Publications by Benedicte A. Lie

159 publications found

Publications 2019

  1. Kjeldsen-Kragh J, Titze TL, Lie BA, Vaage JT, Kjær M (2019)
    HLA-DRB3*01:01 exhibits a dose-dependent impact on HPA-1a antibody levels in HPA-1a-immunized women
    Blood Adv, 3 (7), 945-951
    DOI 10.1182/bloodadvances.2019032227, PubMed 30923048
  2. Tapia G, Mortimer G, Ye J, Gillard BT, Chipper-Keating S, Mårild K, Viken MK, Lie BA, Joner G, Skrivarhaug T, Njølstad PR, Størdal K, Gillespie KM, Stene LC (2019)
    Maternal microchimerism in cord blood and risk of childhood-onset type 1 diabetes
    Pediatr Diabetes (in press)
    DOI 10.1111/pedi.12875, PubMed 31173445
  3. Tapia G, Mårild K, Dahl SR, Lund-Blix NA, Viken MK, Lie BA, Njølstad PR, Joner G, Skrivarhaug T, Cohen AS, Størdal K, Stene LC (2019)
    Maternal and Newborn Vitamin D-Binding Protein, Vitamin D Levels, Vitamin D Receptor Genotype, and Childhood Type 1 Diabetes
    Diabetes Care, 42 (4), 553-559
    DOI 10.2337/dc18-2176, PubMed 30692241

Publications 2018

  1. Guderud K, Mæhlen MT, Nordang GBN, Viken MK, Andreassen BK, Molberg Ø, Flåm ST, Lie BA (2018)
    Lack of Association among Peptidyl Arginine Deiminase Type 4 Autoantibodies, PADI4 Polymorphisms, and Clinical Characteristics in Rheumatoid Arthritis
    J Rheumatol, 45 (9), 1211-1219
    DOI 10.3899/jrheum.170769, PubMed 29858238
  2. Lande A, Andersen I, Egeland T, Lie BA, Viken MK (2018)
    HLA -A, -C, -B, -DRB1, -DQB1 and -DPB1 allele and haplotype frequencies in 4514 healthy Norwegians
    Hum Immunol, 79 (7), 527-529
    DOI 10.1016/j.humimm.2018.04.012, PubMed 29684411
  3. Størdal K, McArdle HJ, Hayes H, Tapia G, Viken MK, Lund-Blix NA, Haugen M, Joner G, Skrivarhaug T, Mårild K, Njølstad PR, Eggesbø M, Mandal S, Page CM, London SJ, Lie BA, Stene LC (2018)
    Prenatal iron exposure and childhood type 1 diabetes
    Sci Rep, 8 (1), 9067
    DOI 10.1038/s41598-018-27391-4, PubMed 29899542

Publications 2017

  1. Henriksen EKK, Viken MK, Wittig M, Holm K, Folseraas T, Mucha S, Melum E, Hov JR, Lazaridis KN, Juran BD, Chazouillères O, Färkkilä M, Gotthardt DN, Invernizzi P, Carbone M, Hirschfield GM, Rushbrook SM, Goode E, UK-PSC Consortium, Ponsioen CY, Weersma RK, Eksteen B, Yimam KK, Gordon SC, Goldberg D et al. (2017)
    HLA haplotypes in primary sclerosing cholangitis patients of admixed and non-European ancestry
    HLA, 90 (4), 228-233
    DOI 10.1111/tan.13076, PubMed 28695657
  2. Mårild K, Tapia G, Haugen M, Dahl SR, Cohen AS, Lundqvist M, Lie BA, Stene LC, Størdal K (2017)
    Maternal and neonatal vitamin D status, genotype and childhood celiac disease
    PLoS One, 12 (7), e0179080
    DOI 10.1371/journal.pone.0179080, PubMed 28686601
  3. Popperud TH, Viken MK, Kerty E, Lie BA (2017)
    Juvenile myasthenia gravis in Norway: HLA-DRB1*04:04 is positively associated with prepubertal onset
    PLoS One, 12 (10), e0186383
    DOI 10.1371/journal.pone.0186383, PubMed 29036181
  4. Størdal K, Mårild K, Tapia G, Haugen M, Cohen AS, Lie BA, Stene LC (2017)
    Fetal and Maternal Genetic Variants Influencing Neonatal Vitamin D Status
    J Clin Endocrinol Metab, 102 (11), 4072-4079
    DOI 10.1210/jc.2017-00827, PubMed 28938476
  5. Viken MK, Flåm ST, Skrivarhaug T, Amundsen SS, Sollid LM, Drivvoll AK, Joner G, Dahl-Jørgensen K, Lie BA (2017)
    HLA class II alleles in Norwegian patients with coexisting type 1 diabetes and celiac disease
    HLA, 89 (5), 278-284
    DOI 10.1111/tan.12986, PubMed 28247576
  6. Witoelar A, Jansen IE, Wang Y, Desikan RS, Gibbs JR, Blauwendraat C, Thompson WK, Hernandez DG, Djurovic S, Schork AJ, Bettella F, Ellinghaus D, Franke A, Lie BA, McEvoy LK, Karlsen TH, Lesage S, Morris HR, Brice A, Wood NW, Heutink P, Hardy J, Singleton AB, Dale AM, Gasser T et al. (2017)
    Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases
    JAMA Neurol, 74 (7), 780-792
    DOI 10.1001/jamaneurol.2017.0469, PubMed 28586827

Publications 2016

  1. Carmona FD, Vaglio A, Mackie SL, Hernández-Rodríguez J, Monach PA, Castañeda S, Solans R, Morado IC, Narváez J, Ramentol-Sintas M, Pease CT, Dasgupta B, Watts R, Khalidi N, Langford CA, Ytterberg S, Boiardi L, Beretta L, Govoni M, Emmi G, Bonatti F, Cimmino MA, Witte T, Neumann T, Holle J et al. (2016)
    A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis
    Am J Hum Genet, 100 (1), 64-74
    DOI 10.1016/j.ajhg.2016.11.013, PubMed 28041642
  2. Dominguez-Valentin M, Gras Navarro A, Rahman AM, Kumar S, Retière C, Ulvestad E, Kristensen V, Lund-Johansen M, Lie BA, Enger PØ, Njølstad G, Kristoffersen E, Lie SA, Chekenya M (2016)
    Identification of a Natural Killer Cell Receptor Allele That Prolongs Survival of Cytomegalovirus-Positive Glioblastoma Patients
    Cancer Res, 76 (18), 5326-36
    DOI 10.1158/0008-5472.CAN-16-1162, PubMed 27406829
  3. Finkel TH, Li J, Wei Z, Wang W, Zhang H, Behrens EM, Reuschel EL, Limou S, Wise C, Punaro M, Becker ML, Munro JE, Flatø B, Førre Ø, Thompson SD, Langefeld CD, Glass DN, Glessner JT, Kim CE, Frackelton E, Shivers DK, Thomas KA, Chiavacci RM, Hou C, Xu K et al. (2016)
    Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility
    BMC Med Genet, 17, 24
    DOI 10.1186/s12881-016-0285-3, PubMed 27005825
  4. Gabrielsen IS, Amundsen SS, Helgeland H, Flåm ST, Hatinoor N, Holm K, Viken MK, Lie BA (2016)
    Genetic risk variants for autoimmune diseases that influence gene expression in thymus
    Hum Mol Genet, 25 (14), 3117-3124
    DOI 10.1093/hmg/ddw152, PubMed 27199374
  5. Gabrielsen IS, Viken MK, Amundsen SS, Helgeland H, Holm K, Flåm ST, Lie BA (2016)
    Autoimmune risk variants in ERAP2 are associated with gene-expression levels in thymus
    Genes Immun, 17 (7), 406-411
    DOI 10.1038/gene.2016.39, PubMed 27829666
  6. Gustavsen MW, Celius EG, Winsvold BS, Moen SM, Nygaard GO, Berg-Hansen P, Lie BA, Zwart JA, Harbo HF (2016)
    Migraine and frequent tension-type headache are not associated with multiple sclerosis in a Norwegian case-control study
    Mult Scler J Exp Transl Clin, 2, 2055217316682976
    DOI 10.1177/2055217316682976, PubMed 28607748
  7. Hov JR, Boberg KM, Taraldsrud E, Vesterhus M, Boyadzhieva M, Solberg IC, Schrumpf E, Vatn MH, Lie BA, Molberg Ø, Karlsen TH (2016)
    Antineutrophil antibodies define clinical and genetic subgroups in primary sclerosing cholangitis
    Liver Int, 37 (3), 458-465
    DOI 10.1111/liv.13238, PubMed 27558072
  8. Wang Y, Bos SD, Harbo HF, Thompson WK, Schork AJ, Bettella F, Witoelar A, Lie BA, Li W, McEvoy LK, Djurovic S, Desikan RS, Dale AM, Andreassen OA (2016)
    Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors
    Mult Scler, 22 (14), 1783-1793
    DOI 10.1177/1352458516635873, PubMed 26920376

