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    Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes von Dornbos, Peter, Chaffin, Mark D., Liu, Dajiang J., Wang, Minxian, Park, Joseph, Aguilar-Salinas, Carlos A., Arnett, Donna K., Barajas-Olmos, Francisco, Barzilai, Nir, Bielak, Lawrence F., Bis, Joshua C., Blangero, John, Boerwinkle, Eric, Bottinger, Erwin, Brody, Jennifer A., Broome, Jai G., Burtt, Noël P., Cade, Brian E., Chang, Yi-Cheng, Chen, Yii-Der I., Choi, Won Jung, Contreras-Cubas, Cecilia, Curran, Joanne E., de Vries, Paul S., DeFronzo, Ralph A., Doddapaneni, Harsha, Duggirala, Ravindranath, Dutcher, Susan K., Emery, Leslie S., Freedman, Barry I., García-Ortiz, Humberto, Gibbs, Richard A., Glaser, Benjamin, Gonzalez, Clicerio, Gonzalez-Villalpando, Maria Elena, Graff, Mariaelisa, Grarup, Niels, Gupta, Namrata, Hansen, Torben, Hung, Yi-Jen, Hwang, Mi Yeong, Irvin, Marguerite R., Kang, Hyun Min, Kardia, Sharon L.R., Kelly, Tanika, Khan, Alyna T., Kim, Bong-Jo, Kim, Young Jin, Lange, Leslie A., Lee, Juyoung, Lee, Seonwook, Lehman, Donna M., Linneberg, Allan, Liu, Jianjun, Lyssenko, Valeriya, Ma, Ronald C.W., Martínez-Hernández, Angélica, Mathias, Rasika A., Meigs, James B., Meitinger, Thomas, Metcalf, Ginger A., Mi, Xuenan, Mohlke, Karen L., Montasser, May E., Moon, Jee-Young, Morrison, Alanna C., Muzny, Donna M., Nelson, Sarah C., Nilsson, Peter M., O’Connell, Jeffrey R., Palmer, Nicholette D., Park, Cheol Joo, Peralta, Juan M., Peyser, Patricia A., Preuss, Michael, Qi, Qibin, Rao, D.C., Reiner, Alexander P., Rich, Stephen S., Samani, Nilesh, Schurmann, Claudia, Seo, Daekwan, Seo, Jeong-Sun, Sim, Xueling, Sladek, Rob, So, Wing Yee, Stilp, Adrienne M., Taylor, Kent D., Teo, Yik Ying, Tsai, Michael Y., Vasan, Ramachandran S., Watkins, Hugh, Weeks, Daniel E., Wilson, James G., Yanek, Lisa R., Rader, Daniel J., Rotter, Jerome I., McCarthy, Mark I., Flannick, Jason A., Khera, Amit V.


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