Holstege, H, Hulsman, M, Charbonnier, C, Grenier-Boley, B, Quenez, O, Grozeva, D, Van Rooij, JGJ, Sims, R, Ahmad, S, Amin, N, Norsworthy, PJ, Dols-Icardo, O, Hummerich, H, Kawalia, A, Amouyel, P, Beecham, GW, Berr, C, Bis, JC, Boland, A, Bossù, P, Bouwman, F, Bras, J, Campion, D, Cochran, JN
, Daniele, A, Dartigues, J-F, Debette, S, Deleuze, J-F, Denning, N, Destefano, AL, Farrer, LA, Fernández, MV, Fox, NC, Galimberti, D, Genin, E, Gille, JJP, Le Guen, Y, Guerreiro, R, Haines, JL, Holmes, C, Ikram, MA, Ikram, MK, Jansen, IE, Kraaij, R, Lathrop, M, Lemstra, AW, Lleó, A, Luckcuck, L, Mannens, MMAM, Marshall, R, Martin, ER, Masullo, C, Mayeux, R, Mecocci, P, Meggy, A, Mol, MO, Morgan, K, Myers, RM, Nacmias, B, Naj, AC, Napolioni, V, Pasquier, F, Pastor, P, Pericak-Vance, MA, Raybould, R, Redon, R, Reinders, MJT, Richard, A-C, Riedel-Heller, SG, Rivadeneira, F, Rousseau, S, Ryan, NS, Saad, S, Sanchez-Juan, P, Schellenberg, GD, Scheltens, P, Schott, JM, Seripa, D, Seshadri, S, Sie, D, Sistermans, EA, Sorbi, S, Van Spaendonk, R, Spalletta, G, Tesi, N, Tijms, B, Uitterlinden, AG, Van Der Lee, SJ, Visser, PJ, Wagner, M, Wallon, D, Wang, L-S, Zarea, A, Clarimon, J, Van Swieten, JC, Greicius, MD, Yokoyama, JS, Cruchaga, C, Hardy, J, Ramirez, A, Mead, S, Van Der Flier, WM, Van Duijn, CM, Williams, J, Nicolas, G, Bellenguez, C & Lambert, J-C 2022, '
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease',
Nature Genetics, pp. N/A-N/A.
https://doi.org/10.1038/s41588-022-01208-7