Publications 2015

  1. Andreassen OA, Desikan RS, Wang Y, Thompson WK, Schork AJ, Zuber V, Doncheva NT, Ellinghaus E, Albrecht M, Mattingsdal M, Franke A, Lie BA, Mills IG, Aukrust P, McEvoy LK, Djurovic S, Karlsen TH, Dale AM (2015)
    Correction: Abundant Genetic Overlap between Blood Lipids and Immune-Mediated Diseases Indicates Shared Molecular Genetic Mechanisms
    PLoS One, 10 (5), e0128048
    DOI 10.1371/journal.pone.0128048, PubMed 25978331
  2. Andreassen OA, Desikan RS, Wang Y, Thompson WK, Schork AJ, Zuber V, Doncheva NT, Ellinghaus E, Albrecht M, Mattingsdal M, Franke A, Lie BA, Mills IG, Aukrust P, McEvoy LK, Djurovic S, Karlsen TH, Dale AM (2015)
    Abundant genetic overlap between blood lipids and immune-mediated diseases indicates shared molecular genetic mechanisms
    PLoS One, 10 (4), e0123057
    DOI 10.1371/journal.pone.0123057, PubMed 25853426
  3. Chiaroni-Clarke RC, Li YR, Munro JE, Chavez RA, Scurrah KJ, Pezic A, Akikusa JD, Allen RC, Piper SE, Becker ML, Thompson SD, Lie BA, Flato B, Forre O, Punaro M, Wise C, Saffery R, Finkel TH, Hakonarson H, Ponsonby AL, Ellis JA (2015)
    The association of PTPN22 rs2476601 with juvenile idiopathic arthritis is specific to females
    Genes Immun, 16 (7), 495-8
    DOI 10.1038/gene.2015.32, PubMed 26291515
  4. Cortes A, Pulit SL, Leo PJ, Pointon JJ, Robinson PC, Weisman MH, Ward M, Gensler LS, Zhou X, Garchon HJ, Chiocchia G, Nossent J, Lie BA, Førre Ø, Tuomilehto J, Laiho K, Bradbury LA, Elewaut D, Burgos-Vargas R, Stebbings S, Appleton L, Farrah C, Lau J, Haroon N, Mulero J et al. (2015)
    Major histocompatibility complex associations of ankylosing spondylitis are complex and involve further epistasis with ERAP1
    Nat Commun, 6, 7146
    DOI 10.1038/ncomms8146, PubMed 25994336
  5. Hov JR, Zhong H, Qin B, Anmarkrud JA, Holm K, Franke A, Lie BA, Karlsen TH (2015)
    The Influence of the Autoimmunity-Associated Ancestral HLA Haplotype AH8.1 on the Human Gut Microbiota: A Cross-Sectional Study
    PLoS One, 10 (7), e0133804
    DOI 10.1371/journal.pone.0133804, PubMed 26207384
  6. Li YR, Li J, Zhao SD, Bradfield JP, Mentch FD, Maggadottir SM, Hou C, Abrams DJ, Chang D, Gao F, Guo Y, Wei Z, Connolly JJ, Cardinale CJ, Bakay M, Glessner JT, Li D, Kao C, Thomas KA, Qiu H, Chiavacci RM, Kim CE, Wang F, Snyder J, Richie MD et al. (2015)
    Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases
    Nat Med, 21 (9), 1018-27
    DOI 10.1038/nm.3933, PubMed 26301688
  7. Li YR, Zhao SD, Li J, Bradfield JP, Mohebnasab M, Steel L, Kobie J, Abrams DJ, Mentch FD, Glessner JT, Guo Y, Wei Z, Connolly JJ, Cardinale CJ, Bakay M, Li D, Maggadottir SM, Thomas KA, Qui H, Chiavacci RM, Kim CE, Wang F, Snyder J, Flatø B, Førre Ø et al. (2015)
    Genetic sharing and heritability of paediatric age of onset autoimmune diseases
    Nat Commun, 6, 8442
    DOI 10.1038/ncomms9442, PubMed 26450413
  8. Omair A, Mannion AF, Holden M, Fairbank J, Lie BA, Hägg O, Fritzell P, Brox JI (2015)
    Catechol-O-methyltransferase (COMT) gene polymorphisms are associated with baseline disability but not long-term treatment outcome in patients with chronic low back pain
    Eur Spine J, 24 (11), 2425-31
    DOI 10.1007/s00586-015-3866-5, PubMed 25772090
  9. Robinson PC, Costello ME, Leo P, Bradbury LA, Hollis K, Cortes A, Lee S, Joo KB, Shim SC, Weisman M, Ward M, Zhou X, Garchon HJ, Chiocchia G, Nossent J, Lie BA, Førre Ø, Tuomilehto J, Laiho K, Jiang L, Liu Y, Wu X, Elewaut D, Burgos-Vargas R, Gensler LS et al. (2015)
    ERAP2 is associated with ankylosing spondylitis in HLA-B27-positive and HLA-B27-negative patients
    Ann Rheum Dis, 74 (8), 1627-9
    DOI 10.1136/annrheumdis-2015-207416, PubMed 25917849
  10. Seldin MF, Alkhairy OK, Lee AT, Lamb JA, Sussman J, Pirskanen-Matell R, Piehl F, Verschuuren JJGM, Kostera-Pruszczyk A, Szczudlik P, McKee D, Maniaol AH, Harbo HF, Lie BA, Melms A, Garchon HJ, Willcox N, Gregersen PK, Hammarstrom L (2015)
    Genome-Wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A and Identification of ZBTB10 and Three Distinct HLA Associations
    Mol Med, 21 (1), 769-781
    DOI 10.2119/molmed.2015.00232, PubMed 26562150

