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D. Undlien · SciRah

Researcher profile · Semantic Scholar

D. Undlien

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D. Undlien — researcher profile on SciRah

h-index: 39
Works: 106
Citations: 7,663

Most-cited papers

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease
H. Ueda, J. Howson, L. Esposito, J. Heward +49 more
2003Nature2,312 citations
Semantic Scholar
Neonatal diabetes mellitus due to complete glucokinase deficiency.
P. Njølstad, O. Søvik, A. Cuesta-Muñoz, L. Bjørkhaug +8 more
2001New England Journal of Medicine396 citations Open access
Semantic Scholar
Clinical, immunological, and genetic features of autoimmune primary adrenal insufficiency: observations from a Norwegian registry.
Martina M. Erichsen, K. Løvås, Beate Skinningsrud, A. B. Wolff +9 more
2009Journal of Clinical Endocrinology and Metabolism395 citations Open access
Semantic Scholar
Detection of a Low-Grade Enteroviral Infection in the Islets of Langerhans of Living Patients Newly Diagnosed With Type 1 Diabetes
L. Krogvold, B. Edwin, T. Buanes, G. Frisk +15 more
2014Diabetes291 citations
Semantic Scholar
Remapping the insulin gene/IDDM2 locus in type 1 diabetes.
B. Barratt, F. Payne, C. Lowe, R. Hermann +18 more
2004Diabetes235 citations Open access
Semantic Scholar
Mutations in the Insulin Gene Can Cause MODY and Autoantibody-Negative Type 1 Diabetes
A. Molven, M. Ringdal, Anita M Nordbø, H. Ræder +11 more
2008Diabetes214 citations Open access
Semantic Scholar
Comparative high-resolution analysis of linkage disequilibrium and tag single nucleotide polymorphisms between populations in the vitamin D receptor gene.
S. Nejentsev, L. Godfrey, Hywel Snook, H. Rance +12 more
2004Human Molecular Genetics200 citations Open access
Semantic Scholar
The predisposition to type 1 diabetes linked to the human leukocyte antigen complex includes at least one non-class II gene.
B. Lie, J. Todd, F. Pociot, J. Nerup +6 more
1999American Journal of Human Genetics192 citations Open access
Semantic Scholar
Autoimmune adrenocortical failure in Norway autoantibodies and human leukocyte antigen class II associations related to clinical features.
A. Myhre, D. Undlien, K. Løvås, S. Uhlving +5 more
2002Journal of Clinical Endocrinology and Metabolism175 citations Open access
Semantic Scholar
HLA-Encoded Genetic Predisposition in IDDM: DR4 Subtypes May Be Associated With Different Degrees of Protection
D. Undlien, T. Friede, H. Rammensee, G. Joner +6 more
1997Diabetes164 citations
Semantic Scholar
DNA Methylation and Gene Expression Changes in Monozygotic Twins Discordant for Psoriasis: Identification of Epigenetically Dysregulated Genes
K. Gervin, M. D. Vigeland, M. Mattingsdal, Martin Hammerø +6 more
2012PLoS Genetics158 citations Open access
Semantic Scholar
Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry
H. U. Irgens, J. Molnes, B. Johansson, M. Ringdal +6 more
2013Diabetologia123 citations Open access
Semantic Scholar
Polymorphisms in the cytotoxic T lymphocyte antigen-4 gene region confer susceptibility to Addison's disease.
A. Blomhoff, B. A. Lie, A. Myhre, E. Kemp +4 more
2004Journal of Clinical Endocrinology and Metabolism116 citations
Semantic Scholar
Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency.
Beate Skinningsrud, E. Husebye, S. Pearce, D. McDonald +5 more
2008Journal of Clinical Endocrinology and Metabolism110 citations
Semantic Scholar
A gene telomeric of the HLA class I region is involved in predisposition to both type 1 diabetes and coeliac disease.
B. Lie, L. Sollid, H. Ascher, J. Ek +4 more
1999Tissue Antigens107 citations
Semantic Scholar
