Screening of GBA Mutations in Nigerian Patients with Parkinson's Disease von Milanowski, Lukasz M., Oshinaike, Olajumoke, Walton, Ronald L., Soto‐Beasley, Alexandra I., Hanna Al‐Shaikh, Rana, Strongosky, Audrey J., Ross, Owen A., Wszolek, Zbigniew K., Ogun, Shamsideen Abayomi

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Association of MAPT subhaplotypes with clinical and demographic features in Parkinson’s disease von Deutschlander, Angela B., Konno, Takuya, Soto‐Beasley, Alexandra I., Walton, Ronald L., Gerpen, Jay A., Uitti, Ryan J., Heckman, Michael G., Wszolek, Zbigniew K., Ross, Owen A.

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Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies von Koga, Shunsuke, Murakami, Aya, Soto-Beasley, Alexandra I, Walton, Ronald L, Baker, Matthew C, Castanedes-Casey, Monica, Josephs, Keith A, Ross, Owen A, Dickson, Dennis W

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PTPA variants are rare in early-onset and familial Parkinson's disease von Dulski, Jarosław, Soto-Beasley, Alexandra I, Uitti, Ryan J, Wszolek, Zbigniew K, Ross, Owen A

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Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson’s disease von Hop, Paul J., Lai, Dongbing, Keagle, Pamela J., Baron, Desiree M., Kenna, Brendan J., Kooyman, Maarten, Shankaracharya, Halter, Cheryl, Straniero, Letizia, Asselta, Rosanna, Bonvegna, Salvatore, Soto-Beasley, Alexandra I., Wszolek, Zbigniew K., Uitti, Ryan J., Isaias, Ioannis Ugo, Pezzoli, Gianni, Ticozzi, Nicola, Ross, Owen A., Veldink, Jan H., Foroud, Tatiana M., Kenna, Kevin P., Landers, John E.

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CLEC3B p.S106G Mutant in a Caucasian Population of Successful Neurological Aging von Kolicheski, Ana, Walton, Ronald L, Soto-Beasley, Alexandra I, Heckman, Michael G, Uitti, Ryan J, Parfitt, Francine, Graff-Radford, Michelle R, Wszolek, Zbigniew K, Graff-Radford, Neill R, Ross, Owen A

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GBA variation and susceptibility to multiple system atrophy von Wernick, Anna I., Walton, Ronald L., Koga, Shunsuke, Soto-Beasley, Alexandra I., Heckman, Michael G., Gan-Or, Ziv, Ren, Yingxue, Rademakers, Rosa, Uitti, Ryan J., Wszolek, Zbigniew K., Cheshire, William P., Dickson, Dennis W., Ross, Owen A.

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Association of mitochondrial genomic background with risk of Multiple System Atrophy von Valentino, Rebecca R., Heckman, Michael G., Johnson, Patrick W., Soto-Beasley, Alexandra I., Walton, Ronald L., Koga, Shunsuke, Uitti, Ryan J., Wszolek, Zbigniew K., Dickson, Dennis W., Ross, Owen A.

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Fine-mapping of the non-coding variation driving the Caucasian LRRK2 GWAS signal in Parkinson's disease von Heckman, Michael G., Labbé, Catherine, Kolicheski, Ana L., Soto-Beasley, Alexandra I., Walton, Ronald L., Valentino, Rebecca R., Brennan, Emily R., Johnson, Patrick W., Baheti, Saurabh, Sarangi, Vivekananda, Ren, Yingxue, Uitti, Ryan J., Wszolek, Zbigniew K., Ross, Owen A.

