The man who mistook his neuropsychologist for a popstar: when configural processing fails in acquired prosopagnosia

بواسطة Jansari, Ashok, Miller, Scott, Pearce, Laura, Cobb, Stephanie, Sagiv, Noam, Williams, Adrian L., Tree, Jeremy J., Hanley, J. Richard
الحاوية / القاعدة Front Hum Neurosci (2015)

Genetic variation of the mitochondrial Complex I subunit NDUFV2 and Parkinson disease

بواسطة Nishioka, Kenya, Vilariño-Güell, Carles, Cobb, Stephanie A., Kachergus, Jennifer M., Ross, Owen A., Hentati, Emna, Hentati, Faycal, Farrer, Matthew J.
الحاوية / القاعدة Parkinsonism Relat Disord (2010)

Glucocerebrosidase mutations are not a common risk factor for Parkinson disease in North Africa

بواسطة Nishioka, Kenya, Vilariño-Güell, Carles, Cobb, Stephanie A., Kachergus, Jennifer M., Ross, Owen A., Wider, Christian, Gibson, Rachel A., Hentati, Faycal, Farrer, Matthew J.
منشور في 2009

Lrrk2 mutations in South America: A study of Chilean Parkinson's disease

بواسطة 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
منشور في 2007

LRRK2 variation and Parkinson's disease in African Americans

بواسطة 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.
منشور في 2010

First neuropathological description of a patient with Parkinson's disease and LRRK2 p.N1437H mutation

بواسطة 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
منشور في 2011

EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population

بواسطة 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
منشور في 2014

PARK2 variability in Polish Parkinson’s disease patients - interaction with mitochondrial haplogroups

بواسطة 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
منشور في 2012

A Swedish family with de novo α-synuclein A53T mutation: Evidence for early cortical dysfunction

بواسطة 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
منشور في 2009

LINGO1 rs9652490 is associated with Essential Tremor and Parkinson Disease

بواسطة 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.
منشور في 2009

Genomewide Association, Parkinson Disease, and PARK10

بواسطة 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
منشور في 2006

Glucocerebrosidase mutations in diffuse Lewy body disease()

بواسطة 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.
الحاوية / القاعدة Parkinsonism Relat Disord (2011)

LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease

بواسطة 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.
منشور في 2010

Novel Pathogenic Lrrk2 p.Asn1437His substitution in familial Parkinson’s disease

بواسطة 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.
منشور في 2010

VPS35 Mutations in Parkinson Disease

بواسطة 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.
منشور في 2011

VPS35 Mutations in Parkinson Disease

بواسطة 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.
منشور في 2011

Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease

بواسطة 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.
منشور في 2011