Pancreatic cancer

Monogenic diabetes

Congenital hyperinsulinism of infancy

Melanoma genetics

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Academic article

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• Bruna Dalmasso; Lorenza Pastorino; Vaishnavi Nathan et al. (2021). Germline ATM variants predispose to melanoma: a joint analysis across the GenoMEL and MelaNostrum consortia. (external link)
• Karianne Fjeld; Anny Gravdal Svanbring; Ranveig Seim Brekke et al. (2022). The genetic risk factor CEL-HYB1 causes proteotoxicity and chronic pancreatitis in mice. (external link)
• Kari Espolin Fladmark; Bjørn Tore Gjertsen; Anders Molven et al. (1997). Gap junctions and growth control in liver regeneration and in isolated rat hepatocytes. (external link)
• B Stern; Anders Molven; D Kamp (1995). Conserved sequence patterns in phages Mu and Lambda. (external link)
• Anders Molven; Jennifer Hollister-Lock; Jiang Hu et al. (2016). The hypoglycemic phenotype is islet cell-autonomous in short-chain hydroxyacyl-CoA dehydrogenase-deficient mice. (external link)
• Xisong Ke; Wencheng Li; Randi Hovland et al. (2011). Reprogramming of cell junction modules during stepwise epithelial to mesenchymal transition and accumulation of malignant features in vitro in a prostate cell model. (external link)
• Bjørn Inge Bertelsen; Solrun Steine; Roar Sandvei et al. (2006). Molecular analysis of the PI3K-AKT pathway in uterine cervical neoplasia: Frequent PIK3CA amplification and AKT phosphorylation. (external link)
• Mark M. Iles; Matthew H. Law; Simon N. Stacey et al. (2013). A variant in FTO shows association with melanoma risk not due to BMI. (external link)
• Ellen Berget; Lars Helgeland; Knut Liseth et al. (2014). Prognostic value of bone marrow involvement by clonal immunoglobulin gene rearrangements in follicular lymphoma. (external link)
• Kjersti Tjensvoll; Morten Lapin; Bjørnar Gilje et al. (2022). Novel hybridization- and tag-based error-corrected method for sensitive ctDNA mutation detection using ion semiconductor sequencing. (external link)
• Heike Immervoll; Dag Hoem; Kalaiarasy Kugarajh et al. (2006). Molecular analysis of the EGFR-RAS-RAF pathway in pancreatic ductal adenocarcinomas: lack of mutations in the BRAF and EGFR genes. (external link)
• Gry Sjøholt; Anders Molven; Roger Løvlie et al. (1997). Genomic structure and chromosomal localization of a human myo-inositol monophosphatase gene (IMPA). (external link)
• Brett M. Cassidy; Sammy Zino; Karianne Fjeld et al. (2020). Single nucleotide polymorphisms in CEL-HYB1 increase risk for chronic pancreatitis through proteotoxic misfolding. (external link)
• Anny Gravdal Svanbring; Xunjun Xiao; Miriam Cnop et al. (2021). The position of single-base deletions in the VNTR sequence of the carboxyl ester lipase (CEL) gene determines proteotoxicity. (external link)
• Jason Flannick; G Thorleifsson; N Beer et al. (2014). Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. (external link)
• Karen Helene Ørstavik; Trine Tangeraas; Anders Molven et al. (2007). Distal phalangeal creases - A distinctive dysmorphic feature in disorders of the RAS signalling pathway?. (external link)
• Marie Holm Solheim; Jonathon N. Winnay; Thiago M. Batista et al. (2018). Mice Carrying a Dominant-Negative Human PI3K Mutation Are Protected From Obesity and Hepatic Steatosis but Not Diabetes. (external link)
• Ingfrid Salvesen Haldorsen; Mette Vesterhus; Helge Ræder et al. (2008). Lack of pancreatic body and tail in HNF1B mutation carriers. (external link)
• Stig Åge Eide; H Ræder; Helge Ræder et al. (2008). Prevalence of HNF1A (MODY3) mutations in a Norwegian population (the HUNT2 Study). (external link)
• Man Hung Choi; Eline Mejlænder-Andersen; Sophia Manueldas et al. (2019). Mutation analysis by deep sequencing of pancreatic juice from patients with pancreatic ductal adenocarcinoma. (external link)
• Ranveig Seim Brekke; Anny Gravdal Svanbring; Khadija el Jellas et al. (2024). Common single-base insertions in the VNTR of the carboxyl ester lipase (CEL) gene are benign and also likely to arise somatically in the exocrine pancreas. (external link)
• Johanna L. St-Louis; Khadija el Jellas; Kelly Velasco et al. (2023). Deficiency of the metabolic enzyme SCHAD in pancreatic β-cells promotes amino acid–sensitive hypoglycemia. (external link)
• Lars A. Akslen; Hanne Eknes Puntervoll; Ingeborg M. Bachmann et al. (2008). Mutation analysis of the EGFR-NRAS-BRAF pathway in melanomas from black Africans and other subgroups of cutaneous melanoma. (external link)
• Jens Kristoffer Hertel; Stefan Johansson; Helge Ræder et al. (2011). Evaluation of four novel genetic variants affecting hemoglobin A1c levels in a population-based type 2 diabetes cohort (the HUNT2 study). (external link)
• Anders Molven; U Rishaug; G E Matre et al. (2002). Hunting for a hypoglyecemia gene:Severe neonatal hypoglyecemia in a consanguineuos family. (external link)
