Genetic counseling for FTD/ALS caused by the C9ORF72 hexanucleotide expansion

le Fong, Jamie C, Karydas, Anna M, Goldman, Jill S
Foilsithe 2012

Frontotemporal Dementia and Psychiatric Illness: Emerging Clinical and Biological Links in Gene Carriers

le Block, Nikolas R., Sha, Sharon J., Karydas, Anna M., Fong, Jamie C., De May, Mary G., Miller, Bruce L., Rosen, Howard J.
Foilsithe in Am J Geriatr Psychiatry (2015)

Genetic prion disease: experience of a rapidly progressive dementia center in the United States and a review of the literature

le Takada, Leonel T., Kim, Mee-Ohk, Cleveland, Ross W., Wong, Katherine, Forner, Sven A., Gala, Ignacio Illán, Fong, Jamie C., Geschwind, Michael D.
Foilsithe in Am J Med Genet B Neuropsychiatr Genet (2017)

Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases

le Kim, Mee-Ohk, Cali, Ignazio, Oehler, Abby, Fong, Jamie C, Wong, Katherine, See, Tricia, Katz, Jonathan S, Gambetti, Pierluigi, Bettcher, Brianne M, DeArmond, Stephen J, Geschwind, Michael D
Foilsithe 2013

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

le 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.
Foilsithe in Ann Clin Transl Neurol (2015)

Ascertainment Bias Causes False Signal of Anticipation in Genetic Prion Disease

le Minikel, Eric Vallabh, Zerr, Inga, Collins, Steven J., Ponto, Claudia, Boyd, Alison, Klug, Genevieve, Karch, André, Kenny, Joanna, Collinge, John, Takada, Leonel T., Forner, Sven, Fong, Jamie C., Mead, Simon, Geschwind, Michael D.
Foilsithe 2014

Frontotemporal dementia in a Brazilian Caucasian kindred with the C9orf72 mutation

le Takada, Leonel T., Pimentel, Maria Lucia V., DeJesus-Hernandez, Mariely, Fong, Jamie C., Yokoyama, Jennifer S., Karydas, Anna, Thibodeau, Marie-Pierre, Rutherford, Nicola J., Baker, Matthew C., Lomen-Hoerth, Catherine, Rademakers, Rosa, Miller, Bruce L.
Foilsithe 2012

Genetic Prion Disease Caused by PRNP Q160X Mutation Presenting with an Orbitofrontal Syndrome, Cyclic Diarrhea, and Peripheral Neuropathy

le Fong, Jamie C., Rojas, Julio C., Bang, Jee, Legati, Andrea, Rankin, Katherine P., Forner, Sven, Miller, Zachary A., Karydas, Anna M., Coppola, Giovanni, Grouse, Carrie K., Ralph, Jeffrey, Miller, Bruce L., Geschwind, Michael D.
Foilsithe in J Alzheimers Dis (2016)

Downregulation of MicroRNA-9 in iPSC-Derived Neurons of FTD/ALS Patients with TDP-43 Mutations

le Zhang, Zhijun, Almeida, Sandra, Lu, Yubing, Nishimura, Agnes L., Peng, Lingtao, Sun, Danqiong, Wu, Bei, Karydas, Anna M., Tartaglia, Maria C., Fong, Jamie C., Miller, Bruce L., Farese, Robert V., Moore, Melissa J., Shaw, Christopher E., Gao, Fen-Biao
Foilsithe 2013

Association of Cognitive and Behavioral Features Between Adults With Tuberous Sclerosis and Frontotemporal Dementia

le Liu, Andy J., Staffaroni, Adam M., Rojas-Martinez, Julio C., Olney, Nicholas T., Alquezar-Burillo, Carolina, Ljubenkov, Peter A., La Joie, Renaud, Fong, Jamie C., Taylor, Joanne, Karydas, Anna, Ramos, Eliana Marisa, Coppola, Giovanni, Boxer, Adam L., Rabinovici, Gil D., Miller, Bruce L., Kao, Aimee W.
Foilsithe in JAMA Neurol (2020)

Frontotemporal dementia due to C9ORF72 mutations: Clinical and imaging features

le Sha, Sharon J., Takada, Leonel T., Rankin, Katherine P., Yokoyama, Jennifer S., Rutherford, Nicola J., Fong, Jamie C., Khan, Baber, Karydas, Anna, Baker, Matt C., DeJesus-Hernandez, Mariely, Pribadi, Mochtar, Coppola, Giovanni, Geschwind, Daniel H., Rademakers, Rosa, Lee, Suzee E., Seeley, William, Miller, Bruce L., Boxer, Adam L.
Foilsithe 2012

Atypical, slowly progressive behavioral variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion

le Khan, Baber K., Yokoyama, Jennifer S., Takada, Leonel T., Sha, Sharon J., Rutherford, Nicola. J., Fong, Jamie C., Karydas, Anna, Wu, Teresa, Ketelle, Robin, Baker, Matt C., Hernandez, Mariely-Dejesus, Coppola, Giovanni, Geschwind, Daniel H., Rademakers, Rosa, Lee, Suzee E., Rosen, Howard J., Rabinovici, Gil D., Seeley, William, Rankin, Katherine P., Boxer, Adam L., Miller, Bruce L.
Foilsithe 2012

