Pancreatic cancer

Monogenic diabetes

Congenital hyperinsulinism of infancy

Melanoma genetics

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Academic article

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• 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. (external link)
• 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. (external link)
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• 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. (external link)
• 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. (external link)
• Hildegunn Høberg Vetti; Anders Molven; Aud Katrin Eliassen et al. (2010). Er farmakogenetisk CYP2D6-testing nyttig?. (external link)
• Anders Molven; Magne B. Grimstvedt; Solrun Steine et al. (2005). A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutation. (external link)
• Anders Molven; Oddmund Søvik; Charlotte von der Lippe et al. (2009). Mutasjonsdiagnostikk ved syndromer knyttet til RAS/MAPK-signalveien. (external link)
• 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. (external link)
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• 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. (external link)
• Tone Sandal; Oddmund Søvik; Pål Rasmus Njølstad et al. (2008). Utredning og behandling av medfødt hyperinsulinisme (1): Molekylære og genetiske aspekter. (external link)
• 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. (external link)
• Kishan Kumar Chudasama; Jonathan Winnay; Stefan Johansson et al. (2013). SHORT syndrome with partial lipodystrophy due to impaired phosphatidylinositol 3 kinase signaling. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• 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?. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• Anders Molven (1996). Fargerik forskar fyller femti. (external link)
• Pål Rasmus Njølstad; Oddmund Søvik; Antonio Cuesta-Munoz et al. (2001). Permanent neonatal diabetes mellitus due to complete glucoinase deficiency. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• 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). (external link)
• Jørn V. Sagen; Lise Bjørkhaug; Janne Molnes et al. (2008). Diagnostic screening of MODY2/GCK mutations in the Norwegian MODY Registry. (external link)
• 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. (external link)
• Anders Molven (1995). Uracil-DNA-glykosylase - en norsk suksesshistorie. (external link)
• Oddmund Søvik; Pål Rasmus Njølstad; Egil Jellum et al. (2008). Wolcott-Rallison syndrome with 3-hydroxydicarboxylic aciduria and lethal outcome. (external link)
• 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?. (external link)
• Anders Molven; Monika Ringdal; Anita-Merete Nordbø et al. (2008). Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. (external link)
• 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. (external link)
• Jørn V. Sagen; Maren E. Baumann; Helga Salvesen et al. (2005). Diagnostic screening of NEUROD1 (MODY6) in subjects with MODY or gestational diabetes mellitus. (external link)
• 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). (external link)
• Maria Negahdar; Ingvild Aukrust; Bente Berg Johansson et al. (2012). GCK-MODY diabetes associated with protein misfolding, cellular self-association and degradation. (external link)
• 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. (external link)
• Mette Vesterhus; Helge Ræder; Stefan Johansson et al. (2008). Pancreatic Exocrine Dysfunction in Maturity-Onset Diabetes of the Young Type 3. (external link)
• 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. (external link)
• 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. (external link)
• Dag Hoem; Oddbjørn Straume; Heike Immervoll et al. (2013). Vascular proliferation is associated with survival in pancreatic ductal adenocarcinoma. (external link)
• 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. (external link)
• 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. (external link)
• Sivaramakrishna Rachakonda; Nalini Srinivas; Seyed Hamidreza Mahmoudpour et al. (2018). Telomere length and survival in primary cutaneous melanoma patients. (external link)
• Anders Molven (1996). Priser til begjær (og #/en til besvær). (external link)
• Anders Molven; Vidar Martin Steen (1996). A retroviral element in the human CYP2D gene cluster. (external link)
• Bruna Dalmasso; Lorenza Pastorino; Vaishnavi Nathan et al. (2021). Germline ATM variants predispose to melanoma: a joint analysis across the GenoMEL and MelaNostrum consortia. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• Brett M. Cassidy; Sammy Zino; Karianne Fjeld et al. (2020). Single nucleotide polymorphisms in CEL-HYB1 increase risk for chronic pancreatitis through proteotoxic misfolding. (external link)
• Jason Flannick; G Thorleifsson; N Beer et al. (2014). Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. (external link)
• Karen Helene Ørstavik; Trine Tangeraas; Anders Molven et al. (2007). Distal phalangeal creases - A distinctive dysmorphic feature in disorders of the RAS signalling pathway?. (external link)
• Ingfrid Salvesen Haldorsen; Mette Vesterhus; Helge Ræder et al. (2008). Lack of pancreatic body and tail in HNF1B mutation carriers. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• 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?. (external link)
• 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. (external link)
