• Pancreas-cancer (kreft i bukspyttkjertelen)
• Kronisk pankreatitt (betennelse i bukspyttkjertelen)
• Arvelig diabetes (sukkersyke)
• Arvelig hypoglykemi (lavt blodsukker)

    For flere opplysninger, se www.pancreas.no

Vitenskapelig artikkel

• Miroslav Vujasinovic; Ihsan Ekin Demir; Giovanni Marchegiani et al. (2026). International Multidisciplinary Consensus Report on Definitions, Diagnostic Criteria, and Management of Fatty Pancreas: A Joint Statement Endorsed by EPC, APA, EASD, EASL, ESGAR, ESGE, ESP, ESPCG, ESPEN, ESPGHAN, IAP, JPS, KPBA, LAPSG, and UEG. (ekstern lenke)
• Miroslav Vujasinovic; Daniel de la Iglesia; J. Enrique Dominguez-Muñoz et al. (2025). Recommendations from the European guidelines for the diagnosis and therapy of pancreatic exocrine insufficiency. (ekstern lenke)
• Kelly Velasco ; Janniche Torsvik; Johanna Lüdeke et al. (2025). Searching for protein partners of short-chain 3-hydroxyacyl-CoA dehydrogenase (SCHAD) reveals keratin 8 as a novel candidate for interaction in pancreatic β-cells. (ekstern lenke)
• Anny Gravdal Svanbring; Steven J. Wilhelm; Ivan Abbedissen et al. (2025). The MODY-Causing Mutation of the Human Carboxyl Ester Lipase Gene (CEL) Triggers Chronic Pancreatitis But Not Diabetes in Mice. (ekstern lenke)
• Jørn V. Sagen; Lise Bjørkhaug; Bjørn Ivar Haukanes et al. (2017). The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes. (ekstern lenke)
• Oddmund Søvik; Pål Rasmus Njølstad; Egil Jellum et al. (2008). Wolcott-Rallison syndrome with 3-hydroxydicarboxylic aciduria and lethal outcome. (ekstern lenke)
• Jennifer H. Barrett; MM Iles; M Harland et al. (2011). Genome-wide association study identifies three new melanoma susceptibility loci. (ekstern lenke)
• Jørn V. Sagen; Helge Ræder; Eba Hathout et al. (2004). Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2 - Patient characteristics and initial response to sulfonylurea therapy. (ekstern lenke)
• Pernille Svalastoga; Alba Kaci; Janne Molnes et al. (2023). Characterisation of HNF1A variants in paediatric diabetes in Norway using functional and clinical investigations to unmask phenotype and monogenic diabetes. (ekstern lenke)
• Heike Immervoll; Dag Hoem; Per Øystein Sakariassen et al. (2008). Expression of the "stem cell marker" CD133 in pancreas and pancreatic ductal adenocarcinomas. (ekstern lenke)
• Matthew H. Law; D. Timothy Bishop; Jeffrey E. Lee et al. (2015). Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. (ekstern lenke)
• JV Sagen; S Odili; L. Bjørkhaug et al. (2006). From clinicogenetic studies of maturity-onset diabetes of the young to unraveling complex mechanisms of glucokinase regulation. (ekstern lenke)
• Helge Raeder; Helge Ræder; Lise Bjorkhaug et al. (2006). A hepatocyte nuclear factor-4 alpha gene (HNF4A) P2 promoter haplotype linked with late-onset diabetes - Studies of HNF4A variants in the Norwegian MODY registry. (ekstern lenke)
• Lise Bj. Gundersen; Jørn V. Sagen; P Thorsby et al. (2003). Hepatocyte nuclear factor-1 alpha gene mutations and diabetes in Norway. (ekstern lenke)
• Anders Molven; GE Matre; M Duran et al. (2004). Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation. (ekstern lenke)
• Stefan Johansson; Henrik Underthun Irgens; Kishankumar Chudasama et al. (2012). Exome sequencing and genetic testing for MODY. (ekstern lenke)
• Monica Dalva; Khadija el Jellas; Solrun Steine et al. (2017). Copy number variants and VNTR length polymorphisms of the carboxyl-ester lipase (CEL) gene as risk factors in pancreatic cancer. (ekstern lenke)
• A Molven; M Ringdal; AM Nordbø et al. (2008). Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. (ekstern lenke)
• Jonathon N. Winnay; Marie Holm Solheim; Ercument Dirice et al. (2016). PI3-kinase mutation linked to insulin and growth factor resistance in vivo. (ekstern lenke)
• Matthew J. Kolar; Siddhesh S. Kamat; William H. Parsons et al. (2016). Branched Fatty Acid Esters of Hydroxy Fatty Acids Are Preferred Substrates of the MODY8 Protein Carboxyl Ester Lipase. (ekstern lenke)
• Henrik Underthun Irgens; Janne Molnes; Bente Berg Johansson et al. (2013). Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry. (ekstern lenke)
• Grzegorz Oracz; Aleksandra Anna Kujko; Karianne Fjeld et al. (2019). The hybrid allele 1 of carboxyl-ester lipase (CEL-HYB1) in Polish pediatric patients with chronic pancreatitis. (ekstern lenke)
• Janniche Torsvik; Bente Berg Johansson; Monica Dalva et al. (2014). Endocytosis of secreted carboxyl ester lipase in a syndrome of diabetes and pancreatic exocrine dysfunction. (ekstern lenke)
• Gry Sjøholt; Anne Karin Gulbrandsen; Roger Løvlie et al. (2000). A human myoinositol monophosphatase gene (IMPA2) localized in a susc eptibility region for bipolar disorder on chromosome 18p11.2: genomic structure and polymorphism screening in manic-depressive patients. (ekstern lenke)
• Gry Sjøholt; RP Ebstein; Rolv Terje Lie et al. (2004). Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder. (ekstern lenke)
• Helge Ræder; Fiona E. McAllister; Erling Tjora et al. (2014). Carboxyl-ester lipase maturity-onset diabetes of the young is associated with development of pancreatic cysts and upregulated MAPK signaling in secretin-stimulated duodenal fluid. (ekstern lenke)
• Lise Bjørkhaug; Pål Rasmus Njølstad; Oddmund Søvik et al. (2001). N EONATAL D IABETES M ELLITUS D UE TO C OMPLETE G LUCOKINASE D EFICIENCY. (ekstern lenke)
• Jun Fang; Jinping Jia; Matthew Makowski et al. (2017). Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148. (ekstern lenke)
• Hilde Gjelberg; Dag Hoem; Caroline Sophie Verbeke et al. (2017). Hypoglycemia and decreased insulin requirement caused by malignant insulinoma in a type 1 diabetic patient: when the hoof beats are from a zebra, not a horse.. (ekstern lenke)
• Sabine Benko; Christopher P. Gordon; Delphine Mallet et al. (2011). Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development. (ekstern lenke)
• L. Bjørkhaug; Stefan Johansson; Helge Ræder et al. (2005). Molekylærgenetisk diagnostikk ved diabetes mellitus. (ekstern lenke)
• Roger Løvlie; Ann K. Daly; Guri E. Matre et al. (2001). Polymorphisms in CYP2D6 duplication-negative individuals with the ultrarapid metabolizer phenotype: a role for the CYP2D6*35 allele in ultrarapid metabolism?. (ekstern lenke)
• Cedric Zeltz; Jahedul Alam; Hengshuo Liu et al. (2019). α11β1 integrin is induced in a subset of cancer- associated fibroblasts in desmoplastic tumor stroma and mediates in vitro cell migration. (ekstern lenke)
• Heike Immervoll; Dag Hoem; Ole Johnny Steffensen et al. (2011). Visualization of CD44 and CD133 in Normal Pancreas and Pancreatic Ductal Adenocarcinomas: Non-overlapping Membrane Expression in Cell Populations Positive for Both Markers. (ekstern lenke)
• Gaute K Wathle; Erling Tjora; Lars Ersland et al. (2014). Assessment of Exocrine Pancreatic Function by Secretin-Stimulated Magnetic Resonance Cholangiopancreaticography and Diffusion-Weighted Imaging in Healthy Controls. (ekstern lenke)
• Pål Rasmus Njølstad; Jørn V. Sagen; Lise Bjørkhaug et al. (2003). Permanent neonatal diabetes caused by glucokinase deficiency; inborn error of the glucose-insulin signaling pathway. (ekstern lenke)
