Maternal, Placental, and Fetal Responses to Intermittent Heat Exposure During Late Gestation in Mice von Olivier, Karike, Reinders, Lauren A., Clarke, Michael W., Crew, Rachael C., Pereira, Gavin, Maloney, Shane K., Wyrwoll, Caitlin S.

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How do adolescents with cerebral palsy participate? Learning from their personal experiences von Wintels, Sophie Catharina, Smits, Dirk‐Wouter, Wesel, Floryt, Verheijden, Johannes, Ketelaar, Marjolijn, Leest, Anna, Groot, Coosje, Snel, Dion, Water, Jesse, Sluiter, Lauren, Bruijn, Nando, Janssen, Nathan, Makkreel, Nienke Heijne, Kramer, Nikita, Bouma, Piotr, Vergeer, Sam, Boer, Thom, Voorman, J.M., Dallmeijer, A.J., Roebroeck, M.E., Reinders‐Messelink, H.A., Gorter, J.W.

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Optimizing MFCC parameters for the automatic detection of respiratory diseases von Yan, Yuyang, Simons, Sami O., van Bemmel, Loes, Reinders, Lauren G., Franssen, Frits M.E., Urovi, Visara

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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

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Reliability of two dissociating tests of phoria in artificially created phoria in normal adults von Helminski, Janet O., Keller, Sarah, Suckow, Melissa, Stein, Amy, Grieco, Lauren, Lintakas, Rima, Reinders, Caroline

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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

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Phenotypic and Genetic Factors Associated with Absence of Cardiomyopathy Symptoms in PLN:c.40_42delAGA Carriers von Lopera-Maya, Esteban A., Li, Shuang, de Brouwer, Remco, Nolte, Ilja M., van Breen, Justin, Jongbloed, Jan D. H., Swertz, Morris A., Snieder, Harold, Franke, Lude, Wijmenga, Cisca, de Boer, Rudolf A., Deelen, Patrick, van der Zwaag, Paul A., Sanna, Serena

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Optimising MFCC parameters for the automatic detection of respiratory diseases von Yan, Yuyang, Simons, Sami O, van Bemmel, Loes, Reinders, Lauren, Franssen, Frits M. E, Urovi, Visara

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Optimising MFCC parameters for the automatic detection of respiratory diseases von Yuyang Yan, Simons, Sami O, Loes van Bemmel, Reinders, Lauren, Franssen, Frits M E, Urovi, Visara

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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 GJ, Sims, Rebecca, Ahmad, Shahzad, Amin, Najaf, Norsworthy, Penny J, Dols-Icardo, Oriol, Hummerich, Holger, Kawalia, Amit, Beecham, Gary W, Berr, Claudine, Bis, Joshua C, Boland, Anne, Bossù, Paola, Bouwman, Femke, Bras, Jose, Campion, Dominique, Cochran, J Nicholas, Daniele, Antonio, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, DeStefano, Anita L, Farrer, Lindsay A, Fernández, Maria Victoria, Fox, Nick C, Galimberti, Daniela, Genin, Emmanuelle, Gille, Johan JP, Le Guen, Yann, Guerreiro, Rita, Haines, Jonathan L, Ikram, M Arfan, Ikram, M Kamran, Jansen, Iris E, Kraaij, Robert, Lathrop, Marc, Lleó, Alberto, Luckcuck, Lauren, Mannens, Marcel MAM, 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, 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, Seshadri, Sudha, Sie, Daoud, Sistermans, Erik A, Sorbi, Sandro, van Spaendonk, Resie, Spalletta, Gianfranco, Tesi, Niccolo, 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, Cruchaga, Carlos, Hardy, John, Ramirez, Alfredo, Mead, Simon, van der Flier, Wiesje 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 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, Norsworthy, Penny J, Dols Icardo, Oriol, Hummerich, Holger, Kawalia, Amit, Beecham, Gary W, Berr, Claudine, Bis, Joshua C, Boland, Anne, Bossù, Paola, Bouwman, Femke, Bras, Jose, Cochran, J. Nicholas, Daniele, Antonio, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, DeStefano, Anita L, Farrer, Lindsay A, Fernández, Maria Victoria, Fox, Nick C, Galimberti, Daniela, Genin, Emmanuelle, Gille, Johan J. P, Le Guen, Yann, Guerreiro, Rita, Haines, Jonathan L, Ikram, M. Arfan, Ikram, M. Kamran, Jansen, Iris E, Kraaij, Robert, Lathrop, Marc, 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, Pericak-Vance, Margaret A, Raybould, Rachel, Redon, Richard, Reinders, Marcel J. T, Richard, Anne-Claire, Riedel-Heller, Steffi, Rivadeneira, Fernando, Rousseau, Stéphane, Ryan, Natalie S, Saad, Salha, Sánchez-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 M, Uitterlinden, André G, van der Lee, Sven J, Visser, Pieter Jelle, Wagner, Michael, Wallon, David, Wang, Li-San, Zarea, Aline, Clarimón, Jordi, van Swieten, John C, Greicius, Michael D, Yokoyama, Jennifer S, Cruchaga, Carlos, Hardy, John, Ramirez, Alfredo, Mead, Simon, van der Flier, Wiesje M, Williams, Julie, Nicolas, Gaël, Bellenguez, Céline, Lambert, Jean-Charles, Universitat Autònoma de Barcelona

