학술논문


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'학술논문' 에서 검색결과 385건 | 목록 1~20
Academic Journal
Bonham, Luke W.Steele, Natasha Z.R.Karch, Celeste M.Manzoni, ClaudiaGeier, Ethan G.Wen, NatalieOfori-Kuragu, AaronMomeni, ParastooHardy, JohnMiller, Zachary A.Hess, Christopher P.Lewis, PatrickMiller, Bruce L.Seeley, William W.Baranzini, Sergio E.Desikan, Rahul S.Ferrari, RaffaeleYokoyama, Jennifer S.Ferrari, RHernandez, D GNalls, M ARohrer, J DRamasamy, AKwok, J B JDobson-Stone, CSchofield, P RHalliday, G MHodges, J RPiguet, OBartley, LThompson, EHernández, IRuiz, ABoada, MBorroni, BPadovani, ACruchaga, CCairns, N JBenussi, LBinetti, GGhidoni, RForloni, GAlbani, DGalimberti, DFenoglio, CSerpente, MScarpini, EClarimón, JLleó, ABlesa, RWaldö, M LandqvistNilsson, KNilsson, CMackenzie, I R AHsiung, G-Y RMann, DGrafman, JMorris, C MAttems, JGriffiths, T DMcKeith, I GThomas, A JPietrini, PHuey, E DWassermann, E MBaborie, AJaros, ETierney, M CPastor, PRazquin, COrtega-Cubero, SAlonso, EPerneczky, RDiehl-Schmid, JAlexopoulos, PKurz, ARainero, IRubino, EPinessi, LRogaeva, ESt George-Hyslop, PRossi, GTagliavini, FGiaccone, GAlbani, D.Rowe, J BSchlachetzki, J C MUphill, JCollinge, JMead, SDanek, AVan Deerlin, V MGrossman, MTrojanowski, J Qvan der Zee, JVan Broeckhoven, CCappa, S FLeber, IHannequin, DGolfier, VVercelletto, MBrice, ANacmias, BSorbi, SBagnoli, SPiaceri, INielsen, J EHjermind, L ERiemenschneider, MMayhaus, MIbach, BGasparoni, GPichler, SGu, WRossor, M NFox, N CWarren, J DSpillantini, M GMorris, H RRizzu, PHeutink, PSnowden, J SRollinson, SRichardson, AGerhard, ABruni, A CMaletta, RFrangipane, FCupidi, CBernardi, LAnfossi, MGallo, MConidi, M ESmirne, NRademakers, RBaker, MDickson, D WGraff-Radford, N RPetersen, R CKnopman, DJosephs, K ABoeve, B FParisi, J ESeeley, W WMiller, B LKarydas, A MRosen, Hvan Swieten, J CDopper, E G PSeelaar, HPijnenburg, Y A LScheltens, PLogroscino, GCapozzo, RNovelli, VPuca, A AFranceschi, MPostiglione, AMilan, GSorrentino, PKristiansen, MChiang, H-HGraff, CPasquier, FRollin, ADeramecourt, VLebouvier, TKapogiannis, DFerrucci, LPickering-Brown, SSingleton, A BHardy, JMomeni, P
Neurology: Genetics. Oct 01, 2018 4(5)
Academic Journal
Zhang M12 3Ferrari R4Tartaglia MC35 6Keith J7Surace EI8Wolf U9Sato C3Grinberg M3Liang Y3Xi Z3Dupont K3McGoldrick P3Weichert A3McKeever PM3Schneider R36 7McCorkindale MD4Manzoni C10Rademakers R11Graff-Radford NR12Dickson DW11Parisi JE13Boeve BF14Petersen RC14Miller BL15Seeley WW16van Swieten JC17van Rooij J17Pijnenburg Y18van der Zee J19Van Broeckhoven C19Le Ber I21Van Deerlin V23Suh E23Rohrer JD24Mead S25Graff C26Öijerstedt L26Pickering-Brown S28Rollinson S28Rossi G29Tagliavini F30Brooks WS31Dobson-Stone C32Halliday GM32Hodges JR32Piguet O34Binetti G36Benussi L37Ghidoni R37Nacmias B38Sorbi S38Bruni AC40Galimberti D41Scarpini E41Rainero I42Rubino E42Clarimon J43Lleó A43Ruiz A45Hernández I45Pastor P46Diez-Fairen M46Borroni B48Pasquier F49Deramecourt V49Lebouvier T49Perneczky R5051 52Diehl-Schmid J50Grafman J53Huey ED55Mayeux R55Nalls MA57Hernandez D57Singleton A57Momeni P58Zeng Z59Hardy J4Robertson J3Zinman L67Rogaeva E36International FTD-Genomics Consortium (IFGC)Ferrari RHernandez DGNalls MARohrer JDRamasamy AKwok JBJDobson-Stone CBrooks WSSchofield PRHalliday GMHodges JRPiguet OBartley