Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Neurodegenerative Diseases and SNCA[original query] |
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| Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's disease. Human molecular genetics 2006 Apr 15 (7): 1151-8. Mizuta Ikuko, Satake Wataru, Nakabayashi Yuko, Ito Chiyomi, Suzuki Satoko, Momose Yoshio, Nagai Yoshitaka, Oka Akira, Inoko Hidetoshi, Fukae Jiro, Saito Yuko, Sawabe Motoji, Murayama Shigeo, Yamamoto Mitsutoshi, Hattori Nobutaka, Murata Miho, Toda Tatsus |
| Genetic variants of SNCA and LRRK2 genes are associated with sporadic PD susceptibility: a replication study in a Taiwanese cohort. Parkinsonism & related disorders 2012 Nov . Wu-Chou YH, Chen YT, Yeh TH, Chang HC, Weng YH, Lai SC, Huang CL, Chen RS, Huang YZ, Chen CC, Hung J, Chuang WL, Lin WY, Chen CH, Lu CS |
| SNCA variants rs2736990 and rs356220 as risk factors for Parkinson's disease but not for amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population. Neurobiology of aging 2014 Dec 35 (12): 2882.e1-6. Guo Xiao Yan, Chen Yong Ping, Song Wei, Zhao Bi, Cao Bei, Wei Qian Qian, Ou Ru Wei, Yang Yuan, Yuan Li Xing, Shang Hui-Fa |
| Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies. Human molecular genetics 2014 Dec 23 (23): 6139-46. Bras Jose, Guerreiro Rita, Darwent Lee, Parkkinen Laura, Ansorge Olaf, Escott-Price Valentina, Hernandez Dena G, Nalls Michael A, Clark Lorraine N, Honig Lawrence S, Marder Karen, Van Der Flier Wiesje M, Lemstra Afina, Scheltens Philip, Rogaeva Ekaterina, St George-Hyslop Peter, Londos Elisabet, Zetterberg Henrik, Ortega-Cubero Sara, Pastor Pau, Ferman Tanis J, Graff-Radford Neill R, Ross Owen A, Barber Imelda, Braae Anne, Brown Kristelle, Morgan Kevin, Maetzler Walter, Berg Daniela, Troakes Claire, Al-Sarraj Safa, Lashley Tammaryn, Compta Yaroslau, Revesz Tamas, Lees Andrew, Cairns Nigel, Halliday Glenda M, Mann David, Pickering-Brown Stuart, Dickson Dennis W, Singleton Andrew, Hardy Jo |
| Genetic Variants of SNCA Are Associated with Susceptibility to Parkinson's Disease but Not Amyotrophic Lateral Sclerosis or Multiple System Atrophy in a Chinese Population. PloS one 2015 10 (7): e0133776. Chen YongPing, Wei Qian-Qian, Ou RuWei, Cao Bei, Chen XuePing, Zhao Bi, Guo XiaoYan, Yang Yuan, Chen Ke, Wu Ying, Song Wei, Shang Hui-Fa |
| MAPT haplotype diversity in multiple system atrophy. Parkinsonism & related disorders 2016 09 30 40-5. Labbé Catherine, Heckman Michael G, Lorenzo-Betancor Oswaldo, Murray Melissa E, Ogaki Kotaro, Soto-Ortolaza Alexandra I, Walton Ronald L, Fujioka Shinsuke, Koga Shunsuke, Uitti Ryan J, van Gerpen Jay A, Petersen Ronald C, Graff-Radford Neill R, Younkin Steven G, Boeve Bradley F, Cheshire William P, Low Phillip A, Sandroni Paola, Coon Elizabeth A, Singer Wolfgang, Wszolek Zbigniew K, Dickson Dennis W, Ross Owen |
| A comprehensive screening of copy number variability in dementia with Lewy bodies. Neurobiology of aging 2019 03 75 223.e1-223.e10. Kun-Rodrigues Celia, Orme Tatiana, Carmona Susana, Hernandez Dena G, Ross Owen A, Eicher John D, Shepherd Claire, Parkkinen Laura, Darwent Lee, Heckman Michael G, Scholz Sonja W, Troncoso Juan C, Pletnikova Olga, Dawson Ted, Rosenthal Liana, 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, Guerreiro Rita, Bras Jo |
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight.
