Treffer 1 - 20 von 274 für Suche 'Sullivan, Caroline M', Suchdauer: 1,90s Treffer weiter einschränken
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    Rare coding variants in ten genes confer substantial risk for schizophrenia von 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, DeLisi, Lynn, Dodge, Sheila, Escamilla, Michael A., Eskelinen, Saana, Fanous, Ayman H., Faraone, Stephen V., Fiorentino, Alessia, Francioli, Laurent, Gabriel, Stacey B., Gage, Diane, Gagliano Taliun, Sarah A., Ganna, Andrea, Genovese, Giulio, Grove, Jakob, Hall, Mei-Hua, 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., Knowles, James A., Lee, Francis S., Lehrer, Douglas S., Lescai, Francesco, Marder, Stephen R., McCarroll, Steven A., McIntosh, Andrew M., Milani, Lili, Morley, Christopher P., Morris, Derek W., Mortensen, Preben Bo, 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., Solomonson, Matthew, Stahl, Eli A., Stevens, Christine R., Suvisaari, Jaana, Watts, Nicholas A., Blackwood, Douglas H., 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., Vawter, Marquis P., Walters, James T., Werge, Thomas M., Ophoff, Roel A., Sullivan, Patrick F., Owen, Michael J., Boehnke, Michael, O’Donovan, Michael C., Neale, Benjamin M., Daly, Mark J.

    Veröffentlicht in Nature (London)

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    Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology von Mullins, Niamh, O’Connell, Kevin S., Coleman, Jonathan R. I., Qiao, Zhen, Bigdeli, Tim B., Hagenaars, Saskia P., Krebs, Kristi, Panagiotaropoulou, Georgia, Schilder, Brian M., Sloofman, Laura G., Winsvold, Bendik S., Al Eissa, Mariam, Albani, Diego, Alliey-Rodriguez, Ney, Antoniou, Anastasia, Beins, Eva C., Boks, Marco P., Brum, Murielle, Byerley, William, Cairns, Murray, Cervantes, Pablo, Cuellar-Barboza, Alfredo, Czerski, Piotr M., Djurovic, Srdjan, Douzenis, Athanassios, Foroud, Tatiana M., Giørtz Pedersen, Marianne, Gordon-Smith, Katherine, Grove, Jakob, Guzman-Parra, José, Haraldsson, Magnus, Herms, Stefan, Hoffmann, Per, Holmans, Peter A., Huckins, Laura, Johnson, Jessica S., Kalman, Janos L., Knowles, James A., Koromina, Maria, Kranzler, Henry R., Lee, Phil H., Lewis, Catrin, Lundberg, Martin, MacIntyre, Donald J., Magnusson, Sigurdur H., Maier, Wolfgang, Medland, Sarah E., Moran, Jennifer L., O’Brien, Niamh, Olde Loohuis, Loes M., Oruc, Lilijana, Papiol, Sergi, Pardiñas, Antonio F., Perry, Amy, Sánchez-Mora, Cristina, Sharp, Sally, Spijker, Anne T., Stein, Dan J., Strauss, John S., Tooney, Paul, Tsermpini, Evangelia-Eirini, Vedder, Helmut, Walters, James T. R., Witt, Stephanie H., Babadjanova, Gulja, Blackwood, Douglas H. R., Carr, Vaughan J., Dannlowski, Udo, Dikeos, Dimitris, Etain, Bruno, Frye, Mark, Gershon, Elliot S., Goes, Fernando S., Grigoroiu-Serbanescu, Maria, Hougaard, David M., Hveem, Kristian, Jablensky, Assen V., Kirov, George, Lewis, Cathryn M., Loughland, Carmel, Martin, Nicholas G., McElroy, Susan L., Melle, Ingrid, Milani, Lili, Nievergelt, Caroline M., Nöthen, Markus M., O’Donovan, Michael C., Oedegaard, Ketil J., Olsson, Tomas, Perlis, Roy H., Ribasés, Marta, Rouleau, Guy A., Schalling, Martin, Schulze, Thomas G., Serretti, Alessandro, Smoller, Jordan W., Stefansson, Kari, Stordal, Eystein, Vieta, Eduard, Nurnberger, John I.

    Veröffentlicht in Nature genetics

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