Anders
Molven
Professor
Visit Address:
Department of Pathology, 2nd floor, Sentralblokken, Haukeland University Hospital, Bergen
Room:
5308
Postal Address:
Postboks 7804
5021 Bergen
Phone:
+47 55 97 31 69
E-mail:
Pancreatic cancer
Monogenic diabetes
Congenital hyperinsulinism of infancy
Melanoma genetics
Books
- 1992. Organochlorines and PAHs in the marine environment: State of art and research needs. Report to NTNF Research Programme on Marine Pollution, 1992.
Journal articles
- 2014. Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions. International Journal of Cancer. doi: 10.1002/ijc.29099
- 2014. Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. Nature Genetics. 46: 357-363. doi: 10.1038/ng.2915
- 2014. First in-mouse development and application of a surgically relevant xenograft model of ovarian carcinoma. PLoS ONE. 9. doi: 10.1371/journal.pone.0089527
- 2014. The effect on melanoma risk of genes previously associated with telomere length. Journal of the National Cancer Institute. 106.
- 2014. Frequency of somatic BRAF mutations in melanocytic lesions from patients in a CDK4 melanoma family. Pigment Cell & Melanoma Research. 27: 149-151. doi: 10.1111/pcmr.12191
- 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. 63: 259-269. doi: 10.2337/db13-1012
- 2014. Assessment of Exocrine Pancreatic Function by Secretin-Stimulated Magnetic Resonance Cholangiopancreaticography and Diffusion-Weighted Imaging in Healthy Controls. Journal of Magnetic Resonance Imaging. 39: 448-454. doi: 10.1002/jmri.24167
- 2013. Detection of B-Cell Lymphoma in Bone Marrow Aspirates Using BIOMED-2 Immunoglobulin Primers. Laboratory Investigation. 93: 320A-320A.
- 2013. Detection of B-Cell Lymphoma in Bone Marrow Aspirates Using BIOMED-2 Immunoglobulin Primers. Modern Pathology. 26: 320A-320A.
- 2013. SHORT syndrome with partial lipodystrophy due to impaired phosphatidylinositol 3 kinase signaling. American Journal of Human Genetics. 93: 150-157. doi: 10.1016/j.ajhg.2013.05.023
- 2013. Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes. Nature Genetics. 45: 1380-1385. doi: 10.1038/ng.2794
- 2013. Type 2 diabetes genes : present status and data from Norwegian studies. Norsk Epidemiologi. 23: 9-22.
- 2013. Vascular proliferation is associated with survival in pancreatic ductal adenocarcinoma. Acta Pathologica, Microbiologica et Immunologica Scandinavica (APMIS). 121: 1037-1046. doi: 10.1111/apm.12057
- 2013. A variant in FTO shows association with melanoma risk not due to BMI. Nature Genetics. 45: 428-432. doi: 10.1038/ng.2571
- 2013. Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry. Diabetologia. 56: 1512-1519. doi: 10.1007/s00125-013-2916-y
- 2013. Cellular re-uptake of secreted carboxyl-ester lipase protein in CEL-MODY, a syndrome of diabetes and pancreatic exocrine dysfunction. Diabetologia. 56: S152-S152.
- 2013. Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants. Journal of Medical Genetics. 50: 264-U82. doi: 10.1136/jmedgenet-2012-101455
- 2013. Generation of prostate tumor-initiating cells is associated with elevation of reactive oxygen species and IL-6/STAT3 signaling. Cancer Research. 73: 7090-7100. doi: 10.1158/0008-5472.CAN-13-1560
- 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). 13: 29-32. doi: 10.1016/j.pan.2012.12.059
- 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. 8. 11 pages. doi: 10.1371/journal.pone.0060229
- 2013. Monogenetic diabetes mellitus in Norway :. Norsk Epidemiologi. 23: 55-60.