Altered network connectivity in frontotemporal dementia with C9orf72 hexanucleotide repeat expansion

le Lee, Suzee E., Khazenzon, Anna M., Trujillo, Andrew J., Guo, Christine C., Yokoyama, Jennifer S., Sha, Sharon J., Takada, Leonel T., Karydas, Anna M., Block, Nikolas R., Coppola, Giovanni, Pribadi, Mochtar, Geschwind, Daniel H., Rademakers, Rosa, Fong, Jamie C., Weiner, Michael W., Boxer, Adam L., Kramer, Joel H., Rosen, Howard J., Miller, Bruce L., Seeley, William W.
Foilsithe 2014

Frequency of frontotemporal dementia gene variants in C9ORF72, MAPT, and GRN in academic versus commercial laboratory cohorts

le Steele, Natasha ZR, Bright, Alison R, Lee, Suzee E, Fong, Jamie C, Bonham, Luke W, Karydas, Anna, Karbassi, Izabela D, Pribadi, Mochtar, Meservey, Marc A, Gallen, Matthew C, Ramos, Eliana Marisa, Liaquat, Khalida, Hoffman, Carol C, Krasner, Meagan R, Dodge, Whitney, L Miller, Bruce, Coppola, Giovanni, Rankin, Katherine P, Yokoyama, Jennifer S, Higgins, Joseph J
Foilsithe in Adv Genomics Genet (2018)

Linking tuberous sclerosis complex, excessive mTOR signaling, and age-related neurodegeneration: a new association between TSC1 mutation and frontotemporal dementia

le Olney, Nicholas T., Alquezar, Carolina, Ramos, Eliana Marisa, Nana, Alissa L., Fong, Jamie C., Karydas, Anna M., Taylor, Joanne B., Stephens, Melanie L., Argouarch, Andrea R., Van Berlo, Victoria A., Dokuru, Deepika R., Sherr, Elliott H., Jicha, Gregory A., Dillon, William P., Desikan, Rahul S., De May, Mary, Seeley, William W., Coppola, Giovanni, Miller, Bruce L., Kao, Aimee W.
Foilsithe in Acta Neuropathol (2017)

Age at onset in genetic prion disease and the design of preventive clinical trials

le Minikel, Eric Vallabh, Vallabh, Sonia M., Orseth, Margaret C., Brandel, Jean-Philippe, Haïk, Stéphane, Laplanche, Jean-Louis, Zerr, Inga, Parchi, Piero, Capellari, Sabina, Safar, Jiri, Kenny, Janna, Fong, Jamie C., Takada, Leonel T., Ponto, Claudia, Hermann, Peter, Knipper, Tobias, Stehmann, Christiane, Kitamoto, Tetsuyuki, Ae, Ryusuke, Hamaguchi, Tsuyoshi, Sanjo, Nobuo, Tsukamoto, Tadashi, Mizusawa, Hidehiro, Collins, Steven J., Chiesa, Roberto, Roiter, Ignazio, de Pedro-Cuesta, Jesús, Calero, Miguel, Geschwind, Michael D., Yamada, Masahito, Nakamura, Yosikazu, Mead, Simon
Foilsithe in Neurology (2019)

Brain volumetric deficits in MAPT mutation carriers: a multisite study

le 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.
Foilsithe in Ann Clin Transl Neurol (2020)

Plasma Neurofilament Light for Prediction of Disease Progression in Familial Frontotemporal Lobar Degeneration

le Rojas, Julio C., Wang, Ping, Staffaroni, Adam M., Heller, Carolin, Cobigo, Yann, Wolf, Amy, Goh, Sheng-Yang M., Ljubenkov, Peter A., Heuer, Hilary W., Fong, Jamie C., Taylor, Joanne B., Veras, Eliseo, Song, Linan, Jeromin, Andreas, Hanlon, David, Yu, Lili, Khinikar, Arvind, Sivasankaran, Rajeev, Kieloch, Agnieszka, Valentin, Marie-Anne, Karydas, Anna M., Mitic, Laura L., Pearlman, Rodney, Kornak, John, Kramer, Joel H., Miller, Bruce L., Kantarci, Kejal, Knopman, David S., Graff-Radford, Neill, Petrucelli, Leonard, Rademakers, Rosa, Irwin, David J., Grossman, Murray, Ramos, Eliana Marisa, Coppola, Giovanni, Mendez, Mario F., Bordelon, Yvette, Dickerson, Bradford C., Ghoshal, Nupur, Huey, Edward D., Mackenzie, Ian R., Appleby, Brian S., Domoto-Reilly, Kimiko, Hsiung, Ging-Yuek R., Toga, Arthur W., Weintraub, Sandra, Kaufer, Daniel I., Kerwin, Diana, Litvan, Irene, Onyike, Chiadikaobi U., Pantelyat, Alexander, Roberson, Erik D., Tartaglia, Maria C., Foroud, Tatiana, Chen, Weiping, Czerkowicz, Julie, Graham, Danielle L., van Swieten, John C., Borroni, Barbara, Sanchez-Valle, Raquel, Moreno, Fermin, Laforce, Robert, Graff, Caroline, Synofzik, Matthis, Galimberti, Daniela, Rowe, James B., Masellis, Mario, Finger, Elizabeth, Vandenberghe, Rik, de Mendonça, Alexandre, Tagliavini, Fabrizio, Santana, Isabel, Ducharme, Simon, Butler, Chris R., Gerhard, Alexander, Levin, Johannes, Danek, Adrian, Otto, Markus, Sorbi, Sandro, Cash, David M., Convery, Rhian S., Bocchetta, Martina, Foiani, Martha, Greaves, Caroline V., Peakman, Georgia, Russell, Lucy, Swift, Imogen, Todd, Emily, Rohrer, Jonathan D., Boeve, Bradley F., Rosen, Howard J., Boxer, Adam L.
Foilsithe in Neurology (2021)