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    Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation von Kitajima, Hidetoshi, Kim, Young Jin, Horikoshi, Momoko, Moon, Sanghoon, Robertson, Neil R., Nano, Jana, Lamri, Amel, Nakatochi, Masahiro, Graff, Mariaelisa, Yao, Jie, Bielak, Lawrence F., Hai, Yang, Schmidt, Ellen M., Nousome, Darryl, Trompet, Stella, Ahmad, Meraj, Noordam, Raymond, Lim, Victor J. Y., Joo, Yoonjung Yoonie, Prins, Bram Peter, Chen, Guanjie, Jensen, Richard A., Kabagambe, Edmond K., Xiang, Anny H., Flanagan, Jack, Adair, Linda S., Akiyama, Masato, Bertoni, Alain, Chee, Miao-Li, Chen, Shyh-Huei, Chen, Yuan-Tsong, Das, Swapan K., de Silva, H. Janaka, Eckardt, Kai-Uwe, Evans, Daniel S., Evans, Michele K., Franco, Oscar H., Fuchsberger, Christian, Genter, Pauline, Goodarzi, Mark O., Gordon-Larsen, Penny, Gorkin, David, Guo, Yu, Howard, Annie-Green, Hung, Yi-Jen, Hwang, Mi Yeong, Ingelsson, Martin, Jonas, Jost B., Jørgensen, Torben, Kamatani, Yoichiro, Kasturiratne, Anuradhani, Katsuya, Tomohiro, Keaton, Jacob M., Kho, Abel N., Khor, Chiea-Chuen, Läll, Kristi, Li-Gao, Ruifang, Liu, Jianjun, Luan, Jian’an, Luo, Xi, Lyssenko, Valeriya, Metspalu, Andres, Morris, Andrew D., Nalls, Michael A., Ntalla, Ioanna, Sattar, Naveed, Shi, Jinxiu, Shriner, Daniel, Stilp, Adrienne M., Takahashi, Atsushi, Taylor, Kent D., Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Varma, Rohit, Yamamoto, Ken, Yoon, Kyungheon, Yusuf, Salim, Zheng, Wei, Cho, Yoon Shin, Lind, Lars, Province, Michael A., Zonderman, Alan B., Becker, Diane M., Yokota, Mitsuhiro, Chen, Yii-Der Ida, Ma, Ronald C. W., Chandak, Giriraj R., Sale, Michèle M., Shu, Xiao-Ou, Jukema, J. Wouter, McKean-Cowdin, Roberta, Kooner, Jaspal S., North, Kari E., Florez, Jose C., Maeda, Shiro, Stefansson, Kari, Mohlke, Karen L., Gloyn, Anna L., Below, Jennifer E., Rotter, Jerome I.