- 2013. Severe pancreatic dysfunction but compensated nutritional status in monogenic pancreatic disease caused by carboxyl-ester lipase mutations. Pancreas. 42: 1078-1084. doi: 10.1097/MPA.0b013e3182920e9c
- 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. 30: 946-955. doi: 10.1111/dme.12190
- 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. 23: 221-226. doi: 10.1097/CMR.0b013e3283608695
- 2012. HNF1B mutation in a Turkish child with renal and exocrine pancreas insufficiency, diabetes and liver disease. Pediatric Diabetes. 13: e1-e5. doi: 10.1111/j.1399-5448.2011.00773.x
- 2012. The role of pancreatic imaging in monogenic diabetes mellitus. Nature Reviews Endocrinology. 8: 148-159. doi: 10.1038/nrendo.2011.197
- 2012. MC1R, ASIP, TYR, and TYRP1 gene variants in a population-based series of multiple primary melanomas. Genes, Chromosomes and Cancer. 51: 654-661. doi: 10.1002/gcc.21952
- 2012. Exome sequencing and genetic testing for MODY. PLoS ONE. 7. 8 pages. doi: 10.1371/journal.pone.0038050
- 2012. GCK-MODY diabetes associated with protein misfolding, cellular self-association and degradation. Biochimica et Biophysica Acta - Molecular Basis of Disease. 1822: 1705-1715. doi: 10.1016/j.bbadis.2012.07.005
- 2012. To test, or not to test: time for a MODY calculator? Diabetologia. 55: 1231-1234. doi: 10.1007/s00125-012-2514-4
- 2012. Skreddersydd medisin eller narsissomikk? Tidsskrift for Den norske legeforening. 132: 1844-1845. Published 2012-09-04. doi: 10.4045/tidsskr.12.0582
- 2012. Clinical efficacy and safety of bevacizumab monotherapy in patients with metastatic melanoma: predictive importance of induced early hypertension. PLoS ONE. 7. 8 pages. doi: 10.1371/journal.pone.0038364
- 2012. Familial occurrence of neonatal diabetes with duplications in chromosome 6q24: treatment with sulfonylurea and 40-yr follow-up. Pediatric Diabetes. 13: 155-162. doi: 10.1111/j.1399-5448.2011.00776.x
- 2011. Genome-wide association study identifies three new melanoma susceptibility loci. Nature Genetics. 43: 1108-U98. doi: 10.1038/ng.959
- 2011. Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development. Journal of Medical Genetics. 48: 825-830. doi: 10.1136/jmedgenet-2011-100255
- 2011. Detection of clonality in follicular lymphoma using formalin-fixed, paraffin-embedded tissue samples and BIOMED-2 immunoglobulin primers. Journal of Clinical Pathology. 64: 37-41. doi: 10.1136/jcp.2010.081109
- 2011. The role of pancreatic imaging in monogenic diabetes. Nature Reviews Endocrinology. doi: 10.1038/nrendo.2011.197
- 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. 12. 6 pages. doi: 10.1186/1471-2350-12-20
- 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. 60: 1637-1644. doi: 10.2337/db10-1340
- 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. 59: 441-455. doi: 10.1369/0022155411398275
- 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. 286: 34593-34605. doi: 10.1074/jbc.M111.222679
- 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. 317: 234-247. doi: 10.1016/j.yexcr.2010.10.009
- 2011. Role of molecular genetics in transforming diagnosis of diabetes mellitus. Expert Review of Molecular Diagnostics. 11: 313-320. doi: 10.1586/ERM.10.123
- 2010. Polygenic risk variants for Type 2 Diabetes susceptibility modify age at diagnosis in Monogenic HNF1A Diabetes. Diabetes. 59: 266-271. doi: 10.2337/db09-0555
- 2010. Evaluation of BIOMED-2 PCR primers for detection of clonality in follicular lymphoma on formalin-fixed, paraffin-embedded samples. Acta Pathologica, Microbiologica et Immunologica Scandinavica (APMIS). 118: 252-253.
- 2010. DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical twins. European Journal of Pediatrics. 169: 207-213. doi: 10.1007/s00431-009-1008-y
- 2010. Monogen diabetes i Norge. Diabetesforum. 23: 10-15.
- 2010. Fremskritt innen diabetesgenetikk. Tidsskrift for Den norske legeforening. 130: 1145-1149.
- 2010. Genetikk i fokus. Diabetesforum. 23: 6-9.