Movement disorders : official journal of the Movement Disorder Society 2019 12 34 (12): 1851-1863. Bandres-Ciga Sara, Ahmed Sarah, Sabir Marya S, Blauwendraat Cornelis, Adarmes-Gómez Astrid D, Bernal-Bernal Inmaculada, Bonilla-Toribio Marta, Buiza-Rueda Dolores, Carrillo Fátima, Carrión-Claro Mario, Gómez-Garre Pilar, Jesús Silvia, Labrador-Espinosa Miguel A, Macias Daniel, Méndez-Del-Barrio Carlota, Periñán-Tocino Teresa, Tejera-Parrado Cristina, Vargas-González Laura, Diez-Fairen Monica, Alvarez Ignacio, Tartari Juan Pablo, Buongiorno Mariateresa, Aguilar Miquel, Gorostidi Ana, Bergareche Jesús Alberto, Mondragon Elisabet, Vinagre-Aragon Ana, Croitoru Ioana, Ruiz-Martínez Javier, Dols-Icardo Oriol, Kulisevsky Jaime, Marín-Lahoz Juan, Pagonabarraga Javier, Pascual-Sedano Berta, Ezquerra Mario, Cámara Ana, Compta Yaroslau, Fernández Manel, Fernández-Santiago Rubén, Muñoz Esteban, Tolosa Eduard, Valldeoriola Francesc, Gonzalez-Aramburu Isabel, Sanchez Rodriguez Antonio, Sierra María, Menéndez-González Manuel, Blazquez Marta, Garcia Ciara, Suarez-San Martin Esther, García-Ruiz Pedro, Martínez-Castrillo Juan Carlos, Vela-Desojo Lydia, Ruz Clara, Barrero Francisco Javier, Escamilla-Sevilla Francisco, Mínguez-Castellanos Adolfo, Cerdan Debora, Tabernero Cesar, Gomez Heredia Maria Jose, Perez Errazquin Francisco, Romero-Acebal Manolo, Feliz Cici, Lopez-Sendon Jose Luis, Mata Marina, Martínez Torres Irene, Kim Jonggeol Jeffrey, Dalgard Clifton L, , Brooks Janet, Saez-Atienzar Sara, Gibbs J Raphael, Jorda Rafael, Botia Juan A, Bonet-Ponce Luis, Morrison Karen E, Clarke Carl, Tan Manuela, Morris Huw, Edsall Connor, Hernandez Dena, Simon-Sanchez Javier, Nalls Mike A, Scholz Sonja W, Jimenez-Escrig Adriano, Duarte Jacinto, Vives Francisco, Duran Raquel, Hoenicka Janet, Alvarez Victoria, Infante Jon, Marti Maria José, Clarimón Jordi, López de Munain Adolfo, Pastor Pau, Mir Pablo, Singleton Andrew, |
| Association study of SNCA gene polymorphisms with schizophrenia in a Chinese North Han population. European review for medical and pharmacological sciences 2020 May 24 (9): 4979-4987. Yang X-P, Yan C, Yuan Z, Zhou J, Miao J-X, He R, Zhu |
| A comprehensive analysis of copy number variation in a Turkish dementia cohort. Human genomics 2021 Jul 15 (1): 48. Dehghani Nadia, Guven Gamze, Kun-Rodrigues Celia, Gouveia Catarina, Foster Kalina, Hanagasi Hasmet, Lohmann Ebba, Samanci Bedia, Gurvit Hakan, Bilgic Basar, Bras Jose, Guerreiro Ri |
| Transcript Variants of Genes Involved in Neurodegeneration Are Differentially Regulated by the APOE and MAPT Haplotypes. Genes 2021 Mar 12 (3): . Koks Sulev, Pfaff Abigail L, Bubb Vivien J, Quinn John |
| Early-Onset Parkinson Disease Screening in Patients From Nigeria. Frontiers in neurology 2021 2 11 594927. Milanowski Lukasz M, Oshinaike Olajumoke, Broadway Benjamin J, Lindemann Jennifer A, Soto-Beasley Alexandra I, Walton Ronald L, Hanna Al-Shaikh Rana, Strongosky Audrey J, Fiesel Fabienne C, Ross Owen A, Springer Wolfdieter, Ogun Shamsideen Abayomi, Wszolek Zbigniew |
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