Treffer 1 - 20 von 33 für Suche 'Neely, Simon R', Suchdauer: 1,16s Treffer weiter einschränken
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    Authenticating the Presence of a Relativistic Massive Black Hole Binary in OJ 287 Using Its General Relativity Centenary Flare: Improved Orbital Parameters von Dey, Lankeswar, Valtonen, M. J., Gopakumar, A., Zola, S., Hudec, R., Pihajoki, P., Ciprini, S., Matsumoto, K., Sadakane, K., Kidger, M., Nilsson, K., Mikkola, S., Sillanpää, A., Takalo, L. O., Lehto, H. J., Berdyugin, A., Piirola, V., Jermak, H., Baliyan, K. S., Pursimo, T., Caton, D. B., Alicavus, F., Baransky, A., Blay, P., Boumis, P., Boyd, D., Torrent, M. Campas, Campos, F., Gómez, J. Carrillo, Chandra, S., Chavushyan, V., Dalessio, J., Debski, B., Drozdz, M., Er, H., Erdem, A., Pérez, A. Escartin, Ramazani, V. Fallah, Filippenko, A. V., Gafton, E., Ganesh, S., Garcia, F., Gazeas, K., Godunova, V., Pinilla, F. Gómez, Gopinathan, M., Haislip, J. B., Harmanen, J., Hurst, G., Jelinek, M., Joshi, A., Kagitani, M., Karjalainen, R., Kaur, N., Keel, W. C., Kouprianov, V. V., Kundera, T., Kurowski, S., Kvammen, A., Lee, B. C., Liakos, A., Lindfors, E., de Haro, J. Lozano, Mugrauer, M., Nogues, R. Naves, Neely, A. W., Nelson, R. H., Ogloza, W., Okano, S., Pajdosz- mierciak, U., Pandey, J. C., Perri, M., Poyner, G., Provencal, J., Raj, A., Reichart, D. E., Reinthal, R., Reynolds, T., Saario, J., Sadegi, S., Sakanoi, T., Sameer, Schweyer, T., Simon, A., Alfaro, F. C. Soldán, Sonbas, E., Steele, I., Stocke, J. T., Strobl, J., Tomov, T., Espasa, L. Tremosa, Valdes, J. R., Pérez, J. Valero, Verrecchia, F., Vasylenko, V., Webb, J. R., Yoneda, M., Zejmo, M., Zheng, W., Zielinski, P.

    Veröffentlicht in The Astrophysical journal

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    SPARK: A US Cohort of 50,000 Families to Accelerate Autism Research von Feliciano, Pamela, Daniels, Amy M., Esler, Amy, Gutierrez, Anibal, Nicholson, Amy, Stephens, Alexandra N., Stedman, Amy, Finucane, Brenda, O’Roak, Brian J., Robertson, Beverly E., Rodriguez, Barbara, Van Metre, Bonnie, Bradley, Catherine, Erickson, Craig A., Harkins, Christina, Ochoa-Lubinoff, Cesar, Rosenberg, Cordelia R., Smith, Christopher J., Taylor, Cora M., White, Loran Casey, Walston, Corrie H., Amaral, David G., Coury, Daniel Lee, Sarver, Dustin E., Li, Deana, Berry-Kravis, Elizabeth, Fombonne, Eric J., Hofammann, Eugenia, Wodka, Ericka L., O’Connor, Eirene, Miller, Fiona, Stein, Gail, Hutter, Hanna, Li, Hai, Lechniak, Holly, Schneider, Hoa Lam, Zaydens, Hana, Arriaga, Ivette, Cubells, Joseph F., Cordova, Jeanette M., Gunderson, Jaclyn, McCracken, James T., Michaelson, Jacob J., Neely, Jason, Orobio, Jessica, Piven, Joseph, Tjernagel, Jennifer, Dent, Katherine, Schweers, Kathryn A., Law, J. Kiely, Lowe, Kathryn, O’Brien, Kaela, Smith, Kaitlin, Pawlowski, Katherine G., Pierce, Karen L., Roeder, Katherine, Coppola, Leigh A., Carpenter, Laura, Huang-Storms, Lark Y., Herbert, Lynette M., Simon, Laura, Soorya, Latha V., Wasserburg, Lucy, Lazar, Maya, Currin, Mary Hannah, Heyman, Michelle, Jones, Mark, Jordy, Michelle, Sahin, Mustafa, Siegel, Matthew S., Yinger, Meredith, Hanna, Nathan, Juarez, A. Pablo, Remington, Rick, Schultz, Robert T., Carpenter, Sarah, Eldred, Sara, Francis, Sunday, Horner, Susannah, Lee, Soo J., Mastel, Sarah A., Myers, Vincent J., Amatya, Alpha, Chatha, Ahmad S., Lash, Alex E., Ridenour, Curtis, Stock, Colleen M., Schmidt, Danielle, Butler, Martin E., Carriero, Nicholas, Volfovsky, Natalia, Edgar, Ron, Chin, Wubin, Jensen, William, Krentz, Anthony D., Astrovskaya, Irina, Gibbs, Richard A., Han, Xinwei, Shen, Yufeng, Reichardt, Louis F.

