Pressure Ulcers and Prolonged Hospital Stay in Hip Fracture Patients Affected by Time-to-Surgery by Rademakers, Leonard M F, Vainas, Tryfon, van Zutphen, Stefan W A M, Brink, Peter R G, van Helden, Sven H

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Unconventional Translation of C9ORF72 GGGGCC Expansion Generates Insoluble Polypeptides Specific to c9FTD/ALS by Ash, Peter E.A., Bieniek, Kevin F., Gendron, Tania F., Caulfield, Thomas, Lin, Wen-Lang, DeJesus-Hernandez, Mariely, van Blitterswijk, Marka M., Jansen-West, Karen, Paul, Joseph W., Rademakers, Rosa, Boylan, Kevin B., Dickson, Dennis W., Petrucelli, Leonard

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Antisense transcripts of the expanded C9ORF72 hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS by Gendron, Tania F., Bieniek, Kevin F., Zhang, Yong-Jie, Jansen-West, Karen, Ash, Peter E. A., Caulfield, Thomas, Daughrity, Lillian, Dunmore, Judith H., Castanedes-Casey, Monica, Chew, Jeannie, Cosio, Danielle M., van Blitterswijk, Marka, Lee, Wing C., Rademakers, Rosa, Boylan, Kevin B., Dickson, Dennis W., Petrucelli, Leonard

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Heterochromatin anomalies and double-stranded RNA accumulation underlie C9orf72 poly(PR) toxicity by Zhang, Yong-Jie, Guo, Lin, Gonzales, Patrick K, Gendron, Tania F, Wu, Yanwei, Jansen-West, Karen, O'Raw, Aliesha D, Pickles, Sarah R, Prudencio, Mercedes, Carlomagno, Yari, Gachechiladze, Mariam A, Ludwig, Connor, Tian, Ruilin, Chew, Jeannie, DeTure, Michael, Lin, Wen-Lang, Tong, Jimei, Daughrity, Lillian M, Yue, Mei, Song, Yuping, Andersen, Jonathan W, Castanedes-Casey, Monica, Kurti, Aishe, Datta, Abhishek, Antognetti, Giovanna, McCampbell, Alexander, Rademakers, Rosa, Oskarsson, Björn, Dickson, Dennis W, Kampmann, Martin, Ward, Michael E, Fryer, John D, Link, Christopher D, Shorter, James, Petrucelli, Leonard

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Association between repeat sizes and clinical and pathological characteristics in carriers of C9ORF72 repeat expansions (Xpansize-72): a cross-sectional cohort study by van Blitterswijk, Marka, PhD, DeJesus-Hernandez, Mariely, BS, Niemantsverdriet, Ellis, BS, Murray, Melissa E, PhD, Heckman, Michael G, MS, Diehl, Nancy N, BS, Brown, Patricia H, MS, Baker, Matthew C, BSc, Finch, NiCole A, MS, Bauer, Peter O, PhD, Serrano, Geidy, PhD, Beach, Thomas G, Prof, Josephs, Keith A, Prof, Knopman, David S, Prof, Petersen, Ronald C, Prof, Boeve, Bradley F, Prof, Graff-Radford, Neill R, Prof, Boylan, Kevin B, MD, Petrucelli, Leonard, Prof, Dickson, Dennis W, Prof, Rademakers, Rosa, Dr

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Truncated stathmin-2 is a marker of TDP-43 pathology in frontotemporal dementia by Prudencio, Mercedes, Humphrey, Jack, Pickles, Sarah, Brown, Anna-Leigh, Hill, Sarah E, Kachergus, Jennifer M, Shi, J, Heckman, Michael G, Spiegel, Matthew R, Cook, Casey, Song, Yuping, Yue, Mei, Daughrity, Lillian M, Carlomagno, Yari, Jansen-West, Karen, de Castro, Cristhoper Fernandez, DeTure, Michael, Koga, Shunsuke, Wang, Ying-Chih, Sivakumar, Prasanth, Bodo, Cristian, Candalija, Ana, Talbot, Kevin, Selvaraj, Bhuvaneish T, Burr, Karen, Chandran, Siddharthan, Newcombe, Jia, Lashley, Tammaryn, Hubbard, Isabel, Catalano, Demetra, Kim, Duyang, Propp, Nadia, Fennessey, Samantha, Fagegaltier, Delphine, Phatnani, Hemali, Secrier, Maria, Fisher, Elizabeth Mc, Oskarsson, Björn, van Blitterswijk, Marka, Rademakers, Rosa, Graff-Radford, Neil R, Boeve, Bradley F, Knopman, David S, Petersen, Ronald C, Josephs, Keith A, Thompson, E Aubrey, Raj, Towfique, Ward, Michael, Dickson, Dennis W, Gendron, Tania F, Fratta, Pietro, Petrucelli, Leonard

