Publications 2024

Carrizosa C, Undlien DE, Vigeland MD (2024)
shinyseg: a web application for flexible cosegregation and sensitivity analysis
Bioinformatics (in press)
DOI 10.1093/bioinformatics/btae201, PubMed 38598476

Publications 2021

Lie BA, Viken MK, Egeland T, Undlien DE, Vaage JT (2021)
OBITUARY Erik Thorsby (1938-2021)
HLA, 98 (1), 3-4
DOI 10.1111/tan.14290

Penna-Martinez M, Meyer G, Wolff AB, Skinningsrud B, Betterle C, Falorni A, Ollier W, Undlien D, Husebye E, Pearce S, Mitchell AL, Badenhoop K (2021)
Vitamin D status and pathway genes in five European autoimmune Addison's disease cohorts
Eur J Endocrinol, 184 (3), 373-381
DOI 10.1530/EJE-20-0956, PubMed 33444227

Publications 2019

Aslaksen S, Methlie P, Vigeland MD, Jøssang DE, Wolff AB, Sheng Y, Oftedal BE, Skinningsrud B, Undlien DE, Selmer KK, Husebye ES, Bratland E (2019)
Coexistence of Congenital Adrenal Hyperplasia and Autoimmune Addison's Disease
Front Endocrinol (Lausanne), 10, 648
DOI 10.3389/fendo.2019.00648, PubMed 31611844

Aslaksen S, Wolff AB, Vigeland MD, Breivik L, Sheng Y, Oftedal BE, Artaza H, Skinningsrud B, Undlien DE, Selmer KK, Husebye ES, Bratland E (2019)
Identification and characterization of rare toll-like receptor 3 variants in patients with autoimmune Addison's disease
J Transl Autoimmun, 1, 100005
DOI 10.1016/j.jtauto.2019.100005, PubMed 32743495

Wikenius E, Myhre AM, Page CM, Moe V, Smith L, Heiervang ER, Undlien DE, LeBlanc M (2019)
Prenatal maternal depressive symptoms and infant DNA methylation: a longitudinal epigenome-wide study
Nord J Psychiatry, 73 (4-5), 257-263
DOI 10.1080/08039488.2019.1613446, PubMed 31070508

Publications 2018

Norum J, Grindedal EM, Heramb C, Karsrud I, Ariansen SL, Undlien DE, Schlichting E, Mæhle L (2018)
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
ESMO Open, 3 (3), e000328
DOI 10.1136/esmoopen-2018-000328, PubMed 29682331

Publications 2017

Grindedal EM, Heramb C, Karsrud I, Ariansen SL, Mæhle L, Undlien DE, Norum J, Schlichting E (2017)
Current guidelines for BRCA testing of breast cancer patients are insufficient to detect all mutation carriers
BMC Cancer, 17 (1), 438
DOI 10.1186/s12885-017-3422-2, PubMed 28637432

Publications 2016

Filges I, Bruder E, Brandal K, Meier S, Undlien DE, Waage TR, Hoesli I, Schubach M, de Beer T, Sheng Y, Hoeller S, Schulzke S, Røsby O, Miny P, Tercanli S, Oppedal T, Meyer P, Selmer KK, Strømme P (2016)
Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF
Hum Mutat, 37 (4), 359-63
DOI 10.1002/humu.22960, PubMed 26820108

Filges I, Bruder E, Brandal K, Meier S, Undlien DE, Waage TR, Hoesli I, Schubach M, de Beer T, Sheng Y, Hoeller S, Schulzke S, Røsby O, Miny P, Tercanli S, Oppedal T, Meyer P, Selmer KK, Strømme P (2016)
Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF
Hum Mutat, 37 (7), 711
DOI 10.1002/humu.22997, PubMed 27300082

Gervin K, Andreassen BK, Hjorthaug HS, Carlsen KCL, Carlsen KH, Undlien DE, Lyle R, Munthe-Kaas MC (2016)
Intra-individual changes in DNA methylation not mediated by cell-type composition are correlated with aging during childhood
Clin Epigenetics, 8, 110
DOI 10.1186/s13148-016-0277-3, PubMed 27785156

Moen MN, Fjær R, Hamdani EH, Laerdahl JK, Menchini RJ, Vigeland MD, Sheng Y, Undlien DE, Hassel B, Salih MA, El Khashab HY, Selmer KK, Chaudhry FA (2016)
Pathogenic variants in KCTD7 perturb neuronal K+ fluxes and glutamine transport
Brain, 139 (Pt 12), 3109-3120
DOI 10.1093/brain/aww244, PubMed 27742667

Publications 2015

Undlien D, Lunde C (2015)
[Not Available]
Tidsskr Nor Laegeforen, 135 (19), 1728-30
DOI 10.4045/tidsskr.15.0968, PubMed 26486666

Wolff AS, Mitchell AL, Cordell HJ, Short A, Skinningsrud B, Ollier W, Badenhoop K, Meyer G, Falorni A, Kampe O, Undlien D, Pearce SH, Husebye ES (2015)
CTLA-4 as a genetic determinant in autoimmune Addison's disease
Genes Immun, 16 (6), 430-6
DOI 10.1038/gene.2015.27, PubMed 26204230

Publications 2014

Brønstad I, Skinningsrud B, Bratland E, Løvås K, Undlien D, Sverre Husebye E, Wolff AS (2014)
CYP21A2 polymorphisms in patients with autoimmune Addison's disease, and linkage disequilibrium to HLA risk alleles
Eur J Endocrinol, 171 (6), 743-50
DOI 10.1530/EJE-14-0432, PubMed 25249698

Krogvold L, Edwin B, Buanes T, Frisk G, Skog O, Anagandula M, Korsgren O, Undlien D, Eike MC, Richardson SJ, Leete P, Morgan NG, Oikarinen S, Oikarinen M, Laiho JE, Hyöty H, Ludvigsson J, Hanssen KF, Dahl-Jørgensen K (2014)
Detection of a low-grade enteroviral infection in the islets of langerhans of living patients newly diagnosed with type 1 diabetes
Diabetes, 64 (5), 1682-7
DOI 10.2337/db14-1370, PubMed 25422108

Mitchell AL, Macarthur KD, Gan EH, Baggott LE, Wolff AS, Skinningsrud B, Platt H, Short A, Lobell A, Kämpe O, Bensing S, Betterle C, Kasperlik-Zaluska A, Zurawek M, Fichna M, Kockum I, Nordling Eriksson G, Ekwall O, Wahlberg J, Dahlqvist P, Hulting AL, Penna-Martinez M, Meyer G, Kahles H, Badenhoop K et al. (2014)
Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European cohorts
PLoS One, 9 (3), e88991
DOI 10.1371/journal.pone.0088991, PubMed 24614117

