Hjem
Anders Molvens bilde

Anders Molven

Professor
  • E-postAnders.Molven@uib.no
  • Telefon+47 55 97 31 69+47 480 21 044
  • Besøksadresse
    Avdeling for patologi, 2. etasje, Sentralblokken, Haukeland Universitets- sjukehus, Bergen
    Rom 
    5308
  • Postadresse
    Postboks 7804
    5020 Bergen
  • Pancreas-cancer (kreft i bukspyttkjertelen)
  • Arvelig diabetes (sukkersyke)
  • Arvelig hypoglykemi (lavt blodsukker)
  • Arvelig malignt melanom (føflekkreft)

    For flere opplysninger, se www.pancreas.no

Vitenskapelig artikkel
  • Vis forfatter(e) 2020. Unsupervised clustering of missense variants in HNF1A using multidimensional functional data aids clinical interpretation. American Journal of Human Genetics. 670-682.
  • Vis forfatter(e) 2020. Single nucleotide polymorphisms in CEL-HYB1 increase risk for chronic pancreatitis through proteotoxic misfolding. Human Mutation. 1967-1978.
  • Vis forfatter(e) 2020. Pathogenic Carboxyl Ester Lipase (CEL) Variants Interact with the Normal CEL Protein in Pancreatic Cells . Cells. 1-19.
  • Vis forfatter(e) 2020. Golgi-Localized PAQR4 Mediates Antiapoptotic Ceramidase Activity in Breast Cancer. Cancer Research. 2163-2174.
  • Vis forfatter(e) 2020. Genome-Wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility . Nature Genetics. 494-504.
  • Vis forfatter(e) 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. The Journal of Inherited Metabolic Disease (JIMD). 1-13.
  • Vis forfatter(e) 2020. Characterization of CEL-DUP2: Complete duplication of the carboxyl ester lipase gene is unlikely to influence risk of chronic pancreatitis. Pancreatology (Print). 377-384.
  • Vis forfatter(e) 2020. Association of HERV-K and LINE-1 hypomethylation with reduced disease-free survival in melanoma patients. Epigenomics. 1689-1706.
  • Vis forfatter(e) 2019. α11β1 integrin is induced in a subset of cancer- associated fibroblasts in desmoplastic tumor stroma and mediates in vitro cell migration. Cancers.
  • Vis forfatter(e) 2019. The hybrid allele 1 of carboxyl-ester lipase (CEL-HYB1) in Polish pediatric patients with chronic pancreatitis. Pancreatology (Print). 531-534.
  • Vis forfatter(e) 2019. Mutation analysis by deep sequencing of pancreatic juice from patients with pancreatic ductal adenocarcinoma. BMC Cancer. 1-12.
  • Vis forfatter(e) 2019. Integrin α11β1 is expressed in breast cancer stroma and associates with aggressive tumor phenotypes. The journal of pathology. Clinical research. 69-82.
  • Vis forfatter(e) 2019. Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth. Nature Communications. 1-10.
  • Vis forfatter(e) 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. Journal of Biological Chemistry. 19476-19491.
  • Vis forfatter(e) 2018. Telomere length and survival in primary cutaneous melanoma patients. Scientific Reports. 1-9.
  • Vis forfatter(e) 2018. Mice Carrying a Dominant-Negative Human PI3K Mutation Are Protected From Obesity and Hepatic Steatosis but Not Diabetes. Diabetes. 1297-1309.
  • Vis forfatter(e) 2017. Tissue MicroRNA profiles as diagnostic and prognostic biomarkers in patients with resectable pancreatic ductal adenocarcinoma and periampullary cancers. Biomarker Research.
  • Vis forfatter(e) 2017. The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes. Diabetes Research and Clinical Practice. 142-149.
  • Vis forfatter(e) 2017. Targeted next-generation sequencing reveals MODY in up to 6.5% of antibody-negative diabetes cases listed in the Norwegian Childhood Diabetes Registry. Diabetologia. 625-635.
  • Vis forfatter(e) 2017. Iris malformation and anterior segment dysgenesis in mice and humans with a mutation in PI 3-Kinase. Investigative Ophthalmology and Visual Science. 3100-3106.
