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Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia

Title: Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia
Authors: Jennifer S. Yokoyama; Celeste M. Karch; Chun C. Fan; Luke W. Bonham; Naomi Kouri; Owen A. Ross; Rosa Rademakers; Jungsu Kim; Yunpeng Wang; Günter U. Höglinger; Ulrich Muller; Raffaele Ferrari; John Hardy; International FTD-Genomics Consortium (IFGC Ferrari R; Hernandez DG; Nalls MA; Rohrer JD; Ramasamy A; Kwok JBJ; Dobson-Stone C; Schofield PR; Halliday GM; Hodges JR; Piguet O; Bartley L; Thompson E; Haan E; Hernández I; Ruiz A; Boada M; Borroni B; Padovani A; Cruchaga C; Cairns NJ; Benussi L; Binetti G; Ghidoni R; Forloni G; Albani D; Galimberti D; Fenoglio C; Serpente M; Scarpini E; Clarimón J; Lleó A; Blesa R; Landqvist Waldö M; Nilsson C; Mackenzie IRA; Hsiung GYR; Mann DMA; Grafman J; Morris CM; Attems J; Griffiths TD; McKeith IG; Thomas AJ; Pietrini P; Huey ED; Wassermann EM; Baborie A; Jaros E; Tierney MC; Pastor P; Razquin C; Ortega-Cubero S; Alonso E; Perneczky R; Diehl-Schmid J; Alexopoulos P; Kurz A; Rainero I; Rubino E; Pinessi L; Rogaeva E; St George-Hyslop P; Rossi G; Tagliavini F; Giaccone G; Rowe JB; Schlachetzki JCM; Uphill J; Collinge J; Mead S; Danek A; Van Deerlin VM; Grossman M; Trojanowski JQ; van der Zee J; Cruts M; Van Broeckhoven C; Cappa SF; Leber I; Hannequin D; Golfier V; Vercelletto M; Brice A; Nacmias B; Sorbi S; Bagnoli S; Piaceri I; Nielsen JE; Hjermind LE; Riemenschneider M; Mayhaus M; Ibach B; Gasparoni G; Pichler S; Gu W; Rossor MN; Fox NC; Warren JD; Spillantini MG; Morris HR; Rizzu P; Heutink P; Snowden JS; Rollinson S; Richardson A; Gerhard A; Bruni AC; Maletta R; Frangipane F; Cupidi C; Bernardi L; Anfossi M; Gallo M; Conidi ME; Smirne N; Rademakers R; Baker M; Dickson DW; Graff-Radford NR; Petersen RC; Knopman D; Josephs KA; Boeve BF; Parisi JE; Seeley WW; Miller BL; Karydas AM; Rosen H; van Swieten JC; Dopper EG; Seelaar H; Pijnenburg YAL; Scheltens P; Logroscino G; Capozzo R; Novelli V; Puca AA; Franceschi M; Postiglione A; Milan G; Sorrentino P; Kristiansen M; Chiang HH; Graff C; Pasquier F; Rollin A; Deramecourt V; Lebouvier T; Kapogiannis D; Ferrucci L; Pickering-Brown S; Singleton AB; Hardy J; Momeni P. ); Parastoo Momeni; Leo P. Sugrue; Christopher P. Hess; A. James Barkovich; Adam L. Boxer; William W. Seele; Gil D. Rabinovici; Howard J. Rosen; Bruce L. Miller; Nicholas J. Schmansky; Bruce Fischl; Bradley T. Hyman; Dennis W. Dickson; Gerard D. Schellenberg; Ole A. Andreassen; Anders M. Dale; and Rahul S. Desikan
