Hardy, J.

(John Hardy)

disease study university mutation department control association alzheimer analysis sample research stroke institute expression region neurology stage table family expansion chromosome medicine health folate variant trial center individual genotype homocysteine allele e ﬀect number brain onset nature hospital protein genetic mthfr genome-wide population genet polymorphism ps -2 gerad school patient hexanucleotide ftld-tdp concentration meta-analysi evidence genome-wide association study randomised trials result randomised dementia folic america homocysteine concentration grn mutations analyses status locus pathology germany finnish neuroscience dataset neuron tmem 106b frontotemporal effect replication tmem 106b expression presenile sequence folic acid ﬁcation

9 Most Recent Publications

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD (Article) Renton, A. Majounie, E. Kalimo, H. Paetau, A. Abramzon, Y. Remes, A. Kaganovich, A. Scholz, S. Duckworth, J. Ding, J. Harmer, D. Hernandez, D.G. Waite, A. Johnson, J. Mok, K. Ryten, M. Trabzuni, D. Guerreiro, R. Orrell, R. Neal, J. Murray, A. Pearson, J. Jansen, I. Simón-Sánchez, J. Sondervan, D. Seelaar, H. Blake, D. Young, K. Halliwell, N. Callister, J. Toulson, G. Richardson, A. Gerhard, A. Snowden, J. Rollinson, S. Mann, D. Neary, D. Nalls, M.A. Peuralinna, T. Jansson, L. Isoviita, V.-M. Kaivorinne, A.-L. Hölttä-Vuori, M. Ikonen, E. Sulkava, R. Gibbs, J. Benatar, M. Wuu, J. Chiò, A. Restagno, G. Borghero, G. Sabatelli, M. Heckerman, D. Rogaeva, E. Zinman, L. Rothstein, J. Schymick, J. Sendtner, M. Drepper, C. Eichler, E. Alkan, C. Abdullaev, Z. Pack, S. Dutra, A. Pak, E. Hardy, J. Singleton, A. Laaksovirta, H. Williams, N. Heutink, P. Pickering-Brown, S. Morris, H. Tienari, P.J. Traynor, B. Swieten, J.C. van Myllykangas, L.	2011-10-20
Effect modification by population dietary folate on the association between MTHFR genotype, homocysteine, and stroke risk: A meta-analysis of genetic studies and randomised trials (Article) Holmes, M.V. Newcomb, P. Smeeth, L. Fowkes, F.G.R. Algra, A. Shmeleva, V. Szolnoki, Z. Roest, M. Linnebank, M. Zacho, J. Nalls, M.A. Singleton, A. Hubacek, J.A. Ferrucci, L. Hardy, J. Worrall, B.B. Rich, S.S. Matarin, M. Norman, P.E. Flicker, L. Almeida, O.P. Bockxmeer, F.M. van Shimokata, H. Sofat, R. Khaw, K-T. Wareham, N.J. Bobak, M. Sterne, J.A.C. Smith, G.D. Talmud, P.J. Tikka-Kleemola, P. Humphries, S.E. Price, J.F. Ebrahim, S. Ricketts, S.L. Lawlor, D.A. Hankey, G.J. Meschia, J.F. Sandhu, M.S. Hingorani, A. Casas, J.P. Cooper, J. Breteler, M.M.B. Bautista, L.E. Sharma, P. Whittaker, J.	2011-08-13
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy (Article) Hoglinger, G. Melhem, N.M. Swieten, J.C. van Pahwa, R. Pezzoli, G. Pickering-Brown, S. Poewe, W. Rabano, A. Rajput, A. Reich, S.G. Respondek, G. Roeber, S. Rohrer, J.D. Heutink, P. Ross, O.A. Rossor, M. Sacilotto, G. Seeley, W.W. Seppi, K. Silveira-Moriyama, L. Spina, S. Srulijes, K. St. George-Hyslop, P. Stamelou, M. Wszolek, Z.K. Standaert, D.G. Tesei, S. Tourtellotte, W.W. Trenkwalder, C. Troakes, C. Trojanowski, J.Q. Troncoso, J.C. Deerlin, V.M. Vonsattel, J.P.G. Wenning, G.K. Uitti, R.J. White, C.L. Winter, P. Zarow, C. Zecchinelli, A.L. Antonini, A. Vandrovcova, J. Hurtig, H.I. Gross, R.G. Maetzler, W. Goldwurm, S. Tolosa, E. Dickson, D. Borroni, B. Pastor, P. Cantwell, L.B. Han, M.R. Dillman, A. Brug, M.P. van der Gibbs, J. Cookson, M.R. Hernandez, D.G. Singleton, A. Sleiman, P.M.A. Farrer, M.J. Yu, C.