Limitations and possibilities of low cell number ChIP-seq
G. Gilfillan, T. Hughes, Y. Sheng, H. Hjorthaug +5 more
2012BMC Genomics97 citations Open access
Semantic Scholar
Analysis of the vitamin D receptor gene sequence variants in type 1 diabetes.
S. Nejentsev, J. Cooper, L. Godfrey, J. Howson +16 more
2004Diabetes95 citations Open access
Semantic Scholar
Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease
Beate Skinningsrud, E. Husebye, Kristina Gervin, K. Løvås +5 more
2008European Journal of Human Genetics94 citations
Semantic Scholar
CTLA-4 polymorphisms in allergy and asthma and the TH1/ TH2 paradigm.
M. Munthe-Kaas, K. Carlsen, P. Helms, J. Gerritsen +8 more
2004Journal of Allergy and Clinical Immunology87 citations Open access
Semantic Scholar
Current guidelines for BRCA testing of breast cancer patients are insufficient to detect all mutation carriers
E. Grindedal, Cecilie Heramb, Inga Karsrud, S. Ariansen +4 more
2017BMC Cancer75 citations Open access
Semantic Scholar
A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insult.
K. Hekman, Guo-Yun Yu, Christopher D. Brown, Haipeng Zhu +10 more
2012Human Molecular Genetics74 citations Open access
Semantic Scholar
Multiple loci in the HLA complex are associated with Addison's disease.
Beate Skinningsrud, B. Lie, Ewa H. Lavant, J. Carlson +8 more
2011Journal of Clinical Endocrinology and Metabolism69 citations
Semantic Scholar
CTLA4 polymorphisms are associated with vitiligo, in patients with concomitant autoimmune diseases.
A. Blomhoff, E. Kemp, D. Gawkrodger, A. Weetman +4 more
2005Pigment Cell Research67 citations
Semantic Scholar
Fine mapping of the diabetes-susceptibility locus, IDDM4, on chromosome 11q13.
Yusuke Nakagawa, Yoshihiko Kawaguchi, R. Twells, C. Muxworthy +22 more
1998American Journal of Human Genetics62 citations Open access
Semantic Scholar
Extensive variation and low heritability of DNA methylation identified in a twin study.
K. Gervin, Martin Hammerø, H. Akselsen, R. Moe +6 more
2011Genome Research60 citations Open access
Semantic Scholar
Joint effects of HLA, INS, PTPN22 and CTLA4 genes on the risk of type 1 diabetes
M. Bjørnvold, D. Undlien, G. Joner, K. Dahl-Jørgensen +5 more
2008Diabetologia58 citations Open access
Semantic Scholar
Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes
D. Smyth, J. Howson, C. Lowe, N. Walker +15 more
2005Nature Genetics57 citations
Semantic Scholar
FOXP3 polymorphisms in type 1 diabetes and coeliac disease.
M. Bjørnvold, S. S. Amundsen, L. C. Stene, G. Joner +11 more
2006Journal of Autoimmunity51 citations
Semantic Scholar
CD14 polymorphisms and serum CD14 levels through childhood: a role for gene methylation?
M. Munthe-Kaas, T. Torjussen, Kristina Gervin, K. Lødrup Carlsen +5 more
2010Journal of Allergy and Clinical Immunology48 citations
Semantic Scholar
Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus
Inger-Lise Mero, M. Ban, Å. R. Lorentzen, C. Smestad +14 more
2011Genes and Immunity46 citations
Semantic Scholar
T cell responses to steroid cytochrome P450 21-hydroxylase in patients with autoimmune primary adrenal insufficiency.
E. Bratland, Beate Skinningsrud, D. Undlien, E. Mozes +1 more
2009Journal of Clinical Endocrinology and Metabolism46 citations
Semantic Scholar
T cell-specific T-box transcription factor haplotype is associated with allergic asthma in children.
M. Munthe-Kaas, K. Carlsen, G. Håland, C. Devulapalli +4 more
2008Journal of Allergy and Clinical Immunology45 citations
Semantic Scholar
HLA Dr‐Dq haplotypes and the TNFA‐308 polymorphism: associations with asthma and allergy
M. Munthe-Kaas, K. Carlsen, K. Carlsen, T. Egeland +4 more