Publications 2013

Irgens HU, Molnes J, Johansson BB, Ringdal M, Skrivarhaug T, Undlien DE, Søvik O, Joner G, Molven A, Njølstad PR (2013)
Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry
Diabetologia, 56 (7), 1512-9
DOI 10.1007/s00125-013-2916-y, PubMed 23624530

Torjussen TM, Munthe-Kaas MC, Mowinckel P, Carlsen KH, Undlien DE, Lødrup Carlsen KC (2013)
Childhood lung function and the association with β2-adrenergic receptor haplotypes
Acta Paediatr, 102 (7), 727-31
DOI 10.1111/apa.12221, PubMed 23463918

Publications 2012

Eike MC, Skinningsrud B, Ronninger M, Stormyr A, Kvien TK, Joner G, Njølstad PR, Førre O, Flatø B, Alfredsson L, Padyukov L, Undlien DE, Lie BA (2012)
CIITA gene variants are associated with rheumatoid arthritis in Scandinavian populations
Genes Immun, 13 (5), 431-6
DOI 10.1038/gene.2012.11, PubMed 22513452

Gervin K, Vigeland MD, Mattingsdal M, Hammerø M, Nygård H, Olsen AO, Brandt I, Harris JR, Undlien DE, Lyle R (2012)
DNA methylation and gene expression changes in monozygotic twins discordant for psoriasis: identification of epigenetically dysregulated genes
PLoS Genet, 8 (1), e1002454
DOI 10.1371/journal.pgen.1002454, PubMed 22291603

Gilfillan GD, Hughes T, Sheng Y, Hjorthaug HS, Straub T, Gervin K, Harris JR, Undlien DE, Lyle R (2012)
Limitations and possibilities of low cell number ChIP-seq
BMC Genomics, 13, 645
DOI 10.1186/1471-2164-13-645, PubMed 23171294

Hekman KE, Yu GY, Brown CD, Zhu H, Du X, Gervin K, Undlien DE, Peterson A, Stevanin G, Clark HB, Pulst SM, Bird TD, White KP, Gomez CM (2012)
A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insult
Hum Mol Genet, 21 (26), 5472-83
DOI 10.1093/hmg/dds392, PubMed 23001565

Munthe-Kaas MC, Bertelsen RJ, Torjussen TM, Hjorthaug HS, Undlien DE, Lyle R, Gervin K, Granum B, Mowinckel P, Carlsen KH, Carlsen KC (2012)
Pet keeping and tobacco exposure influence CD14 methylation in childhood
Pediatr Allergy Immunol, 23 (8), 747-54
DOI 10.1111/pai.12021, PubMed 23194293

Undlien DE (2012)
[Individual genome sequencing]
Tidsskr Nor Laegeforen, 132 (3), 264
DOI 10.4045/tidsskr.11.1490, PubMed 22314723

Publications 2011

Gervin K, Hammerø M, Akselsen HE, Moe R, Nygård H, Brandt I, Gjessing HK, Harris JR, Undlien DE, Lyle R (2011)
Extensive variation and low heritability of DNA methylation identified in a twin study
Genome Res, 21 (11), 1813-21
DOI 10.1101/gr.119685.110, PubMed 21948560

Selmer KK, Gilfillan GD, Strømme P, Lyle R, Hughes T, Hjorthaug HS, Brandal K, Nakken S, Misceo D, Egeland T, Munthe LA, Braekken SK, Undlien DE (2011)
A mild form of Mucopolysaccharidosis IIIB diagnosed with targeted next-generation sequencing of linked genomic regions
Eur J Hum Genet, 20 (1), 58-63
DOI 10.1038/ejhg.2011.126, PubMed 21712855

Skinningsrud B, Lie BA, Lavant E, Carlson JA, Erlich H, Akselsen HE, Gervin K, Wolff AB, Erichsen MM, Løvås K, Husebye ES, Undlien DE (2011)
Multiple loci in the HLA complex are associated with Addison's disease
J Clin Endocrinol Metab, 96 (10), E1703-8
DOI 10.1210/jc.2011-0645, PubMed 21816777

Torjussen TM, Lødrup Carlsen KC, Munthe-Kaas MC, Mowinckel P, Carlsen KH, Helms PJ, Gerritsen J, Whyte MK, Lenney W, Undlien DE, Shianna KV, Zhu G, Pillai SG (2011)
Alpha-nicotinic acetylcholine receptor and tobacco smoke exposure: effects on bronchial hyperresponsiveness in children
Pediatr Allergy Immunol, 23 (1), 40-9
DOI 10.1111/j.1399-3038.2011.01222.x, PubMed 22017462

Publications 2010

Mero IL, Ban M, Lorentzen ÅR, Smestad C, Celius EG, Sæther H, Saeedi H, Viken MK, Skinningsrud B, Undlien DE, Aarseth J, Myhr KM, Granum S, Spurkland A, Sawcer S, Compston A, Lie BA, Harbo HF (2010)
Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus
Genes Immun, 12 (3), 191-8
DOI 10.1038/gene.2010.59, PubMed 21179112

Munthe-Kaas MC, Torjussen TM, Gervin K, Lødrup Carlsen KC, Carlsen KH, Granum B, Hjorthaug HS, Undlien D, Lyle R (2010)
CD14 polymorphisms and serum CD14 levels through childhood: a role for gene methylation?
J Allergy Clin Immunol, 125 (6), 1361-8
DOI 10.1016/j.jaci.2010.02.010, PubMed 20398919

Stene LC, Rønningen KS, Undlien DE, Joner G (2010)
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, 12 (2), 91-4
DOI 10.1111/j.1399-5448.2010.00669.x, PubMed 21352425

Wangensteen T, Akselsen H, Holmen J, Undlien D, Retterstøl L (2010)
A common haplotype in NAPEPLD is associated with severe obesity in a Norwegian population-based cohort (the HUNT study)
Obesity (Silver Spring), 19 (3), 612-7
DOI 10.1038/oby.2010.219, PubMed 20885390

Wangensteen T, Egeland T, Akselsen H, Holmen J, Undlien D, Retterstøl L (2010)
FTO genotype and weight gain in obese and normal weight adults from a Norwegian population based cohort (the HUNT study)
Exp Clin Endocrinol Diabetes, 118 (9), 649-52
DOI 10.1055/s-0030-1249636, PubMed 20373279

Publications 2009

Bjørnvold M, Munthe-Kaas MC, Egeland T, Joner G, Dahl-Jørgensen K, Njølstad PR, Akselsen HE, Gervin K, Carlsen KC, Carlsen KH, Undlien DE (2009)
A TLR2 polymorphism is associated with type 1 diabetes and allergic asthma
Genes Immun, 10 (2), 181-7
DOI 10.1038/gene.2008.100, PubMed 19148143

Bratland E, Skinningsrud B, Undlien DE, Mozes E, Husebye ES (2009)
T cell responses to steroid cytochrome P450 21-hydroxylase in patients with autoimmune primary adrenal insufficiency
J Clin Endocrinol Metab, 94 (12), 5117-24
DOI 10.1210/jc.2009-1115, PubMed 19890026

