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List of works by Dag Undlien

40 EASD Annual Meeting of the European Association for the Study of Diabetes : Munich, Germany, 5-9 September 2004 ⬇️

article

A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis

scientific article

A Common Haplotype in NAPEPLD Is Associated With Severe Obesity in a Norwegian Population‐Based Cohort (the HUNT Study) ⬇️

scientific article published on September 30, 2010

A TLR2 polymorphism is associated with type 1 diabetes and allergic asthma

scientific article published on 15 January 2009

A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes

article

A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insult

scientific article

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

scientific article published in June 2002

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

scientific article published on 4 February 2002

A gene telomeric of the HLA class I region is involved in predisposition to both type 1 diabetes and coeliac disease

scientific article published on 01 August 1999

A mild form of Mucopolysaccharidosis IIIB diagnosed with targeted next-generation sequencing of linked genomic regions ⬇️

scientific article published on June 29, 2011

A novel juvenile idiopathic arthritis (JIA) susceptibility gene in HLA class I region marked by microsatellite D6S265.

scientific article

Alpha‐nicotinic acetylcholine receptor and tobacco smoke exposure: Effects on bronchial hyperresponsiveness in children ⬇️

scientific article published on October 21, 2011

An additional susceptibility gene for juvenile idiopathic arthritis in the HLA class I region on several DR-DQ haplotypes

scientific article (publication date: 2003)

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

scientific article published on 4 November 2009

Analysis of the type 2 diabetes-associated single nucleotide polymorphisms in the genes IRS1, KCNJ11, and PPARG2 in type 1 diabetes

scientific article published in March 2004

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

scientific article published in October 2004

Application and interpretation of transmission/disequilibrium tests: transmission of HLA-DQ haplotypes to unaffected siblings in 526 families with type 1 diabetes

scientific article

Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes

scientific article (publication date: February 2005)

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

scientific article

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

scientific article

Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European cohorts

scientific article published on 10 March 2014

Association of intercellular adhesion molecule-1 gene with type 1 diabetes

scientific article published on November 2003

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

scientific article (publication date: 29 May 2003)

Autoimmune adrenocortical failure in Norway autoantibodies and human leukocyte antigen class II associations related to clinical features

scientific article (publication date: February 2002)

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.

scientific article published on 13 April 2018

CD14 polymorphisms and serum CD14 levels through childhood: a role for gene methylation?

scientific article published on 15 April 2010

CIITA gene variants are associated with rheumatoid arthritis in Scandinavian populations

article

CTLA-4 as a genetic determinant in autoimmune Addison's disease.

scientific article

CTLA-4 polymorphisms in allergy and asthma and the TH1/ TH2 paradigm

scientific article

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

CYP21A2 polymorphisms in patients with autoimmune Addison's disease, and linkage disequilibrium to HLA risk alleles

scientific article published on 23 September 2014

Childhood lung function and the association with β2‐adrenergic receptor haplotypes ⬇️

scientific article published on March 29, 2013

Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor

scientific article published on January 2007

Clinical, immunological, and genetic features of autoimmune primary adrenal insufficiency: observations from a Norwegian registry

scientific article published on 26 October 2009

Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease

scientific article published on 27 September 2019

Common variants in the regulatory region of the insulin gene are associated with fasting plasma insulin levels in juvenile obesity

scientific article

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

scientific article

Construction and analysis of tag single nucleotide polymorphism maps for six human-mouse orthologous candidate genes in type 1 diabetes

scientific article

Current guidelines for BRCA testing of breast cancer patients are insufficient to detect all mutation carriers

scientific article

DNA methylation and gene expression changes in monozygotic twins discordant for psoriasis: identification of epigenetically dysregulated genes

scientific article

DR- and DQ-associated protection from type 1A diabetes: comparison of DRB1*1401 and DQA1*0102-DQB1*0602*.

scientific article

Detection of a low-grade enteroviral infection in the islets of langerhans of living patients newly diagnosed with type 1 diabetes

scientific article

Diabetes mellitus--a complex interaction between heredity and environment

scientific article published on 01 June 1998

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?

