TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal dementia von Nicholson, Alexandra M., Finch, NiCole A., Wojtas, Aleksandra, Baker, Matt C., Perkerson, Ralph B., Castanedes‐Casey, Monica, Rousseau, Linda, Benussi, Luisa, Binetti, Giuliano, Ghidoni, Roberta, Hsiung, Ging‐Yuek R., Mackenzie, Ian R., Finger, Elizabeth, Boeve, Bradley F., Ertekin‐Taner, Nilüfer, Graff‐Radford, Neill R., Dickson, Dennis W., Rademakers, Rosa

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Assessment of Olfactory Function in MAPT-Associated Neurodegenerative Disease Reveals Odor-Identification Irreproducibility as a Non-Disease-Specific, General Characteristic of Olf... von Markopoulou, Katerina, Chase, Bruce A, Robowski, Piotr, Strongosky, Audrey, Narożańska, Ewa, Sitek, Emilia J, Berdynski, Mariusz, Barcikowska, Maria, Baker, Matt C, Rademakers, Rosa, Sławek, Jarosław, Klein, Christine, Hückelheim, Katja, Kasten, Meike, Wszolek, Zbigniew K

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Frontotemporal dementia due to C9ORF72 mutations: Clinical and imaging features von SHA, Sharon J, TAKADA, Leonel T, PRIBADI, Mochtar, COPPOLA, Giovanni, GESCHWIND, Daniel H, RADEMAKERS, Rosa, LEE, Suzee E, SEELEY, William, MILLER, Bruce L, BOXER, Adam L, RANKIN, Katherine P, YOKOYAMA, Jennifer S, RUTHERFORD, Nicola J, FONG, Jamie C, KHAN, Baber, KARYDAS, Anna, BAKER, Matt C, DEJESUS-HERNANDEZ, Mariely

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CSF1R mutations link POLD and HDLS as a single disease entity von NICHOLSON, Alexandra M, BAKER, Matt C, KNOPMAN, David S, RADEMAKERS, Rosa, FINCH, Nicole A, RUTHERFORD, Nicola J, WIDER, Christian, GRAFF-RADFORD, Neill R, NELSON, Peter T, BRENT CLARK, H, WSZOLEK, Zbigniew K, DICKSON, Dennis W

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Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype von Rutherford, Nicola J, Heckman, Michael G, DeJesus-Hernandez, Mariely, Baker, Matt C, Soto-Ortolaza, Alexandra I, Rayaprolu, Sruti, Stewart, Heather, Finger, Elizabeth, Volkening, Kathryn, Seeley, William W, Hatanpaa, Kimmo J, Lomen-Hoerth, Catherine, Kertesz, Andrew, Bigio, Eileen H, Lippa, Carol, Knopman, David S, Kretzschmar, Hans A, Neumann, Manuela, Caselli, Richard J, White, Charles L, Mackenzie, Ian R, Petersen, Ronald C, Strong, Michael J, Miller, Bruce L, Boeve, Bradley F, Uitti, Ryan J, Boylan, Kevin B, Wszolek, Zbigniew K, Graff-Radford, Neill R, Dickson, Dennis W, Ross, Owen A, Rademakers, Rosa

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Diffuse leukoencephalopathy with spheroids presenting as primary progressive aphasia von Oboudiyat, Carly, Bigio, Eileen H, Bonakdarpour, Borna, Baker, Matt C, Rademakers, Rosa, Weintraub, Sandra, Mesulam, M.-Marsel

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Mutations in protein N -arginine methyltransferases are not the cause of FTLD-FUS von Ravenscroft, Thomas A, Baker, Matt C, Rutherford, Nicola J, Neumann, Manuela, Mackenzie, Ian R, Josephs, Keith A, Boeve, Bradley F, Petersen, Ronald, Halliday, Glenda M, Kril, Jillian, van Swieten, John C, Seeley, William W, Dickson, Dennis W, Rademakers, Rosa