• Helge Ræder; Ingfrid Salvesen Haldorsen; Lars Ersland et al. (2007). Pancreatic lipomatosis is a structural marker in nondiabetic children with mutations in carboxyl-Ester lipase. (ekstern lenke)
• Kristine Pettersen; Sonja Benedikte Andersen; Simone Degen et al. (2017). Cancer cachexia associates with a systemic autophagy-inducing activity mimicked by cancer cell-derived IL-6 trans-signaling. (ekstern lenke)
• Hanne Eknes Puntervoll; Xiaohong R. Yang; Hildegunn Høberg Vetti et al. (2013). Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants. (ekstern lenke)
• Roger Løvlie; Anne Karin Gulbrandsen; Anders Molven et al. (1999). Genomic structure and sequence analysis of a human inositol polyphosphate 1-phosphatase gene (INPP1). (ekstern lenke)
• Jennifer H. Barrett; John C. Taylor; C Bright et al. (2015). Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions. (ekstern lenke)
• Khadija el Jellas; Dag Hoem; Kristin Gjerde Hagen et al. (2017). Associations between ABO blood groups and pancreatic ductal adenocarcinoma: influence on resection status and survival. (ekstern lenke)
• Lene Bjerke Laborie; Deborah J.G. Mackay; I. Karen Temple et al. (2010). DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical twins. (ekstern lenke)
• Anders Molven; Monika Ringdal; Anita-Merete Nordbø et al. (2008). Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. (ekstern lenke)
• Jens Kristoffer Hertel; Stefan Johansson; H Ræder et al. (2008). Genetic analysis of recently identified type 2 diabetes loci in 1,638 unselected patients with type 2 diabetes and 1,858 control participants from a Norwegian population-based cohort (the HUNT study). (ekstern lenke)
• Erling Tjora; Gaute K Wathle; Friedemann Erchinger et al. (2013). Exocrine pancreatic function in hepatocyte nuclear factor 1 beta-maturity-onset diabetes of the young (HNF1B-MODY) is only moderately reduced: compensatory hypersecretion from a hypoplastic pancreas. (ekstern lenke)
• Mette Vesterhus; Ingfrid Salvesen Haldorsen; Helge Ræder et al. (2008). Reduced pancreatic volume in hepatocyte nuclear factor 1A-maturity-onset diabetes of the young. (ekstern lenke)
• Lars A. Akslen; Sabrina Angelini; Oddbjørn Straume et al. (2005). BRAF and NRAS mutations are frequent in nodular melanoma but are not associated with tumor cell proliferation or patient survival. (ekstern lenke)
• Line Pedersen; Pouda Panahandeh; Muntequa Ishtiaq Siraji et al. (2020). Golgi-Localized PAQR4 Mediates Antiapoptotic Ceramidase Activity in Breast Cancer. (ekstern lenke)
• Sam Kalungi; Henry Wabinga; Anders Molven et al. (2009). Lymphomas diagnosed in Uganda during the HIB/AIDS pandemic. (ekstern lenke)
• Sam Kalungi; Solrun Steine; Henry Wabinga et al. (2009). pRb2/p130 protein expression and RBL2 mutation analysis in Burkitt lymphoma from Uganda. (ekstern lenke)
• Hildegunn Høberg Vetti; Anders Molven; Aud Katrin Eliassen et al. (2010). Er farmakogenetisk CYP2D6-testing nyttig?. (ekstern lenke)
• Georg Gjorgji Dimcevski; Spiros Kotopoulis; Tormod Karlsen Bjånes et al. (2016). A human clinical trial using ultrasound and microbubbles to enhance gemcitabine treatment of inoperable pancreatic cancer. (ekstern lenke)
• Anders Molven; Magne B. Grimstvedt; Solrun Steine et al. (2005). A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutation. (ekstern lenke)
• Anja Ragvin; Karianne Fjeld; F. Ulrich Weiss et al. (2013). The number of tandem repeats in the carboxyl-ester lipase (CEL) gene as a risk factor in alcoholic and idiopathic chronic pancreatitis. (ekstern lenke)
• Jørn V. Sagen; Maren E. Baumann; Helga Salvesen et al. (2005). Diagnostic screening of NEUROD1 (MODY6) in subjects with MODY or gestational diabetes mellitus. (ekstern lenke)
• Anders Molven; Oddmund Søvik; Charlotte von der Lippe et al. (2009). Mutasjonsdiagnostikk ved syndromer knyttet til RAS/MAPK-signalveien. (ekstern lenke)
• Dace Pjanova; Anders Molven; Lars A. Akslen et al. (2009). Identification of a CDK4 R24H mutation-positive melanoma family by analysis of early-onset melanoma patients in Latvia. (ekstern lenke)
• Tone Sandal; Lene Bjerke Laborie; Klaus Brusgaard et al. (2009). The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy. (ekstern lenke)
• Karianne Fjeld; Frank Ulrich Weiss; Denise Lasher et al. (2015). A recombined allele of the lipase gene CEL and its pseudogene CELP confers susceptibility to chronic pancreatitis. (ekstern lenke)
• Lise Bjørkhaug; Oddmund Søvik; Graeme I. Bell et al. (2000). A simple test for the hot spot mutation P291fsinsC in MODY3. (ekstern lenke)
• Lise Bjørkhaug; Y Horikawa; Hong Ye et al. (2000). MODY associated with two novel hepatocyte nuclear factor 1 alpha loss of function mutations. (ekstern lenke)
• Rūta Veinalde; Aija Ozola; Kristine Azarjana et al. (2013). Analysis of Latvian familial melanoma patients shows novel variants in the noncoding regions of CDKN2A and that the CDK4 mutation R24H is a founder mutation. (ekstern lenke)
• Øystein Helland; Mihaela Lucia Popa; Olav Karsten Vintermyr et al. (2014). First in-mouse development and application of a surgically relevant xenograft model of ovarian carcinoma. (ekstern lenke)
• Helge Ræder; Mette Vesterhus; Abdelfattah El Ouaamari et al. (2013). Absence of diabetes and pancreatic exocrine dysfunction in a transgenic model of carboxyl-ester lipase-MODY (Maturity-Onset Diabetes of the young). (ekstern lenke)
• Henrik Underthun Irgens; Karianne Fjeld; Bente Berg Johansson et al. (2015). Glycogenin-2 is dispensable for liver glycogen synthesis and glucagon-stimulated glucose release. (ekstern lenke)
• Jørgen Gustav Bramness; Svetlana Skurtveit; Lena Fauske et al. (2003). Association between blood carisoprodol/meprobamate concentration ratios and CYP2C19 genotype in carisoprodol drugged drivers: Decreased metabolic capacity in heterozygous CYP2C19*1/CYP2C19*2 subjects?. (ekstern lenke)
• Dag Hoem; Dag Jensen; Solrun Steine et al. (2008). Clinicopathological characteristics and non-adhesive organ culture of insulinomas. (ekstern lenke)
• Maria Teresa Landi; David Timothy Bishop; Stuart MacGregor et al. (2020). Genome-Wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. (ekstern lenke)
• Lise Bj. Gundersen; Andre Bratland; Pål Rasmus Njølstad et al. (2005). Functional dissection of the HNF-1alpha transcription factor: A study on nuclear localization and transcriptional activation. (ekstern lenke)
• Khadija el Jellas; Bente Berg Johansson; Karianne Fjeld et al. (2018). The mucinous domain of pancreatic carboxyl-ester lipase (CEL) contains core 1/core 2 O-glycans that can be modified by ABO blood group determinants. (ekstern lenke)
• Jason Flannick; Nicola L. Beer; Alexander G. Bick et al. (2013). Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes. (ekstern lenke)
• Anja Torsvik; Daniel Stieber; Per Øyvind Enger et al. (2014). U-251 revisited: genetic drift and phenotypic consequences of long-term cultures of glioblastoma cells. (ekstern lenke)
• Maria Negahdar; Ingvild Aukrust; Bente Berg Johansson et al. (2012). GCK-MODY diabetes associated with protein misfolding, cellular self-association and degradation. (ekstern lenke)
