Genetic Examination of SETD7 and SUV39H1/H2 Methyltransferases and the Risk of Diabetes Complications in Patients With Type 1 Diabetes

Por Syreeni, Anna, El-Osta, Assam, Forsblom, Carol, Sandholm, Niina, Parkkonen, Maikki, Tarnow, Lise, Parving, Hans-Henrik, McKnight, Amy J., Maxwell, Alexander P., Cooper, Mark E., Groop, Per-Henrik
Publicado em 2011

Association of Genetic Variants at 3q22 with Nephropathy in Patients with Type 1 Diabetes Mellitus

Por He, Bing, Österholm, Anne-May, Hoverfält, Anna, Forsblom, Carol, Hjörleifsdóttir, Eyrún Edda, Nilsson, Ann-Sofie, Parkkonen, Maikki, Pitkäniemi, Janne, Hreidarsson, Ástrádur, Sarti, Cinzia, McKnight, Amy Jayne, Maxwell, A. Peter, Tuomilehto, Jaakko, Groop, Per-Henrik, Tryggvason, Karl
Publicado em 2009

G/T Substitution in Intron 1 of the UNC13B Gene Is Associated With Increased Risk of Nephropathy in Patients With Type 1 Diabetes

Por Trégouet, David-Alexandre, Groop, Per-Henrik, McGinn, Steven, Forsblom, Carol, Hadjadj, Samy, Marre, Michel, Parving, Hans-Henrik, Tarnow, Lise, Telgmann, Ralph, Godefroy, Tiphaine, Nicaud, Viviane, Rousseau, Rachel, Parkkonen, Maikki, Hoverfält, Anna, Gut, Ivo, Heath, Simon, Matsuda, Fumihiko, Cox, Roger, Kazeem, Gbenga, Farrall, Martin, Gauguier, Dominique, Brand-Herrmann, Stefan-Martin, Cambien, François, Lathrop, Mark, Vionnet, Nathalie
Publicado em 2008