• Mette Vesterhus; Helge Ræder; Amarnath J Kurpad et al. (2010). Pancreatic Function in Carboxyl-Ester Lipase Knockout Mice. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• Jennifer H. Barrett; MM Iles; M Harland et al. (2011). Genome-wide association study identifies three new melanoma susceptibility loci. (external link)
• Heike Immervoll; Dag Hoem; Per Øystein Sakariassen et al. (2008). Expression of the "stem cell marker" CD133 in pancreas and pancreatic ductal adenocarcinomas. (external link)
• 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. (external link)
• 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. (external link)
• Lise Bj. Gundersen; Jørn V. Sagen; P Thorsby et al. (2003). Hepatocyte nuclear factor-1 alpha gene mutations and diabetes in Norway. (external link)
• A Molven; M Ringdal; AM Nordbø et al. (2008). Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. (external link)
• Henrik Underthun Irgens; Janne Molnes; Bente Berg Johansson et al. (2013). Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry. (external link)
• 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. (external link)
• 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. (external link)
• L. Bjørkhaug; Stefan Johansson; Helge Ræder et al. (2005). Molekylærgenetisk diagnostikk ved diabetes mellitus. (external link)
• 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. (external link)
• 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. (external link)
• Line Pedersen; Pouda Panahandeh; Muntequa Ishtiaq Siraji et al. (2020). Golgi-Localized PAQR4 Mediates Antiapoptotic Ceramidase Activity in Breast Cancer. (external link)
• Sam Kalungi; Henry Wabinga; Anders Molven et al. (2009). Lymphomas diagnosed in Uganda during the HIB/AIDS pandemic. (external link)
• Sam Kalungi; Solrun Steine; Henry Wabinga et al. (2009). pRb2/p130 protein expression and RBL2 mutation analysis in Burkitt lymphoma from Uganda. (external link)
• 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. (external link)
• Lise Bjørkhaug; Y Horikawa; Hong Ye et al. (2000). MODY associated with two novel hepatocyte nuclear factor 1 alpha loss of function mutations. (external link)
• 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. (external link)
• 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. (external link)
• 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.. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• Ingfrid S. Haldorsen; Helge Ræder; Mette Vesterhus et al. (2011). The role of pancreatic imaging in monogenic diabetes. (external link)
• 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. (external link)
• Ellen Berget; Lars Helgeland; Knut Liseth et al. (2014). Prognostic value of bone marrow involvement by clonal immunoglobulin gene rearrangements in follicular lymphoma. (external link)
• Gry Sjøholt; Anders Molven; Roger Løvlie et al. (1997). Genomic structure and chromosomal localization of a human myo-inositol monophosphatase gene (IMPA). (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• Per Helsing; Dag André Nyrnoen; Sarah Ariansen et al. (2008). Population-based prevalence of CDKN2A and CDK4 mutations in patients with multiple primary melanomas. (external link)
• 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. (external link)
• Anders Molven; LI Cressey; Ragnar Bøe (1995). Apoptose - når cellene dør. (external link)
• Stefan Johansson; Henrik Underthun Irgens; Kishankumar Chudasama et al. (2012). Exome sequencing and genetic testing for MODY. (external link)
• Jonathon N. Winnay; Marie Holm Solheim; Ercument Dirice et al. (2016). PI3-kinase mutation linked to insulin and growth factor resistance in vivo. (external link)
• 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. (external link)
• 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.. (external link)
• Roger Løvlie; Anne Karin Gulbrandsen; Anders Molven et al. (1999). Genomic structure and sequence analysis of a human inositol polyphosphate 1-phosphatase gene (INPP1). (external link)
• 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). (external link)
• 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. (external link)
• Lise Bjørkhaug; Oddmund Søvik; Graeme I. Bell et al. (2000). A simple test for the hot spot mutation P291fsinsC in MODY3. (external link)
• Henrik Underthun Irgens; Karianne Fjeld; Bente Berg Johansson et al. (2015). Glycogenin-2 is dispensable for liver glycogen synthesis and glucagon-stimulated glucose release. (external link)
• Dag Hoem; Dag Jensen; Solrun Steine et al. (2008). Clinicopathological characteristics and non-adhesive organ culture of insulinomas. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• Anders Molven; Pål Rasmus Njølstad; Anders Fjose (1991). Genomic structure and restricted neural expression of the zebrafish wnt-1 (int-1) gene. (external link)
• 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. (external link)
• Ellen Berget; Anders Molven; Turid Løkeland et al. (2015). IGHV gene usage and mutational status in follicular lymphoma: Correlations with prognosis and patient age. (external link)
• 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. (external link)
• Erling Tjora; Anny Gravdal; Trond Engjom et al. (2021). Protein misfolding in combination with other risk factors in CEL-HYB1-mediated chronic pancreatitis. (external link)
• 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. (external link)
• 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. (external link)