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C9ORF72 repeat expansions in mice cause TDP-43 pathology, neuronal loss, and behavioral deficits by Chew, Jeannie, Gendron, Tania F, Prudencio, Mercedes, Sasaguri, Hiroki, Zhang, Yong-Jie, Castanedes-Casey, Monica, Lee, Chris W, Jansen-West, Karen, Kurti, Aishe, Murray, Melissa E, Bieniek, Kevin F, Bauer, Peter O, Whitelaw, Ena C, Rousseau, Linda, Stankowski, Jeannette N, Stetler, Caroline, Daughrity, Lillian M, Perkerson, Emilie A, Desaro, Pamela, Johnston, Amelia, Overstreet, Karen, Edbauer, Dieter, Rademakers, Rosa, Boylan, Kevin B, Dickson, Dennis W, Fryer, John D, Petrucelli, Leonard

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Phosphorylated neurofilament heavy chain: A biomarker of survival for C9ORF72‐associated amyotrophic lateral sclerosis by Gendron, Tania F., Daughrity, Lillian M., Heckman, Michael G., Diehl, Nancy N., Wuu, Joanne, Miller, Timothy M., Pastor, Pau, Trojanowski, John Q., Grossman, Murray, Berry, James D., Hu, William T., Ratti, Antonia, Benatar, Michael, Silani, Vincenzo, Glass, Jonathan D., Floeter, Mary Kay, Jeromin, Andreas, Boylan, Kevin B., Petrucelli, Leonard

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Targeted manipulation of the sortilin-progranulin axis rescues progranulin haploinsufficiency by Lee, Wing C, Almeida, Sandra, Prudencio, Mercedes, Caulfield, Thomas R, Zhang, Yong-Jie, Tay, William M, Bauer, Peter O, Chew, Jeannie, Sasaguri, Hiroki, Jansen-West, Karen R, Gendron, Tania F, Stetler, Caroline T, Finch, NiCole, Mackenzie, Ian R, Rademakers, Rosa, Gao, Fen-Biao, Petrucelli, Leonard

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Poly(GP) proteins are a useful pharmacodynamic marker for C9ORF72 -associated amyotrophic lateral sclerosis by Gendron, Tania F, Chew, Jeannie, Stankowski, Jeannette N, Hayes, Lindsey R, Zhang, Yong-Jie, Prudencio, Mercedes, Carlomagno, Yari, Daughrity, Lillian M, Jansen-West, Karen, Perkerson, Emilie A, O'Raw, Aliesha, Cook, Casey, Pregent, Luc, Belzil, Veronique, van Blitterswijk, Marka, Tabassian, Lilia J, Lee, Chris W, Yue, Mei, Tong, Jimei, Song, Yuping, Castanedes-Casey, Monica, Rousseau, Linda, Phillips, Virginia, Dickson, Dennis W, Rademakers, Rosa, Fryer, John D, Rush, Beth K, Pedraza, Otto, Caputo, Ana M, Desaro, Pamela, Palmucci, Carla, Robertson, Amelia, Heckman, Michael G, Diehl, Nancy N, Wiggs, Edythe, Tierney, Michael, Braun, Laura, Farren, Jennifer, Lacomis, David, Ladha, Shafeeq, Fournier, Christina N, McCluskey, Leo F, Elman, Lauren B, Toledo, Jon B, McBride, Jennifer D, Tiloca, Cinzia, Morelli, Claudia, Poletti, Barbara, Solca, Federica, Prelle, Alessandro, Wuu, Joanne, Jockel-Balsarotti, Jennifer, Rigo, Frank, Ambrose, Christine, Datta, Abhishek, Yang, Weixing, Raitcheva, Denitza, Antognetti, Giovanna, McCampbell, Alexander, Van Swieten, John C, Miller, Bruce L, Boxer, Adam L, Brown, Robert H, Bowser, Robert, Miller, Timothy M, Trojanowski, John Q, Grossman, Murray, Berry, James D, Hu, William T, Ratti, Antonia, Traynor, Bryan J, Disney, Matthew D, Benatar, Michael, Silani, Vincenzo, Glass, Jonathan D, Floeter, Mary Kay, Rothstein, Jeffrey D, Boylan, Kevin B, Petrucelli, Leonard

