D
Dag E. Undlien
Researcher at Oslo University Hospital
Publications - 139
Citations - 11272
Dag E. Undlien is an academic researcher from Oslo University Hospital. The author has contributed to research in topics: Haplotype & Linkage disequilibrium. The author has an hindex of 49, co-authored 139 publications receiving 10707 citations. Previous affiliations of Dag E. Undlien include University of Oslo.
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Journal ArticleDOI
Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease
H Ueda,Howson Jmm.,Laura Esposito,Joanne M. Heward,Hywel Snook,Giselle Chamberlain,Dan Rainbow,Hunter Kmd.,Anne Smith,G Di Genova,G Di Genova,Mathias H. Herr,Mathias H. Herr,Ingrid Dahlman,Ingrid Dahlman,F Payne,Deborah J. Smyth,Christopher E. Lowe,Twells Rcj.,Sarah Howlett,Barry C. Healy,Sarah Nutland,Helen E. Rance,Vincent H. Everett,Luc J. Smink,A C Lam,Heather J. Cordell,Neil Walker,C Bordin,John S. Hulme,Costantino Motzo,Francesco Cucca,J F Hess,Michael L. Metzker,Michael L. Metzker,Jane Rogers,Simon G. Gregory,Amit Allahabadia,Amit Allahabadia,R Nithiyananthan,Eva Tuomilehto-Wolf,Jaakko Tuomilehto,Polly J. Bingley,Kathleen M Gillespie,Dag E. Undlien,Kjersti S. Rønningen,Cristian Guja,Constantin Ionescu-Tirgoviste,David A. Savage,Alexander P. Maxwell,Dennis Carson,Christopher Patterson,Jayne A. Franklyn,David Clayton,Laurence B. Peterson,Linda S. Wicker,John A. Todd,Gough Scl. +57 more
TL;DR: In this article, the authors identify polymorphisms of the cytotoxic T lymphocyte antigen 4 gene (CTLA4) as candidates for primary determinants of risk of the common autoimmune disorders Graves' disease, autoimmune hypothyroidism and type 1 diabetes.
Journal ArticleDOI
Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus
Simon T. Bennett,Anneke Lucassen,S C Gough,Elizabeth E. Powell,Dag E. Undlien,L E Pritchard,Marilyn E. Merriman,Y Kawaguchi,M J Dronsfield,M J Dronsfield,Flemming Pociot +10 more
TL;DR: Although it is shown that the insulin gene is expressed biallelically in the adult pancreas, it is presented preliminary evidence that the level of transcription in vivo is correlated with allelic variation within the VNTR.
Journal ArticleDOI
Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor.
I. Sadaf Farooqi,Teresia Wangensteen,Stephan C. Collins,Wendy Kimber,Giuseppe Matarese,Julia M. Keogh,Emma Lank,Bill Bottomley,Judith López-Fernández,Iván Ferraz-Amaro,Mehul T. Dattani,Oya Ercan,Anne Grethe Myhre,Lars Retterstøl,Richard Stanhope,J. A. Edge,Sheila A. McKenzie,Nader Lessan,Maryam Ghodsi,Veronica De Rosa,Francesco Perna,Silvia Fontana,Inês Barroso,Dag E. Undlien,Stephen O'Rahilly +24 more
TL;DR: The prevalence of pathogenic LEPR mutations in a cohort of subjects with severe, early-onset obesity was 3%.
Journal ArticleDOI
Neonatal diabetes mellitus due to complete glucokinase deficiency.
Pål R. Njølstad,Oddmund Søvik,A. Cuesta-MuNoz,Lise Bjørkhaug,Ornella Massa,Fabrizio Barbetti,Dag E. Undlien,Chiyo Shiota,Mark A. Magnuson,Anders Molven,Franz M. Matschinsky,Graeme I. Bell +11 more
TL;DR: Two patients in whom complete deficiency of the glycolytic enzyme glucokinase, a key regulator of glucose metabolism in pancreatic beta, is described are described.
Journal ArticleDOI
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 S. B. Wolff,Dag E. Undlien,Dag E. Undlien,Johan Svartberg,Johan Svartberg,Kristian J. Fougner,Tore Julsrud Berg,Jens Bollerslev,Jens Bollerslev,Bjarne Mella,Joyce Carlson,Henry A. Erlich,Eystein S. Husebye,Eystein S. Husebye +18 more
TL;DR: Both anti-21-hydroxylase antibodies and HLA class II can be clinically relevant predictors of AD, and treatment modalities that improve HRQoL are needed.