Publications 2014

  1. Amundsen SS, Viken MK, Sollid LM, Lie BA (2014)
    Coeliac disease-associated polymorphisms influence thymic gene expression
    Genes Immun, 15 (6), 355-60
    DOI 10.1038/gene.2014.26, PubMed 24871462
  2. Andreassen OA, Harbo HF, Wang Y, Thompson WK, Schork AJ, Mattingsdal M, Zuber V, Bettella F, Ripke S, Kelsoe JR, Kendler KS, O'Donovan MC, Sklar P, Psychiatric Genomics Consortium (PGC) Bipolar Disorder and Schizophrenia Work Groups, International Multiple Sclerosis Genetics Consortium (IMSGC), McEvoy LK, Desikan RS, Lie BA, Djurovic S, Dale AM (2014)
    Genetic pleiotropy between multiple sclerosis and schizophrenia but not bipolar disorder: differential involvement of immune-related gene loci
    Mol Psychiatry, 20 (2), 207-14
    DOI 10.1038/mp.2013.195, PubMed 24468824
  3. Avidan N, Le Panse R, Harbo HF, Bernasconi P, Poulas K, Ginzburg E, Cavalcante P, Colleoni L, Baggi F, Antozzi C, Truffault F, Horn-Saban S, Pöschel S, Zagoriti Z, Maniaol A, Lie BA, Bernard I, Saoudi A, Illes Z, Casasnovas Pons C, Melms A, Tzartos S, Willcox N, Kostera-Pruszczyk A, Tallaksen C et al. (2014)
    VAV1 and BAFF, via NFκB pathway, are genetic risk factors for myasthenia gravis
    Ann Clin Transl Neurol, 1 (5), 329-39
    DOI 10.1002/acn3.51, PubMed 25356403
  4. Bossini-Castillo L, de Kovel C, Kallberg H, van 't Slot R, Italiaander A, Coenen M, Tak PP, Posthumus MD, Wijmenga C, Huizinga T, van der Helm-van Mil AH, Stoeken-Rijsbergen G, Rodriguez-Rodriguez L, Balsa A, González-Álvaro I, González-Gay MÁ, Gómez-Vaquero C, Franke B, LifeLines Cohort Study, Vermeulen S, van der Horst-Bruinsma Ie, Dijkmans BA, Wolbink GJ, Ophoff RA, Maehlen MT et al. (2014)
    A genome-wide association study of rheumatoid arthritis without antibodies against citrullinated peptides
    Ann Rheum Dis, 74 (3), e15
    DOI 10.1136/annrheumdis-2013-204591, PubMed 24532677
  5. Ellis JA, Scurrah KJ, Li YR, Ponsonby AL, Chavez RA, Pezic A, Dwyer T, Akikusa JD, Allen RC, Becker ML, Thompson SD, Lie BA, Flatø B, Førre O, Punaro M, Wise C, Finkel TH, Hakonarson H, Munro JE (2014)
    Epistasis amongst PTPN2 and genes of the vitamin D pathway contributes to risk of juvenile idiopathic arthritis
    J Steroid Biochem Mol Biol, 145, 113-20
    DOI 10.1016/j.jsbmb.2014.10.012, PubMed 25460303
  6. Flåm ST, Gunnarsson R, Garen T, Norwegian MCTD Study Group, Lie BA, Molberg Ø (2014)
    The HLA profiles of mixed connective tissue disease differ distinctly from the profiles of clinically related connective tissue diseases
    Rheumatology (Oxford), 54 (3), 528-35
    DOI 10.1093/rheumatology/keu310, PubMed 25187641
  7. Gustavsen MW, Celius EG, Moen SM, Bjølgerud A, Berg-Hansen P, Nygaard GO, Sandvik L, Lie BA, Harbo HF (2014)
    No association between multiple sclerosis and periodontitis after adjusting for smoking habits
    Eur J Neurol, 22 (3), 588-90
    DOI 10.1111/ene.12520, PubMed 25041906
  8. Gustavsen MW, Page CM, Moen SM, Bjølgerud A, Berg-Hansen P, Nygaard GO, Sandvik L, Lie BA, Celius EG, Harbo HF (2014)
    Environmental exposures and the risk of multiple sclerosis investigated in a Norwegian case-control study
    BMC Neurol, 14, 196
    DOI 10.1186/s12883-014-0196-x, PubMed 25274070
  9. Gustavsen MW, Viken MK, Celius EG, Berge T, Mero IL, Berg-Hansen P, Aarseth JH, Myhr KM, Søndergaard HB, Sellebjerg F, Oturai AB, Hillert J, Alfredsson L, Olsson T, Kockum I, Lie BA, Harbo HF (2014)
    Oligoclonal band phenotypes in MS differ in their HLA class II association, while specific KIR ligands at HLA class I show association to MS in general
    J Neuroimmunol, 274 (1-2), 174-9
    DOI 10.1016/j.jneuroim.2014.06.024, PubMed 25037176
  10. Moreno-Mayar JV, Rasmussen S, Seguin-Orlando A, Rasmussen M, Liang M, Flåm ST, Lie BA, Gilfillan GD, Nielsen R, Thorsby E, Willerslev E, Malaspinas AS (2014)
    Genome-wide ancestry patterns in Rapanui suggest pre-European admixture with Native Americans
    Curr Biol, 24 (21), 2518-25
    DOI 10.1016/j.cub.2014.09.057, PubMed 25447991
  11. Naess S, Björnsson E, Anmarkrud JA, Al Mamari S, Juran BD, Lazaridis KN, Chapman R, Bergquist A, Melum E, Marsh SG, Schrumpf E, Lie BA, Boberg KM, Karlsen TH, Hov JR (2014)
    Small duct primary sclerosing cholangitis without inflammatory bowel disease is genetically different from large duct disease
    Liver Int, 34 (10), 1488-95
    DOI 10.1111/liv.12492, PubMed 24517468
  12. Næss S, Lie BA, Melum E, Olsson M, Hov JR, Croucher PJ, Hampe J, Thorsby E, Bergquist A, Traherne JA, Schrumpf E, Boberg KM, Schreiber S, Franke A, Karlsen TH (2014)
    Refinement of the MHC risk map in a scandinavian primary sclerosing cholangitis population
    PLoS One, 9 (12), e114486
    DOI 10.1371/journal.pone.0114486, PubMed 25521205
  13. Tinholt M, Viken MK, Dahm AE, Vollan HK, Sahlberg KK, Garred O, Børresen-Dale AL, Jacobsen AF, Kristensen V, Bukholm I, Kåresen R, Schlichting E, Skretting G, Lie BA, Sandset PM, Iversen N (2014)
    Increased coagulation activity and genetic polymorphisms in the F5, F10 and EPCR genes are associated with breast cancer: a case-control study
    BMC Cancer, 14, 845
    DOI 10.1186/1471-2407-14-845, PubMed 25407022

