Dag E Undlien

Dag E Undlien

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Dag E Undlien

Dag E Undlien

Publications by authors named "Dag E Undlien"

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42Publications

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Childhood lung function and the association with β2-adrenergic receptor haplotypes.

Acta Paediatr 2013 Jul 29;102(7):727-31. Epub 2013 Mar 29.

Department of Paediatrics, Women and Children's Division, Oslo University Hospital, Oslo, Norway.

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http://dx.doi.org/10.1111/apa.12221DOI Listing
July 2013

Limitations and possibilities of low cell number ChIP-seq.

BMC Genomics 2012 Nov 21;13:645. Epub 2012 Nov 21.

Department of Medical Genetics, Oslo University Hospital, Norway.

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http://dx.doi.org/10.1186/1471-2164-13-645DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3533509PMC
November 2012

[Individual genome sequencing].

Authors:
Dag E Undlien

Tidsskr Nor Laegeforen 2012 Feb;132(3):264

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http://dx.doi.org/10.4045/tidsskr.11.1490DOI Listing
February 2012

Extensive variation and low heritability of DNA methylation identified in a twin study.

Genome Res 2011 Nov 26;21(11):1813-21. Epub 2011 Sep 26.

Department of Medical Genetics, Oslo University Hospital and University of Oslo, 0407 Oslo, Norway;

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http://dx.doi.org/10.1101/gr.119685.110DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3205566PMC
November 2011

Multiple loci in the HLA complex are associated with Addison's disease.

J Clin Endocrinol Metab 2011 Oct 3;96(10):E1703-8. Epub 2011 Aug 3.

Department of Medical Genetics, Oslo University Hospital, Ullevål, N-0407 Oslo, Norway.

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http://dx.doi.org/10.1210/jc.2011-0645DOI Listing
October 2011

Does the relative risk for type 1 diabetes conferred by HLA-DQ, INS, and PTPN22 polymorphisms vary with maternal age, birth weight, or cesarean section?

Pediatr Diabetes 2011 Mar 6;12(2):91-4. Epub 2010 Sep 6.

Division of Epidemiology, Norwegian Institute of Public Health, Oslo, Norway.

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http://doi.wiley.com/10.1111/j.1399-5448.2010.00669.x
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http://dx.doi.org/10.1111/j.1399-5448.2010.00669.xDOI Listing
March 2011

An inverse association between history of childhood eczema and subsequent risk of type 1 diabetes that is not likely to be explained by HLA-DQ, PTPN22, or CTLA4 polymorphisms.

Pediatr Diabetes 2010 Sep 4;11(6):386-93. Epub 2009 Nov 4.

Division of Epidemiology, Norwegian Institute of Public Health, NO-0403 Oslo, Norway.

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http://dx.doi.org/10.1111/j.1399-5448.2009.00605.xDOI Listing
September 2010

T cell responses to steroid cytochrome P450 21-hydroxylase in patients with autoimmune primary adrenal insufficiency.

J Clin Endocrinol Metab 2009 Dec 4;94(12):5117-24. Epub 2009 Nov 4.

Department of Medicine, Haukeland University Hospital, N-5021 Bergen, Norway.

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https://academic.oup.com/jcem/article-lookup/doi/10.1210/jc.
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http://dx.doi.org/10.1210/jc.2009-1115DOI Listing
December 2009

Genome-wide linkage analysis with clustered SNP markers.

J Biomol Screen 2009 Jan;14(1):92-6

Institute of Medical Genetics, University of Oslo, Oslo, Norway.

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http://dx.doi.org/10.1177/1087057108327327DOI Listing
January 2009

Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency.

J Clin Endocrinol Metab 2008 Sep 1;93(9):3310-7. Epub 2008 Jul 1.

Department of Medical Genetics, Ullevål University Hospital, University of Oslo, Kirkeveien 166, N-0407 Oslo, Norway.

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http://dx.doi.org/10.1210/jc.2008-0821DOI Listing
September 2008

Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease.

Eur J Hum Genet 2008 Aug 27;16(8):977-82. Epub 2008 Feb 27.

Institute of Medical Genetics, University of Oslo, Department of Medical Genetics, Ullevaal University Hospital, Oslo, Norway.

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http://dx.doi.org/10.1038/ejhg.2008.33DOI Listing
August 2008

Association analysis in type 1 diabetes of the PRSS16 gene encoding a thymus-specific serine protease.

Hum Immunol 2007 Jul 13;68(7):592-8. Epub 2007 Apr 13.

Institute of Immunology, Rikshospitalet-Radiumhospitalet Medical Center, and Institute of Medical Genetics, University of Oslo, Norway.