  • Vis forfatter(e) 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. Clinical Case Reports. 761-768.
  • Vis forfatter(e) 2017. Heterogeneity of proliferative markers in pancreatic β-cells of patients with severe hypoglycemia following Roux-en-Y gastric bypass. Acta Diabetologica. 737-747.
  • Vis forfatter(e) 2017. Functional investigations of HNF1A identify rare variants as risk factors for type 2 diabetes in the general population. Diabetes. 335-346.
  • Vis forfatter(e) 2017. Functional characterization of a multi-cancer risk locus on chr5p15.33 reveals regulation of TERT by ZNF148. Nature Communications. 1-15.
  • Vis forfatter(e) 2017. Copy number variants and VNTR length polymorphisms of the carboxyl-ester lipase (CEL) gene as risk factors in pancreatic cancer. Pancreatology (Print). 83-88.
  • Vis forfatter(e) 2017. Cancer cachexia associates with a systemic autophagy-inducing activity mimicked by cancer cell-derived IL-6 trans-signaling. Scientific Reports. 1-16.
  • Vis forfatter(e) 2017. Associations between ABO blood groups and pancreatic ductal adenocarcinoma: influence on resection status and survival. Cancer Medicine. 1531-1540.
  • Vis forfatter(e) 2016. The hypoglycemic phenotype is islet cell-autonomous in short-chain hydroxyacyl-CoA dehydrogenase-deficient mice. Diabetes. 1672-1678.
  • Vis forfatter(e) 2016. PI3-kinase mutation linked to insulin and growth factor resistance in vivo. Journal of Clinical Investigation. 1401-1412.
  • Vis forfatter(e) 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. PLOS ONE.
  • Vis forfatter(e) 2016. Branched Fatty Acid Esters of Hydroxy Fatty Acids Are Preferred Substrates of the MODY8 Protein Carboxyl Ester Lipase. Biochemistry. 4636-4641.
  • Vis forfatter(e) 2016. A human clinical trial using ultrasound and microbubbles to enhance gemcitabine treatment of inoperable pancreatic cancer. Journal of Controlled Release. 172-181.
  • Vis forfatter(e) 2015. IGHV gene usage and mutational status in follicular lymphoma: Correlations with prognosis and patient age. Leukemia Research. 702-708.
  • Vis forfatter(e) 2015. Glycogenin-2 is dispensable for liver glycogen synthesis and glucagon-stimulated glucose release. Journal of Clinical Endocrinology and Metabolism. E767-E775.
  • Vis forfatter(e) 2015. Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. Nature Genetics. 987-995.
  • Vis forfatter(e) 2015. Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions. International Journal of Cancer. 1351-1360.
  • Vis forfatter(e) 2015. A recombined allele of the lipase gene CEL and its pseudogene CELP confers susceptibility to chronic pancreatitis. Nature Genetics. 518-522.
  • Vis forfatter(e) 2014. U-251 revisited: genetic drift and phenotypic consequences of long-term cultures of glioblastoma cells . Cancer Medicine. 812-824.
  • Vis forfatter(e) 2014. The effect on melanoma risk of genes previously associated with telomere length. Journal of the National Cancer Institute.
  • Vis forfatter(e) 2014. Prognostic value of bone marrow involvement by clonal immunoglobulin gene rearrangements in follicular lymphoma. Journal of Clinical Pathology. 1072-1077.
  • Vis forfatter(e) 2014. Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. Nature Genetics. 357-363.
  • Vis forfatter(e) 2014. First in-mouse development and application of a surgically relevant xenograft model of ovarian carcinoma. PLOS ONE.
  • Vis forfatter(e) 2014. Endocytosis of secreted carboxyl ester lipase in a syndrome of diabetes and pancreatic exocrine dysfunction. Journal of Biological Chemistry. 29097-29111.
  • Vis forfatter(e) 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. Diabetes. 259-269.
  • Vis forfatter(e) 2014. Assessment of Exocrine Pancreatic Function by Secretin-Stimulated Magnetic Resonance Cholangiopancreaticography and Diffusion-Weighted Imaging in Healthy Controls. Journal of Magnetic Resonance Imaging. 448-454.
