Dancing Feet Dyskinesia in a Patient with GBA-PD

por Olszewska, Diana A., McCarthy, Allan, Soto-Beasley, Alexandra I., Walton, Ronald L., Ross, Owen A., Lynch, Tim
Publicado 2022

Systematic Functional Analysis of PINK1 and PRKN Coding Variants

por 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.
Publicado 2022

Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies

por 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.
Publicado 2023

Publisher Correction to: Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS path...

por 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.
Publicado 2023

Association Between Glucocerebrosidase Mutations and Parkinson's Disease in Ireland

por Olszewska, Diana A., McCarthy, Allan, Soto-Beasley, Alexandra I., Walton, Ronald L., Magennis, Brian, McLaughlin, Russell L., Hardiman, Orla, Ross, Owen A., Lynch, Tim
Publicado 2020

Association of MAPT subhaplotypes with clinical and demographic features in Parkinson’s disease

por Deutschlander, Angela B., Konno, Takuya, Soto‐Beasley, Alexandra I., Walton, Ronald L., van Gerpen, Jay A., Uitti, Ryan J., Heckman, Michael G., Wszolek, Zbigniew K., Ross, Owen A.
Publicado 2020

Associations of mitochondrial genomic variation with corticobasal degeneration, progressive supranuclear palsy, and neuropathological tau measures

por Valentino, Rebecca R., Tamvaka, Nikoleta, 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.
Publicado 2020

Early-Onset Parkinson Disease Screening in Patients From Nigeria

por Milanowski, Lukasz M., Oshinaike, Olajumoke, Broadway, Benjamin J., Lindemann, Jennifer A., Soto-Beasley, Alexandra I., Walton, Ronald L., Hanna Al-Shaikh, Rana, Strongosky, Audrey J., Fiesel, Fabienne C., Ross, Owen A., Springer, Wolfdieter, Ogun, Shamsideen Abayomi, Wszolek, Zbigniew K.
Publicado 2021

MAPT subhaplotypes in corticobasal degeneration: assessing associations with disease risk, severity of tau pathology, and clinical features

por Valentino, Rebecca R., Koga, Shunsuke, Walton, Ronald L., Soto-Beasley, Alexandra I., Kouri, Naomi, DeTure, Michael A., Murray, Melissa E., Johnson, Patrick W., Petersen, Ronald C., Boeve, Bradley F., Uitti, Ryan J., Wszolek, Zbigniew K., Dickson, Dennis W., Ross, Owen A., Heckman, Michael G.
Publicado 2020

Case report of a patient with unclassified tauopathy with molecular and neuropathological features of both progressive supranuclear palsy and corticobasal degeneration

por Koga, Shunsuke, Metrick, Michael A., Golbe, Lawrence I., Santambrogio, Alessia, Kim, Minji, Soto-Beasley, Alexandra I., Walton, Ronald L., Baker, Matthew C., De Castro, Cristhoper Fernandez, DeTure, Michael, Russell, David, Navia, Bradford A., Sandiego, Christine, Ross, Owen A., Vendruscolo, Michele, Caughey, Byron, Dickson, Dennis W.
Publicado 2023

CWH43 Variants Are Associated With Disease Risk and Clinical Phenotypic Measures in Patients With Normal Pressure Hydrocephalus

por 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
Publicado 2023

Latent trait modeling of tau neuropathology in progressive supranuclear palsy

por Kouri, Naomi, Murray, Melissa E., Reddy, Joseph S., Serie, Daniel J., Soto-Beasley, Alexandra, Allen, Mariet, Carrasquillo, Minerva M., Wang, Xue, Castanedes, Monica Casey, Baker, Matthew C., Rademakers, Rosa, Uitti, Ryan J., Graff-Radford, Neill R., Wszolek, Zbigniew K., Schellenberg, Gerard D., Crook, Julia E., Ertekin-Taner, Nilüfer, Ross, Owen A., Dickson, Dennis W.
Publicado 2021

Mitochondrial genomic variation in dementia with Lewy bodies: association with disease risk and neuropathological measures

por 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.
Publicado 2022

Cathepsin B p.Gly284Val Variant in Parkinson’s Disease Pathogenesis

por Milanowski, Lukasz M., Hou, Xu, Bredenberg, Jenny M., Fiesel, Fabienne C., Cocker, Liam T., Soto-Beasley, Alexandra I., Walton, Ronald L., Strongosky, Audrey J., Faroqi, Ayman H., Barcikowska, Maria, Boczarska-Jedynak, Magdalena, Dulski, Jaroslaw, Fedoryshyn, Lyuda, Janik, Piotr, Potulska-Chromik, Anna, Karpinsky, Katherine, Krygowska-Wajs, Anna, Lynch, Tim, Olszewska, Diana A., Opala, Grzegorz, Pulyk, Aleksander, Rektorova, Irena, Sanotsky, Yanosh, Siuda, Joanna, Widlak, Mariusz, Slawek, Jaroslaw, Rudzinska-Bar, Monika, Uitti, Ryan, Figura, Monika, Szlufik, Stanislaw, Rzonca-Niewczas, Sylwia, Podgorska, Elzbieta, McLean, Pamela J., Koziorowski, Dariusz, Ross, Owen A., Hoffman-Zacharska, Dorota, Springer, Wolfdieter, Wszolek, Zbigniew K.
Publicado 2022

Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis

por 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.
Publicado 2022

Creating the Pick’s disease International Consortium: Association study of MAPT H2 haplotype with risk of Pick’s disease

por Valentino, Rebecca R, Scotton, William J, Roemer, Shanu F, Lashley, Tammaryn, Heckman, Michael G, Shoai, Maryam, Martinez-Carrasco, Alejandro, Tamvaka, Nicole, Walton, Ronald L, Baker, Matthew C, Macpherson, Hannah L, Real, Raquel, Soto-Beasley, Alexandra I, Mok, Kin, Revesz, Tamas, Warner, Thomas T, Jaunmuktane, Zane, Boeve, Bradley F, Christopher, Elizabeth A, DeTure, Michael, Duara, Ranjan, Graff-Radford, Neill R, Josephs, Keith A, Knopman, David S, Koga, Shunsuke, Murray, Melissa E, Lyons, Kelly E, Pahwa, Rajesh, Parisi, Joseph E, Petersen, Ronald C, Whitwell, Jennifer, Grinberg, Lea T, Miller, Bruce, Schlereth, Athena, Seeley, William W, Spina, Salvatore, Grossman, Murray, Irwin, David J, Lee, Edward B, Suh, EunRan, Trojanowski, John Q, Van Deerlin, Vivianna M, Wolk, David A, Connors, Theresa R, Dooley, Patrick M, Frosch, Matthew P, Oakley, Derek H, Aldecoa, Iban, Balasa, Mircea, Gelpi, Ellen, Borrego-Écija, Sergi, de Eugenio Huélamo, Rosa Maria, Gascon-Bayarri, Jordi, Sánchez-Valle, Raquel, Sanz-Cartagena, Pilar, Piñol-Ripoll, Gerard, Molina-Porcel, Laura, Bigio, Eileen H, Flanagan, Margaret E, Gefen, Tamar, Rogalski, Emily J, Weintraub, Sandra, Redding-Ochoa, Javier, Chang, Koping, Troncoso, Juan C, Prokop, Stefan, Newell, Kathy L, Ghetti, Bernardino, Jones, Matthew, Richardson, Anna, Robinson, Andrew C, Roncaroli, Federico, Snowden, Julie, Allinson, Kieren, Green, Oliver, Rowe, James B, Singh, Poonam, Beach, Thomas G, Serrano, Geidy E, Flowers, Xena E, Goldman, James E, Heaps, Allison C, Leskinen, Sandra P, Teich, Andrew F, Black, Sandra E, Keith, Julia L, Masellis, Mario, Bodi, Istvan, King, Andrew, Sarraj, Safa-Al, Troakes, Claire, Halliday, Glenda M, Hodges, John R, Kril, Jillian J, Kwok, John B, Piguet, Olivier, Gearing, Marla, Arzberger, Thomas, Roeber, Sigrun, Attems, Johannes, Morris, Christopher M, Thomas, Alan J, Evers, Bret M., White, Charles L, Mechawar, Naguib, Sieben, Anne A, Cras, Patrick P, De Vil, Bart B, De Deyn, Peter Paul P.P., Duyckaerts, Charles, Le Ber, Isabelle, Seihean, Danielle, Turbant-Leclere, Sabrina, MacKenzie, Ian R, McLean, Catriona, Cykowski, Matthew D, Ervin, John F, Wang, Shih-Hsiu J, Graff, Caroline, Nennesmo, Inger, Nagra, Rashed M, Riehl, James, Kovacs, Gabor G, Giaccone, Giorgio, Nacmias, Benedetta, Neumann, Manuela, Ang, Lee-Cyn, Finger, Elizabeth C, Blauwendraat, Cornelis, Nalls, Mike A, Singleton, Andrew B, Vitale, Dan, Cunha, Cristina, Carvalho, Agostinho, Wszolek, Zbigniew K, Morris, Huw R, Rademakers, Rosa, Hardy, John A, Dickson, Dennis W, Rohrer, Jonathan D, Ross, Owen A
Publicado 2023