Publications 2013

  1. Andersen IM, Tengesdal G, Lie BA, Boberg KM, Karlsen TH, Hov JR (2013)
    Effects of coffee consumption, smoking, and hormones on risk for primary sclerosing cholangitis
    Clin Gastroenterol Hepatol, 12 (6), 1019-28
    DOI 10.1016/j.cgh.2013.09.024, PubMed 24076415
  2. International Genetics of Ankylosing Spondylitis Consortium (IGAS), Cortes A, Hadler J, Pointon JP, Robinson PC, Karaderi T, Leo P, Cremin K, Pryce K, Harris J, Lee S, Joo KB, Shim SC, Weisman M, Ward M, Zhou X, Garchon HJ, Chiocchia G, Nossent J, Lie BA, Førre Ø, Tuomilehto J, Laiho K, Jiang L, Liu Y et al. (2013)
    Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci
    Nat Genet, 45 (7), 730-8
    DOI 10.1038/ng.2667, PubMed 23749187
  3. International Multiple Sclerosis Genetics Consortium (IMSGC), Beecham AH, Patsopoulos NA, Xifara DK, Davis MF, Kemppinen A, Cotsapas C, Shah TS, Spencer C, Booth D, Goris A, Oturai A, Saarela J, Fontaine B, Hemmer B, Martin C, Zipp F, D'Alfonso S, Martinelli-Boneschi F, Taylor B, Harbo HF, Kockum I, Hillert J, Olsson T, Ban M et al. (2013)
    Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
    Nat Genet, 45 (11), 1353-60
    DOI 10.1038/ng.2770, PubMed 24076602
  4. Maehlen MT, Olsen IC, Andreassen BK, Viken MK, Jiang X, Alfredsson L, Källberg H, Brynedal B, Kurreeman F, Daha N, Toes R, Zhernakova A, Gutierrez-Achury J, de Bakker PI, Martin J, Teruel M, Gonzalez-Gay MA, Rodríguez-Rodríguez L, Balsa A, Uhlig T, Kvien TK, Lie BA (2013)
    Genetic risk scores and number of autoantibodies in patients with rheumatoid arthritis
    Ann Rheum Dis, 74 (4), 762-8
    DOI 10.1136/annrheumdis-2013-204173, PubMed 24336335
  5. Maehlen MT, Provan SA, de Rooy DP, van der Helm-van Mil AH, Krabben A, Saxne T, Lindqvist E, Semb AG, Uhlig T, van der Heijde D, Mero IL, Olsen IC, Kvien TK, Lie BA (2013)
    Associations between APOE genotypes and disease susceptibility, joint damage and lipid levels in patients with rheumatoid arthritis
    PLoS One, 8 (4), e60970
    DOI 10.1371/journal.pone.0060970, PubMed 23613766
  6. Mero IL, Gustavsen MW, Sæther HS, Flåm ST, Berg-Hansen P, Søndergaard HB, Jensen PE, Berge T, Bjølgerud A, Muggerud A, Aarseth JH, International Multiple Sclerosis Genetics Consortium, Myhr KM, Celius EG, Sellebjerg F, Hillert J, Alfredsson L, Olsson T, Oturai AB, Kockum I, Lie BA, Andreassen BK, Harbo HF (2013)
    Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles
    PLoS One, 8 (3), e58352
    DOI 10.1371/journal.pone.0058352, PubMed 23472185
  7. Nordang GB, Flåm ST, Maehlen MT, Kvien TK, Viken MK, Lie BA (2013)
    HLA-C alleles confer risk for anti-citrullinated peptide antibody-positive rheumatoid arthritis independent of HLA-DRB1 alleles
    Rheumatology (Oxford), 52 (11), 1973-82
    DOI 10.1093/rheumatology/ket252, PubMed 23901134
  8. Omair A, Holden M, Lie BA, Reikeras O, Brox JI (2013)
    Treatment outcome of chronic low back pain and radiographic lumbar disc degeneration are associated with inflammatory and matrix degrading gene variants: a prospective genetic association study
    BMC Musculoskelet Disord, 14, 105
    DOI 10.1186/1471-2474-14-105, PubMed 23522322
  9. Serrano A, Márquez A, Mackie SL, Carmona FD, Solans R, Miranda-Filloy JA, Hernández-Rodríguez J, Cid MC, Castañeda S, Morado IC, Narváez J, Blanco R, Sopeña B, García-Villanueva MJ, Monfort J, Ortego-Centeno N, Unzurrunzaga A, Marí-Alfonso B, Sánchez Martín J, de Miguel E, Magro C, Raya E, UK GCA Consortium, Spanish GCA Consortium, Braun N et al. (2013)
    Identification of the PTPN22 functional variant R620W as susceptibility genetic factor for giant cell arteritis
    Ann Rheum Dis, 72 (11), 1882-1886
    DOI 10.1136/annrheumdis-2013-203641, PubMed 23946333
  10. Teruel M, McKinney C, Balsa A, Pascual-Salcedo D, Rodriguez-Rodriguez L, Ortiz AM, Gómez-Vaquero C, González-Gay MA, Smith M, Witte T, Merriman T, Lie BA, Martin J (2013)
    Association of CD247 polymorphisms with rheumatoid arthritis: a replication study and a meta-analysis
    PLoS One, 8 (7), e68295
    DOI 10.1371/journal.pone.0068295, PubMed 23861880
  11. Vang T, Landskron J, Viken MK, Oberprieler N, Torgersen KM, Mustelin T, Tasken K, Tautz L, Rickert RC, Lie BA (2013)
    The autoimmune-predisposing variant of lymphoid tyrosine phosphatase favors T helper 1 responses
    Hum Immunol, 74 (5), 574-85
    DOI 10.1016/j.humimm.2012.12.017, PubMed 23333624

Publications 2012

  1. Daha NA, Lie BA, Trouw LA, Stoeken G, Schonkeren JJ, Ding B, Kvien TK, Schilham MW, Padyukov L, Huizinga TW, Toes R (2012)
    Novel genetic association of the VTCN1 region with rheumatoid arthritis
    Ann Rheum Dis, 71 (4), 567-71
    DOI 10.1136/annrheumdis-2011-200574, PubMed 22323440
  2. 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
  3. Elbarbary NS, Tjora E, Molnes J, Lie BA, Habib MA, Salem MA, Njølstad PR (2012)
    An Egyptian family with H syndrome due to a novel mutation in SLC29A3 illustrating overlapping features with pigmented hypertrichotic dermatosis with insulin-dependent diabetes and Faisalabad histiocytosis
    Pediatr Diabetes, 14 (6), 466-72
    DOI 10.1111/j.1399-5448.2012.00925.x, PubMed 22989030
  4. Gregersen PK, Kosoy R, Lee AT, Lamb J, Sussman J, McKee D, Simpfendorfer KR, Pirskanen-Matell R, Piehl F, Pan-Hammarstrom Q, Verschuuren JJ, Titulaer MJ, Niks EH, Marx A, Ströbel P, Tackenberg B, Pütz M, Maniaol A, Elsais A, Tallaksen C, Harbo HF, Lie BA, Raychaudhuri S, de Bakker PI, Melms A et al. (2012)
    Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08
    Ann Neurol, 72 (6), 927-35
    DOI 10.1002/ana.23691, PubMed 23055271
  5. Leikfoss IS, Mero IL, Dahle MK, Lie BA, Harbo HF, Spurkland A, Berge T (2012)
    Multiple sclerosis-associated single-nucleotide polymorphisms in CLEC16A correlate with reduced SOCS1 and DEXI expression in the thymus
    Genes Immun, 14 (1), 62-6
    DOI 10.1038/gene.2012.52, PubMed 23151489
  6. Link J, Kockum I, Lorentzen AR, Lie BA, Celius EG, Westerlind H, Schaffer M, Alfredsson L, Olsson T, Brynedal B, Harbo HF, Hillert J (2012)
    Importance of human leukocyte antigen (HLA) class I and II alleles on the risk of multiple sclerosis
    PLoS One, 7 (5), e36779
    DOI 10.1371/journal.pone.0036779, PubMed 22586495
  7. Maniaol AH, Elsais A, Lorentzen ÅR, Owe JF, Viken MK, Sæther H, Flåm ST, Bråthen G, Kampman MT, Midgard R, Christensen M, Rognerud A, Kerty E, Gilhus NE, Tallaksen CM, Lie BA, Harbo HF (2012)
    Late onset myasthenia gravis is associated with HLA DRB1*15:01 in the Norwegian population
    PLoS One, 7 (5), e36603
    DOI 10.1371/journal.pone.0036603, PubMed 22590574
  8. Mero IL, Smestad C, Lie BA, Lorentzen ÅR, Sandvik L, Landrø NI, Aarseth JH, Myhr KM, Celius EG, Harbo HF (2012)
    Polymorphisms of the BDNF gene show neither association with multiple sclerosis susceptibility nor clinical course
    J Neuroimmunol, 244 (1-2), 107-10
    DOI 10.1016/j.jneuroim.2012.01.011, PubMed 22341604
  9. Nordang GB, Carpenter D, Viken MK, Kvien TK, Armour JA, Lie BA (2012)
    Association analysis of the CCL3L1 copy number locus by paralogue ratio test in Norwegian rheumatoid arthritis patients and healthy controls
    Genes Immun, 13 (7), 579-82
    DOI 10.1038/gene.2012.30, PubMed 22785612
  10. Omair A, Lie BA, Reikeras O, Brox JI (2012)
    An Association Study of Interleukin 18 Receptor Genes (IL18R1 and IL18RAP) in Lumbar Disc Degeneration
    Open Orthop J, 6, 164-71
    DOI 10.2174/1874325001206010164, PubMed 22550553
  11. Omair A, Lie BA, Reikeras O, Holden M, Brox JI (2012)
    Genetic contribution of catechol-O-methyltransferase variants in treatment outcome of low back pain: a prospective genetic association study
    BMC Musculoskelet Disord, 13, 76
    DOI 10.1186/1471-2474-13-76, PubMed 22612913
  12. Ronninger M, Seddighzadeh M, Eike MC, Plant D, Daha NA, Skinningsrud B, Worthington J, Kvien TK, Toes RE, Lie BA, Alfredsson L, Padyukov L (2012)
    Interaction analysis between HLA-DRB1 shared epitope alleles and MHC class II transactivator CIITA gene with regard to risk of rheumatoid arthritis
    PLoS One, 7 (3), e32861
    DOI 10.1371/journal.pone.0032861, PubMed 22461888
  13. Rønningen KS, Yap SE, Brandal K, Stormyr A, Lie BA, Rasmussen T, Stray-Pedersen B, Akselsen HE (2012)
    HLA-DRB1, -DQA1 and -DQB1 alleles and haplotypes in first-generation Pakistani immigrants in Norway
    Scand J Immunol, 75 (4), 426-30
    DOI 10.1111/j.1365-3083.2011.02669.x, PubMed 22171671
  14. Vang T, Liu WH, Delacroix L, Wu S, Vasile S, Dahl R, Yang L, Musumeci L, Francis D, Landskron J, Tasken K, Tremblay ML, Lie BA, Page R, Mustelin T, Rahmouni S, Rickert RC, Tautz L (2012)
    LYP inhibits T-cell activation when dissociated from CSK
    Nat Chem Biol, 8 (5), 437-46
    DOI 10.1038/nchembio.916, PubMed 22426112