Erichsen MM, Løvås K, Skinningsrud B, Wolff AB, Undlien DE, Svartberg J, Fougner KJ, Berg TJ, Bollerslev J, Mella B, Carlson JA, Erlich H, Husebye ES (2009)
Clinical, immunological, and genetic features of autoimmune primary adrenal insufficiency: observations from a Norwegian registry
J Clin Endocrinol Metab, 94 (12), 4882-90
DOI 10.1210/jc.2009-1368, PubMed 19858318

Mitchell AL, Cordell HJ, Soemedi R, Owen K, Skinningsrud B, Wolff AB, Ericksen M, Undlien D, Husebye E, Pearce SH (2009)
Programmed death ligand 1 (PD-L1) gene variants contribute to autoimmune Addison's disease and Graves' disease susceptibility
J Clin Endocrinol Metab, 94 (12), 5139-45
DOI 10.1210/jc.2009-1404, PubMed 19850680

Selmer KK, Brandal K, Olstad OK, Birkenes B, Undlien DE, Egeland T (2009)
Genome-wide linkage analysis with clustered SNP markers
J Biomol Screen, 14 (1), 92-6
DOI 10.1177/1087057108327327, PubMed 19171925

Selmer KK, Eriksson AS, Brandal K, Egeland T, Tallaksen C, Undlien DE (2009)
Parental SCN1A mutation mosaicism in familial Dravet syndrome
Clin Genet, 76 (4), 398-403
DOI 10.1111/j.1399-0004.2009.01208.x, PubMed 19673951

Selmer KK, Grøndahl J, Riise R, Brandal K, Braaten O, Bragadottir R, Undlien DE (2009)
Autosomal dominant pericentral retinal dystrophy caused by a novel missense mutation in the TOPORS gene
Acta Ophthalmol, 88 (3), 323-8
DOI 10.1111/j.1755-3768.2008.01465.x, PubMed 19183411

Selmer KK, Lund C, Brandal K, Undlien DE, Brodtkorb E (2009)
SCN1A mutation screening in adult patients with Lennox-Gastaut syndrome features
Epilepsy Behav, 16 (3), 555-7
DOI 10.1016/j.yebeh.2009.08.021, PubMed 19782004

Skinningsrud B, Husebye ES, Gilfillan GD, Frengen E, Erichsen A, Gervin K, Ormerod E, Egeland T, Undlien DE (2009)
X-linked congenital adrenal hypoplasia with hypogonadotropic hypogonadism caused by an inversion disrupting a conserved noncoding element upstream of the NR0B1 (DAX1) gene
J Clin Endocrinol Metab, 94 (10), 4086-93
DOI 10.1210/jc.2009-0923, PubMed 19773398

Skinningsrud B, Lie BA, Husebye ES, Kvien TK, Førre Ø, Flatø B, Stormyr A, Joner G, Njølstad PR, Egeland T, Undlien DE (2009)
A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis
Ann Rheum Dis, 69 (8), 1471-4
DOI 10.1136/ard.2009.114934, PubMed 19734133

Stene LC, Rønningen KS, Bjørnvold M, Undlien DE, Joner G (2009)
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, 11 (6), 386-93
DOI 10.1111/j.1399-5448.2009.00605.x, PubMed 19895409

Viken MK, Blomhoff A, Olsson M, Akselsen HE, Pociot F, Nerup J, Kockum I, Cambon-Thomsen A, Thorsby E, Undlien DE, Lie BA (2009)
Reproducible association with type 1 diabetes in the extended class I region of the major histocompatibility complex
Genes Immun, 10 (4), 323-33
DOI 10.1038/gene.2009.13, PubMed 19295542

Wangensteen T, Kolsgaard ML, Mattingsdal M, Joner G, Tonstad S, Undlien D, Retterstol L (2009)
Mutations in the melanocortin 4 receptor (MC4R) gene in obese patients in Norway
Exp Clin Endocrinol Diabetes, 117 (6), 266-73
DOI 10.1055/s-0028-1102942, PubMed 19301229

Publications 2008

Bjørnvold M, Undlien DE, Joner G, Dahl-Jørgensen K, Njølstad PR, Akselsen HE, Gervin K, Rønningen KS, Stene LC (2008)
Joint effects of HLA, INS, PTPN22 and CTLA4 genes on the risk of type 1 diabetes
Diabetologia, 51 (4), 589-96
DOI 10.1007/s00125-008-0932-0, PubMed 18292987

Eike MC, Olsson M, Undlien DE, Dahl-Jørgensen K, Joner G, Rønningen KS, Thorsby E, Lie BA (2008)
Genetic variants of the HLA-A, HLA-B and AIF1 loci show independent associations with type 1 diabetes in Norwegian families
Genes Immun, 10 (2), 141-50
DOI 10.1038/gene.2008.88, PubMed 18987644

Gilfillan GD, Selmer KK, Roxrud I, Smith R, Kyllerman M, Eiklid K, Kroken M, Mattingsdal M, Egeland T, Stenmark H, Sjøholm H, Server A, Samuelsson L, Christianson A, Tarpey P, Whibley A, Stratton MR, Futreal PA, Teague J, Edkins S, Gecz J, Turner G, Raymond FL, Schwartz C, Stevenson RE et al. (2008)
SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome
Am J Hum Genet, 82 (4), 1003-10
DOI 10.1016/j.ajhg.2008.01.013, PubMed 18342287

Magitta NF, Bøe Wolff AS, Johansson S, Skinningsrud B, Lie BA, Myhr KM, Undlien DE, Joner G, Njølstad PR, Kvien TK, Førre Ø, Knappskog PM, Husebye ES (2008)
A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes
Genes Immun, 10 (2), 120-4
DOI 10.1038/gene.2008.85, PubMed 18946481

Molven A, Ringdal M, Nordbø AM, Raeder H, Støy J, Lipkind GM, Steiner DF, Philipson LH, Bergmann I, Aarskog D, Undlien DE, Joner G, Søvik O, Norwegian Childhood Diabetes Study Group, Bell GI, Njølstad PR (2008)
Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes
Diabetes, 57 (4), 1131-5
DOI 10.2337/db07-1467, PubMed 18192540

Selmer KK, Egeland T, Solaas MH, Nakken KO, Kjeldsen MJ, Friis ML, Brandal K, Corey LA, Undlien DE (2008)
SCN1A variant in a Scandinavian GEFS+ family: a wolf in sheep's clothing? Comment
Acta Neurol. Scand., 118 (5), 346
DOI 10.1111/j.1600-0404.2008.01061.x

Skinningsrud B, Husebye ES, Gervin K, Løvås K, Blomhoff A, Wolff AB, Kemp EH, Egeland T, Undlien DE (2008)
Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease
Eur J Hum Genet, 16 (8), 977-82
DOI 10.1038/ejhg.2008.33, PubMed 18301444

