D. Undlien

发表

Pathogenic variants in KCTD7 perturb neuronal K+ fluxes and glutamine transport.

F. Chaudhry, M. N. Moen, Roar Fjær, 2016, Brain : a journal of neurology.

Limitations and possibilities of low cell number ChIP-seq

Jennifer R. Harris, R. Lyle, G. Gilfillan, 2012, BMC Genomics.

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

R. Lyle, K. Carlsen, B. K. Andreassen, 2016, Clinical Epigenetics.

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

Kristian Løvås, D. Undlien, A. Wolff, 2014, European journal of endocrinology.

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

Luc J. Smink, Neil M. Walker, Linda S. Wicker, 2003, Nature.

Remapping the insulin gene/IDDM2 locus in type 1 diabetes.

Mark I McCarthy, Heather J Cordell, Jaakko Tuomilehto, 2004, Diabetes.

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

P. Bingley, J. Todd, S. Nutland, 2003, The Lancet.

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

T. Egeland, D. Undlien, L. Retterstøl, 2010, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

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

J. Todd, S. Nutland, N. Walker, 2005, Biochemical and biophysical research communications.

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

D. Strachan, J. Todd, S. Nutland, 2005, BMC Genetics.

The clinical expression of hemochromatosis in Oslo, Norway. Excessive oral iron intake may lead to secondary hemochromatosis even in HFE C282Y mutation negative subjects.

E. Thorsby, J. Berg, H. E. Heier, 2000, Scandinavian journal of gastroenterology.

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

B. Lie, A. Weetman, D. Undlien, 2004, The Journal of clinical endocrinology and metabolism.

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

J. Berg, D. Undlien, 2001, European journal of endocrinology.

Lack of Association of the Ala45Thr Polymorphism and Other Common Variants of the NeuroD Gene With Type 1 Diabetes

J. Todd, S. Nutland, J. Tuomilehto, 2004 .

Autosomal dominant pericentral retinal dystrophy caused by a novel missense mutation in the TOPORS gene

Ø. Braaten, D. Undlien, K. Selmer, 2009, Acta ophthalmologica.

Mutations in the Insulin Gene Can Cause MODY and Autoantibody-Negative Type 1 Diabetes

Geir Joner, Graeme I. Bell, D. Steiner, 2008, Diabetes.

High Frequency of Coeliac Disease among Patients with Autoimmune Adrenocortical Failure

E. Husebye, D. Undlien, L. Aksnes, 2003, Scandinavian journal of gastroenterology.

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

R. Lyle, K. Carlsen, K. L. Lødrup Carlsen, 2010, The Journal of allergy and clinical immunology.

Reply to “Insulin expression: is VNTR allele 698 really anomalous?”

J. Todd, S. Gough, A. Cambon-Thomsen, 1995, Nature Genetics.

Brief Genetics Report Lack of Association of the Ala 45 Thr Polymorphism and Other Common Variants of the NeuroD Gene With Type 1 Diabetes

J. Todd, S. Nutland, J. Tuomilehto, 2004 .

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

J. Todd, S. Nutland, J. Tuomilehto, 2004, Diabetes.

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

S. Tonstad, M. Mattingsdal, D. Undlien, 2009, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Pet keeping and tobacco exposure influence CD14 methylation in childhood

R. Lyle, K. Carlsen, P. Mowinckel, 2012, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

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

E. Thorsby, B. Lie, A. Cambon-Thomsen, 2003, Human immunology.

Vitamin D status and pathway genes in five European autoimmune Addison's disease cohorts.

K. Badenhoop, W. Ollier, S. Pearce, 2021, European journal of endocrinology.

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

E. Husebye, D. Undlien, A. Myhre, 2002, The Journal of clinical endocrinology and metabolism.

No association of multiple sclerosis to alleles at the TAP2 locus.

