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    Cortical abnormalities in bipolar disorder: an MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group von Westlye, L T, Jahanshad, N, Cheung, J W, Ching, C R K, Versace, A, Bilderbeck, A C, Uhlmann, A, Overs, B, Dima, D, Grotegerd, D, Sprooten, E, Bøen, E, Jimenez, E, Howells, F M, Delvecchio, G, Starke, J, Goikolea, J M, Houenou, J, Beard, L M, Rauer, L, Abramovic, L, Bonnin, M, Ponteduro, M F, Keil, M, Rive, M M, Yao, N, Rosa, P G, Redlich, R, Trost, S, Fears, S C, van Erp, T G M, Nickson, T, Chaim-Avancini, T M, Elvsåshagen, T, Haukvik, U K, Lee, W H, Schene, A H, Lloyd, A J, Young, A H, Nugent, A, Dale, A M, Pfennig, A, Lafer, B, Baune, B T, Ekman, C J, Zarate, C A, Bearden, C E, Henry, C, Simhandl, C, McDonald, C, Bourne, C, Stein, D J, Wolf, D H, Cannon, D M, Glahn, D C, Veltman, D J, Vieta, E, Canales-Rodriguez, E J, Nery, F G, Duran, F L S, Busatto, G F, Roberts, G, Pearlson, G D, Goodwin, G M, Ruhe, H G, Soares, J C, Fullerton, J M, Rybakowski, J K, Chaim, K T, Fatjó-Vilas, M, Soeiro-de-Souza, M G, Boks, M P, Zanetti, M V, Otaduy, M C G, Schaufelberger, M S, Ingvar, M, Phillips, M L, Bauer, M, Landén, M, Lawrence, N S, van Haren, N E M, Horn, N R, Freimer, N B, Schofield, P R, Mitchell, P B, Kahn, R S, Lenroot, R, Machado-Vieira, R, Ophoff, R A, Sarró, S, Frangou, S, Satterthwaite, T D, Hajek, T, Dannlowski, U, Arolt, V, Gattaz, W F, Drevets, W C, Agartz, I, Thompson, P M, Andreassen, O A

    Veröffentlicht in Molecular psychiatry

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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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    Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis von Wheeler, Eleanor, Leong, Aaron, Liu, Ching-Ti, Hivert, Marie-France, Strawbridge, Rona J, Podmore, Clara, Li, Man, Yao, Jie, Sim, Xueling, Hong, Jaeyoung, Chu, Audrey Y, Zhang, Weihua, Wang, Xu, Chen, Peng, Maruthur, Nisa M, Porneala, Bianca C, Sharp, Stephen J, Jia, Yucheng, Kabagambe, Edmond K, Chang, Li-Ching, Chen, Wei-Min, Elks, Cathy E, Evans, Daniel S, Fan, Qiao, Giulianini, Franco, Go, Min Jin, Hottenga, Jouke-Jan, Hu, Yao, Jackson, Anne U, Kanoni, Stavroula, Kim, Young Jin, Kleber, Marcus E, Ladenvall, Claes, Lecoeur, Cecile, Lim, Sing-Hui, Lu, Yingchang, Mahajan, Anubha, Marzi, Carola, Nalls, Mike A, Navarro, Pau, Nolte, Ilja M, Rose, Lynda M, Rybin, Denis V, Sanna, Serena, Shi, Yuan, Stram, Daniel O, Takeuchi, Fumihiko, Tan, Shu Pei, van der Most, Peter J, Van Vliet-Ostaptchouk, Jana V, Wong, Andrew, Yengo, Loic, Zhao, Wanting, Goel, Anuj, Martinez Larrad, Maria Teresa, Radke, Dörte, Salo, Perttu, Tanaka, Toshiko, van Iperen, Erik P A, Abecasis, Goncalo, Afaq, Saima, Alizadeh, Behrooz Z, Bertoni, Alain G, Bonnefond, Amelie, Böttcher, Yvonne, Bottinger, Erwin P, Campbell, Harry, Carlson, Olga D, Chen, Chien-Hsiun, Cho, Yoon Shin, Garvey, W Timothy, Gieger, Christian, Goodarzi, Mark O, Grallert, Harald, Hamsten, Anders, Hartman, Catharina A, Herder, Christian, Hsiung, Chao Agnes, Huang, Jie, Igase, Michiya, Isono, Masato, Katsuya, Tomohiro, Khor, Chiea-Chuen, Kiess, Wieland, Kohara, Katsuhiko, Kovacs, Peter, Lee, Juyoung, Lee, Wen-Jane, Lehne, Benjamin, Li, Huaixing, Liu, Jianjun, Lobbens, Stephane, Luan, Jian'an, Lyssenko, Valeriya, Meitinger, Thomas, Miki, Tetsuro, Miljkovic, Iva, Moon, Sanghoon, Mulas, Antonella, Müller, Gabriele

    Veröffentlicht in PLoS medicine

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