Skinningsrud B, Husebye ES, Pearce SH, McDonald DO, Brandal K, Wolff AB, Løvås K, Egeland T, Undlien DE (2008)
Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency
J Clin Endocrinol Metab, 93 (9), 3310-7
DOI 10.1210/jc.2008-0821, PubMed 18593762

Publications 2007

Eike MC, Nordang GB, Karlsen TH, Boberg KM, Vatn MH, IBSEN study group, Dahl-Jørgensen K, Rønningen KS, Joner G, Flatø B, Bergquist A, Thorsby E, Førre O, Kvien TK, Undlien DE, Lie BA (2007)
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
Ann Rheum Dis, 67 (9), 1287-91
DOI 10.1136/ard.2007.077826, PubMed 18065500

Farooqi IS, Wangensteen T, Collins S, Kimber W, Matarese G, Keogh JM, Lank E, Bottomley B, Lopez-Fernandez J, Ferraz-Amaro I, Dattani MT, Ercan O, Myhre AG, Retterstol L, Stanhope R, Edge JA, McKenzie S, Lessan N, Ghodsi M, De Rosa V, Perna F, Fontana S, Barroso I, Undlien DE, O'Rahilly S (2007)
Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor
N Engl J Med, 356 (3), 237-47
DOI 10.1056/NEJMoa063988, PubMed 17229951

Lie BA, Viken MK, Akselsen HE, Flåm ST, Pociot F, Nerup J, Kockum I, Cambon-Thomsen A, Thorsby E, Undlien DE (2007)
Association analysis in type 1 diabetes of the PRSS16 gene encoding a thymus-specific serine protease
Hum Immunol, 68 (7), 592-8
DOI 10.1016/j.humimm.2007.03.009, PubMed 17584581

Munthe-Kaas MC, Carlsen KH, Håland G, Devulapalli CS, Gervin K, Egeland T, Carlsen KL, Undlien D (2007)
T cell-specific T-box transcription factor haplotype is associated with allergic asthma in children
J Allergy Clin Immunol, 121 (1), 51-6
DOI 10.1016/j.jaci.2007.07.068, PubMed 17949803

Munthe-Kaas MC, Carlsen KL, Carlsen KH, Egeland T, Håland G, Devulapalli CS, Akselsen H, Undlien D (2007)
HLA Dr-Dq haplotypes and the TNFA-308 polymorphism: associations with asthma and allergy
Allergy, 62 (9), 991-8
DOI 10.1111/j.1398-9995.2007.01377.x, PubMed 17686102

Munthe-Kaas MC, Gerritsen J, Carlsen KH, Undlien D, Egeland T, Skinningsrud B, Tørres T, Carlsen KL (2007)
Eosinophil cationic protein (ECP) polymorphisms and association with asthma, s-ECP levels and related phenotypes
Allergy, 62 (4), 429-36
DOI 10.1111/j.1398-9995.2007.01327.x, PubMed 17362255

Selmer KK, Egeland T, Solaas MH, Nakken KO, Kjeldsen MJ, Friis ML, Brandal K, Corey LA, Undlien DE (2007)
Genetic screening of Scandinavian families with febrile seizures and epilepsy or GEFS+
Acta Neurol Scand, 117 (4), 289-92
DOI 10.1111/j.1600-0404.2007.00941.x, PubMed 17927801

Thomson G, Valdes AM, Noble JA, Kockum I, Grote MN, Najman J, Erlich HA, Cucca F, Pugliese A, Steenkiste A, Dorman JS, Caillat-Zucman S, Hermann R, Ilonen J, Lambert AP, Bingley PJ, Gillespie KM, Lernmark A, Sanjeevi CB, Rønningen KS, Undlien DE, Thorsby E, Petrone A, Buzzetti R, Koeleman BP et al. (2007)
Relative predispositional effects of HLA class II DRB1-DQB1 haplotypes and genotypes on type 1 diabetes: a meta-analysis
Tissue Antigens, 70 (2), 110-27
DOI 10.1111/j.1399-0039.2007.00867.x, PubMed 17610416

Viken MK, Sollid HD, Joner G, Dahl-Jørgensen K, Rønningen KS, Undlien DE, Flatø B, Selvaag AM, Førre Ø, Kvien TK, Thorsby E, Melms A, Tolosa E, Lie BA (2007)
Polymorphisms in the cathepsin L2 (CTSL2) gene show association with type 1 diabetes and early-onset myasthenia gravis
Hum Immunol, 68 (9), 748-55
DOI 10.1016/j.humimm.2007.05.009, PubMed 17869649

Publications 2006

Bjørnvold M, Amundsen SS, Stene LC, Joner G, Dahl-Jørgensen K, Njølstad PR, Ek J, Ascher H, Gudjònsdòttir AH, Lie BA, Skinningsrud B, Akselsen HE, Rønningen KS, Sollid LM, Undlien DE (2006)
FOXP3 polymorphisms in type 1 diabetes and coeliac disease
J Autoimmun, 27 (2), 140-4
DOI 10.1016/j.jaut.2006.06.007, PubMed 16996248

Blomhoff A, Olsson M, Johansson S, Akselsen HE, Pociot F, Nerup J, Kockum I, Cambon-Thomsen A, Thorsby E, Undlien DE, Lie BA (2006)
Linkage disequilibrium and haplotype blocks in the MHC vary in an HLA haplotype specific manner assessed mainly by DRB1*03 and DRB1*04 haplotypes
Genes Immun, 7 (2), 130-40
DOI 10.1038/sj.gene.6364272, PubMed 16395395

Stene LC, Thorsby PM, Berg JP, Rønningen KS, Undlien DE, Joner G, Norwegian Childhood Diabetes Study Group (2006)
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
Diabetologia, 49 (9), 2068-73
DOI 10.1007/s00125-006-0292-6, PubMed 16691379

Publications 2005

Bjørkhaug L, Johansson S, Raeder H, Thorsby PM, Undlien DE, Søvik O, Molven A, Sagen JV, Njølstad PR (2005)
[Molecular diagnostics in diabetes mellitus]
Tidsskr Nor Laegeforen, 125 (21), 2968-72
PubMed 16276383

Blomhoff A, Kemp EH, Gawkrodger DJ, Weetman AP, Husebye ES, Akselsen HE, Lie BA, Undlien DE (2005)
CTLA4 polymorphisms are associated with vitiligo, in patients with concomitant autoimmune diseases
Pigment Cell Res, 18 (1), 55-8
DOI 10.1111/j.1600-0749.2004.00196.x, PubMed 15649153