Contributors: Jennifer S. Yokoyama, Celeste M. Karch, Chun C. Fan, Luke W. Bonham, Naomi Kouri, Owen A. Ross, Rosa Rademakers, Jungsu Kim, Yunpeng Wang, Günter U. Höglinger, Ulrich Muller, Raffaele Ferrari, John Hardy, International FTD-Genomics Consortium (IFGC Ferrari R, Hernandez DG, Nalls MA, Rohrer JD, Ramasamy A, Kwok JBJ, Dobson-Stone C, Schofield PR, Halliday GM, Hodges JR, Piguet O, Bartley L, Thompson E, Haan E, Hernández I, Ruiz A, Boada M, Borroni B, Padovani A, Cruchaga C, Cairns NJ, Benussi L, Binetti G, Ghidoni R, Forloni G, Albani D, Galimberti D, Fenoglio C, Serpente M, Scarpini E, Clarimón J, Lleó A, Blesa R, Landqvist Waldö M, Nilsson C, Mackenzie IRA, Hsiung GYR, Mann DMA, Grafman J, Morris CM, Attems J, Griffiths TD, McKeith IG, Thomas AJ, Pietrini P, Huey ED, Wassermann EM, Baborie A, Jaros E, Tierney MC, Pastor P, Razquin C, Ortega-Cubero S, Alonso E, Perneczky R, Diehl-Schmid J, Alexopoulos P, Kurz A, Rainero I, Rubino E, Pinessi L, Rogaeva E, St George-Hyslop P, Rossi G, Tagliavini F, Giaccone G, Rowe JB, Schlachetzki JCM, Uphill J, Collinge J, Mead S, Danek A, Van Deerlin VM, Grossman M, Trojanowski JQ, van der Zee J, Cruts M, Van Broeckhoven C, Cappa SF, Leber I, Hannequin D, Golfier V, Vercelletto M, Brice A, Nacmias B, Sorbi S, Bagnoli S, Piaceri I, Nielsen JE, Hjermind LE, Riemenschneider M, Mayhaus M, Ibach B, Gasparoni G, Pichler S, Gu W, Rossor MN, Fox NC, Warren JD, Spillantini MG, Morris HR, Rizzu P, Heutink P, Snowden JS, Rollinson S, Richardson A, Gerhard A, Bruni AC, Maletta R, Frangipane F, Cupidi C, Bernardi L, Anfossi M, Gallo M, Conidi ME, Smirne N, Rademakers R, Baker M, Dickson DW, Graff-Radford NR, Petersen RC, Knopman D, Josephs KA, Boeve BF, Parisi JE, Seeley WW, Miller BL, Karydas AM, Rosen H, van Swieten JC, Dopper EG, Seelaar H, Pijnenburg YAL, Scheltens P, Logroscino G, Capozzo R, Novelli V, Puca AA, Franceschi M, Postiglione A, Milan G, Sorrentino P, Kristiansen M, Chiang HH, Graff C, Pasquier F, Rollin A, Deramecourt V, Lebouvier T, Kapogiannis D, Ferrucci L, Pickering-Brown S, Singleton AB, Hardy J, Momeni P. ), Parastoo Momeni, Leo P. Sugrue, Christopher P. Hess, A. James Barkovich, Adam L. Boxer, William W. Seele, Gil D. Rabinovici, Howard J. Rosen, Bruce L. Miller, Nicholas J. Schmansky, Bruce Fischl, Bradley T. Hyman, Dennis W. Dickson, Gerard D. Schellenberg, Ole A. Andreassen, Anders M. Dale, and Rahul S. Desikan
Publication Year: 2017
Collection: Università degli studi di Torino: AperTo (Archivio Istituzionale ad Accesso Aperto)
Subject Terms: Neurology (clinical); Cellular and Molecular Neuroscience
Time: 2734
Document Type: article in journal/newspaper
Language: English
Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000399397300009; volume:133; issue:5; firstpage:825; lastpage:837; numberofpages:13; journal:ACTA NEUROPATHOLOGICA; http://hdl.handle.net/2318/1678636; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85014531490; link.springer.de/link/service/journals/00401/index.htm
DOI: 10.1007/s00401-017-1693-y
Availability: http://hdl.handle.net/2318/1678636; https://doi.org/10.1007/s00401-017-1693-y
Rights: info:eu-repo/semantics/openAccess
Accession Number: edsbas.EFA8E134
Database: BASE