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Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study by Perkerson, Ralph B, Jenkins, Gregory D, Serie, Daniel J, Ghidoni, Roberta, Benussi, Luisa, López de Munain, Adolfo, Zulaica, Miren, Moreno, Fermin, Le Ber, Isabelle, Pasquier, Florence, Hannequin, Didier, Sánchez-Valle, Raquel, Antonell, Anna, Lladó, Albert, Parsons, Tammee M, Finch, NiCole A, Finger, Elizabeth C, Lippa, Carol F, Huey, Edward D, Neumann, Manuela, Heutink, Peter, Synofzik, Matthis, Wilke, Carlo, Slawek, Jaroslaw, Sitek, Emilia, Johannsen, Peter, Nielsen, Jørgen E, Ren, Yingxue, DeJesus-Hernandez, Mariely, Murray, Melissa E, Bieniek, Kevin F, Evers, Bret M, Richardson, Anna, Scarpini, Elio, Hardy, John, Frangipane, Francesca, Maletta, Raffaele, Anfossi, Maria, Gallo, Maura, Suh, EunRan, Lopez, Oscar L, Wong, Tsz H, van Rooij, Jeroen G J, Seelaar, Harro, Caselli, Richard J, Reiman, Eric M, Noel Sabbagh, Marwan, Kjolby, Mads, Nykjaer, Anders, Karydas, Anna M, Boxer, Adam L, Spina, Salvatore, Oblak, Adrian, Mesulam, M-Marsel, Weintraub, Sandra, Geula, Changiz, Hodges, John R, Piguet, Olivier, Irwin, David J, Trojanowski, John Q, Lee, Edward B, Josephs, Keith A, Knopman, David S, Piaceri, Irene, Bagnoli, Silvia, Sorbi, Sandro, Gearing, Marla, Beach, Thomas G, Black, Sandra E, Masellis, Mario, Rogaeva, Ekaterina, Honig, Lawrence S, Bruni, Amalia C, Snowden, Julie, Pickering-Brown, Stuart, Diehl-Schmid, Janine, Winkelmann, Juliane, Galimberti, Daniela, Graff, Caroline, Öijerstedt, Linn, Troakes, Claire, Al-Sarraj, Safa, Cruchaga, Carlos, Cairns, Nigel J, Rohrer, Jonathan D, Halliday, Glenda M, Kwok, John B, van Swieten, John C, White, Charles L, Ghetti, Bernardino, Murell, Jill R, Borroni, Barbara, Tagliavini, Fabrizio, Bigio, Eileen H, Grossman, Murray, Van Deerlin, Vivianna M, Miller, Bruce L, Dickson, Dennis W, Biernacka, Joanna M, Rademakers, Rosa

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Repetitive element transcripts are elevated in the brain of C9orf72 ALS/FTLD patients by Prudencio, Mercedes, Gonzales, Patrick K, Cook, Casey N, Gendron, Tania F, Daughrity, Lillian M, Song, Yuping, Ebbert, Mark T W, van Blitterswijk, Marka, Zhang, Yong-Jie, Jansen-West, Karen, Baker, Matthew C, DeTure, Michael, Rademakers, Rosa, Boylan, Kevin B, Dickson, Dennis W, Petrucelli, Leonard, Link, Christopher D

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Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degeneration by Kouri, Naomi, Carlomagno, Yari, Baker, Matthew, Liesinger, Amanda M., Caselli, Richard J., Wszolek, Zbigniew K., Petrucelli, Leonard, Boeve, Bradley F., Parisi, Joseph E., Josephs, Keith A., Uitti, Ryan J., Ross, Owen A., Graff-Radford, Neill R., DeTure, Michael A., Dickson, Dennis W., Rademakers, Rosa