LThompson EHernández IRuiz ABoada MBorroni BPadovani ACruchaga CCairns NJBenussi LBinetti GGhidoni RForloni GAlbani DGalimberti DFenoglio CSerpente MScarpini EClarimón JLleó ABlesa RWald Ouml MLNilsson KNilsson CMackenzie IRAHsiung GRMann DMAGrafman JMorris CMAttems JGriffiths TDMcKeith IGThomas AJPietrini PHuey EDWassermann EMBaborie AJaros ETierney MCPastor PRazquin COrtega-Cubero SAlonso EPerneczky RDiehl-Schmid JAlexopoulos PKurz ARainero IRubino EPinessi LRogaeva ESt George-Hyslop PRossi GTagliavini FGiaccone GRowe JBSchlachetzki JCMUphill JCollinge JMead SDanek AVan Deerlin VMGrossman MTrojanowski JQvan der Zee JVan Broeckhoven CCappa SFLeber IHannequin DGolfier VVercelletto MBrice ANacmias BSorbi SBagnoli SPiaceri INielsen JEHjermind LERiemenschneider MMayhaus MIbach BGasparoni GPichler SGu WRossor MNFox NCWarren JDGrazia Spillantini MMorris HRRizzu PHeutink PSnowden JSRollinson SRichardson AGerhard ABruni ACMaletta RFrangipane FCupidi CBernardi LAnfossi MGallo MElena Conidi MSmirne NRademakers RBaker MDickson DWGraff-Radford NRPetersen RCKnopman DJosephs KABoeve BFParisi JESeeley WWMiller BLKarydas AMRosen Hvan Swieten JCDopper EGPSeelaar HPijnenburg YALScheltens PLogroscino GCapozzo RNovelli VPuca AAFranceschi MPostiglione AMilan GSorrentino PKristiansen MChiang HHGraff CPasquier FRollin ADeramecourt VLebouvier TKapogiannis DFerrucci LPickering-Brown SSingleton ABHardy JMomeni P
Brain
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
BRAIN
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
instname
Zhang, M, Ferrari, R, Tartaglia, M C, Keith, J, Surace, E I, Wolf, U, Sato, C, Grinberg, M, Liang, Y, Xi, Z, Dupont, K, McGoldrick, P, Weichert, A, McKeever, P M, Schneider, R, McCorkindale, M D, Manzoni, C, Rademakers, R, Graff-Radford, N R, Dickson, D W, Parisi, J E, Boeve, B F, Petersen, R C, Miller, B L, Seeley, W W, van Swieten, J C, van Rooij, J, Pijnenburg, Y, van der Zee, J, van Broeckhoven, C, le Ber, I, van Deerlin, V, Suh, E, Rohrer, J D, Mead, S, Graff, C, Öijerstedt, L, Pickering-Brown, S, Rollinson, S, Rossi, G, Tagliavini, F, Brooks, W S, Dobson-Stone, C, Halliday, G M, Hodges, J R, Piguet, O, Binetti, G, Benussi, L, Ghidoni, R, Nacmias, B, Sorbi, S, Bruni, A C, Galimberti, D, Scarpini, E, Rainero, I, Rubino, E, Clarimon, J, Lleó, A, Ruiz, A, Hernández, I, Pastor, P, Diez-Fairen, M, Borroni, B, Pasquier, F, Deramecourt, V, Lebouvier, T, Perneczky, R, Diehl-Schmid, J, Grafman, J, Huey, E D, Mayeux, R, Nalls, M A, Hernandez, D, Singleton, A, Momeni, P, Zeng, Z, Hardy, J, Robertson, J, Zinman, L & Rogaeva, E 2018, 'A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers', Brain, vol. 141, no. 10, pp. 2895-2907. https://doi.org/10.1093/brain/awy238
International FTD-Genomics Consortium (IFGC) 2018, 'A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers', Brain, vol. 141, no. 10, pp. 2895-2907. https://doi.org/10.1093/brain/awy238
Academic Journal
