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New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

by Jackson, Anne U, Wheeler, Eleanor, Bouatia-Naji, Nabila, Morris, Andrew P, Rybin, Denis, Thorleifsson, Gudmar, Steinthorsdottir, Valgerdur, Grallert, Harald, Dehghan, Abbas, Franklin, Christopher S, Song, Kijoung, Egan, Josephine M, Lajunen, Taina, Doney, Alex, Kanoni, Stavroula, Qi, Lu, Gieger, Christian, Payne, Felicity, Roccasecca, Rosa Maria, Sethupathy, Praveen, Balkau, Beverley, Barter, Philip, Beilby, John P, Benediktsson, Rafn, Bergmann, Sven, Bumpstead, Suzannah J, Chines, Peter, Cornelis, Marilyn, Day, Ian N M, de Geus, Eco J C, Dina, Christian, Erdos, Michael R, Fedson, Annette C, Fischer-Rosinsky, Antje, Graessler, Jürgen, Grundy, Scott, Hartikainen, Anna-Liisa, Hassanali, Neelam, Hayward, Caroline, Heath, Simon C, Herder, Christian, Hicks, Andrew A, Hillman, David R, Hingorani, Aroon D, Hui, Jennie, Isomaa, Bo, Johnson, Paul R V, Jula, Antti, Kaakinen, Marika, Kesaniemi, Y Antero, Kivimaki, Mika, Knight, Beatrice, Mahley, Robert, Mangino, Massimo, McAteer, Jarred B, McPherson, Ruth, Morken, Mario A, Mukherjee, Sutapa, Naitza, Silvia, Narisu, Narisu, Pattaro, Cristian, Pedersen, Nancy L, Pichler, Irene, Polasek, Ozren, Posthuma, Danielle, Province, Michael A, Psaty, Bruce M, Roden, Michael, Sanna, Serena, Sayer, Avan Aihie, Scheet, Paul, Scott, Laura J, Seedorf, Udo, Shields, Beverley, Simpson, Laila, Swift, Amy, Syvänen, Ann-Christine, Tanaka, Toshiko, Thorand, Barbara, Tichet, Jean, Varma, Dhiraj, Vitart, Veronique, Waeber, Gérard, Walley, Andrew, Walters, G Bragi, Wild, Sarah H, Zelenika, Diana, Zhai, Guangju, Zillikens, M Carola, Meneton, Pierre, Magnusson, Patrik K E, Salomaa, Veikko, Schwarz, Peter, Karpe, Fredrik, Dedoussis, George V, Kuusisto, Johanna, Pedersen, Oluf, Pramstaller, Peter Paul, Wichmann, H Erich, Stumvoll, Michael
Published in Nature genetics (01.02.2010)

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Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases

by Coppola, Giovanni, Chinnathambi, Subashchandrabose, Lee, Jason JiYong, Dombroski, Beth A., Baker, Matt C., Soto-Ortolaza, Alexandra I., Lee, Suzee E., Klein, Eric, Huang, Alden Y., Sears, Renee, Lane, Jessica R., Karydas, Anna M., Kenet, Robert O., Biernat, Jacek, Wang, Li-San, Cotman, Carl W., DeCarli, Charles S., Levey, Allan I., Ringman, John M., Mendez, Mario F., Chui, Helena C., Le Ber, Isabelle, Brice, Alexis, Lupton, Michelle K., Preza, Elisavet, Lovestone, Simon, Powell, John, Graff-Radford, Neill, Petersen, Ronald C., Boeve, Bradley F., Lippa, Carol F., Bigio, Eileen H., Mackenzie, Ian, Finger, Elizabeth, Kertesz, Andrew, Caselli, Richard J., Gearing, Marla, Juncos, Jorge L., Ghetti, Bernardino, Spina, Salvatore, Bordelon, Yvette M., Tourtellotte, Wallace W., Frosch, Matthew P., Vonsattel, Jean Paul G., Zarow, Chris, Beach, Thomas G., Albin, Roger L., Lieberman, Andrew P., Lee, Virginia M., Trojanowski, John Q., Van Deerlin, Vivianna M., Bird, Thomas D., Galasko, Douglas R., Masliah, Eliezer, White, Charles L., Troncoso, Juan C., Hannequin, Didier, Boxer, Adam L., Geschwind, Michael D., Kumar, Satish, Mandelkow, Eva-Maria, Wszolek, Zbigniew K., Uitti, Ryan J., Dickson, Dennis W., Haines, Jonathan L., Mayeux, Richard, Pericak-Vance, Margaret A., Farrer, Lindsay A., Ross, Owen A., Rademakers, Rosa, Schellenberg, Gerard D., Miller, Bruce L., Mandelkow, Eckhard, Geschwind, Daniel H.
Published in Human molecular genetics (01.08.2012)

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