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Spt4 selectively regulates the expression of C9orf72 sense and antisense mutant transcripts by Kramer, Nicholas J., Carlomagno, Yari, Zhang, Yong-Jie, Almeida, Sandra, Cook, Casey N., Gendron, Tania F., Prudencio, Mercedes, Van Blitterswijk, Marka, Belzil, Veronique, Couthouis, Julien, Paul, Joseph West, Goodman, Lindsey D., Daughrity, Lillian, Chew, Jeannie, Garrett, Aliesha, Pregent, Luc, Jansen-West, Karen, Tabassian, Lilia J., Rademakers, Rosa, Boylan, Kevin, Graff-Radford, Neill R., Josephs, Keith A., Parisi, Joseph E., Knopman, David S., Petersen, Ronald C., Boeve, Bradley F., Deng, Ning, Feng, Yanan, Cheng, Tzu-Hao, Dickson, Dennis W., Cohen, Stanley N., Bonini, Nancy M., Link, Christopher D., Gao, Fen-Biao, Petrucelli, Leonard, Gitler, Aaron D.

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Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTL... by Pottier, Cyril, Ren, Yingxue, Perkerson, Ralph B., Baker, Matt, Jenkins, Gregory D., van Blitterswijk, Marka, DeJesus-Hernandez, Mariely, van Rooij, Jeroen G. J., Murray, Melissa E., Christopher, Elizabeth, McDonnell, Shannon K., Fogarty, Zachary, Batzler, Anthony, Tian, Shulan, Vicente, Cristina T., Matchett, Billie, Karydas, Anna M., Hsiung, Ging-Yuek Robin, Seelaar, Harro, Mol, Merel O., Finger, Elizabeth C., Graff, Caroline, Öijerstedt, Linn, Neumann, Manuela, Heutink, Peter, Synofzik, Matthis, Wilke, Carlo, Prudlo, Johannes, Rizzu, Patrizia, Simon-Sanchez, Javier, Edbauer, Dieter, Diehl-Schmid, Janine, Evers, Bret M., King, Andrew, Mesulam, M. Marsel, Weintraub, Sandra, Geula, Changiz, Bieniek, Kevin F., Petrucelli, Leonard, Ahern, Geoffrey L., Reiman, Eric M., Woodruff, Bryan K., Caselli, Richard J., Huey, Edward D., Farlow, Martin R., Grafman, Jordan, Mead, Simon, Grinberg, Lea T., Spina, Salvatore, Irwin, David J., Lee, Edward B., Suh, EunRan, Snowden, Julie, Mann, David, Ertekin-Taner, Nilufer, Uitti, Ryan J., Wszolek, Zbigniew K., Josephs, Keith A., Parisi, Joseph E., Knopman, David S., Petersen, Ronald C., Hodges, John R., Piguet, Olivier, Geier, Ethan G., Yokoyama, Jennifer S., Rissman, Robert A., Rogaeva, Ekaterina, Keith, Julia, Zinman, Lorne, Tartaglia, Maria Carmela, Cairns, Nigel J., Cruchaga, Carlos, Kofler, Julia, Lopez, Oscar L., Beach, Thomas G., Arzberger, Thomas, Herms, Jochen, Honig, Lawrence S., Vonsattel, Jean Paul, Halliday, Glenda M., Kwok, John B., White, Charles L., Gearing, Marla, Glass, Jonathan, Rollinson, Sara, Pickering-Brown, Stuart, Rohrer, Jonathan D., Trojanowski, John Q., Van Deerlin, Vivianna, Bigio, Eileen H., Troakes, Claire, Asmann, Yan, Miller, Bruce L., Boeve, Bradley F., Seeley, William W., Mackenzie, Ian R. A., van Swieten, John C., Dickson, Dennis W., Biernacka, Joanna M., Rademakers, Rosa

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Novel clinical associations with specific C9ORF72 transcripts in patients with repeat expansions in C9ORF72 by van Blitterswijk, Marka, Gendron, Tania F., Baker, Matthew C., DeJesus-Hernandez, Mariely, Finch, NiCole A., Brown, Patricia H., Daughrity, Lillian M., Murray, Melissa E., Heckman, Michael G., Jiang, Jie, Lagier-Tourenne, Clotilde, Edbauer, Dieter, Cleveland, Don W., Josephs, Keith A., Parisi, Joseph E., Knopman, David S., Petersen, Ronald C., Petrucelli, Leonard, Boeve, Bradley F., Graff-Radford, Neill R., Boylan, Kevin B., Dickson, Dennis W., Rademakers, Rosa