Publications 2011

  1. Eerligh P, Koeleman BP, Lie BA, Roep BO, Thorsby E (2011)
    No extreme genetic risk for type 1 diabetes among DR3/4-DQ8 siblings sharing both extended HLA haplotypes with their diabetic proband
    Tissue Antigens, 77 (4), 338-40
    DOI 10.1111/j.1399-0039.2011.01636.x, PubMed 21388358
  2. Gorlova O, Martin JE, Rueda B, Koeleman BP, Ying J, Teruel M, Diaz-Gallo LM, Broen JC, Vonk MC, Simeon CP, Alizadeh BZ, Coenen MJ, Voskuyl AE, Schuerwegh AJ, van Riel PL, Vanthuyne M, van 't Slot R, Italiaander A, Ophoff RA, Hunzelmann N, Fonollosa V, Ortego-Centeno N, González-Gay MA, García-Hernández FJ, González-Escribano MF et al. (2011)
    Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy
    PLoS Genet, 7 (7), e1002178
    DOI 10.1371/journal.pgen.1002178, PubMed 21779181
  3. Harbo HF, Lorentzen AR, Lie BA, Celius EG, Spurkland A (2011)
    [New gene map for multiple sclerosis]
    Tidsskr Nor Laegeforen, 131 (21), 2126-30
    DOI 10.4045/tidsskr.10.0823, PubMed 22048209
  4. Hov JR, Kosmoliaptsis V, Traherne JA, Olsson M, Boberg KM, Bergquist A, Schrumpf E, Bradley JA, Taylor CJ, Lie BA, Trowsdale J, Karlsen TH (2011)
    Electrostatic modifications of the human leukocyte antigen-DR P9 peptide-binding pocket and susceptibility to primary sclerosing cholangitis
    Hepatology, 53 (6), 1967-76
    DOI 10.1002/hep.24299, PubMed 21413052
  5. Maehlen MT, Nordang GB, Syversen SW, van der Heijde DM, Kvien TK, Uhlig T, Lie BA (2011)
    FCRL3 -169C/C genotype is associated with anti-citrullinated protein antibody-positive rheumatoid arthritis and with radiographic progression
    J Rheumatol, 38 (11), 2329-35
    DOI 10.3899/jrheum.110489, PubMed 21885492
  6. Martín JE, Alizadeh BZ, González-Gay MA, Balsa A, Pascual-Salcedo D, González-Escribano MF, Rodriguez-Rodriguez L, Fernández-Gutiérrez B, Raya E, Coenen MJ, van Riel P, Radstake TR, Kvien TK, Viken MK, Lie BA, Koeleman BP, Martín J (2011)
    Evidence for PTPN22 R620W polymorphism as the sole common risk variant for rheumatoid arthritis in the 1p13.2 region
    J Rheumatol, 38 (11), 2290-6
    DOI 10.3899/jrheum.110361, PubMed 21965649
  7. Nordang GB, Viken MK, Amundsen SS, Sanchez ES, Flatø B, Førre OT, Martin J, Kvien TK, Lie BA (2011)
    Interferon regulatory factor 5 gene polymorphism confers risk to several rheumatic diseases and correlates with expression of alternative thymic transcripts
    Rheumatology (Oxford), 51 (4), 619-26
    DOI 10.1093/rheumatology/ker364, PubMed 22179739
  8. Rodríguez-Rodríguez L, Taib WR, Topless R, Steer S, González-Escribano MF, Balsa A, Pascual-Salcedo D, González-Gay MA, Raya E, Fernandez-Gutierrez B, González-Álvaro I, Bottini N, Witte T, Viken MK, Coenen MJ, van Riel PL, Franke B, den Heijer M, Radstake TR, Wordsworth P, Lie BA, Merriman TR, Martín J (2011)
    The PTPN22 R263Q polymorphism is a risk factor for rheumatoid arthritis in Caucasian case-control samples
    Arthritis Rheum, 63 (2), 365-72
    DOI 10.1002/art.30145, PubMed 21279993
  9. 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
  10. Zaiss DM, Bekker CP, Gröne A, Lie BA, Sijts AJ (2011)
    Proteasome immunosubunits protect against the development of CD8 T cell-mediated autoimmune diseases
    J Immunol, 187 (5), 2302-9
    DOI 10.4049/jimmunol.1101003, PubMed 21804012

