TMEM161B-AS1/hsa-miR-27a-3p/GCH1 Regulatory Network. Frontiers in genetics 2022 3 13 829384. Lu Min, Li Jiaqi, Fan Xin, Xie Fei, Fan Jie, Xiong Yuanpi |
Influence of genetic variants on remifentanil sensitivity in Chinese women. Journal of clinical pharmacy and therapeutics 2022 Oct . Niu Haojie, Zhao Shuai, Wang Yafeng, Huang Shiqian, Zhou Ruihui, Wu Zhouyang, Song Wentao, Chen Xiangdo |
Detection of Single-Nucleotide and Copy Number Defects Underlying Hyperphenylalaninemia by Next-Generation Sequencing. Biomedicines 2023 7 11 (7): . Elisabetta Anna Tendi, Giovanna Morello, Maria Guarnaccia, Valentina La Cognata, Salvatore Petralia, Maria Anna Messina, Concetta Meli, Agata Fiumara, Martino Ruggieri, Sebastiano Cavalla |
The genetic spectrum of a cohort of patients clinically diagnosed as Parkinson's disease in mainland China. NPJ Parkinson's disease 2023 5 9 (1): 76. Yi-Min Sun, Xin-Yue Zhou, Xiao-Niu Liang, Jin-Ran Lin, Yi-Dan Xu, Chen Chen, Si-Di Wei, Qi-Si Chen, Feng-Tao Liu, Jue Zhao, Yi-Lin Tang, Bo Shen, Lin-Hua Gan, Boxun Lu, Zheng-Tong Ding, Yu An, Jian-Jun Wu, Jian Wa |
Heterozygous pathogenic variant in GCH1 associated with treatable severe spastic tetraplegia: Expert opinion. Parkinsonism & related disorders 2023 3 105370. Salles Philippe |
Genetic screening of Filipinos suspected with familial Parkinson's disease: A pilot study. Parkinsonism & related disorders 2023 2 108 105319. Caritativo Erin Camille A, Yu Jeryl Ritzi T, Bautista Juan Miguel P, Nishioka Kenya, Jamora Roland Dominic G, Yalung Patrick M, Ng Arlene R, Hattori Nobuta |
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- Page last updated:Apr 22, 2024
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