A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan

Por Fung, Hon-Chung, Chen, Chiung-Mei, Hardy, John, Singleton, Andrew B, Wu, Yih-Ru
Publicado em 2006

The Need for Appropriate Genotyping Strategies for Glucocerebrosidase Mutations in Cohorts With Parkinson Disease

Por Gutti, Usha, Fung, Hon-Chung, Hruska, Kathleen S., LaMarca, Mary E., Chen, Chiung-Mei, Wu, Yih-Ru, Sidransky, Ellen
Publicado em 2008

STK39, But Not BST1, HLA-DQB1, and SPPL2B Polymorphism, Is Associated With Han-Chinese Parkinson's Disease in Taiwan

Por Chang, Kuo-Hsuan, Wu, Yih-Ru, Chen, Yi-Chun, Fung, Hon-Chung, Lee-Chen, Guey-Jen, Chen, Chiung-Mei
Publicado no Medicine (Baltimore) (2015)

Digit symbol substitution test score and hyperhomocysteinemia in older adults

Por Hsu, Wen-Chuin, Chu, Yi-Chuan, Fung, Hon-Chung, Wai, Yau-Yau, Wang, Jiun-Jie, Lee, Jiann-Der, Chen, Yi-Chun
Publicado no Medicine (Baltimore) (2016)

Conflicting Results Regarding the Semaphorin Gene (SEMA5A) and the Risk for Parkinson Disease

Por Clarimon, Jordi, Scholz, Sonja, Fung, Hon-Chung, Hardy, John, Eerola, Johanna, Hellström, Olli, Chen, Chiung-Mei, Wu, Yih-Ru, Tienari, Pentti J., Singleton, Andrew
Publicado em 2006

Tract-Based Spatial Statistics: Application to Mild Cognitive Impairment

Por Wai, Yau-Yau, Hsu, Wen-Chuin, Fung, Hon-Chung, Lee, Jiann-Der, Chan, Hsiao-Lung, Tsai, Ming-Lun, Lin, Yu-Chun, Wu, Yih-Ru, Ying, Leslie, Wang, Jiun-Jie
Publicado em 2014

Sex dimorphism of cortical water diffusion in normal aging measured by magnetic resonance imaging

Por Ng, Shu-Hang, Hsu, Wen-Chiun, Wai, Yau-Yau, Lee, Jiann-Der, Chan, Hsiao-Lung, Chen, Yao-Liang, Fung, Hon-Chung, Wu, Yih-Ru, Tsai, Ming-Lun, Wang, Jiun-Jie
Publicado em 2013

Structural genomic variation in ischemic stroke

Por Matarin, Mar, Simon-Sanchez, Javier, Fung, Hon-Chung, Scholz, Sonja, Gibbs, J. Raphael, Hernandez, Dena G., Crews, Cynthia, Britton, Angela, Wavrant De Vrieze, Fabienne, Brott, Thomas G., Brown, Robert D., Worrall, Bradford B., Silliman, Scott, Case, L. Douglas, Hardy, John A., Rich, Stephen S., Meschia, James F., Singleton, Andrew B.
Publicado em 2008

Evolutionary Toggling of the MAPT 17q21.31 Inversion Region

Por Zody, Michael C., Jiang, Zhaoshi, Fung, Hon-Chung, Antonacci, Francesca, Hillier, LaDeana W., Cardone, Maria Francesca, Graves, Tina A., Kidd, Jeffrey M., Cheng, Ze, Abouelleil, Amr, Chen, Lin, Wallis, John, Glasscock, Jarret, Wilson, Richard K., Reily, Amy Denise, Duckworth, Jaime, Ventura, Mario, Hardy, John, Warren, Wesley C., Eichler, Evan E.
Publicado em 2008

A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release

Por Matarín, Mar, Brown, W Mark, Scholz, Sonja, Simón-Sánchez, Javier, Fung, Hon-Chung, Hernandez, Dena, Gibbs, J Raphael, De Vrieze, Fabienne Wavrant, Crews, Cynthia, Britton, Angela, Langefeld, Carl D, Brott, Thomas G, Brown, Robert D, Worrall, Bradford B, Frankel, Michael, Silliman, Scott, Case, L Douglas, Singleton, Andrew, Hardy, John A, Rich, Stephen S, Meschia, James F
Publicado em 2007

Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD

Por Momeni, Parastoo, Schymick, Jennifer, Jain, Shushant, Cookson, Mark R, Cairns, Nigel J, Greggio, Elisa, Greenway, Matthew J, Berger, Stephen, Pickering-Brown, Stuart, Chiò, Adriano, Fung, Hon Chung, Holtzman, David M, Huey, Edward D, Wassermann, Eric M, Adamson, Jennifer, Hutton, Michael L, Rogaeva, Ekaterina, St George-Hyslop, Peter, Rothstein, Jeffrey D, Hardiman, Orla, Grafman, Jordan, Singleton, Andrew, Hardy, John, Traynor, Bryan J
Publicado em 2006