Publications 2010

  1. Bossini-Castillo L, Broen JC, Simeon CP, Beretta L, Vonk MC, Ortego-Centeno N, Espinosa G, Carreira P, Camps MT, Navarrete N, González-Escribano MF, Vicente-Rabaneda E, Rodríguez L, Tolosa C, Román-Ivorra JA, Gómez-Gracia I, García-Hernández FJ, Castellví I, Gallego M, Fernández-Nebro A, García-Portales R, Egurbide MV, Fonollosa V, de la Peña PG, Pros A et al. (2010)
    A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with systemic sclerosis in a large European cohort
    Ann Rheum Dis, 70 (4), 638-41
    DOI 10.1136/ard.2010.141838, PubMed 21187296
  2. Bowlus CL, Li CS, Karlsen TH, Lie BA, Selmi C (2010)
    Primary sclerosing cholangitis in genetically diverse populations listed for liver transplantation: unique clinical and human leukocyte antigen associations
    Liver Transpl, 16 (11), 1324-30
    DOI 10.1002/lt.22161, PubMed 21031548
  3. Hov JR, Keitel V, Laerdahl JK, Spomer L, Ellinghaus E, ElSharawy A, Melum E, Boberg KM, Manke T, Balschun T, Schramm C, Bergquist A, Weismüller T, Gotthardt D, Rust C, Henckaerts L, Onnie CM, Weersma RK, Sterneck M, Teufel A, Runz H, Stiehl A, Ponsioen CY, Wijmenga C, Vatn MH et al. (2010)
    Mutational characterization of the bile acid receptor TGR5 in primary sclerosing cholangitis
    PLoS One, 5 (8), e12403
    DOI 10.1371/journal.pone.0012403, PubMed 20811628
  4. Link J, Lorentzen AR, Kockum I, Duvefelt K, Lie BA, Celius EG, Harbo HF, Hillert J, Brynedal B (2010)
    Two HLA class I genes independently associated with multiple sclerosis
    J Neuroimmunol, 226 (1-2), 172-6
    DOI 10.1016/j.jneuroim.2010.07.006, PubMed 20678810
  5. Lorentzen AR, Melum E, Ellinghaus E, Smestad C, Mero IL, Aarseth JH, Myhr KM, Celius EG, Lie BA, Karlsen TH, Franke A, Harbo HF (2010)
    Association to the Glypican-5 gene in multiple sclerosis
    J Neuroimmunol, 226 (1-2), 194-7
    DOI 10.1016/j.jneuroim.2010.07.003, PubMed 20692050
  6. 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
  7. Radstake TR, Gorlova O, Rueda B, Martin JE, Alizadeh BZ, Palomino-Morales R, Coenen MJ, Vonk MC, Voskuyl AE, Schuerwegh AJ, Broen JC, van Riel PL, van 't Slot R, Italiaander A, Ophoff RA, Riemekasten G, Hunzelmann N, Simeon CP, Ortego-Centeno N, González-Gay MA, González-Escribano MF, Spanish Scleroderma Group, Airo P, van Laar J, Herrick A et al. (2010)
    Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus
    Nat Genet, 42 (5), 426-9
    DOI 10.1038/ng.565, PubMed 20383147
  8. Sanner H, Kirkhus E, Merckoll E, Tollisen A, Røisland M, Lie BA, Taraldsrud E, Gran JT, Flatø B (2010)
    Long-term muscular outcome and predisposing and prognostic factors in juvenile dermatomyositis: A case-control study
    Arthritis Care Res (Hoboken), 62 (8), 1103-11
    DOI 10.1002/acr.20203, PubMed 20506141
  9. van der Woude D, Lie BA, Lundström E, Balsa A, Feitsma AL, Houwing-Duistermaat JJ, Verduijn W, Nordang GB, Alfredsson L, Klareskog L, Pascual-Salcedo D, Gonzalez-Gay MA, Lopez-Nevot MA, Valero F, Roep BO, Huizinga TW, Kvien TK, Martín J, Padyukov L, de Vries RR, Toes RE (2010)
    Protection against anti-citrullinated protein antibody-positive rheumatoid arthritis is predominantly associated with HLA-DRB1*1301: a meta-analysis of HLA-DRB1 associations with anti-citrullinated protein antibody-positive and anti-citrullinated protein antibody-negative rheumatoid arthritis in four European populations
    Arthritis Rheum, 62 (5), 1236-45
    DOI 10.1002/art.27366, PubMed 20131291

Publications 2009

  1. Amundsen SS, Rundberg J, Adamovic S, Gudjónsdóttir AH, Ascher H, Ek J, Nilsson S, Lie BA, Naluai AT, Sollid LM (2009)
    Four novel coeliac disease regions replicated in an association study of a Swedish-Norwegian family cohort
    Genes Immun, 11 (1), 79-86
    DOI 10.1038/gene.2009.67, PubMed 19693089
  2. Eike MC, Humphreys K, Becker T, Olsson M, Lie BA, Type 1 Diabetes Genetics Consortium (2009)
    Three microsatellites from the T1DGC MHC data set show highly significant association with type 1 diabetes, independent of the HLA-DRB1, -DQA1 and -DQB1 genes
    Diabetes Obes Metab, 11 Suppl 1, 17-24
    DOI 10.1111/j.1463-1326.2008.00999.x, PubMed 19143811
  3. Harbo HF, Riccio ME, Lorentzen AR, Utsi E, Myhr KM, Mellgren SI, Flåm ST, Thorsby E, Sanchez-Mazas A, Lie BA (2009)
    Norwegian Sami differs significantly from other Norwegians according to their HLA profile
    Tissue Antigens, 75 (3), 207-17
    DOI 10.1111/j.1399-0039.2009.01425.x, PubMed 20047643
  4. Karlsen TH, Franke A, Melum E, Kaser A, Hov JR, Balschun T, Lie BA, Bergquist A, Schramm C, Weismüller TJ, Gotthardt D, Rust C, Philipp EE, Fritz T, Henckaerts L, Weersma RK, Stokkers P, Ponsioen CY, Wijmenga C, Sterneck M, Nothnagel M, Hampe J, Teufel A, Runz H, Rosenstiel P et al. (2009)
    Genome-wide association analysis in primary sclerosing cholangitis
    Gastroenterology, 138 (3), 1102-11
    DOI 10.1053/j.gastro.2009.11.046, PubMed 19944697
  5. Lorentzen AR, Karlsen TH, Olsson M, Smestad C, Mero IL, Woldseth B, Sun JY, Senitzer D, Celius EG, Thorsby E, Spurkland A, Lie BA, Harbo HF (2009)
    Killer immunoglobulin-like receptor ligand HLA-Bw4 protects against multiple sclerosis
    Ann Neurol, 65 (6), 658-66
    DOI 10.1002/ana.21695, PubMed 19630074
  6. Mero IL, Lorentzen AR, Ban M, Smestad C, Celius EG, Aarseth JH, Myhr KM, Link J, Hillert J, Olsson T, Kockum I, Masterman T, Oturai AB, Søndergaard HB, Sellebjerg F, Saarela J, Kemppinen A, Elovaara I, Spurkland A, Dudbridge F, Lie BA, Harbo HF (2009)
    A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis
    Eur J Hum Genet, 18 (4), 502-4
    DOI 10.1038/ejhg.2009.195, PubMed 19888296
  7. Nordang GB, Viken MK, Hollis-Moffatt JE, Merriman TR, Førre ØT, Helgetveit K, Kvien TK, Lie BA (2009)
    Association analysis of the interleukin 17A gene in Caucasian rheumatoid arthritis patients from Norway and New Zealand
    Rheumatology (Oxford), 48 (4), 367-70
    DOI 10.1093/rheumatology/ken512, PubMed 19208686
  8. Ramagopalan SV, Link J, Byrnes JK, Dyment DA, Giovannoni G, Hintzen RQ, Sundqvist E, Kockum I, Smestad C, Lie BA, Harbo HF, Padyukov L, Alfredsson L, Olsson T, Sadovnick AD, Hillert J, Ebers GC (2009)
    HLA-DRB1 and month of birth in multiple sclerosis
    Neurology, 73 (24), 2107-11
    DOI 10.1212/WNL.0b013e3181c679f3, PubMed 20018638
  9. 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
  10. Syversen SW, Goll GL, van der Heijde D, Landewé R, Lie BA, Odegård S, Uhlig T, Gaarder PI, Kvien TK (2009)
    Prediction of radiographic progression in rheumatoid arthritis and the role of antibodies against mutated citrullinated vimentin: results from a 10-year prospective study
    Ann Rheum Dis, 69 (2), 345-51
    DOI 10.1136/ard.2009.113092, PubMed 19648126
  11. 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