2007Allergy. European Journal of Allergy and Clinical Immunology43 citations
Semantic Scholar
Analysis of the type 2 diabetes-associated single nucleotide polymorphisms in the genes IRS1, KCNJ11, and PPARG2 in type 1 diabetes.
C. Eftychi, J. Howson, B. Barratt, A. Vella +13 more
2004Diabetes43 citations Open access
Semantic Scholar
HLA associations in type 1 diabetes among patients not carrying high-risk DR3-DQ2 or DR4-DQ8 haplotypes.
D. Undlien, I. Kockum, K. S. Rønningen, R. Lowe +6 more
1999Tissue Antigens42 citations
Semantic Scholar
Association of intercellular adhesion molecule-1 gene with type 1 diabetes.
S. Nejentsev, C. Guja, Rose McCormack, J. Cooper +17 more
2003The Lancet41 citations
Semantic Scholar
SCN1A mutation screening in adult patients with Lennox-Gastaut syndrome features.
K. Selmer, C. Lund, K. Brandal, D. Undlien +1 more
2009Epilepsy & Behavior39 citations
Semantic Scholar
Pathogenic variants in KCTD7 perturb neuronal K+ fluxes and glutamine transport.
M. N. Moen, Roar Fjær, El Hassan Hamdani, J. K. Laerdahl +9 more
2016Brain : a journal of neurology37 citations Open access
Semantic Scholar
Polymorphisms in the cathepsin L2 (CTSL2) gene show association with type 1 diabetes and early-onset myasthenia gravis.
M. K. Viken, Hege Dahlen Sollid, G. Joner, K. Dahl-Jørgensen +10 more
2007Human Immunology35 citations
Semantic Scholar
Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF
I. Filges, E. Bruder, K. Brandal, S. Meier +15 more
2016Human Mutation34 citations Open access
Semantic Scholar
A Common Haplotype in NAPEPLD Is Associated With Severe Obesity in a Norwegian Population‐Based Cohort (the HUNT Study)
T. Wangensteen, H. Akselsen, J. Holmen, D. Undlien +1 more
2011Obesity33 citations Open access
Semantic Scholar
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
M. C. Eike, G. B. Nordang, T. Karlsen, K. Boberg +11 more
2007Annals of the Rheumatic Diseases33 citations
Semantic Scholar
Association of Autoimmune Addison's Disease with Alleles of STAT4 and GATA3 in European Cohorts
A. Mitchell, K. Macarthur, Earn H. Gan, Lucy E. Baggott +32 more
2014PLoS ONE31 citations Open access
Semantic Scholar
CTLA-4 as a genetic determinant in autoimmune Addison’s disease
A. B. Wolff, A. L. Mitchell, Heather J. Cordell, A. Short +9 more
2015Genes and Immunity30 citations Open access
Semantic Scholar
A gene in the telomeric HLA complex distinct from HLA-A is involved in predisposition to juvenile idiopathic arthritis.
A. Smerdel, B. Lie, R. Płoski, B. Koeleman +3 more
2002Arthritis & Rheumatism30 citations
Semantic Scholar
No Independent Associations of LMP2 and LMP7 Polymorphisms With Susceptibility to Develop IDDM
D. Undlien, H. Akselsen, G. Joner, K. Dahl-Jørgensen +3 more
1997Diabetes29 citations
Semantic Scholar
Mutations in the melanocortin 4 receptor (MC4R) gene in obese patients in Norway.
T. Wangensteen, M. L. Pollestad Kolsgaard, M. Mattingsdal, G. Joner +3 more
2009Experimental and clinical endocrinology & diabetes28 citations
Semantic Scholar
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
L. C. Stene, P. Thorsby, J. Berg, K. S. Rønningen +2 more
2006Diabetologia28 citations Open access
Semantic Scholar
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
J. Norum, E. Grindedal, Cecilie Heramb, Inga Karsrud +4 more
2018ESMO Open26 citations Open access
Semantic Scholar
Pet keeping and tobacco exposure influence CD14 methylation in childhood
M. Munthe-Kaas, R. Bertelsen, Tale Maehre Torjussen, Hanne Sagsveen Hjorthaug +7 more
2012Pediatric Allergy and Immunology26 citations
Semantic Scholar

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