Search Results - Bieniek, K

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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

    Published in Lancet neurology
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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

    Published in Acta neuropathologica
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