Publications from Dr. Harald Grallert
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Fisher, E. ; Nitz, I. ; Gieger, C. ; Grallert, H. ; Gohlke, H. ; Lindner, I. ; Dahm, S. ; Boeing, H. ; Burwinkel, B. ; Rathmann, W. ; Wichmann, H.-E. ; Schrezenmeir, J. ; Illig, T. ; Döring, F.
Association of acyl-CoA-binding protein (ACBP) single nucleotide polymorphisms and type 2 diabetes in two German study populations.Nitz, I. ; Fisher, E. ; Grallert, H. ; Li, Y. ; Gieger, C. ; Rubin, D. ; Boeing, H. ; Spranger, J. ; Lindner, I. ; Schreiber, S. ; Rathmann, W. ; Gohlke, H. ; Döring, A. ; Wichmann, H.-E. ; Schrezenmeir, J. ; Döring, F. ; Illig, T.
Association of prostaglandin E synthase 2 (PTGES2) Arg298His polymorphism with type 2 diabetes in two German study populations.Hinney, A. ; Nguyen, T.T. ; Scherag, A. ; Friedel, S. ; Brönner, G. ; Müller, T.D. ; Grallert, H. ; Illig, T. ; Wichmann, H.-E. ; Rief, W. ; Schäfer, H. ; Hebebrand, J.
Genome wide association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants.Grallert, H. ; Sedlmeier, E.-M. ; Huth, C. ; Kolz, M. ; Heid, I.M. ; Meisinger, C. ; Herder, C. ; Strassburger, K. ; Gehringer, A. ; Haak, M. ; Giani, G. ; Kronenberg, F. ; Wichmann, H.-E. ; Adamski, J. ; Paulweber, B. ; Illig, T. ; Rathmann, W.
APOA5 variants and metabolic syndrome in Caucasians.Holzapfel, C. ; Klopp, N. ; Grallert, H. ; Huth, C. ; Gieger, C. ; Meisinger, C. ; Strassburger, K. ; Giani, G. ; Wichmann, H.-E. ; Laumen, H. ; Hauner, H. ; Herder, C. ; Rathmann, W. ; Illig, T.
Genetic variants in the leukemia-associated Rho guanine nucleotide exchange factor (ARHGEF12) gene are not associated with T2DM and related parameters in Caucasians (KORA study).Sedlmeier, E.-M. ; Grallert, H. ; Huth, C. ; Löwel, H. ; Herder, C. ; Strassburger, K. ; Giani, G. ; Wichmann, H.-E. ; Hauner, H. ; Illig, T. ; Rathmann, W.
Gene variants of monocyte chemoattractant protein 1 and components of metabolic syndrome in KORA S4, Augsburg.Marzi, C. ; Huth, C. ; Kolz, M. ; Grallert, H. ; Meisinger, C. ; Wichmann, H.-E. ; Rathmann, W. ; Herder, C. ; Illig, T.
Variants of the transcription factor 7-like 2 gene (TCF7L2) are strongly associated with type 2 diabetes but not with the metabolic syndrome in the MONICA/KORA surveys.