Jørn V. Sagen

Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction

Helge Ræder, Stefan Johansson, Pål I. Holm et al. · Nature Genetics · 2005 · 377 citations

Medicine, Genetics, Molecular Genetics +13

Permanent Neonatal Diabetes due to Mutations in <i>KCNJ11</i> Encoding Kir6.2

Jørn V. Sagen, Helge Ræder, Eba Hathout et al. · Diabetes · 2004 · 334 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Permanent Neonatal Diabetes Caused by Glucokinase Deficiency

Pål R. Njølstad, Jørn V. Sagen, Lise Bjørkhaug et al. · Diabetes · 2003 · 194 citations

Medicine, Endocrinology, Genetics +17

SHORT Syndrome with Partial Lipodystrophy Due to Impaired Phosphatidylinositol 3 Kinase Signaling

Kishan Chudasama, Jonathon N. Winnay, Stefan Johansson et al. · The American Journal of Human Genetics · 2013 · 159 citations · Full text

Life Sciences, Biochemistry, Molecular Genetics +16

Switch from Stress Response to Homeobox Transcription Factors in Adipose Tissue After Profound Fat Loss

Simon N. Dankel, Dag Fadnes, Anne-Kristin Stavrum et al. · PLoS ONE · 2010 · 118 citations · Full text

Life Sciences, Molecular Biology, Molecular Genetics +17