van der Lee, Sven JConway, Olivia JZettergren, AnnaChristensen, KaareErtekin-Taner, NilüferScholz, Sonja WRamirez, AlfredoRuiz, AgustínSlagboom, Elinevan der Flier, Wiesje MHolstege, HenneMead, S.Synofzik, M.Andlauer, Till F Mvan Swieten, J. C.Leber, I.Ferrari, R.Hernandez, D. G.Nalls, M. A.Rohrer, J. D.Ramasamy, A.Kwok, J. B. J.Dobson-Stone, C.Schofield, P. R.Diez-Fairen, MonicaHalliday, G. M.Hodges, J. R.Piguet, O.Bartley, L.Thompson, E.Borroni, B.Padovani, A.Cruchaga, C.Cairns, N. J.Benussi, L.Simon-Sanchez, JavierBinetti, G.Ghidoni, R.Forloni, G.Albani, D.Galimberti, D.Fenoglio, C.Serpente, M.Scarpini, E.Blesa, R.Landqvist Waldö, M.Lleó, AlbertoNilsson, K.Nilsson, C.Mackenzie, I. R. A.Hsiung, G-Y RMann, D. M. A.Grafman, J.Morris, C. M.Attems, J.Griffiths, T. D.McKeith, I. G.Zetterberg, HenrikThomas, A. J.Pietrini, P.Huey, E. D.Wassermann, E. M.Baborie, A.Jaros, E.Tierney, M. C.Razquin, C.Ortega-Cubero, S.Alonso, E.Nygaard, MariannePerneczky, R.Diehl-Schmid, J.Alexopoulos, P.Kurz, A.Rainero, I.Rubino, E.Pinessi, L.Rogaeva, E.St George-Hyslop, P.Rossi, G.Blauwendraat, CornelisTagliavini, F.Giaccone, G.Rowe, J. B.Schlachetzki, J. C. M.Uphill, J.Collinge, J.Danek, A.Van Deerlin, V. M.Grossman, M.Trojanowski, J. Q.Savage, Jeanne Evan der Zee, J.Van Broeckhoven, C.Cappa, S. F.Hannequin, D.Golfier, V.Vercelletto, M.Brice, A.Nacmias, B.Sorbi, S.Bagnoli, S.Mengel-From, JonasPiaceri, I.Nielsen, J. E.Hjermind, L. E.Riemenschneider, M.Mayhaus, M.Ibach, B.Gasparoni, G.Pichler, S.Gu, W.Rossor, M. N.Jansen, IrisMoreno-Grau, SoniaFox, N. C.Warren, J. D.Spillantini, M. G.Morris, H. R.Rizzu, P.Snowden, J. S.Rollinson, S.Richardson, A.Gerhard, A.Bruni, A. C.Wagner, MichaelMaletta, R.Frangipane, F.Cupidi, C.Bernardi, L.Anfossi, M.Gallo, M.Conidi, M. E.Smirne, N.Baker, M.Josephs, K. A.Fortea, JuanParisi, J. E.Seeley, W. W.Miller, B. L.Karydas, A. M.Rosen, H.Dopper, E. G. P.Seelaar, H.Logroscino, G.Capozzo, R.Novelli, V.Keogh, Michael JPuca, A. A.Franceschi, M.Postiglione, A.Milan, G.Sorrentino, P.Kristiansen, M.Chiang, H-HGraff, C.Pasquier, F.Rollin, A.Blennow, KajDeramecourt, V.Lebouvier, T.Kapogiannis, D.Ferrucci, L.Pickering-Brown, S.Singleton, A. B.Hardy, J.Momeni, P.Coppola, G.Skoog, IngmarVarpetian, A.Foroud, T. M.Levey, A. I.Kukull, W. A.Mendez, M. F.Ringman, J.Chui, H.Cotman, C.DeCarli, C.Friese, Manuel AGeschwind, D. H.Pletnikova, OlgaZulaica, MirenLage, CarmenCarrasquillo, Minerva Mde Rojas, ItziarRiedel-Heller, SteffiIllán-Gala, IgnacioWei, WeiJeune, BernardOrellana, AdelinaThen Bergh, FlorianWang, XueHulsman, MarcBeker, NinaKleineidam, LucaTesi, NiccoloMorris, Christopher MIndakoetxea, BegoñaCollij, Lyduine EScherer, MartinMorenas-Rodríguez, EstrellaIronside, James Wvan Berckel, Bart N MAlcolea, DanielWiendl, Heinzvan den Akker, ErikStrickland, Samantha LPastor, PauRodríguez Rodríguez, EloyDESGESCOEADBIFGCIPDGCRiMod-FTDBank, Netherlands BrainBoeve, Bradley FHernández, IsabelPetersen, Ronald CFerman, Tanis Jvan Gerpen, Jay AReinders, Marcel J TUitti, Ryan JTárraga, LluísMaier, WolfgangDols-Icardo, OriolKawalia, AmitDalmasso, Maria Carolinavan Eijk, Kristel RBoada, MercèZettl, Uwe Kvan Schoor, Natasja MBeekman, MarianAllen, MarietMasliah, Eliezerde Munain, Adolfo LópezPantelyat, AlexanderWszolek, Zbigniew KRoss, Owen AStringa, NajadaDickson, Dennis WGraff-Radford, Neill RKnopman, DavidRademakers, RosaLemstra, Afina WPijnenburg, Yolande A LScheltens, PhilipGasser, ThomasChinnery, Patrick FHemmer, BernhardChen, Jason AHuisman, Martijn ATroncoso, JuanMoreno, FerminNohr, Ellen ASørensen, Thorkild I AHeutink, PeterSánchez-Juan, PascualPosthuma, DanielleGIFTClarimón, Jordi
Acta Neuropathol
Acta Neuropathol . 2019 Aug;138(2):237-250.