- 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. 10. doi: 10.1186/1472-6823-10-16
- 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 Science of the United States of America. 107: 775-780. doi: 10.1073/pnas.0911591107
- 2010. Spontaneous Malignant Transformation of Human Mesenchymal Stem Cells Reflects Cross-Contamination: Putting the Research Field on Track - Letter. Cancer Research. 70: 6393-6396. doi: 10.1158/0008-5472.CAN-10-1305
- 2010. Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes. Human Genetics. 127: 55-64. doi: 10.1007/s00439-009-0740-8
- 2010. Pancreatic Function in Carboxyl-Ester Lipase Knockout Mice. Pancreatology (Print). 10: 467-476. doi: 10.1159/000266284
- 2010. Er farmakogenetisk CYP2D6-testing nyttig? Tidsskrift for Den norske legeforening. 130: 2224-2228.
- 2010. Er formakogenetisk CYP2D6-testing nyttig? Tidsskrift for Den norske legeforening. 130: 2224-2228. doi: 10.4045/tidsskr.09.1445
- 2009. Polygenic risk variants for type 2 diabetes susceptibility modify age at diagnosis in monogenic HNF1A diabetes. Journal of Medical Genetics. 46: S26-S26.
- 2009. Evaluation of BIOMED-2 PCR primers for detection of clonality in follicular lymphoma on formalin-fixed, paraffin-embedded samples. Virchows Archiv. 455: 395-395.
- 2009. pRb2/p130 protein expression and RBL2 mutation analysis in Burkitt lymphoma from Uganda. BMC Clinical Pathology. 9. Published 2009-08-19. doi: 10.1186/1472-6890-9-6
- 2009. Lymphomas diagnosed in Uganda during the HIB/AIDS pandemic. East African Medical Journal. 86: 226-32.
- 2009. Improved diagnostic segregation of mantle cell lymphoma by determination of cyclin D1/D3 expression ratio in formalin-fixed tissue. Diagnostic molecular pathology. 18: 150-155. doi: 10.1097/PDM.0b013e31818935d2
- 2009. Mutasjonsdiagnostikk ved syndromer knyttet til RAS/MAPK-signalveien. Tidsskrift for Den norske legeforening. 129: 2358-2361.
- 2009. The Genotypes and Phenotypes of Diabetes. Journal of the Pancreas. 10.
- 2009. Identification of a CDK4 R24H mutation-positive melanoma family by analysis of early-onset melanoma patients in Latvia. Melanoma research. 19: 119-122. doi: 10.1097/CMR.0b013e3283287d3e
- 2009. The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy. Clinical Genetics. 75: 440-448. doi: 10.1111/j.1399-0004.2009.01152.x
- 2008. Mutation analysis of the EGFR-NRAS-BRAF pathway in melanomas from black Africans and other subgroups of cutaneous melanoma. Melanoma research. 18: 29-35.
- 2008. Congenital Hyperinsullnism: Prevalence Prevalence of activating glucokinase mutations and a novel mutation. Hormone Research. 70: 41-41.
- 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. 159: 27-34. doi: 10.1530/EJE-08-0203
- 2008. Prevalence of HNF1A (MODY3) mutations in a Norwegian population (the HUNT2 Study). Diabetic Medicine. 25: 775-781. doi: 10.1111/j.1464-5491.2008.02459.x
- 2008. Structural changes in the repeated region of the carboxyl-ester lipase (CEL) gene and the development of diabetes. Diabetologia. 51: S123-S123. doi: 10.1007/s00125-008-1117-6
- 2008. Lack of pancreatic body and tail in HNF1B mutation carriers. Diabetic Medicine. 25: 782-787. doi: 10.1111/j.1464-5491.2008.02460.x
- 2008. Population-based prevalence of CDKN2A and CDK4 mutations in patients with multiple primary melanomas. Genes, Chromosomes and Cancer. 47: 175-184. doi: 10.1002/gcc.20518
- 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. 51: 971-977. doi: 10.1007/s00125-008-0982-3
- 2008. Clinicopathological characteristics and non-adhesive organ culture of insulinomas. Scandinavian Journal of Surgery. 97: 42-49.
