Human Genome Epidemiology Literature Finder
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Records 1 - 20 (of 20 Records) |
| Query Trace: Disease and DNAJC13[original query] |
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| DNAJC13 mutations in Parkinson disease. Human molecular genetics 2014 Apr 23 (7): 1794-801. Vilariño-Güell Carles, Rajput Alex, Milnerwood Austen J, Shah Brinda, Szu-Tu Chelsea, Trinh Joanne, Yu Irene, Encarnacion Mary, Munsie Lise N, Tapia Lucia, Gustavsson Emil K, Chou Patrick, Tatarnikov Igor, Evans Daniel M, Pishotta Frederick T, Volta Mattia, Beccano-Kelly Dayne, Thompson Christina, Lin Michelle K, Sherman Holly E, Han Heather J, Guenther Bruce L, Wasserman Wyeth W, Bernard Virginie, Ross Colin J, Appel-Cresswell Silke, Stoessl A Jon, Robinson Christopher A, Dickson Dennis W, Ross Owen A, Wszolek Zbigniew K, Aasly Jan O, Wu Ruey-Meei, Hentati Faycal, Gibson Rachel A, McPherson Peter S, Girard Martine, Rajput Michele, Rajput Ali H, Farrer Matthew |
| 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 |
| VPS35 and DNAJC13 disease-causing variants in essential tremor. European journal of human genetics : EJHG 2015 Jun 23 (6): 887-8. Rajput Alex, Ross Jay P, Bernales Cecily Q, Rayaprolu Sruti, Soto-Ortolaza Alexandra I, Ross Owen A, van Gerpen Jay, Uitti Ryan J, Wszolek Zbigniew K, Rajput Ali H, Vilariño-Güell Carl |
| DNAJC13 genetic variants in parkinsonism. Movement disorders : official journal of the Movement Disorder Society 2015 Feb 30 (2): 273-8. Gustavsson Emil K, Trinh Joanne, Guella Ilaria, Vilariño-Güell Carles, Appel-Cresswell Silke, Stoessl A Jon, Tsui Joseph K, McKeown Martin, Rajput Alex, Rajput Ali H, Aasly Jan O, Farrer Matthew |
| Disease penetrance of late-onset parkinsonism: a meta-analysis. JAMA neurology 2014 Dec 71 (12): 1535-9. Trinh Joanne, Guella Ilaria, Farrer Matthew Jam |
| 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 |
| Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease. Neurobiology of aging 2016 09 45 212.e13-212.e17. Ross Jay P, Dupre Nicolas, Dauvilliers Yves, Strong Stephanie, Ambalavanan Amirthagowri, Spiegelman Dan, Dionne-Laporte Alexandre, Pourcher Emanuelle, Langlois Melanie, Boivin Michel, Leblond Claire S, Dion Patrick A, Rouleau Guy A, Gan-Or Z |
| DNAJC13 mutation screening in patients with Parkinson's disease from South Italy. Parkinsonism & related disorders 2018 Jun . Gagliardi Monica, Annesi Grazia, Procopio Radha, Morelli Maurizio, Iannello Grazia, Bonapace Giuseppe, Mancini Manuela, Nicoletti Giuseppe, Quattrone Al |
| Utility and implications of exome sequencing in early-onset Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2019 01 34 (1): 133-137. Trinh Joanne, Lohmann Katja, Baumann Hauke, Balck Alexander, Borsche Max, Brüggemann Norbert, Dure Leon, Dean Marissa, Volkmann Jens, Tunc Sinem, Prasuhn Jannik, Pawlack Heike, Imhoff Sophie, Lill Christina M, Kasten Meike, Bauer Peter, Rolfs Arndt, , Klein Christi |
| A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing. Movement disorders : official journal of the Movement Disorder Society 2019 2 34 (4): 506-515. Lin Chin-Hsien, Chen Pei-Lung, Tai Chun-Hwei, Lin Hang-I, Chen Chih-Shan, Chen Meng-Ling, Wu Ruey-Me |
| 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 |
| Systematically analyzing rare variants of autosomal-dominant genes for sporadic Parkinson's disease in a Chinese cohort. Neurobiology of aging 2019 1 76 215.e1-215.e7. Yang Nannan, Zhao Yuwen, Liu Zhenhua, Zhang Rui, He Yan, Zhou Yangjie, Xu Qian, Sun Qiying, Yan Xinxiang, Guo Jifeng, Tang Beis |
| Analysis of rare variants of autosomal-dominant genes in a Chinese population with sporadic Parkinson's disease. Molecular genetics & genomic medicine 2020 Aug e1449. Zheng Ran, Jin Chong-Yao, Chen Ying, Ruan Yang, Gao Ting, Lin Zhi-Hao, Dong Jia-Xian, Yan Ya-Ping, Tian Jun, Pu Jia-Li, Zhang Bao-Ro |
| 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 |
| Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease. Neurobiology of aging 2020 Oct . Saini Prabhjyot, Rudakou Uladzislau, Yu Eric, Ruskey Jennifer A, Asayesh Farnaz, Laurent Sandra B, Spiegelman Dan, Fahn Stanley, Waters Cheryl, Monchi Oury, Dauvilliers Yves, Dupré Nicolas, Greenbaum Lior, Hassin-Baer Sharon, Espay Alberto J, Rouleau Guy A, Alcalay Roy N, Fon Edward A, Postuma Ronald B, Gan-Or Z |
| 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 |
| Genetic Analysis of Patients With Early-Onset Parkinson's Disease in Eastern China. Frontiers in aging neuroscience 2022 14 849462. Hua Ping, Zhao Yuwen, Zeng Qian, Li Lanting, Ren Jingru, Guo Jifeng, Tang Beisha, Liu Weig |
| Genetic variants associated with circulating liver injury markers in Mexican Americans, a population at risk for non-alcoholic fatty liver disease. Frontiers in genetics 2022 11 13 995488. Sabotta Caroline M, Kwan Suet-Ying, Petty Lauren E, Below Jennifer E, Joon Aron, Wei Peng, Fisher-Hoch Susan P, McCormick Joseph B, Beretta Lau |
| 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 |
| Parkinson's Disease Gene Screening in Familial Cases from Central and South America. Movement disorders : official journal of the Movement Disorder Society 2024 7 . Oswaldo Lorenzo-Betancor, Seysha Mehta, Janvi Ramchandra, Sekinat Mumuney, Artur F Schumacher-Schuh, Mario Cornejo-Olivas, Elison H Sarapura-Castro, Luis Torres, Miguel A Inca-Martinez, Pilar Mazzetti, Carlos Cosentino, Federico Micheli, Vitor Tumas, Elena Dieguez, Victor Raggio, Vanderci Borges, Henrique B Ferraz, Pedro Chana-Cuevas, Marlene Jimenez-Del-Rio, Carlos Velez-Pardo, Sonia Moreno, Francisco Lopera, Jorge L Orozco-Velez, Beatriz Muñoz-Ospina, Carlos R M Rieder, Alex Medina-Escobar, Dora Yearout, Cyrus P Zabetian, Ignacio F Mata, |
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