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http://dx.doi.org/10.1016/j.humimm.2007.03.009DOI Listing
July 2007

FOXP3 polymorphisms in type 1 diabetes and coeliac disease.

J Autoimmun 2006 Sep 20;27(2):140-4. Epub 2006 Sep 20.

Institute of Medical Genetics, Faculty Division Ullevål University Hospital, University of Oslo, Oslo, Norway.

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http://dx.doi.org/10.1016/j.jaut.2006.06.007DOI Listing
September 2006

[Molecular diagnostics in diabetes mellitus].

Tidsskr Nor Laegeforen 2005 Nov;125(21):2968-72

Seksjon for medisinsk genetikk og molekylaermedisin, Institutt for klinisk medisin, Universitetet i Bergen.

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November 2005

No evidence for association of the TATA-box binding protein glutamine repeat sequence or the flanking chromosome 6q27 region with type 1 diabetes.

Biochem Biophys Res Commun 2005 Jun;331(2):435-41

Juvenile Diabetes Research Foundation/Wellcome Trust Diabetes and Inflammation Laboratory, Cambridge Institute for Medical Research, University of Cambridge, Wellcome Trust/MRC Building, Hills Road, Cambridge, UK.

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http://dx.doi.org/10.1016/j.bbrc.2005.03.203DOI Listing
June 2005

CTLA4 polymorphisms are associated with vitiligo, in patients with concomitant autoimmune diseases.

Pigment Cell Res 2005 Feb;18(1):55-8

Institute and Department of Medical Genetics, Ullevål University Hospital, University of Oslo, Oslo, Norway.

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http://dx.doi.org/10.1111/j.1600-0749.2004.00196.xDOI Listing
February 2005

Analysis of the vitamin D receptor gene sequence variants in type 1 diabetes.

Diabetes 2004 Oct;53(10):2709-12

Juvenile Diabetes Research Foundation/Wellcome Trust DiabetesInflammation Laboratory, Cambridge Institute for Medical Research, University of Cambridge, WT/MRC building, Addenbrooke's Hospital, Cambridge, CB2 2XY, UK.

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http://dx.doi.org/10.2337/diabetes.53.10.2709DOI Listing
October 2004

Association analysis of the lymphocyte-specific protein tyrosine kinase (LCK) gene in type 1 diabetes.

Diabetes 2004 Sep;53(9):2479-82

JDRF/WT Diabetes and Inflammation Laboratory, Cambridge Institute for Medical Research, Wellcome Trust/MRC Building, Addenbrooke's Hospital, Hills Road, Cambridge, CB2 2XY, UK.

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http://diabetes.diabetesjournals.org/content/53/9/2479.full.
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http://dx.doi.org/10.2337/diabetes.53.9.2479DOI Listing
September 2004

Comparative high-resolution analysis of linkage disequilibrium and tag single nucleotide polymorphisms between populations in the vitamin D receptor gene.

Hum Mol Genet 2004 Aug 2;13(15):1633-9. Epub 2004 Jun 2.

Juvenile Diabetes Research Foundation/Wellcome Trust Diabetes and Inflammation Laboratory, Cambridge Institute for Medical Research, University of Cambridge, UK.

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http://dx.doi.org/10.1093/hmg/ddh169DOI Listing
August 2004

Polymorphisms in the cytotoxic T lymphocyte antigen-4 gene region confer susceptibility to Addison's disease.

J Clin Endocrinol Metab 2004 Jul;89(7):3474-6

Institute of Medical Genetics, University of Oslo, P.O. Box 1036, Blindern, NO-0315 Oslo, Norway.

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http://dx.doi.org/10.1210/jc.2003-031854DOI Listing
July 2004

Lack of association of the Ala(45)Thr polymorphism and other common variants of the NeuroD gene with type 1 diabetes.

Diabetes 2004 Apr;53(4):1158-61

Juvenile Diabetes Research Foundation/Wellcome Trust Diabetes and Inflammation Laboratory, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK.

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http://dx.doi.org/10.2337/diabetes.53.4.1158DOI Listing
April 2004

No evidence of type 1 diabetes susceptibility genes in the region centromeric of the HLA complex.

Hum Immunol 2003 Oct;64(10):951-9

Institute of Immunology, Rikshospitalet University Hospital, Oslo, Norway.

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http://dx.doi.org/10.1016/s0198-8859(03)00172-1DOI Listing
October 2003

A gene in the telomeric HLA complex distinct from HLA-A is involved in predisposition to juvenile idiopathic arthritis.

Arthritis Rheum 2002 Jun;46(6):1614-9

Institute of Immunology and Center for Rheumatic Diseases, Rikshospitalet University Hospital, N-0027 Oslo, Norway.

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http://dx.doi.org/10.1002/art.10337DOI Listing
June 2002