Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry von Irgens, H. U., Molnes, J., Johansson, B. B., Ringdal, M., Skrivarhaug, T., Undlien, D. E., Søvik, O., Joner, G., Molven, A., Njølstad, P. R.

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Clinical and molecular characterization of neonatal diabetes and monogenic syndromic diabetes in Asian Indian children von Jahnavi, S, Poovazhagi, V, Mohan, V, Bodhini, D, Raghupathy, P, Amutha, A, Suresh Kumar, P, Adhikari, P, Shriraam, M, Kaur, T, Das, AK, Molnes, J, Njolstad, PR, Unnikrishnan, R, Radha, V

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Independent mutational events in the hypervariable region of the carboxyl ester lipase gene: Identification of two new CEL-MODY families from Sweden and the Czech Republic von El Jellas, K., Dušátková, P., Molnes, J., Haldorsen, I., Tjora, E., Johansson, B., Fjeld, K., Johansson, S., Ů, Prúhová, Groop, L., Njølstad, P., Molven, A.

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The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes von Sagen, J.V., Bjørkhaug, L., Haukanes, B.I., Grevle, L., Molnes, J., Nedrebø, B.G., Søvik, O., Njølstad, P.R., Johansson, S., Molven, A.

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Two New Mutations in the CEL Gene Causing Diabetes and Hereditary Pancreatitis: How to Correctly Identify MODY8 Cases von El Jellas, Khadija, Dušátková, Petra, Haldorsen, Ingfrid S, Molnes, Janne, Tjora, Erling, Johansson, Bente B, Fjeld, Karianne, Johansson, Stefan, Průhová, Štěpánka, Groop, Leif, Löhr, J Matthias, Njølstad, Pål R, Molven, Anders

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Activating Mutations in the Gene Encoding the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal Diabetes von Gloyn, Anna L, Pearson, Ewan R, Antcliff, Jennifer F, Proks, Peter, Bruining, G. Jan, Slingerland, Annabelle S, Howard, Neville, Srinivasan, Shubha, Silva, José M.C.L, Molnes, Janne, Edghill, Emma L, Frayling, Timothy M, Temple, I. Karen, Mackay, Deborah, Shield, Julian P.H, Sumnik, Zdenek, van Rhijn, Adrian, Wales, Jerry K.H, Clark, Penelope, Gorman, Shaun, Aisenberg, Javier, Ellard, Sian, Njølstad, Pål R, Ashcroft, Frances M, Hattersley, Andrew T

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Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: Patient characteristics and initial response to sulfonylurea therapy von SAGEN, Jørn V, RAEDER, Helge, GLOYN, Anna L, HATTERSLEY, Andrew T, MOLVEN, Anders, SØVIK, Oddmund, NJØLSTAD, Pal R, HATHOUT, Eba, SHEHADEH, Naim, GUDMUNDSSON, Kolbeinn, BAEVRE, Halvor, ABUELO, Dianne, PHORNPHUTKUL, Chanika, MOLNES, Janne, BELL, Graeme I

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Permanent neonatal diabetes caused by glucokinase deficiency: Inborn error of the glucose-insulin signaling pathway von NJØLSTAD, Pal R, SAGEN, Jørn V, SØVIK, Oddmund, MATSCHINSKY, Franz M, BJØRKHAUG, Lise, ODILI, Stella, SHEHADEH, Naim, BAKRY, Doua, SARICI, S. Umit, ALPAY, Faruk, MOLNES, Janne, MOLVEN, Anders

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Kir6.2 mutations causing neonatal diabetes provide new insights into Kir6.2-SUR1 interactions von Tammaro, Paolo, Girard, Christophe, Molnes, Janne, Njølstad, Pål R, Ashcroft, Frances M

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Epidermal Growth Factor Receptor Efficiently Activates Mitogen-Activated Protein Kinase in HeLa Cells and Hep2 Cells Conditionally Defective in Clathrin-Dependent Endocytosis von Johannessen, Lene Elisabeth, Ringerike, Tove, Molnes, Janne, Madshus, Inger Helene

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The Impact of the West Africa Ebola Outbreak on Obstetric Health Care in Sierra Leone von Brolin Ribacke, Kim J, van Duinen, Alex J, Nordenstedt, Helena, Höijer, Jonas, Molnes, Ragnhild, Froseth, Torunn Wigum, Koroma, A P, Darj, Elisabeth, Bolkan, Håkon Angel, Ekström, AnnaMia

