Lista de obras - Dag Undlien - Dominio Público Uruguay

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

artículo científico publicado en 2010

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

artículo científico publicado el 30 de septiembre de 2010

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

artículo científico publicado en 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

artículo científico publicado en 2012

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

artículo científico publicado en 2002

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

artículo científico publicado en 2002

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

artículo científico publicado en 1999

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

artículo científico publicado el 29 de junio de 2011

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

artículo científico publicado en 2003

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

artículo científico publicado el 21 de octubre de 2011

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

artículo científico publicado en 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

artículo científico publicado en 2009

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

artículo científico publicado en 2004

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

artículo científico publicado en 2004

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

artículo científico publicado en 2000

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

artículo científico publicado en 2005

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

artículo científico publicado en 2007

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

artículo científico publicado en 2004

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

artículo científico publicado en 2014

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

artículo científico publicado en 2003

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

artículo científico publicado en 2003

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

artículo científico publicado en 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

artículo científico publicado en 2018

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

artículo científico publicado en 2010

CIITA gene variants are associated with rheumatoid arthritis in Scandinavian populations

article

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

artículo científico publicado en 2015

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

artículo científico publicado en 2004

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

artículo científico publicado en 2014

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

artículo científico publicado el 29 de marzo de 2013

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

artículo científico publicado en 2007

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

artículo científico publicado en 2009

Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease

artículo científico publicado en 2019

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

artículo científico publicado en 2001

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

artículo científico publicado en 2004

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

artículo científico publicado en 2005

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

artículo científico publicado en 2017

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

artículo científico publicado en 2012

DR- and DQ-associated protection from type 1A diabetes: comparison of DRB11401 and DQA10102-DQB10602.

artículo científico publicado en 2000

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

artículo científico publicado en 2014

Diabetes mellitus--a complex interaction between heredity and environment

artículo científico publicado en 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?

artículo científico publicado en 2010

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

artículo científico publicado en 2007

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

artículo científico publicado en 1997

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

artículo científico publicado en 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

artículo científico publicado en 2003

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

artículo científico publicado en 2010

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

artículo científico publicado en 2011

FOXP3 polymorphisms in type 1 diabetes and coeliac disease

artículo científico publicado en 2006

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

artículo científico publicado en 2010

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

artículo científico publicado en 1998

Genetic diagnostic test for hemochromatosis

artículo científico publicado el 20 de enero de 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

artículo científico publicado en 2008

Genome-wide linkage analysis with clustered SNP markers

artículo científico publicado en 2009

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

artículo científico publicado en 2004

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

artículo científico publicado el 1 de julio de 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

artículo científico publicado en 2003

HLA associations in type 1 diabetes: merging genetics and immunology

artículo científico publicado en 2001

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

artículo científico publicado en 2001

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

artículo científico publicado en 1997

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

artículo científico publicado en 1994

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

artículo científico publicado en 2019

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

artículo científico publicado en 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

artículo científico publicado en 1993

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

artículo científico publicado en 1995

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

artículo científico publicado el 1 de noviembre de 1992

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

artículo científico publicado en 2016

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

artículo científico publicado en 2008

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

artículo científico

Limitations and possibilities of low cell number ChIP-seq.

artículo científico publicado en 2012

Linkage disequilibrium and haplotype blocks in the MHC vary in an HLA haplotype specific manner assessed mainly by DRB103 and DRB104 haplotypes

artículo científico publicado en 2006

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.

artículo científico publicado en 1995

Molecular diagnostics in diabetes mellitus

artículo científico publicado en 2005

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

artículo científico publicado en 2011

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

artículo científico publicado en 2008

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

artículo científico publicado en 2008

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

artículo científico publicado en 2009

Neonatal diabetes mellitus due to complete glucokinase deficiency

artículo científico publicado en 2001

No association of multiple sclerosis to alleles at the TAP2 locus

artículo científico publicado en 1994

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

artículo científico publicado en 1995

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

artículo científico publicado en 2005

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

artículo científico publicado en 2003

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

artículo científico publicado en 1997

Pet keeping and tobacco exposure influence CD14 methylation in childhood

artículo científico publicado en 2012

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

artículo científico publicado en 2008

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

artículo científico publicado en 2007

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

artículo científico publicado en 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

artículo científico publicado en 2002

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

artículo científico publicado en 2013

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

artículo científico publicado en 2009

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

artículo científico publicado en 2009

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

artículo científico publicado en 2007

Remapping the insulin gene/IDDM2 locus in type 1 diabetes

artículo científico publicado en 2004

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

artículo científico publicado en 2009

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

artículo científico publicado en 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

artículo científico publicado en 2009

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

artículo científico publicado en 2007

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

artículo científico publicado en 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

artículo científico publicado en 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

artículo científico publicado en 2007

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

artículo científico publicado en 1996

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

artículo científico publicado en 2001

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

artículo científico publicado en 1999

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

artículo científico publicado en 2006

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

artículo científico publicado en 1998

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

artículo científico publicado en 2009

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

artículo científico publicado en 2000

[Genetic causes of obesity]

scientific article published on 01 November 2005

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

artículo

Lista de obras de Dag Undlien

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

CIITA gene variants are associated with rheumatoid arthritis in Scandinavian populations

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

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

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

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

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

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

Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease

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

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

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

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

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

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

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

Diabetes mellitus--a complex interaction between heredity and environment

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?

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

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

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

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

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

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

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

FOXP3 polymorphisms in type 1 diabetes and coeliac disease

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

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

Genetic diagnostic test for hemochromatosis

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

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

Genome-wide linkage analysis with clustered SNP markers

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

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

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

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

HLA associations in type 1 diabetes: merging genetics and immunology

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

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

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

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

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

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

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

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

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

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

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

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

Limitations and possibilities of low cell number ChIP-seq.

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

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

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

DR- and DQ-associated protection from type 1A diabetes: comparison of DRB11401 and DQA10102-DQB10602.

Linkage disequilibrium and haplotype blocks in the MHC vary in an HLA haplotype specific manner assessed mainly by DRB103 and DRB104 haplotypes