Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 30 Records) |
| Query Trace: Disease and meta-analysis and SNCA[original query] |
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Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
Human genetics 2009 Jan 124 (6): 593-605. Pankratz Nathan, Wilk Jemma B, Latourelle Jeanne C, DeStefano Anita L, Halter Cheryl, Pugh Elizabeth W, Doheny Kimberly F, Gusella James F, Nichols William C, Foroud Tatiana, Myers Richard H, |
| Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.
Nature genetics 2010 Sep 42 (9): 781-5. Hamza Taye H, Zabetian Cyrus P, Tenesa Albert, Laederach Alain, Montimurro Jennifer, Yearout Dora, Kay Denise M, Doheny Kimberly F, Paschall Justin, Pugh Elizabeth, Kusel Victoria I, Collura Randall, Roberts John, Griffith Alida, Samii Ali, Scott William K, Nutt John, Factor Stewart A, Payami Hayd |
| Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.
BMC medical genetics 2011 12 (1): 104. Liu Xinmin, Cheng Rong, Verbitsky Miguel, Kisselev Sergey, Browne Andrew, Mejia-Sanatana Helen, Louis Elan D, Cote Lucien J, Andrews Howard, Waters Cheryl, Ford Blair, Frucht Steven, Fahn Stanley, Marder Karen, Clark Lorraine N, Lee Joseph |
| Independent and joint effects of the MAPT and SNCA genes in Parkinson disease. Annals of neurology 2011 May 69 (5): 778-92. Elbaz Alexis, Ross Owen A, Ioannidis John P A, Soto-Ortolaza Alexandra I, Moisan Frédéric, Aasly Jan, Annesi Grazia, Bozi Maria, Brighina Laura, Chartier-Harlin Marie-Christine, Destée Alain, Ferrarese Carlo, Ferraris Alessandro, Gibson J Mark, Gispert Suzana, Hadjigeorgiou Georgios M, Jasinska-Myga Barbara, Klein Christine, Krüger Rejko, Lambert Jean-Charles, Lohmann Katja, van de Loo Simone, Loriot Marie-Anne, Lynch Timothy, Mellick George D, Mutez Eugénie, Nilsson Christer, Opala Grzegorz, Puschmann Andreas, Quattrone Aldo, Sharma Manu, Silburn Peter A, Stefanis Leonidas, Uitti Ryan J, Valente Enza Maria, Vilariño-Güell Carles, Wirdefeldt Karin, Wszolek Zbigniew K, Xiromerisiou Georgia, Maraganore Demetrius M, Farrer Matthew J, |
| Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.
Lancet (London, England) 2011 Feb 377 (9766): 641-9. , Nalls Michael A, Plagnol Vincent, Hernandez Dena G, Sharma Manu, Sheerin Una-Marie, Saad Mohamad, Simón-Sánchez J, Schulte Claudia, Lesage Suzanne, Sveinbjörnsdóttir Sigurlaug, Stefánsson Kári, Martinez Maria, Hardy John, Heutink Peter, Brice Alexis, Gasser Thomas, Singleton Andrew B, Wood Nicholas |
| Genetic variants of a-synuclein are not associated with essential tremor. Movement disorders : official journal of the Movement Disorder Society 2011 Dec 26 (14): 2552-6. Ross Owen A, Conneely Karen N, Wang Tao, Vilarino-Guell Carles, Soto-Ortolaza Alexandra I, Rajput Alex, Wszolek Zbigniew K, Uitti Ryan J, Louis Elan D, Clark Lorraine N, Farrer Matthew J, Testa Claudia |
| 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 |
| Large-scale replication and heterogeneity in Parkinson disease genetic loci. Neurology 2012 Aug 79 (7): 659-67. Sharma Manu, Ioannidis John P A, Aasly Jan O, Annesi Grazia, Brice Alexis, Van Broeckhoven Christine, Bertram Lars, Bozi Maria, Crosiers David, Clarke Carl, Facheris Maurizio, Farrer Matthew, Garraux Gaetan, Gispert Suzana, Auburger Georg, Vilariño-Güell Carles, Hadjigeorgiou Georgios M, Hicks Andrew A, Hattori Nobutaka, Jeon Beom, Lesage Suzanne, Lill Christina M, Lin Juei-Jueng, Lynch Timothy, Lichtner Peter, Lang Anthony E, Mok Vincent, Jasinska-Myga Barbara, Mellick George D, Morrison Karen E, Opala Grzegorz, Pramstaller Peter P, Pichler Irene, Park Sung Sup, Quattrone Aldo, Rogaeva Ekaterina, Ross Owen A, Stefanis Leonidas, Stockton Joanne D, Satake Wataru, Silburn Peter A, Theuns Jessie, Tan Eng-King, Toda Tatsushi, Tomiyama Hiroyuki, Uitti Ryan J, Wirdefeldt Karin, Wszolek Zbigniew, Xiromerisiou Georgia, Yueh Kuo-Chu, Zhao Yi, Gasser Thomas, Maraganore Demetrius, Krüger Rejko, |
| Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
PLoS genetics 2012 8 (3): e1002548. Lill Christina M, Roehr Johannes T, McQueen Matthew B, Kavvoura Fotini K, Bagade Sachin, Schjeide Brit-Maren M, Schjeide Leif M, Meissner Esther, Zauft Ute, Allen Nicole C, Liu Tian, Schilling Marcel, Anderson Kari J, Beecham Gary, Berg Daniela, Biernacka Joanna M, Brice Alexis, DeStefano Anita L, Do Chuong B, Eriksson Nicholas, Factor Stewart A, Farrer Matthew J, Foroud Tatiana, Gasser Thomas, Hamza Taye, Hardy John A, Heutink Peter, Hill-Burns Erin M, Klein Christine, Latourelle Jeanne C, Maraganore Demetrius M, Martin Eden R, Martinez Maria, Myers Richard H, Nalls Michael A, Pankratz Nathan, Payami Haydeh, Satake Wataru, Scott William K, Sharma Manu, Singleton Andrew B, Stefansson Kari, Toda Tatsushi, Tung Joyce Y, Vance Jeffery, Wood Nick W, Zabetian Cyrus P, , , , , Young Peter, Tanzi Rudolph E, Khoury Muin J, Zipp Frauke, Lehrach Hans, Ioannidis John P A, Bertram La |
| SNCA rs356219 variant increases risk of sporadic Parkinson's disease in ethnic Chinese. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2013 Jul 162B (5): 452-6. Li Nan-Nan, Mao Xue-Ye, Chang Xue-Li, Zhao Dong-Mei, Zhang Jin-Hong, Liao Qiao, Yu Wen-Juan, Tan Eng-King, Peng Ro |
| Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.
Nature genetics 2014 Sep 46 (9): 989-93. Nalls Mike A, Pankratz Nathan, Lill Christina M, Do Chuong B, Hernandez Dena G, Saad Mohamad, DeStefano Anita L, Kara Eleanna, Bras Jose, Sharma Manu, Schulte Claudia, Keller Margaux F, Arepalli Sampath, Letson Christopher, Edsall Connor, Stefansson Hreinn, Liu Xinmin, Pliner Hannah, Lee Joseph H, Cheng Rong, , , , , , , , , , , , , Ikram M Arfan, Ioannidis John P A, Hadjigeorgiou Georgios M, Bis Joshua C, Martinez Maria, Perlmutter Joel S, Goate Alison, Marder Karen, Fiske Brian, Sutherland Margaret, Xiromerisiou Georgia, Myers Richard H, Clark Lorraine N, Stefansson Kari, Hardy John A, Heutink Peter, Chen Honglei, Wood Nicholas W, Houlden Henry, Payami Haydeh, Brice Alexis, Scott William K, Gasser Thomas, Bertram Lars, Eriksson Nicholas, Foroud Tatiana, Singleton Andrew |
| SNP rs11931074 of the SNCA gene may not be associated with multiple system atrophy in Chinese population. The International journal of neuroscience 2015 Aug 125 (8): 612-5. Sun ZhanFang, Xiang XiaoShuang, Tang BeiSha, Chen Zhao, Peng HuiRong, Xia Kun, Jiang Ho |
| Alpha-synuclein (SNCA) polymorphisms and susceptibility to Parkinson's disease: a meta-analysis. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Mar 168B (2): 123-34. Han Wei, Liu Yingli, Mi Yingjun, Zhao Jing, Liu Dianwu, Tian Qingb |
| [SNCA rs356219 AND rs356165 VARIANTS ARE ASSOCIATED WITH PARKINSON'S DISEASE AND INCREASED ALPHA-SYNUCLEIN GENE EXPRESSION IN THE CD45(+)-BLOOD CELLS]. Tsitologiia 2016 58 (2): 99-104. Emelyanov A K, Andoskin P A, Miliukhina I V, Timofeeva A A, Yakimovskii A F, Senkevich K A, Nikolaev M A, Pchelina S |
| Genome-wide association study of Parkinson's disease in East Asians.