Maier LM, Smyth DJ, Vella A, Payne F, Cooper JD, Pask R, Lowe C, Hulme J, Smink LJ, Fraser H, Moule C, Hunter KM, Chamberlain G, Walker N, Nutland S, Undlien DE, Rønningen KS, Guja C, Ionescu-Tîrgoviste C, Savage DA, Strachan DP, Peterson LB, Todd JA, Wicker LS, Twells RC (2005)
Construction and analysis of tag single nucleotide polymorphism maps for six human-mouse orthologous candidate genes in type 1 diabetes
BMC Genet, 6, 9
DOI 10.1186/1471-2156-6-9, PubMed 15720714

Payne F, Smyth DJ, Pask R, Cooper JD, Masters J, Wang WY, Godfrey LM, Bowden G, Szeszko J, Smink LJ, Lam AC, Burren O, Walker NM, Nutland S, Rance H, Undlien DE, Rønningen KS, Guja C, Ionescu-Tîrgovişte C, Todd JA, Twells RC (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, 331 (2), 435-41
DOI 10.1016/j.bbrc.2005.03.203, PubMed 15850778

Smyth DJ, Howson JM, Lowe CE, Walker NM, Lam AC, Nutland S, Hutchings J, Tuomilehto-Wolf E, Tuomilehto J, Guja C, Ionescu-Tîrgoviste C, Undlien DE, Rønningen KS, Savage D, Dunger DB, Twells RC, McArdle WL, Strachan DP, Todd JA (2005)
Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes
Nat Genet, 37 (2), 110-1; author reply 112-3
DOI 10.1038/ng0205-110, PubMed 15678134

Undlien D (2005)
Din unike arv: genetikk og helse
Aschehoug, Oslo, 236 s.
BIBSYS 051715015, ISBN 978-82-03-23248-0

Wangensteen T, Undlien D, Tonstad S, Retterstøl L (2005)
[Genetic causes of obesity]
Tidsskr Nor Laegeforen, 125 (22), 3090-3
PubMed 16299561

Publications 2004

Barratt BJ, Payne F, Lowe CE, Hermann R, Healy BC, Harold D, Concannon P, Gharani N, McCarthy MI, Olavesen MG, McCormack R, Guja C, Ionescu-Tîrgovişte C, Undlien DE, Rønningen KS, Gillespie KM, Tuomilehto-Wolf E, Tuomilehto J, Bennett ST, Clayton DG, Cordell HJ, Todd JA (2004)
Remapping the insulin gene/IDDM2 locus in type 1 diabetes
Diabetes, 53 (7), 1884-9
DOI 10.2337/diabetes.53.7.1884, PubMed 15220214

Blomhoff A, Lie BA, Myhre AG, Kemp EH, Weetman AP, Akselsen HE, Huseby ES, Undlien DE (2004)
Polymorphisms in the cytotoxic T lymphocyte antigen-4 gene region confer susceptibility to Addison's disease
J Clin Endocrinol Metab, 89 (7), 3474-6
DOI 10.1210/jc.2003-031854, PubMed 15240634

Eftychi C, Howson JM, Barratt BJ, Vella A, Payne F, Smyth DJ, Twells RC, Walker NM, Rance HE, Tuomilehto-Wolf E, Tuomilehto J, Undlien DE, Rønningen KS, Guja C, Ionescu-Tîirgovişte C, Savage DA, Todd JA (2004)
Analysis of the type 2 diabetes-associated single nucleotide polymorphisms in the genes IRS1, KCNJ11, and PPARG2 in type 1 diabetes
Diabetes, 53 (3), 870-3
DOI 10.2337/diabetes.53.3.870, PubMed 14988278

Hulme JS, Barratt BJ, Twells RC, Cooper JD, Lowe CE, Howson JM, Lam AC, Smink LJ, Savage DA, Undlien DE, Guja C, Ionescu-Tîirgoviste C, Tuomilehto-Wolf E, Tuomilehto J, Todd JA (2004)
Association analysis of the lymphocyte-specific protein tyrosine kinase (LCK) gene in type 1 diabetes
Diabetes, 53 (9), 2479-82
DOI 10.2337/diabetes.53.9.2479, PubMed 15331563

Koeleman BP, Lie BA, Undlien DE, Dudbridge F, Thorsby E, de Vries RR, Cucca F, Roep BO, Giphart MJ, Todd JA (2004)
Genotype effects and epistasis in type 1 diabetes and HLA-DQ trans dimer associations with disease
Genes Immun, 5 (5), 381-8
DOI 10.1038/sj.gene.6364106, PubMed 15164102

Munthe-Kaas MC, Carlsen KH, Helms PJ, Gerritsen J, Whyte M, Feijen M, Skinningsrud B, Main M, Kwong GN, Lie BA, Lødrup Carlsen KC, Undlien DE (2004)
CTLA-4 polymorphisms in allergy and asthma and the TH1/ TH2 paradigm
J Allergy Clin Immunol, 114 (2), 280-7
DOI 10.1016/j.jaci.2004.03.050, PubMed 15316504

Nejentsev S, Cooper JD, Godfrey L, Howson JM, Rance H, Nutland S, Walker NM, Guja C, Ionescu-Tirgovişte C, Savage DA, Undlien DE, Rønningen KS, Tuomilehto-Wolf E, Tuomilehto J, Gillespie KM, Ring SM, Strachan DP, Widmer B, Dunger D, Todd JA (2004)
Analysis of the vitamin D receptor gene sequence variants in type 1 diabetes
Diabetes, 53 (10), 2709-12
DOI 10.2337/diabetes.53.10.2709, PubMed 15448105

Nejentsev S, Godfrey L, Snook H, Rance H, Nutland S, Walker NM, Lam AC, Guja C, Ionescu-Tirgoviste C, Undlien DE, Rønningen KS, Tuomilehto-Wolf E, Tuomilehto J, Newport MJ, Clayton DG, Todd JA (2004)
Comparative high-resolution analysis of linkage disequilibrium and tag single nucleotide polymorphisms between populations in the vitamin D receptor gene
Hum Mol Genet, 13 (15), 1633-9
DOI 10.1093/hmg/ddh169, PubMed 15175274

Undlien DE (2004)
Forebygging av type 1 diabetes
In Diabeteshåndboken, Gyldendal akademisk, Oslo, s. 42-50
BIBSYS 041953398

Undlien DE, Følling I (2004)
Arv, miljø og mekanismer ved utvikling av type 1 diabetes
In Diabeteshåndboken, Gyldendal akademisk, Oslo, s. 26-35
BIBSYS 041953347

Vella A, Howson JM, Barratt BJ, Twells RC, Rance HE, Nutland S, Tuomilehto-Wolf E, Tuomilehto J, Undlien DE, Rønningen KS, Guja C, Ionescu-Tîrgovişte C, Savage DA, Todd JA (2004)
Lack of association of the Ala(45)Thr polymorphism and other common variants of the NeuroD gene with type 1 diabetes
Diabetes, 53 (4), 1158-61
DOI 10.2337/diabetes.53.4.1158, PubMed 15047635