  • Vis forfatter(e) 2013. Vascular proliferation is associated with survival in pancreatic ductal adenocarcinoma. APMIS - Journal of Pathologiy, Microbiology and Immunology. 1037-1046.
  • Vis forfatter(e) 2013. Type 2 diabetes genes : present status and data from Norwegian studies. Norsk Epidemiologi. 9-22.
  • Vis forfatter(e) 2013. The number of tandem repeats in the carboxyl-ester lipase (CEL) gene as a risk factor in alcoholic and idiopathic chronic pancreatitis. Pancreatology (Print). 29-32.
  • Vis forfatter(e) 2013. Severe pancreatic dysfunction but compensated nutritional status in monogenic pancreatic disease caused by carboxyl-ester lipase mutations. Pancreas. 1078-1084.
  • Vis forfatter(e) 2013. SHORT syndrome with partial lipodystrophy due to impaired phosphatidylinositol 3 kinase signaling. American Journal of Human Genetics. 150-157.
  • Vis forfatter(e) 2013. Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry. Diabetologia. 1512-1519.
  • Vis forfatter(e) 2013. Monogenetic diabetes mellitus in Norway :. Norsk Epidemiologi. 55-60.
  • Vis forfatter(e) 2013. Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants. Journal of Medical Genetics. 264-U82.
  • Vis forfatter(e) 2013. Generation of prostate tumor-initiating cells is associated with elevation of reactive oxygen species and IL-6/STAT3 signaling. Cancer Research. 7090-7100.
  • Vis forfatter(e) 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. Diabetic Medicine. 946-955.
  • Vis forfatter(e) 2013. Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes. Nature Genetics. 1380-1385.
  • Vis forfatter(e) 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. Melanoma research. 221-226.
  • Vis forfatter(e) 2013. Absence of diabetes and pancreatic exocrine dysfunction in a transgenic model of carboxyl-ester lipase-MODY (Maturity-Onset Diabetes of the young). PLOS ONE. 11 sider.
  • Vis forfatter(e) 2013. A variant in FTO shows association with melanoma risk not due to BMI. Nature Genetics. 428-432.
  • Vis forfatter(e) 2012. MC1R, ASIP, TYR, and TYRP1 gene variants in a population-based series of multiple primary melanomas. Genes, Chromosomes and Cancer. 654-661.
  • Vis forfatter(e) 2012. HNF1B mutation in a Turkish child with renal and exocrine pancreas insufficiency, diabetes and liver disease. Pediatric Diabetes. e1-e5.
  • Vis forfatter(e) 2012. GCK-MODY diabetes associated with protein misfolding, cellular self-association and degradation. Biochimica et Biophysica Acta - Molecular Basis of Disease. 1705-1715.
  • Vis forfatter(e) 2012. Familial occurrence of neonatal diabetes with duplications in chromosome 6q24: treatment with sulfonylurea and 40-yr follow-up. Pediatric Diabetes. 155-162.
  • Vis forfatter(e) 2012. Exome sequencing and genetic testing for MODY. PLOS ONE. 8 sider.
  • Vis forfatter(e) 2012. Clinical efficacy and safety of bevacizumab monotherapy in patients with metastatic melanoma: predictive importance of induced early hypertension. PLOS ONE. 8 sider.
  • Vis forfatter(e) 2011. Visualization of CD44 and CD133 in Normal Pancreas and Pancreatic Ductal Adenocarcinomas: Non-overlapping Membrane Expression in Cell Populations Positive for Both Markers. Journal of Histochemistry and Cytochemistry. 441-455.
  • Vis forfatter(e) 2011. The role of pancreatic imaging in monogenic diabetes. Nature Reviews Endocrinology.
  • Vis forfatter(e) 2011. Reprogramming of cell junction modules during stepwise epithelial to mesenchymal transition and accumulation of malignant features in vitro in a prostate cell model. Experimental Cell Research. 234-247.
  • Vis forfatter(e) 2011. Genome-wide association study identifies three new melanoma susceptibility loci. Nature Genetics. 1108-U98.
  • Vis forfatter(e) 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. Diabetes. 1637-1644.
