Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Neurodegenerative Diseases and PARK2[original query] |
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| A PARK2 polymorphism associated with delayed neuropsychological sequelae after carbon monoxide poisoning. BMC medical genetics 2013 14 99. Liang Fei, Li Wenqiang, Zhang Ping, Zhang Yanxia, Gu Jiapeng, Wang Xiahong, Zhang Hongxing, Gu Renj |
Genome-wide Network-assisted Association and Enrichment Study of Amyloid Imaging Phenotype in Alzheimer's Disease.
Current Alzheimer research 2019 16 (13): 1163-1174. Li Jin, Chen Feng, Zhang Qiushi, Meng Xianglian, Yao Xiaohui, Risacher Shannon L, Yan Jingwen, Saykin Andrew J, Liang Hong, Shen Li, |
| 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, |
| Contribution of rare variant associations to neurodegenerative disease presentation. NPJ genomic medicine 2021 9 6 (1): 80. Dilliott Allison A, Abdelhady Abdalla, Sunderland Kelly M, Farhan Sali M K, Abrahao Agessandro, Binns Malcolm A, Black Sandra E, Borrie Michael, Casaubon Leanne K, Dowlatshahi Dar, Finger Elizabeth, Fischer Corinne E, Frank Andrew, Freedman Morris, Grimes David, Hassan Ayman, Jog Mandar, Kumar Sanjeev, Kwan Donna, Lang Anthony E, Mandzia Jennifer, Masellis Mario, McIntyre Adam D, Pasternak Stephen H, Pollock Bruce G, Rajji Tarek K, Rogaeva Ekaterina, Sahlas Demetrios J, Saposnik Gustavo, Sato Christine, Seitz Dallas, Shoesmith Christen, Steeves Thomas D L, Swartz Richard H, Tan Brian, Tang-Wai David F, Tartaglia Maria C, Turnbull John, Zinman Lorne, , Hegele Robert |
- Page last reviewed:Feb 1, 2024
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