Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease von Aasly, Jan O., Vilariño-Güell, Carles, Dachsel, Justus C., Webber, Philip J., West, Andrew B., Haugarvoll, Kristoffer, Johansen, Krisztina K., Toft, Mathias, Nutt, John G., Payami, Haydeh, Kachergus, Jennifer M., Lincoln, Sarah J., Felic, Amela, Wider, Christian, Soto-Ortolaza, Alexandra I., Cobb, Stephanie A., White, Linda R., Ross, Owen A., Farrer, Matthew J.

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Lrrk2 pathogenic substitutions in Parkinson's disease von MATA, Ignacio F, KACHERGUS, Jennifer M, LAHOZ, Carlos, WSZOLEK, Zbigniew K, FARRER, Matthew J, TAYLOR, Julie P, LINCOLN, Sarah, AASLY, Jan, LYNCH, Timothy, HULIHAN, Mary M, COBB, Stephanie A, WU, Ruey-Meei, LU, Chin-Song

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Genomewide Association, Parkinson Disease, and PARK10 von Farrer, Matthew J., Haugarvoll, Kristoffer, Ross, Owen A., Stone, Jeremy T., Milkovic, Nicole M., Cobb, Stephanie A., Whittle, Andrew J., Lincoln, Sarah J., Hulihan, Mary M., Heckman, Michael G., White, Linda R., Aasly, Jan O., Gibson, J. Mark, Gosal, David, Lynch, Timothy, Wszolek, Zbigniew K., Uitti, Ryan J., Toft, Mathias

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LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease von Vilariño-Güell, Carles, Wider, Christian, Ross, Owen A., Jasinska-Myga, Barbara, Kachergus, Jennifer, Cobb, Stephanie A., Soto-Ortolaza, Alexandra I., Behrouz, Bahareh, Heckman, Michael G., Diehl, Nancy N., Testa, Claudia M., Wszolek, Zbigniew K., Uitti, Ryan J., Jankovic, Joseph, Louis, Elan D., Clark, Lorraine N., Rajput, Alex, Farrer, Matthew J.

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A Swedish family with de novo α-synuclein A53T mutation: Evidence for early cortical dysfunction von Puschmann, Andreas, Ross, Owen A, Vilariño-Güell, Carles, Lincoln, Sarah J, Kachergus, Jennifer M, Cobb, Stephanie A, Lindquist, Suzanne G, Nielsen, Jørgen E, Wszolek, Zbigniew K, Farrer, Matthew, Widner, Håkan, van Westen, Danielle, Hägerström, Douglas, Markopoulou, Katerina, Chase, Bruce A, Nilsson, Karin, Reimer, Jan, Nilsson, Christer

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First neuropathological description of a patient with Parkinson’s disease and LRRK2 p.N1437H mutation von Puschmann, Andreas, Englund, Elisabet, Ross, Owen A, Vilariño-Güell, Carles, Lincoln, Sarah J, Kachergus, Jennifer M, Cobb, Stephanie A, Törnqvist, Anna-Lena, Rehncrona, Stig, Widner, Håkan, Wszolek, Zbigniew K, Farrer, Matthew J, Nilsson, Christer

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LINGO1 rs9652490 is associated with essential tremor and Parkinson disease von Vilariño-Güell, Carles, Ross, Owen A, Wider, Christian, Jasinska-Myga, Barbara, Cobb, Stephanie A, Soto-Ortolaza, Alexandra I, Kachergus, Jennifer M, Keeling, Brett H, Dachsel, Justus C, Melrose, Heather L, Behrouz, Bahareh, Wszolek, Zbigniew K, Uitti, Ryan J, Aasly, Jan O, Rajput, Alex, Farrer, Matthew J

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Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson’s disease von Nishioka, Kenya, Vilariño-Güell, Carles, Cobb, Stephanie A, Kachergus, Jennifer M, Ross, Owen A, Hentati, Emna, Hentati, Faycal, Farrer, Matthew J

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EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population von Nishioka, Kenya, Funayama, Manabu, Vilariño-Güell, Carles, Ogaki, Kotaro, Li, Yuanzhe, Sasaki, Ryogen, Kokubo, Yasumasa, Kuzuhara, Shigeki, Kachergus, Jennifer M, Cobb, Stephanie A, Takahashi, Hirohide, Mizuno, Yoshikuni, Farrer, Matthew J, Ross, Owen A, Hattori, Nobutaka

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Glucocerebrosidase mutations in diffuse Lewy body disease von Nishioka, Kenya, Ross, Owen A, Vilariño-Güell, Carles, Cobb, Stephanie A, Kachergus, Jennifer M, Mann, David M.A, Snowden, Julie, Richardson, Anna M.T, Neary, David, Robinson, Christopher A, Rajput, Alex, Papapetropoulos, Spiridon, Mash, Deborah C, Pahwa, Rajesh, Lyons, Kelly E, Wszolek, Zbigniew K, Dickson, Dennis W, Farrer, Matthew J

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Glucocerebrosidase mutations are not a common risk factor for Parkinson disease in North Africa von Nishioka, Kenya, Vilariño-Güell, Carles, Cobb, Stephanie A., Kachergus, Jennifer M., Ross, Owen A., Wider, Christian, Gibson, Rachel A., Hentati, Faycal, Farrer, Matthew J.