Publications 2003

Johansson S, Lie BA, Cambon-Thomsen A, Pociot F, Nerup J, Kockum I, Thorsby E, Undlien DE (2003)
No evidence of type 1 diabetes susceptibility genes in the region centromeric of the HLA complex
Hum Immunol, 64 (10), 951-9
DOI 10.1016/s0198-8859(03)00172-1, PubMed 14522092

Johansson S, Lie BA, Pociot F, Nerup J, Cambon-Thomsen A, Kockum I, Thorsby E, Undlien DE (2003)
HLA associations in type 1 diabetes: DPB1 alleles may act as markers of other HLA-complex susceptibility genes
Tissue Antigens, 61 (5), 344-51
DOI 10.1034/j.1399-0039.2003.00055.x, PubMed 12753653

Johansson S, Lie BA, Todd JA, Pociot F, Nerup J, Cambon-Thomsen A, Kockum I, Akselsen HE, Thorsby E, Undlien DE (2003)
Evidence of at least two type 1 diabetes susceptibility genes in the HLA complex distinct from HLA-DQB1, -DQA1 and -DRB1
Genes Immun, 4 (1), 46-53
DOI 10.1038/sj.gene.6363917, PubMed 12595901

Maier LM, Twells RC, Howson JM, Lam AC, Clayton DG, Smyth DJ, Savage D, Carson D, Patterson CC, Smink LJ, Walker NM, Burren OS, Nutland S, Rance H, Tuomilehto-Wolf E, Tuomilehto J, Guja C, Ionescu-Tirgoviste C, Undlien DE, Rønningen KS, Cucca F, Todd JA (2003)
Testing the possible negative association of type 1 diabetes and atopic disease by analysis of the interleukin 4 receptor gene
Genes Immun, 4 (7), 469-75
DOI 10.1038/sj.gene.6364007, PubMed 14551599

Myhre AG, Aarsetøy H, Undlien DE, Hovdenak N, Aksnes L, Husebye ES (2003)
High frequency of coeliac disease among patients with autoimmune adrenocortical failure
Scand J Gastroenterol, 38 (5), 511-5
DOI 10.1080/00365520310002544, PubMed 12795461

Nejentsev S, Guja C, McCormack R, Cooper J, Howson JM, Nutland S, Rance H, Walker N, Undlien D, Ronningen KS, Tuomilehto-Wolf E, Tuomilehto J, Ionescu-Tirgoviste C, Gale EA, Bingley PJ, Gillespie KM, Savage DA, Carson DJ, Patterson CC, Maxwell AP, Todd JA (2003)
Association of intercellular adhesion molecule-1 gene with type 1 diabetes
Lancet, 362 (9397), 1723-4
DOI 10.1016/S0140-6736(03)14847-7, PubMed 14643123

Smerdel A, Lie BA, Finholt C, Ploski R, Førre Ø, Undlien DE, Thorsby E (2003)
An additional susceptibility gene for juvenile idiopathic arthritis in the HLA class I region on several DR-DQ haplotypes
Tissue Antigens, 61 (1), 80-4
DOI 10.1034/j.1399-0039.2003.610107.x, PubMed 12622778

Ueda H, Howson JM, Esposito L, Heward J, Snook H, Chamberlain G, Rainbow DB, Hunter KM, Smith AN, Di Genova G, Herr MH, Dahlman I, Payne F, Smyth D, Lowe C, Twells RC, Howlett S, Healy B, Nutland S, Rance HE, Everett V, Smink LJ, Lam AC, Cordell HJ, Walker NM et al. (2003)
Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease
Nature, 423 (6939), 506-11
DOI 10.1038/nature01621, PubMed 12724780

Publications 2002

Lie BA, Akselsen HE, Bowlus CL, Gruen JR, Thorsby E, Undlien DE (2002)
Polymorphisms in the gene encoding thymus-specific serine protease in the extended HLA complex: a potential candidate gene for autoimmune and HLA-associated diseases
Genes Immun, 3 (5), 306-12
DOI 10.1038/sj.gene.6363858, PubMed 12140752

Myhre AG, Undlien DE, Løvås K, Uhlving S, Nedrebø BG, Fougner KJ, Trovik T, Sørheim JI, Husebye ES (2002)
Autoimmune adrenocortical failure in Norway autoantibodies and human leukocyte antigen class II associations related to clinical features
J Clin Endocrinol Metab, 87 (2), 618-23
DOI 10.1210/jcem.87.2.8192, PubMed 11836294

Smerdel A, Lie BA, Ploski R, Koeleman BP, Førre Ø, Thorsby E, Undlien DE (2002)
A gene in the telomeric HLA complex distinct from HLA-A is involved in predisposition to juvenile idiopathic arthritis
Arthritis Rheum, 46 (6), 1614-9
DOI 10.1002/art.10337, PubMed 12115193

Publications 2001

Johansson S, Lie BA, Thorsby E, Undlien DE (2001)
The polymorphism in the 3' untranslated region of IL12B has a negligible effect on the susceptibility to develop type 1 diabetes in Norway
Immunogenetics, 53 (7), 603-5
DOI 10.1007/s002510100370, PubMed 11685474

Merriman TR, Cordell HJ, Eaves IA, Danoy PA, Coraddu F, Barber R, Cucca F, Broadley S, Sawcer S, Compston A, Wordsworth P, Shatford J, Laval S, Jirholt J, Holmdahl R, Theofilopoulos AN, Kono DH, Tuomilehto J, Tuomilehto-Wolf E, Buzzetti R, Marrosu MG, Undlien DE, Rønningen KS, Ionesco-Tirgoviste C, Shield JP et al. (2001)
Suggestive evidence for association of human chromosome 18q12-q21 and its orthologue on rat and mouse chromosome 18 with several autoimmune diseases
Diabetes, 50 (1), 184-94
DOI 10.2337/diabetes.50.1.184, PubMed 11147786

Njølstad PR, Søvik O, Cuesta-Muñoz A, Bjørkhaug L, Massa O, Barbetti F, Undlien DE, Shiota C, Magnuson MA, Molven A, Matschinsky FM, Bell GI (2001)
Neonatal diabetes mellitus due to complete glucokinase deficiency
N Engl J Med, 344 (21), 1588-92
DOI 10.1056/NEJM200105243442104, PubMed 11372010

Undlien DE, Berg JP (2001)
Common variants in the regulatory region of the insulin gene are associated with fasting plasma insulin levels in juvenile obesity
Eur J Endocrinol, 144 (5), 457-9
DOI 10.1530/eje.0.1440457, PubMed 11331210

Undlien DE, Berg JP (2001)
Common variants in the regulatory region of the insulin gene are associated with fasting plasma insulin levels in juvenile obesity
In European journal of endocrinology, BioScientifa Ltd., Bristol, 144(2001)nr 5, s.457-459
BIBSYS 02206138x