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
instname
ACTA NEUROPATHOLOGICA
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
Acta Neuropathologica
van der Lee, S J, Conway, O J, Jansen, I, Carrasquillo, M M, Kleineidam, L, van den Akker, E, Hernández, I, van Eijk, K R, Stringa, N, Chen, J A, Zettergren, A, Andlauer, T F M, Diez-Fairen, M, Simon-Sanchez, J, Lleó, A, Zetterberg, H, Nygaard, M, Blauwendraat, C, Savage, J E, Mengel-From, J, Moreno-Grau, S, Wagner, M, Fortea, J, Keogh, M J, Blennow, K, Skoog, I, Friese, M A, Pletnikova, O, Zulaica, M, Lage, C, de Rojas, I, Riedel-Heller, S, Illán-Gala, I, Wei, W, Jeune, B, Hulsman, M, Beker, N, Tesi, N, Collij, L E, van Berckel, B N M, Reinders, M J T, van Schoor, N M, Lemstra, A W, Pijnenburg, Y A L, Scheltens, P, Huisman, M A, Heutink, P, Posthuma, D, van der Flier, W M, Holstege, H, DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer Disease European DNA biobank), EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementia), Netherlands Brain Bank (NBB) & The GIFT (Genetic Investigation in Frontotemporal Dementia and Alzheimer’s Disease) Study Group 2019, 'A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity', Acta Neuropathologica, vol. 138, no. 2, pp. 237-250. https://doi.org/10.1007/s00401-019-02026-8
Acta neuropathologica 138(2), 237-250 (2019). doi:10.1007/s00401-019-02026-8
Acta neuropathologica 139(5), 959-962 (2020). doi:10.1007/s00401-019-02107-8
2019, 'A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity', Acta Neuropathologica, vol. 138, no. 2, pp. 237-250. https://doi.org/10.1007/s00401-019-02026-8
van der Lee, S J, Conway, O J, Jansen, I, Carrasquillo, M M, Kleineidam, L, van den Akker, E, Hernandez, I, van Eijk, K R, Stringa, N, Chen, J A, Zettergren, A, Andlauer, T F M, Diez-Fairen, M, Simon-Sanchez, J, Lleo, A, Zetterberg, H, Nygaard, M, Blauwendraat, C, Savage, J E, Mengel-From, J, Moreno-Grau, S, Wagner, M, Fortea, J, Keogh, M J, Blennow, K, Skoog, I, Friese, M A, Pletnikova, O, Zulaica, M, Lage, C, de Rojas, I, Riedel-Heller, S, Illan-Gala, I, Wei, W, Jeune, B, Orellana, A, Bergh, F T, Wang, X, Hulsman, M, Beker, N, Tesi, N, Morris, C M, Indakoetxea, B, Collij, L E, Scherer, M, Morenas-Rodriguez, E, Ironside, J W, van Berckel, B N M, Alcolea, D, Wiendl, H, Strickland, S L, Pastor, P, Rodriguez Rodriguez, E, Boeve, B F, Petersen, R C, Ferman, T J, van Gerpen, J A, Reinders, M J T, Uitti, R J, Tarraga, L, Maier, W, Dols-Icardo, O, Kawalia, A, Dalmasso, M C, Boada, M, Zettl, U K, van Schoor, N M, Beekman, M, Allen, M, Masliah, E, Lopez de Munain, A, Pantelyat, A, Wszolek, Z K, Ross, O A, Dickson, D W, Graff-Radford, N R, Knopman, D, Rademakers, R, Lemstra, A W, Pijnenburg, Y A L, Scheltens, P, Gasser, T, Chinnery, P F, Hemmer, B, Huisman, M A, Troncoso, J, Moreno, F, Nohr, E A, Sørensen, T I A, Heutink, P, Sanchez-Juan, P, Posthuma, D, Clarimon, J, Christensen, K, Ertekin-Taner, N, Scholz, S W, Ramirez, A, Ruiz, A, Slagboom, E, van der Flier, W M & Holstege, H 2019, ' A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity ', Acta Neuropathologica, vol. 138, no. 2, pp. 237-250 . https://doi.org/10.1007/s00401-019-02026-8