    Veröffentlicht in Nature genetics

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    Genetic drivers of heterogeneity in type 2 diabetes pathophysiology von Southam, Lorraine, Yin, Xianyong, Melloni, Giorgio E. M., Rayner, Nigel W., Bocher, Ozvan, Namba, Shinichi, Lee, Simon S. K., Petty, Lauren E., Schroeder, Philip, Kals, Mart, Zhang, Weihua, Graff, Mariaelisa, Lamri, Amel, Parra, Esteban J., Bielak, Lawrence F., Hai, Yang, Sofer, Tamar, Nousome, Darryl, Sun, Meng, Noordam, Raymond, Lim, Victor J. Y., Yanek, Lisa R., An, Ping, Tan, Jingyi, Canouil, Mickaël, Chee, Miao-Li, Chen, Shyh-Huei, Chen, Yuan-Tsong, Dimitrov, Latchezar, Doumatey, Ayo P., Du, Shufa, Eckardt, Kai-Uwe, Gerstein, Hertzel C., Han, Sohee, Herder, Christian, Howard, Annie-Green, Hsueh, Willa, Ichihara, Sahoko, Ikram, Mohammad Arfan, Jang, Hye-Mi, Jonas, Jost B., Kandeel, Fouad R., Kaur, Varinderpal, Lange, Leslie A., Lee, Myung-Shik, Leong, Aaron, Liu, Ching-Ti, Louie, Tin, Luo, Xi, Maeda, Shiro, Mansuri, Sohail Rafik, Nalls, Michael A., Nayak, Uma, Okada, Yukinori, Patil, Snehal, Prasad, Gauri, Roden, Michael, Rohde, Rebecca, Sandow, Kevin, Sankareswaran, Alagu, So, Wing Yee, Stilp, Adrienne M., Taylor, Kent D., Thorand, Barbara, Valladares-Salgado, Adan, Wheeler, Eleanor, Raffel, Leslie J., Igase, Michiya, Province, Michael A., Rotimi, Charles N., Peyser, Patricia A., Pankow, James S., Wilson, James G., Sheu, Wayne H. H., Mook-Kanamori, Dennis O., Collins, Francis S., Paré, Guillaume, Shu, Xiao-Ou, Dupuis, Josee, Kato, Norihiro, Laakso, Markku, Wareham, Nicholas J., Kim, Bong-Jo, Stefansson, Kari, Goodarzi, Mark O., Mohlke, Karen L., Florez, Jose C., Zöllner, Sebastian, Mägi, Reedik, van Heel, David A., Finer, Sarah, Ng, Maggie C. Y., Sim, Xueling, Below, Jennifer E., Chang, Kyong-Mi, Meigs, James B., Mahajan, Anubha, Vujkovic, Marijana, Voight, Benjamin F., Morris, Andrew P.

    Veröffentlicht in Nature (London)

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    Rare genetic variants explain missing heritability in smoking von Jang, Seon-Kyeong, Evans, Luke, Fialkowski, Allison, Arnett, Donna K., Ashley-Koch, Allison E., Barnes, Kathleen C., Becker, Diane M., Bis, Joshua C., Blangero, John, Bleecker, Eugene R., Boorgula, Meher Preethi, Bowden, Donald W., Brody, Jennifer A., Cade, Brian E., Jenkins, Brenda W. Campbell, Carson, April P., Chavan, Sameer, Cupples, L. Adrienne, Custer, Brian, Damrauer, Scott M., David, Sean P., de Andrade, Mariza, Dinardo, Carla L., Fingerlin, Tasha E., Fornage, Myriam, Freedman, Barry I., Garrett, Melanie E., Gharib, Sina A., Glahn, David C., Haessler, Jeffrey, Heckbert, Susan R., Hokanson, John E., Hou, Lifang, Hwang, Shih-Jen, Hyman, Matthew C., Judy, Renae, Justice, Anne E., Kaplan, Robert C., Kardia, Sharon L. R., Kelly, Shannon, Kim, Wonji, Kooperberg, Charles, Levy, Daniel, Lloyd-Jones, Donald M., Loos, Ruth J. F., Manichaikul, Ani W., Gladwin, Mark T., Martin, Lisa Warsinger, Nouraie, Mehdi, Melander, Olle, Meyers, Deborah A., Montgomery, Courtney G., North, Kari E., Oelsner, Elizabeth C., Palmer, Nicholette D., Payton, Marinelle, Peljto, Anna L., Peyser, Patricia A., Preuss, Michael, Psaty, Bruce M., Qiao, Dandi, Rader, Daniel J., Rafaels, Nicholas, Redline, Susan, Reed, Robert M., Reiner, Alexander P., Rich, Stephen S., Rotter, Jerome I., Schwartz, David A., Shadyab, Aladdin H., Silverman, Edwin K., Smith, Nicholas L., Smith, J. Gustav, Smith, Albert V., Smith, Jennifer A., Tang, Weihong, Taylor, Kent D., Telen, Marilyn J., Vasan, Ramachandran S., Gordeuk, Victor R., Wang, Zhe, Wiggins, Kerri L., Yanek, Lisa R., Yang, Ivana V., Young, Kendra A., Young, Kristin L., Zhang, Yingze, Liu, Dajiang J., Keller, Matthew C., Vrieze, Scott

    Veröffentlicht in Nature human behaviour

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