Recent Publications

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The following papers have been supported by the CEED3 project:

Lead Author Other Authors Publication Title Date Publishedsort icon Journal Volume Pages
Lango H UK Type 2 Diabetes Genetics Consortium, Palmer CN, Morris AD, Zeggini E, Hattersley AT, McCarthy MI, Frayling TM, Weedon MN. Assessing the combined impact of 18 common genetic variants of modest effect sizes on type 2 diabetes risk June 2008 Diabetes Nov;57(11) 3129-35
Schwarz PE Li J, Lindstrom J, Tuomilehto J Tools for predicting the risk of type 2 diabetes in daily practice November 2008 Hormone and Metabolic Research Feb;41(2) 86-97
Schwarz PE Li J, Reimann M, Schutte AE, Bergmann A, Hanefeld M, Bornstein SR, Schulze J, Tuomilehto J, Lindström J The Finnish Diabetes Risk Score Is Associated with Insulin Resistance and Progression towards Type 2 Diabetes. December 2008 Journal of Clinical Endocrinology & Metabolism Mar;94(3) 920-6
Boj SF Servitja JM, Martin D, Rios M, Talianidis I, Guigo R, Ferrer J. Functional targets of the monogenic diabetes transcription factors HNF-1alpha and HNF-4alpha are highly conserved between mice and humans. February 2009 Diabetes May 2009;58(5) 1245-53
Pilgaard K The T allele of rs7903146 TCF7L2 is associated with impaired insulinotropic action of incretin hormones, reduced 24 h profiles of plasma insulin and glucagon, and increased hepatic glucose production in young healthy men. March 2009 Diabetologia Jul;52(7) 1298-307
Boj SF Servitja JM, Martin D, Rios M, Talianidis I, Guigo R, Ferrer J Functional targets of the monogenic diabetes transcription factors HNF-1apha and HNF-4alpha are high conserved between mice and humans May 2009 Diabetes 58(5) 1245-53
Klupa T Skupien J, Mirkiewicz-Sieradzka B, Gach A, Noczynska A, Szalecki M, Kozek E, Sieradzki J, Mlynarski W, Malecki MT Diabetic retinopathy in permanent neonatal diabetes due to Kir6.2 gene mutations: the results of a minimum 2-year follow-up after the transfer from insulin to sulphonylurea June 2009 Diabet Med 26(6) 663-4
Servitja JM Pignatelli M, Maestro MA, Cardalda C, Boj SF, Lozano J, Blanco E, Lafuente A, McCarthy MI, Sumoy L, Guigó R, Ferrer J Hnf1alpha (MODY3) controls tissue-specific transcriptional programs and exerts opposed effects on cell growth in pancreatic islets and liver June 2009 Mol Cell Biol 29(11) 2945-59
Servitja JM Hnf1alpha (MODY3) controls tissue-specific transcriptional programs and exerts opposed effects on cell growth in pancreatic islets and liver. June 2009 Molecular Cell Biology 2009 Jul;29(11) 2945-59
Cervin C Axler O, Holmkvist J, Almgren P, Rantala E, Tuomi T, Groop L, Dahlbäck B, Karlsson E. An investigation of serum concentration of apoM as a potential MODY3 marker using a novel ELISA. June 2009 Journal of International Medicine Mar 2009;267(3) 316-21
Pilgaard K Jensen CB, Schou JH, Lyssenko V, Wegner L, Brøns C, Vilsbøll T, Hansen T, Madsbad S, Holst JJ, Vølund A, Poulsen P, Groop L, Pedersen O, Vaag AA The T allele of rs7903146 TCF7L2 is associated with impaired insulintropic action of incretin hormones, reduced 24 h profiles of plasma insulin and glucagon, and increased hepatic glucose production in young health men July 2009 Diabetologia 52(7) 1298-307
Jonsson A, Isomaa B, Tuomi T, Taneera J, Salehi A, Nilsson P, Groop L, Lyssenko V. A variant in the KCNQ1 gene predicts future type 2 diabetes and mediates impaired insulin secretion. July 2009 Diabetes Oct 2009;58(10) 2409-13
Klupa T Skupien J, Mirkiewicz-Sieradzka B, Gach A, Noczynska A, Szalecki M, Kozek E, Sieradzki J, Mlynarski W, Malecki MT. Diabetic retinopathy in permanent neonatal diabetes due to Kir6.2 gene mutations: the results of a minimum 2-year follow-up after the transfer from insulin to sulphonylurea. July 2009 Diabetic Medicine Jun 2009;26(6); 663-4 663-4
Jafar-Mohammadi B Groves CJ, Owen KR, Frayling TM, Hattersley AT, McCarthy MI, Gloyn AL Low frequency variants in the exons only encoding isoform A of HNF1A do not contribute to susceptibility to type 2 diabetes August 2009 PLoS One 4(8) e6615
Jafar-Mohammadi B Groves CJ, Owen KR, Frayling TM, Hattersley AT, McCarthy MI, Gloyn AL. Low frequency variants in the exons only encoding isoform A of HNF1A do not contribute to susceptibility to type 2 diabetes. August 2009 PLoS One 2009 4(8) e6615