- 2008. Expression of the "stem cell marker" CD133 in pancreas and pancreatic ductal adenocarcinomas. BMC Cancer. 8. 14 pages. doi: 10.1186/1471-2407-8-48
- 2008. The role of confirmed type 2 diabetes risk alleles on age-of-diagnosis in a Norwegian population based sample: the HUNT Study. Diabetologia. 51: S129-S129. doi: 10.1007/s00125-008-1117-6
- 2008. Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. Diabetes. 57: 1131-1135.
- 2008. Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes. Diabetes. 57: 1131-1135. doi: 10.2337/db07-1467
- 2008. SUR mutation in type 1 diabetes: autoimmunity prevents sulfonylurea rescue of diabetes caused by SUR1 mutation. Results from the Hvidore Study Group. Diabetologia. 51: S116-S116. doi: 10.1007/s00125-008-1117-6
- 2008. Diagnostic screening of MODY2/GCK mutations in the Norwegian MODY Registry. Pediatric Diabetes. 9: 442-449. doi: 10.1111/j.1399-5448.2008.00399.x
- 2008. Utredning og behandling av medfødt hyperinsulinisme (1): Molekylære og genetiske aspekter. Pediatrisk Endokrinologi. 28: 37-43.
- 2008. Wolcott-Rallison syndrome with 3-hydroxydicarboxylic aciduria and lethal outcome. Journal of Inherited Metabolic Disease. doi: 10.1007/s10545-008-0866-1
- 2008. Pancreatic exocrine dysfunction in diabetes: functional characterisation of the carboxyl-ester lipase gene. Diabetologia. 51: S123-S124. doi: 10.1007/s00125-008-1117-6
- 2008. Reduced pancreatic volume in hepatocyte nuclear factor 1A-maturity-onset diabetes of the young. Journal of Clinical Endocrinology and Metabolism. 93: 3505-3509. doi: 10.1210/jc.2008-0340
- 2008. Neurological features and enzyme therapy in patients with endocrine and exocrine pancreas dysfunction due to CEL mutations. Diabetes Care. 31: 1738-1740. doi: 10.2337/dc07-2217
- 2008. Pancreatic Exocrine Dysfunction in Maturity-Onset Diabetes of the Young Type 3. Diabetes Care. 31: 306-310. doi: 10.2337/dc07-1002
- 2008. CD133 negative glioma cells form tumors in nude rats and give rise to CD133 positive cells. International Journal of Cancer. 122: 761-768. doi: 10.1002/ijc.23130
- 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. 56: 3112-3117. doi: 10.2337/db07-0513
- 2007. Pancreatic lipomatosis is a structural marker in nondiabetic children with mutations in carboxyl-Ester lipase. Diabetes. 56: 444-449. doi: 10.2337/db06-0859
- 2007. Biochemical and functional characterization of germ line KRAS mutations. Molecular and Cellular Biology. 27: 7765-7770. doi: 10.1128/MCB.00965-07
- 2007. De novo HRAS and KRAS mutations in two siblings with short stature and neuro-cardio-facio-cutaneous features. Journal of Medical Genetics. 44. 6 pages. doi: 10.1136/jmg.2007.049361
- 2007. Pancreatic exocrine deficiency is common in MODY 3. Diabetologia. 50: S123-S123. doi: 10.1007/s00125-007-0809-7
- 2007. Distal phalangeal creases - A distinctive dysmorphic feature in disorders of the RAS signalling pathway? European Journal of Medical Genetics. 50: 155-158. doi: 10.1016/j.ejmg.2006.12.003
- 2006. Molecular analysis of the PI3K-AKT pathway in uterine cervical neoplasia: Frequent PIK3CA amplification and AKT phosphorylation. International Journal of Cancer. 118: 1877-1883. doi: 10.1002/ijc.21461
- 2006. AKT phosphorylation and PIK3CA amplification are common in cervical neoplasia. Laboratory Investigation. 86: 172A-172A.
- 2006. AKT phosphorylation and PIK3CA amplification are common in cervical neoplasia. Modern Pathology. 19: 172A-172A.