• Henrik B.T. Christesen; Nicholas D. Tribble; Anders Molven et al. (2008). Activating glucokinase (GCK) Mutations as a cause of medically responsive congenital hyperinsulinism: prevalence in children and characterisation of a novel GCK mutation. (ekstern lenke)
• Laila S. Nilssen; John Ødegård; G. Hege Thoresen et al. (2004). G protein-coupled receptor agonist-stimulated expression of ATF3/LRF-1 and c-myc and comitogenic effects in hepatocytes do not require EGF receptor transactivation. (ekstern lenke)
• Anders Molven; Pål Rasmus Njølstad; Anders Fjose (1991). Genomic structure and restricted neural expression of the zebrafish wnt-1 (int-1) gene. (ekstern lenke)
• Anders Molven; Gunnar Houge; R. Berger (1996). Chromosomal assignment of the human gene encoding the Fos-related antigen-2 (FRA-2) to chromosome 2p22-p23. (ekstern lenke)
• Hilde Ytre-Hauge Smeland; Cecilie Askeland; Elisabeth Wik et al. (2019). Integrin α11β1 is expressed in breast cancer stroma and associates with aggressive tumor phenotypes.. (ekstern lenke)
• Helge Ræder; Stefan Johansson; Pål I. Holm et al. (2006). Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction. (ekstern lenke)
• Tone Sandal; Oddmund Søvik; Pål Rasmus Njølstad et al. (2008). Utredning og behandling av medfødt hyperinsulinisme (1): Molekylære og genetiske aspekter. (ekstern lenke)
• Mette Vesterhus; Helge Ræder; Stefan Johansson et al. (2008). Pancreatic Exocrine Dysfunction in Maturity-Onset Diabetes of the Young Type 3. (ekstern lenke)
• Ellen Berget; Anders Molven; Turid Løkeland et al. (2015). IGHV gene usage and mutational status in follicular lymphoma: Correlations with prognosis and patient age. (ekstern lenke)
• Karianne Fjeld; Sebastian Beer; Marianne Johnstone et al. (2016). Length of variable numbers of tandem repeats in the carboxyl ester lipase (CEL) gene may confer susceptibility to alcoholic liver cirrhosis but not alcoholic chronic pancreatitis. (ekstern lenke)
• Erling Tjora; Gaute K Wathle; Trond Engjom et al. (2013). Severe pancreatic dysfunction but compensated nutritional status in monogenic pancreatic disease caused by carboxyl-ester lipase mutations. (ekstern lenke)
• Jørgen Bramnes; Svetlana Skurtveit; Lars Fauske et al. (2003). Association between blood carisoprodol:meprobamate concentration ratios and CYP2C19 genotype in carisoprodol-drugged drivers: decreased metabolic capacity in heterozygous CYP2C19*1/CYP2C19*2 subjects?. (ekstern lenke)
• Maurizio Cardelli; Remco van Doorn; Lares Larcher et al. (2020). Association of HERV-K and LINE-1 hypomethylation with reduced disease-free survival in melanoma patients. (ekstern lenke)
• Erling Tjora; Anny Gravdal; Trond Engjom et al. (2021). Protein misfolding in combination with other risk factors in CEL-HYB1-mediated chronic pancreatitis. (ekstern lenke)
• Oddmund Søvik; Henrik Underthun Irgens; Janne Molnes et al. (2013). Monogenetic diabetes mellitus in Norway :. (ekstern lenke)
• Karianne Fjeld; Emmanuelle Masson; Jin-Huan Lin et al. (2020). Characterization of CEL-DUP2: Complete duplication of the carboxyl ester lipase gene is unlikely to influence risk of chronic pancreatitis. (ekstern lenke)
• Dan Calatayud; Christian Dehlendorff; Heike Immervoll et al. (2017). Tissue MicroRNA profiles as diagnostic and prognostic biomarkers in patients with resectable pancreatic ductal adenocarcinoma and periampullary cancers.. (ekstern lenke)
• Monica Dalva Valvatne; Ida Marie Kjærefjord Lavik; Khadija el Jellas et al. (2020). Pathogenic Carboxyl Ester Lipase (CEL) Variants Interact with the Normal CEL Protein in Pancreatic Cells. (ekstern lenke)
• Mark M. Iles; D. Timothy Bishop; John C. Taylor et al. (2014). The effect on melanoma risk of genes previously associated with telomere length. (ekstern lenke)
• Roger Løvlie; Ann K. Daly; Anders Molven et al. (1996). Ultrarapid metabilizers of debrisoquine : characterization and PCR-based detection of alleles with duplication of the CYP2D6 gene. (ekstern lenke)
• Anders Molven; Ivar Hordvik; Pål Rasmus Njølstad et al. (1992). The zebrafish homeobox gene Hox(zf-114): primary structure, expression pattern and evolutionary aspects. (ekstern lenke)
• Christoffer Drabløs Velde; Hallvard Reigstad; Erling Tjora et al. (2023). Medfødt hyperinsulinisme. (ekstern lenke)
• Kishan Kumar Chudasama; Jonathan Winnay; Stefan Johansson et al. (2013). SHORT syndrome with partial lipodystrophy due to impaired phosphatidylinositol 3 kinase signaling. (ekstern lenke)
• Anders Fjose; Pål Rasmus Njølstad; S. Nornes et al. (1992). Structure and early embryonic expression of the zebrafish engrailed-2 gene. (ekstern lenke)
• Jens Kristoffer Hertel; Stefan Johansson; Kristian Midthjell et al. (2013). Type 2 diabetes genes : present status and data from Norwegian studies. (ekstern lenke)
• Bente Berg Johansson; Janniche Torsvik; Lise Bjørkhaug et al. (2011). Diabetes and pancreatic exocrine dysfunction due to mutations in the carboxyl ester lipase gene-maturity onset diabetes of the young (CEL-MODY) A PROTEIN MISFOLDING DISEASE. (ekstern lenke)
• Bente Berg Johansson; Henrik Underthun Irgens; Janne Molnes et al. (2017). Targeted next-generation sequencing reveals MODY in up to 6.5% of antibody-negative diabetes cases listed in the Norwegian Childhood Diabetes Registry. (ekstern lenke)
• Kelly Velasco Pinto; Johanna Lüdeke St-Louis; Henrikke Nilsen Hovland et al. (2020). Functional evaluation of 16 SCHAD missense variants: Only amino acid substitutions causing congenital hyperinsulinism of infancy lead to loss-of-function phenotypes in vitro. (ekstern lenke)
• Xiaozheng Liu; Anastasiia Rulina; Man Hung Choi et al. (2022). C/EBPB-dependent adaptation to palmitic acid promotes tumor formation in hormone receptor negative breast cancer. (ekstern lenke)
• Yi Qu; Anne Margrete Øyan; Run-hui Liu et al. (2013). Generation of prostate tumor-initiating cells is associated with elevation of reactive oxygen species and IL-6/STAT3 signaling. (ekstern lenke)
• Per Helsing; Dag Andre Nymoen; Helge Rootwelt et al. (2012). MC1R, ASIP, TYR, and TYRP1 gene variants in a population-based series of multiple primary melanomas. (ekstern lenke)
• Moses Musiime; Pugazendhi Murugan Erusappan; Edna Cukierman et al. (2024). Fibroblast integrin α11β1 is a collagen assembly receptor in mechanoregulated fibrillar adhesions. (ekstern lenke)
• Oddmund Søvik; Suzanne Schubbert; Gunnar Houge et al. (2007). De novo HRAS and KRAS mutations in two siblings with short stature and neuro-cardio-facio-cutaneous features. (ekstern lenke)
• Pål Rasmus Njølstad; Anders Molven (2003). Forskere diskuterte diabetes. (ekstern lenke)
• Mary Elizabeth Patti; Allison B. Goldfine; Jiang Hu et al. (2017). Heterogeneity of proliferative markers in pancreatic β-cells of patients with severe hypoglycemia following Roux-en-Y gastric bypass. (ekstern lenke)
• Sara Althari; Laeya Abdoli Najmi; Amanda J. Bennett et al. (2020). Unsupervised clustering of missense variants in HNF1A using multidimensional functional data aids clinical interpretation. (ekstern lenke)
• Anders Molven (2000). MGM - Medisin, Gener og Mennesker. (ekstern lenke)
