Twenty-first century brain banking. Processing brains for research: the Columbia University methods

por Vonsattel, Jean Paul G., del Amaya, Maria Pilar, Keller, Christian E.
Publicado 2007

Cerebellar Pathology of a Dual Clinical Diagnosis: Patients with Essential Tremor and Dystonia

por Ma, Karen, Babij, Rachel, Cortés, Etty, Vonsattel, Jean‐Paul G., Louis, Elan D.
Publicado 2012

What is It? Difficult to Pigeon Hole Tremor: a Clinical–Pathological Study of a Man with Jaw Tremor

por Louis, Elan D., Bain, Peter G., Hallett, Mark, Jankovic, Joseph, Vonsattel, Jean-Paul G.
Publicado 2013

Essential tremor with ubiquitinated intranuclear inclusions and cerebellar degeneration

por Louis, Elan D., Mazzoni, Pietro, Ma, Karen J., Moskowitz, Carol B., Lawton, Arlene, Garber, Anthony, Vonsattel, Jean-Paul G.
Publicado 2012

Inferior Olivary nucleus degeneration does not lessen tremor in essential tremor

por Louis, Elan D., Diaz, Daniel Trujillo, Kuo, Sheng-Han, Gan, Shi-Rui, Cortes, Etty P., Vonsattel, Jean Paul G., Faust, Phyllis L.
Publicado 2018

A soluble truncated tau species related to cognitive dysfunction and caspase-2 is elevated in the brain of Huntington’s disease patients

por Liu, Peng, Smith, Benjamin R., Huang, Eric S., Mahesh, Abhishek, Vonsattel, Jean Paul G., Petersen, Ashley J., Gomez-Pastor, Rocio, Ashe, Karen H.
Publicado 2019

Macroautophagy Abnormality in Essential Tremor

por Kuo, Sheng-Han, Tang, Guomei, Ma, Karen, Babij, Rachel, Cortes, Etty, Vonsattel, Jean-Paul G., Faust, Phyllis L., Sulzer, David, Louis, Elan D.
Publicado 2012

Generation of iPSC lines from archived non-cryoprotected biobanked dura mater

por Sproul, Andrew A, Vensand, Lauren B, Dusenberry, Carmen R, Jacob, Samson, Vonsattel, Jean Paul G, Paull, Daniel J, Shelanski, Michael L, Crary, John F, Noggle, Scott A
Publicado 2014

Changes of peripheral TGF-β1 depend on monocytes-derived macrophages in Huntington disease

por Di Pardo, Alba, Alberti, Silvia, Maglione, Vittorio, Amico, Enrico, Cortes, Etty P, Elifani, Francesca, Battaglia, Giuseppe, Busceti, Carla L, Nicoletti, Ferdinando, Vonsattel, Jean Paul G, Squitieri, Ferdinando
Publicado 2013

Reduced LRRK2 in association with retromer dysfunction in post-mortem brain tissue from LRRK2 mutation carriers

por Zhao, Ye, Perera, Gayathri, Takahashi-Fujigasaki, Junko, Mash, Deborah C, Vonsattel, Jean Paul G, Uchino, Akiko, Hasegawa, Kazuko, Jeremy Nichols, R, Holton, Janice L, Murayama, Shigeo, Dzamko, Nicolas, Halliday, Glenda M
Publicado 2018

Soluble amyloid beta levels are elevated in the white matter of Alzheimer’s patients, independent of cortical plaque severity

por Collins-Praino, Lyndsey E, Francis, Yitshak I, Griffith, Erica Y, Wiegman, Anne F, Urbach, Jonathan, Lawton, Arlene, Honig, Lawrence S, Cortes, Etty, Vonsattel, Jean Paul G, Canoll, Peter D, Goldman, James E, Brickman, Adam M
Publicado 2014

Single cell RNA sequencing of human microglia uncovers a subset associated with Alzheimer’s disease

por Olah, Marta, Menon, Vilas, Habib, Naomi, Taga, Mariko F., Ma, Yiyi, Yung, Christina J., Cimpean, Maria, Khairallah, Anthony, Coronas-Samano, Guillermo, Sankowski, Roman, Grün, Dominic, Kroshilina, Alexandra A., Dionne, Danielle, Sarkis, Rani A., Cosgrove, Garth R., Helgager, Jeffrey, Golden, Jeffrey A., Pennell, Page B., Prinz, Marco, Vonsattel, Jean Paul G., Teich, Andrew F., Schneider, Julie A., Bennett, David A., Regev, Aviv, Elyaman, Wassim, Bradshaw, Elizabeth M., De Jager, Philip L.
Publicado 2020

Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregates

por Ling, Helen, Gelpi, Ellen, Davey, Karen, Jaunmuktane, Zane, Mok, Kin Y., Jabbari, Edwin, Simone, Roberto, R’Bibo, Lea, Brandner, Sebastian, Ellis, Matthew J., Attems, Johannes, Mann, David, Halliday, Glenda M., Al-Sarraj, S., Hedreen, J., Ironside, James W., Kovacs, Gabor G., Kovari, E., Love, S., Vonsattel, Jean Paul G., Allinson, Kieren S. J., Hansen, Daniela, Bradshaw, Teisha, Setó-Salvia, Núria, Wray, Selina, de Silva, Rohan, Morris, Huw R., Warner, Thomas T., Hardy, John, Holton, Janice L., Revesz, Tamas
Publicado 2020

