Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 35 Records) |
Query Trace: UCHL1[original query] |
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The G2019S LRRK2 mutation is rare in Korean patients with Parkinson's disease. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2007 Feb 34 (1): 53-5. Cho Jin-Whan, Kim Sung-Yeon, Park Sung-Sup, Kim Han-Jun, Ahn Tae-Beom, Kim Jong-Min, Jeon Beom-Se |
Lack of evidence for an association between UCHL1 S18Y and Parkinson's disease. European journal of neurology : the official journal of the European Federation of Neurological Societies 2008 Feb 15 (2): 134-9. Hutter Carolyn M, Samii Ali, Factor Stewart A, Nutt John G, Higgins Donald S, Bird Thomas D, Griffith Alida, Roberts John W, Leis Berta C, Montimurro Jennifer S, Kay Denise M, Edwards Karen L, Payami Haydeh, Zabetian Cyrus |
Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease. Neurogenetics 2008 Oct 9 (4): 263-9. Choi Jung Mi, Woo Myoung Soo, Ma Hyeo-Il, Kang Suk Yun, Sung Young-Hee, Yong Seok Woo, Chung Sun Ju, Kim Joong-Seok, Shin Hae-won, Lyoo Chul Hyoung, Lee Phil Hyu, Baik Jong Sam, Kim Sang-Jin, Park Mee Young, Sohn Young Ho, Kim Jin-Ho, Kim Jae Woo, Lee Myung Sik, Lee Myoung Chong, Kim Dong-Hyun, Kim Yun Joo |
Exploring gene-environment interactions in Parkinson's disease. Human genetics 2008 Apr 123 (3): 257-65. McCulloch Colin C, Kay Denise M, Factor Stewart A, Samii Ali, Nutt John G, Higgins Donald S, Griffith Alida, Roberts John W, Leis Berta C, Montimurro Jennifer S, Zabetian Cyrus P, Payami Hayd |
Analysis of the UCHL1 genetic variant in Parkinson's disease among Chinese. Neurobiology of aging 2010 Dec 31 (12): 2194-6. Tan E K, Lu C S, Peng R, Teo Y Y, Wu-Chou Y H, Chen R S, Weng Y H, Chen C M, Fung H C, Tan L C, Zhang Z J, An X K, Lee-Chen G J, Lee M C, Fook-Chong S, Burgunder J M, Wu R M, Wu Y |
Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease? Movement disorders : official journal of the Movement Disorder Society 2009 Apr 24 (6): 833-8. Sutherland Greg T, Halliday Glenda M, Silburn Peter A, Mastaglia Frank L, Rowe Dominic B, Boyle Richard S, O'Sullivan John D, Ly Tina, Wilton Steve D, Mellick George |
Association between the ubiquitin carboxyl-terminal esterase L1 gene (UCHL1) S18Y variant and Parkinson's Disease: a HuGE review and meta-analysis. American journal of epidemiology 2009 Dec 170 (11): 1344-57. Ragland Margaret, Hutter Carolyn, Zabetian Cyrus, Edwards Kar |
Ubiquitin specific proteases USP24 and USP40 and ubiquitin thiolesterase UCHL1 polymorphisms have synergic effect on the risk of Parkinson's disease among Taiwanese. Clinica chimica acta; international journal of clinical chemistry 2010 Jul 411 (13-14): 955-8. Wu Yih-Ru, Chen Chiung-Mei, Chen Yi-Chun, Chao Chih-Ying, Ro Long Sun, Fung Hon-Chung, Hsiao Ya-Chin, Hu Fen-Ju, Lee-Chen Guey-J |
Ubiquitin carboxy-terminal hydrolase L1 (UCHL1) S18Y polymorphism in Alzheimer's disease. Molecular neurodegeneration 2010 5 (1): 11. Zetterberg Madeleine, Sjölander Annica, von Otter Malin, Palmér Mona Seibt, Landgren Sara, Minthon Lennart, Wallin Anders, Andreasen Niels, Blennow Kaj, Zetterberg Henr |
Common variants in PARK loci and related genes and Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2011 Feb 26 (2): 280-8. Chung Sun Ju, Armasu Sebastian M, Biernacka Joanna M, Lesnick Timothy G, Rider David N, Lincoln Sarah J, Ortolaza Alexandra I, Farrer Matthew J, Cunningham Julie M, Rocca Walter A, Maraganore Demetrius |
The UCHL1 S18Y polymorphism and Parkinson's disease in a Japanese population. Parkinsonism & related disorders 2011 Jul 17 (6): 473-5. Snapinn Katherine W, Larson Eric B, Kawakami Hideshi, Ujike Hiroshi, Borenstein Amy R, Izumi Yuishin, Kaji Ryuji, Maruyama Hirofumi, Mata Ignacio F, Morino Hiroyuki, Oda Masaya, Tsuang Debby W, Yearout Dora, Edwards Karen L, Zabetian Cyrus |
Ubiquitin carboxyl-terminal esterase L1 (UCHL1) S18Y polymorphism in patients with cataracts. Ophthalmic genetics 2011 Jun 32 (2): 75-9. Rudolph Thiemo, Sjölander Annica, Palmér Mona Seibt, Minthon Lennart, Wallin Anders, Andreasen Niels, Tasa Gunnar, Juronen Erkki, Blennow Kaj, Zetterberg Henrik, Zetterberg Madelei |