  • Vis forfatter(e) 2011. Evaluation of four novel genetic variants affecting hemoglobin A1c levels in a population-based type 2 diabetes cohort (the HUNT2 study). BMC Medical Genetics. 6 sider.
  • Vis forfatter(e) 2011. Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development. Journal of Medical Genetics. 825-830.
  • Vis forfatter(e) 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. Journal of Biological Chemistry. 34593-34605.
  • Vis forfatter(e) 2011. Detection of clonality in follicular lymphoma using formalin-fixed, paraffin-embedded tissue samples and BIOMED-2 immunoglobulin primers. Journal of Clinical Pathology. 37-41.
  • Vis forfatter(e) 2010. Polygenic risk variants for Type 2 Diabetes susceptibility modify age at diagnosis in Monogenic HNF1A Diabetes. Diabetes. 266-271.
  • Vis forfatter(e) 2010. Pancreatic Function in Carboxyl-Ester Lipase Knockout Mice. Pancreatology (Print). 467-476.
  • Vis forfatter(e) 2010. Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes. Human Genetics. 55-64.
  • Vis forfatter(e) 2010. Long-range gene regulation links genomic type 2 diabetes and obesity risk regions to HHEX, SOX4, and IRX3. Proceedings of the National Academy of Sciences of the United States of America. 775-780.
  • Vis forfatter(e) 2010. Er formakogenetisk CYP2D6-testing nyttig? Tidsskrift for Den norske legeforening. 2224-2228.
  • Vis forfatter(e) 2010. Er farmakogenetisk CYP2D6-testing nyttig? Tidsskrift for Den norske legeforening. 2224-2228.
  • Vis forfatter(e) 2010. Disease progression and search for monogenic diabetes among children with new onset type 1 diabetes negative for ICA, GAD- and IA-2 antibodies. BMC Endocrine Disorders.
  • Vis forfatter(e) 2010. DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical twins. European Journal of Pediatrics. 207-213.
  • Vis forfatter(e) 2009. pRb2/p130 protein expression and RBL2 mutation analysis in Burkitt lymphoma from Uganda. BMC Clinical Pathology.
  • Vis forfatter(e) 2009. The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy. Clinical Genetics. 440-448.
  • Vis forfatter(e) 2009. Mutasjonsdiagnostikk ved syndromer knyttet til RAS/MAPK-signalveien. Tidsskrift for Den norske legeforening. 2358-2361.
  • Vis forfatter(e) 2009. Lymphomas diagnosed in Uganda during the HIB/AIDS pandemic. East African Medical Journal. 226-32.
  • Vis forfatter(e) 2009. Improved diagnostic segregation of mantle cell lymphoma by determination of cyclin D1/D3 expression ratio in formalin-fixed tissue. Diagnostic molecular pathology (Print). 150-155.
  • Vis forfatter(e) 2009. Identification of a CDK4 R24H mutation-positive melanoma family by analysis of early-onset melanoma patients in Latvia. Melanoma research. 119-122.
  • Vis forfatter(e) 2008. Wolcott-Rallison syndrome with 3-hydroxydicarboxylic aciduria and lethal outcome. The Journal of Inherited Metabolic Disease (JIMD).
  • Vis forfatter(e) 2008. Utredning og behandling av medfødt hyperinsulinisme (1): Molekylære og genetiske aspekter. Pediatrisk Endokrinologi. 37-43.
  • Vis forfatter(e) 2008. Reduced pancreatic volume in hepatocyte nuclear factor 1A-maturity-onset diabetes of the young. Journal of Clinical Endocrinology and Metabolism. 3505-3509.
  • Vis forfatter(e) 2008. Prevalence of HNF1A (MODY3) mutations in a Norwegian population (the HUNT2 Study). Diabetic Medicine. 775-781.
  • Vis forfatter(e) 2008. Population-based prevalence of CDKN2A and CDK4 mutations in patients with multiple primary melanomas. Genes, Chromosomes and Cancer. 175-184.
  • Vis forfatter(e) 2008. Pancreatic Exocrine Dysfunction in Maturity-Onset Diabetes of the Young Type 3. Diabetes Care. 306-310.
