Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: DNAJC6[original query] |
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A genome-wide association study of the Protein C anticoagulant pathway.
PloS one 2011 6 (12): e29168. Athanasiadis Georgios, Buil Alfonso, Souto Juan Carlos, Borrell Montserrat, López Sonia, Martinez-Perez Angel, Lathrop Mark, Fontcuberta Jordi, Almasy Laura, Soria José Manu |
DNAJ mutations are rare in Chinese Parkinson's disease patients and controls. Neurobiology of aging 2014 Apr 35 (4): 935.e1-2. Foo Jia Nee, Liany Herty, Tan Louis C, Au Wing-Lok, Prakash Kumar-M, Liu Jianjun, Tan Eng-Ki |
Systematic analysis of genetic variants in Han Chinese patients with sporadic Parkinson's disease. Scientific reports 0 6 33850. Yuan Lamei, Song Zhi, Deng Xiong, Zheng Wen, Guo Yi, Yang Zhijian, Deng H |
Genome-wide association scans for idiopathic osteonecrosis of the femoral head in a Korean population.
Molecular medicine reports 2016 Dec . Baek Seung-Hoon, Kim Kang-Il, Yoon Kyung-Sik, Kim Tae-Ho, Kim Shin-Yo |
DNAJC6 mutations are not common causes of early onset Parkinson's disease in Chinese Han population. Neuroscience letters 2016 Sep . Shi Changhe, Li Fang, Yang Jing, Zhang Shuyu, Mao Chengyuan, Wang Hui, Shi Mengmeng, Liu Yutao, Song Bong, Xu Yumi |
Haplotype Analysis on the Relationship of the DNAJC6 Gene with Early-Onset Parkinson's Disease Risk in a Chinese Population. Journal of Parkinson's disease 2019 9 (1): 109-120. Shen Ting, Zhao Shuai, Jiang Yasi, Pu Jiali, Lai Hsin-Yi, Yan Yaping, Tian Jun, Chen Yanxin, Zhang Baoro |
The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improving Chances in Stratification for Clinical Trials. Frontiers in genetics 2019 11 10 1061. Illés Anett, Csabán Dóra, Grosz Zoltán, Balicza Péter, Gézsi András, Molnár Viktor, Bencsik Renáta, Gál Anikó, Klivényi Péter, Molnar Maria Jud |
A genetic analysis of a Spanish population with early onset Parkinson's disease. PloS one 2020 15 (9): e0238098. Cristina Tejera-Parrado, Pablo Mir, Teresa Periñán María, Lydia Vela-Desojo, Irene Abreu-Rodríguez, Araceli Alonso-Cánovas, Inmaculada Bernal-Bernal, Marta Bonilla-Toribio, Dolores Buiza-Rueda, José Catalán-Alonso María, Rocío García-Ramos, José García-Ruiz Pedro, Ismael Huertas-Fernández, Silvia Jesús, Labrador Miguel A-Espinosa, Lydia López-Manzanares, Carlos Martínez-Castrillo Juan, Posada Ignacio J, Ana Rojo-Sebastián, Cristina Ruiz-Huete, Javier Del Val, Gómez-Garre Pil |
Mutation Analysis of DNAJC Family for Early-Onset Parkinson's Disease in a Chinese Cohort. Movement disorders : official journal of the Movement Disorder Society 2020 Jul . Li ChunYu, Ou RuWei, Chen YongPing, Gu XiaoJing, Wei QianQian, Cao Bei, Zhang LingYu, Hou YanBing, Liu KunCheng, Chen XuePing, Song Wei, Zhao Bi, Wu Ying, Shang HuiFa |
When does postural instability appear in monogenic parkinsonisms? An individual-patient meta-analysis. Journal of neurology 2020 5 268 (9): 3203-3211. Marsili Luca, Vizcarra Joaquin A, Sturchio Andrea, Dwivedi Alok K, Keeling Elizabeth G, Patel Dhiren, Mishra Murli, Farooqi Ashar, Merola Aristide, Fasano Alfonso, Mata Ignacio F, Kauffman Marcelo A, Espay Alberto |
First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery. European journal of human genetics : EJHG 2020 Mar . Hengel Holger, Buchert Rebecca, Sturm Marc, Haack Tobias B, Schelling Yvonne, Mahajnah Muhammad, Sharkia Rajech, Azem Abdussalam, Balousha Ghassan, Ghanem Zaid, Falana Mohammed, Balousha Osama, Ayesh Suhail, Keimer Reinhard, Deigendesch Werner, Zaidan Jimmy, Marzouqa Hiyam, Bauer Peter, Schöls Ludg |
Identification of sixteen novel candidate genes for late onset Parkinson's disease. Molecular neurodegeneration 2021 6 16 (1): 35. Gialluisi Alessandro, Reccia Mafalda Giovanna, Modugno Nicola, Nutile Teresa, Lombardi Alessia, Di Giovannantonio Luca Giovanni, Pietracupa Sara, Ruggiero Daniela, Scala Simona, Gambardella Stefano, , Iacoviello Licia, Gianfrancesco Fernando, Acampora Dario, D'Esposito Maurizio, Simeone Antonio, Ciullo Marina, Esposito Tere |
Investigating the Endo-Lysosomal System in Major Neurocognitive Disorders Due to Alzheimer's Disease, Frontotemporal Lobar Degeneration and Lewy Body Disease: Evidence for SORL1 as a Cross-Disease Gene. International journal of molecular sciences 2021 12 22 (24): . Benussi Luisa, Longobardi Antonio, Kocoglu Cemile, Carrara Matteo, Bellini Sonia, Ferrari Clarissa, Nicsanu Roland, Saraceno Claudia, Bonvicini Cristian, Fostinelli Silvia, Zanardini Roberta, Catania Marcella, Moisse Matthieu, Van Damme Philip, Di Fede Giuseppe, Binetti Giuliano, Van Broeckhoven Christine, van der Zee Julie, Ghidoni Rober |
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 |
Whole Exome Sequencing Study in Isolated South-Eastern Moravia (Czechia) Population Indicates Heterogenous Genetic Background for Parkinsonism Development. Frontiers in neuroscience 2022 4 16 817713. Kolarikova Kristyna, Vodicka Radek, Vrtel Radek, Stellmachova Julia, Prochazka Martin, Mensikova Katerina, Kanovsky Pe |
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- Page last updated:Apr 22, 2024
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