• Christoffer Drabløs Velde; Hallvard Reigstad; Erling Tjora et al. (2023). Medfødt hyperinsulinisme. (external link)
• 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. (external link)
• Moses Musiime; Pugazendhi Murugan Erusappan; Edna Cukierman et al. (2024). Fibroblast integrin α11β1 is a collagen assembly receptor in mechanoregulated fibrillar adhesions. (external link)
• Pål Rasmus Njølstad; Anders Molven (2003). Forskere diskuterte diabetes. (external link)
• Anders Molven (2000). MGM - Medisin, Gener og Mennesker. (external link)
• L Bjørkhaug; Jørn V. Sagen; P Thorsby et al. (2003). Hepatocyte nuclear factor- 1 alpha gene mutations and diabetes in Norway. (external link)
• Christoffer Drabløs Velde; Janne Molnes; Siren Berland et al. (2025). Clinical and Genetic Characteristics of Congenital Hyperinsulinism in Norway: A Nationwide Cohort Study. (external link)
• Lise Bj. Gundersen; Stefan Johansson; Helge Ræder et al. (2005). Molekylærgenetisk diagnostikk ved diabetes mellitus. (external link)
• 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. (external link)
• 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. (external link)
• Anders Molven (1996). Fusk og fanteri i forskningen. (external link)
• Anders Molven (1996). Priser til begjær -del II. (external link)
• Suzanne Schubbert; Gideon Bollag; Natalya Lyubynska et al. (2007). Biochemical and functional characterization of germ line KRAS mutations. (external link)
• 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. (external link)
• Kari Espolin Fladmark; Bjørn Tore Gjertsen; Anders Molven et al. (1997). Gap junctions and growth control in liver regeneration and in isolated rat hepatocytes. (external link)
• B Stern; Anders Molven; D Kamp (1995). Conserved sequence patterns in phages Mu and Lambda. (external link)
• Anders Molven; U Rishaug; G E Matre et al. (2002). Hunting for a hypoglyecemia gene:Severe neonatal hypoglyecemia in a consanguineuos family. (external link)
• 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. (external link)
• 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. (external link)
• Anders Molven (1995). Med Goksøyr inn i genalderen. (external link)
• 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. (external link)
• 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. (external link)
• B Stern; Anders Molven; D Kamp (1995). Conserved sequence patterns in phages Mu and Lambda. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• Mette Vesterhus; Ingfrid Salvesen Haldorsen; Helge Ræder et al. (2008). Reduced pancreatic volume in hepatocyte nuclear factor 1A-maturity-onset diabetes of the young. (external link)
• 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. (external link)
• 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. (external link)
• Tone Sandal; Lene Bjerke Laborie; Klaus Brusgaard et al. (2009). The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy. (external link)
• 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. (external link)
• Helge Ræder; Stefan Johansson; Pål I. Holm et al. (2006). Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction. (external link)
• 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?. (external link)
• Oddmund Søvik; Henrik Underthun Irgens; Janne Molnes et al. (2013). Monogenetic diabetes mellitus in Norway :. (external link)
• 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.. (external link)
• Mark M. Iles; D. Timothy Bishop; John C. Taylor et al. (2014). The effect on melanoma risk of genes previously associated with telomere length. (external link)
• Anders Molven; Ivar Hordvik; Pål Rasmus Njølstad et al. (1992). The zebrafish homeobox gene Hox(zf-114): primary structure, expression pattern and evolutionary aspects. (external link)
• Anders Fjose; Pål Rasmus Njølstad; S. Nornes et al. (1992). Structure and early embryonic expression of the zebrafish engrailed-2 gene. (external link)
• Jens Kristoffer Hertel; Stefan Johansson; Kristian Midthjell et al. (2013). Type 2 diabetes genes : present status and data from Norwegian studies. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• Hildegunn Høberg Vetti; Anders Molven; Aud Katrin Eliassen et al. (2010). Er formakogenetisk CYP2D6-testing nyttig?. (external link)
• Pål Rasmus Njølstad; Lars Fredrik Engebretsen; Anders Molven et al. (2001). MODY-prosjektet ved Haukeland Sykehus: fra forskning til diagnostikk. (external link)
• Karianne Fjeld; Anny Gravdal Svanbring; Ranveig Seim Brekke et al. (2022). The genetic risk factor CEL-HYB1 causes proteotoxicity and chronic pancreatitis in mice. (external link)
• 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. (external link)
• 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. (external link)
• Stig Åge Eide; H Ræder; Helge Ræder et al. (2008). Prevalence of HNF1A (MODY3) mutations in a Norwegian population (the HUNT2 Study). (external link)
• Sevim Kahraman; Ercument Dirice; Giorgio Basile et al. (2022). Abnormal exocrine–endocrine cell cross-talk promotes β-cell dysfunction and loss in MODY8. (external link)
• Anders Molven (1997). Forfatterskap til besvær. (external link)
• K.E. Flatmark; B.T. Gjertsen; Anders Molven et al. (1997). Gap junctions and growth control in liver regeneration and in isolated rat hepatocytes. (external link)
• Anders Molven (1995). Aarskog-genet endelig klonet. (external link)
• Anders Molven (1995). Protein-folding med konsekvensar. Om scrapie, prionar og degenerative hjernesjukdomar. (external link)

