Genome-wide association meta-analysis identifies five loci associated with postpartum hemorrhage von Westergaard, David, Steinthorsdottir, Valgerdur, Stefansdottir, Lilja, Rohde, Palle Duun, Wu, Xiaoping, Geller, Frank, Tyrmi, Jaakko, Havulinna, Aki S., Solé-Navais, Pol, Flatley, Christopher, Ostrowski, Sisse Rye, Pedersen, Ole Birger, Erikstrup, Christian, Sørensen, Erik, Mikkelsen, Christina, Bruun, Mie Topholm, Aagaard Jensen, Bitten, Brodersen, Thorsten, Ullum, Henrik, Magnus, Per, Andreassen, Ole A., Njolstad, Pål R., Kolte, Astrid Marie, Krebs, Lone, Nyegaard, Mette, Hansen, Thomas Folkmann, Feenstra, Bjarke, Daly, Mark, Lindgren, Cecilia M., Thorleifsson, Gudmar, Stefansson, Olafur A., Sveinbjornsson, Gardar, Gudbjartsson, Daniel F., Thorsteinsdottir, Unnur, Banasik, Karina, Jacobsson, Bo, Laisk, Triin, Laivuori, Hannele, Stefansson, Kari, Brunak, Søren, Nielsen, Henriette Svarre

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Assessment of exocrine pancreatic function by secretin-stimulated magnetic resonance cholangiopancreaticography and diffusion-weighted imaging in healthy controls von Wathle, Gaute K., Tjora, Erling, Ersland, Lars, Dimcevski, Georg, Salvesen, Øyvind O., Molven, Anders, Njølstad, Pål R., Haldorsen, Ingfrid S.

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Lipase gene fusion: a new route to chronic pancreatitis von Molven, Anders, Njølstad, Pål R, Weiss, Frank Ulrich

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ISPAD Clinical Practice Consensus Guidelines 2018: The diagnosis and management of monogenic diabetes in children and adolescents von Hattersley, Andrew T, Greeley, Siri A W, Polak, Michel, Rubio-Cabezas, Oscar, Njølstad, Pål R, Mlynarski, Wojciech, Castano, Luis, Carlsson, Annelie, Raile, Klemens, Chi, Dung V, Ellard, Sian, Craig, Maria E

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ISPAD Clinical Practice Consensus Guidelines 2022: The diagnosis and management of monogenic diabetes in children and adolescents von Greeley, Siri Atma W, Polak, Michel, Njølstad, Pål R, Barbetti, Fabrizio, Williams, Rachel, Castano, Luis, Raile, Klemens, Chi, Dung Vu, Habeb, Abdelhadi, Hattersley, Andrew T, Codner, Ethel

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Switching from Insulin to Oral Sulfonylureas in Patients with Diabetes Due to Kir6.2 Mutations von Pearson, Ewan R, Flechtner, Isabelle, Njølstad, Pål R, Malecki, Maciej T, Flanagan, Sarah E, Larkin, Brian, Ashcroft, Frances M, Klimes, Iwar, Codner, Ethel, Iotova, Violeta, Slingerland, Annabelle S, Shield, Julian, Robert, Jean-Jacques, Holst, Jens J, Clark, Penny M, Ellard, Sian, Søvik, Oddmund, Polak, Michel, Hattersley, Andrew T

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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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A recombined allele of the lipase gene CEL and its pseudogene CELP confers susceptibility to chronic pancreatitis von Fjeld, Karianne, Weiss, Frank Ulrich, Lasher, Denise, Rosendahl, Jonas, Chen, Jian-Min, Johansson, Bente B, Kirsten, Holger, Ruffert, Claudia, Masson, Emmanuelle, Steine, Solrun J, Bugert, Peter, Cnop, Miriam, Grützmann, Robert, Mayerle, Julia, Mössner, Joachim, Ringdal, Monika, Schulz, Hans-Ulrich, Sendler, Matthias, Simon, Peter, Sztromwasser, Paweł, Torsvik, Janniche, Scholz, Markus, Tjora, Erling, Férec, Claude, Witt, Heiko, Lerch, Markus M, Njølstad, Pål R, Johansson, Stefan, Molven, Anders

