The need for a tailored national dementia plan in Ethiopia: A call for action

por Ayele, Biniyam A., Ali, Seid, Anbessie, Mohammed, Zewde, Yared Z., Yoseph, Selam, Lee, Suzee, Valcour, Victor, Miller, Bruce
Publicado 2023

C9orf72 gene networks in the human brain correlate with cortical thickness in C9-FTD and implicate vulnerable cell types

por Broce, Iris J., Sirkis, Daniel W., Nillo, Ryan M., Bonham, Luke W., Lee, Suzee E., Miller, Bruce, Castruita, Patricia, Sturm, Virginia E., Sugrue, Leo S., Desikan, Rahul S., Yokoyama, Jennifer S.
Publicado 2023

Young‐onset frontotemporal dementia in a homozygous tau R406W mutation carrier

por Ng, Adeline S. L., Sias, Ana C., Pressman, Peter S., Fong, Jamie C., Karydas, Anna M., Zanto, Theodore P., De May, Mary, Coppola, Giovanni, Geschwind, Daniel H., Miller, Bruce L., Lee, Suzee E.
Publicado 2015

The unexpected co-occurrence of GRN and MAPT p.A152T in Basque families: Clinical and pathological characteristics

por Moreno, Fermin, Indakoetxea, Begoña, Barandiaran, Myriam, Caballero, María Cristina, Gorostidi, Ana, Calafell, Francesc, Gabilondo, Alazne, Tainta, Mikel, Zulaica, Miren, Martí Massó, José F., López de Munain, Adolfo, Sánchez-Juan, Pascual, Lee, Suzee E.
Publicado 2017

Advancing functional dysconnectivity and atrophy in progressive supranuclear palsy

por Brown, Jesse A., Hua, Alice Y., Trujillo, Andrew, Attygalle, Suneth, Binney, Richard J., Spina, Salvatore, Lee, Suzee E., Kramer, Joel H., Miller, Bruce L., Rosen, Howard J., Boxer, Adam L., Seeley, William W.
Publicado 2017

Gyrification abnormalities in presymptomatic c9orf72 expansion carriers

por Caverzasi, Eduardo, Battistella, Giovanni, Chu, Stephanie A, Rosen, Howie, Zanto, Theodore P, Karydas, Anna, Shwe, Wendy, Coppola, Giovanni, Geschwind, Daniel H, Rademakers, Rosa, Miller, Bruce L, Gorno-Tempini, Maria Luisa, Lee, Suzee E
Publicado 2019

Single-cell RNA-seq reveals alterations in peripheral CX3CR1 and nonclassical monocytes in familial tauopathy

por Sirkis, Daniel W., Warly Solsberg, Caroline, Johnson, Taylor P., Bonham, Luke W., Sturm, Virginia E., Lee, Suzee E., Rankin, Katherine P., Rosen, Howard J., Boxer, Adam L., Seeley, William W., Miller, Bruce L., Geier, Ethan G., Yokoyama, Jennifer S.
Publicado 2023

Predicting amyloid status in corticobasal syndrome using modified clinical criteria, magnetic resonance imaging and fluorodeoxyglucose positron emission tomography

por Sha, Sharon J, Ghosh, Pia M, Lee, Suzee E, Corbetta-Rastelli, Chiara, Jagust, Willian J, Kornak, John, Rankin, Katherine P, Grinberg, Lea T, Vinters, Harry V, Mendez, Mario F, Dickson, Dennis W, Seeley, William W, Gorno-Tempini, Marilu, Kramer, Joel, Miller, Bruce L, Boxer, Adam L, Rabinovici, Gil D
Publicado 2015

A152T tau allele causes neurodegeneration that can be ameliorated in a zebrafish model by autophagy induction

por Lopez, Ana, Lee, Suzee E., Wojta, Kevin, Ramos, Eliana Marisa, Klein, Eric, Chen, Jason, Boxer, Adam L., Gorno-Tempini, Maria Luisa, Geschwind, Daniel H., Schlotawa, Lars, Ogryzko, Nikolay V., Bigio, Eileen H., Rogalski, Emily, Weintraub, Sandra, Mesulam, Marsel M., Fleming, Angeleen, Coppola, Giovanni, Miller, Bruce L., Rubinsztein, David C.
Publicado 2017