Publications 2008

  1. Adamovic S, Amundsen SS, Lie BA, Gudjónsdóttir AH, Ascher H, Ek J, van Heel DA, Nilsson S, Sollid LM, Torinsson Naluai A (2008)
    Association study of IL2/IL21 and FcgRIIa: significant association with the IL2/IL21 region in Scandinavian coeliac disease families
    Genes Immun, 9 (4), 364-7
    DOI 10.1038/gene.2008.27, PubMed 18418394
  2. Eike MC, Becker T, Humphreys K, Olsson M, Lie BA (2008)
    Conditional analyses on the T1DGC MHC dataset: novel associations with type 1 diabetes around HLA-G and confirmation of HLA-B
    Genes Immun, 10 (1), 56-67
    DOI 10.1038/gene.2008.74, PubMed 18830248
  3. 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
  4. Lorentzen AR, Smestad C, Lie BA, Oturai AB, Akesson E, Saarela J, Myhr KM, Vartdal F, Celius EG, Sørensen PS, Hillert J, Spurkland A, Harbo HF (2008)
    The SH2D2A gene and susceptibility to multiple sclerosis
    J Neuroimmunol, 197 (2), 152-8
    DOI 10.1016/j.jneuroim.2008.04.037, PubMed 18554728
  5. 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
  6. Melum E, Karlsen TH, Schrumpf E, Bergquist A, Thorsby E, Boberg KM, Lie BA (2008)
    Cholangiocarcinoma in primary sclerosing cholangitis is associated with NKG2D polymorphisms
    Hepatology, 47 (1), 90-6
    DOI 10.1002/hep.21964, PubMed 18023027

Publications 2007

  1. Adamovic S, Amundsen SS, Lie BA, Hellqvist A, Gudjónsdóttir AH, Ek J, Nilsson S, Wahlström J, Ascher H, Sollid LM, Naluai AT (2007)
    Fine mapping study in Scandinavian families suggests association between coeliac disease and haplotypes in chromosome region 5q32
    Tissue Antigens, 71 (1), 27-34
    DOI 10.1111/j.1399-0039.2007.00955.x, PubMed 17971050
  2. Amundsen SS, Adamovic S, Hellqvist A, Nilsson S, Gudjónsdóttir AH, Ascher H, Ek J, Larsson K, Wahlström J, Lie BA, Sollid LM, Naluai AT (2007)
    A comprehensive screen for SNP associations on chromosome region 5q31-33 in Swedish/Norwegian celiac disease families
    Eur J Hum Genet, 15 (9), 980-7
    DOI 10.1038/sj.ejhg.5201870, PubMed 17551518
  3. 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
  4. Harbo HF, Utsi E, Lorentzen AR, Kampman MT, Celius EG, Myhr KM, Lie BA, Mellgren SI, Thorsby E (2007)
    Low frequency of the disease-associated DRB1*15-DQB1*06 haplotype may contribute to the low prevalence of multiple sclerosis in Sami
    Tissue Antigens, 69 (4), 299-304
    DOI 10.1111/j.1399-0039.2007.00803.x, PubMed 17389012
  5. Karlsen TH, Boberg KM, Olsson M, Sun JY, Senitzer D, Bergquist A, Schrumpf E, Thorsby E, Lie BA (2007)
    Particular genetic variants of ligands for natural killer cell receptors may contribute to the HLA associated risk of primary sclerosing cholangitis
    J Hepatol, 46 (5), 899-906
    DOI 10.1016/j.jhep.2007.01.032, PubMed 17383044
  6. Karlsen TH, Boberg KM, Vatn M, Bergquist A, Hampe J, Schrumpf E, Thorsby E, Schreiber S, Lie BA, IBSEN Study Group (2007)
    Different HLA class II associations in ulcerative colitis patients with and without primary sclerosing cholangitis
    Genes Immun, 8 (3), 275-8
    DOI 10.1038/sj.gene.6364377, PubMed 17301827
  7. Lie BA, Dupuy BM, Spurkland A, Fernández-Viña MA, Hagelberg E, Thorsby E (2007)
    Molecular genetic studies of natives on Easter Island: evidence of an early European and Amerindian contribution to the Polynesian gene pool
    Tissue Antigens, 69 (1), 10-8
    DOI 10.1111/j.1399-0039.2006.00717.x, PubMed 17212703
  8. 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
  9. Lie BA, Viken MK, Odegård S, van der Heijde D, Landewé R, Uhlig T, Kvien TK (2007)
    Associations between the PTPN22 1858C->T polymorphism and radiographic joint destruction in patients with rheumatoid arthritis: results from a 10-year longitudinal study
    Ann Rheum Dis, 66 (12), 1604-9
    DOI 10.1136/ard.2006.067892, PubMed 17472988
  10. Lindner E, Nordang GB, Melum E, Flatø B, Selvaag AM, Thorsby E, Kvien TK, Førre OT, Lie BA (2007)
    Lack of association between the chemokine receptor 5 polymorphism CCR5delta32 in rheumatoid arthritis and juvenile idiopathic arthritis
    BMC Med Genet, 8, 33
    DOI 10.1186/1471-2350-8-33, PubMed 17565662
  11. Smestad C, Brynedal B, Jonasdottir G, Lorentzen AR, Masterman T, Akesson E, Spurkland A, Lie BA, Palmgren J, Celius EG, Hillert J, Harbo HF (2007)
    The impact of HLA-A and -DRB1 on age at onset, disease course and severity in Scandinavian multiple sclerosis patients
    Eur J Neurol, 14 (8), 835-40
    DOI 10.1111/j.1468-1331.2007.01825.x, PubMed 17662002
  12. Viken MK, Olsson M, Flåm ST, Førre O, Kvien TK, Thorsby E, Lie BA (2007)
    The PTPN22 promoter polymorphism -1123G>C association cannot be distinguished from the 1858C>T association in a Norwegian rheumatoid arthritis material
    Tissue Antigens, 70 (3), 190-7
    DOI 10.1111/j.1399-0039.2007.00871.x, PubMed 17661906
  13. 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
  14. Wiencke K, Karlsen TH, Boberg KM, Thorsby E, Schrumpf E, Lie BA, Spurkland A (2007)
    Primary sclerosing cholangitis is associated with extended HLA-DR3 and HLA-DR6 haplotypes
    Tissue Antigens, 69 (2), 161-9
    DOI 10.1111/j.1399-0039.2006.00738.x, PubMed 17257319