Human molecular genetics 2016 Dec . Foo Jia Nee, Tan Louis C, Irwan Ishak D, Au Wing-Lok, Low Hui Qi, Prakash Kumar-M, Ahmad-Annuar Azlina, Bei Jinxin, Chan Anne Yy, Chen Chiung Mei, Chen Yi-Chun, Chung Sun Ju, Deng Hao, Lim Shen-Yang, Mok Vincent, Pang Hao, Pei Zhong, Peng Rong, Shang Hui-Fang, Song Kyuyoung, Tan Ai Huey, Wu Yih-Ru, Aung Tin, Cheng Ching-Yu, Chew Fook Tim, Chew Soo-Hong, Chong Siow-Ann, Ebstein Richard P, Lee Jimmy, Saw Seang-Mei, Seow Adeline, Subramaniam Mythily, Tai E-Shyong, Vithana Eranga N, Wong Tien-Yin, Heng Khai Koon, Meah Wee-Yang, Khor Chiea Chuen, Liu Hong, Zhang Furen, Liu Jianjun, Tan Eng-Ki |
| Parkinson's disease susceptibility variants and severity of Lewy body pathology. Parkinsonism & related disorders 2017 Sep . Heckman Michael G, Kasanuki Koji, Diehl Nancy N, Koga Shunsuke, Soto Alexandra, Murray Melissa E, Dickson Dennis W, Ross Owen |
| Association between SNCA rs2736990 polymorphism and Parkinson's disease: a meta-analysis. Neuroscience letters 2017 Aug 658 102-107. Fang Jinni, Hou Binghui, Liu Hongxin, Zhang Xiaona, Wang Jing, Zhou Chang, Xie An |
| Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study.
The Lancet. Neurology 2018 Jan 17 (1): 64-74. Guerreiro Rita, Ross Owen A, Kun-Rodrigues Celia, Hernandez Dena G, Orme Tatiana, Eicher John D, Shepherd Claire E, Parkkinen Laura, Darwent Lee, Heckman Michael G, Scholz Sonja W, Troncoso Juan C, Pletnikova Olga, Ansorge Olaf, Clarimon Jordi, Lleo Alberto, Morenas-Rodriguez Estrella, Clark Lorraine, Honig Lawrence S, Marder Karen, Lemstra Afina, Rogaeva Ekaterina, St George-Hyslop Peter, Londos Elisabet, Zetterberg Henrik, Barber Imelda, Braae Anne, Brown Kristelle, Morgan Kevin, Troakes Claire, Al-Sarraj Safa, Lashley Tammaryn, Holton Janice, Compta Yaroslau, Van Deerlin Vivianna, Serrano Geidy E, Beach Thomas G, Lesage Suzanne, Galasko Douglas, Masliah Eliezer, Santana Isabel, Pastor Pau, Diez-Fairen Monica, Aguilar Miquel, Tienari Pentti J, Myllykangas Liisa, Oinas Minna, Revesz Tamas, Lees Andrew, Boeve Brad F, Petersen Ronald C, Ferman Tanis J, Escott-Price Valentina, Graff-Radford Neill, Cairns Nigel J, Morris John C, Pickering-Brown Stuart, Mann David, Halliday Glenda M, Hardy John, Trojanowski John Q, Dickson Dennis W, Singleton Andrew, Stone David J, Bras Jo |
| An updated analysis with 45,078 subjects confirms the association between SNCA rs11931074 and Parkinson's disease. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2018 Aug . Liu Xu, Zhu Ruixia, Xiao Tongling, Li Qu, Zhu Ying, He Zhi |
| A Comprehensive Analysis of the Association Between SNCA Polymorphisms and the Risk of Parkinson's Disease. Frontiers in molecular neuroscience 2018 11 11 391. Zhang Yuan, Shu Li, Sun Qiying, Pan Hongxu, Guo Jifeng, Tang Beis |
| Association of rs356219 and rs3822086 polymorphisms with the risk of Parkinson's disease: A meta-analysis. Neuroscience letters 2019 Jul 709 134380. Hou Binghui, Zhang Xue, Liu Zongchao, Wang Jing, Xie An |
| Association between SNCA rs356220 polymorphism and Parkinson's disease: A meta-analysis. Neuroscience letters 2019 Dec 717 134703. Bi Mingxia, Kang Shan, Du Xixun, Jiao Qian, Jiang Ho |