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PARK2 variability in Polish Parkinson’s disease patients - interaction with mitochondrial haplogroups von Gaweda-Walerych, Katarzyna, Safranow, Krzysztof, Jasinska-Myga, Barbara, Bialecka, Monika, Klodowska-Duda, Gabriela, Rudzinska, Monika, Czyzewski, Krzysztof, Cobb, Stephanie A, Slawek, Jaroslaw, Styczynska, Maria, Opala, Grzegorz, Drozdzik, Marek, Nishioka, Kenya, Farrer, Matthew J, Ross, Owen A, Wszolek, Zbigniew K, Barcikowska, Maria, Zekanowski, Cezary

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Alpha-synuclein polymorphisms are associated with Parkinson's disease in a Saskatchewan population von Rajput, Alex, Vilariño-Güell, Carles, Rajput, Michele L., Ross, Owen A., Soto-Ortolaza, Alexandra I., Lincoln, Sarah J., Cobb, Stephanie A., Heckman, Michael G., Farrer, Matthew J., Rajput, Ali

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LRRK2 variation and Parkinson's disease in African Americans von Ross, Owen A., Wilhoite, Greggory J., Bacon, Justin A., Soto-Ortolaza, Alexandra, Kachergus, Jennifer, Cobb, Stephanie A., Puschmann, Andreas, Vilariño-Güell, Carles, Farrer, Matthew J., Graff-Radford, Neill, Meschia, James F., Wszolek, Zbigniew K.

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GCH1 in early-onset Parkinson's disease von Cobb, Stephanie A., Wider, Christian, Ross, Owen A., Mata, Ignacio F., Adler, Charles H., Rajput, Alex, Rajput, Ali H., Wu, Ruey-Meei, Hauser, Robert, Josephs, Keith A., Carr, Jonathan, Gwinn, Katrina, Heckman, Michael G., Aasly, Jan O., Lynch, Timothy, Uitti, Ryan J., Wszolek, Zbigniew K., Kapatos, Gregory, Farrer, Matthew J.

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Lrrk2 mutations in South America: A study of Chilean Parkinson's disease von Perez-Pastene, Carolina, Cobb, Stephanie A., Díaz-Grez, Fernando, Hulihan, Mary M., Miranda, Marcelo, Venegas, Pablo, Godoy, Osvaldo Trujillo, Kachergus, Jennifer M., Ross, Owen A., Layson, Luis, Farrer, Matthew J., Segura-Aguilar, Juan

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VPS35 Mutations in Parkinson Disease von Vilariño-Güell, Carles, Wider, Christian, Ross, Owen A., Dachsel, Justus C., Kachergus, Jennifer M., Lincoln, Sarah J., Soto-Ortolaza, Alexandra I., Cobb, Stephanie A., Wilhoite, Greggory J., Bacon, Justin A., Behrouz, Bahareh, Melrose, Heather L., Hentati, Emna, Puschmann, Andreas, Evans, Daniel M., Conibear, Elizabeth, Wasserman, Wyeth W., Aasly, Jan O., Burkhard, Pierre R., Djaldetti, Ruth, Ghika, Joseph, Hentati, Faycal, Krygowska-Wajs, Anna, Lynch, Tim, Melamed, Eldad, Rajput, Alex, Rajput, Ali H., Solida, Alessandra, Wu, Ruey-Meei, Uitti, Ryan J., Wszolek, Zbigniew K., Vingerhoets, François, Farrer, Matthew J.

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Independent and joint effects of the MAPT and SNCA genes in Parkinson disease von 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.

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Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease von Chartier-Harlin, Marie-Christine, Dachsel, Justus C., Vilariño-Güell, Carles, Lincoln, Sarah J., Leprêtre, Frédéric, Hulihan, Mary M., Kachergus, Jennifer, Milnerwood, Austen J., Tapia, Lucia, Song, Mee-Sook, Le Rhun, Emilie, Mutez, Eugénie, Larvor, Lydie, Duflot, Aurélie, Vanbesien-Mailliot, Christel, Kreisler, Alexandre, Ross, Owen A., Nishioka, Kenya, Soto-Ortolaza, Alexandra I., Cobb, Stephanie A., Melrose, Heather L., Behrouz, Bahareh, Keeling, Brett H., Bacon, Justin A., Hentati, Emna, Williams, Lindsey, Yanagiya, Akiko, Sonenberg, Nahum, Lockhart, Paul J., Zubair, Abba C., Uitti, Ryan J., Aasly, Jan O., Krygowska-Wajs, Anna, Opala, Grzegorz, Wszolek, Zbigniew K., Frigerio, Roberta, Maraganore, Demetrius M., Gosal, David, Lynch, Tim, Hutchinson, Michael, Bentivoglio, Anna Rita, Valente, Enza Maria, Nichols, William C., Pankratz, Nathan, Foroud, Tatiana, Gibson, Rachel A., Hentati, Faycal, Dickson, Dennis W., Destée, Alain, Farrer, Matthew J.

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Genetic variation of the mitochondrial Complex I subunit NDUFV2 and Parkinson disease von Nishioka, Kenya, Vilariño-Güell, Carles, Cobb, Stephanie A., Kachergus, Jennifer M., Ross, Owen A., Hentati, Emna, Hentati, Faycal, Farrer, Matthew J.

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