Human Genome Epidemiology Literature Finder
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Records 1 - 27 (of 27 Records) |
| Query Trace: Disease and EIF4G1[original query] |
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| Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's disease. Neurogenetics 2012 Aug 13 (3): 281-5. Schulte Eva C, Mollenhauer Brit, Zimprich Alexander, Bereznai Benjamin, Lichtner Peter, Haubenberger Dietrich, Pirker Walter, Brücke Thomas, Molnar Maria J, Peters Annette, Gieger Christian, Trenkwalder Claudia, Winkelmann Julia |
| Study of the genetic variability in a Parkinson's Disease gene: EIF4G1. Neuroscience letters 2012 Jun 518 (1): 19-22. Tucci Arianna, Charlesworth Gavin, Sheerin Una-Marie, Plagnol Vincent, Wood Nicholas W, Hardy Jo |
| VPS35 Asp620Asn and EIF4G1 Arg1205His mutations are rare in Parkinson disease from southwest China. Neurobiology of aging 2012 Dec . Chen Y, Chen K, Song W, Chen X, Cao B, Huang R, Zhao B, Guo X, Burgunder J, Li J, Shang HF |
| Analysis of EIF4G1 in Parkinson's disease among Asians. Neurobiology of aging 2013 Apr 34 (4): 1311.e5-6. Zhao Yi, Ho Patrick, Prakash Kumar-M, Foo Jia-Nee, Liu Jian-Jun, Au Wing-Lok, Tan Louis C, Tan Eng-Ki |
| VPS35 and EIF4G1 mutations are rare in Parkinson's disease among Indians. Neurobiology of aging 2013 Oct 34 (10): 2442.e1-3. Sudhaman Sumedha, Behari Madhuri, Govindappa Shyla T, Muthane Uday B, Juyal Ramesh C, Thelma B |
| EIF4G1 Ala502Val and Arg1205His variants in Chinese patients with Parkinson disease. Neuroscience letters 2013 May 543 69-71. Yuan Lamei, Song Zhi, Xu Hongbo, Gu Shaojuan, Zhu Anding, Gong Lina, Zhao Yongxiang, Deng H |
| Analysis of EIF4G1 in ethnic Chinese. BMC neurology 2013 13 (1): 38. Li Kai, Tang Bei-sha, Guo Ji-feng, Lou Ming-xing, Lv Zhan-yun, Liu Zhen-hua, Tian Yun, Song Cheng-yuan, Xia Kun, Yan Xin-xia |
| Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease. Neurology 2013 Mar 80 (11): 982-9. Nuytemans Karen, Bademci Guney, Inchausti Vanessa, Dressen Amy, Kinnamon Daniel D, Mehta Arpit, Wang Liyong, Züchner Stephan, Beecham Gary W, Martin Eden R, Scott William K, Vance Jeffery |
| EIF4G1 R1205H and VPS35 D620N mutations are rare in Parkinson's disease from South Africa. Neurobiology of aging 2014 Feb 35 (2): 445.e1-3. Blanckenberg Janine, Ntsapi Claudia, Carr Jonathan A, Bardien Sora |
| Frequency of the ASP620ASN mutation in VPS35 and Arg1205His mutation in EIF4G1 in familial Parkinson's disease from South Italy. Neurobiology of aging 2014 Oct 35 (10): 2422.e1-2. Gagliardi Monica, Annesi Grazia, Tarantino Patrizia, Nicoletti Giuseppe, Quattrone Al |
| EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population. Parkinsonism & related disorders 2014 Jun 20 (6): 659-61. Nishioka Kenya, Funayama Manabu, Vilariño-Güell Carles, Ogaki Kotaro, Li Yuanzhe, Sasaki Ryogen, Kokubo Yasumasa, Kuzuhara Shigeki, Kachergus Jennifer M, Cobb Stephanie A, Takahashi Hirohide, Mizuno Yoshikuni, Farrer Matthew J, Ross Owen A, Hattori Nobuta |
| EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohorts. Journal of medical genetics 2015 Jan 52 (1): 37-41. Huttenlocher Johanna, Krüger Rejko, Capetian Philipp, Lohmann Katja, Brockmann Kathrin, Csoti Ilona, Klein Christine, Berg Daniela, Gasser Thomas, Bonin Michael, Riess Olaf, Bauer Pet |
| Disease penetrance of late-onset parkinsonism: a meta-analysis. JAMA neurology 2014 Dec 71 (12): 1535-9. Trinh Joanne, Guella Ilaria, Farrer Matthew Jam |
| D620N mutation in the VPS35 gene and R1205H mutation in the EIF4G1 gene are uncommon in the Greek population. Neuroscience letters 2015 Aug 606 113-116. Kalinderi Kallirhoe, Bostantjopoulou Sevasti, Katsarou Zoe, Dimikiotou Maria, Fidani Lia |
| EIF4G1 mutations do not cause Parkinson's disease. Neurobiology of aging 2015 Aug 36 (8): 2444.e1-4. Nichols Noah, Bras Jose M, Hernandez Dena G, Jansen Iris E, Lesage Suzanne, Lubbe Steven, Singleton Andrew B, |
| The EIF4G1 gene and Parkinson's disease. Acta neurologica Scandinavica 2015 Aug 132 (2): 73-8. Deng H, Wu Y, Jankovic |
| Genetic Mutation Analysis of Parkinson's Disease Patients Using Multigene Next-Generation Sequencing Panels. Molecular diagnosis & therapy 2016 Jun . Gorostidi Ana, Martí-Massó José Félix, Bergareche Alberto, Rodríguez-Oroz Mari Cruz, de Munain Adolfo López, Ruiz-Martínez Javi |
| A novel TCF7L2 type 2 diabetes SNP identified from fine mapping in African American women. PloS one 2017 12 (3): e0172577. Haddad Stephen A, Palmer Julie R, Lunetta Kathryn L, Ng Maggie C Y, , Ruiz-Narváez Edward |
| Association analysis of EIF4G1 and Parkinson disease in Xinjiang Uygur and Han nationality. Medicine 2018 May 97 (18): e0234. Ma Yu, Zheng Daxiong, Li Hongy |
| 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 |
| Novel and reported variants in Parkinson's disease genes confer high disease burden among Indians. Parkinsonism & related disorders 2020 7 78 46-52. Kumar Sumeet, Yadav Navneesh, Pandey Sanjay, Muthane Uday B, Govindappa Shyla T, Abbas Masoom M, Behari Madhuri, Thelma B |
| 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 |
| A genetic analysis of Chinese patients with early-onset Parkinson' s disease. Neuroscience letters 2022 9 790 136880. Liu Qi, Jiang Bin, Zou Min, Wan Hui-Juan, Yu Zi-Wen, Wang Jing, Xu Chu-Chuan, Lin Si-Ning, Zheng Kun-Mu, Xiao Nai-An, Bi Min, Li Jian-Pe |
| High-Throughput Sequencing Haplotype Analysis Indicates in LRRK2 Gene a Potential Risk Factor for Endemic Parkinsonism in Southeastern Moravia, Czech Republic. Life (Basel, Switzerland) 2022 1 12 (1): . Kolarikova Kristyna, Vodicka Radek, Vrtel Radek, Stellmachova Julia, Prochazka Martin, Mensikova Katerina, Bartonikova Tereza, Furst Tomas, Kanovsky Petr, Geryk J |
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