van der Lee, S J, Conway, O J, Jansen, I, Carrasquillo, M M, Kleineidam, L, van den Akker, E, Hernández, I, van Eijk, K R, Stringa, N, Chen, J A, Zettergren, A, Andlauer, T F M, Diez-Fairen, M, Simon-Sanchez, J, Lleó, A, Zetterberg, H, Nygaard, M, Blauwendraat, C, Savage, J E, Mengel-From, J, Moreno-Grau, S, Wagner, M, Fortea, J, Keogh, M J, Blennow, K, Skoog, I, Friese, M A, Pletnikova, O, Zulaica, M, Lage, C, de Rojas, I, Riedel-Heller, S, Illán-Gala, I, Wei, W, Jeune, B, Orellana, A, Then Bergh, F, Wang, X, Hulsman, M, Beker, N, Tesi, N, Morris, C M, Indakoetxea, B, Collij, L E, Scherer, M, Morenas-Rodríguez, E, Ironside, J W, van Berckel, B N M, Nohr, E A, Sørensen, T I A, Christensen, K & DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer Disease European DNA biobank) 2019, ' A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity ', Acta Neuropathologica, vol. 138, no. 2, pp. 237-250 . https://doi.org/10.1007/s00401-019-02026-8
van der Lee, S J, Conway, O J, Jansen, I, Carrasquillo, M M, Kleineidam, L, van den Akker, E, Hernández, I, van Eijk, K R, Stringa, N, Chen, J A, Zettergren, A, Andlauer, T F M, Diez-Fairen, M, Simon-Sanchez, J, Lleó, A, Zetterberg, H, Nygaard, M, Blauwendraat, C, Savage, J E, Mengel-From, J, Moreno-Grau, S, Wagner, M, Fortea, J, Keogh, M J, Blennow, K, Skoog, I, Friese, M A, Pletnikova, O, Zulaica, M, Lage, C, de Rojas, I, Riedel-Heller, S, Illán-Gala, I, Wei, W, Jeune, B, Orellana, A, Then Bergh, F, Wang, X, Hulsman, M, Beker, N, Tesi, N, Morris, C M, Indakoetxea, B, Collij, L E, Scherer, M, Morenas-Rodríguez, E, Ironside, J W, van Berckel, B N M, Alcolea, D & Wiendl, H 2019, ' Correction to : A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity ', Acta Neuropathologica . https://doi.org/10.1007/s00401-019-02107-8
Acta Neuropathologica, vol 138, iss 2
Acta Neuropathologica, vol 139, iss 5
Academic Journal
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Journal of Neurology, Neurosurgery & Psychiatry. Feb 01, 2017 88(2):152-164
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Beghi, EttorePupillo, ElisabettaBianchi, ElisaBonetto, ValentinaLuotti, SilviaPasetto, LauraBendotti, CaterinaTortarolo, MassimoSironi, FrancescaCamporeale, LauraSherman, Alexander VPaganoni, SabrinaScognamiglio, AdaDe Marchi, FabiolaBongioanni, PaoloDel Carratore, RenataCaponnetto, ClaudiaDiamanti, LucaMartinelli, DanieleCalvo, AndreaFilosto, MassimilianoPadovani, AlessandroPiccinelli, Stefano CottiRicci, ClaudiaDalla Giacoma, StefaniaDe Angelis, NicolettaInghilleri, MaurizioSpataro, RossellaLa Bella, VincenzoLogroscino, GiancarloLunetta, ChristianTarlarini, ClaudiaMandrioli, JessicaMartinelli, IlariaSimonini, CeciliaZucchi, ElisabettaMonsurrò, Maria RosariaRicciardi, DarioTrojsi, FrancescaRiva, NiloFilippi, MassimoSimone, Isabella LauraSorarù, GianniSpera, CristinaFlorio, LuciaMessina, SoniaRusso, MassimoSiciliano, GabrieleConte, AmeliaSaddi, Maria ValeriaCarboni, NicolaMazzini LetiziaRN S60-ALS Study Group (Gabriele EniaAndrea ZucchellaLorenzo PinzaniLorena De GiorgiCeleste NicolettiElisa SemprucciEmilio Davide ArippolGiorgia GiussaniMonica GrazianiCinzia FerrariRoberto CantelloEnrica BersanoCristina DolciottiSilvia Maria MasciandaroIlaria Da PratoCorrado CabonaGiuseppe MeoMauro CeroniBeatrice Dal FabbroAdriano ChiòCristina MogliaUmberto ManeraGiuseppe FudaFederico CasaleGiovanni De MarcoPaolina SalamoneFabio GianniniSilvia BocciMarco CeccantiChiara CambieriLaura LibonatiFederica MoretVittorio FrascaTiziana ColettiRosanna TortelliRosa CapozzoFrancesca GerardiValeria SansoneNicola FiniGiulia GianferrariAnnalisa GessaniYuri FalzoneParide SchitoLaura PozziTeuta DomiEustachio D'ErricoAntonella MoreaGianmarco MilellaMatteo GizziFrancesca PaciSimonetta FerracchiatoMichele ZarrelliNino DesinaAlessandra GovoniErika SchirinziCostanza SimonciniMario SabatelliDaniela BernardoGiulia BisogniGiovanna PirasMaria MonneElisabetta Manca)
