Dag E. Undlien - Concepedia

Author

Dag E. Undlien

Also Known As

D E Undlien, D Undlien, D. E. Undlien, D. Undlien, D.E. Undlien, Dag E Undlien, Dag E. Undlien, Dag Erik Undlien, Dag Undlien, Nourdine Bouzekri

128

Publications

10.6K

Citations

H-Index

Concepts

All Affiliations

Oslo University Hospital University of Oslo Haukeland University Hospital Norwegian Institute of Public Health University of Bergen

About

Dag E. Undlien is an author at Oslo University Hospital specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	29	43	6.1K
2	Public Health	15	16	1.7K
3	Allergy	5	5	366
4	Allergy Medicine	2	2	124
5	Natural Sciences	1	1	207

Dag E. Undlien

Publications

9.8K

Citations

H-Index

Page 1

	Year	Citations
Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease Hironori Ueda, Joanna M. M. Howson, Laura Esposito, Nature ImmunogeneticsAutoimmune DiseaseT-regulatory CellImmunologyPathology	2003	2.2K
Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus S. T. Bennett, Anneke Lucassen, Stephen Gough, Nature Genetics Insulin ResistanceMetabolic SyndromeTandem Repeat VariationDiabetes EpidemiologyGenetic Determinant	1995	754
Clinical and Molecular Genetic Spectrum of Congenital Deficiency of the Leptin Receptor I. Sadaf Farooqi, Teresia Wangensteen, Stephan C. Collins, New England Journal of Medicine	2007	717
Neonatal Diabetes Mellitus Due to Complete Glucokinase Deficiency Pål R. Njølstad, Antonio L. Cuesta‐Muñoz, Lise Bjørkhaug, New England Journal of Medicine Metabolic SyndromeDevelopmental BiologyComplete Glucokinase DeficiencyDiabetesGlycobiology	2001	424
Clinical, Immunological, and Genetic Features of Autoimmune Primary Adrenal Insufficiency: Observations from a Norwegian Registry Martina M. Erichsen, Kristian Løvås, Beate Skinningsrud, The Journal of Clinical Endocrinology & Metabolism	2009	419
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, Trond Buanes, Diabetes	2014	304
SLC9A6 Mutations Cause X-Linked Mental Retardation, Microcephaly, Epilepsy, and Ataxia, a Phenotype Mimicking Angelman Syndrome Gregor D. Gilfillan, Kaja Kristine Selmer, Ingrid Roxrud, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPsychiatric GeneticsFragile X Spectrum	2008	235
Remapping the Insulin Gene/<i>IDDM2</i> Locus in Type 1 Diabetes Bryan J. Barratt, Felicity Payne, Chris Lowe, Diabetes GeneticsGenetic EpidemiologyHuman PolymorphismDisease Gene IdentificationInsulin Signaling	2004	223
Mutations in the Insulin Gene Can Cause MODY and Autoantibody-Negative Type 1 Diabetes Anders Molven, Monika Ringdal, Anita M. Nordbø, Diabetes	2008	208
Linkage disequilibrium mapping of a type 1 diabetes susceptibility gene (IDDM7) to chromosome 2q31–q33 James Copeman, Francesco Cucca, Catherine M. Hearne, Nature Genetics Type 1Linkage DisequilibriumGenetic DeterminantLinkage Disequilibrium MappingDiabetes Susceptibility Gene	1995	207

Page 1