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  1. No Access

    Article

    Genetic risk scores for body fat distribution attenuate weight loss in women during dietary intervention

    The well-established link between body fat distribution and metabolic health has been suggested to act through an impact on the remodeling capacity of the adipose tissue. Remodeling of the adipose tissue has b...

    M Svendstrup, K H Allin, T I A Sørensen, T H Hansen in International Journal of Obesity (2018)

  2. No Access

    Article

    Association studies of genetic scores of serum vitamin B12 and folate levels with symptoms of depression and anxiety in two danish population studies

    Observational studies have suggested low serum levels of vitamin B12 or folate to be risk factors of depression and anxiety. However, these results may be biased by confounding and reverse causation. Mendelian...

    L T Møllehave, T Skaaby, K S Simonsen in European Journal of Clinical Nutrition (2017)

  3. No Access

    Article

    Mendelian randomisation study of the associations of vitamin B12 and folate genetic risk scores with blood pressure and fasting serum lipid levels in three Danish population-based studies

    The aim was to examine the association of genetic risk scores (GRSs) of vitamin B12 and folate-associated variants with blood pressure and lipids.

    L L N Husemoen, T Skaaby, B H Thuesen, N Grarup in European Journal of Clinical Nutrition (2016)

  4. Article

    Open Access

    EHMTI-0380. The association of migraine susceptibility loci with severe migraine characteristics in a clinic-based migraine sample

    A Esserlind, AF Christensen, S Steinberg, N Grarup in The Journal of Headache and Pain (2014)

  5. Article

    Open Access

    Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes

    Human complex metabolic traits are in part regulated by genetic determinants. Here we applied exome sequencing to identify novel associations of coding polymorphisms at minor allele frequencies (MAFs) >1% with...

    A. Albrechtsen, N. Grarup, Y. Li, T. Sparsø, G. Tian, H. Cao, T. Jiang in Diabetologia (2013)

  6. Article

    Common variation in oxidative phosphorylation genes is not a major cause of insulin resistance or type 2 diabetes

    There is substantial evidence that mitochondrial dysfunction is linked to insulin resistance and is present in several tissues relevant to the pathogenesis of type 2 diabetes. Here, we examined whether common ...

    L. S. Snogdal, M. Wod, N. Grarup, M. Vestmar, T. Sparsø, T. Jørgensen in Diabetologia (2012)

  7. Article

    Association studies of novel obesity-related gene variants with quantitative metabolic phenotypes in a population-based sample of 6,039 Danish individuals

    Genome-wide association studies have identified novel WHR and BMI susceptibility loci. The aim of this study was to elucidate if any of these loci had an effect on quantitative measures of glucose homeostasis,...

    K. S. Burgdorf, A. P. Gjesing, N. Grarup, J. M. Justesen, C. H. Sandholt in Diabetologia (2012)

  8. Article

    Homozygous carriers of the G allele of rs4664447 of the glucagon gene (GCG) are characterised by decreased fasting and stimulated levels of insulin, glucagon and glucagon-like peptide (GLP)-1

    The glucagon gene (GCG) encodes several hormones important for energy metabolism: glucagon, oxyntomodulin and glucagon-like peptide (GLP)-1 and -2. Variants in GCG may associate with type 2 diabetes, obesity and/...

    S. S. Torekov, L. Ma, N. Grarup, B. Hartmann, I. A. Hainerová, U. Kielgast in Diabetologia (2011)

  9. Article

    Erratum to: Type 2 diabetes risk allele near CENTD2 is associated with decreased glucose-stimulated insulin release

    T. Nielsen, T. Sparsø, N. Grarup, T. Jørgensen, C. Pisinger, D. R. Witte in Diabetologia (2011)

  10. Article

    Type 2 diabetes risk allele near CENTD2 is associated with decreased glucose-stimulated insulin release

    By combining multiple genome-wide association (GWA) studies and comprehensive replication efforts, 12 novel type 2 diabetes associated loci have recently been discovered. Here we evaluate the effect of lead va...

    T. Nielsen, T. Sparsø, N. Grarup, T. Jørgensen, C. Pisinger, D. R. Witte in Diabetologia (2011)

  11. Article

    The diabetogenic VPS13C/C2CD4A/C2CD4B rs7172432 variant impairs glucose-stimulated insulin response in 5,722 non-diabetic Danish individuals

    A genome-wide association study in the Japanese population reported two genome-wide significant loci associated with type 2 diabetes of which the VPS13C/C2CD4A/C2CD4B locus was replicated in Europeans. We looked ...