Conference abstract

• Ellen Berget; Lars Helgeland; Anders Molven et al. (2013). Detection of B-Cell Lymphoma in Bone Marrow Aspirates Using BIOMED-2 Immunoglobulin Primers. (external link)
• Bjørn Inge Bertelsen; Solrun Steine; Roar Sandvei et al. (2006). AKT phosphorylation and PIK3CA amplification are common in cervical neoplasia. (external link)
• 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. (external link)
• Mette Vesterhus; Stefan Johansson; Helge Ræder et al. (2007). Pancreatic exocrine deficiency is common in MODY 3. (external link)
• Georg Gjorgji Dimcevski; Spiros Kotopoulis; Tormod Karlsen Bjånes et al. (2016). Ultrasound and microbubble enhanced treatment of inoperable pancreatic adeonocarcinoma. (external link)
• 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. (external link)
• Janniche Torsvik; Bente Berg Johansson; Stefan Johansson et al. (2008). Pancreatic exocrine dysfunction in diabetes: functional characterisation of the carboxyl-ester lipase gene. (external link)
• 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. (external link)
• Pål Rasmus Njølstad; Anders Molven; Leif Groop (2009). The Genotypes and Phenotypes of Diabetes. (external link)
• Henrik B. Thybo Christesen; Nicholas D. Tribble; Anders Molven et al. (2008). Congenital Hyperinsullnism: Prevalence Prevalence of activating glucokinase mutations and a novel mutation. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• Ellen Berget; Lars Helgeland; Anders Molven et al. (2013). Detection of B-Cell Lymphoma in Bone Marrow Aspirates Using BIOMED-2 Immunoglobulin Primers. (external link)
• Bjørn Inge Bertelsen; Solrun Steine; Roar Sandvei et al. (2006). AKT phosphorylation and PIK3CA amplification are common in cervical neoplasia. (external link)

Editorial/Leader article

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

Media feature article

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

Doctoral thesis (PhD)