  • Vis forfatter(e) 2008. Neurological features and enzyme therapy in patients with endocrine and exocrine pancreas dysfunction due to CEL mutations. Diabetes Care. 1738-1740.
  • Vis forfatter(e) 2008. Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. Diabetes. 1131-1135.
  • Vis forfatter(e) 2008. Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. Diabetes. 1131-1135.
  • Vis forfatter(e) 2008. Mutation analysis of the EGFR-NRAS-BRAF pathway in melanomas from black Africans and other subgroups of cutaneous melanoma. Melanoma research. 29-35.
  • Vis forfatter(e) 2008. Lack of pancreatic body and tail in HNF1B mutation carriers. Diabetic Medicine. 782-787.
  • Vis forfatter(e) 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). Diabetologia. 971-977.
  • Vis forfatter(e) 2008. Expression of the "stem cell marker" CD133 in pancreas and pancreatic ductal adenocarcinomas. BMC Cancer. 14 sider.
  • Vis forfatter(e) 2008. Diagnostic screening of MODY2/GCK mutations in the Norwegian MODY Registry. Pediatric Diabetes. 442-449.
  • Vis forfatter(e) 2008. Clinicopathological characteristics and non-adhesive organ culture of insulinomas. Scandinavian Journal of Surgery. 42-49.
  • Vis forfatter(e) 2008. CD133 negative glioma cells form tumors in nude rats and give rise to CD133 positive cells. International Journal of Cancer. 761-768.
  • Vis forfatter(e) 2008. Activating glucokinase (GCK) Mutations as a cause of medically responsive congenital hyperinsulinism: prevalence in children and characterisation of a novel GCK mutation. European Journal of Endocrinology (EJE). 27-34.
  • Vis forfatter(e) 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. Diabetes. 3112-3117.
  • Vis forfatter(e) 2007. Pancreatic lipomatosis is a structural marker in nondiabetic children with mutations in carboxyl-Ester lipase. Diabetes. 444-449.
  • Vis forfatter(e) 2007. Biochemical and functional characterization of germ line KRAS mutations. Molecular and Cellular Biology. 7765-7770.
  • Vis forfatter(e) 2006. Molecular analysis of the PI3K-AKT pathway in uterine cervical neoplasia: Frequent PIK3CA amplification and AKT phosphorylation. International Journal of Cancer. 1877-1883.
  • Vis forfatter(e) 2006. From clinicogenetic studies of maturity-onset diabetes of the young to unraveling complex mechanisms of glucokinase regulation. Diabetes. 1713-1722.
  • Vis forfatter(e) 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. Diabetes. 1899-1903.
  • Vis forfatter(e) 2005. Molekylærgenetisk diagnostikk ved diabetes mellitus. Tidsskrift for Den norske legeforening. 2968-72.
  • Vis forfatter(e) 2005. Molekylærgenetisk diagnostikk ved diabetes mellitus. Tidsskrift for Den norske legeforening. 2968-2972.
  • Vis forfatter(e) 2005. Functional dissection of the HNF-1alpha transcription factor: A study on nuclear localization and transcriptional activation. DNA and Cell Biology. 661-669.
  • Vis forfatter(e) 2005. Diagnostic screening of NEUROD1 (MODY6) in subjects with MODY or gestational diabetes mellitus. Diabetic Medicine. 1012-1015.
  • Vis forfatter(e) 2005. BRAF and NRAS mutations are frequent in nodular melanoma but are not associated with tumor cell proliferation or patient survival. Journal of Investigative Dermatology. 312-317.
  • Vis forfatter(e) 2004. Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2 - Patient characteristics and initial response to sulfonylurea therapy. Diabetes. 2713-2718.
  • Vis forfatter(e) 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. Journal of Cellular Physiology. 349-358.
  • Vis forfatter(e) 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. Journal of Cellular Physiology. 349-358.
  • Vis forfatter(e) 2004. Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation. Diabetes. 221-227.
  • Vis forfatter(e) 2004. Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder. Molecular Psychiatry. 621-629.
  • Vis forfatter(e) 2003. Permanent neonatal diabetes mellitus due to glucokinase deficiency- an inborn error of the glucose-insulin signalling pathway. Diabetes. 2854-2860.
