Janne Molnes

Activating Mutations in the Gene Encoding the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal Diabetes

Anna L. Gloyn, Ewan R. Pearson, Jennifer F. Antcliff et al. · New England Journal of Medicine · 2004 · 1.1K citations

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

Permanent Neonatal Diabetes Caused by Glucokinase Deficiency

Pål R. Njølstad, Jørn V. Sagen, Lise Bjørkhaug et al. · Diabetes · 2003 · 191 citations

Genetic Disorder, Genetics, Diabetes +13

Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes

Jason Flannick, Nicola L. Beer, Alexander G. Bick et al. · Nature Genetics · 2013 · 139 citations

Allelic Variant, Phenotypic Variation, Genetic Determinant +13

Targeted next-generation sequencing reveals MODY in up to 6.5% of antibody-negative diabetes cases listed in the Norwegian Childhood Diabetes Registry

Bente B. Johansson, Henrik Irgens, Janne Molnes et al. · Diabetologia · 2016 · 124 citations · Full text

Sequencing, Medicine, Next-generation Sequencing +10