Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease
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.
Published in Movement disorders (15.10.2010)
Published in Movement disorders (15.10.2010)
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Lrrk2 pathogenic substitutions in Parkinson's disease
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
Published in Neurogenetics (01.12.2005)
Published in Neurogenetics (01.12.2005)
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Genomewide Association, Parkinson Disease, and PARK10
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
Published in American journal of human genetics (01.06.2006)
Published in American journal of human genetics (01.06.2006)
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LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease
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.
Published in Neurogenetics (01.10.2010)
Published in Neurogenetics (01.10.2010)
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A Swedish family with de novo α-synuclein A53T mutation: Evidence for early cortical dysfunction
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
Published in Parkinsonism & related disorders (01.11.2009)
Published in Parkinsonism & related disorders (01.11.2009)
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First neuropathological description of a patient with Parkinson’s disease and LRRK2 p.N1437H mutation
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
Published in Parkinsonism & related disorders (01.05.2012)
Published in Parkinsonism & related disorders (01.05.2012)
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LINGO1 rs9652490 is associated with essential tremor and Parkinson disease
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
Published in Parkinsonism & related disorders (01.02.2010)
Published in Parkinsonism & related disorders (01.02.2010)
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Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson’s disease
Nishioka, Kenya, Vilariño-Güell, Carles, Cobb, Stephanie A, Kachergus, Jennifer M, Ross, Owen A, Hentati, Emna, Hentati, Faycal, Farrer, Matthew J
Published in Parkinsonism & related disorders (01.12.2010)
Published in Parkinsonism & related disorders (01.12.2010)
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EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population
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
Published in Parkinsonism & related disorders (01.06.2014)
Published in Parkinsonism & related disorders (01.06.2014)
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Glucocerebrosidase mutations in diffuse Lewy body disease
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
Published in Parkinsonism & related disorders (01.01.2011)
Published in Parkinsonism & related disorders (01.01.2011)
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Glucocerebrosidase mutations are not a common risk factor for Parkinson disease in North Africa
Nishioka, Kenya, Vilariño-Güell, Carles, Cobb, Stephanie A., Kachergus, Jennifer M., Ross, Owen A., Wider, Christian, Gibson, Rachel A., Hentati, Faycal, Farrer, Matthew J.
Published in Neuroscience letters (21.06.2010)
Published in Neuroscience letters (21.06.2010)
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PARK2 variability in Polish Parkinson’s disease patients - interaction with mitochondrial haplogroups
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
Published in Parkinsonism & related disorders (01.06.2012)
Published in Parkinsonism & related disorders (01.06.2012)
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Alpha-synuclein polymorphisms are associated with Parkinson's disease in a Saskatchewan population
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
Published in Movement disorders (15.12.2009)
Published in Movement disorders (15.12.2009)
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LRRK2 variation and Parkinson's disease in African Americans
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.
Published in Movement disorders (15.09.2010)
Published in Movement disorders (15.09.2010)
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GCH1 in early-onset Parkinson's disease
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.
Published in Movement disorders (30.10.2009)
Published in Movement disorders (30.10.2009)
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Lrrk2 mutations in South America: A study of Chilean Parkinson's disease
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
Published in Neuroscience letters (18.07.2007)
Published in Neuroscience letters (18.07.2007)
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VPS35 Mutations in Parkinson Disease
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.
Published in American journal of human genetics (15.07.2011)
Published in American journal of human genetics (15.07.2011)
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Journal Article
Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease
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.
Published in American journal of human genetics (09.09.2011)
Published in American journal of human genetics (09.09.2011)
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Journal Article
Genetic variation of the mitochondrial Complex I subunit NDUFV2 and Parkinson disease
Nishioka, Kenya, Vilariño-Güell, Carles, Cobb, Stephanie A., Kachergus, Jennifer M., Ross, Owen A., Hentati, Emna, Hentati, Faycal, Farrer, Matthew J.
Published in Parkinsonism & related disorders (23.10.2010)
Published in Parkinsonism & related disorders (23.10.2010)
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Journal Article
VPS35 Mutations in Parkinson Disease
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.
Published in American journal of human genetics (12.08.2011)
Published in American journal of human genetics (12.08.2011)
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