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Modeling assortative mating and genetic similarities between partners, siblings, and in-laws von Torvik, Fartein Ask, Eilertsen, Espen Moen, Hannigan, Laurie J., Cheesman, Rosa, Howe, Laurence J., Magnus, Per, Reichborn-Kjennerud, Ted, Andreassen, Ole A., Njølstad, Pål R., Havdahl, Alexandra, Ystrom, Eivind

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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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Targeted next-generation sequencing reveals MODY in up to 6.5% of antibody-negative diabetes cases listed in the Norwegian Childhood Diabetes Registry von Johansson, Bente B., Irgens, Henrik U., Molnes, Janne, Sztromwasser, Paweł, Aukrust, Ingvild, Juliusson, Petur B., Søvik, Oddmund, Levy, Shawn, Skrivarhaug, Torild, Joner, Geir, Molven, Anders, Johansson, Stefan, Njølstad, Pål R.

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Mutations in the Insulin Gene Can Cause MODY and Autoantibody-Negative Type 1 Diabetes von Molven, Anders, Ringdal, Monika, Nordbø, Anita M, Raeder, Helge, Støy, Julie, Lipkind, Gregory M, Steiner, Donald F, Philipson, Louis H, Bergmann, Ines, Aarskog, Dagfinn, Undlien, Dag E, Joner, Geir, Søvik, Oddmund, Bell, Graeme I, Njølstad, Pål R

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SeeCiTe: a method to assess CNV calls from SNP arrays using trio data von Lavrichenko, Ksenia, Helgeland, Øyvind, Njølstad, Pål R, Jonassen, Inge, Johansson, Stefan

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The diagnosis and management of monogenic diabetes in children and adolescents von Rubio-Cabezas, Oscar, Hattersley, Andrew T, Njølstad, Pål R, Mlynarski, Wojciech, Ellard, Sian, White, Neil, Chi, Dung Vu, Craig, Maria E

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Maternal and Newborn Vitamin D-Binding Protein, Vitamin D Levels, Vitamin D Receptor Genotype, and Childhood Type 1 Diabetes von Tapia, German, Mårild, Karl, Dahl, Sandra R, Lund-Blix, Nicolai A, Viken, Marte K, Lie, Benedicte A, Njølstad, Pål R, Joner, Geir, Skrivarhaug, Torild, Cohen, Arieh S, Størdal, Ketil, Stene, Lars C

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Infant Feeding and Risk of Type 1 Diabetes in Two Large Scandinavian Birth Cohorts von Lund-Blix, Nicolai A, Dydensborg Sander, Stine, Størdal, Ketil, Nybo Andersen, Anne-Marie, Rønningen, Kjersti S, Joner, Geir, Skrivarhaug, Torild, Njølstad, Pål R, Husby, Steffen, Stene, Lars C

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Social and genetic associations with educational performance in a Scandinavian welfare state von Isungset, Martin A, Conley, Dalton, Zachrisson, Henrik D, Ystrom, Eivind, Havdahl, Alexandra, Njølstad, Pål R, Lyngstad, Torkild Hovde

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The position of single-base deletions in the VNTR sequence of the carboxyl ester lipase (CEL) gene determines proteotoxicity von Gravdal, Anny, Xiao, Xunjun, Cnop, Miriam, El Jellas, Khadija, Johansson, Stefan, Njølstad, Pål R., Lowe, Mark E., Johansson, Bente B., Molven, Anders, Fjeld, Karianne

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The role of the carboxyl ester lipase (CEL) gene in pancreatic disease von Johansson, Bente B., Fjeld, Karianne, El Jellas, Khadija, Gravdal, Anny, Dalva, Monica, Tjora, Erling, Ræder, Helge, Kulkarni, Rohit N., Johansson, Stefan, Njølstad, Pål R., Molven, Anders

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How important are parents in the development of child anxiety and depression? A genomic analysis of parent-offspring trios in the Norwegian Mother Father and Child Cohort Study (Mo... von Cheesman, Rosa, Eilertsen, Espen Moen, Ahmadzadeh, Yasmin I., Gjerde, Line C., Hannigan, Laurie J., Havdahl, Alexandra, Young, Alexander I., Eley, Thalia C., Njolstad, Pal R., Magnus, Per, Andreassen, Ole A., Ystrom, Eivind, McAdams, Tom A.

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