F. Vartdal, D. Undlien, A. Spurkland, 1994, Human immunology.

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

J. Todd, N. Walker, J. Tuomilehto, 2004, Diabetes.

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

J. Carlson, J. Svartberg, H. Erlich, 2009, The Journal of clinical endocrinology and metabolism.

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

B. Lie, D. Gawkrodger, E. Husebye, 2005, Pigment cell research.

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

T. Egeland, G. Gilfillan, E. Ormerod, 2009, The Journal of clinical endocrinology and metabolism.

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

Spain, S. O’Rahilly, M. Dattani, 2007, The New England journal of medicine.

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

Sergey Nejentsev, Constantin Ionescu-Tirgoviste, Jaakko Tuomilehto, 2004, Human molecular genetics.

No Independent Associations of LMP2 and LMP7 Polymorphisms With Susceptibility to Develop IDDM

E. Thorsby, O. Søvik, K. Rønningen, 1997, Diabetes.

HLA-Encoded Genetic Predisposition in IDDM: DR4 Subtypes May Be Associated With Different Degrees of Protection

H. Rammensee, E. Thorsby, D. Undlien, 1997, Diabetes.

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

Amanda J. Wilson, J. Todd, C. Polychronakos, 1997, Nature Genetics.

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

J. Gécz, M. Stratton, P. Futreal, 2008, American journal of human genetics.

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

Christopher D. Brown, K. White, S. Pulst, 2012, Human molecular genetics.

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

E. Thorsby, B. Lie, R. Płoski, 2002, Arthritis and rheumatism.

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

L. C. Stene, K. Rønningen, D. Undlien, 2010, Pediatric diabetes.

DNA Methylation and Gene Expression Changes in Monozygotic Twins Discordant for Psoriasis: Identification of Epigenetically Dysregulated Genes

Morten Mattingsdal, Jennifer R. Harris, Kristina Gervin, 2012, PLoS genetics.

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

Jennifer R Harris, Kristina Gervin, Robert Lyle, 2011, Genome research.

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?

K. Rønningen, D. Undlien, L. C. Stene, 2011, Pediatric diabetes.

Neonatal diabetes mellitus due to complete glucokinase deficiency.

A. Molven, P. Njølstad, O. Søvik, 2001, The New England journal of medicine.

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

E. Thorsby, D. Monos, J. Strominger, 1993, European journal of immunology.

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

H. Cordell, S. Pearce, E. Husebye, 2009, The Journal of clinical endocrinology and metabolism.

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

T. Egeland, S. Pearce, E. Husebye, 2008, The Journal of clinical endocrinology and metabolism.

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

T. Egeland, E. Husebye, D. Undlien, 2008, European Journal of Human Genetics.

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

J. Todd, J. Tuomilehto, J. Howson, 2004, Diabetes.

FOXP3 polymorphisms in type 1 diabetes and coeliac disease.

B. Lie, P. Njølstad, L. Sollid, 2006, Journal of autoimmunity.

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

A. Molven, P. Njølstad, O. Søvik, 2013, Diabetologia.

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

K. Carlsen, K. L. Lødrup Carlsen, P. Mowinckel, 2013, Acta paediatrica.

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

E. Schlichting, L. Mæhle, D. Undlien, 2017, BMC Cancer.

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

E. Schlichting, L. Mæhle, D. Undlien, 2017, BMC Cancer.

Detection of a Low-Grade Enteroviral Infection in the Islets of Langerhans of Living Patients Newly Diagnosed With Type 1 Diabetes

N. Morgan, S. Richardson, B. Edwin, 2014, Diabetes.

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

B. Lie, K. Carlsen, K. L. Lødrup Carlsen, 2004, The Journal of allergy and clinical immunology.

Association of Autoimmune Addison's Disease with Alleles of STAT4 and GATA3 in European Cohorts