Genetic Risk Underlying Psychiatric and Cognitive Symptoms in Huntington’s Disease

por Ellis, Natalie, Tee, Amelia, McAllister, Branduff, Massey, Thomas, McLauchlan, Duncan, Stone, Timothy, Correia, Kevin, Loupe, Jacob, Kim, Kyung-Hee, Barker, Douglas, Hong, Eun Pyo, Chao, Michael J., Long, Jeffrey D., Lucente, Diane, Vonsattel, Jean Paul G., Pinto, Ricardo Mouro, Elneel, Kawther Abu, Ramos, Eliana Marisa, Mysore, Jayalakshmi Srinidhi, Gillis, Tammy, Wheeler, Vanessa C., Medway, Christopher, Hall, Lynsey, Kwak, Seung, Sampaio, Cristina, Ciosi, Marc, Maxwell, Alastair, Chatzi, Afroditi, Monckton, Darren G., Orth, Michael, Landwehrmeyer, G. Bernhard, Paulsen, Jane S., Shoulson, Ira, Myers, Richard H., van Duijn, Erik, Rickards, Hugh, MacDonald, Marcy E., Lee, Jong-min, Gusella, James F., Jones, Lesley, Holmans, Peter
Publicado 2020

Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy

por Kouri, Naomi, Ross, Owen A., Dombroski, Beth, Younkin, Curtis S., Serie, Daniel J., Soto-Ortolaza, Alexandra, Baker, Matthew, Finch, Ni Cole A., Yoon, Hyejin, Kim, Jungsu, Fujioka, Shinsuke, McLean, Catriona A., Ghetti, Bernardino, Spina, Salvatore, Cantwell, Laura B., Farlow, Martin R., Grafman, Jordan, Huey, Edward D., Ryung Han, Mi, Beecher, Sherry, Geller, Evan T., Kretzschmar, Hans A., Roeber, Sigrun, Gearing, Marla, Juncos, Jorge L., Vonsattel, Jean Paul G., Van Deerlin, Vivianna M., Grossman, Murray, Hurtig, Howard I., Gross, Rachel G., Arnold, Steven E., Trojanowski, John Q., Lee, Virginia M., Wenning, Gregor K., White, Charles L., Höglinger, Günter U., Müller, Ulrich, Devlin, Bernie, Golbe, Lawrence I., Crook, Julia, Parisi, Joseph E., Boeve, Bradley F., Josephs, Keith A., Wszolek, Zbigniew K., Uitti, Ryan J., Graff-Radford, Neill R., Litvan, Irene, Younkin, Steven G., Wang, Li-San, Ertekin-Taner, Nilüfer, Rademakers, Rosa, Hakonarsen, Hakon, Schellenberg, Gerard D., Dickson, Dennis W.
Publicado 2015

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

por Van Deerlin, Vivianna M., Sleiman, Patrick M. A., Martinez-Lage, Maria, Chen-Plotkin, Alice, Wang, Li-San, Graff-Radford, Neill R, Dickson, Dennis W., Rademakers, Rosa, Boeve, Bradley F., Grossman, Murray, Arnold, Steven E., Mann, David M.A., Pickering-Brown, Stuart M., Seelaar, Harro, Heutink, Peter, van Swieten, John C., Murrell, Jill R., Ghetti, Bernardino, Spina, Salvatore, Grafman, Jordan, Hodges, John, Spillantini, Maria Grazia, Gilman, Sid', Lieberman, Andrew P., Kaye, Jeffrey A., Woltjer, Randall L., Bigio, Eileen H, Mesulam, Marsel, al-Sarraj, Safa, Troakes, Claire, Rosenberg, Roger N., White, Charles L., Ferrer, Isidro, Lladó, Albert, Neumann, Manuela, Kretzschmar, Hans A., Hulette, Christine Marie, Welsh-Bohmer, Kathleen A., Miller, Bruce L, Alzualde, Ainhoa, de Munain, Adolfo Lopez, McKee, Ann C., Gearing, Marla, Levey, Allan I., Lah, James J., Hardy, John, Rohrer, Jonathan D., Lashley, Tammaryn, Mackenzie, Ian R.A., Feldman, Howard H., Hamilton, Ronald L., Dekosky, Steven T., van der Zee, Julie, Kumar-Singh, Samir, Van Broeckhoven, Christine, Mayeux, Richard, Vonsattel, Jean Paul G., Troncoso, Juan C., Kril, Jillian J, Kwok, John B.J., Halliday, Glenda M., Bird, Thomas D., Ince, Paul G., Shaw, Pamela J., Cairns, Nigel J., Morris, John C., McLean, Catriona Ann, DeCarli, Charles, Ellis, William G., Freeman, Stefanie H., Frosch, Matthew P., Growdon, John H., Perl, Daniel P., Sano, Mary, Bennett, David A., Schneider, Julie A., Beach, Thomas G., Reiman, Eric M., Woodruff, Bryan K., Cummings, Jeffrey, Vinters, Harry V., Miller, Carol A., Chui, Helena C., Alafuzoff, Irina, Hartikainen, Päivi, Seilhean, Danielle, Galasko, Douglas, Masliah, Eliezer, Cotman, Carl W., Tuñón, M. Teresa, Martínez, M. Cristina Caballero, Munoz, David G., Carroll, Steven L., Marson, Daniel, Riederer, Peter F., Bogdanovic, Nenad, Schellenberg, Gerard D., Hakonarson, Hakon, Trojanowski, John Q., Lee, Virginia M.-Y.
Publicado 2010