- 2006. Molecular analysis of the EGFR-RAS-RAF pathway in pancreatic ductal adenocarcinomas: lack of mutations in the BRAF and EGFR genes. Virchows Archiv. 448: 788-796. doi: 10.1007/s00428-006-0191-8
- 2006. Historiske norske arbeider: Jostein Goksøyr(1967): Evolution of eucaryotic cells. NBS-nytt. 30: 6-7.
- 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. 55: 1899-1903. doi: 10.2337/db05-1677
- 2006. Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction. Nature Genetics. 38: 54-62. doi: 10.1038/ng1708
- 2006. From clinicogenetic studies of maturity-onset diabetes of the young to unraveling complex mechanisms of glucokinase regulation. Diabetes. 55: 1713-1722.
- 2006. From clinicogenetic studies of maturity-onset diabetes of the young to unraveling complex mechanisms of glucokinase regulation. Diabetes. 55: 1713-1722. doi: 10.2337/db05-1513
- 2006. Forstadier til kreft i bukspyttkjertelen. Tidsskrift for Den norske legeforening. 126: 905-908.
- 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. 125: 312-317.
- 2005. Molekylærgenetisk diagnostikk ved diabetes mellitus. Tidsskrift for Den norske legeforening. 125: 2968-72.
- 2005. Molekylærgenetisk diagnostikk ved diabetes mellitus. Tidsskrift for Den norske legeforening. 125: 2968-2972.
- 2005. Functional dissection of the HNF-1alpha transcription factor: A study on nuclear localization and transcriptional activation. DNA and Cell Biology. 24: 661-669.
- 2005. Molekylærgenetisk diagnostikk ved diabetes mellitus. Tidsskrift for Den norske legeforening. 125: 2968-2972.
- 2005. A score of 25 in 1. The Scientist (Philadelphia, Pa.). 19: 8-8.
- 2005. A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutation. Genes, Chromosomes and Cancer. 44: 10-18. doi: 10.1002/gcc.20202
- 2005. Diagnostic screening of NEUROD1 (MODY6) in subjects with MODY or gestational diabetes mellitus. Diabetic Medicine. 22: 1012-1015.
- 2004. Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation. Diabetes. 53: 221-227.
- 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. 201: 349-358.
- 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. 201: 349-358.
- 2004. Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2 - Patient characteristics and initial response to sulfonylurea therapy. Diabetes. 53: 2713-2718.
- 2004. Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder. Molecular Psychiatry. 9: 621-629.
- 2003. Hepatocyte nuclear factor- 1 alpha gene mutations and diabetes in Norway. Journal of Clinical Endocrinology and Metabolism. 88: 920-931.
- 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 & Genomics. 13: 383-388.
- 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 & Genomics. 12: 383-388.
- 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 & Genomics. 13: 383-388.
- 2003. Hepatocyte nuclear factor-1 alpha gene mutations and diabetes in Norway. Journal of Clinical Endocrinology and Metabolism. 88: 920-931.
- 2003. Forskere diskuterte arv og diabetes. Diabetes for helsepersonell. 4. 12-14.
- 2003. Forskere diskuterte arv og diabetes. Diabetes for helsepersonell. 4: 12-14.
- 2003. Forskere diskuterte diabetes. Diabetes for helsepersonell. 4: 12-14.
- 2003. Permanent neonatal diabetes caused by glucokinase deficiency; inborn error of the glucose-insulin signaling pathway. Diabetes. 52: 2854-2860.
- 2003. Permanent neonatal diabetes mellitus due to glucokinase deficiency- an inborn error of the glucose-insulin signalling pathway. Diabetes. 52: 2854-2860.
- 2003. Examination of IMPA1- and IMPA2 genes in manic-depressive patients: Association between IMPA2 promoter polymorphisms and bipolar disorder. Molecular Psychiatry. Epub-23Dec2003.
- 2002. Hunting for a hypoglyecemia gene:Severe neonatal hypoglyecemia in a consanguineuos family. American Journal of Medical Genetics. 113: 40-46.
- 2001. Polymorphisms in CYP2D6 duplication-negative individuals with the ultrarapid metabolizer phenotype: a role for the CYP2D6*35 allele in ultrarapid metabolism? Pharmacogenetics & Genomics. 11: 45-55.