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

Conference poster

• Gry Sjøholt; Anne Karin Gulbrandsen; Roger Løvlie et al. (2000). Searching for genetic variations in inositol monophosphatase genes in lithium-treated manic-depressive patients. (external link)
• 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. (external link)
• 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. (external link)
• 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. (external link)
• L Bjørkhaug; Jørn Sagen; P Thorsby et al. (2002). Hepatocyte nuclear factor-1alpha gene mutations and diabetes in Norway. (external link)
• Lado Lako Loro; Salah Osman Ibrahim; Olav Karsten Vintermyr et al. (2004). Molecular analysis of the Ras-Raf signalling pathway in oral cancers. (external link)
• Morten Lapin; Kjersti Tjensvoll; Yves Rozenholc et al. (2019). Sensitive detection of plasma mutations using a novel tag-based error suppression sequencing method. (external link)
• Kristine Pettersen; Sonja Benedikte Andersen; Almaz Nigatu Tesfahun et al. (2013). A role of autophagy in cancer cachexia. (external link)
• 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. (external link)
• Kristine Pettersen; Sonja Benedikte Andersen; Siver Andreas Moestue et al. (2013). Systemically accelerated autophagy causal in cancer cachexia?. (external link)
• Gry Sjøholt; Anne Karin Gulbrandsen; Roger Løvlie et al. (1999). Searching for genetic variations in inositol monophosphatase genes in lithium-treated manic-depressive patients. (external link)
• 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. (external link)
• Miguel Angel Juarez Garzon; Ksenia Kuznetsova; Divya Sri Priyanka Tallapragada et al. (2024). Pediatric Diabetes Clustering: Phenotypic and polygenic risk analysis. (external link)
• 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. (external link)
• Kristine Pettersen; Sonja Benedikte Andersen; Almaz Nigatu Tesfahun et al. (2012). A role of autophagy in cancer cachexia. (external link)
• Gry Sjøholt; Anne Karin Gulbrandsen; Roger Løvlie et al. (2000). Searching for genetic variations in inositol monophosphatase genes in lithium-treated manic-depressive patients. (external link)

Research report

• 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. (external link)
• Pål Rasmus Njølstad; Anders Molven; Leif Groop (2009). Diabetes Genetics. A Seventh Sense for the Successful Sequel of ‘Come Together’. (external link)

Popular science article

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

Academic book chapter

• Pål Rasmus Njølstad; Anders Molven; Oddmund Søvik (2005). Diagnosis and mangement of MODY in a pediatric setting. (external link)
• 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. (external link)
• Georg Gjorgji Dimcevski; Spiros Kotopoulis; Dag Hoem et al. (2013). Ultrasound-assisted treatment of an inoperable pancreatic cancer. (external link)
• Anders Molven (1997). p53 er vår indre vaktmester. (external link)
• Anders Molven; Anders Goksøyr (1993). Biological effects and biomonitoring of organochlorines and polycyclic aromatic hydrocarbons in the marine environment. (external link)
• Anders Molven; Pål Rasmus Njølstad; Anders Fjose (1993). Pattern formation in fish embryos: Characterization of homebox genes from the zebrafish (Brachydranio rerio). (external link)

Conference lecture

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

Lecture

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

Academic literature review

• Ingfrid S. Haldorsen; Helge Ræder; Mette Vesterhus et al. (2012). The role of pancreatic imaging in monogenic diabetes mellitus. (external link)
• Bente Berg Johansson; Karianne Fjeld; Khadija el Jellas et al. (2018). The role of the carboxyl ester lipase (CEL) gene in pancreatic disease. (external link)
• 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). (external link)
• Anders Molven; Pål Rasmus Njølstad (2011). Role of molecular genetics in transforming diagnosis of diabetes mellitus. (external link)
• Pål Rasmus Njølstad; Jens Kristoffer Hertel; Oddmund Søvik et al. (2010). Fremskritt innen diabetesgenetikk. (external link)
• Kjetil Søreide; Heike Immervoll; Anders Molven (2006). Forstadier til kreft i bukspyttkjertelen. (external link)

Master’s thesis

• 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. (external link)
• Alexander Williams; Nils Henrik Halberg; Anders Molven (2023). The Effect of Alternate Day Fasting on a Mouse Model of Pancreatic Ductal Adenocarcinoma. (external link)

Letter to the editor

• Sahba Shafiee; Pascal Francois Gelebart; Mihaela-Lucia Popa et al. (2021). Preclinical characterisation and development of a novel myelodysplastic syndrome-derived cell line. (external link)
• Hanne Eknes Puntervoll; Anders Molven; Lars A. Akslen (2014). Frequency of somatic BRAF mutations in melanocytic lesions from patients in a CDK4 melanoma family. (external link)
• 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. (external link)
• Hanne Eknes Puntervoll; Anders Molven; Lars A. Akslen (2014). Frequencies of KIT and GNAQ mutations in acral melanoma. (external link)
• Anders Molven (2005). A score of 25 in 1. (external link)

Journal corrigendum

• 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). (external link)
• Sivaramakrishna Rachakonda; Nalini Srinivas; Seyed Hamidreza Mahmoudpour et al. (2018). Erratum to: Telomere length and survival in primary cutaneous melanoma patients. (external link)

Non-fiction monograph

• 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. (external link)

See a complete overview of publications in Cristin.