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 FTLD

作者：Cyril Pottier, Yingxue Ren, Ralph B. Perkerson, Matt Baker, Gregory D. Jenkins, Marka van Blitterswijk, Mariely DeJesus‐Hernandez, Jeroen van Rooij, Melissa E. Murray, Elizabeth Christopher, Shannon K. McDonnell, Zachary C. Fogarty, Anthony Batzler, Shulan Tian, Cristina T. Vicente, Billie J. Matchett, Anna M. Karydas, Ging‐Yuek Robin Hsiung, Harro Seelaar, Merel O. Mol, Elizabeth Finger, Caroline Graff, Linn Öijerstedt, Manuela Neumann, Peter Heutink, Matthis Synofzik, Carlo Wilke, Johannes Prudlo, Patrizia Rizzu, Javier Simón‐Sánchez, Dieter Edbauer, Sigrun Roeber, Janine Diehl‐Schmid, Bret M. Evers, Andrew King, Marsel Mesulam, Sandra Weıntraub, Changiz Geula, Kevin F. Bieniek, Leonard Petrucelli, Geoffrey L. Ahern, Eric M. Reiman, Bryan K. Woodruff, Richard J. Caselli, Edward D. Huey, Martin R. Farlow, Jordan Grafman, Simon Mead, Lea T. Grinberg, Salvatore Spina, Murray Grossman, David J. Irwin, Edward B. Lee, EunRan Suh, Julie S. Snowden, David Mann, Nilüfer Ertekin‐Taner, Ryan J. Uitti, Zbigniew K. Wszołek, Keith A. Josephs, Joseph E. Parisi, David S. Knopman, Ronald C. Petersen, John R. Hodges, Olivier Piguet, Ethan G. Geier, Jennifer S. Yokoyama, Robert A. Rissman, Ekaterina Rogaeva, Julia Keith, Lorne Zinman, Maria Carmela Tartaglia, Nigel J. Cairns, Carlos Cruchaga, Bernardino Ghetti, Julia Kofler, Oscar L. López, Thomas G. Beach, Thomas Arzberger, Jochen Herms, Lawrence S. Honig, Jean Paul Vonsattel, Glenda M. Halliday, John B. Kwok, Charles L. White, Marla Gearing, Jonathan D. Glass, Sara Rollinson, Stuart Pickering‐Brown, Jonathan D. Rohrer, John Q. Trojanowski, Vivianna Van Deerlin, Eileen H. Bigio, Claire Troakes, Safa Al‐Sarraj, Yan W. Asmann, Bruce L. Miller, Neill R. Graff‐Radford, Bradley F. Boeve, William W. Seeley, Ian R. Mackenzie, John C. van Swieten, Dennis W. Dickson, Joanna M. Biernacka, Rosa Rademakers · 发表于：Acta Neuropathologica · 年份：2019 · DOI：10.1007/s00401-019-01962-9 · 被引用次数：130 · 研究领域：Neurological diseases and metabolism、Genomics and Rare Diseases、Genetics and Neurodevelopmental Disorders