• L Bjørkhaug; Jørn V. Sagen; P Thorsby et al. (2003). Hepatocyte nuclear factor- 1 alpha gene mutations and diabetes in Norway. (ekstern lenke)
• Pål Rasmus Njølstad; Jørn Sagen; Lise Bjørkhaug et al. (2003). Permanent neonatal diabetes mellitus due to glucokinase deficiency- an inborn error of the glucose-insulin signalling pathway. (ekstern lenke)
• Dag Hoem; Oddbjørn Straume; Heike Immervoll et al. (2013). Vascular proliferation is associated with survival in pancreatic ductal adenocarcinoma. (ekstern lenke)
• Ellen Berget; Lars Helgeland; Anders Molven et al. (2011). Detection of clonality in follicular lymphoma using formalin-fixed, paraffin-embedded tissue samples and BIOMED-2 immunoglobulin primers. (ekstern lenke)
• Jørgen Bramness; S Skurtveit; Lars Fauske et al. (2003). Association between blood carisoprodol/meprobamate concentration ratios and CYP2C19 genotype in carisoprodol-drugged drivers: Decreased metabolic capacity in heterozygous CYP2C19*1/CYP2C19*2 subjects?. (ekstern lenke)
• Christoffer Drabløs Velde; Janne Molnes; Siren Berland et al. (2025). Clinical and Genetic Characteristics of Congenital Hyperinsulinism in Norway: A Nationwide Cohort Study. (ekstern lenke)
• Roger Løvlie; A. K. Daly; Anders Molven et al. (1996). Ultrarapid metabolizers of debrisoquine: Characterization and PCR-based detection of alleles with duplication of the CYP2D6 gene. (ekstern lenke)
• Anders Molven; Gunnar Houge; R. Berger (1996). Chromosomal assignment of the human gene encoding the Fos-related antigen-2 (FRA-2) to chromosome 2p22-p23. (ekstern lenke)
• Oddmund Søvik; Øystein Aagenæs; Stig Åge Eide et al. (2012). Familial occurrence of neonatal diabetes with duplications in chromosome 6q24: treatment with sulfonylurea and 40-yr follow-up. (ekstern lenke)
• Lise Bj. Gundersen; Stefan Johansson; Helge Ræder et al. (2005). Molekylærgenetisk diagnostikk ved diabetes mellitus. (ekstern lenke)
• Laeya Abdoli Najmi; Ingvild Aukrust; Jason Flannick et al. (2017). Functional investigations of HNF1A identify rare variants as risk factors for type 2 diabetes in the general population. (ekstern lenke)
• Anja Ragvin; Enrico Moro; David Fredman et al. (2010). Long-range gene regulation links genomic type 2 diabetes and obesity risk regions to HHEX, SOX4, and IRX3. (ekstern lenke)
• Janniche Torsvik; Stefan Johansson; Anders Johansen et al. (2010). Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes. (ekstern lenke)
• Hana Lango Allen; Stefan Johansson; Sian Ellard et al. (2010). Polygenic risk variants for Type 2 Diabetes susceptibility modify age at diagnosis in Monogenic HNF1A Diabetes. (ekstern lenke)
• Sivaramakrishna Rachakonda; Nalini Srinivas; Seyed Hamidreza Mahmoudpour et al. (2018). Telomere length and survival in primary cutaneous melanoma patients. (ekstern lenke)
• Laila S. Nilssen; John Ødegård; G. Hege Thoresen et al. (2004). G protein-coupled receptor agonist-stimulated expression of ATF3/LRF-1 and c-myc and comitogenic effects in hepatocytes do not require EGF receptor transactivation. (ekstern lenke)
• Sven Pörksen; Lene Bjerke Laborie; Lotte B. Nielsen et al. (2010). Disease progression and search for monogenic diabetes among children with new onset type 1 diabetes negative for ICA, GAD- and IA-2 antibodies. (ekstern lenke)
• Hildegunn Høberg Vetti; Anders Molven; Aud Katrin Eliassen et al. (2010). Er formakogenetisk CYP2D6-testing nyttig?. (ekstern lenke)
• Ingfrid S. Haldorsen; Helge Ræder; Mette Vesterhus et al. (2011). The role of pancreatic imaging in monogenic diabetes. (ekstern lenke)
• E. Nazli Gonc; Burcu Bulum Ozturk; Ingfrid S. Haldorsen et al. (2012). HNF1B mutation in a Turkish child with renal and exocrine pancreas insufficiency, diabetes and liver disease. (ekstern lenke)
• Anders Molven (1996). Fusk og fanteri i forskningen. (ekstern lenke)
• Anders Molven (1996). Fargerik forskar fyller femti. (ekstern lenke)
• Anders Molven (1996). Priser til begjær (og #/en til besvær). (ekstern lenke)
• Anders Molven; Vidar Martin Steen (1996). A retroviral element in the human CYP2D gene cluster. (ekstern lenke)
• Anders Molven (1996). Priser til begjær -del II. (ekstern lenke)
• Pål Rasmus Njølstad; Oddmund Søvik; Antonio Cuesta-Munoz et al. (2001). Permanent neonatal diabetes mellitus due to complete glucoinase deficiency. (ekstern lenke)
• Vidar Martin Steen; Anders Molven; Nina Karin Aarskog et al. (1995). Homologous unequal cross-over involving a 2.8 kb direct repeat as a mechanism for the generation of allelic variants of human cytochrome P450 CYP2D6 gene. (ekstern lenke)
• Stefan Johansson; Helge Ræder; Stig Åge Eide et al. (2007). Studies in 3,523 Norwegians and meta-analysis in 11,571 subjects indicate that variants in the hepatocyte nuclear factor 4 alpha (HNF4A) P2 region are associated with type 2 diabetes in Scandinavians. (ekstern lenke)
• Suzanne Schubbert; Gideon Bollag; Natalya Lyubynska et al. (2007). Biochemical and functional characterization of germ line KRAS mutations. (ekstern lenke)
• Marie Holm Solheim; Allen C. Clermont; Jonathon N. Winnay et al. (2017). Iris malformation and anterior segment dysgenesis in mice and humans with a mutation in PI 3-Kinase. (ekstern lenke)
• Jens Kristoffer Hertel; Stefan Johansson; Emily Sonestedt et al. (2011). FTO, type 2 diabetes, and weight gain throughout adult life A meta-analysis of 41,504 subjects from the Scandinavian HUNT, MDC, and MPP studies. (ekstern lenke)
• Pål Rasmus Njølstad; Lars Fredrik Engebretsen; Anders Molven et al. (2001). MODY-prosjektet ved Haukeland Sykehus: fra forskning til diagnostikk. (ekstern lenke)
• Gry Sjøholt; RP Ebstein; Rolv Terje Lie et al. (2003). Examination of IMPA1- and IMPA2 genes in manic-depressive patients: Association between IMPA2 promoter polymorphisms and bipolar disorder. (ekstern lenke)
• Bruna Dalmasso; Lorenza Pastorino; Vaishnavi Nathan et al. (2021). Germline ATM variants predispose to melanoma: a joint analysis across the GenoMEL and MelaNostrum consortia. (ekstern lenke)
• Karianne Fjeld; Anny Gravdal Svanbring; Ranveig Seim Brekke et al. (2022). The genetic risk factor CEL-HYB1 causes proteotoxicity and chronic pancreatitis in mice. (ekstern lenke)
• Kari Espolin Fladmark; Bjørn Tore Gjertsen; Anders Molven et al. (1997). Gap junctions and growth control in liver regeneration and in isolated rat hepatocytes. (ekstern lenke)
• B Stern; Anders Molven; D Kamp (1995). Conserved sequence patterns in phages Mu and Lambda. (ekstern lenke)
• Anders Molven; Jennifer Hollister-Lock; Jiang Hu et al. (2016). The hypoglycemic phenotype is islet cell-autonomous in short-chain hydroxyacyl-CoA dehydrogenase-deficient mice. (ekstern lenke)
• Xisong Ke; Wencheng Li; Randi Hovland et al. (2011). Reprogramming of cell junction modules during stepwise epithelial to mesenchymal transition and accumulation of malignant features in vitro in a prostate cell model. (ekstern lenke)
• Bjørn Inge Bertelsen; Solrun Steine; Roar Sandvei et al. (2006). Molecular analysis of the PI3K-AKT pathway in uterine cervical neoplasia: Frequent PIK3CA amplification and AKT phosphorylation. (ekstern lenke)