Publications 2006

  1. Amundsen SS, Monsuur AJ, Wapenaar MC, Lie BA, Ek J, Gudjónsdóttir AH, Ascher H, Wijmenga C, Sollid LM (2006)
    Association analysis of MYO9B gene polymorphisms with celiac disease in a Swedish/Norwegian cohort
    Hum Immunol, 67 (4-5), 341-5
    DOI 10.1016/j.humimm.2006.03.020, PubMed 16720215
  2. Amundsen SS, Vatn M, IBSEN study group, Wijmenga C, Sollid LM, Lie BA (2006)
    Association analysis of MYO9B gene polymorphisms and inflammatory bowel disease in a Norwegian cohort
    Tissue Antigens, 68 (3), 249-52
    DOI 10.1111/j.1399-0039.2006.00665.x, PubMed 16948647
  3. 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
  4. 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
  5. Bowlus CL, Karlsen TH, Broomé U, Thorsby E, Vatn M, Schrumpf E, Lie BA, Boberg KM (2006)
    Analysis of MAdCAM-1 and ICAM-1 polymorphisms in 365 Scandinavian patients with primary sclerosing cholangitis
    J Hepatol, 45 (5), 704-10
    DOI 10.1016/j.jhep.2006.03.012, PubMed 16750586
  6. Karlsen TH, Hampe J, Wiencke K, Schrumpf E, Thorsby E, Lie BA, Broomé U, Schreiber S, Boberg KM (2006)
    Genetic polymorphisms associated with inflammatory bowel disease do not confer risk for primary sclerosing cholangitis
    Am J Gastroenterol, 102 (1), 115-21
    DOI 10.1111/j.1572-0241.2006.00928.x, PubMed 17100974
  7. Karlsen TH, Lie BA, Frey Frøslie K, Thorsby E, Broomé U, Schrumpf E, Boberg KM (2006)
    Polymorphisms in the steroid and xenobiotic receptor gene influence survival in primary sclerosing cholangitis
    Gastroenterology, 131 (3), 781-7
    DOI 10.1053/j.gastro.2006.05.057, PubMed 16952547
  8. Melum E, Karlsen TH, Broomé U, Thorsby E, Schrumpf E, Boberg KM, Lie BA (2006)
    The 32-base pair deletion of the chemokine receptor 5 gene (CCR5-Delta32) is not associated with primary sclerosing cholangitis in 363 Scandinavian patients
    Tissue Antigens, 68 (1), 78-81
    DOI 10.1111/j.1399-0039.2006.00604.x, PubMed 16774544

Publications 2005

  1. 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
  2. Lie BA, Thorsby E (2005)
    Several genes in the extended human MHC contribute to predisposition to autoimmune diseases
    Curr Opin Immunol, 17 (5), 526-31
    DOI 10.1016/j.coi.2005.07.001, PubMed 16054351
  3. Lorentzen AR, Celius EG, Ekstrøm PO, Wiencke K, Lie BA, Myhr KM, Ling V, Thorsby E, Vartdal F, Spurkland A, Harbo HF (2005)
    Lack of association with the CD28/CTLA4/ICOS gene region among Norwegian multiple sclerosis patients
    J Neuroimmunol, 166 (1-2), 197-201
    DOI 10.1016/j.jneuroim.2005.06.002, PubMed 16005527
  4. Smerdel-Ramoya A, Finholt C, Lilleby V, Gilboe IM, Harbo HF, Maslinski S, Førre Ø, Thorsby E, Lie BA (2005)
    Systemic lupus erythematosus and the extended major histocompatibility complex--evidence for several predisposing loci
    Rheumatology (Oxford), 44 (11), 1368-73
    DOI 10.1093/rheumatology/kei015, PubMed 16174649
  5. Sollid LM, Lie BA (2005)
    Celiac disease genetics: current concepts and practical applications
    Clin Gastroenterol Hepatol, 3 (9), 843-51
    DOI 10.1053/S1542-3565(05)00532-X, PubMed 16234020
  6. Thorsby E, Lie BA (2005)
    HLA associated genetic predisposition to autoimmune diseases: Genes involved and possible mechanisms
    Transpl Immunol, 14 (3-4), 175-82
    DOI 10.1016/j.trim.2005.03.021, PubMed 15982560
  7. Viken MK, Amundsen SS, Kvien TK, Boberg KM, Gilboe IM, Lilleby V, Sollid LM, Førre OT, Thorsby E, Smerdel A, Lie BA (2005)
    Association analysis of the 1858C>T polymorphism in the PTPN22 gene in juvenile idiopathic arthritis and other autoimmune diseases
    Genes Immun, 6 (3), 271-3
    DOI 10.1038/sj.gene.6364178, PubMed 15759012

Publications 2004

  1. Amundsen SS, Naluai AT, Ascher H, Ek J, Gudjónsdóttir AH, Wahlström J, Lie BA, Sollid LM (2004)
    Genetic analysis of the CD28/CTLA4/ICOS (CELIAC3) region in coeliac disease
    Tissue Antigens, 64 (5), 593-9
    DOI 10.1111/j.1399-0039.2004.00312.x, PubMed 15496203
  2. 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
  3. Harbo HF, Lie BA, Sawcer S, Celius EG, Dai KZ, Oturai A, Hillert J, Lorentzen AR, Laaksonen M, Myhr KM, Ryder LP, Fredrikson S, Nyland H, Sørensen PS, Sandberg-Wollheim M, Andersen O, Svejgaard A, Edland A, Mellgren SI, Compston A, Vartdal F, Spurkland A (2004)
    Genes in the HLA class I region may contribute to the HLA class II-associated genetic susceptibility to multiple sclerosis
    Tissue Antigens, 63 (3), 237-47
    DOI 10.1111/j.0001-2815.2004.00173.x, PubMed 14989713
  4. 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
  5. 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

Publications 2003

  1. Bowlus CL, Lie BA (2003)
    Discussion of the role of hemochromatosis susceptibility gene mutation in protecting against iron deficiency in celiac disease
    Gastroenterology, 124 (5), 1562-3; author reply 1564
    DOI 10.1016/S0016-5085(03)00354-8, PubMed 12744238
  2. Etokebe GE, Opsahl M, Tveter AK, Lie BA, Thorsby E, Vartdal F, Spurkland A (2003)
    Physical separation of HLA-A alleles by denaturing high-performance liquid chromatography
    Tissue Antigens, 61 (6), 443-50
    DOI 10.1034/j.1399-0039.2003.00058.x, PubMed 12823768
  3. 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
  4. 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
  5. 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
  6. Louka AS, Lie BA, Talseth B, Ascher H, Ek J, Gudjónsdóttir AH, Sollid LM (2003)
    Coeliac disease patients carry conserved HLA-DR3-DQ2 haplotypes revealed by association of TNF alleles
    Immunogenetics, 55 (5), 339-43
    DOI 10.1007/s00251-003-0586-5, PubMed 12845502
  7. 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
  8. Twells RC, Mein CA, Phillips MS, Hess JF, Veijola R, Gilbey M, Bright M, Metzker M, Lie BA, Kingsnorth A, Gregory E, Nakagawa Y, Snook H, Wang WY, Masters J, Johnson G, Eaves I, Howson JM, Clayton D, Cordell HJ, Nutland S, Rance H, Carr P, Todd JA (2003)
    Haplotype structure, LD blocks, and uneven recombination within the LRP5 gene
    Genome Res, 13 (5), 845-55
    DOI 10.1101/gr.563703, PubMed 12727905

Publications 2002

  1. 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
  2. Louka AS, Nilsson S, Olsson M, Talseth B, Lie BA, Ek J, Gudjónsdóttir AH, Ascher H, Sollid LM (2002)
    HLA in coeliac disease families: a novel test of risk modification by the 'other' haplotype when at least one DQA1*05-DQB1*02 haplotype is carried
    Tissue Antigens, 60 (2), 147-54
    DOI 10.1034/j.1399-0039.2002.600205.x, PubMed 12392509
  3. 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

  1. 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
  2. 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

Publications 2000

  1. 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
  2. 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

Publications 1999

  1. 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
  2. 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
  3. 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 1997

  1. 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

Publications 1996

  1. Jacobsen T, Lie BA, Lysvand H, Wiig M, Pettersen HB, Iversen OJ (1996)
    Detection of psoriasis-associated antigen pso p27 in sarcoidosis bronchoalveolar lavage fluid using monoclonal antibodies
    Clin Immunol Immunopathol, 81 (1), 82-7
    DOI 10.1006/clin.1996.0161, PubMed 8808646

Publications 1995

  1. Iversen OJ, Lysvand H, Jacobsen T, Bergh K, Lie BA (1995)
    The psoriasis-associated antigen, pso p27, is expressed by tryptase-positive cells in psoriatic lesions
    Arch Dermatol Res, 287 (5), 503-5
    DOI 10.1007/BF00373437, PubMed 7625863