Universität zu Köln

Belloy, Michael E., Eger, Sarah J., Le Guen, Yann, Damotte, Vincent, Ahmad, Shahzad, Ikram, M. Arfan, Ramirez, Alfredo ORCID: 0000-0003-4991-763X, Tsolaki, Anthoula C., Rossi, Giacomina, Jansen, Iris E., de Rojas, Itziar, Parveen, Kayenat, Sleegers, Kristel, Ingelsson, Martin, Hiltunen, Mikko, Amin, Najaf, Andreassen, Ole, Sanchez-Juan, Pascual, Kehoe, Patrick ORCID: 0000-0002-7542-1139, Amouyel, Philippe, Sims, Rebecca, Frikke-Schmidt, Ruth, van der Flier, Wiesje M., Lambert, Jean-Charles, He, Zihuai ORCID: 0000-0002-8220-4183, Han, Summer S., Napolioni, Valerio and Greicius, Michael D. (2022). Challenges at the APOE locus: a robust quality control approach for accurate APOE genotyping. Alzheimers Res. Ther., 14 (1). LONDON: BMC. ISSN 1758-9193

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

Le Guen, Yann, Belloy, Michael E., Grenier-Boley, Benjamin, de Rojas, Itziar, Castillo-Morales, Atahualpa, Jansen, Iris, Nicolas, Aude, Bellenguez, Celine, Dalmasso, Carolina, Kucukali, Fahri, Eger, Sarah J., Rasmussen, Katrine Laura, Thomassen, Jesper Qvist ORCID: 0000-0003-3484-9531, Deleuze, Jean-Francois, He, Zihuai ORCID: 0000-0002-8220-4183, Napolioni, Valerio, Amouyel, Philippe, Jessen, Frank, Kehoe, Patrick G., van Duijn, Cornelia, Tsolaki, Magda, Sanchez-Juan, Pascual, Sleegers, Kristel, Ingelsson, Martin, Rossi, Giacomina, Hiltunen, Mikko, Sims, Rebecca, van der Flier, Wiesje M., Ramirez, Alfredo ORCID: 0000-0003-4991-763X, Andreassen, Ole A., Frikke-Schmidt, Ruth, Williams, Julie, Ruiz, Agustin, Lambert, Jean-Charles and Greicius, Michael D. (2022). Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease. JAMA Neurol., 79 (7). S. 652 - 664. CHICAGO: AMER MEDICAL ASSOC. ISSN 2168-6157