  • Vis forfatter(e) 2003. Permanent neonatal diabetes caused by glucokinase deficiency; inborn error of the glucose-insulin signaling pathway. Diabetes. 2854-2860.
  • Vis forfatter(e) 2003. Hepatocyte nuclear factor-1 alpha gene mutations and diabetes in Norway. Journal of Clinical Endocrinology and Metabolism. 920-931.
  • Vis forfatter(e) 2003. Hepatocyte nuclear factor- 1 alpha gene mutations and diabetes in Norway. Journal of Clinical Endocrinology and Metabolism. 920-931.
  • Vis forfatter(e) 2003. Forskere diskuterte diabetes. Diabetes for helsepersonell. 12-14.
  • Vis forfatter(e) 2003. Examination of IMPA1- and IMPA2 genes in manic-depressive patients: Association between IMPA2 promoter polymorphisms and bipolar disorder. Molecular Psychiatry. Epub-23Dec2003.
  • Vis forfatter(e) 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? Pharmacogenetics (London). 383-388.
  • Vis forfatter(e) 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? Pharmacogenetics (London). 383-388.
  • Vis forfatter(e) 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? Pharmacogenetics (London). 383-388.
  • Vis forfatter(e) 2002. Hunting for a hypoglyecemia gene:Severe neonatal hypoglyecemia in a consanguineuos family. American Journal of Medical Genetics. 40-46.
  • Vis forfatter(e) 2001. Polymorphisms in CYP2D6 duplication-negative individuals with the ultrarapid metabolizer phenotype: a role for the CYP2D6*35 allele in ultrarapid metabolism? Pharmacogenetics (London). 45-55.
  • Vis forfatter(e) 2001. Polymorphisms in CYP2D6 duplication-negative individuals with the ultrarapid metabolizer phenotype: a role for the CYP2D6*35 allele in ultrarapid metabolism? Pharmacogenetics (London). 45-55.
  • Vis forfatter(e) 2001. Permanent neonatal diabetes mellitus due to complete glucoinase deficiency. New England Journal of Medicine. 1588-1592.
  • Vis forfatter(e) 2001. N EONATAL D IABETES M ELLITUS D UE TO C OMPLETE G LUCOKINASE D EFICIENCY. New England Journal of Medicine. 1588-1592.
  • Vis forfatter(e) 2001. MODY-prosjektet ved Haukeland Sykehus: fra forskning til diagnostikk. Diabetes for helsepersonell. 23-24.
  • Vis forfatter(e) 2000. MODY associated with two novel hepatocyte nuclear factor 1 alpha loss of function mutations. Biochemical and Biophysical Research Communications - BBRC. 792-798.
  • Vis forfatter(e) 2000. MGM - Medisin, Gener og Mennesker. NBS-nytt. 25-27.
  • Vis forfatter(e) 2000. A simple test for the hot spot mutation P291fsinsC in MODY3. Diabetologia. 818-819.
  • Vis forfatter(e) 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. Molecular Psychiatry. 172-180.
  • Vis forfatter(e) 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. Molecular Psychiatry.
  • Vis forfatter(e) 1999. Genomic structure and sequence analysis of a human inositol polyphosphate 1-phosphatase gene (INPP1). Pharmacogenetics (London). 517-528.
  • Vis forfatter(e) 1997. Genomic structure and chromosomal localization of a human myo-inositol monophosphatase gene (IMPA). Genomics. 113-122.
  • Vis forfatter(e) 1997. Gap junctions and growth control in liver regeneration and in isolated rat hepatocytes. Hepatology. 847-855.
  • Vis forfatter(e) 1997. Gap junctions and growth control in liver regeneration and in isolated rat hepatocytes. Hepatology. 847-855.
  • Vis forfatter(e) 1997. Forfatterskap til besvær. Klinisk Biokemi i Norden. 7-10.
  • Vis forfatter(e) 1996. Ultrarapid metabolizers of debrisoquine: Characterization and PCR-based detection of alleles with duplication of the CYP2D6 gene. FEBS Letters. 30-34.