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C9ORF72 hexanucleotide repeat expansions in patients with ALS from the Coriell Cell Repository von Rutherford, Nicola J, DeJesus-Hernandez, Mariely, Baker, Matt C, Kryston, Thomas B, Brown, Patricia E, Lomen-Hoerth, Catherine, Boylan, Kevin, Wszolek, Zbigniew K, Rademakers, Rosa

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A Novel GRN Mutation (GRN c.708+6_+9delTGAG) in Frontotemporal Lobar Degeneration With TDP-43–Positive Inclusions: Clinicopathologic Report of 6 Cases von Bit-Ivan, Esther N, Suh, Eunran, Shim, Hyung-Sub, Weintraub, Sandra, Hyman, Bradley T, Arnold, Steven E, McCarty-Wood, Elisabeth, Van Deerlin, Viviana M, Schneider, Julie A, Trojanowski, John Q, Frosch, Matthew P, Baker, Matt C, Rademakers, Rosa, Mesulam, Marsel, Bigio, Eileen H

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MRS in Early and Presymptomatic Carriers of a Novel Octapeptide Repeat Insertion in the Prion Protein Gene von McDade, Eric M, Boeve, Bradley F., Fields, Julie A, Kumar, Neeraj, Rademakers, Rosa, Baker, Matt C., Knopman, BSc, David S., Petersen, Ronald C., Jack Jr, Clifford R., Kantarci, Kejal

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Atypical, slowly progressive behavioural variant frontotemporal dementia associated with C9ORF72 hexanucleotide expansion von Khan, Baber K, Yokoyama, Jennifer S, Takada, Leonel T, Sha, Sharon J, Rutherford, Nicola J, Fong, Jamie C, Karydas, Anna M, Wu, Teresa, Ketelle, Robin S, Baker, Matthew C, Hernandez, Mariely-Dejesus, Coppola, Giovanni, Geschwind, Daniel H, Rademakers, Rosa, Lee, Suzee E, Rosen, Howard J, Rabinovici, Gil D, Seeley, William W, Rankin, Katherine P, Boxer, Adam L, Miller, Bruce L

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Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases von COPPOLA, Giovanni, CHINNATHAMBI, Subashchandrabose, LANE, Jessica R, KARYDAS, Anna M, KENET, Robert O, BIERNAT, Jacek, WANG, Li-San, COTMAN, Carl W, DECARLI, Charles S, LEVEY, Allan I, RINGMAN, John M, MENDEZ, Mario F, JIYONG LEE, Jason, CHUI, Helena C, LE BER, Isabelle, BRICE, Alexis, LUPTON, Michelle K, PREZA, Elisavet, LOVESTONE, Simon, POWELL, John, GRAFF-RADFORD, Neill, PETERSEN, Ronald C, BOEVE, Bradley F, DOMBROSKI, Beth A, LIPPA, Carol F, BIGIO, Eileen H, MACKENZIE, Ian, FINGER, Elizabeth, KERTESZ, Andrew, CASELLI, Richard J, GEARING, Marla, JUNCOS, Jorge L, GHETTI, Bernardino, SPINA, Salvatore, BAKER, Matt C, BORDELON, Yvette M, TOURTELLOTTE, Wallace W, FROSCH, Matthew P, VONSATTEL, Jean Paul G, ZAROW, Chris, BEACH, Thomas G, ALBIN, Roger L, LIEBERMAN, Andrew P, LEE, Virginia M, TROJANOWSKI, John Q, SOTO-ORTOLAZA, Alexandra I, VAN DEERLIN, Vivianna M, BIRD, Thomas D, GALASKO, Douglas R, MASLIAH, Eliezer, WHITE, Charles L, TRONCOSO, JuanC, HANNEQUIN, Didier, BOXER, Adam L, GESCHWIND, Michael D, KUMAR, Satish, LEE, Suzee E, KLEIN, Eric, HUANG, Alden Y, SEARS, Renee