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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, Norsworthy, Penny J, Dols Icardo, Oriol, Hummerich, Holger, Kawalia, Amit, Beecham, Gary W, Berr, Claudine, Bis, Joshua C, Boland, Anne, Bossù, Paola, Bouwman, Femke, Bras, Jose, Campion, Dominique, Cochran, J. Nicholas, Daniele, Antonio, Dartigues, Jean-François, Debette, Stéphanie, Deleuze, Jean-François, DeStefano, Anita L, Farrer, Lindsay A, Fernández, Maria Victoria, Fox, Nick C, Galimberti, Daniela, Genin, Emmanuelle, Gille, Johan J. P, Le Guen, Yann, Guerreiro, Rita, Haines, Jonathan L, Ikram, M. Arfan, Ikram, M. Kamran, Jansen, Iris E, Kraaij, Robert, Lathrop, Marc, 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, 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, Sánchez-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, Uitterlinden, André G, van der Lee, Sven J, Visser, Pieter Jelle, Wagner, Michael, Wallon, David, Wang, Li-San, Zarea, Aline, Clarimón, Jordi, van Swieten, John C, Greicius, Michael D, Yokoyama, Jennifer S, Cruchaga, Carlos, Hardy, John, Ramirez, Alfredo, Mead, Simon, van der Flier, Wiesje M, Williams, Julie, Nicolas, Gaël, Bellenguez, Céline, Lambert, Jean-Charles, Universitat Autònoma de Barcelona

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Corezilla: Build and Tame the Multicore Beast? von Sarno, Lauren, Hwu, Wen-mei W., Lund, Craig, Levy, Markus, Larus, James R., Reinders, James, Cameron, Gordon, Lennard, Chris, Yoshimori, Takashi

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Summary statistics for "Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's Disease" von Henne Holstege, Hulsman, Marc, Charbonnier, Camille, Grenier-Boley, Benjamin, Quenez, Olivier, Grozeva, Detelina, Van Rooij, Jeroen G.J., Sims, Rebecca, Ahmad, Shahzad, Norsworthy, Penny J., Dols-Icardo, Oriol, Hummerich, Holger, Kawalia, Amit, Alzheimer's Disease Neuroimaging Initiative (ADNI) Database, Beecham, Gary W., Berr, Claudine, Bis, Joshua C., Boland, Anne, Bossù, Paola, Bouwman, Femke, Bras, Jose, Campion, Dominique, J. Nicholas Cochran, Daniele, Antonio, Jean-François Dartigues, Debette, Stéphanie, Jean-François Deleuze, Denning, Nicola, Fernandez, Maria Victoria, Fox, Nick C., Galimberti, Daniela, Gille, Hans, Guen, Yann Le, Guerreiro, Rita, Haines, Jonathan L., Holmes, Clive, M. Arfan Ikram, M. Kamran Ikram, Jansen, Iris, Kraaij, Robert, Lathrop, Marc, Afina W. Lemstra, 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., Myers, Richard M., Nacmias, Benedetta, Naj, Adam C, Napolioni, Valerio, Pasquier, Florence, Pau Pastor, Pericak-Vance, Margaret A., Raybould, Rachel, Redon, Richard, Reinders, Marcel J.T., Anne-Claire Richard, Riedel-Heller, Steffi G, Rivadeneira, Fernando, Rousseau, Stéphane, Ryan, Natalie S., 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, Niccólo Tesi, Tijms, Betty, Uitterlinden, André G, Van Der Lee, Sven J., De Visser, Pieter Jelle, Wagner, Michael, Wallon, David, Li-San Wang, Zarea, Aline, Van Swieten, John C., Greicius, Michael, 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, Jean-Charles Lambert

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