| Association between alpha-synuclein (SNCA) rs11931074 variability and susceptibility to Parkinson's disease: an updated meta-analysis of 41,811 patients. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2019 Nov . Du Bingying, Xue Qiang, Liang Caiquan, Fan Cunxiu, Liang Meng, Zhang Yanbo, Bi Xiaoying, Hou Lij |
| SNPs in SNCA, MCCC1, DLG2, GBF1 and MBNL2 are associated with Parkinson's disease in southern Chinese population. Journal of cellular and molecular medicine 2020 Jul . Zhao Aonan, Li Yuanyuan, Niu Mengyue, Li Guanglu, Luo Ningdi, Zhou Liche, Kang Wenyan, Liu J |
| 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 |
| 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 |
| Alpha synuclein (SNCA) rs7684318 variant contributes to Parkinson's disease risk by altering transcription factor binding related with Notch and Wnt signaling. Neuroscience letters 2021 04 750 135802. Naushad Shaik Mohammad, Hussain Tajamul, Alrokayan Salman, Kutala Vijay Kum |
| Genetic Modifiers of Age at Onset for Parkinson's Disease in Asians: A Genome-Wide Association Study.
Movement disorders : official journal of the Movement Disorder Society 2021 4 36 (9): 2077-2084. 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, Li Tao, Dong Xianjun, Shang Huifa |
| Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence From the COURAGE-PD Consortium.
Neurology 2022 8 99 (7): e698-e710. Grover Sandeep, Kumar Sreelatha Ashwin Ashok, Pihlstrom Lasse, Domenighetti Cloé, Schulte Claudia, Sugier Pierre-Emmanuel, Radivojkov-Blagojevic Milena, Lichtner Peter, Mohamed Océane, Portugal Berta, Landoulsi Zied, May Patrick, Bobbili Dheeraj, Edsall Connor, Bartusch Felix, Hanussek Maximilian, Krüger Jens, Hernandez Dena G, Blauwendraat Cornelis, Mellick George D, Zimprich Alexander, Pirker Walter, Tan Manuela, Rogaeva Ekaterina, Lang Anthony, Koks Sulev, Taba Pille, Lesage Suzanne, Brice Alexis, Corvol Jean-Christophe, Chartier-Harlin Marie-Christine, Mutez Eugenie, Brockmann Kathrin, Deutschländer Angela B, Hadjigeorgiou Georges M, Dardiotis Efthimos, Stefanis Leonidas, Simitsi Athina Maria, Valente Enza Maria, Petrucci Simona, Straniero Letizia, Zecchinelli Anna, Pezzoli Gianni, Brighina Laura, Ferrarese Carlo, Annesi Grazia, Quattrone Andrea, Gagliardi Monica, Burbulla Lena F, Matsuo Hirotaka, Kawamura Yusuke, Hattori Nobutaka, Nishioka Kenya, Chung Sun Ju, Kim Yun Joong, Pavelka Lukas, van de Warrenburg Bart P C, Bloem Bastiaan R, Singleton Andrew B, Aasly Jan, Toft Mathias, Guedes Leonor Correia, Ferreira Joaquim J, Bardien Soraya, Carr Jonathan, Tolosa Eduardo, Ezquerra Mario, Pastor Pau, Diez-Fairen Monica, Wirdefeldt Karin, Pedersen Nancy L, Ran Caroline, Belin Andrea C, Puschmann Andreas, Hellberg Clara, Clarke Carl E, Morrison Karen E, Krainc Dimitri, Farrer Matt J, Kruger Rejko, Elbaz Alexis, Gasser Thomas, Sharma Manu, |
| Machine Learning Identifies Six Genetic Variants and Alterations in the Heart Atrial Appendage as Key Contributors to PD Risk Predictivity. Frontiers in genetics 2021 12 785436. Ho Daniel, Schierding William, Farrow Sophie L, Cooper Antony A, Kempa-Liehr Andreas W, O'Sullivan Justin |
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