Eur J Neurol
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Mishra, AniketFerrari, RaffaeleRohrer, J. D.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.Ramasamy, A.Heutink, P.Snowden, J. S.Rollinson, S.Richardson, A.Gerhard, A.Bruni, A. C.Maletta, R.Frangipane, F.Cupidi, C.Bernardi, L.Kwok, J. B. J.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.Dobson-Stone, C.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.Schofield, P. R.Pijnenburg, Y. A. L.Scheltens, P.Logroscino, G.Capozzo, R.Novelli, V.Puca, A. A.Franceschi, M.Postiglione, A.Milan, G.Sorrentino, P.Halliday, G. M.Kristiansen, M.Chiang, H-HGraff, C.Pasquier, F.Rollin, A.Deramecourt, V.Lebouvier, T.Kapogiannis, D.Ferrucci, L.Pickering-Brown, S.Hodges, J. R.Singleton, A. B.Hardy, J.Momeni, P.Piguet, O.Bartley, L.Thompson, E.Heutink, PeterHaan, E.Hernández, I.Ruiz, A.Boada, M.Borroni, B.Padovani, A.Cruchaga, C.Cairns, N. J.Benussi, L.Binetti, G.Hardy, JohnGhidoni, R.Forloni, G.Albani, D.Galimberti, D.Fenoglio, C.Serpente, M.Scarpini, E.Clarimón, J.Lleó, A.Blesa, R.Pijnenburg, YolandeLandqvist Waldö, M.Nilsson, K.Nilsson, C.Mackenzie, I. R. A.Hsiung, G-Y RMann, D. M. A.Grafman, J.Morris, C. M.Attems, J.Griffiths, T. D.Posthuma, DanielleMcKeith, I. G.Thomas, A. J.Pietrini, P.Huey, E. D.Wassermann, E. M.Baborie, A.Jaros, E.Tierney, M. C.Pastor, P.Razquin, C.Consortium, International FTD-GenomicsOrtega-Cubero, S.Alonso, E.Perneczky, R.Diehl-Schmid, J.Alexopoulos, P.Kurz, A.Rainero, I.Rubino, E.Pinessi, L.Rogaeva, E.Ferrari, R.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.Hernandez, D. G.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.Nalls, M. A.Vercelletto, M.Brice, A.Nacmias, B.Sorbi, S.Bagnoli, S.Piaceri, I.Nielsen, J. E.Hjermind, L. E.Riemenschneider, M.Mayhaus, M.
Mishra, A, Ferrari, R, Heutink, P, Hardy, J, Pijnenburg, Y & Posthuma, D 2017, 'Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia', Brain, vol. 140, pp. 1437-1446. https://doi.org/10.1093/brain/awx066
Brain 140(5), 1437-1446 (2017). doi:10.1093/brain/awx066
Academic Journal
Ferrari RWang YVandrovcova JGuelfi SWiteolar AKarch CMSchork AJFan CCBrewer JBInternational FTD-Genomics Consortium (IFGC)International Parkinson's Disease Genomics Consortium (IPDGC)International Genomics of Alzheimer's Project (IGAP)Momeni PSchellenberg GDDillon WPSugrue LPHess CPYokoyama JSBonham LWRabinovici GDMiller BLAndreassen OADale AMHardy JDesikan RSCollaborators: Ferrari RHernandez DGNalls MARohrer JDRamasamy AKwok JBJDobson-Stone CSchofield PRHalliday GMHodges JRPiguet OBartley LThompson EHaan EHernández IRuiz ABoada MBorroni BPadovani ACruchaga CCairns NJBenussi LBinetti GGhidoni RForloni GAlbani DGalimberti DFenoglio CSerpente MScarpini EClarimón JLleó ABlesa RLandqvist Waldö MNilsson CMackenzie IRAHsiung GYRMann DMAGrafman JMorris CMAttems JGriffiths TDMcKeith IGThomas AJPietrini PHuey EDWassermann EMBaborie AJaros ETierney MCPastor