Search Results - Glatt, Andrew

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    Analysis of protein-coding genetic variation in 60,706 humans by Lek, Monkol, Karczewski, Konrad J., Minikel, Eric V., Samocha, Kaitlin E., Banks, Eric, Fennell, Timothy, O’Donnell-Luria, Anne H., Ware, James S., Hill, Andrew J., Cummings, Beryl B., Tukiainen, Taru, Birnbaum, Daniel P., Kosmicki, Jack A., Duncan, Laramie E., Estrada, Karol, Zhao, Fengmei, Zou, James, Pierce-Hoffman, Emma, Berghout, Joanne, Cooper, David N., Deflaux, Nicole, DePristo, Mark, Do, Ron, Flannick, Jason, Fromer, Menachem, Gauthier, Laura, Goldstein, Jackie, Gupta, Namrata, Howrigan, Daniel, Kiezun, Adam, Kurki, Mitja I., Moonshine, Ami Levy, Natarajan, Pradeep, Orozco, Lorena, Peloso, Gina M., Poplin, Ryan, Rivas, Manuel A., Ruano-Rubio, Valentin, Rose, Samuel A., Ruderfer, Douglas M., Shakir, Khalid, Stenson, Peter D., Stevens, Christine, Thomas, Brett P., Tiao, Grace, Tusie-Luna, Maria T., Weisburd, Ben, Won, Hong-Hee, Yu, Dongmei, Altshuler, David M., Ardissino, Diego, Boehnke, Michael, Danesh, John, Donnelly, Stacey, Elosua, Roberto, Florez, Jose C., Gabriel, Stacey B., Getz, Gad, Glatt, Stephen J., Hultman, Christina M., Kathiresan, Sekar, Laakso, Markku, McCarroll, Steven, McCarthy, Mark I., McGovern, Dermot, McPherson, Ruth, Neale, Benjamin M., Palotie, Aarno, Purcell, Shaun M., Saleheen, Danish, Scharf, Jeremiah M., Sklar, Pamela, Sullivan, Patrick F., Tuomilehto, Jaakko, Tsuang, Ming T., Watkins, Hugh C., Wilson, James G., Daly, Mark J., MacArthur, Daniel G.

    Published in Nature (London)
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    Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts by Schwantes-An, Tae-Hwi, Zhang, Juan, Chen, Li-Shiun, Hartz, Sarah M., Chen, Xiangning, Coon, Hilary, Frank, Josef, Kamens, Helen M., Konte, Bettina, Kovanen, Leena, Latvala, Antti, Legrand, Lisa N., Maher, Brion S., Melroy, Whitney E., Nelson, Elliot C., Reid, Mark W., Shen, Pei-Hong, Yang, Bao-Zhu, Andrews, Judy A., Aveyard, Paul, Brown, Sandra A., Cichon, Sven, Corley, Robin P., Dahmen, Norbert, Degenhardt, Louisa, Gaebel, Wolfgang, Giegling, Ina, Glatt, Stephen J., Grucza, Richard A., Hardin, Jill, Hartmann, Annette M., Heath, Andrew C., Herms, Stefan, Hoffmann, Per, Hops, Hyman, Ising, Marcus, Johnson, Eric O., Johnstone, Elaine, Kaneva, Radka P., Kendler, Kenneth S., Kiefer, Falk, Kranzler, Henry R., Krauter, Ken S., Levran, Orna, Lucae, Susanne, Maier, Wolfgang, Mann, Karl, Martin, Nicholas G., Mattheisen, Manuel, Montgomery, Grant W., Murphy, Michael F., Neale, Michael C., Nikolov, Momchil A., Nishita, Denise, Nöthen, Markus M., Nurnberger, John, Partonen, Timo, Pergadia, Michele L., Reynolds, Maureen, Ridinger, Monika, Rose, Richard J., Rouvinen-Lagerström, Noora, Scherbaum, Norbert, Schmäl, Christine, Soyka, Michael, Stallings, Michael C., Steffens, Michael, Treutlein, Jens, Tsuang, Ming, Wall, Tamara L., Wodarz, Norbert, Yuferov, Vadim, Zill, Peter, Bergen, Andrew W., Chen, Jingchun, Cinciripini, Paul M., Edenberg, Howard J., Ehringer, Marissa A., Ferrell, Robert E., Gelernter, Joel, Goldman, David, Hewitt, John K., Hopfer, Christian J., Iacono, William G., Kaprio, Jaakko, Kremensky, Ivo M., Madden, Pamela A.F., McGue, Matt, Munafò, Marcus R., Philibert, Robert A., Rietschel, Marcella, Roy, Alec, Rujescu, Dan, Saarikoski, Sirkku T., Swan, Gary E., Todorov, Alexandre A., Vanyukov, Michael M., Weiss, Robert B., Bierut, Laura J., Saccone, Nancy L.

    Published in Behavior genetics
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    Rare coding variants in 10 genes confer substantial risk for schizophrenia by Singh, Tarjinder, Poterba, Timothy, Curtis, David, Akil, Huda, Al Eissa, Mariam, Barchas, Jack D., Bass, Nicholas, Bigdeli, Tim B., Breen, Gerome, Bromet, Evelyn J., Buckley, Peter F., Bunney, William E., Bybjerg-Grauholm, Jonas, Byerley, William F., Chapman, Sinéad B., Chen, Wei J., Churchhouse, Claire, Craddock, Nicholas, Cusick, Caroline M., DeLisi, Lynn, Dodge, Sheila, Escamilla, Michael A., Eskelinen, Saana, Fanous, Ayman H., Faraone, Stephen V., Fiorentino, Alessia, Francioli, Laurent, Gabriel, Stacey B., Gage, Diane, Taliun, Sarah A. Gagliano, Ganna, Andrea, Genovese, Giulio, Glahn, David C., Grove, Jakob, Hall, Mei-Hua, Hämäläinen, Eija, Heyne, Henrike O., Holi, Matti, Hougaard, David M., Howrigan, Daniel P., Huang, Hailiang, Hwu, Hai-Gwo, Kahn, René S., Kang, Hyun Min, Karczewski, Konrad J., Kirov, George, Knowles, James A., Lee, Francis S., Lehrer, Douglas S., Lescai, Francesco, Malaspina, Dolores, Marder, Stephen R., McCarroll, Steven A., McIntosh, Andrew M., Medeiros, Helena, Milani, Lili, Morley, Christopher P., Morris, Derek W., Bo Mortensen, Preben, Myers, Richard M., Nordentoft, Merete, O’Brien, Niamh L., Olivares, Ana Maria, Ongur, Dost, Ouwehand, Willem H., Palmer, Duncan S., Paunio, Tiina, Quested, Digby, Rapaport, Mark H., Rees, Elliott, Rollins, Brandi, Satterstrom, F. Kyle, Schatzberg, Alan, Scolnick, Edward, Scott, Laura J., Sharp, Sally I., Sklar, Pamela, Smoller, Jordan W., Sobell, Janet l., Solomonson, Matthew, Stevens, Christine R., Suvisaari, Jaana, Tiao, Grace, Watson, Stanley J., Watts, Nicholas A., Blackwood, Douglas H., Børglum, Anders D., Cohen, Bruce M., Corvin, Aiden P., Esko, Tõnu, Freimer, Nelson B., Glatt, Stephen J., Hultman, Christina M., McQuillin, Andrew, Palotie, Aarno, Pato, Carlos N., Pato, Michele T., Pulver, Ann E., St. Clair, David, Tsuang, Ming T.

    Published in Nature (London)
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