Treffer 1 - 20 von 172 für Suche 'Quinn, Chad J', Suchdauer: 1,68s Treffer weiter einschränken
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    Common genetic variants influence human subcortical brain structures von Hibar, Derrek P., Desrivières, Sylvane, Toro, Roberto, Wittfeld, Katharina, Abramovic, Lucija, Bernard, Manon, Chen, Qiang, Giddaluru, Sudheer, Janowitz, Deborah, Lee, Phil H., Ramasamy, Adaikalavan, Risacher, Shannon L., Rose, Emma J., Salami, Alireza, Schmaal, Lianne, Schork, Andrew J., Strike, Lachlan T., Walters, Raymond K., Winkler, Anderson M., Zwiers, Marcel P., Athanasiu, Lavinia, Hakobjan, Marina M. H., Hartberg, Cecilie B., Heister, Angelien J. G. A. M., Hoehn, David, Kasperaviciute, Dalia, Makkinje, Remco R. R., Reese McKay, D., Shen, Li, Walton, Esther, Ames, David, Corvin, Aiden, Curran, Joanne E., Dillman, Allissa, Erk, Susanne, Foroud, Tatiana M., Guelfi, Sebastian, Hegenscheid, Katrin, Hernandez, Dena G., Heslenfeld, Dirk J., Hottenga, Jouke-Jan, Jenkinson, Mark, Kanai, Ryota, Kent, Jack W., McMahon, Katie L., Meisenzahl, Eva, Mohnke, Sebastian, Mühleisen, Thomas W., Nalls, Michael A., Nichols, Thomas E., Potkin, Steven G., Reppermund, Simone, Rujescu, Dan, Schnell, Knut, Thalamuthu, Anbupalam, Turner, Jessica A., van 't Ent, Dennis, Wassink, Thomas H., Westman, Eric, Ashbrook, David G., Lu, Lu, Williams, Robert W., Buckner, Randy L., Calhoun, Vince D., Cavalleri, Gianpiero L., Dale, Anders M., Espeseth, Thomas, Hoffmann, Wolfgang, Le Hellard, Stephanie, Meyer-Lindenberg, Andreas, Müller-Myhsok, Bertram, Nyberg, Lars, Penninx, Brenda W. J. H., van Bokhoven, Hans, van Haren, Neeltje E. M., Völzke, Henry, Weiner, Michael W., White, Tonya, Agartz, Ingrid, Blangero, John, Boomsma, Dorret I., Fernández, Guillén, Fisher, Simon E., Francks, Clyde, Grabe, Hans J., Hashimoto, Ryota, Hulshoff Pol, Hilleke E., Jönsson, Erik G., McIntosh, Andrew M., Singleton, Andrew, Schmidt, Reinhold, Satizabal, Claudia L., Ebling, Maritza, Nyquist, Paul, Vinke, Louis N., Xue, Luting, Mazoyer, Bernard, Martin, Nicholas G., Wright, Margaret J., Schumann, Gunter

    Veröffentlicht in Nature (London)

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    Returning integrated genomic risk and clinical recommendations: The eMERGE study von Chisholm, Rex L., Clayton, Ellen Wright, DiVietro, Alanna, Green, Richard, Harden, Maegan V., Limdi, Nita A., Rasmussen, Luke V., Schmidlen, Tara, Cimino, James J., Guiducci, Candace, Harr, Margaret, Larkin, Katie, Mooney, Sean D., Mutai, Brenda, Namjou, Bahram, Perez, Emma F., Saadatagah, Seyedmohammad, Seabolt, Lynn, Shaibi, Gabriel Q., Sharp, Richard R., Sterling, Rene, Tiwari, Hemant K., Allworth, Aimee, DiVietro, Alanna, Khera, Amit, Kontorovich, Amy, Prince, Anya, Iverson, Ayuko, Khales, Bahram Namjou, Benoit, Barbara, Satterfield, Benjamin, Devine, Beth, Grundmeier, Bob, Piening, Brian, Korf, Bruce, Hammack, Catherine, Gascoigne, Caytie, Lange, Christoph, Liu, Cong, Shimbo, Daichi, Singh, Davinder, Edwards, Digna Velez, Morales, Eduardo, Cohn, Elizabeth, Karlson, Elizabeth, DeFranco, Emily, Perez, Emma, Cash, Erin, Berner, Eta, Wang, Fei, Mentch, Frank, Wiesner, Georgia, Belbin, Gillian, Hakonarson, Hakon, Tiwari, Hemant, Thomas, Hope, Hellwege, Jacklyn, Snyder, James, Olson, Janet, Glessner, Joe, Alsip, Jorge, Kannry, Joseph, Peterson, Josh, Galasso, Julia, Starren, Justin, Mittendorf, Kate, Anderson, Katherine, Bonini, Katherine, Rasmussen-Torvik, Laura, Gomez, Lizbeth, Petukhova, Lynn, Beasley, Mark, Horike, Martha, Hamed, Marwan, Davis, Matthew, Preuss, Michael, Shi, Mingjian, Perera, Minoli, Elkind, Mitch, Saadatagah, Mohammad, Netherly, Neil, Lennon, Niall, Limdi, Nita, Robinson, Nora, Elsekaily, Omar, Kovatch, Patricia, O’Reilly, Paul, Murali, Priyanka, Sharp, Richard, Peters, Riki, Rowley, Robb, Freimuth, Robert, Green, Robert, Winter, Robert, Irvin, Ryan, Knerr, Sarah, Bland, S.T., Booth, Stuart James, Desai, Vimi, Luo, Yuan

    Veröffentlicht in Genetics in medicine

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