scientific article published on 6 September 2010

Evidence by allelic association-dependent methods for a type 1 diabetes polygene (IDDM6) on chromosome 18q21

scientific article published on 12 September 2007

Evidence by allelic association-dependent methods for a type 1 diabetes polygene (IDDM6) on chromosome 18q21.

scientific article published on July 1997

Evidence for a type 1 diabetes susceptibility locus (IDDM10) on human chromosome 10p11-q11

scientific article published on 12 September 2007

Evidence for a type 1 diabetes susceptibility locus (IDDM10) on human chromosome 10p11-q11

article

Evidence of at least two type 1 diabetes susceptibility genes in the HLA complex distinct from HLA-DQB1, -DQA1 and –DRB1

scientific article

Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus

scientific article published on 23 December 2010

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

scientific article

FOXP3 polymorphisms in type 1 diabetes and coeliac disease.

scientific article

FTO genotype and weight gain in obese and normal weight adults from a Norwegian population based cohort (the HUNT study).

scientific article

Fine mapping of the diabetes-susceptibility locus, IDDM4, on chromosome 11q13.

scientific article published in August 1998

Genetic diagnostic test for hemochromatosis

scientific article published on January 20, 1998

Genetic screening of Scandinavian families with febrile seizures and epilepsy or GEFS+

scientific article published on 10 October 2007

Genetic variants of the HLA-A, HLA-B and AIF1 loci show independent associations with type 1 diabetes in Norwegian families

scientific article published on 06 November 2008

Genome-wide linkage analysis with clustered SNP markers

scientific article published on 01 January 2009

Genotype effects and epistasis in type 1 diabetes and HLA-DQ trans dimer associations with disease

scientific article published in August 2004

HLA Associations in Insulin-Dependent Diabetes Mellitus: No Independent Association to Particular DP Genes ⬇️

scientific article published on 01 July 1997

HLA associations in type 1 diabetes among patients not carrying high-risk DR3-DQ2 or DR4-DQ8 haplotypes

scientific article published on 01 December 1999

HLA associations in type 1 diabetes: DPB1 alleles may act as markers of other HLA-complex susceptibility genes

scientific article

HLA associations in type 1 diabetes: merging genetics and immunology

scientific article published on 01 September 2001

HLA complex genes in type 1 diabetes and other autoimmune diseases. Which genes are involved?

scientific article

HLA-encoded genetic predisposition in IDDM: DR4 subtypes may be associated with different degrees of protection

scientific article

HLA-encoded genetic predisposition in IDDM: DR4 subtypes may be associated with different degrees of protection

IDDM susceptibility associated with polymorphisms in the insulin gene region. A study of blacks, Caucasians and orientals

scientific article

Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's disease

scientific article published on 01 April 2019

Influence of genetic factors (HLA class II genes, insulin-gene region polymorphisms) and metabolic control on the development of diabetic nephropathy

scientific article published on 01 January 1993

Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele

article

Insulin autoimmune syndrome; HLA genes may be a marker of disease heterogeneity

scientific article published on 01 January 1993

Insulin gene region-encoded susceptibility to IDDM maps upstream of the insulin gene

scientific article published on 01 June 1995

Insulin gene region-encoded susceptibility to type 1 diabetes is not restricted to HLA-DR4-positive individuals

scientific article published on November 1, 1992

Intra-individual changes in DNA methylation not mediated by cell-type composition are correlated with aging during childhood

scientific article published on 21 October 2016

Joint effects of HLA, INS, PTPN22 and CTLA4 genes on the risk of type 1 diabetes

scientific article published on 22 February 2008

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

scientific article published on April 2004

Limitations and possibilities of low cell number ChIP-seq.

scientific article

Linkage disequilibrium and haplotype blocks in the MHC vary in an HLA haplotype specific manner assessed mainly by DRB1*03 and DRB1*04 haplotypes

scientific article

Linkage disequilibrium between TAP2 variants and HLA class II alleles; no primary association between TAP2 variants and insulin-dependent diabetes mellitus

article

Linkage disequilibrium mapping of a type 1 diabetes susceptibility gene (IDDM7) to chromosome 2q31-q33.

