List of works - Anders Molven

CD133 negative glioma cells form tumors in nude rats and give rise to CD133 positive cells

scientific article

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

scientific article

Genome-wide association study identifies three new melanoma susceptibility loci

scientific article

Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy

scientific article published in October 2004

Neonatal diabetes mellitus due to complete glucokinase deficiency

scientific article published in May 2001

Spontaneous Malignant Transformation of Human Mesenchymal Stem Cells Reflects Cross-Contamination: Putting the Research Field on Track - Letter

scientific article published on 14 July 2010

Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction

scientific article

Expression of the "stem cell marker" CD133 in pancreas and pancreatic ductal adenocarcinomas

scientific article

Long-range gene regulation links genomic type 2 diabetes and obesity risk regions to HHEX, SOX4, and IRX3

scientific article

Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes

scientific article

Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma

scientific article

Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation

scientific article

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

scientific article published on 11 March 2011

Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development

scientific article

A human clinical trial using ultrasound and microbubbles to enhance gemcitabine treatment of inoperable pancreatic cancer

scientific article published on 12 October 2016

Molecular analysis of the PI3K-AKT pathway in uterine cervical neoplasia: frequent PIK3CA amplification and AKT phosphorylation

scientific article published in April 2006

The effect on melanoma risk of genes previously associated with telomere length

scientific article

A variant in FTO shows association with melanoma risk not due to BMI

scientific article

Ultrarapid metabolizers of debrisoquine: Characterization and PCR-based detection of alleles with duplication of the CYP2D6 gene

article

Permanent neonatal diabetes caused by glucokinase deficiency: inborn error of the glucose-insulin signaling pathway

scientific article published in November 2003

Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes

scientific article

BRAF and NRAS Mutations Are Frequent in Nodular Melanoma but Are not Associated with Tumor Cell Proliferation or Patient Survival

article

A recombined allele of the lipase gene CEL and its pseudogene CELP confers susceptibility to chronic pancreatitis

scientific article published on 16 March 2015

Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants

scientific article published on 5 February 2013

Biochemical and functional characterization of germ line KRAS mutations

scientific article published on 17 September 2007

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).

scientific article published on 24 April 2008

SHORT syndrome with partial lipodystrophy due to impaired phosphatidylinositol 3 kinase signaling

scientific article published on 27 June 2013

Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder

scientific article

Molecular analysis of the EGFR-RAS-RAF pathway in pancreatic ductal adenocarcinomas: lack of mutations in the BRAF and EGFR genes

scientific article

Exome sequencing and genetic testing for MODY.

scientific article

A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutation

scientific article published on September 2005

Generation of prostate tumor-initiating cells is associated with elevation of reactive oxygen species and IL-6/STAT3 signaling

scientific article

Activating glucokinase (GCK) mutations as a cause of medically responsive congenital hyperinsulinism: prevalence in children and characterisation of a novel GCK mutation

scientific article published in May 2008

Pancreatic lipomatosis is a structural marker in nondiabetic children with mutations in carboxyl-ester lipase

scientific article published on 01 February 2007

A human myo-inositol monophosphatase gene (IMPA2) localized in a putative susceptibility region for bipolar disorder on chromosome 18p11.2: genomic structure and polymorphism screening in manic-depressive patients

scientific article

Mutation analysis of the EGFR-NRAS-BRAF pathway in melanomas from black Africans and other subgroups of cutaneous melanoma

scientific article

Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry

scientific article published on 27 April 2013

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

scientific article

Genomic Structure and Chromosomal Localization of a Humanmyo-Inositol Monophosphatase Gene (IMPA)

scientific article published on October 1, 1997

From Clinicogenetic Studies of Maturity-Onset Diabetes of the Young to Unraveling Complex Mechanisms of Glucokinase Regulation

scientific article published on 01 June 2006

U-251 revisited: genetic drift and phenotypic consequences of long-term cultures of glioblastoma cells

scientific article

Lack of pancreatic body and tail in HNF1B mutation carriers

scientific article published on 01 July 2008

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

scientific article published in December 1995

Hepatocyte nuclear factor-1 alpha gene mutations and diabetes in Norway

scientific article published on 01 February 2003

A zebrafish engrailed-like homeobox sequence expressed during embryogenesis

scientific article published on 01 April 1988

Prevalence ofHNF1A(MODY3) mutations in a Norwegian population (the HUNT2 Study)

scientific article

Polymorphisms in CYP2D6 duplication-negative individuals with the ultrarapid metabolizer phenotype: a role for the CYP2D6*35 allele in ultrarapid metabolism?

