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

Holstege, Henne; Hulsman, Marc; Charbonnier, Camille; Grenier-Boley, Benjamin; Quenez, Olivier; Grozeva, Detelina; van Rooij, Jeroen G. J.; Sims, Rebecca; Ahmad, Shahzad; Amin, Najaf; Norsworthy, Penny J.; Dols-Icardo, Oriol; Hummerich, Holger; Kawalia, Amit; Amouyel, Philippe; Beecham, Gary W.; Berr, Claudine; Bis, Joshua C.; Boland, Anne; Bossù, Paola; Bouwman, Femke; Bras, Jose; Campion, Dominique; Nicholas Cochran, J.; Daniele, Antonio; Dartigues, Jean-François; Debette, Stéphanie; Deleuze, Jean-François; Denning, Nicola; DeStefano, Anita L.; Farrer, Lindsay A.; Fernandez, Maria Victoria; Fox, Nick C.; Galimberti, Daniela; Genin, Emmanuelle; Gille, Hans; Guen, Yann Le; Guerreiro, Rita; Haines, Jonathan L.; Holmes, Clive; Arfan Ikram, M.; Kamran Ikram, M.; Jansen, Iris E.; Kraaij, Robert; Lathrop, Marc; Lemstra, Afina W.; Lleó, Alberto; Luckcuck, Lauren; Mannens, Marcel M. A. M.; Marshall, Rachel; Martin, Eden R.; Masullo, Carlo; Mayeux, Richard; Mecocci, Patrizia; Meggy, Alun; Mol, Merel O.; Morgan, Kevin; Myers, Richard M.; Nacmias, Benedetta; Naj, Adam C.; Napolioni, Valerio; Pasquier, Florence; Pastor, Pau; Pericak Vance, Margaret A.; Raybould, Rachel; Redon, Richard; Reinders, Marcel J. T.; Richard, Anne-Claire; Riedel Heller, Steffi G.; Rivadeneira, Fernando; Rousseau, Stéphane; Ryan, Natalie S.; Saad, Salha; Sanchez-Juan, Pascual; Schellenberg, Gerard D.; Scheltens, Philip; Schott, Jonathan M.; Seripa, Davide; Seshadri, Sudha; Sie, Daoud; Sistermans, Erik; Sorbi, Sandro; van Spaendonk, Resie; Spalletta, Gianfranco; Tesi, Niccólo; Tijms, Betty; Uitterlinden, André G.; van der Lee, Sven J.; de Visser, Pieter Jelle; Wagner, Michael; Wallon, David; Wang, Li-San; Zarea, Aline; Clarimon, Jordi; van Swieten, John C.; Greicius, Michael D.; Yokoyama, Jennifer S.; Cruchaga, Carlos; Hardy, John; Ramirez, Alfredo; Mead, Simon; van der Flier, Wiesje M.; van Duijn, Cornelia M.; Williams, Julie; Nicolas, Gaël; Bellenguez, Céline; Lambert, Jean-Charles

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

Published in 2020 by Henne Holstege, Marc Hulsman

, Camille Charbonnier, Benjamin Grenier-Boley, Olivier Quenez, Detelina Grozeva, Jeroen G. J. van Rooij, Rebecca Sims, Shahzad Ahmad, Najaf Amin, Penny J. Norsworthy, Oriol Dols-Icardo, Holger Hummerich, Amit Kawalia, Philippe Amouyel and other authors.

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