Dag E. Undlien

Oslo University Hospital — Norway

Biochemistry, Genetics and Molecular Biology · Life Sciences

44h-index10.6kcitations128works0.02yr avg
OpenAlex↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Diabetes and associated disorders(57), Pancreatic function and diabetes(32), T-cell and B-cell Immunology(21), Immune Cell Function and Interaction(19), Adrenal Hormones and Disorders(18)

Publications128 total

Artificial intelligence (AI) tools in genetics
Open Access Government·2024Open Access
shinyseg: a web application for flexible cosegregation and sensitivity analysis
Bioinformatics·2024Open Access
Erik Thorsby (1938–2021)
HLA·2021
Vitamin D status and pathway genes in five European autoimmune Addison’s disease cohorts
European Journal of Endocrinology·2021· 6 citedOpen Access
Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease
Frontiers in Endocrinology·2019· 5 citedOpen Access
Prenatal maternal depressive symptoms and infant DNA methylation: a longitudinal epigenome-wide study
Nordic Journal of Psychiatry·2019· 25 cited
Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's disease
Journal of Translational Autoimmunity·2019· 6 citedOpen Access
Quality improvement in clinical NGS through a peer-driven Nordic collaboration
European Journal of Human Genetics·2019
Målrettet ut fra genetisk variasjon
Tidsskrift for Den Norske Laegeforening·2018
BRCA mutation carrier detection. A model-based cost-effectiveness analysis comparing the traditional family history approach and the testing of all patients with breast cancer
ESMO Open·2018· 25 citedOpen Access
Current guidelines for BRCA testing of breast cancer patients are insufficient to detect all mutation carriers
BMC Cancer·2017· 94 citedOpen Access
Intra-individual changes in DNA methylation not mediated by cell-type composition are correlated with aging during childhood
Clinical Epigenetics·2016· 19 citedOpen Access
Pathogenic variants in<i>KCTD7</i>perturb neuronal K<sup>+</sup>fluxes and glutamine transport
Brain·2016· 36 citedOpen Access
Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF
Human Mutation·2016· 10 citedOpen Access
Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in<i>CENPF</i>
Human Mutation·2016· 34 cited
Additional file 4: Table S1. of Intra-individual changes in DNA methylation not mediated by cell-type composition are correlated with aging during childhood
Figshare·2016Open Access
Additional file 6: Table S2. of Intra-individual changes in DNA methylation not mediated by cell-type composition are correlated with aging during childhood
Figshare·2016Open Access
Additional file 1: Figure S1. of Intra-individual changes in DNA methylation not mediated by cell-type composition are correlated with aging during childhood
Figshare·2016Open Access
CTLA-4 as a genetic determinant in autoimmune Addison’s disease
Genes and Immunity·2015· 31 citedOpen Access
Detection of a Low-Grade Enteroviral Infection in the Islets of Langerhans of Living Patients Newly Diagnosed With Type 1 Diabetes
Diabetes·2014· 304 citedOpen Access
page 1 of 7Next →

Frequent Co-authors

Kjersti S. Rønningen(16), John A. Todd(15), Hanne E. Akselsen(12), Beate Skinningsrud(10), Eystein S. Husebye(10), Geir Joner(10), Erik Thorsby(9), Kristina Gervin(9), Eva Tuomilehto‐Wolf(8), Flemming Pociot(8), Benedicte A. Lie(8), Francesco Cucca(7), Jaakko Tuomilehto(7), Pål R. Njølstad(7), Cristian Guja(6), Jørn Nerup(6), Anette S. B. Wolff(6), Knut Dahl‐Jørgensen(6), Neil Walker(5), C Ionescu-Tîrgovişte(5)