Undlien DE, Lie BA, Thorsby E (2001)
HLA complex genes in type 1 diabetes and other autoimmune diseases. Which genes are involved?
Trends Genet, 17 (2), 93-100
DOI 10.1016/s0168-9525(00)02180-6, PubMed 11173119

Undlien DE, Thorsby E (2001)
HLA associations in type 1 diabetes: merging genetics and immunology
Trends Immunol, 22 (9), 467-9
DOI 10.1016/s1471-4906(01)01997-4, PubMed 11525926

Publications 2000

Bell H, Berg JP, Undlien DE, Distante S, Raknerud N, Heier HE, Try K, Thomassen Y, Haug E, Raha-Chowdhury R, Thorsby E (2000)
The clinical expression of hemochromatosis in Oslo, Norway. Excessive oral iron intake may lead to secondary hemochromatosis even in HFE C282Y mutation negative subjects
Scand J Gastroenterol, 35 (12), 1301-7
DOI 10.1080/003655200453665, PubMed 11199371

Bell H, Berg JP, Undlien DE, Distante S, Raknerud N, Heier HE, Try K, Thomassen Y, Haug E, Raha-Chowdhury R, Thorsby E (2000)
The clinical expression of hemachromatosis in Oslo, Norway. Excessive oral iron intake may lead to secondary hemachromatosis even in the HFE C282Y mutation negative subjects
In Scandinavian journal of gastroenterology, Taylor & Francis, Basingstoke, 35(2000)nr 12, s. 1301-1307
BIBSYS 010706097

Lie BA, Ronningen KS, Akselsen HE, Thorsby E, Undlien DE (2000)
Application and interpretation of transmission/disequilibrium tests: transmission of HLA-DQ haplotypes to unaffected siblings in 526 families with type 1 diabetes
Am J Hum Genet, 66 (2), 740-3
DOI 10.1086/302780, PubMed 10677335

Redondo MJ, Kawasaki E, Mulgrew CL, Noble JA, Erlich HA, Freed BM, Lie BA, Thorsby E, Eisenbarth GS, Undlien DE, Ronningen KS (2000)
DR- and DQ-associated protection from type 1A diabetes: comparison of DRB1*1401 and DQA1*0102-DQB1*0602*
J Clin Endocrinol Metab, 85 (10), 3793-7
DOI 10.1210/jcem.85.10.6920, PubMed 11061540

Undlien D, Borch-Iohnsen B, Bell H (2000)
Hemokromatose: en medisinsk utfordring : en sammenstilling av vår kunnskap om hemokromatose
Norsk hemokromatoseforbund, Oslo, 24 s.
BIBSYS 010291458, ISBN 82-995850-0-7

Undlien DE, Joner G, Dahl-Jørgensen K, Rønningen KS, Nicol-Smith L, Torjesen PA, Søvik O (2000)
[Genetic and immunologic risks for development of type 1 diabetes--experiences from an intervention trial]
Tidsskr Nor Laegeforen, 120 (23), 2799-803
PubMed 11107929

Undlien DE, Joner G, Dahl-Jørgensen K, Rønningen KS, Nicol-Smith L, Torjesen PA, Søvik O (2000)
Genetisk og immunologisk risiko for type 1-diabetes: erfaringer fra en intervensjonsstudie
In Tidsskrift for Den norske legeforening, Foreningen, Oslo, 120(2000)nr. 23, S. 2799-2803
BIBSYS 010831932

Publications 1999

Lie BA, Sollid LM, Ascher H, Ek J, Akselsen HE, Rønningen KS, Thorsby E, Undlien DE (1999)
A gene telomeric of the HLA class I region is involved in predisposition to both type 1 diabetes and coeliac disease
Tissue Antigens, 54 (2), 162-8
DOI 10.1034/j.1399-0039.1999.540207.x, PubMed 10488743

Lie BA, Todd JA, Pociot F, Nerup J, Akselsen HE, Joner G, Dahl-Jørgensen K, Rønningen KS, Thorsby E, Undlien DE (1999)
The predisposition to type 1 diabetes linked to the human leukocyte antigen complex includes at least one non-class II gene
Am J Hum Genet, 64 (3), 793-800
DOI 10.1086/302283, PubMed 10053014

Undlien DE, Kockum I, Rønningen KS, Lowe R, Saanjeevi CB, Graham J, Lie BA, Akselsen HE, Lernmark A, Thorsby E (1999)
HLA associations in type 1 diabetes among patients not carrying high-risk DR3-DQ2 or DR4-DQ8 haplotypes
Tissue Antigens, 54 (6), 543-51
DOI 10.1034/j.1399-0039.1999.540602.x, PubMed 10674967

Publications 1998

Merriman TR, Eaves IA, Twells RC, Merriman ME, Danoy PA, Muxworthy CE, Hunter KM, Cox RD, Cucca F, McKinney PA, Shield JP, Baum JD, Tuomilehto J, Tuomilehto-Wolf E, Ionesco-Tirgoviste C, Joner G, Thorsby E, Undlien DE, Pociot F, Nerup J, Ronningen KS, Bain SC, Todd JA (1998)
Transmission of haplotypes of microsatellite markers rather than single marker alleles in the mapping of a putative type 1 diabetes susceptibility gene (IDDM6)
Hum Mol Genet, 7 (3), 517-24
DOI 10.1093/hmg/7.3.517, PubMed 9467012

Nakagawa Y, Kawaguchi Y, Twells RC, Muxworthy C, Hunter KM, Wilson A, Merriman ME, Cox RD, Merriman T, Cucca F, McKinney PA, Shield JP, Tuomilehto J, Tuomilehto-Wolf E, Ionesco-Tirgoviste C, Nisticò L, Buzzetti R, Pozzilli P, Joner G, Thorsby E, Undlien DE, Pociot F, Nerup J, Rönningen KS, Bain SC et al. (1998)
Fine mapping of the diabetes-susceptibility locus, IDDM4, on chromosome 11q13
Am J Hum Genet, 63 (2), 547-56
DOI 10.1086/301974, PubMed 9683605

Thorsby P, Undlien DE, Berg JP, Thorsby E, Birkeland KI (1998)
[Diabetes mellitus--a complex interaction between heredity and environment]
Tidsskr Nor Laegeforen, 118 (16), 2519-24
PubMed 9667132

Undlien DE, Bell H, Heier HE, Akselsen HE, Thorsby E (1998)
[Genetic diagnostic test for hemochromatosis]
Tidsskr Nor Laegeforen, 118 (2), 238-40
PubMed 9485619

Publications 1997

Bennett ST, Wilson AJ, Esposito L, Bouzekri N, Undlien DE, Cucca F, Nisticò L, Buzzetti R, Bosi E, Pociot F, Nerup J, Cambon-Thomsen A, Pugliese A, Shield JP, McKinney PA, Bain SC, Polychronakos C, Todd JA (1997)
Insulin VNTR allele-specific effect in type 1 diabetes depends on identity of untransmitted paternal allele. The IMDIAB Group
Nat Genet, 17 (3), 350-2
DOI 10.1038/ng1197-350, PubMed 9354805

