Evaluation of the Role of SNCA Variants in Survival without Neurological Disease

por Heckman, Michael G., Soto-Ortolaza, Alexandra I., Diehl, Nancy N., Carrasquillo, Minerva M., Uitti, Ryan J., Wszolek, Zbigniew K., Graff-Radford, Neill R., Ross, Owen A.
Publicado 2012

NOTCH3 Variants and Risk of Ischemic Stroke

por Ross, Owen A., Soto-Ortolaza, Alexandra I., Heckman, Michael G., Verbeeck, Christophe, Serie, Daniel J., Rayaprolu, Sruti, Rich, Stephen S., Nalls, Michael A., Singleton, Andrew, Guerreiro, Rita, Kinsella, Emma, Wszolek, Zbigniew K., Brott, Thomas G., Brown, Robert D., Worrall, Bradford B., Meschia, James F.
Publicado 2013

Analysis of COQ2 gene in multiple system atrophy

por Ogaki, Kotaro, Fujioka, Shinsuke, Heckman, Michael G, Rayaprolu, Sruti, Soto-Ortolaza, Alexandra I, Labbé, Catherine, Walton, Ronald L, Lorenzo-Betancor, Oswaldo, Wang, Xue, Asmann, Yan, Rademakers, Rosa, Graff-Radford, Neill, Uitti, Ryan, Cheshire, William P, Wszolek, Zbigniew K, Dickson, Dennis W, Ross, Owen A
Publicado 2014

Identification of genetic modifiers of age-at-onset for familial Parkinson’s disease

por Hill-Burns, Erin M., Ross, Owen A., Wissemann, William T., Soto-Ortolaza, Alexandra I., Zareparsi, Sepideh, Siuda, Joanna, Lynch, Timothy, Wszolek, Zbigniew K., Silburn, Peter A., Mellick, George D., Ritz, Beate, Scherzer, Clemens R., Zabetian, Cyrus P., Factor, Stewart A., Breheny, Patrick J., Payami, Haydeh
Publicado 2016

Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson’s Disease Locus

por Labbé, Catherine, Ogaki, Kotaro, Lorenzo-Betancor, Oswaldo, Carrasquillo, Minerva M., Heckman, Michael G., McCarthy, Allan, Soto-Ortolaza, Alexandra I., Walton, Ronald L., Lynch, Timothy, Siuda, Joanna, Opala, Grzegorz, Krygowska-Wajs, Anna, Barcikowska, Maria, Czyzewski, Krzysztof, Dickson, Dennis W., Uitti, Ryan J., Wszolek, Zbigniew K., Ross, Owen A.
Publicado 2015

TREM2 p.R47H substitution is not associated with dementia with Lewy bodies

por Walton, Ronald L., Soto-Ortolaza, Alexandra I., Murray, Melissa E., Lorenzo-Betancor, Oswaldo, Ogaki, Kotaro, Heckman, Michael G., Rayaprolu, Sruti, Rademakers, Rosa, Ertekin-Taner, Nilüfer, Uitti, Ryan J., van Gerpen, Jay A., Wszolek, Zbigniew K., Smith, Glenn E., Kantarci, Kejal, Lowe, Val J., Parisi, Joseph E., Jones, David T., Savica, Rodolfo, Graff-Radford, Jonathan, Knopman, David S., Petersen, Ronald C., Graff-Radford, Neill R., Ferman, Tanis J., Dickson, Dennis W., Boeve, Bradley F., Ross, Owen A., Labbé, Catherine
Publicado 2016

Genome-wide association study in essential tremor identifies three new loci

por Müller, Stefanie H., Girard, Simon L., Hopfner, Franziska, Merner, Nancy D., Bourassa, Cynthia V., Lorenz, Delia, Clark, Lorraine N., Tittmann, Lukas, Soto-Ortolaza, Alexandra I., Klebe, Stephan, Hallett, Mark, Schneider, Susanne A., Hodgkinson, Colin A., Lieb, Wolfgang, Wszolek, Zbigniew K., Pendziwiat, Manuela, Lorenzo-Betancor, Oswaldo, Poewe, Werner, Ortega-Cubero, Sara, Seppi, Klaus, Rajput, Alex, Hussl, Anna, Rajput, Ali H., Berg, Daniela, Dion, Patrick A., Wurster, Isabel, Shulman, Joshua M., Srulijes, Karin, Haubenberger, Dietrich, Pastor, Pau, Vilariño-Güell, Carles, Postuma, Ronald B., Bernard, Geneviève, Ladwig, Karl-Heinz, Dupré, Nicolas, Jankovic, Joseph, Strauch, Konstantin, Panisset, Michel, Winkelmann, Juliane, Testa, Claudia M., Reischl, Eva, Zeuner, Kirsten E., Ross, Owen A., Arzberger, Thomas, Chouinard, Sylvain, Deuschl, Günther, Louis, Elan D., Kuhlenbäumer, Gregor, Rouleau, Guy A.
Publicado 2016