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| Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes A Molven, M Ringdal, AM Nordbø, H Ræder, J Støy, GM Lipkind, ... Diabetes 57 (4), 1131-1135, 2008 | 262 | 2008 |
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| Exome sequencing reveals FAM20c mutations associated with fibroblast growth factor 23–related hypophosphatemia, dental anomalies, and ectopic calcification SH Rafaelsen, H Ræder, AK Fagerheim, P Knappskog, TO Carpenter, ... Journal of Bone and Mineral Research 28 (6), 1378-1385, 2013 | 168 | 2013 |
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| A large multi-centre European study validates high-sensitivity C-reactive protein (hsCRP) as a clinical biomarker for the diagnosis of diabetes subtypes G Thanabalasingham, N Shah, M Vaxillaire, T Hansen, T Tuomi, ... Diabetologia 54, 2801-2810, 2011 | 138 | 2011 |
| Anatomy and evolution of database search engines—a central component of mass spectrometry based proteomic workflows K Verheggen, H Ræder, FS Berven, L Martens, H Barsnes, M Vaudel Mass spectrometry reviews 39 (3), 292-306, 2020 | 135 | 2020 |
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| Genetic analysis of recently identified type 2 diabetes loci in 1,638 unselected patients with type 2 diabetes and 1,858 control participants from a Norwegian population-based … JK Hertel, S Johansson, H Raeder, K Midthjell, V Lyssenko, L Groop, ... Diabetologia 51, 971-977, 2008 | 125 | 2008 |
| Diabetes and pancreatic exocrine dysfunction due to mutations in the carboxyl ester lipase gene-maturity onset diabetes of the young (CEL-MODY): a protein misfolding disease BB Johansson, J Torsvik, L Bjørkhaug, M Vesterhus, A Ragvin, E Tjora, ... Journal of Biological Chemistry 286 (40), 34593-34605, 2011 | 121 | 2011 |
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| A case of X-linked hypophosphatemic rickets: complications and the therapeutic use of cinacalcet H Ræder, N Shaw, C Netelenbos, R Bjerknes European Journal of Endocrinology 159 (Supplement_1), S101-S105, 2008 | 64 | 2008 |
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