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    Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease von 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, Cochran, J. Nicholas, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, Denning, Nicola, DeStefano, Anita L., Farrer, Lindsay A., Fox, Nick C., Galimberti, Daniela, 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., 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., 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 A., Spalletta, Gianfranco, Tesi, Niccolo’, Tijms, Betty, Uitterlinden, André 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., Hardy, John, Ramirez, Alfredo, Mead, Simon, van der Flier, Wiesje M., van Duijn, Cornelia M., Williams, Julie, Nicolas, Gaël, Bellenguez, Céline, Lambert, Jean-Charles

    Veröffentlicht in Nature genetics

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    Exome sequencing identifies rare damaging variants in the ATB8B4 and ABCA1 genes as novel risk factors for Alzheimer’s disease von 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, Dols‐Icardo, Oriol, Hummerich, Holger, Kawalia, Amit, Amouyel, Philippe, Berr, Claudine, Bis, Josh C, Boland, Anne, Bossù, Paola, Bouwman, Femke H., Bras, Jose, Campion, Dominique, Cochran, J. Nicholas, Daniele, Antonio, Dartigues, Jean‐François, Debette, Stéphanie, Deleuze, Jean‐François, Denning, Nicola, Destefano, Anita L., Farrer, Lindsay A., Fernandez, Victoria, Fox, Nick C, Génin, Emmanuelle, Gille, Hans, Guen, Yann Le, Guerreiro, Rita, Haines, Jonathan L., Holmes, Clive, Ikram, M. Arfan, Ikram, Mohammed Kamran, Jansen, Iris E., Kraaij, Robert, Lathrop, Mark, Lemstra, Afina W., Lleó, Alberto, Luckcuck, Lauren, 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, Pastor, Pau, Pericak‐Vance, Margaret A., Raybould, Rachel, Redon, Richard, Reinders, Marcel JT, 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, Sie, Daoud, Sistermans, Erik, Sorbi, Sandro, van Spaendonk, Rosalina M.L., Spalletta, Gianfranco, Tesi, Niccoló, Tijms, Betty M., Van Der Lee, Sven J, Uitterlinden, André G., Visser, Pieter Jelle, Wagner, Michael, Wallon, David, Wang, Li‐San, Clarimón, Jordi, van Swieten, John C, Hardy, John, Greicius, Michael D, Ramirez, Alfredo, Yokoyama, Jennifer S., van der Flier, Wiesje M, Cruchaga, Carlos, Van Duijn, Cornelia M, Williams, Julie, Nicolas, Gaël, Bellenguez, Céline, Lambert, Jean‐Charles

    Veröffentlicht in Alzheimer's & dementia

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