Search Results - Wray, Simon N.*

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    Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia by Kendler, Kenneth S., Walters, James, Blackwell, Jenefer M., Bramon, Elvira, Markus, Hugh S., Rautanen, Anna, Freeman, Colin, Hopkins, Lucinda, Edkins, Sarah, Bumpstead, Suzannah J., Dronov, Serge, Gillman, Matthew, Gray, Emma, Liddle, Jennifer, Potter, Simon C., Weston, Paul, Ripke, Stephan, Farh, Kai‐How, Holmans, Peter A., Lee, Phil, Huang, Hailiang, Bacanu, Silviu A., Belliveau, Richard A., Bene, Judit, Bigdeli, Tim B., Bruggeman, Richard, Cahn, Wiepke, Carrera, Noa, Cheung, Eric F. C., Cohen, David, Craddock, Nick, Davis, Kenneth L., Dinan, Timothy, Drapeau, Elodie, Dudbridge, Frank, Durmishi, Naser, Eichhammer, Peter, Farrell, Martilias S., Franke, Lude, Freimer, Nelson B., Friedman, Joseph I., Fromer, Menachem, Gratten, Jacob, Haroutunian, Vahram, Hartmann, Annette M., Henskens, Frans A., Hofman, Andrea, Hollegaard, Mads V., Joa, Inge, Keller, Matthew C., Klovins, Janis, Konte, Bettina, Kucinskiene, Zita Ausrele, Laurent, Claudine, Loughland, Carmel M., Mallet, Jacques, Mattheisen, Manuel, McCarley, Robert W., McDonald, Colm, Meier, Sandra, Meijer, Carin J., Metspalu, Andres, Milani, Lili, Milanova, Vihra, Mokrab, Younes, Myin‐Germeys, Inez, Nenadic, Igor, Nikitina‐Zake, Liene, O'Callaghan, Eadbhard, O'Neill, F. Anthony, Paunio, Tiina, Pejovic‐Milovancevic, Milica, Perkins, Diana O., Pietiläinen, Olli, Quested, Digby, Reichenberg, Abraham, Salomaa, Veikko, Scolnick, Edward M., Silagadze, Teimuraz, So, Hon‐Cheong, Spencer, Chris C. A., Suvisaari, Jaana, Szatkiewicz, Jin P., Thirumalai, Srinivas, Tosato, Sarah, Waddington, John, Wang, Qiang, Williams, Nigel M., Witt, Stephanie H., Wormley, Brandon K., Zheng, Xuebin, Zimprich, Fritz, Wray, Naomi R., Buxbaum, Joseph D., Jablensky, Assen V., Knight, Jo, Levinson, Douglas F., Malhotra, Anil K., Weinberger, Daniel R., Werge, Thomas

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    Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture by Davis, Lea K, Yu, Dongmei, Keenan, Clare L, Gamazon, Eric R, Konkashbaev, Anuar I, Derks, Eske M, Neale, Benjamin M, Yang, Jian, Lee, S Hong, Evans, Patrick, Barr, Cathy L, Bellodi, Laura, Benarroch, Fortu, Berrio, Gabriel Bedoya, Bienvenu, Oscar J, Bloch, Michael H, Blom, Rianne M, Bruun, Ruth D, Budman, Cathy L, Camarena, Beatriz, Campbell, Desmond, Cappi, Carolina, Cardona Silgado, Julio C, Cath, Danielle C, Cavallini, Maria C, Chavira, Denise A, Chouinard, Sylvain, Conti, David V, Cook, Edwin H, Coric, Vladimir, Cullen, Bernadette A, Deforce, Dieter, Delorme, Richard, Dion, Yves, Edlund, Christopher K, Egberts, Karin, Falkai, Peter, Fernandez, Thomas V, Gallagher, Patience J, Garrido, Helena, Geller, Daniel, Girard, Simon L, Grabe, Hans J, Grados, Marco A, Greenberg, Benjamin D, Gross-Tsur, Varda, Haddad, Stephen, Heiman, Gary A, Hemmings, Sian M J, Hounie, Ana G, Illmann, Cornelia, Jankovic, Joseph, Jenike, Michael A, Kennedy, James L, King, Robert A, Kremeyer, Barbara, Kurlan, Roger, Lanzagorta, Nuria, Leboyer, Marion, Leckman, James F, Lennertz, Leonhard, Liu, Chunyu, Lochner, Christine, Lowe, Thomas L, Macciardi, Fabio, McCracken, James T, McGrath, Lauren M, Mesa Restrepo, Sandra C, Moessner, Rainald, Morgan, Jubel, Muller, Heike, Murphy, Dennis L, Naarden, Allan L, Ochoa, William Cornejo, Ophoff, Roel A, Osiecki, Lisa, Pakstis, Andrew J, Pato, Michele T, Pato, Carlos N, Piacentini, John, Pittenger, Christopher, Pollak, Yehuda, Rauch, Scott L, Renner, Tobias J, Reus, Victor I, Richter, Margaret A, Riddle, Mark A, Robertson, Mary M, Romero, Roxana, Rosàrio, Maria C, Rosenberg, David, Rouleau, Guy A, Ruhrmann, Stephan, Ruiz-Linares, Andres, Sampaio, Aline S, Samuels, Jack, Sandor, Paul, Sheppard, Brooke, Singer, Harvey S, Smit, Jan H

    Published in PLoS genetics
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