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mutation department disease university ftld-tdp expression control grn mutations association tmem 106b research tmem 106b expression center neurology medicine sample frontotemporal lobar degeneration individual alzheimer pathology study grn mutation table genotype nature analysis chromosome frontotemporal hospital brain locus school allele number genome-wide genetic institute replication cohort dementia california frontotemporal dementia pennsylvania value variant health 7 p 21 degeneration lobar status population family arizona model genomic grn locus ftld-tdp cases inclusion laboratory medicine genet genotyping disease status -43 pennsylvania school phase effect philadelphia region method tmem 106b locus gene expression data genome-wide association study america neuroscience regression san diego risk factor spain criteria quality
3 Most Recent Publications
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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
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Evidence for major gene inheritance of Alzheimer disease in families of patients with and without apolipoprotein E ε 4.
(Article)
Rao, V. Cupples, L.A. Growdon, J.H. Haines, J.L. Farrer, L.A. Broeckhoven, C. van Duijn, C.M. van Kurz, A. Green, R.C. Chui, H. Duara, R. Auerbach, S.A. Volicer, L. Wells, J. |
1996-01-01
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Apolipoprotein E genotype in patients with Alzheimer's disease: implications for the risk of dementia among relatives.
(Article)
Farrer, L.A. Cupples, L.A. Chui, H. Flanagan, S.D. Duara, R. St George-Hyslop, P.H. Auerbach, S.A. Volicer, L. Well, J.M. Growdon, J.H. Haines, J.L. Broeckhoven, C. van Duijn, C.M. van Kurz, A. Zimmer, R. Mulller, U. Green, R.C. Clarke, V. Shoffner, J. Wallace, D.C. |
1995-01-01
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