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Autor:
Holstege, Henne, Hulsman, Marc, Charbonnier, Camille, Grenier-Boley, Benjamin, Quenez, Olivier, Grozeva, Detelina, van Rooij, Jeroen, Sims, Rebecca, Ahmad, Shahzad, Amin, Najaf, Norsworthy, Penny, Dols-Icardo, Oriol, Hummerich, Holger, Kawalia, Amit, Amouyel, Philippe, Beecham, Gary, Berr, Claudine, Bis, Joshua, Boland, Anne, Bossu, Paola, Bouwman, Femke, Bras, Jose, Campion, Dominique, Cochran, Jesse Nicholas, Daniele, Antonio, Dartigues, Jean-Francois, Debette, Stephanie, Deleuze, Jean-Francois, Denning, Nicola, Destefano, Anita, Farrer, Lindsay, Fernandez, Maria-Victoria, Fox, Nick, Galimberti, Daniela, Genin, Emmanuelle, Gille, Johan JP, Le Guen, Yann, Guerreiro, Rita, Haines, Jonathan, Holmes, Clive, Ikram, M. Arfan, Ikram, M. Kamran, Jansen, Iris E., Kraaij, Robert, Lathrop, Mark, Lemstra, Afina W., Lleo, Alberto, Luckcuck, Lauren, Mannens, Marcel M.A.M., Marschall, Rachel, Martin, Eden, Masullo, Carlo, Mayeux, Richard, Mecocci, Patrizia, Meggy, Alun, Mol, Merel, Morgan, Kevin, Myers, Richard M., Nacmias, Benedetta, Naj, Adam, Napolioni, Valerio, Pasquier, Florence, Pastor, Pau, Pericak-Vance, Margaret, Raybould, Rachel, Redon, Richard, Reinders, Marcel J.T., Richard, Anne-Claire, Riedel-Heller, Steffi, Rivadeneira, Fernando, Rousseau, Stephane, Ryan, Natalie, Saad, Salha, Sanchez-Juan, Pascual, Schellenberg, Gerard, Scheltens, Philip, Schott, Jonathan M., Seripa, Davide, Seshadri, Sudha, Sie, Daoud, Sistermans, Erik A, Sorbi, Sandro, van Spaendonk, Resie, Spalletta, Gianfranco, Tesi, Niccolo, Tijms, Betty, Uitterlinden, Andre, van der Lee, Sven, Wagner, Michael, Wallon, David, Wang, Li San, Zarea, Aline, Clarimon, Jordi, van Swieten, John, Greicius, Michael D., Yokoyama, Jennifer S., Cruchaga, Carlos, Hardy, John, Ramirez, Alfredo, Mead, Simon H, van der Flier, Wiesje, van Duijn, Cornelia, Williams, Julie, Nicolas, Gael, Bellenguez, Celine, Lambert, Jean-Charles
The genetic component of Alzheimer’s disease (AD) has been mainly assessed using Genome Wide Association Studies (GWAS), which do not capture the risk contributed by rare variants. Here, we compared the gene-based burden of rare damaging variants i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::5eb71320d50d12bedaff0b381889150b