Deletion at ITPR1 Underlies Ataxia in Mice and Spinocerebellar Ataxia 15 in Humans

Por van de Leemput, Joyce, Chandran, Jayanth, Knight, Melanie A, Holtzclaw, Lynne A, Scholz, Sonja, Cookson, Mark R, Houlden, Henry, Gwinn-Hardy, Katrina, Fung, Hon-Chung, Lin, Xian, Hernandez, Dena, Simon-Sanchez, Javier, Wood, Nick W, Giunti, Paola, Rafferty, Ian, Hardy, John, Storey, Elsdon, Gardner, R. J. McKinlay, Forrest, Susan M, Fisher, Elizabeth M. C, Russell, James T, Cai, Huaibin, Singleton, Andrew B
Publicado em 2007

Multi-center analysis of glucocerebrosidase mutations in Parkinson disease

Por Sidransky, Ellen, Nalls, Michael A., Aasly, Jan O., Aharon-Peretz, Judith, Annesi, Grazia, Barbosa, Egberto Reis, Bar-Shira, Anat, Berg, Daniela, Bras, Jose, Brice, Alexis, Chen, Chiung-Mei, Clark, Lorraine N., Condroyer, Christel, De Marco, Elvira Valeria, Dürr, Alexandra, Eblan, Michael J., Fahn, Stanley, Farrer, Matthew, Fung, Hon-Chung, Gan-Or, Ziv, Gasser, Thomas, Gershoni-Baruch, Ruth, Giladi, Nir, Griffith, Alida, Gurevich, Tanya, Januario, Cristina, Kropp, Peter, Lang, Anthony E., Lee-Chen, Guey-Jen, Lesage, Suzanne, Marder, Karen, Mata, Ignacio F., Mirelman, Anat, Mitsui, Jun, Mizuta, Ikuko, Nicoletti, Giuseppe, Oliveira, Catarina, Ottman, Ruth, Orr-Urtreger, Avi, Pereira, Lygia V., Quattrone, Aldo, Rogaeva, Ekaterina, Rolfs, Arndt, Rosenbaum, Hanna, Rozenberg, Roberto, Samii, Ali, Samaddar, Ted, Schulte, Claudia, Sharma, Manu, Singleton, Andrew, Spitz, Mariana, Tan, Eng-King, Tayebi, Nahid, Toda, Tatsushi, Troiano, André, Tsuji, Shoji, Wittstock, Matthias, Wolfsberg, Tyra G., Wu, Yih-Ru, Zabetian, Cyrus P., Zhao, Yi, Ziegler, Shira G.
Publicado em 2009

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

Por Chiò, Adriano, Schymick, Jennifer C., Restagno, Gabriella, Scholz, Sonja W., Lombardo, Federica, Lai, Shiao-Lin, Mora, Gabriele, Fung, Hon-Chung, Britton, Angela, Arepalli, Sampath, Gibbs, J. Raphael, Nalls, Michael, Berger, Stephen, Kwee, Lydia Coulter, Oddone, Eugene Z., Ding, Jinhui, Crews, Cynthia, Rafferty, Ian, Washecka, Nicole, Hernandez, Dena, Ferrucci, Luigi, Bandinelli, Stefania, Guralnik, Jack, Macciardi, Fabio, Torri, Federica, Lupoli, Sara, Chanock, Stephen J., Thomas, Gilles, Hunter, David J., Gieger, Christian, Wichmann, H. Erich, Calvo, Andrea, Mutani, Roberto, Battistini, Stefania, Giannini, Fabio, Caponnetto, Claudia, Mancardi, Giovanni Luigi, La Bella, Vincenzo, Valentino, Francesca, Monsurrò, Maria Rosaria, Tedeschi, Gioacchino, Marinou, Kalliopi, Sabatelli, Mario, Conte, Amelia, Mandrioli, Jessica, Sola, Patrizia, Salvi, Fabrizio, Bartolomei, Ilaria, Siciliano, Gabriele, Carlesi, Cecilia, Orrell, Richard W., Talbot, Kevin, Simmons, Zachary, Connor, James, Pioro, Erik P., Dunkley, Travis, Stephan, Dietrich A., Kasperaviciute, Dalia, Fisher, Elizabeth M., Jabonka, Sibylle, Sendtner, Michael, Beck, Marcus, Bruijn, Lucie, Rothstein, Jeffrey, Schmidt, Silke, Singleton, Andrew, Hardy, John, Traynor, Bryan J.
Publicado em 2009