UCHL1 S18Y variant is a risk factor for Parkinson's disease in Japan. BMC neurology 2012 Jul 12 (1): 1. Miyake Y, Tanaka K, Fukushima W, Kiyohara C, Sasaki S, Tsuboi Y, Yamada T, Oeda T, Shimada H, Kawamura N, Sakae N, Fukuyama H, Hirota Y, Nagai M, Study Group TF |
Lack of genetic association of the UCHL1 gene with Alzheimer's disease and Parkinson's disease with dementia. Dementia and geriatric cognitive disorders 2012 33 (4): 250-4. Shibata Nobuto, Motoi Yumiko, Tomiyama Hiroyuki, Ohnuma Tohru, Kuerban Bolati, Tomson Katrin, Komatsu Miwa, Hattori Nobutaka, Arai He |
Mutation analysis of LRRK2, SCNA, UCHL1, HtrA2 and GIGYF2 genes in Chinese patients with autosomal dorminant Parkinson's disease. Neuroscience letters 2012 May 516 (2): 207-11. Tian Jin-yong, Guo Ji-feng, Wang Lei, Sun Qi-ying, Yao Ling-yan, Luo Lin-zi, Shi Chang-he, Hu Ya-cen, Yan Xin-xiang, Tang Bei-s |
Association between ubiquitin carboxy-terminal hydrolase-L1 S18Y variant and risk of Parkinson's disease: the impact of ethnicity and onset age. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2015 Feb 36 (2): 179-88. Liu Ying, Chen Yan-Yan, Liu Hui, Yao Ci-Jiang, Zhu Xiao-Xia, Chen Dao-Jun, Yang Jin, Lu You-Jin, Cao Ji- |
Lack of association between UCHL1 S18Y gene polymorphism and Parkinson's disease in the Asian population: a meta-analysis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2014 Dec 35 (12): 1867-76. Sun Shuang, Zhao Yan, Jin Guojiang, Kang H |
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 |
Variation in Candidate Traumatic Brain Injury Biomarker Genes Are Associated with Gross Neurological Outcomes after Severe Traumatic Brain Injury. Journal of neurotrauma 2018 Jul . Osier Nicole D, Conley Yvette P, Okonkwo David O, Puccio Ava |
The rs13388259 Intergenic Polymorphism in the Genomic Context of the BCYRN1 Gene Is Associated with Parkinson's Disease in the Hungarian Population. Parkinson's disease 2018 2018 9351598. Márki Sándor, Göblös Anikó, Szlávicz Eszter, Török Nóra, Balicza Péter, Bereznai Benjamin, Takáts Annamária, Engelhardt József, Klivényi Péter, Vécsei László, Molnár Mária Judit, Nagy Nikoletta, Széll Már |
Proteomics in cerebrospinal fluid and spinal cord suggests UCHL1, MAP2 and GPNMB as biomarkers and underpins importance of transcriptional pathways in amyotrophic lateral sclerosis. Acta neuropathologica 2019 11 139 (1): 119-134. Oeckl Patrick, Weydt Patrick, Thal Dietmar R, Weishaupt Jochen H, Ludolph Albert C, Otto Mark |
Analysis of Exon Dosage Using Multiplex Ligation-Dependent Probe Amplification in Chinese Patients with Early-Onset Parkinson's Disease. European neurology 2019 10 81 (5-6): 246-253. Lin Yu, Zeng Yi-Fang, Cai Nai-Qing, Lin Xiao-Zhen, Wang Ning, He J |
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 |
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 the Genes Associated with Parkinson's Disease in a Finnish Cohort of Early-Onset Dementia. Journal of Alzheimer's disease : JAD 2020 6 76 (3): 955-965. Luukkainen Laura, Huttula Samuli, Väyrynen Henri, Helisalmi Seppo, Kytövuori Laura, Haapasalo Annakaisa, Hiltunen Mikko, Remes Anne M, Krüger Johan |
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 |
A novel c.-652C>T mutation in UCHL1 gene is associated with the growth performance in Yangzhou goose. Poultry science 2021 5 100 (7): 101089. Wang Qin, Wang Qiushi, Melak Sherif, Lin Xiangsheng, Wei Wei, Zhang Lifan, Chen J |
Characterization of molecular biomarkers in cerebrospinal fluid and serum of E46K-SNCA mutation carriers. Parkinsonism & related disorders 2022 2 96 29-35. Murueta-Goyena Ane, Cipriani Raffaela, Carmona-Abellán Mar, Acera Marian, Ayo Naia, Del Pino Rocío, Tijero Beatriz, Fernández-Valle Tamara, Gabilondo Iñigo, Zallo Fátima, Matute Carlos, Sánchez-Pernaute Rosario, Khurana Vikram, Cavaliere Fabio, Capetillo-Zarate Estibaliz, Gómez-Esteban Juan Carl |
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 |
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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