• Øyvind Helgeland; Marc Vaudel; Petur Benedikt Juliusson et al. (2019). Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth. (external link)
• Per Helsing; Dag André Nyrnoen; Sarah Ariansen et al. (2008). Population-based prevalence of CDKN2A and CDK4 mutations in patients with multiple primary melanomas. (external link)
• Khadija el Jellas; Petra Dušátková; Ingfrid S. Haldorsen et al. (2022). Two New Mutations in the CEL Gene Causing Diabetes and Hereditary Pancreatitis: How to Correctly Identify MODY8 Cases. (external link)
• Jørn V. Sagen; Lise Bjørkhaug; Janne Molnes et al. (2008). Diagnostic screening of MODY2/GCK mutations in the Norwegian MODY Registry. (external link)
• Gry Sjøholt; Anne Karin Gulbrandsen; Roger Løvlie et al. (2000). A human myoinositol monophosphatase gene (IMPA2) localized in a susc eptibility region for bipolar disorder on chromosome 18p11.2: genomic structure and polymorphism screening in manic-depressive patients. (external link)
• Roger Løvlie; Ann K. Daly; Guri E. Matre et al. (2001). Polymorphisms in CYP2D6 duplication-negative individuals with the ultrarapid metabolizer phenotype: a role for the CYP2D6*35 allele in ultrarapid metabolism?. (external link)
• Sevim Kahraman; Ercument Dirice; Giorgio Basile et al. (2022). Abnormal exocrine–endocrine cell cross-talk promotes β-cell dysfunction and loss in MODY8. (external link)
• Mette Vesterhus; Helge Ræder; Harald Aurlien et al. (2008). Neurological features and enzyme therapy in patients with endocrine and exocrine pancreas dysfunction due to CEL mutations. (external link)
• Mette Vesterhus; Helge Ræder; Amarnath J Kurpad et al. (2010). Pancreatic Function in Carboxyl-Ester Lipase Knockout Mice. (external link)
• Jian Wang; Per Øystein Sakariassen; Oleg Tsinkalovsky et al. (2008). CD133 negative glioma cells form tumors in nude rats and give rise to CD133 positive cells. (external link)
• Kjersti Mangseth; Lars Inge Helgeland; Jan Klos et al. (2009). Improved diagnostic segregation of mantle cell lymphoma by determination of cyclin D1/D3 expression ratio in formalin-fixed tissue. (external link)
• Anders Molven (1997). Forfatterskap til besvær. (external link)
• K.E. Flatmark; B.T. Gjertsen; Anders Molven et al. (1997). Gap junctions and growth control in liver regeneration and in isolated rat hepatocytes. (external link)
• Jørn Sagen; Stella Odili; Lise Bjørkhaug et al. (2006). From clinicogenetic studies of maturity-onset diabetes of the young to unraveling complex mechanisms of glucokinase regulation. (external link)
• Vidar Martin Steen; Anders Molven; NK Aarskog et al. (1995). Homologous unequal cross-over involving a 2.8 kb direct repeat as a mechanism for the generation of allelic variants of the human cytochrome P450 CYP2D6 gene. (external link)
• Anders Molven (1995). Med Goksøyr inn i genalderen. (external link)
• Anders Molven (1995). Uracil-DNA-glykosylase - en norsk suksesshistorie. (external link)
• Cornelia Schuster; Hans Petter Eikesdal; Hanne Eknes Puntervoll et al. (2012). Clinical efficacy and safety of bevacizumab monotherapy in patients with metastatic melanoma: predictive importance of induced early hypertension. (external link)
• Man Hung Choi; Erling Tjora; Rakel Brendsdal Forthun et al. (2021). KRAS mutation analysis by droplet digital PCR of duodenal juice from patients with MODY8 and other pancreatic diseases. (external link)
• Anders Molven; LI Cressey; Ragnar Bøe (1995). Apoptose - når cellene dør. (external link)
• B Stern; Anders Molven; D Kamp (1995). Conserved sequence patterns in phages Mu and Lambda. (external link)
• Anders Molven (1995). Aarskog-genet endelig klonet. (external link)
• Anders Molven (1995). Protein-folding med konsekvensar. Om scrapie, prionar og degenerative hjernesjukdomar. (external link)

Academic literature review

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

Conference lecture

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

Editorial/Leader article

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

Academic book chapter

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

Doctoral thesis (PhD)

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

Conference abstract

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

Conference poster

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

Journal corrigendum

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

Media feature article

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

Non-fiction monograph

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

Letter to the editor

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

Popular science article

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

Master’s thesis

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

Research report

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

Lecture

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

See a complete overview of publications in NVA.