His primary scientific interests are in Genetics, Type 1 diabetes, Gene, Immunology and Linkage disequilibrium. His research related to Haplotype, Allele, Gene mapping, Locus and Major histocompatibility complex might be considered part of Genetics. The Gene mapping study combines topics in areas such as T cell, PTPN22 and Regulator gene.
The concepts of his Type 1 diabetes study are interwoven with issues in Autoantibody, Vitiligo and Adrenal insufficiency. His Immunology research is multidisciplinary, incorporating perspectives in Epigenetics and CpG site. His Linkage disequilibrium research includes themes of HLA Complex, Human leukocyte antigen and Microsatellite.
His scientific interests lie mostly in Genetics, Immunology, Haplotype, Allele and Linkage disequilibrium. His study involves Gene, Human leukocyte antigen, Single-nucleotide polymorphism, Locus and HLA Complex, a branch of Genetics. His research in Immunology intersects with topics in Internal medicine and Type 1 diabetes.
His work in Haplotype tackles topics such as Candidate gene which are related to areas like Genetic association. His Allele research incorporates themes from Disease, Genetic predisposition and Genotype. The study incorporates disciplines such as Transmission disequilibrium test, Variable number tandem repeat, Genetic marker, Microsatellite and Gene mapping in addition to Linkage disequilibrium.
Dag E. Undlien spends much of his time researching Immunology, Genetics, Single-nucleotide polymorphism, Allele and Human leukocyte antigen. His Immunology research integrates issues from Missense mutation, Type 1 diabetes and Epigenetics. His work on Genetics deals in particular with Locus, Medical genetics, Phenotype, Compound heterozygosity and Gene.
Dag E. Undlien has included themes like Genotyping, Case-control study and Polymorphism in his Single-nucleotide polymorphism study. His research on Allele focuses in particular on Haplotype. Dag E. Undlien interconnects RNA, Immunohistochemistry, Diabetes mellitus and Pancreatic islets in the investigation of issues within Human leukocyte antigen.
His primary areas of study are Genetics, Diabetes mellitus, Type 1 diabetes, Immunology and Islet. His Genetics study frequently draws connections between adjacent fields such as Myoclonus. His Childhood diabetes study, which is part of a larger body of work in Diabetes mellitus, is frequently linked to Permanent neonatal diabetes mellitus, bridging the gap between disciplines.
His work carried out in the field of Immunology brings together such families of science as Gene expression, DNA methylation, Human genome, Concordance and Regulation of gene expression. He combines subjects such as Immunohistochemistry, Human leukocyte antigen and RNA with his study of Islet. Dag E. Undlien has researched Gene in several fields, including Autoimmunity and Case-control study.
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Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease
H Ueda;Howson Jmm.;L Esposito;J Heward.
Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus
Bennett;A M Lucassen;S C Gough;E E Powell.
Nature Genetics (1995)
Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor.
I. Sadaf Farooqi;Teresia Wangensteen;Stephan Collins;Wendy Kimber.
The New England Journal of Medicine (2007)
Neonatal diabetes mellitus due to complete glucokinase deficiency.
Pål R. Njølstad;Oddmund Søvik;Antonio Cuesta-Muñoz;Lise Bjørkhaug.
The New England Journal of Medicine (2001)
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers.
Suna Onengut-Gumuscu;Wei-Min Chen;Oliver Burren;Nick J Cooper.
Nature Genetics (2015)
Clinical, Immunological, and Genetic Features of Autoimmune Primary Adrenal Insufficiency: Observations from a Norwegian Registry
Martina M. Erichsen;Kristian Løvås;Kristian Løvås;Beate Skinningsrud;Beate Skinningsrud;Anette B. Wolff.
The Journal of Clinical Endocrinology and Metabolism (2009)
Linkage disequilibrium mapping of a type 1 diabetes susceptibility gene (IDDM7) to chromosome 2q31-q33.
J B Copeman;F Cucca;C M Hearne;R J Cornall.
Nature Genetics (1995)
Remapping the insulin gene/IDDM2 locus in type 1 diabetes.
Bryan J. Barratt;Felicity Payne;Chris E. Lowe;Robert Hermann.
Detection of a Low-Grade Enteroviral Infection in the Islets of Langerhans of Living Patients Newly Diagnosed With Type 1 Diabetes
Lars Krogvold;Bjørn Edwin;Bjørn Edwin;Trond Buanes;Trond Buanes;Gun Frisk.
Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele
Simon T. Bennett;Amanda J. Wilson;Laura Esposito;Nourdine Bouzekri.
Nature Genetics (1997)
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