scientific article published on 01 February 2001

Studies in 3,523 Norwegians and Meta-Analysis in 11,571 Subjects Indicate That Variants in the Hepatocyte Nuclear Factor 4 (HNF4A) P2 Region Are Associated With Type 2 Diabetes in Scandinavians

scientific article

Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes

scientific article published on 17 September 2009

Structure and early embryonic expression of the zebrafish engrailed-2 gene

scientific article

List of works by Anders Molven

CD133 negative glioma cells form tumors in nude rats and give rise to CD133 positive cells

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

Genome-wide association study identifies three new melanoma susceptibility loci

Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy

Neonatal diabetes mellitus due to complete glucokinase deficiency

Spontaneous Malignant Transformation of Human Mesenchymal Stem Cells Reflects Cross-Contamination: Putting the Research Field on Track - Letter

Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction

Expression of the "stem cell marker" CD133 in pancreas and pancreatic ductal adenocarcinomas

Long-range gene regulation links genomic type 2 diabetes and obesity risk regions to HHEX, SOX4, and IRX3

Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes

Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma

Familial hyperinsulinemic hypoglycemia caused by a defect in the SCHAD enzyme of mitochondrial fatty acid oxidation

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

Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development

A human clinical trial using ultrasound and microbubbles to enhance gemcitabine treatment of inoperable pancreatic cancer

Molecular analysis of the PI3K-AKT pathway in uterine cervical neoplasia: frequent PIK3CA amplification and AKT phosphorylation

The effect on melanoma risk of genes previously associated with telomere length

A variant in FTO shows association with melanoma risk not due to BMI

Ultrarapid metabolizers of debrisoquine: Characterization and PCR-based detection of alleles with duplication of the CYP2D6 gene

Permanent neonatal diabetes caused by glucokinase deficiency: inborn error of the glucose-insulin signaling pathway

Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes

BRAF and NRAS Mutations Are Frequent in Nodular Melanoma but Are not Associated with Tumor Cell Proliferation or Patient Survival

A recombined allele of the lipase gene CEL and its pseudogene CELP confers susceptibility to chronic pancreatitis

Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants

Biochemical and functional characterization of germ line KRAS mutations

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).

SHORT syndrome with partial lipodystrophy due to impaired phosphatidylinositol 3 kinase signaling

Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder

Molecular analysis of the EGFR-RAS-RAF pathway in pancreatic ductal adenocarcinomas: lack of mutations in the BRAF and EGFR genes

Exome sequencing and genetic testing for MODY.

A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutation

Generation of prostate tumor-initiating cells is associated with elevation of reactive oxygen species and IL-6/STAT3 signaling

Activating glucokinase (GCK) mutations as a cause of medically responsive congenital hyperinsulinism: prevalence in children and characterisation of a novel GCK mutation

Pancreatic lipomatosis is a structural marker in nondiabetic children with mutations in carboxyl-ester lipase

A human myo-inositol monophosphatase gene (IMPA2) localized in a putative susceptibility region for bipolar disorder on chromosome 18p11.2: genomic structure and polymorphism screening in manic-depressive patients

Mutation analysis of the EGFR-NRAS-BRAF pathway in melanomas from black Africans and other subgroups of cutaneous melanoma

Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry

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

Genomic Structure and Chromosomal Localization of a Humanmyo-Inositol Monophosphatase Gene (IMPA)

From Clinicogenetic Studies of Maturity-Onset Diabetes of the Young to Unraveling Complex Mechanisms of Glucokinase Regulation

U-251 revisited: genetic drift and phenotypic consequences of long-term cultures of glioblastoma cells

Lack of pancreatic body and tail in HNF1B mutation carriers

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

Hepatocyte nuclear factor-1 alpha gene mutations and diabetes in Norway

A zebrafish engrailed-like homeobox sequence expressed during embryogenesis

Prevalence ofHNF1A(MODY3) mutations in a Norwegian population (the HUNT2 Study)

Polymorphisms in CYP2D6 duplication-negative individuals with the ultrarapid metabolizer phenotype: a role for the CYP2D6*35 allele in ultrarapid metabolism?

Studies in 3,523 Norwegians and Meta-Analysis in 11,571 Subjects Indicate That Variants in the Hepatocyte Nuclear Factor 4 (HNF4A) P2 Region Are Associated With Type 2 Diabetes in Scandinavians

Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes

Structure and early embryonic expression of the zebrafish engrailed-2 gene