Anders Molven

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Publications in SciGraph latest 50 shown

  • 2019-12 Mutation analysis by deep sequencing of pancreatic juice from patients with pancreatic ductal adenocarcinoma in BMC CANCER
  • 2018-12 Author Correction: Telomere length and survival in primary cutaneous melanoma patients in SCIENTIFIC REPORTS
  • 2018-12 Telomere length and survival in primary cutaneous melanoma patients in SCIENTIFIC REPORTS
  • 2017-12 Cancer cachexia associates with a systemic autophagy-inducing activity mimicked by cancer cell-derived IL-6 trans-signaling in SCIENTIFIC REPORTS
  • 2017-12 Tissue MicroRNA profiles as diagnostic and prognostic biomarkers in patients with resectable pancreatic ductal adenocarcinoma and periampullary cancers in BIOMARKER RESEARCH
  • 2017-08 Heterogeneity of proliferative markers in pancreatic β-cells of patients with severe hypoglycemia following Roux-en-Y gastric bypass in ACTA DIABETOLOGICA
  • 2017-04 Targeted next-generation sequencing reveals MODY in up to 6.5% of antibody-negative diabetes cases listed in the Norwegian Childhood Diabetes Registry in DIABETOLOGIA
  • 2015-09 Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma in NATURE GENETICS
  • 2015-05 A recombined allele of the lipase gene CEL and its pseudogene CELP confers susceptibility to chronic pancreatitis in NATURE GENETICS
  • 2014-04 Loss-of-function mutations in SLC30A8 protect against type 2 diabetes in NATURE GENETICS
  • 2013-11 Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes in NATURE GENETICS
  • 2013-07 Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry in DIABETOLOGIA
  • 2013-04 A variant in FTO shows association with melanoma risk not due to BMI in NATURE GENETICS
  • 2012-05 To test, or not to test: time for a MODY calculator? in DIABETOLOGIA
  • 2012-03 The role of pancreatic imaging in monogenic diabetes mellitus in NATURE REVIEWS ENDOCRINOLOGY
  • 2011-12 Evaluation of four novel genetic variants affecting hemoglobin A1c levels in a population-based type 2 diabetes cohort (the HUNT2 study) in BMC MEDICAL GENETICS
  • 2011-11 Genome-wide association study identifies three new melanoma susceptibility loci in NATURE GENETICS
  • 2010-12 Disease progression and search for monogenic diabetes among children with new onset type 1 diabetes negative for ICA, GAD- and IA-2 Antibodies in BMC ENDOCRINE DISORDERS
  • 2010-02 DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical twins in EUROPEAN JOURNAL OF PEDIATRICS
  • 2010-01 Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes in HUMAN GENETICS
  • 2009-12 pRb2/p130 protein expression and RBL2 mutation analysis in Burkitt lymphoma from Uganda in BMC CLINICAL PATHOLOGY
  • 2008-12 Expression of the "stem cell marker" CD133 in pancreas and pancreatic ductal adenocarcinomas in BMC CANCER
  • 2008-12 Wolcott–Rallison syndrome with 3-hydroxydicarboxylic aciduria and lethal outcome in JOURNAL OF INHERITED METABOLIC DISEASE
  • 2008-06 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) in DIABETOLOGIA
  • 2006-06 Molecular analysis of the EGFR-RAS-RAF pathway in pancreatic ductal adenocarcinomas: lack of mutations in the BRAF and EGFR genes in VIRCHOWS ARCHIV
  • 2006-01 Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction in NATURE GENETICS
  • 2005-08 BRAF and NRAS Mutations Are Frequent in Nodular Melanoma but Are not Associated with Tumor Cell Proliferation or Patient Survival in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2004-06 Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder in MOLECULAR PSYCHIATRY
  • 2000-03 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 in MOLECULAR PSYCHIATRY
  • 1999-08 35th Annual Meeting of the European Association for the Study of Diabetes in DIABETOLOGIA
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