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Prevalence of GBA p.K198E mutation in Colombian and Hispanic populations von Tipton, Philip W., Soto-Beasley, Alexandra I., Walton, Ronald L., Soler-Rangel, Silvia, Romero-Osorio, Óscar, Díaz, Cindy, Moreno-López, Claudia Lucía, Ross, Owen A., Wszolek, Zbigniew K., Cerquera-Cleves, Catalina

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CWH43 Variants Are Associated With Disease Risk and Clinical Phenotypic Measures in Patients With Normal Pressure Hydrocephalus von Tipton, Philip W, Atik, Merve, Soto-Beasley, Alexandra I, Day, Gregory S, Grewal, Sanjeet S, Chaichana, Kaisorn, Fermo, Olga P, Ball, Colleen T, Heckman, Michael G, White, Launia J, Quicksall, Zachary S, Reddy, Joseph S, Ramanan, Vijay K, Vemuri, Prashanthi, Elder, Benjamin D, Ertekin-Taner, Nilufer, Ross, Owen, Graff-Radford, Neill

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Spinocerebellar ataxia type 6 family with phenotypic overlap with Multiple System Atrophy von Al-Shaikh, Rana Hanna, Wernick, Anna, Strongosky, Audrey J., Soto-Beasley, Alexandra, van Gerpen, Jay A., Cheshire, William P., Uitti, Ryan J., Ross, Owen A., Wszolek, Zbigniew K.

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Mitochondrial genomic variation in dementia with Lewy bodies: association with disease risk and neuropathological measures von Valentino, Rebecca R, Ramnarine, Chloe, Heckman, Michael G, Johnson, Patrick W, Soto-Beasley, Alexandra I, Walton, Ronald L, Koga, Shunsuke, Kasanuki, Koji, Murray, Melissa E, Uitti, Ryan J, Fields, Julie A, Botha, Hugo, Ramanan, Vijay K, Kantarci, Kejal, Lowe, Val J, Jack, Clifford R, Ertekin-Taner, Nilufer, Savica, Rodolfo, Graff-Radford, Jonathan, Petersen, Ronald C, Parisi, Joseph E, Reichard, R Ross, Graff-Radford, Neill R, Ferman, Tanis J, Boeve, Bradley F, Wszolek, Zbigniew K, Dickson, Dennis W, Ross, Owen A

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Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis von Liao, Calwing, Castonguay, Charles-Etienne, Heilbron, Karl, Vuokila, Veikko, Medeiros, Miranda, Houle, Gabrielle, Akçimen, Fulya, Ross, Jay P, Catoire, Helene, Diez-Fairen, Monica, Kang, Jooeun, Mueller, Stefanie H, Girard, Simon L, Hopfner, Franziska, Lorenz, Delia, Clark, Lorraine N, Soto-Beasley, Alexandra I, Klebe, Stephan, Hallett, Mark, Wszolek, Zbigniew K, Pendziwiat, Manuela, Lorenzo-Betancor, Oswaldo, Seppi, Klaus, Berg, Daniela, Vilariño-Güell, Carles, Postuma, Ronald B, Bernard, Geneviève, Dupré, Nicolas, Jankovic, Joseph, Testa, Claudia M, Ross, Owen A, Arzberger, Thomas, Chouinard, Sylvain, Louis, Elan D, Mandich, Paola, Vitale, Carmine, Barone, Paolo, García-Martín, Elena, Alonso-Navarro, Hortensia, Agúndez, José A. G, Jiménez-Jiménez, Félix Javier, Pastor, Pau, Rajput, Alex, Deuschl, Günther, Kuhlenbaümer, Gregor, Meijer, Inge A, Dion, Patrick A, Rouleau, Guy A

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Association of Mitochondrial DNA Genomic Variation with Risk of Pick’s disease von Valentino, Rebecca R., Heckman, Michael G., Johnson, Patrick W., Baker, Matthew C., Soto-Beasley, Alexandra I., Walton, Ronald L., Koga, Shunsuke, Roemer, Shanu F., Suh, EunRan, Uitti, Ryan J., Trojanowski, John Q., Grossman, Murray, Van Deerlin, Vivianna M., Rademakers, Rosa, Wszolek, Zbigniew K., Dickson, Dennis W., Ross, Owen A.

