Unraveling the effects of 1,25(OH)2D3 on global gene expression in pancreatic islets von Wolden-Kirk, H., Overbergh, L., Gysemans, C., Brusgaard, K., Naamane, N., Van Lommel, L., Schuit, F., Eizirik, D.L., Christesen, H., Mathieu, C.

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Whole genome sequencing identifies rare variants enriched in cancer related genes in first-degree relatives of familial pancreatic cancer von Tan, M., Brusgaard, K., Gerdes, A.A., Mortensen, M.B., Detlefsen, S., Schaffalitzky deMuckadell, O.B., Joergensen, M.T.

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JP-HHT phenotype in Danish patients with SMAD4 mutations von Jelsig, A. M., Tørring, P. M., Kjeldsen, A. D., Qvist, N., Bojesen, A., Jensen, U. B., Andersen, M. K., Gerdes, A. M., Brusgaard, K., Ousager, L. B.

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Heredity of familial pancreatic cancer in a Danish national family cohort von Tan, M., Brusgaard, K., Gerdes, A., Mortensen, M., Detlefsen, S., Schaffalitzky De Muckadell, O., Joergensen, M.

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National mutation study among Danish patients with hereditary haemorrhagic telangiectasia von Tørring, P.M., Brusgaard, K., Ousager, L.B., Andersen, P.E., Kjeldsen, A.D.

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Disease pattern in Danish patients with Peutz-Jeghers syndrome von Jelsig, A. M., Qvist, N., Sunde, L., Brusgaard, K., Hansen, Tvo, Wikman, F. P., Nielsen, C. B., Nielsen, I. K., Gerdes, A. M., Bojesen, A., Ousager, L. B.

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Transcriptional profiling of myotubes from patients with type 2 diabetes: no evidence for a primary defect in oxidative phosphorylation genes von Frederiksen, C. M, Højlund, K, Hansen, L, Oakeley, E. J, Hemmings, B, Abdallah, B. M, Brusgaard, K, Beck-Nielsen, H, Gaster, M

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Discovery of Molecular Pathways Mediating 1,25-Dihydroxyvitamin D3 Protection Against Cytokine-Induced Inflammation and Damage of Human and Male Mouse Islets of Langerhans von Wolden-Kirk, H, Rondas, D, Bugliani, M, Korf, H, Van Lommel, L, Brusgaard, K, Christesen, H.T, Schuit, F, Proost, P, Masini, M, Marchetti, P, Eizirik, D.L, Overbergh, L, Mathieu, C

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Intraoperative ultrasound imaging in the surgical treatment of congenital hyperinsulinism: prospective, blinded study von Bjarnesen, A P, Dahlin, P, Globa, E, Petersen, H, Brusgaard, K, Rasmussen, L, Melikian, M, Detlefsen, S, Christesen, H T, Mortensen, M B

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Clinical symptoms according to genotype amongst patients with hereditary haemorrhagic telangiectasia von KJELDSEN, A. D., MØLLER, T. R., BRUSGAARD, K., VASE, P., ANDERSEN, P. E.

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Non-insulinoma persistent hyperinsulinaemic hypoglycaemia caused by an activating glucokinase mutation: hypoglycaemia unawareness and attacks von Christesen, H. B. T., Brusgaard, K., Beck Nielsen, H., Brock Jacobsen, B.

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Hyperinsulinemic Hypoglycemia in Beckwith-Wiedemann Syndrome due to Defects in the Function of Pancreatic β-Cell Adenosine Triphosphate-Sensitive Potassium Channels von Hussain, K., Cosgrove, K. E., Shepherd, R. M., Luharia, A., Smith, V. V., Kassem, S., Gregory, J. W., Sivaprasadarao, A., Christesen, H. T., Jacobsen, B. B., Brusgaard, K., Glaser, B., Maher, E. A., Lindley, K. J., Hindmarsh, P., Dattani, M., Dunne, M. J.

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Significantly Higher Adrenocorticotropin-Stimulated Cortisol and 17-Hydroxyprogesterone Levels in 337 Consecutive, Premenopausal, Caucasian, Hirsute Patients Compared with Healthy... von Glintborg, D., Hermann, A. P., Brusgaard, K., Hangaard, J., Hagen, C., Andersen, M.

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Genetic diversity and population structure of 20 north European cattle breeds von Kantanen, J, Olsaker, I, Holm, L-E, Lien, S, Vilkki, J, Brusgaard, K, Eythorsdottir, E, Danell, B, Adalsteinsson, S

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The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy von Sandal, T, Laborie, LB, Brusgaard, K, Eide, SÅ, Christesen, HBT, Søvik, O, Njølstad, PR, Molven, A

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Mutations in endoglin and in activin receptor-like kinase 1 among Danish patients with hereditary haemorrhagic telangiectasia von Brusgaard, K, Kjeldsen, AD, Poulsen, L, Moss, H, Vase, P, Rasmussen, K, Kruse, TA, Hørder, M

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Hereditary pancreatitis caused by a three amino-acid insertion within the activation peptide of human cationic trypsinogen ( PRSS1 ) von Geisz, A, Joergensen, M.T, Brusgaard, K, Schaffalitzky de Muckadell, O.B, Gerdes, A.-M, Hegyi, P, Sahin-Tóth, M

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18F-DOPA PET/CT and 68Ga-DOTANOC PET/CT scans as diagnostic tools in focal congenital hyperinsulinism: a blinded evaluation von Christiansen, Charlotte Dahl, Petersen, Henrik, Nielsen, Anne Lerberg, Detlefsen, Sönke, Brusgaard, Klaus, Rasmussen, Lars, Melikyan, Maria, Ekström, Klas, Globa, Evgenia, Rasmussen, Annett Helleskov, Hovendal, Claus, Christesen, Henrik Thybo

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Effect of insulin on protein phosphatase 2A expression in muscle in type 2 diabetes von Højlund, K., Poulsen, M., Staehr, P., Brusgaard, K., Beck-Nielsen, H.

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Incidence of nutritional and hereditary rickets among children living in Denmark von Beck-Nielsen, S, Jensen, T, Gram, J, Brixen, K, Brusgaard, K, Brock-Jacobsen, B

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