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Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases

Title: Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases
Authors: Ferrari R; Wang Y; Vandrovcova J; Guelfi S; Witeolar A; Karch CM; Schork AJ; Fan CC; Brewer JB; International FTD-Genomics Consortium (IFGC); International Parkinson's Disease Genomics Consortium (IPDGC); International Genomics of Alzheimer's Project (IGAP); Momeni P; Schellenberg GD; Dillon WP; Sugrue LP; Hess CP; Yokoyama JS; Bonham LW; Rabinovici GD; Miller BL; Andreassen OA; Dale AM; Hardy J; Desikan RS; Collaborators: 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; 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; Momeni P.
Contributors: Ferrari, R; Wang, Y; Vandrovcova, J; Guelfi, S; Witeolar, A; Karch, Cm; Schork, Aj; Fan, Cc; Brewer, Jb; International FTD-Genomics Consortium, (IFGC); International Parkinson's Disease Genomics Consortium, (IPDGC); International Genomics of Alzheimer's Project, (IGAP); Momeni, P; Schellenberg, Gd; Dillon, Wp; Sugrue, Lp; Hess, Cp; Yokoyama, J; Bonham, Lw; Rabinovici, Gd; Miller, Bl; Andreassen, Oa; Dale, Am; Hardy, J; Desikan, R; Collaborators: 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
Publication Year: 2017
Collection: IRIS Università degli Studi di Napoli Federico II
Description: Clinical, pathological and genetic overlap between sporadic frontotemporal dementia (FTD), Alzheimer's disease (AD) and Parkinson's disease (PD) has been suggested; however, the relationship between these disorders is still not well understood. Here we evaluated genetic overlap between FTD, AD and PD to assess shared pathobiology and identify novel genetic variants associated with increased risk for FTD.
Document Type: article in journal/newspaper
Language: English
Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000393903700012; volume:88; issue:2; firstpage:152; lastpage:164; numberofpages:13; journal:JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY; https://hdl.handle.net/11588/717132
DOI: 10.1136/jnnp-2016-314411
Availability: https://hdl.handle.net/11588/717132; https://doi.org/10.1136/jnnp-2016-314411
Accession Number: edsbas.71DB17F9
Database: BASE