T. Merriman, K. Badenhoop, H. Cordell, 2014, PloS one.

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

E. Mozes, E. Husebye, D. Undlien, 2009, The Journal of clinical endocrinology and metabolism.

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

E. Thorsby, B. Lie, S. Johansson, 2001, Immunogenetics.

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

E. Thorsby, B. Lie, A. Cambon-Thomsen, 2007, Human immunology.

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

E. Thorsby, B. Lie, K. Dahl-Jørgensen, 2007, Human immunology.

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

B. Lie, J. Carlson, H. Erlich, 2011, The Journal of clinical endocrinology and metabolism.

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

E. Husebye, B. Oftedal, M. D. Vigeland, 2019, Journal of translational autoimmunity.

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

B. Lie, T. Egeland, P. Njølstad, 2009, Annals of the rheumatic diseases.

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

D. Strachan, J. Todd, S. Nutland, 2005, Nature Genetics.

Title: Detection of a low-grade enteroviral infection in the islets of Langerhans of living patients newly diagnosed with type 1 diabetes Short running title: Enterovirus in pancreas in patients with T1D

S. Richardson, B. Edwin, H. Hyöty, 2014 .

Prenatal maternal depressive symptoms and infant DNA methylation: a longitudinal epigenome-wide study

E. Heiervang, D. Undlien, A. Myhre, 2019, Nordic journal of psychiatry.

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

D. Undlien, L. Retterstøl, J. Holmen, 2011, Obesity.

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

D. Misceo, R. Lyle, S. Nakken, 2011, European Journal of Human Genetics.

Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF

M. Schubach, S. Hoeller, S. Schulzke, 2016, Human Mutation.

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

K. Carlsen, T. Egeland, D. Undlien, 2008, The Journal of allergy and clinical immunology.

Correction: Association of Autoimmune Addison's Disease with Alleles of STAT4 and GATA3 in European Cohorts

H. Cordell, S. Pearce, E. Husebye, 2014, PLoS ONE.

SCN1A mutation screening in adult patients with Lennox–Gastaut syndrome features

E. Brodtkorb, D. Undlien, K. Selmer, 2009, Epilepsy & Behavior.

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

D. Strachan, J. Todd, S. Nutland, 2004, Diabetes.

Insulin Gene Region-Encoded Susceptibility to IDDM Maps Upstream of the Insulin Gene

M. Knip, J. Todd, E. Thorsby, 1995, Diabetes.

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

K. Carlsen, T. Egeland, P. Njølstad, 2009, Genes and Immunity.

The HLA Associated Predisposition to Type 1 Diabetes and Other Autoimmune Diseases

E. Thorsby, D. Undlien, D. Undlien, 1996, Journal of pediatric endocrinology & metabolism : JPEM.

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

B. Lie, P. Njølstad, S. Johansson, 2009, Genes and Immunity.

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

P. Bingley, J. Ilonen, Å. Lernmark, 2007, Tissue antigens.

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

J. Todd, E. Thorsby, B. Lie, 1999, American journal of human genetics.

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

K. Shianna, K. Carlsen, K. L. Lødrup Carlsen, 2012, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

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

T. Karlsen, K. Boberg, M. Vatn, 2007, Annals of the rheumatic diseases.

Correction: Association of Autoimmune Addison's Disease with Alleles of STAT4 and GATA3 in European Cohorts

H. Cordell, S. Pearce, E. Husebye, 2014, PLoS ONE.

[Genetic causes of obesity].

S. Tonstad, D. Undlien, L. Retterstøl, 2005, Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke.

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

Christopher D. Brown, K. White, S. Pulst, 2012, Human molecular genetics.

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

K. Carlsen, K. L. Lødrup Carlsen, P. Mowinckel, 2013, Acta paediatrica.

[Diabetes mellitus--a complex interaction between heredity and environment].

E. Thorsby, K. Birkeland, J. Berg, 1998, Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke.

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?

K. Rønningen, D. Undlien, L. C. Stene, 2011, Pediatric diabetes.

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

E. Schlichting, L. Mæhle, D. Undlien, 2018, ESMO Open.