Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease

H. Holstege, M. Hulsman, C. Charbonnier, B. Grenier-Boley, O. Quenez, D. Grozeva, J.G.J. van Rooij, R. Sims, S. Ahmad, N. Amin, P.J. Norsworthy, O. Dols-Icardo, H. Hummerich, A. Kawalia, P. Amouyel, G.W. Beecham, C. Berr, J.C. Bis, A. Boland, P. BossùF. Bouwman, J. Bras, D. Campion, J.N. Cochran, A. Daniele, J.-F. Dartigues, S. Debette, J.-F. Deleuze, N. Denning, A.L. DeStefano, L.A. Farrer, M.V. Fernández, N.C. Fox, D. Galimberti, E. Genin, J.J.P. Gille, Y. Le Guen, R. Guerreiro, J.L. Haines, C. Holmes, M.A. Ikram, M.K. Ikram, I.E. Jansen, R. Kraaij, M. Lathrop, A.W. Lemstra, A. Lleó, L. Luckcuck, M.M.A.M. Mannens, R. Marshall, E.R. Martin, C. Masullo, R. Mayeux, P. Mecocci, A. Meggy, M.O. Mol, K. Morgan, R.M. Myers, B. Nacmias, A.C. Naj, V. Napolioni, F. Pasquier, P. Pastor, M.A. Pericak-Vance, R. Raybould, R. Redon, M.J.T. Reinders, A.-C. Richard, S.G. Riedel-Heller, F. Rivadeneira, S. Rousseau, N.S. Ryan, S. Saad, P. Sanchez-Juan, G.D. Schellenberg, P. Scheltens, J.M. Schott, D. Seripa, S. Seshadri, D. Sie, E.A. Sistermans, S. Sorbi, R. van Spaendonk, G. Spalletta, N. Tesi, B. Tijms, A.G. Uitterlinden, S.J. van der Lee, P.J. Visser, M. Wagner, D. Wallon, L.-S. Wang, A. Zarea, J. Clarimon, J.C. van Swieten, M.D. Greicius, J.S. Yokoyama, C. Cruchaga, J. Hardy, A. Ramirez, S. Mead, W.M. van der Flier, C.M. van Duijn, J. Williams, G. Nicolas, C. Bellenguez, J.-C. Lambert

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Biochemistry, Genetics and Molecular Biology