Detection of clonality in follicular lymphoma using formalin-fixed, paraffin-embedded tissue samples and BIOMED-2 immunoglobulin primersBERGET, Ellen; HELGELAND, Lars; MOLVEN, Anders et al.Journal of clinical pathology. 2011, Vol 64, Num 1, pp 37-41, issn 0021-9746, 5 p.Article

Distal phalangeal creases : A distinctive dysmorphic feature in disorders of the RAS signalling pathway?ØRSTAVIK, Karen Helene; TANGERAAS, Trine; MOLVEN, Anders et al.European journal of medical genetics. 2007, Vol 50, Num 2, pp 155-158, issn 1769-7212, 4 p.Article

Polymorphisms in CYP2D6 duplication-negative individuals with the ultrarapid metabolizer phenotype : a role for the CYP2D6*35 allele in ultrarapid metabolism?LØVLIE, Roger; DALY, Ann K; MATRE, Guri E et al.Pharmacogenetics (London). 2001, Vol 11, Num 1, pp 45-55, issn 0960-314XArticle

Pancreatic Exocrine Dysfunction in Maturity-Onset Diabetes of the Young Type 3VESTERHUS, Mette; RAEDER, Helge; JOHANSSON, Stefan et al.Diabetes care. 2008, Vol 31, Num 2, pp 306-310, issn 0149-5992, 5 p.Article

Hepatocyte nuclear factor-1α gene mutations and diabetes in NorwayBJØRKHAUG, Lise; SAGEN, Jørn V; THORSBY, Per et al.The Journal of clinical endocrinology and metabolism. 2003, Vol 88, Num 2, pp 920-931, issn 0021-972X, 12 p.Article

Genome-wide association study identifies three new melanoma susceptibility lociBARRETT, Jennifer H; ILES, Markm; BAKKER, Bert et al.Nature genetics. 2011, Vol 43, Num 11, pp 1108-1113, issn 1061-4036, 6 p.Article

The Effect on Melanoma Risk of Genes Previously Associated With Telomere LengthILES, Mark M; BISHOP, D. Timothy; ANDRESEN, Per A et al.Journal of the National Cancer Institute. 2014, Vol 106, Num 10, issn 0027-8874, 267.1-267.5Article

DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical twinsLABORIE, Lene Bjerke; MACKAY, Deborah J. G; TEMPLE, I. Karen et al.European journal of pediatrics. 2010, Vol 169, Num 2, pp 207-213, issn 0340-6199, 7 p.Article

Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetesTORSVIK, Janniche; JOHANSSON, Stefan; MOLVEN, Anders et al.Human genetics. 2010, Vol 127, Num 1, pp 55-64, issn 0340-6717, 10 p.Article

BRAF and NRAS mutations are frequent in nodular melanoma but are not associated with tumor cell proliferation or patient survivalAKSLEN, Lars A; ANGELINI, Sabrina; STRAUME, Oddbjørn et al.Journal of investigative dermatology. 2005, Vol 125, Num 2, pp 312-317, issn 0022-202X, 6 p.Article

Permanent neonatal diabetes caused by glucokinase deficiency: Inborn error of the glucose-insulin signaling pathwayNJØLSTAD, Pal R; SAGEN, Jørn V; SØVIK, Oddmund et al.Diabetes (New York, NY). 2003, Vol 52, Num 11, pp 2854-2860, issn 0012-1797, 7 p.Article

Generation of Prostate Tumor―Initiating Cells Is Associated with Elevation of Reactive Oxygen Species and IL-6/STAT3 SignalingYI QU; OYAN, Anne Margrete; MOLVEN, Anders et al.Cancer research (Chicago, Ill.). 2013, Vol 73, Num 23, pp 7090-7100, issn 0008-5472, 11 p.Article

Pancreatic lipomatosis is a structural marker in nondiabetic children with mutations in carboxyl-ester lipaseRAEDER, Helge; HALDORSEN, Ingfrid S; ERSLAND, Lars et al.Diabetes (New York, NY). 2007, Vol 56, Num 2, pp 444-449, issn 0012-1797, 6 p.Article

Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunctionRAEDER, Helge; JOHANSSON, Stefan; SAGEN, Jørn V et al.Nature genetics. 2006, Vol 38, Num 1, pp 54-62, issn 1061-4036, 9 p.Article

Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidationMOLVEN, Anders; MATRE, Guri E; DURAN, Marinus et al.Diabetes (New York, NY). 2004, Vol 53, Num 1, pp 221-227, issn 0012-1797, 7 p.Article

Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: Patient characteristics and initial response to sulfonylurea therapySAGEN, Jørn V; RAEDER, Helge; GLOYN, Anna L et al.Diabetes (New York, NY). 2004, Vol 53, Num 10, pp 2713-2718, issn 0012-1797, 6 p.Article