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TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia by van Blitterswijk, Marka, Mullen, Bianca, Nicholson, Alexandra M., Bieniek, Kevin F., Heckman, Michael G., Baker, Matthew C., DeJesus-Hernandez, Mariely, Finch, NiCole A., Brown, Patricia H., Murray, Melissa E., Hsiung, Ging-Yuek R., Stewart, Heather, Karydas, Anna M., Finger, Elizabeth, Kertesz, Andrew, Bigio, Eileen H., Weintraub, Sandra, Mesulam, Marsel, Hatanpaa, Kimmo J., White III, Charles L., Strong, Michael J., Beach, Thomas G., Wszolek, Zbigniew K., Lippa, Carol, Caselli, Richard, Petrucelli, Leonard, Josephs, Keith A., Parisi, Joseph E., Knopman, David S., Petersen, Ronald C., Mackenzie, Ian R., Seeley, William W., Grinberg, Lea T., Miller, Bruce L., Boylan, Kevin B., Graff-Radford, Neill R., Boeve, Bradley F., Dickson, Dennis W., Rademakers, Rosa

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ATXN2 Trinucleotide Repeat Length Correlates with Risk of ALS by Sproviero, William, Shatunov, Aleksey, Stahl, Daniel, Shoai, Maryam, van Rheenen, Wouter, Jones, Ashley R, Al-Sarraj, Safa, Andersen, Peter M, Bonini, Nancy M, Conforti, Francesca L, Van Damme, Philip, Daoud, Hussein, Del Mar Amador, Maria, Fogh, Isabella, Forzan, Monica, Gaastra, Ben, Gellera, Cinzia, Gitler, Aaron D, Hardy, John, Fratta, Pietro, La Bella, Vincenzo, Le Ber, Isabelle, Van Langenhove, Tim, Lattante, Serena, Lee, Yi-Chung, Malaspina, Andrea, Meininger, Vincent, Millecamps, Stèphanie, Orrell, Richard, Rademakers, Rosa, Robberecht, Wim, Rouleau, Guy, Ross, Owen A, Salachas, Francois, Sidle, Katie, Smith, Bradley N, Soong, Bing-Wen, Sorarù, Gianni, Stevanin, Giovanni, Kabashi, Edor, Troakes, Claire, van Broeckhoven, Christine, Veldink, Jan H, van den Berg, Leonard H, Shaw, Christopher E, Powell, John F, Al-Chalabi, Ammar

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Cerebellar c9RAN proteins associate with clinical and neuropathological characteristics of C9ORF72 repeat expansion carriers by Gendron, Tania F., van Blitterswijk, Marka, Bieniek, Kevin F., Daughrity, Lillian M., Jiang, Jie, Rush, Beth K., Pedraza, Otto, Lucas, John A., Murray, Melissa E., Desaro, Pamela, Robertson, Amelia, Overstreet, Karen, Thomas, Colleen S., Crook, Julia E., Castanedes-Casey, Monica, Rousseau, Linda, Josephs, Keith A., Parisi, Joseph E., Knopman, David S., Petersen, Ronald C., Boeve, Bradley F., Graff-Radford, Neill R., Rademakers, Rosa, Lagier-Tourenne, Clotilde, Edbauer, Dieter, Cleveland, Don W., Dickson, Dennis W., Petrucelli, Leonard, Boylan, Kevin B.

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Shared brain transcriptomic signature in TDP-43 type A FTLD patients with or without GRN mutations by Pottier, Cyril, Mateiu, Ligia, Baker, Matthew C, DeJesus-Hernandez, Mariely, Teixeira Vicente, Cristina, Finch, NiCole A, Tian, Shulan, van Blitterswijk, Marka, Murray, Melissa E, Ren, Yingxue, Petrucelli, Leonard, Oskarsson, Björn, Biernacka, Joanna M, Graff-Radford, Neill R, Boeve, Bradley F, Petersen, Ronald C, Josephs, Keith A, Asmann, Yan W, Dickson, Dennis W, Rademakers, Rosa

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