    Veröffentlicht in Neuron (Cambridge, Mass.)

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    Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders von Gillentine, Madelyn A., Wang, Tianyun, Hoekzema, Kendra, Rosenfeld, Jill, Liu, Pengfei, Guo, Hui, Kim, Chang N., De Vries, Bert B. A., Vissers, Lisenka E. L. M., Nordenskjold, Magnus, Kvarnung, Malin, Lindstrand, Anna, Nordgren, Ann, Gecz, Jozef, Iascone, Maria, Cereda, Anna, Scatigno, Agnese, Maitz, Silvia, Zanni, Ginevra, Bertini, Enrico, Zweier, Christiane, Schuhmann, Sarah, Wiesener, Antje, Pepper, Micah, Panjwani, Heena, Torti, Erin, Abid, Farida, Anselm, Irina, Srivastava, Siddharth, Atwal, Paldeep, Bacino, Carlos A., Bhat, Gifty, Cobian, Katherine, Bird, Lynne M., Friedman, Jennifer, Wright, Meredith S., Callewaert, Bert, Petit, Florence, Mathieu, Sophie, Afenjar, Alexandra, Christensen, Celenie K., White, Kerry M., Elpeleg, Orly, Berger, Itai, Espineli, Edward J., Fagerberg, Christina, Brasch-Andersen, Charlotte, Hansen, Lars Kjaersgaard, Feyma, Timothy, Hughes, Susan, Thiffault, Isabelle, Sullivan, Bonnie, Yan, Shuang, Keller, Kory, Keren, Boris, Mignot, Cyril, Kooy, Frank, Meuwissen, Marije, Basinger, Alice, Kukolich, Mary, Philips, Meredith, Ortega, Lucia, Drummond-Borg, Margaret, Lauridsen, Mathilde, Sorensen, Kristina, Lehman, Anna, Lopez-Rangel, Elena, Levy, Paul, Lessel, Davor, Lotze, Timothy, Madan-Khetarpal, Suneeta, Sebastian, Jessica, Vento, Jodie, Vats, Divya, Benman, L. Manace, Mckee, Shane, Mirzaa, Ghayda M., Muss, Candace, Pappas, John, Peeters, Hilde, Romano, Corrado, Elia, Maurizio, Galesi, Ornella, Simon, Marleen E. H., van Gassen, Koen L. I., Simpson, Kara, Stratton, Robert, Syed, Sabeen, Thevenon, Julien, Palafoll, Irene Valenzuela, Vitobello, Antonio, Bournez, Marie, Faivre, Laurence, Xia, Kun, Earl, Rachel K., Nowakowski, Tomasz, Bernier, Raphael A., Eichler, Evan E.

    Veröffentlicht in Genome medicine

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