scientific article

Molecular diagnostics in diabetes mellitus

scientific article published in November 2005

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

scientific article published on 03 August 2011

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

scientific article

Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes

scientific article

Mutations in the melanocortin 4 receptor (MC4R) gene in obese patients in Norway

scientific article published on 19 March 2009

Neonatal diabetes mellitus due to complete glucokinase deficiency

scientific article published in May 2001

No association of multiple sclerosis to alleles at the TAP2 locus

scientific article published on 01 April 1994

No difference in the parental origin of susceptibility HLA class II haplotypes among Norwegian patients with insulin-dependent diabetes mellitus

scientific article published on December 1995

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

scientific article published in June 2005

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

scientific article published in October 2003

No independent associations of LMP2 and LMP7 polymorphisms with susceptibility to develop IDDM.

scientific article published in February 1997

Pet keeping and tobacco exposure influence CD14 methylation in childhood

scientific article

Polymorphism of human major histocompatibility complex-encoded transporter associated with antigen processing (TAP) genes and susceptibility to juvenile rheumatoid arthritis

article

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

scientific article

Polymorphisms in the cathepsin L2 (CTSL2) gene show association with type 1 diabetes and early-onset myasthenia gravis

scientific article

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

scientific article published in July 2004

Polymorphisms in the gene encoding thymus-specific serine protease in the extended HLA complex: a potential candidate gene for autoimmune and HLA-associated diseases

scientific article

Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry

scientific article published on 27 April 2013

Programmed Death Ligand 1 (PD-L1) Gene Variants Contribute to Autoimmune Addison’s Disease and Graves’ Disease Susceptibility

scientific article published in November 2009

Programmed death ligand 1 (PD-L1) gene variants contribute to autoimmune Addison's disease and Graves' disease susceptibility

scientific article published on 22 October 2009

Relative predispositional effects of HLA class II DRB1-DQB1 haplotypes and genotypes on type 1 diabetes: a meta-analysis

scientific article

Remapping the insulin gene/IDDM2 locus in type 1 diabetes

scientific article published in July 2004

Reproducible association with type 1 diabetes in the extended class I region of the major histocompatibility complex

scientific article

SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome

scientific article published on 13 March 2008

Suggestive Evidence for Association of Human Chromosome 18q12-q21 and Its Orthologue on Rat and Mouse Chromosome 18 With Several Autoimmune Diseases

article

Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus

article

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

scientific article published on 04 November 2009

T cell-specific T-box transcription factor haplotype is associated with allergic asthma in children

scientific article published on 18 October 2007

Testing the possible negative association of type 1 diabetes and atopic disease by analysis of the interleukin 4 receptor gene.

scientific article published in October 2003

The Clinical Expression of Hemochromatosis in Oslo, Norway: Excessive Oral Iron Intake May Lead to Secondary Hemochromatosis Even in HFE C282Y Mutation Negative Subjects

scientific article published on 01 December 2000

The FCRL3 -169T>C polymorphism is associated with rheumatoid arthritis and shows suggestive evidence of involvement with juvenile idiopathic arthritis in a Scandinavian panel of autoimmune diseases

scientific article published on 07 December 2007

The HLA associated predisposition to type 1 diabetes and other autoimmune diseases

scientific article published on March 1996

The polymorphism in the 3' untranslated region of IL12B has a negligible effect on the susceptibility to develop type 1 diabetes in Norway

scientific article published on 01 September 2001

The predisposition to type 1 diabetes linked to the human leukocyte antigen complex includes at least one non-class II gene

scientific article

The relation between size at birth and risk of type 1 diabetes is not influenced by adjustment for the insulin gene (-23HphI) polymorphism or HLA-DQ genotype

scientific article

Transmission of haplotypes of microsatellite markers rather than single marker alleles in the mapping of a putative type 1 diabetes susceptibility gene (IDDM6)

scientific article

X-linked congenital adrenal hypoplasia with hypogonadotropic hypogonadism caused by an inversion disrupting a conserved noncoding element upstream of the NR0B1 (DAX1) gene

scientific article published on 22 September 2009

[Genetic and immunologic risks for development of type 1 diabetes--experiences from an intervention trial]

scientific article published on 01 September 2000

[Genetic causes of obesity]

scientific article published on 01 November 2005

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