  • Vis forfatter(e) 1996. Ultrarapid metabilizers of debrisoquine : characterization and PCR-based detection of alleles with duplication of the CYP2D6 gene. FEBS Letters. 30-34.
  • Vis forfatter(e) 1996. Priser til begjær -del II. NBS-nytt. 20-21.
  • Vis forfatter(e) 1996. Priser til begjær (og #/en til besvær). NBS-nytt. 21-22.
  • Vis forfatter(e) 1996. Fusk og fanteri i forskningen. NBS-nytt. 16-22.
  • Vis forfatter(e) 1996. Fargerik forskar fyller femti. NBS-nytt. 20-21.
  • Vis forfatter(e) 1996. Chromosomal assignment of the human gene encoding the Fos-related antigen-2 (FRA-2) to chromosome 2p22-p23. Genomics. 72-75.
  • Vis forfatter(e) 1996. Chromosomal assignment of the human gene encoding the Fos-related antigen-2 (FRA-2) to chromosome 2p22-p23. Genomics. 72-75.
  • Vis forfatter(e) 1996. A retroviral element in the human CYP2D gene cluster. Pharmacogenetics (London). 375-377.
  • Vis forfatter(e) 1995. Uracil-DNA-glykosylase - en norsk suksesshistorie. NBS-nytt. 40-44.
  • Vis forfatter(e) 1995. Protein-folding med konsekvensar. Om scrapie, prionar og degenerative hjernesjukdomar. NBS-nytt. 12-15.
  • Vis forfatter(e) 1995. Med Goksøyr inn i genalderen. NBS-nytt. 23-24.
  • Vis forfatter(e) 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. Hum Molecul Genet. 2251-2257.
  • Vis forfatter(e) 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. Human Molecular Genetics. 2251-2257.
  • Vis forfatter(e) 1995. Conserved sequence patterns in phages Mu and Lambda. Biochimica et Biophysica Acta. 115-120.
  • Vis forfatter(e) 1995. Conserved sequence patterns in phages Mu and Lambda. Biochimica et Biophysica Acta. 115-120.
  • Vis forfatter(e) 1995. Apoptose - når cellene dør. Naturen. 18-26.
  • Vis forfatter(e) 1995. Aarskog-genet endelig klonet. NBS-nytt. 12-13.
  • Vis forfatter(e) 1992. The zebrafish homeobox gene Hox(zf-114): primary structure, expression pattern and evolutionary aspects. International Journal of Developmental Biology. 229-237.
  • Vis forfatter(e) 1992. Structure and early embryonic expression of the zebrafish engrailed-2 gene. Mechanisms of Development. 51-62.
  • Vis forfatter(e) 1991. Genomic structure and restricted neural expression of the zebrafish wnt-1 (int-1) gene. EMBO Journal. 799-807.
Vitenskapelig foredrag
  • Vis forfatter(e) 2004. PI3K/Akt signalveien ved livmorhalskreft.
  • Vis forfatter(e) 2004. HRAS, KRAS, NRAS and BRAF mutation analysis in oral squamous cell carcinomas from the Sudan.
  • Vis forfatter(e) 2003. Mutation analysis of the RAS-RAF pathway in pancreatic adenocarcinomas and malignant melanomas.
  • Vis forfatter(e) 2003. BRAF mutational analysis in oral dysplastic and neoplastic epithelial lesions.
  • Vis forfatter(e) 2001. Autosomal recessive glucagon deficiency and severe neonatal hypoglycemia: A candidate gene approach.
  • Vis forfatter(e) 1999. Searching for genetic variations in inositol monophosphatase genes in lithium-treated manic-depressive patients.
  • Vis forfatter(e) 1999. Molecular genetic analyses of Norwegian families with maturity-onset diabetes of the young.
  • Vis forfatter(e) 1999. Maturity onset diabetes of the young (MODY): A Norwegian experience.
  • Vis forfatter(e) 1998. Genomic structure and sequence analysis of a human inositol polyphosphate 1-phosphatase gene (INPP1).
  • Vis forfatter(e) 1998. Genomic characterization of genes encoding human myo-inositol monophosphatase enzymes.
  • Vis forfatter(e) 1998. Gene mutations of the phosphatidylinositol signaking system in lithium-treated manic-depressive patients.