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Activating Mutations in the Gene Encoding the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal Diabetes von Gloyn, A.L, Pearson, E.R, Antcliff, J.F, Proks, P, Bruining, G.J, Slingerland, A.S, Howard, N, Srinivasan, S, Silva, J.M.C.L, Molnes, J, Edghill, E.L, Frayling, T.M, Temple, K, Mackay, D, Shield, J.P.H, Sumnik, Z, van Rhijn, A, Wales, J.K.H, Clark, P, Gorman, S, Aisenberg, J, Ellard, S, Njolstad, P.R, Ashcroft, F.M, Hattersley, A.T

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Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes von Flannick, Jason, Beer, Nicola L, Bick, Alexander G, Agarwala, Vineeta, Molnes, Janne, Gupta, Namrata, Burtt, Noël P, Florez, Jose C, Meigs, James B, Taylor, Herman, Lyssenko, Valeriya, Irgens, Henrik, Fox, Ervin, Burslem, Frank, Johansson, Stefan, Brosnan, M Julia, Trimmer, Jeff K, Newton-Cheh, Christopher, Tuomi, Tiinamaija, Molven, Anders, Wilson, James G, O'Donnell, Christopher J, Kathiresan, Sekar, Hirschhorn, Joel N, Njølstad, Pål R, Rolph, Tim, Seidman, J G, Gabriel, Stacey, Cox, David R, Seidman, Christine E, Groop, Leif, Altshuler, David

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Unsupervised Clustering of Missense Variants in HNF1A Using Multidimensional Functional Data Aids Clinical Interpretation von Althari, Sara, Najmi, Laeya A., Bennett, Amanda J., Aukrust, Ingvild, Rundle, Jana K., Colclough, Kevin, Molnes, Janne, Kaci, Alba, Nawaz, Sameena, van der Lugt, Timme, Hassanali, Neelam, Mahajan, Anubha, Molven, Anders, Ellard, Sian, McCarthy, Mark I., Bjørkhaug, Lise, Njølstad, Pål Rasmus, Gloyn, Anna L.

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In Vitro Functional Analysis Can Aid Precision Diagnostics of HNF1B-MODY von Pavithram, Aishwarya, Zhang, Haichen, Maloney, Kristin A., Ringdal, Monika, Kaci, Alba, Sagen, Jørn V., Kleinberger, Jeffrey, Jeng, Linda J.B., Njølstad, Pål R., Pollin, Toni I., Molnes, Janne, Johansson, Bente B.

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Interfacial and rheological properties of gelatin based solid emulsions prepared with acid or alkali pretreated gelatins von Hattrem, Magnus N., Molnes, Silje, Haug, Ingvild J., Draget, Kurt I.

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Unsupervised clustering of missense variants in HNF1A using multidimensional functional data aids clinical interpretation von Althari, Sara, Najmi, Laeya Abdoli, Bennett, Amanda J., Aukrust, Ingvild, Rundle, Jana K., Colclough, Kevin, Molnes, Janne, Kaci, Alba, Nawaz, Sameena, van der Lugt, Timme, Hassanali, Neelam, Mahajan, Anubha, Molven, Anders, Ellard, Sian, McCarthy, Mark I., Bjørkhaug, Lise, Njølstad, Pål Rasmus, Gloyn, Anna L.

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Importance of liver biopsy findings in immunosuppression management: Biopsy monitoring and working criteria for patients with operational tolerance von Demetris, Anthony

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Two New Mutations in the CEL Gene Causing Diabetes and Hereditary Pancreatitis: How to Correctly Identify MODY8 Cases von Jellas, Khadija el, Dušátková, Petra, Haldorsen, Ingfrid S, Molnes, Janne, Tjora, Erling, Johansson, Bente Berg, Fjeld, Karianne, Johansson, Stefan, Průhová, Štěpánka, Groop, Leif, Löhr, J. Matthias, Njølstad, Pål Rasmus, Molven, Anders

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Unsupervised clustering of missense variants in HNF1A using multidimensional functional data aids clinical interpretation von Althari, Sara, Najmi, Laeya Abdoli, Bennett, Amanda J, Aukrust, Ingvild, Rundle, Jana K, Colclough, Kevin, Molnes, Janne, Kaci, Alba, Nawaz, Sameena, van der Lugt, Timme, Hassanali, Neelam, Mahajan, Anubha, Molven, Anders, Ellard, Sian, McCarthy, Mark I, Bjørkhaug, Lise, Njølstad, Pål Rasmus, Gloyn, Anna L

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