• Mark M. Iles; Matthew H. Law; Simon N. Stacey et al. (2013). A variant in FTO shows association with melanoma risk not due to BMI. (ekstern lenke)
• Ellen Berget; Lars Helgeland; Knut Liseth et al. (2014). Prognostic value of bone marrow involvement by clonal immunoglobulin gene rearrangements in follicular lymphoma. (ekstern lenke)
• Kjersti Tjensvoll; Morten Lapin; Bjørnar Gilje et al. (2022). Novel hybridization- and tag-based error-corrected method for sensitive ctDNA mutation detection using ion semiconductor sequencing. (ekstern lenke)
• Heike Immervoll; Dag Hoem; Kalaiarasy Kugarajh et al. (2006). Molecular analysis of the EGFR-RAS-RAF pathway in pancreatic ductal adenocarcinomas: lack of mutations in the BRAF and EGFR genes. (ekstern lenke)
• Gry Sjøholt; Anders Molven; Roger Løvlie et al. (1997). Genomic structure and chromosomal localization of a human myo-inositol monophosphatase gene (IMPA). (ekstern lenke)
• Brett M. Cassidy; Sammy Zino; Karianne Fjeld et al. (2020). Single nucleotide polymorphisms in CEL-HYB1 increase risk for chronic pancreatitis through proteotoxic misfolding. (ekstern lenke)
• Anny Gravdal Svanbring; Xunjun Xiao; Miriam Cnop et al. (2021). The position of single-base deletions in the VNTR sequence of the carboxyl ester lipase (CEL) gene determines proteotoxicity. (ekstern lenke)
• Jason Flannick; G Thorleifsson; N Beer et al. (2014). Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. (ekstern lenke)
• Karen Helene Ørstavik; Trine Tangeraas; Anders Molven et al. (2007). Distal phalangeal creases - A distinctive dysmorphic feature in disorders of the RAS signalling pathway?. (ekstern lenke)
• Marie Holm Solheim; Jonathon N. Winnay; Thiago M. Batista et al. (2018). Mice Carrying a Dominant-Negative Human PI3K Mutation Are Protected From Obesity and Hepatic Steatosis but Not Diabetes. (ekstern lenke)
• Ingfrid Salvesen Haldorsen; Mette Vesterhus; Helge Ræder et al. (2008). Lack of pancreatic body and tail in HNF1B mutation carriers. (ekstern lenke)
• Stig Åge Eide; H Ræder; Helge Ræder et al. (2008). Prevalence of HNF1A (MODY3) mutations in a Norwegian population (the HUNT2 Study). (ekstern lenke)
• Man Hung Choi; Eline Mejlænder-Andersen; Sophia Manueldas et al. (2019). Mutation analysis by deep sequencing of pancreatic juice from patients with pancreatic ductal adenocarcinoma. (ekstern lenke)
• Ranveig Seim Brekke; Anny Gravdal Svanbring; Khadija el Jellas et al. (2024). Common single-base insertions in the VNTR of the carboxyl ester lipase (CEL) gene are benign and also likely to arise somatically in the exocrine pancreas. (ekstern lenke)
• Johanna L. St-Louis; Khadija el Jellas; Kelly Velasco et al. (2023). Deficiency of the metabolic enzyme SCHAD in pancreatic β-cells promotes amino acid–sensitive hypoglycemia. (ekstern lenke)
• Lars A. Akslen; Hanne Eknes Puntervoll; Ingeborg M. Bachmann et al. (2008). Mutation analysis of the EGFR-NRAS-BRAF pathway in melanomas from black Africans and other subgroups of cutaneous melanoma. (ekstern lenke)
• Jens Kristoffer Hertel; Stefan Johansson; Helge Ræder et al. (2011). Evaluation of four novel genetic variants affecting hemoglobin A1c levels in a population-based type 2 diabetes cohort (the HUNT2 study). (ekstern lenke)
• Anders Molven; U Rishaug; G E Matre et al. (2002). Hunting for a hypoglyecemia gene:Severe neonatal hypoglyecemia in a consanguineuos family. (ekstern lenke)
• Øyvind Helgeland; Marc Vaudel; Petur Benedikt Juliusson et al. (2019). Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth. (ekstern lenke)
• Per Helsing; Dag André Nyrnoen; Sarah Ariansen et al. (2008). Population-based prevalence of CDKN2A and CDK4 mutations in patients with multiple primary melanomas. (ekstern lenke)
• Khadija el Jellas; Petra Dušátková; Ingfrid S. Haldorsen et al. (2022). Two New Mutations in the CEL Gene Causing Diabetes and Hereditary Pancreatitis: How to Correctly Identify MODY8 Cases. (ekstern lenke)
• Jørn V. Sagen; Lise Bjørkhaug; Janne Molnes et al. (2008). Diagnostic screening of MODY2/GCK mutations in the Norwegian MODY Registry. (ekstern lenke)
• Gry Sjøholt; Anne Karin Gulbrandsen; Roger Løvlie et al. (2000). A human myoinositol monophosphatase gene (IMPA2) localized in a susc eptibility region for bipolar disorder on chromosome 18p11.2: genomic structure and polymorphism screening in manic-depressive patients. (ekstern lenke)
• Roger Løvlie; Ann K. Daly; Guri E. Matre et al. (2001). Polymorphisms in CYP2D6 duplication-negative individuals with the ultrarapid metabolizer phenotype: a role for the CYP2D6*35 allele in ultrarapid metabolism?. (ekstern lenke)
• Sevim Kahraman; Ercument Dirice; Giorgio Basile et al. (2022). Abnormal exocrine–endocrine cell cross-talk promotes β-cell dysfunction and loss in MODY8. (ekstern lenke)
• Mette Vesterhus; Helge Ræder; Harald Aurlien et al. (2008). Neurological features and enzyme therapy in patients with endocrine and exocrine pancreas dysfunction due to CEL mutations. (ekstern lenke)
• Mette Vesterhus; Helge Ræder; Amarnath J Kurpad et al. (2010). Pancreatic Function in Carboxyl-Ester Lipase Knockout Mice. (ekstern lenke)
• Jian Wang; Per Øystein Sakariassen; Oleg Tsinkalovsky et al. (2008). CD133 negative glioma cells form tumors in nude rats and give rise to CD133 positive cells. (ekstern lenke)
• Kjersti Mangseth; Lars Inge Helgeland; Jan Klos et al. (2009). Improved diagnostic segregation of mantle cell lymphoma by determination of cyclin D1/D3 expression ratio in formalin-fixed tissue. (ekstern lenke)
• Anders Molven (1997). Forfatterskap til besvær. (ekstern lenke)
• K.E. Flatmark; B.T. Gjertsen; Anders Molven et al. (1997). Gap junctions and growth control in liver regeneration and in isolated rat hepatocytes. (ekstern lenke)
• Jørn Sagen; Stella Odili; Lise Bjørkhaug et al. (2006). From clinicogenetic studies of maturity-onset diabetes of the young to unraveling complex mechanisms of glucokinase regulation. (ekstern lenke)
• Vidar Martin Steen; Anders Molven; NK Aarskog et al. (1995). Homologous unequal cross-over involving a 2.8 kb direct repeat as a mechanism for the generation of allelic variants of the human cytochrome P450 CYP2D6 gene. (ekstern lenke)
• Anders Molven (1995). Med Goksøyr inn i genalderen. (ekstern lenke)
• Anders Molven (1995). Uracil-DNA-glykosylase - en norsk suksesshistorie. (ekstern lenke)
• Cornelia Schuster; Hans Petter Eikesdal; Hanne Eknes Puntervoll et al. (2012). Clinical efficacy and safety of bevacizumab monotherapy in patients with metastatic melanoma: predictive importance of induced early hypertension. (ekstern lenke)
• Man Hung Choi; Erling Tjora; Rakel Brendsdal Forthun et al. (2021). KRAS mutation analysis by droplet digital PCR of duodenal juice from patients with MODY8 and other pancreatic diseases. (ekstern lenke)
• Anders Molven; LI Cressey; Ragnar Bøe (1995). Apoptose - når cellene dør. (ekstern lenke)
• B Stern; Anders Molven; D Kamp (1995). Conserved sequence patterns in phages Mu and Lambda. (ekstern lenke)
• Anders Molven (1995). Aarskog-genet endelig klonet. (ekstern lenke)
• Anders Molven (1995). Protein-folding med konsekvensar. Om scrapie, prionar og degenerative hjernesjukdomar. (ekstern lenke)

