Search Results - Paterson, Jennifer M

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    Genetic insights into resting heart rate and its role in cardiovascular disease by van de Vegte, Yordi J., Eppinga, Ruben N., van der Ende, M. Yldau, Hagemeijer, Yanick P., Mahendran, Yuvaraj, Tan, Vanessa Y., Ntalla, Ioanna, Brody, Jennifer A., Lecoeur, Cecile, Hwang, Shih-Jen, Mononen, Nina, Auro, Kirsi, Jackson, Anne U., Zeng, Linyao, Nethander, Maria, Pechlivanis, Sonali, Qi, Lu, Zhao, Wei, Rizzi, Federica, Tanaka, Toshiko, Robino, Antonietta, Lange, Leslie, Zhang, Weihua, Guo, Xiuqing, Lin, Henry J., Noordam, Raymond, Milaneschi, Yuri, Schraut, Katharina E., den Hoed, Marcel, Trompet, Stella, van den Berg, Marten E., Pistis, Giorgio, Weiss, Stefan, Nolte, Ilja M., Lyytikäinen, Leo-Pekka, Iribarren, Carlos, Ring, Susan M., de Vries, Paul S., Sever, Peter, Linneberg, Allan, Bottinger, Erwin P., Sotoodehnia, Nona, Kolcic, Ivana, Gudbjartsson, Daniel F., Newton-Cheh, Christopher H., Nikus, Kjell, Salo, Perttu, Peyser, Patricia A., Schunkert, Heribert, Lorentzon, Mattias, Lahti, Jari, Rao, Dabeeru C., Cornelis, Marilyn C., Faul, Jessica D., Smith, Jennifer A., Concas, Maria Pina, Sinagra, Gianfranco, Delgado, Graciela E., Foco, Luisa, Melander, Olle, de Mutsert, Renée, de Geus, Eco J. C., Joshi, Peter K., Macfarlane, Peter W., Tan, Nicholas, Felix, Stephan B., Quek, Debra Q., Ingelsson, Martin, Raitakari, Olli T., Timpson, Nicholas J., Morrison, Alanna C., Heckbert, Susan R., Hayward, Caroline, Stefansson, Kari, Wareham, Nicholas J., van Duijn, Cornelia M., Feitosa, Mary F., Boehnke, Michael, Kardia, Sharon L. R., Ohlsson, Claes, Eriksson, Johan G., Moebus, Susanne, Cusi, Daniele, Girotto, Giorgia, Kääb, Stefan, Peters, Annette, März, Winfried, Smith, J. Gustav, Mook-Kanamori, Dennis O., Gyllensten, Ulf, Wilson, James F., Burgess, Stephen, Sundström, Johan, Lieb, Wolfgang, Eijgelsheim, Mark, Cheng, Ching-Yu, Dörr, Marcus, Wong, Tien-Yin, Riese, Harriette, Verweij, Niek

    Published in Nature communications
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    Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia by The Psychiatric Genomics Consortium, The Autism Spectrum Disorders Working Group Of, Anney, Richard J L, Ripke, Stephan, Anttila, Verneri, Grove, Jakob, Holmans, Peter, Huang, Hailiang, Klei, Lambertus, Lee, Phil H, Medland, Sarah E, Neale, Benjamin, Robinson, Elise, Weiss, Lauren A, Zwaigenbaum, Lonnie, Yu, Timothy W, Wittemeyer, Kerstin, Willsey, a Jeremy, Wijsman, Ellen M, Werge, Thomas, Wassink, Thomas H, Waltes, Regina, Walsh, Christopher A, Wallace, Simon, Vorstman, Jacob a S, Vieland, Veronica J, Vicente, Astrid M, Vanengeland, Herman, Tsang, Kathryn, Thompson, Ann P, Szatmari, Peter, Svantesson, Oscar, Steinberg, Stacy, Stefansson, Kari, Stefansson, Hreinn, State, Matthew W, Soorya, Latha, Silagadze, Teimuraz, Scherer, Stephen W, Schellenberg, Gerard D, Sandin, Sven, Sanders, Stephan J, Saemundsen, Evald, Rouleau, Guy A, Rogé, Bernadette, Roeder, Kathryn, Roberts, Wendy, Reichert, Jennifer, Reichenberg, Abraham, Rehnström, Karola, Regan, Regina, Poustka, Fritz, Poultney, Christopher S, Piven, Joseph, Pinto, Dalila, Pericak-Vance, Margaret A, Pejovic-Milovancevic, Milica, Pedersen, Marianne Giørtz, Pedersen, Carsten Bøcker, Paterson, Andrew D, Parr, Jeremy R, Pagnamenta, Alistair T, Oliveira, Guiomar, Nurnberger, John I, Nordentoft, Merete, Murtha, Michael T, Mouga, Susana, Mortensen, Preben Bo, Mors, Ole, Morrow, Eric M, Moreno-De-Luca, Daniel, Monaco, Anthony P, Minshew, Nancy, Merikangas, Alison, Mcmahon, William M, Mcgrew, Susan G, Mattheisen, Manuel, Martsenkovsky, Igor, Martin, Donna M, Mane, Shrikant M, Magnusson, Pall, Magalhaes, Tiago, Maestrini, Elena, Lowe, Jennifer K, Lord, Catherine, Levitt, Pat, Martin, Christa Lese, Ledbetter, David H, Leboyer, Marion, Lecouteur, Ann S, Ladd-Acosta, Christine, Kolevzon, Alexander, Klauck, Sabine M, Jacob, Suma, Iliadou, Bozenna, Hultman, Christina M, Hougaard, David M, Hertz-Picciotto, Irva, Hendren, Robert, Hansen, Christine Søholm, Haines, Jonathan L

    Published in Molecular autism
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