• 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

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

Mastergradsoppgave

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

Brev til redaktøren

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

Errata

• Duffy, David L.; Zhu, Gu; Li, Xin 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)
• Rachakonda, Sivaramakrishna; Srinivas, Nalini; Mahmoudpour, Seyed Hamidreza et al. (2018). Erratum to: Telomere length and survival in primary cutaneous melanoma patients. (ekstern lenke)

Poster

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

Vitenskapelig oversiktsartikkel/review

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

Doktorgradsavhandling

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

Sammendrag/abstract

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

Leder

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

Kronikk

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

Vitenskapelig Kapittel/Artikkel/Konferanseartikkel

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

Populærvitenskapelig artikkel

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

Leserinnlegg

• Torsvik, Anja; Røsland, Gro Vatne; Svendsen, Agnete et al. (2010). Spontaneous Malignant Transformation of Human Mesenchymal Stem Cells Reflects Cross-Contamination: Putting the Research Field on Track - Letter. (ekstern lenke)
• Molven, Anders (2005). A score of 25 in 1. (ekstern lenke)

Rapport

• Njølstad, Pål Rasmus; Molven, Anders; Groop, Leif (2009). Diabetes Genetics. A Seventh Sense for the Successful Sequel of ‘Come Together’. (ekstern lenke)
• Molven, Anders; Goksøyr, Anders; Næss, K. 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)

Vitenskapelig foredrag

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

Populærvitenskapelig foredrag

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

Fagbok

• Molven, Anders; Goksøyr, Anders (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)

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