Vitenskapelig litteraturgjennomgang

• Ingfrid S. Haldorsen; Helge Ræder; Mette Vesterhus et al. (2012). The role of pancreatic imaging in monogenic diabetes mellitus. (ekstern lenke)
• Øyvind Helgeland; Jens Kristoffer Hertel; Anders Molven et al. (2015). The chromosome 9p21 CVD- and T2D-associated regions in a Norwegian population (the HUNT2 survey). (ekstern lenke)
• Anders Molven; Pål Rasmus Njølstad (2011). Role of molecular genetics in transforming diagnosis of diabetes mellitus. (ekstern lenke)
• Pål Rasmus Njølstad; Jens Kristoffer Hertel; Oddmund Søvik et al. (2010). Fremskritt innen diabetesgenetikk. (ekstern lenke)
• Bente Berg Johansson; Karianne Fjeld; Khadija el Jellas et al. (2018). The role of the carboxyl ester lipase (CEL) gene in pancreatic disease. (ekstern lenke)
• Kjetil Søreide; Heike Immervoll; Anders Molven (2006). Forstadier til kreft i bukspyttkjertelen. (ekstern lenke)

Konferanseforedrag

• Oddmund Søvik; PR Njølstad; Lene Bjørkhaug et al. (1999). Maturity onset diabetes of the young (MODY): A Norwegian experience. (ekstern lenke)
• Roger Løvlie; Anne Karin Gulbrandsen; Anders Molven et al. (1998). Genomic structure and sequence analysis of a human inositol polyphosphate 1-phosphatase gene (INPP1). (ekstern lenke)
• Gry Sjøholt; Anne Karin Gulbrandsen; Roger Løvlie et al. (1998). Genomic characterization of genes encoding human myo-inositol monophosphatase enzymes. (ekstern lenke)
• Lado Lako Loro; Salah Osman Ibrahim; Anne Chr. Johannessen et al. (2004). HRAS, KRAS, NRAS and BRAF mutation analysis in oral squamous cell carcinomas from the Sudan. (ekstern lenke)
• Bjørn Inge Bertelsen; Solrun Steine; Roar Sandvei et al. (2004). PI3K/Akt signalveien ved livmorhalskreft. (ekstern lenke)
• Gry Sjøholt; Anders Molven; Roger Løvlie et al. (1998). Gene mutations of the phosphatidylinositol signaking system in lithium-treated manic-depressive patients. (ekstern lenke)
• Gry Sjøholt; Anne Karin Gulbrandsen; Roger Løvlie et al. (1999). Searching for genetic variations in inositol monophosphatase genes in lithium-treated manic-depressive patients. (ekstern lenke)
• Lado Lako Loro; Olav Karsten Vintermyr; Anders Molven et al. (2003). BRAF mutational analysis in oral dysplastic and neoplastic epithelial lesions. (ekstern lenke)
• Anders Molven; U Rishaug; G E Matre et al. (2001). Autosomal recessive glucagon deficiency and severe neonatal hypoglycemia: A candidate gene approach. (ekstern lenke)
• Anders Molven; H Immervold; K Kugarajh et al. (2003). Mutation analysis of the RAS-RAF pathway in pancreatic adenocarcinomas and malignant melanomas. (ekstern lenke)
• Lene Bjørkhaug; PR Njølstad; P Thorsby et al. (1999). Molecular genetic analyses of Norwegian families with maturity-onset diabetes of the young. (ekstern lenke)

Lederartikkel

• Anders Molven; Karianne Fjeld; Mark E. Lowe (2016). Lipase genetic variants in chronic pancreatitis: when the end is wrong, all's not well. (ekstern lenke)
• Helge Ræder; Anders Molven; Pål Rasmus Njølstad (2012). Skreddersydd medisin eller narsissomikk?. (ekstern lenke)
• Pål Rasmus Njølstad; Anders Molven (2012). To test, or not to test: time for a MODY calculator?. (ekstern lenke)
• PR Njølstad; Anders Molven (2003). Forskere diskuterte arv og diabetes. (ekstern lenke)
• Anders Molven; Pål Rasmus Njølstad; Frank Ulrich Weiss (2015). Lipase gene fusion: a new route to chronic pancreatitis. (ekstern lenke)