-E. Golbe, L.I. Revesz, T. Hardy, J. Lees, A.J. Devlin, B. Hakonarson, H. Müller, U. Schellenberg, G.D. Wang, L.-S. Albin, R.L. Alonso, E. Apfelbacher, M. Arnold, S.E. Avila, J. Beach, T.G. Beecher, S. Berg, D. Bird, T.D. Bogdanovic, N. Klei, L. Boon, A.J.W. Bordelon, Y. Brice, A. Budka, H. Canesi, M. Chiu, W.Z. Cilia, R. Colosimo, C. Deyn, P.P. de Yebenes, J.G. de Rademakers, R. Donker Kaat, L. Duara, R. Durr, A. Engelborghs, S. Fabbrini, G. Finch, N.A. Flook, R. Frosch, M.P. Gaig, C. Galasko, D. Silva, R. de Gasser, T. Gearing, M. Geller, E.T. Ghetti, B. Graff-Radford, N.R. Grossman, M. Hall, D.A. Hazrati, L.-N. Höllerhage, M. Jankovic, J. Litvan, I. Juncos, J.L. Karydas, A. Kretzschmar, H.A. Leber, I. Lee, V.M.Y. Lieberman, A.P. Lyons, K.E. Mariani, C. Masliah, E. Massey, L.A. Riley, D.E. McLean, C.A. Meucci, N. Miller, B.L. Mollenhauer, B. Möller, J.C. Morris, H. O'Sullivan, S.S. Oertel, W. Ottaviani, D. Padovani, A.	2011-07-01
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease (Article) Hollingworth, P. Harold, D. Dowzell, K. Tikka-Kleemola, P. Breteler, M.M.B. Ikram, M.A. DeStefano, A.L. Fitzpatrick, A.L. Lopez, O.L. Launer, L.J. Seshadri, S. Berr, C. Campion, D. Jones, N. Epelbaum, J. Dartigues, J.-F. Tzourio, C. Alperovitch, A. Lathrop, G.M. Feulner, T.M. Friedrich, P. Riehle, C. Krawczak, M. Schreiber, S. Stretton, A. Mayhaus, M. Nicolhaus, S. Wagenpfeil, S. Steinberg, S. Kallela, M. SnÆdal, J. Björnsson, S. Jonsson, P.V. Chouraki, V. Genier-Boley, B. Thomas, C. Hiltunen, M. Soininen, H. Combarros, O. Zelenika, D. Delepine, M. Bullido, M.J. Pasquier, F. Mateo, I. Frank-Garcia, A. Porcellini, E. Richards, A. Hanon, O. Coto, E. Alvarez, V. Bosco, P. Siciliano, G. Mancuso, M. Panza, F. Solfrizzi, V. Nacmias, B. Sorbi, S. Ivanov, D. Bossù, P. Piccardi, P. Arosio, B. Annoni, G. Seripa, D. Pilotto, A. Scarpini, E. Galimberti, D. Brice, A. Hannequin, D. Widdowson, C. Licastro, F. Holmans, P.A. Riemenschneider, M. Morgan, K. Younkin, S. Owen, M.J. O'Donovan, M. Amouyel, P. Williams, J. Chapman, J. Lovestone, S. Powell, J. Sims, R. Proitsi, P. Lupton, M.K. Brayne, C. Rubinsztein, D.C. Gill, M. Lawlor, B. Lynch, A. Brown, K. Passmore, P.A. Craig, D. Gerrish, A. McGuinness, B. Todd, S. Holmes, C. Mann, D. Smith, A.D. Beaumont, H. Warden, D.R. Wilcock, G.K. Love, S. Kehoe, P.G. Lambert, J.C. Hooper, N.M. Vardy, E.R.L.C. Hardy, J. Mead, S. Fox, N.C. Rossor, M. Collinge, J. Maier, W. Jessen, F. Rüther, E. Carrasquillo, M.M. Schürmann, B. Heun, R. Kölsch, H. Bussche, H. van den Heuser, I. Kornhuber, J. Wiltfang, J. Dichgans, M. Frölich, L. Hampel, H. Abraham, R. Gallacher, J. Hüll, M. Rujescu, D. Giegling, I. Goate, A.M. Kauwe, J.S.K. Cruchaga, C. Nowotny, P. Morris, J.C. Mayo, K. Hamshere, M.L. Sleegers, K. Bettens, K. Engelborghs, S. Deyn, P.P. de Broeckhoven, C. van Livingston, G. Bass, N.J. Gurling, H. McQuillin, A. Gwilliam, R. Pahwa, J.S. Deloukas, P. Al-Chalabi, A. Shaw, C.E. Tsolaki, M. Singleton, A.B. Guerreiro, R. Mühleisen, T.W. Nöthen, M.M. Moebus, S. Jöckel, K.-H. Moskvina, V. Klopp, N. Wichmann, H.E. Pankratz, V.S. Sando, S.B. Aasly, J.O. Barcikowska, M. Wszolek, Z.K. Dickson, D. Graff-Radford, N.R. Petersen, R.C.	2011-05-01