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Systematic Functional Analysis of IPINK1/I and IPRKN/I Coding Variants von Broadway, Benjamin J, Boneski, Paige K, Bredenberg, Jenny M, Kolicheski, Ana, Hou, Xu, Soto-Beasley, Alexandra I, Ross, Owen A, Springer, Wolfdieter, Fiesel, Fabienne C

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Frequency of Mutations in PRKN, PINK1, and DJ1 in Patients With Early-Onset Parkinson Disease From Neighboring Countries in Central Europea von Milanowski, Lukasz M., Lindemann, Jennifer A., Hoffman-Zacharska, Dorota, Soto-Beasley, Alexandra I., Barcikowska, Maria, Boczarska-Jedynak, Magdalena, Deutschlander, Angela, Klodowska, Gabriela, Dulski, Jaroslaw, Fedoryshyn, Lyuda, Friedman, Andrzej, Jamrozik, Zygmunt, Janik, Piotr, Karpinsky, Katherine, Koziorowski, Dariusz, Krygowska-Wajs, Anna, Jasinska-Myga, Barbara, Opala, Grzegorz, Potulska-Chromik, Anna, Pulyk, Aleksander, Rektorova, Irena, Sanotsky, Yanosh, Siuda, Joanna, Slawek, Jaroslaw, Smilowska, Katarzyna, Szczechowski, Lech, Rudzinska-Bar, Monika, Walton, Ronald L., Ross, Owen A., Wszolek, Zbigniew K.

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MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association study von Valentino, Rebecca R, Heckman, Michael G, Shoai, Maryam, Martinez-Carrasco, Alejandro, Tamvaka, Nicole, Walton, Ronald L, Real, Raquel, Mok, Kin, Christopher, Elizabeth A, Lee, Edward B, Frosch, Matthew P, Molina-Porcel, Laura, Gefen, Tamar, Robinson, Andrew C, Kobylecki, Christopher, Rowe, James B, Beach, Thomas G, Teich, Andrew F, Keith, Julia L, Bodi, Istvan, Gearing, Marla, Arzberger, Thomas, Morris, Christopher M, White, Charles L, Mechawar, Naguib, MacKenzie, Ian R, McLean, Catriona, Wang, Shih-Hsiu J, Nagra, Rashed M, Kovacs, Gabor G, Giaccone, Giorgio, Ang, Lee-Cyn, Morris, Huw R, Hardy, John A, Dickson, Dennis W, Ross, Owen A, Warner, Thomas T, Boeve, Bradley F, Duara, Ranjan, Josephs, Keith A, Murray, Melissa E, Lyons, Kelly E, Whitwell, Jennifer L, Miller, Bruce, Schlereth, Athena, Van Deerlin, Vivianna M, Wolk, David A, Connors, Theresa R, Dooley, Patrick M, Aldecoa, Iban, Gelpi, Ellen, Sánchez-Valle, Raquel, Sanz-Cartagena, Pilar, Bigio, Eileen H, Weintraub, Sandra, Schneider, Julie A, Chang, Koping, Troncoso, Juan C, Jones, Matthew, Richardson, Anna, Roncaroli, Federico, Snowden, Julie, Serrano, Geidy E, Goldman, James E, Leskinen, Sandra P, Masellis, Mario, King, Andrew, Al-Sarraj, Safa, Troakes, Claire, Hodges, John R, Kril, Jillian J, Kwok, John B, Roeber, Sigrun, Attems, Johannes, Thomas, Alan J, Evers, Bret M., Bieniek, Kevin F, Sieben, Anne A, Cras, Patrick P, De Vil, Bart B, Castellani, Rudolph J, Chaffee, Ann, Franklin, Erin, Jacobsen, Max, Keene, Dirk, Latimer, Caitlin S, Purohit, Dushyant P, Schantz, Aimee, Walker, Jamie, De Deyn, Peter P, Duyckaerts, Charles, Seilhean, Danielle, Turbant-Leclere, Sabrina, Nennesmo, Inger, Riehl, James, Nacmias, Benedetta, Finger, Elizabeth C, Blauwendraat, Cornelis, Nalls, Mike A, Singleton, Andrew B

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