PRazquin COrtega-Cubero SAlonso EPerneczky RDiehl-Schmid JAlexopoulos PKurz ARainero IRubino EPinessi LRogaeva ESt George-Hyslop PRossi GTagliavini FGiaccone GRowe JBSchlachetzki JCMUphill JCollinge JMead SDanek AVan Deerlin VMGrossman MTrojanowski JQvan der Zee JCruts MVan Broeckhoven CCappa SFLeber IHannequin DGolfier VVercelletto MBrice ANacmias BSorbi SBagnoli SPiaceri INielsen JEHjermind LERiemenschneider MMayhaus MIbach BGasparoni GPichler SGu WRossor MNFox NCWarren JDSpillantini MGMorris HRRizzu PHeutink PSnowden JSRollinson SRichardson AGerhard ABruni ACMaletta RFrangipane FCupidi CBernardi LAnfossi MGallo MConidi MESmirne NRademakers RBaker MDickson DWGraff-Radford NRPetersen RCKnopman DJosephs KABoeve BFParisi JESeeley WWKarydas AMRosen Hvan Swieten JCDopper EGSeelaar HPijnenburg YALScheltens PLogroscino GCapozzo RNovelli VPuca AAFranceschi MPostiglione AMilan GSorrentino PKristiansen MChiang HHGraff CPasquier FRollin ADeramecourt VLebouvier TKapogiannis DFerrucci LPickering-Brown SSingleton ABMomeni P.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
The IFGC and IPDGC members 2017, 'Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases', Journal of Neurology, Neurosurgery and Psychiatry, vol. 88, no. 2, pp. 152-164. https://doi.org/10.1136/jnnp-2016-314411
Journal of Neurology Neurosurgery & Psychiatry, vol 88, iss 2
Academic Journal
Lin, KPulit, SLVan Rheenen, WShatunov, ADekker, AMMcLaughlin, RLDiekstra, FPVan Der Spek, RAAVõsa, UDe Jong, SRobinson, MRYang, JFogh, IVan Doormaal, PTTazelaar, GHPKoppers, MBlokhuis, AMSproviero, WJones, ARKenna, KPVan Eijk, KRHarschnitz, OSchellevis, RDBrands, WJMedic, JMenelaou, AVajda, ATicozzi, NRogelj, BVrabec, KRavnik-Glavač, MKoritnik, BZidar, JLeonardis, LGrošelj, LDMillecamps, SSalachas, FMeininger, VDe Carvalho, MPinto, SMora, JSRojas-García, RPolak, MChandran, SColville, SSwingler, RMorrison, KEShaw, PJHardy, JOrrell, RWPittman, ASidle, KFratta, PMalaspina, ATopp, SPetri, SAbdulla, SDrepper, CSendtner, MMeyer, TOphoff, RAStaats, KAWiedau-Pazos, MLomen-Hoerth, CVan Deerlin, VMTrojanowski, JQElman, LMcCluskey, LBasak, ANTunca, CHamzeiy, HParman, YMeitinger, TLichtner, PRadivojkov-Blagojevic, MAndres, CRMaurel, CBensimon, GLandwehrmeyer, BBrice, APayan, CAMSaker-Delye, SDürr, AWood, NWTittmann, LLieb, WFranke, ARietschel, MCichon, SNöthen, MMAmouyel, PTzourio, CDartigues, J-FUitterlinden, AGRivadeneira, FEstrada, KHofman, ACurtis, CBlauw, HMVan Der Kooi, AJDe Visser, MGoris, AWeber, MShaw, CESmith, BNPansarasa, OCereda, CDel Bo, RComi, GPD'Alfonso, SBertolin, CSorarù, GMazzini, LPensato, VGellera, CTiloca, CRatti, ACalvo, AMoglia, CBrunetti, MArcuti, SCapozzo, RZecca, CLunetta, CPenco, SRiva, NPadovani, AFilosto, MMuller, BStuit, RJRegistry, PGroup, SlalomRegistry, SConsortium, Fals SequencingConsortium, SlagenGroup, Nnipps StudyBlair, IZhang, KMcCann, EPFifita, JANicholson, GARowe, DBPamphlett, RKiernan, MCGrosskreutz, JWitte, OWRinger, TPrell, TStubendorff, BKurth, IHübner, CALeigh, PNCasale, FChio, ABeghi, EPupillo, ETortelli, RLogroscino, GPowell, JLudolph, ACWeishaupt, JHRobberecht, WVan Damme, PFranke, LPers, THBrown, RHGlass, JDLanders, JEHardiman, OAndersen, PMCorcia, PVourc'H, PSilani, VWray, NRVisscher, PMDe Bakker, PIWVan Es, MAPasterkamp, RJLewis, CMBreen, GAl-Chalabi, AVan Den Berg, LHVeldink, JH
NATURE GENETICS