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions (Article) Deerlin, V.M. Sleiman, P.M.A. Arnold, S.E. Mann, D. Pickering-Brown, S. Seelaar, H. Heutink, P. Swieten, J.C. van Murrell, J.R. Ghetti, B. Spina, S. Grafman, J. Martinez-Lage, M. Hodges, J. Spillantini, M.G. Gilman, S. Lieberman, A.P. Kaye, J.A. Woltjer, R.L. Bigio, E.H. Mesulam, M. Al-Sarraj, S. Troakes, C. Chen-Plotkin, A. Rosenberg, R.N. White, C.L. Ferrer, I. Lladó, A. Neumann, H.A.M. Kretzschmar, H.A. Hulette, C. Welsh-Bohmer, K.A. Miller, B.L. Alzualde, A. Wang, L. Munain, A.L. de McKee, A.C. Gearing, M. Levey, A.I. Lah, J.J. Hardy, J. Rohrer, J.D. Lashley, T. Mackenzie, I.R.A. Feldman, H.H. Graff-Radford, N.R. Hamilton, R.L. Dekosky, S.T. Zee, J. van der Kumar-Singh, S. Broeckhoven, C. van Mayeux, R. Vonsattel, J.P. Troncoso, J.C. Kril, J.J. Kwok, J.B.J. Dickson, D. Halliday, G.M. Bird, T.D. Ince, P.G. Shaw, P.J. Cairns, N.J. Morris, J.C. McLean, C.A. DeCarli, C. Ellis, W.G. Freeman, S.H. Rademakers, R. Frosch, M.P. Growdon, J.H. Perl, D.P. Sano, M. Bennett, D.A. Schneider, J.A. Beach, T.G. Reiman, E.M. Woodruff, B.K. Cummings, J.F. Boeve, B. Vinters, H.V. Miller, C.A. Chui, H. Alafuzoff, I. Hartikainen, P. Seilhean, D. Galasko, D. Masliah, E. Cotman, C.W. Tũón, M.T. Grossman, M. Martínez, M.C.C. Munoz, D.G. Carroll, S.L. Marson, D. Riederer, P.F. Bogdanovic, N. Schellenberg, G.D. Hakonarson, H. Trojanowski, J.Q. Lee, V.M.Y.	2010-03-01
Apolipoprotein E genotype does not affect the age of onset of dementia in families with define tau mutations (Article) Houlden, H. Stevens, M. Jannsen, J.C. Petersen, R.C. Dodd, P. Dark, F. Boeve, B. Dickson, D. Davies, P. Pickering-Brown, S. Mann, D. Adamson, J. Knijff, P. de Lynch, T. Payami, H. Poorkaj, P. Bird, T.D. Schellenberg, G.D. Chadraverty, S. Norton, J. Morris, F.C. Goate, A.M. Hutton, M. Duijn, C.M. van Hardy, J. Rizzu, P. Swieten, J.C. van Heutink, P. Perez-Tur, J. Thomas, V. Baker, M.C. Morris, H. Rossor, M.	1999-02-05
Estimation of the genetic contribution of presenilin-1 and -2 mutations in a population-based study of presenile Alzheimer disease (Article) Cruts, M. St George-Hyslop, P.H. Broeckhoven, C. van Hofman, A. Duijn, C.M. van Wehnert, A. Serneels, S. Sherrington, R. Hutton, M. Hardy, J. Backhovens, H. Broeck, M. van den	1998-01-01
Amyloid precursor protein gene mutation in early-onset Alzheimer's disease. (Letter To Editor) Duijn, C.M. van Cruts, M. Hardy, J. Hendriks, L. Broeckhoven, C. van Hofman, A.	1991-01-01
Evidence for allelic heterogeneity in familial early-onset Alzheimer's disease (Article) Duijn, C.M. van Hardy, J. Goate, A.M. Rossor, M.N. Vandenberghe, A. Martin, J-J. Mullan, M.J. Broeckhoven, C. van Hofman, A.	1991-01-01

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