Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases
- Ferrari, Raffaele
- Wang, Yunpeng
- Vandrovcova, Jana
- Guelfi, Sebastian
- Witeolar, Aree
- Karch, Celeste M.
- Schork, Andrew J.
- Fan, Chun C.
- Brewer, James B.
- Momeni, Parastoo
- Schellenberg, Gerard D.
- Dillon, William P.
- Sugrue, Leo P.
- Hess, Christopher P.
- Yokoyama, Jennifer S.
- Bonham, Luke W.
- Rabinovici, Gil D.
- Miller, Bruce L.
- Andreassen, Ole A.
- Dale, Anders M.
- Hardy, John
- Desikan, Rahul S.
- Ferrari, R.
- Hernandez, D. G.
- Nalls, M. A.
- Rohrer, J. D.
- Ramasamy, A.
- Kwok, J. B. J.
- Dobson-Stone, C.
- Schofield, P. R.
- Halliday, G. M.
- Hodges, J. R.
- Piguet, O.
- Bartley, L.
- Thompson, E.
- Haan, E.
- Hernández, I.
- Ruiz, A.
- Boada, M.
- Borroni, B.
- Padovani, A.
- Cruchaga, C.
- Cairns, N. J.
- 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, K.
- Nilsson, C.
- Mackenzie, I. R. A.
- Hsiung, G-Y. R.
- Mann, D. M. A.
- Grafman, J.
- Morris, C. M.
- Attems, J.
- Griffiths, T. D.
- McKeith, I. G.
- Thomas, A. J.
- Pietrini, P.
- Huey, E. D.
- Wassermann, E. M.
- Baborie, A.
- Jaros, E.
- Tierney, M. C.
- 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, J. B.
- Schlachetzki, J. C. M.
- Uphill, J.
- Collinge, J.
- Mead, S.
- Danek, A.
- Van Deerlin, V. M.
- Grossman, M.
- Trojanowski, J. Q.
- van der Zee, J.
- Cruts, M.
- Van Broeckhoven, C.
- Cappa, S. F.
- Leber, I.
- Hannequin, D.
- Golfier, V.
- Vercelletto, M.
- Brice, A.
- Nacmias, B.
- Sorbi, S.
- Bagnoli, S.
- Piaceri, I.
- Nielsen, J. E.
- Hjermind, L. E.
- Riemenschneider, M.
- Mayhaus, M.
- Ibach, B.
- Gasparoni, G.
- Pichler, S.
- Gu, W.
- Rossor, M. N.
- Fox, N. C.
- Warren, J. D.
- Spillantini, M. G.
- Morris, H. R.
- Rizzu, P.
- Heutink, P.
- Snowden, J. S.
- Rollinson, S.
- Richardson, A.
- Gerhard, A.
- Bruni, A. C.
- Maletta, R.
- Frangipane, F.
- Cupidi, C.
- Bernardi, L.
- Anfossi, M.
- Gallo, M.
- Conidi, M. E.
- Smirne, N.
- Rademakers, R.
- Baker, M.
- Dickson, D. W.
- Graff-Radford, N. R.
- Petersen, R. C.
- Knopman, D.
- Josephs, K. A.
- Boeve, B. F.
- Parisi, J. E.
- Seeley, W. W.
- Miller, B. L.
- Karydas, A. M.
- Rosen, H.
- van Swieten, J. C.
- Dopper, E. G. P.
- Seelaar, H.
- Pijnenburg, Y. A. L.
- Scheltens, P.
- Logroscino, G.
- Capozzo, R.
- Novelli, V.
- PUCA, Annibale Alessandro
- Franceschi, M.
- Postiglione, A.
- Milan, G.
- Sorrentino, P.
- Kristiansen, M.
- Chiang, H-H.
- Graff, C.
- Pasquier, F.
- Rollin, A.
- Deramecourt, V.
- Lebouvier, T.
- Kapogiannis, D.
- Ferrucci, L.
- Pickering-Brown, S.
- Singleton, A. B.
- Hardy, J.
- Momeni, P.
DOIAbstract
Background 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. Methods Summary statistics were obtained from the International FTD Genomics Consortium, International PD Genetics Consortium and International Genomics of AD Project (n>75000 cases and controls). We used conjunction false discovery rate (FDR) to evaluate genetic pleiotropy and conditional FDR to identify novel FTD-associated ...
Add to ORKG