    N. Grarup, M. Overvad, T. Sparsø, D. R. Witte, C. Pisinger, T. Jørgensen in Diabetologia (2011)

  12. Article

    Glucose tolerance, insulin sensitivity and insulin release in European non-diabetic carriers of a polymorphism upstream of CDKN2A and CDKN2B

    The aim of this study was to investigate the association of the rs10811661 polymorphism near the CDKN2B/CDKN2A genes with glucose tolerance, insulin sensitivity and insulin release in three samples of white peopl...

    M. L. Hribal, I. Presta, T. Procopio, M. A. Marini, A. Stančáková in Diabetologia (2011)

  13. Article

    Carriers of the TCF7L2 rs7903146 TT genotype have elevated levels of plasma glucose, serum proinsulin and plasma gastric inhibitory polypeptide (GIP) during a meal test

    The transcription factor 7-like 2 (TCF7L2) rs7903146 T allele associates with type 2 diabetes in several populations, possibly mediated via decreased incretin secretion and/or action and altered beta and alpha ce...

    A. P. Gjesing, L. L. Kjems, M. A. Vestmar, N. Grarup, A. Linneberg in Diabetologia (2011)

  14. Article

    Type 2 diabetes risk alleles near ADCY5, CDKAL1 and HHEX-IDE are associated with reduced birthweight

    The fetal insulin hypothesis suggests that variation in the fetal genotype influencing insulin secretion or action may predispose to low birthweight and type 2 diabetes. We examined associations between 25 con...

    E. A. Andersson, K. Pilgaard, C. Pisinger, M. N. Harder, N. Grarup in Diabetologia (2010)

  15. Article

    Variants at DGKB/TMEM195, ADRA2A, GLIS3 and C2CD4B loci are associated with reduced glucose-stimulated beta cell function in middle-aged Danish people

    A meta-analysis of 21 genome-wide association studies identified 11 novel genetic loci implicated in fasting glucose homeostasis. We aimed to evaluate the impact of these variants on insulin release and insuli...

    T. W. Boesgaard, N. Grarup, T. Jørgensen, K. Borch-Johnsen, T. Hansen in Diabetologia (2010)

  16. Article

    A variant in the G6PC2/ABCB11 locus is associated with increased fasting plasma glucose, increased basal hepatic glucose production and increased insulin release after oral and intravenous glucose loads

    An association between elevated fasting plasma glucose and the common rs560887 G allele in the G6PC2/ABCB11 locus has been reported. In Danes we aimed to examine rs560887 in relation to plasma glucose and serum i...

    C. S. Rose, N. Grarup, N. T. Krarup, P. Poulsen, L. Wegner, T. Nielsen in Diabetologia (2009)

  17. Article

    Combined analysis of 19 common validated type 2 diabetes susceptibility gene variants shows moderate discriminative value and no evidence of gene–gene interaction

    The list of validated type 2 diabetes susceptibility variants has recently been expanded from three to 19. The variants identified are common and have low penetrance in the general population. The aim of the s...

    T. Sparsø, N. Grarup, C. Andreasen, A. Albrechtsen, J. Holmkvist in Diabetologia (2009)

  18. Article

    Variation in the peroxisome proliferator-activated receptor δ gene in relation to common metabolic traits in 7,495 middle-aged white people

    Studies in animals reveal that peroxisome proliferator-activated receptor δ (PPARδ) regulates glucose metabolism and insulin sensitivity in both the liver and skeletal muscles. Moreover, PPARδ augments physical e...

    N. Grarup, A. Albrechtsen, J. Ek, K. Borch-Johnsen, T. Jørgensen in Diabetologia (2007)

  19. No Access

    Article

    Genetic analysis of the estrogen-related receptor α and studies of association with obesity and type 2 diabetes

    The estrogen-related receptor α (ERRα or NR3B1) is a transcription factor from the nuclear receptor super-family, group III. The gene encoding ERRα (ESRRA) is located on chromosome 11q13, a region showing genetic...

    L H Larsen, C S Rose, T Sparsø, J Overgaard in International Journal of Obesity (2007)

  20. Article

    Studies of the relationship between the ENPP1 K121Q polymorphism and type 2 diabetes, insulin resistance and obesity in 7,333 Danish white subjects

    Plasma cell membrane glycoprotein 1 (PC-1) inhibits insulin signalling by direct interaction with the insulin receptor α subunit. This inhibition is enhanced by the minor Q allele of the K121Q polymorphism (rs...

    N. Grarup, S. A. Urhammer, J. Ek, A. Albrechtsen, C. Glümer in Diabetologia (2006)

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