Sammendrag/abstract
  • Vis forfatter(e) 2016. Ultrasound and microbubble enhanced treatment of inoperable pancreatic adeonocarcinoma. Journal of Clinical Oncology.
  • Vis forfatter(e) 2013. Detection of B-Cell Lymphoma in Bone Marrow Aspirates Using BIOMED-2 Immunoglobulin Primers. Laboratory Investigation. 320A-320A.
  • Vis forfatter(e) 2013. Detection of B-Cell Lymphoma in Bone Marrow Aspirates Using BIOMED-2 Immunoglobulin Primers. Modern Pathology. 320A-320A.
  • Vis forfatter(e) 2013. Cellular re-uptake of secreted carboxyl-ester lipase protein in CEL-MODY, a syndrome of diabetes and pancreatic exocrine dysfunction. Diabetologia. S152-S152.
  • Vis forfatter(e) 2010. Evaluation of BIOMED-2 PCR primers for detection of clonality in follicular lymphoma on formalin-fixed, paraffin-embedded samples. APMIS - Journal of Pathologiy, Microbiology and Immunology. 252-253.
  • Vis forfatter(e) 2009. The Genotypes and Phenotypes of Diabetes. Journal of the Pancreas.
  • Vis forfatter(e) 2009. Polygenic risk variants for type 2 diabetes susceptibility modify age at diagnosis in monogenic HNF1A diabetes. Journal of Medical Genetics. S26-S26.
  • Vis forfatter(e) 2009. Evaluation of BIOMED-2 PCR primers for detection of clonality in follicular lymphoma on formalin-fixed, paraffin-embedded samples. Virchows Archiv. 395-395.
  • Vis forfatter(e) 2008. The role of confirmed type 2 diabetes risk alleles on age-of-diagnosis in a Norwegian population based sample: the HUNT Study. Diabetologia. S129-S129.
  • Vis forfatter(e) 2008. Structural changes in the repeated region of the carboxyl-ester lipase (CEL) gene and the development of diabetes. Diabetologia. S123-S123.
  • Vis forfatter(e) 2008. SUR mutation in type 1 diabetes: autoimmunity prevents sulfonylurea rescue of diabetes caused by SUR1 mutation. Results from the Hvidore Study Group. Diabetologia. S116-S116.
  • Vis forfatter(e) 2008. Pancreatic exocrine dysfunction in diabetes: functional characterisation of the carboxyl-ester lipase gene. Diabetologia. S123-S124.
  • Vis forfatter(e) 2008. Congenital Hyperinsullnism: Prevalence Prevalence of activating glucokinase mutations and a novel mutation. Hormone Research. 41-41.
  • Vis forfatter(e) 2007. Pancreatic exocrine deficiency is common in MODY 3. Diabetologia. S123-S123.
  • Vis forfatter(e) 2006. AKT phosphorylation and PIK3CA amplification are common in cervical neoplasia. Modern Pathology. 172A-172A.
  • Vis forfatter(e) 2006. AKT phosphorylation and PIK3CA amplification are common in cervical neoplasia. Laboratory Investigation. 172A-172A.
Vitenskapelig oversiktsartikkel/review
  • Vis forfatter(e) 2018. The role of the carboxyl ester lipase (CEL) gene in pancreatic disease. Pancreatology (Print). 12-19.
  • Vis forfatter(e) 2015. The chromosome 9p21 CVD- and T2D-associated regions in a Norwegian population (the HUNT2 survey). International Journal of Endocrinology. 9 sider.
  • Vis forfatter(e) 2012. The role of pancreatic imaging in monogenic diabetes mellitus. Nature Reviews Endocrinology. 148-159.
  • Vis forfatter(e) 2011. Role of molecular genetics in transforming diagnosis of diabetes mellitus. Expert Review of Molecular Diagnostics. 313-320.
  • Vis forfatter(e) 2010. Fremskritt innen diabetesgenetikk. Tidsskrift for Den norske legeforening. 1145-1149.
  • Vis forfatter(e) 2006. Forstadier til kreft i bukspyttkjertelen. Tidsskrift for Den norske legeforening. 905-908.

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