Lie BA, Akselsen HE, Joner G, Dahl-Jørgensen K, Rønningen KS, Thorsby E, Undlien DE (1997)
HLA associations in insulin-dependent diabetes mellitus: no independent association to particular DP genes
Hum Immunol, 55 (2), 170-5
DOI 10.1016/s0198-8859(97)00095-5, PubMed 9361969

Merriman T, Twells R, Merriman M, Eaves I, Cox R, Cucca F, McKinney P, Shield J, Baum D, Bosi E, Pozzilli P, Nisticò L, Buzzetti R, Joner G, Rønningen KS, Thorsby E, Undlien D, Pociot F, Nerup J, Bain S, Barnett A, Todd J (1997)
Evidence by allelic association-dependent methods for a type 1 diabetes polygene (IDDM6) on chromosome 18q21
Hum Mol Genet, 6 (7), 1003-10
DOI 10.1093/hmg/6.7.1003, PubMed 9215667

Reed P, Cucca F, Jenkins S, Merriman M, Wilson A, McKinney P, Bosi E, Joner G, Rønningen KS, Thorsby E, Undlien D, Merriman T, Barnett A, Bain S, Todd J (1997)
Evidence for a type 1 diabetes susceptibility locus (IDDM10) on human chromosome 10p11-q11
Hum Mol Genet, 6 (7), 1011-6
DOI 10.1093/hmg/6.7.1011, PubMed 9215668

Undlien DE (1997)
Genetic predisposition to insulin-dependent diabetes mellitus (IDDM): susceptibility and resistance conferred by HLA complex genes and polymorphisms in the insulin gene region
Institute of Transplantation Immunology, the National Hospital and University of Oslo, [Oslo], 1 b. (flere pag.)
BIBSYS 97140223x, ISBN 82-7633-088-6

Undlien DE, Akselsen HE, Joner G, Dahl-Jørgensen K, Søvik O, Rønningen KS, Thorsby E (1997)
No independent associations of LMP2 and LMP7 polymorphisms with susceptibility to develop IDDM
Diabetes, 46 (2), 307-12
DOI 10.2337/diab.46.2.307, PubMed 9000709

Undlien DE, Friede T, Rammensee HG, Joner G, Dahl-Jørgensen K, Søvik O, Akselsen HE, Knutsen I, Rønningen KS, Thorsby E (1997)
HLA-encoded genetic predisposition in IDDM: DR4 subtypes may be associated with different degrees of protection
Diabetes, 46 (1), 143-9
DOI 10.2337/diab.46.1.143, PubMed 8971095

Publications 1996

Thorsby E, Undlien D (1996)
The HLA associated predisposition to type 1 diabetes and other autoimmune diseases
J Pediatr Endocrinol Metab, 9 Suppl 1, 75-88
DOI 10.1515/jpem.1996.9.s1.75, PubMed 8887157

Publications 1995

Bennett ST, Lucassen AM, Gough SC, Powell EE, Undlien DE, Pritchard LE, Merriman ME, Kawaguchi Y, Dronsfield MJ, Pociot F (1995)
Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus
Nat Genet, 9 (3), 284-92
DOI 10.1038/ng0395-284, PubMed 7773291

Copeman JB, Cucca F, Hearne CM, Cornall RJ, Reed PW, Rønningen KS, Undlien DE, Nisticò L, Buzzetti R, Tosi R (1995)
Linkage disequilibrium mapping of a type 1 diabetes susceptibility gene (IDDM7) to chromosome 2q31-q33
Nat Genet, 9 (1), 80-5
DOI 10.1038/ng0195-80, PubMed 7704030

Undlien DE, Akselsen HE, Joner G, Dahl-Jorgensen K, Aagenaes O, Sovik O, Thorsby E, Rønningen KS (1995)
No difference in the parental origin of susceptibility HLA class II haplotypes among Norwegian patients with insulin-dependent diabetes mellitus
Am J Hum Genet, 57 (6), 1511-4
PubMed 8533785

Undlien DE, Bennett ST, Todd JA, Akselsen HE, Ikäheimo I, Reijonen H, Knip M, Thorsby E, Rønningen KS (1995)
Insulin gene region-encoded susceptibility to IDDM maps upstream of the insulin gene
Diabetes, 44 (6), 620-5
DOI 10.2337/diab.44.6.620, PubMed 7789624

Publications 1994

Ploski R, Undlien DE, Vinje O, Førre O, Thorsby E, Rønningen KS (1994)
Polymorphism of human major histocompatibility complex-encoded transporter associated with antigen processing (TAP) genes and susceptibility to juvenile rheumatoid arthritis
Hum Immunol, 39 (1), 54-60
DOI 10.1016/0198-8859(94)90101-5, PubMed 8181963

Spurkland A, Knutsen I, Undlien DE, Vartdal F (1994)
No association of multiple sclerosis to alleles at the TAP2 locus
Hum Immunol, 39 (4), 299-301
DOI 10.1016/0198-8859(94)90273-9, PubMed 8071104

Undlien DE, Hamaguchi K, Kimura A, Tuomilehto-Wolf E, Swai AB, McLarty DG, Tuomilehto J, Thorsby E, Rønningen KS (1994)
IDDM susceptibility associated with polymorphisms in the insulin gene region. A study of blacks, Caucasians and orientals
Diabetologia, 37 (8), 745-9
DOI 10.1007/BF00404330, PubMed 7988775

Publications 1993

Rønningen KS, Bangstad HJ, Undlien DE, Thorsby E (1993)
Influence of genetic factors (HLA class II genes, insulin-gene region polymorphisms) and metabolic control on the development of diabetic nephropathy
Diabetes Res, 23 (1), 31-40
PubMed 7924146

Rønningen KS, Undlien DE, Ploski R, Maouni N, Konrad RJ, Jensen E, Hornes E, Reijonen H, Colonna M, Monos DS (1993)
Linkage disequilibrium between TAP2 variants and HLA class II alleles; no primary association between TAP2 variants and insulin-dependent diabetes mellitus
Eur J Immunol, 23 (5), 1050-6
DOI 10.1002/eji.1830230511, PubMed 8477801

Rønningen KS, Undlien DE, Thorsby E, Følling I (1993)
Insulin autoimmune syndrome; HLA genes may be a marker of disease heterogeneity
Autoimmunity, 14 (4), 343
PubMed 8347777

Publications 1992

Bain SC, Prins JB, Hearne CM, Rodrigues NR, Rowe BR, Pritchard LE, Ritchie RJ, Hall JR, Undlien DE, Ronningen KS (1992)
Insulin gene region-encoded susceptibility to type 1 diabetes is not restricted to HLA-DR4-positive individuals
Nat Genet, 2 (3), 212-5
DOI 10.1038/ng1192-212, PubMed 1345171