Treffer 1 - 20 von 51 für Suche 'Kerr, Annette M.', Suchdauer: 1,39s Treffer weiter einschränken
  1. 1
  2. 2
  3. 3
  4. 4
  5. 5
  6. 6
  7. 7
  8. 8

    Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels von Li, Yong, Wuttke, Matthias, Kirsten, Holger, Qiu, Chengxiang, Gorski, Mathias, Giri, Ayush, Li, Man, Noce, Damia, van der Most, Peter J., Horn, Katrin, Xu, Yizhe, Fuchsberger, Christian, Baptista, Daniela, Brumat, Marco, Campana, Eric, Campbell, Archie, Campbell, Harry, Carroll, Robert J., Catamo, Eulalia, Ciullo, Marina, Concas, Maria Pina, Coresh, Josef, De Grandi, Alessandro, Dittrich, Katalin, Eckardt, Kai-Uwe, Endlich, Karlhans, Evans, Michele K., Gieger, Christian, Gudbjartsson, Daniel F., Hicks, Andrew A., Hofer, Edith, Huang, Wei, Hutri-Kähönen, Nina, Hwang, Shih-Jen, Ikram, M. Arfan, Jakobsdottir, Johanna, Jonsson, Helgi, Joshi, Peter K., Josyula, Navya Shilpa, Jung, Bettina, Kähönen, Mika, Kamatani, Yoichiro, Kanai, Masahiro, Kooner, Jaspal S., Körner, Antje, Kovacs, Peter, Krämer, Bernhard K., Kronenberg, Florian, Kubo, Michiaki, Kühnel, Brigitte, Lange, Leslie A., Loeffler, Markus, Loos, Ruth J. F., Lyytikäinen, Leo-Pekka, Matsuda, Koichi, Meitinger, Thomas, Mishra, Pashupati P., Montgomery, Grant W., Müller-Nurasyid, Martina, Nadkarni, Girish N., Nolte, Ilja M., Noordam, Raymond, Perls, Thomas, Pirastu, Mario, Pistis, Giorgio, Ponte, Belen, Poulain, Tanja, Rabelink, Ton J., Rettig, Rainer, Rheinberger, Myriam, Rice, Kenneth M., Rudan, Igor, Rueedi, Rico, Ryan, Kathleen A., Saba, Yasaman, Shaffer, Christian M., Smith, Albert V., Stumvoll, Michael, Thiery, Joachim, Thio, Chris H. L., Thorsteinsdottir, Unnur, Uitterlinden, André G., Völker, Uwe, Waldenberger, Melanie, Whitfield, John B., Wilson, James F., Zonderman, Alan B., Wilson, James G., Ho, Kevin, Parsa, Afshin, Psaty, Bruce M., Böger, Carsten A., Butterworth, Adam S., Stefansson, Kari, Heid, Iris M., Hung, Adriana M., Teumer, Alexander, Pattaro, Cristian, Woodward, Owen M., Vitart, Veronique

    Veröffentlicht in Nature genetics

    Volltext
    Artikel
  9. 9
  10. 10
  11. 11
  12. 12
  13. 13
  14. 14
  15. 15
  16. 16
  17. 17
  18. 18
  19. 19

    Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk von Shrine, Nick, Chen, Jing, Packer, Richard, Hall, Robert J., Guyatt, Anna L., Batini, Chiara, Thompson, Rebecca J., Malik, Vidhi, Moll, Matthew, Tal-Singer, Ruth, Bakke, Per, Fawcett, Katherine A., John, Catherine, Piga, Noemi Nicole, Pozarickij, Alfred, Lin, Kuang, Chen, Zhengming, Li, Liming, Lahousse, Lies, Uitterlinden, Andre G., Oelsner, Elizabeth C., Rich, Stephen S., Kerr, Shona M., Vitart, Veronique, Brown, Michael R., Wielscher, Matthias, Imboden, Medea, Bartz, Traci M., Gharib, Sina A., Flexeder, Claudia, Karrasch, Stefan, Peters, Annette, Hu, Xiaowei, Ortega, Victor E., Meyers, Deborah A., Bleecker, Eugene R., Gupta, Namrata, Smith, Albert Vernon, Luan, Jian’an, Zhao, Jing-Hua, Hansen, Ailin F., Langhammer, Arnulf, Willer, Cristen, Bhatta, Laxmi, Porteous, David, Smith, Blair H., Lee, Jiwon, Daviglus, Martha L., Yu, Bing, Lim, Elise, Xu, Hanfei, O’Connor, George T., Thareja, Gaurav, Suhre, Karsten, Granell, Raquel, Faquih, Tariq O., Hiemstra, Pieter S., Hui, Jennie, James, Alan, Beilby, John, Hysi, Pirro, Koskela, Jukka T., Jin, Jianping, Sikdar, Sinjini, May-Wilson, Sebastian, Kentistou, Katherine A., Free, Robert C., Wang, Xueyang, Gilliland, Frank D., Chen, Zhanghua, Foong, Rachel E., Harris, Sarah E., Taylor, Adele, Redmond, Paul, Cook, James P., Lind, Lars, Lehtimäki, Terho, Pietiläinen, Kirsi H., Pennell, Craig E., Hall, Graham L., Gauderman, W. James, Wilson, James F., Laitinen, Tarja, Salomaa, Veikko, Timpson, Nicholas J., Zeggini, Eleftheria, Dupuis, Josée, Hayward, Caroline, Brumpton, Ben, Weiss, Stefan, Homuth, Georg, Probst-Hensch, Nicole, Jarvelin, Marjo-Riitta, Morrison, Alanna C., Sayers, Ian, Rawlins, Emma L., Strachan, David P., Walters, Robin G., Morris, Andrew P., Tobin, Martin D.

    Veröffentlicht in Nature genetics

    Volltext
    Artikel
  20. 20