- 2001. Polymorphisms in CYP2D6 duplication-negative individuals with the ultrarapid metabolizer phenotype: a role for the CYP2D6*35 allele in ultrarapid metabolism? Pharmacogenetics & Genomics. 11: 45-55.
- 2001. MODY-prosjektet ved Haukeland Sykehus: fra forskning til diagnostikk. Diabetes for helsepersonell. 3: 23-24.
- 2001. Permanent neonatal diabetes mellitus due to complete glucoinase deficiency. New England Journal of Medicine. 344: 1588-1592.
- 2000. MODY associated with two novel hepatocyte nuclear factor 1 alpha loss of function mutations. Biochemical and Biophysical Research Communications - BBRC. 279: 792-798.
- 2000. A simple test for the hot spot mutation P291fsinsC in MODY3. Diabetologia. 43: 818-819.
- 2000. MGM - Medisin, Gener og Mennesker. NBS-nytt. 24: 25-27.
- 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. In press.
- 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. 5: 172-180.
- 2000. CYP2D6-gentest: ny rutineanalyse for identifisering av langsomme og ultraraske legemiddelomsettere. Norsk Farmaceutisk Tidsskrift. 2. 14-15.
- 2000. CYP2D6-gentest: ny rutineanalyse for identifisering av langsomme og ultraraske legemiddelomsettere. Norsk Farmaceutisk Tidsskrift. 2. 14-15.
- 1999. Genomic structure and sequence analysis of a human inositol polyphosphate 1-phosphatase gene (INPP1). Pharmacogenetics & Genomics. 9: 517-528.
- 1998. Stein Ove Døskeland: Vestlandsk vitenskapsmann med virketrang og visjoner. NBS-nytt. 22: 16-18.
- 1997. Gap junctions and growth control in liver regeneration and in isolated rat hepatocytes. Hepatology. 25: 847-855.
- 1997. Gap junctions and growth control in liver regeneration and in isolated rat hepatocytes. Hepatology. 25: 847-855.
- 1997. Forfatterskap til besvær. Klinisk kemi i Norden. 9: 7-10.
- 1997. Et mekka for molekylær marinbiologi. NSB-nytt. 21: 28-29.
- 1997. Genomic structure and chromosomal localization of a human myo-inositol monophosphatase gene (IMPA). Genomics. 45: 113-122.
- 1996. Ultrarapid metabolizers of debrisoquine: Characterization and PCR-based detection of alleles with duplication of the CYP2D6 gene. FEBS Letters. 39266: 30-34.
- 1996. Ultrarapid metabilizers of debrisoquine : characterization and PCR-based detection of alleles with duplication of the CYP2D6 gene. FEBS Letters. 392: 30-34.
- 1996. Priser til begjær -del II. NBS-nytt. 20: 20-21.
- 1996. Fargerik forskar fyller femti. NBS-nytt. 20: 20-21.
- 1996. Priser til begjær (og #/en til besvær). NBS-nytt. 20: 21-22.
- 1996. Jens Gabliel Hauge: Hvordan genene virker (Bokanmeldelse). Naturen. 120: 334-335.
- 1996. Nytt DNA-sekvenseringslaboratorium opna i Bergen. NBS-nytt. 20: 22.
- 1996. Fusk og fanteri i forskningen. NBS-nytt. 20: 16-22.
- 1996. Nobelprisen i medisin 1995 - genene gir oss form. Naturen. 120: 46-48.
- 1996. Chromosomal assignment of the human gene encoding the Fos-related antigen-2 (FRA-2) to chromosome 2p22-p23. Genomics. 38: 72-75.
- 1996. Chromosomal assignment of the human gene encoding the Fos-related antigen-2 (FRA-2) to chromosome 2p22-p23. Genomics. 38: 72-75.
- 1996. A retroviral element in the human CYP2D gene cluster. Pharmacogenetics & Genomics. 6: 375-377.
- 1995. Med Goksøyr inn i genalderen. NBS-nytt. 19: 23-24.