Vitenskapelig bokkapittel

• Anders Molven (1997). p53 er vår indre vaktmester. (ekstern lenke)
• Anders Molven; Geir Helgeland; Tone Sandal et al. (2012). The molecular genetics and pathophysiology of congenital hyperinsulinism caused by short-chain 3-hydroxyacyl-CoA dehydrogenase (SCHAD) deficiency. (ekstern lenke)
• Anders Molven; Anders Goksøyr (1993). Biological effects and biomonitoring of organochlorines and polycyclic aromatic hydrocarbons in the marine environment. (ekstern lenke)
• Pål Rasmus Njølstad; Anders Molven; Oddmund Søvik (2005). Diagnosis and mangement of MODY in a pediatric setting. (ekstern lenke)
• Anders Molven; Pål Rasmus Njølstad; Anders Fjose (1993). Pattern formation in fish embryos: Characterization of homebox genes from the zebrafish (Brachydranio rerio). (ekstern lenke)
• Georg Gjorgji Dimcevski; Spiros Kotopoulis; Dag Hoem et al. (2013). Ultrasound-assisted treatment of an inoperable pancreatic cancer. (ekstern lenke)

Doktorgradsavhandling

• Anders Molven (1991). Pattern formation and neurogenesis in a vertebrate embryo: study of developmentally regulated genes in the zebrafish. (dr.scient.). (ekstern lenke)
• Khadija el Jellas; Anders Molven (2018). Carboxyl-ester lipase in human pancreatic disease. A study with focus on genetics, glycosylation and ABO blood groups. (ekstern lenke)
• Monica Dalva Valvatne; Anders Molven (2018). Genetic and cellular studies of carboxyl-ester lipase (CEL), a protein involved in exocrine and endocrine pancreatic disease. (ekstern lenke)
• Henrik Underthun Irgens; Pål Rasmus Njølstad; Anders Molven (2017). Targeted clinical and genetic investigations to identify monogenic diabetes. (ekstern lenke)

Konferanseabstrakt

• Ellen Berget; Lars Helgeland; Anders Molven et al. (2010). Evaluation of BIOMED-2 PCR primers for detection of clonality in follicular lymphoma on formalin-fixed, paraffin-embedded samples. (ekstern lenke)
• HL Allen; Stefan Johansson; S Ellard et al. (2009). Polygenic risk variants for type 2 diabetes susceptibility modify age at diagnosis in monogenic HNF1A diabetes. (ekstern lenke)
• Anders Molven; Janniche Torsvik; Bente Berg Johansson et al. (2013). Cellular re-uptake of secreted carboxyl-ester lipase protein in CEL-MODY, a syndrome of diabetes and pancreatic exocrine dysfunction. (ekstern lenke)
• Ellen Berget; Lars Helgeland; Anders Molven et al. (2013). Detection of B-Cell Lymphoma in Bone Marrow Aspirates Using BIOMED-2 Immunoglobulin Primers. (ekstern lenke)
• Ellen Berget; Lars Helgeland; Anders Molven et al. (2009). Evaluation of BIOMED-2 PCR primers for detection of clonality in follicular lymphoma on formalin-fixed, paraffin-embedded samples. (ekstern lenke)
• Ellen Berget; Lars Helgeland; Anders Molven et al. (2013). Detection of B-Cell Lymphoma in Bone Marrow Aspirates Using BIOMED-2 Immunoglobulin Primers. (ekstern lenke)
• Pål Rasmus Njølstad; Anders Molven; Leif Groop (2009). The Genotypes and Phenotypes of Diabetes. (ekstern lenke)
• Mette Vesterhus; Stefan Johansson; Helge Ræder et al. (2007). Pancreatic exocrine deficiency is common in MODY 3. (ekstern lenke)
• Georg Gjorgji Dimcevski; Spiros Kotopoulis; Tormod Karlsen Bjånes et al. (2016). Ultrasound and microbubble enhanced treatment of inoperable pancreatic adeonocarcinoma. (ekstern lenke)
• Henrik B. Thybo Christesen; Nicholas D. Tribble; Anders Molven et al. (2008). Congenital Hyperinsullnism: Prevalence Prevalence of activating glucokinase mutations and a novel mutation. (ekstern lenke)
• Bjørn Inge Bertelsen; Solrun Steine; Roar Sandvei et al. (2006). AKT phosphorylation and PIK3CA amplification are common in cervical neoplasia. (ekstern lenke)
• Bjørn Inge Bertelsen; Solrun Steine; Roar Sandvei et al. (2006). AKT phosphorylation and PIK3CA amplification are common in cervical neoplasia. (ekstern lenke)
• Janniche Torsvik; Bente Berg Johansson; Stefan Johansson et al. (2008). Pancreatic exocrine dysfunction in diabetes: functional characterisation of the carboxyl-ester lipase gene. (ekstern lenke)
• Sven Pörksen; Lene Bjerke Laborie; Lotte B. Nielsen et al. (2008). SUR mutation in type 1 diabetes: autoimmunity prevents sulfonylurea rescue of diabetes caused by SUR1 mutation. Results from the Hvidore Study Group. (ekstern lenke)
• Karianne Fjeld; Janniche Torsvik; Stefan Johansson et al. (2008). Structural changes in the repeated region of the carboxyl-ester lipase (CEL) gene and the development of diabetes. (ekstern lenke)
• Stefan Johansson; Jens Kristoffer Hertel; Kristian Midthjell et al. (2008). The role of confirmed type 2 diabetes risk alleles on age-of-diagnosis in a Norwegian population based sample: the HUNT Study. (ekstern lenke)

Konferanseposter

• Miguel Angel Juarez Garzon; Ksenia Kuznetsova; Divya Sri Priyanka Tallapragada et al. (2024). Pediatric Diabetes Clustering: Phenotypic and polygenic risk analysis. (ekstern lenke)
• Oddmund Søvik; G E Matre; U Rishaug et al. (2002). familial hyperinsulinemic hypoglycemia with a mutation in the gene encoding short-chain 3-hydroxyacyl-coa dehydrogenase. (ekstern lenke)
• Anders Molven; G E Matre; E Jellum et al. (2002). A link between fatty acid oxidation and insulin secretion in the gen for short-chain 3-hydrozyacyl-CoA dehydrogenase leads to severe neonatal hypoglycemia with hyperinsulinism. (ekstern lenke)
• Pål Rasmus Njølstad; Knut Dahl-Jørgensen; U Sarici et al. (2002). Mild diabetes or permanent neonatal diabetes: Localization of glukoinase mutations linked to severity of phenotype. (ekstern lenke)
• L Bjørkhaug; Jørn Sagen; P Thorsby et al. (2002). Hepatocyte nuclear factor-1alpha gene mutations and diabetes in Norway. (ekstern lenke)
• Pål Rasmus Njølstad; Knut Dahl-Jørgensen; U Sarici et al. (2002). Mild diabetes or permanent neonatal diabetes: Localization of glucoinase mutations linked to severity of phenotype. (ekstern lenke)
• Lado Lako Loro; Salah Osman Ibrahim; Olav Karsten Vintermyr et al. (2004). Molecular analysis of the Ras-Raf signalling pathway in oral cancers. (ekstern lenke)
• Morten Lapin; Kjersti Tjensvoll; Yves Rozenholc et al. (2019). Sensitive detection of plasma mutations using a novel tag-based error suppression sequencing method. (ekstern lenke)
• Gry Sjøholt; Anne Karin Gulbrandsen; Roger Løvlie et al. (2000). Searching for genetic variations in inositol monophosphatase genes in lithium-treated manic-depressive patients. (ekstern lenke)
• Kristine Pettersen; Sonja Benedikte Andersen; Siver Andreas Moestue et al. (2013). Systemically accelerated autophagy causal in cancer cachexia?. (ekstern lenke)
• Kristine Pettersen; Sonja Benedikte Andersen; Almaz Nigatu Tesfahun et al. (2013). A role of autophagy in cancer cachexia. (ekstern lenke)
• Gry Sjøholt; Anne Karin Gulbrandsen; Roger Løvlie et al. (1999). Searching for genetic variations in inositol monophosphatase genes in lithium-treated manic-depressive patients. (ekstern lenke)
• Gry Sjøholt; Roger Løvlie; Anne Karin Gulbrandsen et al. (1999). The role of gene mutations of the inositol phospholipid signaling system in lithium-treated bipolar disorder. (ekstern lenke)
• Kristine Pettersen; Sonja Benedikte Andersen; Almaz Nigatu Tesfahun et al. (2012). A role of autophagy in cancer cachexia. (ekstern lenke)
• Gry Sjøholt; Anne Karin Gulbrandsen; Roger Løvlie et al. (2000). Searching for genetic variations in inositol monophosphatase genes in lithium-treated manic-depressive patients. (ekstern lenke)
• A Brendehaug; GO Ness; G Houge et al. (2003). Sox9 and human sex differentiation: Molecular and cytogenetic studies in a family with a case of true hermaphroditism. (ekstern lenke)

