| Genetic diversity and population structure of 20 North European cattle breeds J Kantanen, I Olsaker, LE Holm, S Lien, J Vilkki, K Brusgaard, ... Journal of heredity 91 (6), 446-457, 2000 | 323 | 2000 |
| Vitamin D and diabetes: its importance for beta cell and immune function H Wolden-Kirk, L Overbergh, HT Christesen, K Brusgaard, C Mathieu Molecular and cellular endocrinology 347 (1-2), 106-120, 2011 | 296 | 2011 |
| The second activating glucokinase mutation (A456V) implications for glucose homeostasis and diabetes therapy HBT Christesen, BB Jacobsen, S Odili, C Buettger, A Cuesta-Munoz, ... Diabetes 51 (4), 1240-1246, 2002 | 260 | 2002 |
| Reduced expression of nuclear-encoded genes involved in mitochondrial oxidative metabolism in skeletal muscle of insulin-resistant women with polycystic ovary syndrome V Skov, D Glintborg, S Knudsen, T Jensen, TA Kruse, Q Tan, K Brusgaard, ... Diabetes 56 (9), 2349-2355, 2007 | 219 | 2007 |
| Hamartomatous polyposis syndromes: a review AM Jelsig, N Qvist, K Brusgaard, CB Nielsen, TP Hansen, LB Ousager Orphanet journal of rare diseases 9, 1-10, 2014 | 149 | 2014 |
| Phenotype presentation of hypophosphatemic rickets in adults SS Beck-Nielsen, K Brusgaard, LM Rasmussen, K Brixen, ... Calcified tissue international 87, 108-119, 2010 | 138 | 2010 |
| Clinical symptoms according to genotype amongst patients with hereditary haemorrhagic telangiectasia AD Kjeldsen, TR Møller, K Brusgaard, P Vase, PE Andersen Journal of internal medicine 258 (4), 349-355, 2005 | 127 | 2005 |
| Gene panel testing in epileptic encephalopathies and familial epilepsies RS Møller, LHG Larsen, KM Johannesen, I Talvik, T Talvik, U Vaher, ... Molecular syndromology 7 (4), 210-219, 2016 | 121 | 2016 |
| Activating glucokinase (GCK) mutations as a cause of medically responsive congenital hyperinsulinism: prevalence in children and characterisation of a novel GCK mutation. HBT Christesen, ND Tribble, A Molven, J Siddiqui, T Sandal, K Brusgaard, ... European Journal of Endocrinology 159 (1), 27-34, 2008 | 110 | 2008 |
| Update of variants identified in the pancreatic β‐cell KATP channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes E De Franco, C Saint‐Martin, K Brusgaard, AE Knight Johnson, ... Human mutation 41 (5), 884-905, 2020 | 105 | 2020 |
| The etiology of multiple sclerosis: genetic evidence for the involvement of the human endogenous retrovirus HERV-Fc1 BA Nexø, T Christensen, J Frederiksen, A Møller-Larsen, AB Oturai, ... PloS one 6 (2), e16652, 2011 | 89 | 2011 |
| Hyperinsulinemic hypoglycemia in Beckwith-Wiedemann syndrome due to defects in the function of pancreatic β-cell adenosine triphosphate-sensitive potassium channels K Hussain, KE Cosgrove, RM Shepherd, A Luharia, VV Smith, S Kassem, ... The Journal of Clinical Endocrinology & Metabolism 90 (7), 4376-4382, 2005 | 88 | 2005 |
| Significantly higher adrenocorticotropin-stimulated cortisol and 17-hydroxyprogesterone levels in 337 consecutive, premenopausal, caucasian, hirsute patients compared with … D Glintborg, AP Hermann, K Brusgaard, J Hangaard, C Hagen, ... The Journal of Clinical Endocrinology & Metabolism 90 (3), 1347-1353, 2005 | 85 | 2005 |
| Incidence, prevalence, etiology, and prognosis of first-time chronic pancreatitis in young patients: a nationwide cohort study M Joergensen, K Brusgaard, DG Crüger, AM Gerdes, OBS de Muckadell Digestive diseases and sciences 55, 2988-2998, 2010 | 80 | 2010 |
| Mutational analysis of PHEX, FGF23, DMP1, SLC34A3 and CLCN5 in patients with hypophosphatemic rickets SS Beck-Nielsen, K Brixen, J Gram, K Brusgaard Journal of human genetics 57 (7), 453-458, 2012 | 75 | 2012 |
| Genetic, epidemiological, and clinical aspects of hereditary pancreatitis: a population-based cohort study in Denmark MT Joergensen, K Brusgaard, DG Crüger, AM Gerdes, OSB de Muckadell Official journal of the American College of Gastroenterology| ACG 105 (8 …, 2010 | 70 | 2010 |
| Both low blood glucose and insufficient treatment confer risk of neurodevelopmental impairment in congenital hyperinsulinism: a multinational cohort study A Helleskov, M Melikyan, E Globa, I Shcherderkina, F Poertner, ... Frontiers in endocrinology 8, 156, 2017 | 68 | 2017 |
| Association of polycystic ovary syndrome susceptibility single nucleotide polymorphism rs2479106 and PCOS in Caucasian patients with PCOS or hirsutism as referral diagnosis MB Eriksen, K Brusgaard, M Andersen, Q Tan, ML Altinok, M Gaster, ... European Journal of Obstetrics & Gynecology and Reproductive Biology 163 (1 …, 2012 | 66 | 2012 |
| Serum glucagon counterregulatory hormonal response to hypoglycemia is blunted in congenital hyperinsulinism K Hussain, J Bryan, HT Christesen, K Brusgaard, L Aguilar-Bryan Diabetes 54 (10), 2946-2951, 2005 | 66 | 2005 |
| Transcriptional profiling of myotubes from patients with type 2 diabetes: no evidence for a primary defect in oxidative phosphorylation genes CM Frederiksen, K Højlund, L Hansen, EJ Oakeley, B Hemmings, ... Diabetologia 51, 2068-2077, 2008 | 65 | 2008 |
Qihua TanUniversity of Southern DenmarkVerified email at health.sdu.dk
