Search Results - Skotte, G

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    Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women by Steinthorsdottir, Valgerdur, McGinnis, Ralph, Williams, Nicholas O., Stefansdottir, Lilja, Thorleifsson, Gudmar, Shooter, Scott, Fadista, João, Sigurdsson, Jon K., Auro, Kirsi M., Berezina, Galina, Borges, Maria-Carolina, Bumpstead, Suzannah, Bybjerg-Grauholm, Jonas, Colgiu, Irina, Dolby, Vivien A., Dudbridge, Frank, Engel, Stephanie M., Franklin, Christopher S., Frigge, Michael L., Frisbaek, Yr, Geirsson, Reynir T., Geller, Frank, Gretarsdottir, Solveig, Gudbjartsson, Daniel F., Harmon, Quaker, Hougaard, David Michael, Hegay, Tatyana, Helgadottir, Anna, Hjartardottir, Sigrun, Jääskeläinen, Tiina, Johannsdottir, Hrefna, Jonsdottir, Ingileif, Juliusdottir, Thorhildur, Kalsheker, Noor, Kasimov, Abdumadjit, Kemp, John P., Kivinen, Katja, Klungsøyr, Kari, Lee, Wai K., Melbye, Mads, Miedzybrodska, Zosia, Moffett, Ashley, Najmutdinova, Dilbar, Nishanova, Firuza, Olafsdottir, Thorunn, Perola, Markus, Pipkin, Fiona Broughton, Poston, Lucilla, Prescott, Gordon, Saevarsdottir, Saedis, Salimbayeva, Damilya, Scaife, Paula Juliet, Skotte, Line, Staines-Urias, Eleonora, Stefansson, Olafur A., Sørensen, Karina Meden, Thomsen, Liv Cecilie Vestrheim, Tragante, Vinicius, Trogstad, Lill, Simpson, Nigel A. B., Aripova, Tamara, Casas, Juan P., Dominiczak, Anna F., Walker, James J., Thorsteinsdottir, Unnur, Iversen, Ann-Charlotte, Feenstra, Bjarke, Lawlor, Deborah A., Boyd, Heather Allison, Magnus, Per, Laivuori, Hannele, Zakhidova, Nodira, Svyatova, Gulnara, Stefansson, Kari, Morgan, Linda

    Published in Nature communications
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    Associations of autozygosity with a broad range of human phenotypes by Mason, Dan, Pirastu, Nicola, Gandin, Ilaria, Lin, Kuang, Deelen, Patrick, Schurmann, Claudia, Baumbach, Clemens, Fuchsberger, Christian, Gao, He, Jia, Yucheng, van der Most, Peter J, Priyanka, Tallapragada Divya Sri, Salvi, Erika, Smart, Melissa C, Spracklen, Cassandra N, Verweij, Niek, Warren, Helen R, Yousri, Noha A, Zhao, Wei, Borja, Judith B, Bottinger, Erwin P, Broer, Linda, Concas, Maria Pina, Damulina, Anna, Daneshpour, Maryam S, Delgado, Graciela E, Freedman, Barry I, Goel, Anuj, Goodarzi, Mark O, Graff, Mariaelisa, Grodstein, Francine, Guo, Yu, Halevy, Avner, Höfer, Imo, Huang, Jinyan, Kanai, Masahiro, Kessler, Thorsten, Khor, Chiea Chuen, Kutalik, Zoltán, Launer, Lenore J, Lerch, Markus M, London, Stephanie J, Loomis, Stephanie, Luan, Jian’an, Manichaikul, Ani W, Meitinger, Thomas, Milani, Lili, Millwood, Iona Y, Ong, Ken K, Orozco, Lorena, Pattaro, Cristian, Pattie, Alison, Räikkönen, Katri, Ralhan, Sarju, van Rooij, Frank J A, Sabanayagam, Charumathi, van Setten, Jessica, Sever, Peter J, Shi, Yuan, Shrestha, Smeeta, Starr, John M, Tham, Yih-Chung, Tillander, Annika, Yuan, Jian-Min, Zhang, Liang, Bennett, David A, van den Berg, Leonard H, Berndt, Sonja I, Bielak, Lawrence F, Bouchard, Claude, Bradfield, Jonathan P, Brody, Jennifer A, Caulfield, Mark J, Cesarini, David, Eriksson, Johan G, Feitosa, Mary, Gieger, Christian, Goyette, Philippe, Gyllensten, Ulf, Hakonarson, Hakon, Hunt, Steven C, Jaddoe, Vincent W V, Karpe, Fredrik, März, Winfried, McCarthy, Mark I, Metspalu, Andres, Oldehinkel, Albertine J, Palmas, Walter, Pasterkamp, Gerard G, Porteous, David J, Rotimi, Charles, Sanghera, Dharambir K, Toniolo, Daniela, Wang, Carol A, Magnusson, Patrik K. E., Uitterlinden, André G, Franceschini, Nora, Hayward, Caroline, Walters, Robin G, Perry, John R. B.

    Published in Nature communications
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    Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes by Albrechtsen, A., Grarup, N., Li, Y., Sparsø, T., Cao, H., Jiang, T., Kim, S. Y., Korneliussen, T., Li, Q., Nie, C., Wu, R., Morris, A. P., Ladenvall, C., Cauchi, S., Stančáková, A., Andersen, G., Astrup, A., Banasik, K., Bennett, A. J., Bolund, L., Charpentier, G., Chen, Y., Dekker, J. M., Doney, A. S. F., Dorkhan, M., Forsen, T., Frayling, T. M., Gui, Y., Hallmans, G., Hattersley, A. T., He, K., Hitman, G. A., Holmkvist, J., Huang, S., Jiang, H., Jin, X., Justesen, J. M., Kristiansen, K., Kuusisto, J., Lajer, M., Lantieri, O., Li, W., Liao, Q., Liu, X., Ma, T., Ma, X., Marre, M., Mokrosiński, J., Morris, A. D., Mu, B., Nielsen, A. A., Nijpels, G., Nilsson, P., Palmer, C. N. A., Rayner, N. W., Renström, F., Ribel-Madsen, R., Robertson, N., Rolandsson, O., Rossing, P., Schwartz, T. W., Slagboom, P. E., Sterner, M., Tang, M., Tarnow, L., Tuomi, T., van’t Riet, E., van Leeuwen, N., Varga, T. V., Vestmar, M. A., Walker, M., Wang, B., Wang, Y., Wu, H., Xi, F., Yengo, L., Yu, C., Zhang, J., Zhang, Q., Zhang, W., Zheng, H., Zhou, Y., Altshuler, D., ‘t Hart, L. M., Franks, P. W., Balkau, B., Froguel, P., McCarthy, M. I., Laakso, M., Groop, L., Christensen, C., Brandslund, I., Lauritzen, T., Witte, D. R., Linneberg, A., Jørgensen, T., Hansen, T., Wang, J., Nielsen, R., Pedersen, O.

    Published in Diabetologia
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