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C90RF72 HEXANUCLEOTIDE REPEAT EXPANSIONS IN PATIENTS WITH ALS FROM THE CORIELL CELL REPOSITORY von RUTHERFORD, Nicola J, DEJESUS-HERNANDEZ, Mariely, BAKER, Matt C, KRYSTON, Thomas B, BROWN, Patricia E, LOMEN-HOERTH, Catherine, BOYLAN, Kevin, WSZOLEK, Zbigniew K, RADEMAKERS, Rosa

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TMEM 106B p.T185S regulates TMEM 106B protein levels: implications for frontotemporal dementia von Nicholson, Alexandra M., Finch, NiCole A., Wojtas, Aleksandra, Baker, Matt C., Perkerson, Ralph B., Castanedes‐Casey, Monica, Rousseau, Linda, Benussi, Luisa, Binetti, Giuliano, Ghidoni, Roberta, Hsiung, Ging‐Yuek R., Mackenzie, Ian R., Finger, Elizabeth, Boeve, Bradley F., Ertekin‐Taner, Nilüfer, Graff‐Radford, Neill R., Dickson, Dennis W., Rademakers, Rosa

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Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype von Rutherford, Nicola J, Heckman, Michael G, Dejesus-Hernandez, Mariely, Baker, Matt C, Soto-Ortolaza, Alexandra I, Rayaprolu, Sruti, Stewart, Heather, Finger, Elizabeth, Volkening, Kathryn, Seeley, William W, Hatanpaa, Kimmo J, Lomen-Hoerth, Catherine, Kertesz, Andrew, Bigio, Eileen H, Lippa, Carol, Knopman, David S, Kretzschmar, Hans A, Neumann, Manuela, Caselli, Richard J, White, Charles L, Mackenzie, Ian R, Petersen, Ronald C, Strong, Michael J, Miller, Bruce L, Boeve, Bradley F, Uitti, Ryan J, Boylan, Kevin B, Wszolek, Zbigniew K, Graff-Radford, Neill R, Dickson, Dennis W, Ross, Owen A, Rademakers, Rosa

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1H MR Spectroscopy in Presymptomatic MAPT mutation carriers: A Biomarker for Tau Mediated Pathology von Kantarci, Kejal, Boeve, Bradley F., Wszolek, Zbigniew K., Rademakers, Rosa, Whitwell, Jennifer L., Baker, Matt C., Senjem, Matthew L., Knopman, David S., Petersen, Ronald C., Jack, Clifford R.

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P1‐411: 1H MR spectroscopy in presymptomatic MAPT mutation carriers: A biomarker for tau mediated pathology von Kantarci, Kejal, Boeve, Bradley F., Wszolek, Zbigniew K., Rademakers, Rosa, Whitwell, Jennifer L., Baker, Matt C., Senjem, Matthew L., Knopman, David S., Petersen, Ronald C., Jack, Clifford R.

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IC‐P‐105: 1H MR Spectroscopy in Presymptomatic MAPT mutation carriers: A Biomarker for Tau Mediated Pathology von Kantarci, Kejal, Boeve, Bradley F., Wszolek, Zbigniew K., Rademakers, Rosa, Whitwell, Jennifer L., Baker, Matt C., Senjem, Matthew L., Knopman, David S., Petersen, Ronald C., Jack, Clifford R.

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1H MR spectroscopy in presymptomatic MAPT mutation carriers: A biomarker for tau mediated pathology von Kantarci, Kejal, Boeve, Bradley F., Wszolek, Zbigniew K., Rademakers, Rosa, Whitwell, Jennifer L., Baker, Matt C., Senjem, Matthew L., Knopman, David S., Petersen, Ronald C., Jack, Clifford R.

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IC‐P‐105: 1 H MR Spectroscopy in Presymptomatic MAPT mutation carriers: A Biomarker for Tau Mediated Pathology von Kantarci, Kejal, Boeve, Bradley F., Wszolek, Zbigniew K., Rademakers, Rosa, Whitwell, Jennifer L., Baker, Matt C., Senjem, Matthew L., Knopman, David S., Petersen, Ronald C., Jack, Clifford R.

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