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Number of items: 2.

Journal Article

Corominas, Jordi, Colijn, Johanna M., Geerlings, Maartje J., Pauper, Marc ORCID: 0000-0001-6274-9891, Bakker, Bjorn, Amin, Najaf, Motta, Laura Lores, Kersten, Eveline, Garanto, Alejandro ORCID: 0000-0001-5721-1560, Verlouw, Joost A. M., van Rooij, Jeroen G. J., Kraaij, Robert, de Jong, Paulus T. V. M., Hofman, Albert, Vingerling, Johannes R., Schick, Tina, Fauser, Sascha, de Jong, Eiko K., van Duijn, Cornelia M., Hoyng, Carel B., Klaver, Caroline C. W. and den Hollander, Anneke I. (2018). Whole-Exome Sequencing in Age-Related Macular Degeneration Identifies Rare Variants in COL8A1, a Component of Bruch's Membrane. Ophthalmology, 125 (9). S. 1433 - 1444. NEW YORK: ELSEVIER SCIENCE INC. ISSN 1549-4713

Holstege, Henne, Hulsman, Marc ORCID: 0000-0002-9889-3606, Charbonnier, Camille ORCID: 0000-0003-1172-0196, Grenier-Boley, Benjamin, Quenez, Olivier ORCID: 0000-0002-8273-8505, Grozeva, Detelina ORCID: 0000-0003-3239-8415, van Rooij, Jeroen G. J., Sims, Rebecca ORCID: 0000-0002-3885-1199, Ahmad, Shahzad ORCID: 0000-0002-8658-3790, Amin, Najaf, Norsworthy, Penny J., Dols-Icardo, Oriol ORCID: 0000-0003-2656-8748, Hummerich, Holger, Kawalia, Amit, Amouyel, Philippe, Beecham, Gary W., Berr, Claudine, Bis, Joshua C., Boland, Anne, Bossu, Paola, Bouwman, Femke, Bras, Jose, Campion, Dominique, Cochran, J. Nicholas, Daniele, Antonio, Dartigues, Jean-Francois, Debette, Stephanie, Deleuze, Jean-Francois, Denning, Nicola, DeStefano, Anita L., Farrer, Lindsay A., Fernandez, Maria Victoria, Fox, Nick C., Galimberti, Daniela ORCID: 0000-0002-9284-5953, Genin, Emmanuelle, Gille, Johan J. P., Le Guen, Yann, Guerreiro, Rita, Haines, Jonathan L., Holmes, Clive, Ikram, M. Arfan, Ikram, M. Kamran, Jansen, Iris E., Kraaij, Robert, Lathrop, Marc, Lemstra, Afina W., Lleo, 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 ORCID: 0000-0002-7493-8777, Pericak-Vance, Margaret A., Raybould, Rachel, Redon, Richard, Reinders, Marcel J. T., Richard, Anne-Claire, Riedel-Heller, Steffi G., Rivadeneira, Fernando, Rousseau, Stephane, Ryan, Natalie S., Saad, Salha, Sanchez-Juan, Pascual, Schellenberg, Gerard D., 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 G., van der Lee, Sven J., 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 ORCID: 0000-0002-3122-0423, Ramirez, Alfredo ORCID: 0000-0003-4991-763X, Mead, Simon ORCID: 0000-0002-4326-1468, van der Flier, Wiesje M., van Duijn, Cornelia M., Williams, Julie, Nicolas, Gael, Bellenguez, Celine ORCID: 0000-0002-1240-7874 and Lambert, Jean-Charles . Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease. Nature Genet.. BERLIN: NATURE PORTFOLIO. ISSN 1546-1718

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