Rettelse i tidsskrift

• Sivaramakrishna Rachakonda; Nalini Srinivas; Seyed Hamidreza Mahmoudpour et al. (2018). Erratum to: Telomere length and survival in primary cutaneous melanoma patients. (ekstern lenke)
• David L. Duffy; Gu Zhu; Xin Li et al. (2019). Erratum to: Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (Nature Communications, (2018), 9, 1, (4774), 10.1038/s41467-018-06649-5). (ekstern lenke)

Fremhevet artikkel i media

• Anders Molven (1996). Nytt DNA-sekvenseringslaboratorium opna i Bergen. (ekstern lenke)
• Karianne Fjeld; Anders Molven (2015). Du vet nesten ingenting om det, men dette er et av kroppens mest sentrale organer. (ekstern lenke)
• Anders Molven (1997). Et mekka for molekylær marinbiologi. (ekstern lenke)
• Anders Molven (1995). Nobelprisen i fysiologi og medisin 1995 - fosterutviklingens mysterium. (ekstern lenke)
• Anders Molven (1995). Nobelprisen i medisin 1995 - genene som styrer fosterutviklingen. (ekstern lenke)
• Anders Molven; Rein Aasland (1991). Fakta om transkripsjonsfaktorer. (ekstern lenke)
• Anders Molven (1998). Stein Ove Døskeland: Vestlandsk vitenskapsmann med virketrang og visjoner. (ekstern lenke)

Fagbok

• Anders Molven; Anders Goksøyr (1992). Organochlorines and PAHs in the marine environment: State of art and research needs. Report to NTNF Research Programme on Marine Pollution, 1992. (ekstern lenke)

Leserbrev

• Sahba Shafiee; Pascal Francois Gelebart; Mihaela-Lucia Popa et al. (2021). Preclinical characterisation and development of a novel myelodysplastic syndrome-derived cell line. (ekstern lenke)
• Hanne Eknes Puntervoll; Anders Molven; Lars A. Akslen (2014). Frequency of somatic BRAF mutations in melanocytic lesions from patients in a CDK4 melanoma family. (ekstern lenke)
• Anders Molven (2005). A score of 25 in 1. (ekstern lenke)
• Anja Torsvik; Gro Vatne Røsland; Agnete Svendsen et al. (2010). Spontaneous Malignant Transformation of Human Mesenchymal Stem Cells Reflects Cross-Contamination: Putting the Research Field on Track - Letter. (ekstern lenke)
• Hanne Eknes Puntervoll; Anders Molven; Lars A. Akslen (2014). Frequencies of KIT and GNAQ mutations in acral melanoma. (ekstern lenke)

Populærvitenskapelig artikkel

• Anders Molven; Pål Rasmus Njølstad (1991). Når beina sitter på hodet! Om bananfluer, fosterutvikling og homeobokser. (ekstern lenke)
• Anders Molven (2006). Historiske norske arbeider: Jostein Goksøyr(1967): Evolution of eucaryotic cells. (ekstern lenke)
• Vidar Martin Steen; Anders Molven (2000). CYP2D6-gentest: ny rutineanalyse for identifisering av langsomme og ultraraske legemiddelomsettere. (ekstern lenke)
• Pål Rasmus Njølstad; Anders Molven (2010). Genetikk i fokus. (ekstern lenke)
• Anders Molven; Pål Rasmus Njølstad (2010). Monogen diabetes i Norge. (ekstern lenke)
• Anders Molven (1995). Scrapie - meir enn sauesjukdom. (Kronikk). (ekstern lenke)
• Anders Molven (1996). Jens Gabliel Hauge: Hvordan genene virker (Bokanmeldelse). (ekstern lenke)
• Anders Molven (1996). Nobelprisen i medisin 1995 - genene gir oss form. (ekstern lenke)
• Anders Molven (1995). Aarskog-genet endelig funnet. (ekstern lenke)
• Vidar Martin Steen; Anders Molven (2000). CYP2D6-gentest: ny rutineanalyse for identifisering av langsomme og ultraraske legemiddelomsettere. (ekstern lenke)
• Anders Molven (1995). Mikrobiologi-pionerer møttes i Bergen. (ekstern lenke)
• Anders Molven; LI Cressey; Ragnar Bøe (1995). Apoptose - når cellene dør. (ekstern lenke)
• Pål Rasmus Njølstad; Anders Molven (2003). Forskere diskuterte arv og diabetes. (ekstern lenke)

Masteroppgave

• Diego Iglesias Lopez; Anders Molven; Nils Henrik Halberg et al. (2024). Interplay of the proteotoxic CEL-MODY protein and oncogenic KRAS in pancreatic cancer development. (ekstern lenke)
• Alexander Williams; Nils Henrik Halberg; Anders Molven (2023). The Effect of Alternate Day Fasting on a Mouse Model of Pancreatic Ductal Adenocarcinoma. (ekstern lenke)

Forskningsrapport

• Pål Rasmus Njølstad; Anders Molven; Leif Groop (2009). Diabetes Genetics. A Seventh Sense for the Successful Sequel of ‘Come Together’. (ekstern lenke)
• Anders Molven; Anders Goksøyr; K. Næss et al. (1992). PAH og klororganiske forbindelser i det marine miljø: oppsummering av forskningsbehov med vekt på norske forhold. Rapport til Forskningsprogram om marin forurensing, NTNF, 1992. (ekstern lenke)

Forelesning

• Vidar Martin Steen; Ole A. Andreassen; Roger Løvlie et al. (1996). Detection of poor and ultrarapid metabolizers of psychopharmacological drugs. (ekstern lenke)
• Anders Molven; Roger Løvlie; Aud K. Eliassen et al. (1998). Pharmacogenetics: how genes influence drug response. (ekstern lenke)
• Roger Løvlie; Anne Karin Gulbrandsen; Anders Molven et al. (1998). Genomic structure and sequence analysis of a human inositol polyphosphate 1-phosphatase gene (INPP1). (ekstern lenke)
• Gry Sjøholt; Anders Molven; Roger Løvlie et al. (1998). Gene mutations of the phosphatidylinositol signaling system in lithium-treated manic-depressive patients. (ekstern lenke)
• Gry Sjøholt; Anne Karin Gulbrandsen; Roger Løvlie et al. (1998). Genomic characterization of genes encoding human myo-inositol monophosphatase enzymes. (ekstern lenke)

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