Network degeneration and dysfunction in presymptomatic C9ORF72 expansion carriers

por Lee, Suzee E., Sias, Ana C., Mandelli, Maria Luisa, Brown, Jesse A., Brown, Alainna B., Khazenzon, Anna M., Vidovszky, Anna A., Zanto, Theodore P., Karydas, Anna M., Pribadi, Mochtar, Dokuru, Deepika, Coppola, Giovanni, Geschwind, Dan H., Rademakers, Rosa, Gorno-Tempini, Maria Luisa, Rosen, Howard J., Miller, Bruce L., Seeley, William W.
Publicado 2016

Thalamo-cortical network hyperconnectivity in preclinical progranulin mutation carriers

por Lee, Suzee E., Sias, Ana C., Kosik, Eena L., Flagan, Taru M., Deng, Jersey, Chu, Stephanie A., Brown, Jesse A., Vidovszky, Anna A., Ramos, Eliana Marisa, Gorno-Tempini, Maria Luisa, Karydas, Anna M., Coppola, Giovanni, Geschwind, Daniel H., Rademakers, Rosa, Boeve, Bradley F., Boxer, Adam L., Rosen, Howard J., Miller, Bruce L., Seeley, William W.
Publicado 2019

A novel temporal‐predominant neuro‐astroglial tauopathy associated with TMEM106B gene polymorphism in FTLD/ALS‐TDP

por Llibre‐Guerra, Jorge J., Lee, Suzee E., Suemoto, Claudia K., Ehrenberg, Alexander J., Kovacs, Gabor G., Karydas, Anna, Staffaroni, Adam, Franca Resende, Elisa De Paula, Kim, Eun‐Joo, Hwang, Ji‐Hye, Ramos, Eliana Marisa, Wojta, Kevin J., Pasquini, Lorenzo, Pang, Shirley Yin‐Yu, Spina, Salvatore, Allen, Isabel E., Kramer, Joel, Miller, Bruce L., Seeley, William W., Grinberg, Lea T.
Publicado 2021

(18)F-flortaucipir (AV-1451) tau PET in frontotemporal dementia syndromes

por Tsai, Richard M., Bejanin, Alexandre, Lesman-Segev, Orit, LaJoie, Renaud, Visani, Adrienne, Bourakova, Viktoriya, O’Neil, James P., Janabi, Mustafa, Baker, Suzanne, Lee, Suzee E., Perry, David C., Bajorek, Lynn, Karydas, Anna, Spina, Salvatore, Grinberg, Lea T., Seeley, William W., Ramos, Eliana M., Coppola, Giovanni, Gorno-Tempini, Maria Luisa, Miller, Bruce L., Rosen, Howard J., Jagust, William, Boxer, Adam L., Rabinovici, Gil D.
Publicado 2019

Radiogenomics of C9orf72 Expansion Carriers Reveals Global Transposable Element Derepression and Enables Prediction of Thalamic Atrophy and Clinical Impairment

por Bonham, Luke W., Geier, Ethan G., Sirkis, Daniel W., Leong, Josiah K., Ramos, Eliana Marisa, Wang, Qing, Karydas, Anna, Lee, Suzee E., Sturm, Virginia E., Sawyer, Russell P., Friedberg, Adit, Ichida, Justin K., Gitler, Aaron D., Sugrue, Leo, Cordingley, Michael, Bee, Walter, Weber, Eckard, Kramer, Joel H., Rankin, Katherine P., Rosen, Howard J., Boxer, Adam L., Seeley, William W., Ravits, John, Miller, Bruce L., Yokoyama, Jennifer S.
Publicado 2023

Rates of Brain Atrophy Across Disease Stages in Familial Frontotemporal Dementia Associated With MAPT, GRN, and C9orf72 Pathogenic Variants

por Staffaroni, Adam M., Goh, Sheng-Yang M., Cobigo, Yann, Ong, Elise, Lee, Suzee E., Casaletto, Kaitlin B., Wolf, Amy, Forsberg, Leah K., Ghoshal, Nupur, Graff-Radford, Neill R., Grossman, Murray, Heuer, Hilary W., Hsiung, Ging-Yuek R., Kantarci, Kejal, Knopman, David S., Kremers, Walter K., Mackenzie, Ian R., Miller, Bruce L., Pedraza, Otto, Rascovsky, Katya, Tartaglia, M. Carmela, Wszolek, Zbigniew K., Kramer, Joel H., Kornak, John, Boeve, Bradley F., Boxer, Adam L., Rosen, Howard J.
Publicado 2020