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
instname
van Rheenen, W, Shatunov, A, Dekker, A M, McLaughlin, R L, Diekstra, F P, Pulit, S L, van der Spek, R A A, Võsa, U, de Jong, S, Robinson, M R, Yang, J, Fogh, I, van Doormaal, P T, Tazelaar, G H P, Koppers, M, Blokhuis, A M, Sproviero, W, Jones, A R, Kenna, K P, van Eijk, K R, Harschnitz, O, Schellevis, R D, Brands, W J, Medic, J, Menelaou, A, Vajda, A, Ticozzi, N, Lin, K, Rogelj, B, Vrabec, K, Ravnik-Glavač, M, Koritnik, B, Zidar, J, Leonardis, L, Grošelj, L D, Millecamps, S, Salachas, F, Meininger, V, de Carvalho, M, Pinto, S, Fratta, P, Topp, S, Curtis, C, Shaw, C E, Smith, B N, Leigh, P N, Powell, J, Lewis, C M, Breen, G, Al-Chalabi, A 2016, ' Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis ', Nature Genetics, vol. 48, pp. 1043–1048 . https://doi.org/10.1038/ng.3622
Van Rheenen, W, Shatunov, A, Dekker, A M, Mclaughlin, R L, Diekstra, F P, Pulit, S L, Van Der Spek, R A A, Võsa, U, De Jong, S, Robinson, M R, Yang, J, Fogh, I, Van Doormaal, P T, Tazelaar, G H P, Koppers, M, Blokhuis, A M, Sproviero, W, Jones, A R, Kenna, K P, Van Eijk, K R, Harschnitz, O, Schellevis, R D, Brands, W J, Medic, J, Menelaou, A, Vajda, A, Ticozzi, N, Lin, K, Rogelj, B, Vrabec, K, Ravnik-glavač, M, Koritnik, B, Zidar, J, Leonardis, L, Grošelj, L D, Millecamps, S, Salachas, F, Meininger, V, De Carvalho, M, Pinto, S, Mora, J S, Rojas-garcía, R, Polak, M, Chandran, S, Colville, S, Swingler, R, Morrison, K E, Shaw, P J, Hardy, J, Orrell, R W, Pittman, A, Sidle, K, Fratta, P, Malaspina, A, Topp, S, Petri, S, Abdulla, S, Drepper, C, Sendtner, M, Meyer, T, Ophoff, R A, Staats, K A, Wiedau-pazos, M, Lomen-hoerth, C, Van Deerlin, V M, Trojanowski, J Q, Elman, L, Mccluskey, L, Basak, A N, Tunca, C, Hamzeiy, H, Parman, Y, Meitinger, T, Lichtner, P, Radivojkov-blagojevic, M, Andres, C R, Maurel, C, Bensimon, G, Landwehrmeyer, B, Brice, A, Payan, C A M, Saker-delye, S, Dürr, A, Wood, N W, Tittmann, L, Lieb, W, Franke, A, Rietschel, M, Cichon, S, Nöthen, M M, Amouyel, P, Tzourio, C, Dartigues, J, Uitterlinden, A G, Rivadeneira, F, Estrada, K, Hofman, A, Curtis, C, Blauw, H M, Van Der Kooi, A J, De Visser, M, Goris, A, Weber, M, Shaw, C E, Smith, B N, Pansarasa, O, Cereda, C, Del Bo, R, Comi, G P, D'alfonso, S, Bertolin, C, Sorarù, G, Mazzini, L, Pensato, V, Gellera, C, Tiloca, C, Ratti, A, Calvo, A, Moglia, C, Brunetti, M, Arcuti, S, Capozzo, R, Zecca, C, Lunetta, C, Penco, S, Riva, N, Padovani, A, Filosto, M, Muller, B, Stuit, R J, Blair, I, Zhang, K, Mccann, E P, Fifita, J A, Nicholson, G A, Rowe, D B, Pamphlett, R, Kiernan, M C, Grosskreutz, J, Witte, O W, Ringer, T, Prell, T, Stubendorff, B, Kurth, I, Hübner, C A, Leigh, P N, Casale, F, Chio, A, Beghi, E, Pupillo, E, Tortelli, R, Logroscino, G, Powell, J, Ludolph, A C, Weishaupt, J H, Robberecht, W, Van Damme, P, Franke, L, Pers, T H, Brown, R H, Glass, J D, Landers, J E, Hardiman, O, Andersen, P M, Corcia, P, Vourc'h, P, Silani, V, Wray, N R, Visscher, P M, De Bakker, P I W, Van Es, M A, Pasterkamp, R J, Lewis, C M, Breen, G, Al-chalabi, A, Van Den Berg, L H & Veldink, J H 2016, ' Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis ', Nature Genetics . https://doi.org/10.1038/ng.3622
Nat. Genet. 48, 1043-1048 (2016)
Nature Genetics
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