- 1995. Aarskog-genet endelig klonet. NBS-nytt. 19: 12-13.
- 1995. Protein-folding med konsekvensar. Om scrapie, prionar og degenerative hjernesjukdomar. NBS-nytt. 19: 12-15.
- 1995. Uracil-DNA-glykosylase - en norsk suksesshistorie. NBS-nytt. 19: 40-44.
- 1995. Scrapie - meir enn sauesjukdom. (Kronikk). Bergens Tidende. 20. Published 1995-07-21.
- 1995. Nobelprisen i medisin 1995 - genene som styrer fosterutviklingen. NBS-nytt. 19: 24.
- 1995. Aarskog-genet endelig funnet. Innsyn. 4: 8-9.
- 1995. Mikrobiologi-pionerer møttes i Bergen. UiB-magasinet : nytt fra Universitetet i Bergen. 4. 33-34.
- 1995. Nobelprisen i fysiologi og medisin 1995 - fosterutviklingens mysterium. Tidsskrift for Den norske legeforening. 3712-3713.
- 1995. Apoptose - når cellene dør. Naturen. 1: 18-26.
- 1995. Apoptose - når cellene dør. Naturen. 1. 18-26.
- 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. 4: 2251-2257.
- 1995. Conserved sequence patterns in phages Mu and Lambda. Biochimica et Biophysica Acta. 1264: 115-120.
- 1995. Conserved sequence patterns in phages Mu and Lambda. Biochimica et Biophysica Acta. 1264: 115-120.
- 1992. Structure and early embryonic expression of the zebrafish engrailed-2 gene. Mechanisms of Development. 39: 51-62.
- 1992. The zebrafish homeobox gene Hox(zf-114): primary structure, expression pattern and evolutionary aspects. International Journal of Developmental Biology. 36: 229-237.
- 1991. Fakta om transkripsjonsfaktorer. NBS-nytt. 4: 9-13.
- 1991. Når beina sitter på hodet! Om bananfluer, fosterutvikling og homeobokser. Naturen. 5: 203-211.
- 1991. Genomic structure and restricted neural expression of the zebrafish wnt-1 (int-1) gene. EMBO Journal. 10: 799-807.
Reports and theses
- 2009. Diabetes Genetics. A Seventh Sense for the Successful Sequel of ‘Come Together’. Journal of the Pancreas. 10: 4. Journal of the Pancreas. -466471 pages.
- 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. Universitetet i Bergen, inst. for fiskeri- og marinbiologi.
- 1991. Pattern formation and neurogenesis in a vertebrate embryo: study of developmentally regulated genes in the zebrafish. (dr.scient.). [Mangler utgivernavn], Bergen Universitetet i Bergen.
Book sections
- 2013. Ultrasound-assisted treatment of an inoperable pancreatic cancer. Session 2, pages 49-52. In:
- 2013. MedViz Conference 2013. 146 pages. ISBN: 978-82-998920-1-8.
- 2012. The molecular genetics and pathophysiology of congenital hyperinsulinism caused by short-chain 3-hydroxyacyl-CoA dehydrogenase (SCHAD) deficiency. Chapt 13, pages 137-145. In:
- 2012. Frontiers in Diabetes, Vol 21. Monogenic Hyperinsulinemic Hypoglycemia Disorders. S. Karger. 192 pages. ISBN: 978-3-8055-9943-6.
- 2005. Diagnosis and mangement of MODY in a pediatric setting. Chapter 5, pages 84-93. In:
- 2005. Diabetes in Childhood and Adolescence. S. Karger. 400 pages. ISBN: 3-8055-7766-4.
- 1997. p53 er vår indre vaktmester. 24-26. In:
- 1997. Prosjektkatalog for kreftforskning.
- 1993. Biological effects and biomonitoring of organochlorines and polycyclic aromatic hydrocarbons in the marine environment. 137-162. In:
- 1993. Ecotoxicology monitoring.
- 1993. Pattern formation in fish embryos: Characterization of homebox genes from the zebrafish (Brachydranio rerio). 30-39. In:
- 1993. Physiological and biochemical aspects of fish development. (Red.: Walther, B. T., Fyhn, H. J.).
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