A Comprehensive Resource for Induced Pluripotent Stem Cells from Patients with Primary Tauopathies

por Karch, Celeste M., Kao, Aimee W., Karydas, Anna, Onanuga, Khadijah, Martinez, Rita, Argouarch, Andrea, Wang, Chao, Huang, Cindy, Sohn, Peter Dongmin, Bowles, Kathryn R., Spina, Salvatore, Silva, M. Catarina, Marsh, Jacob A., Hsu, Simon, Pugh, Derian A., Ghoshal, Nupur, Norton, Joanne, Huang, Yadong, Lee, Suzee E., Seeley, William W., Theofilas, Panagiotis, Grinberg, Lea T., Moreno, Fermin, McIlroy, Kathryn, Boeve, Bradley F., Cairns, Nigel J., Crary, John F., Haggarty, Stephen J., Ichida, Justin K., Kosik, Kenneth S., Miller, Bruce L., Gan, Li, Goate, Alison M., Temple, Sally
Publicado 2019

Poly(GP), neurofilament and grey matter deficits in C9orf72 expansion carriers

por Meeter, Lieke H.H., Gendron, Tania F., Sias, Ana C., Jiskoot, Lize C., Russo, Silvia P., Donker Kaat, Laura, Papma, Janne M., Panman, Jessica L., van der Ende, Emma L., Dopper, Elise G., Franzen, Sanne, Graff, Caroline, Boxer, Adam L., Rosen, Howard J., Sanchez‐Valle, Raquel, Galimberti, Daniela, Pijnenburg, Yolande A. L., Benussi, Luisa, Ghidoni, Roberta, Borroni, Barbara, Laforce, Robert, del Campo, Marta, Teunissen, Charlotte E., van Minkelen, Rick, Rojas, Julio C., Coppola, Giovanni, Geschwind, Dan H., Rademakers, Rosa, Karydas, Anna M., Öijerstedt, Linn, Scarpini, Elio, Binetti, Giuliano, Padovani, Alessandro, Cash, David M., Dick, Katrina M., Bocchetta, Martina, Miller, Bruce L., Rohrer, Jonathan D., Petrucelli, Leonard, van Swieten, John C., Lee, Suzee E.
Publicado 2018

Brain volumetric deficits in MAPT mutation carriers: a multisite study

por Chu, Stephanie A., Flagan, Taru M., Staffaroni, Adam M., Jiskoot, Lize C., Deng, Jersey, Spina, Salvatore, Zhang, Liwen, Sturm, Virginia E., Yokoyama, Jennifer S., Seeley, William W., Papma, Janne M., Geschwind, Dan H., Rosen, Howard J., Boeve, Bradley F., Boxer, Adam L., Heuer, Hilary W., Forsberg, Leah K., Brushaber, Danielle E., Grossman, Murray, Coppola, Giovanni, Dickerson, Bradford C., Bordelon, Yvette M., Faber, Kelley, Feldman, Howard H., Fields, Julie A., Fong, Jamie C., Foroud, Tatiana, Gavrilova, Ralitza H., Ghoshal, Nupur, Graff‐Radford, Neill R., Hsiung, Ging‐Yuek Robin, Huey, Edward D., Irwin, David J., Kantarci, Kejal, Kaufer, Daniel I., Karydas, Anna M., Knopman, David S., Kornak, John, Kramer, Joel H., Kukull, Walter A., Lapid, Maria I., Litvan, Irene, Mackenzie, Ian R.A., Mendez, Mario F., Miller, Bruce L., Onyike, Chiadi U., Pantelyat, Alexander Y., Rademakers, Rosa, Marisa Ramos, Eliana, Roberson, Erik D., Carmela Tartaglia, Maria, Tatton, Nadine A., Toga, Arthur W., Vetor, Ashley, Weintraub, Sandra, Wong, Bonnie, Wszolek, Zbigniew K., Van Swieten, John C., Lee, Suzee E.
Publicado 2020