Publications by Marte Kathrine Viken
56 publications found
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 Killer cell immunoglobulin-like receptor (KIR) alleles suggested to be associated with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)
 Brain Behav Immun, 130, 106098
 DOI 10.1016/j.bbi.2025.106098, PubMed 40897283
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 Foetal Microchimerism Correlates With Foetal-Maternal Histocompatibility Both During Pregnancy and Postpartum
 HLA, 104 (4), e15717
 DOI 10.1111/tan.15717, PubMed 39435899
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 HLA-DQ2 is associated with anti-drug antibody formation to infliximab in patients with immune-mediated inflammatory diseases
 J Intern Med, 293 (5), 648-655
 DOI 10.1111/joim.13616, PubMed 36843323
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 Increased muscle activity during sleep and more RBD symptoms in H1N1-(Pandemrix)-vaccinated narcolepsy type 1 patients compared with their non-narcoleptic siblings
 Sleep, 46 (3)
 DOI 10.1093/sleep/zsac316, PubMed 36562330
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 No replication of previously reported association with genetic variants in the T cell receptor alpha (TRA) locus for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)
 Transl Psychiatry, 12 (1), 277
 DOI 10.1038/s41398-022-02046-1, PubMed 35821115
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 Genetic association study in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) identifies several potential risk loci
 Brain Behav Immun, 102, 362-369
 DOI 10.1016/j.bbi.2022.03.010, PubMed 35318112
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 Allele imputation for the killer cell immunoglobulin-like receptor KIR3DL1/S1
 PLoS Comput Biol, 18 (2), e1009059
 DOI 10.1371/journal.pcbi.1009059, PubMed 35192601
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 Fine mapping of the HLA locus in Parkinson's disease in Europeans
 NPJ Parkinsons Dis, 7 (1), 84
 DOI 10.1038/s41531-021-00231-5, PubMed 34548497
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 Fine mapping of the major histocompatibility complex (MHC) in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) suggests involvement of both HLA class I and class II loci
 Brain Behav Immun, 98, 101-109
 DOI 10.1016/j.bbi.2021.08.219, PubMed 34403736
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 Narcolepsy type 1 patients have lower levels of effector memory CD4+ T cells compared to their siblings when controlling for H1N1-(Pandemrix™)-vaccination and HLA DQB1∗06:02 status
 Sleep Med, 85, 271-279
 DOI 10.1016/j.sleep.2021.07.024, PubMed 34388506
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 HLA-B*27 typing using a triplex real time PCR in routine laboratory
 HLA, 98 (4), 366-369
 DOI 10.1111/tan.14386, PubMed 34342381
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 High nocturnal sleep fragmentation is associated with low T lymphocyte P2Y11 protein levels in narcolepsy type 1
 Sleep, 44 (8)
 DOI 10.1093/sleep/zsab062, PubMed 33710305
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 Maternal Microchimerism in Cord Blood and Risk of Celiac Disease in Childhood
 J Pediatr Gastroenterol Nutr, 71 (3), 321-327
 DOI 10.1097/MPG.0000000000002811, PubMed 32833392
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 Intravenous Cyclophosphamide in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome. An Open-Label Phase II Study
 Front Med (Lausanne), 7, 162
 DOI 10.3389/fmed.2020.00162, PubMed 32411717
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 Human Leukocyte Antigen alleles associated with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
 Sci Rep, 10 (1), 5267
 DOI 10.1038/s41598-020-62157-x, PubMed 32210306
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 HLA and sleep parameter associations in post-H1N1 narcolepsy type 1 patients and first-degree relatives
 Sleep, 43 (3)
 DOI 10.1093/sleep/zsz239, PubMed 31606740
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 Maternal microchimerism in cord blood and risk of childhood-onset type 1 diabetes
 Pediatr Diabetes, 20 (6), 728-735
 DOI 10.1111/pedi.12875, PubMed 31173445
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 The novel HLA-A*01 variant, HLA-A*01:308N, detected by sequencing-based typing
 HLA, 94 (3), 312
 DOI 10.1111/tan.13606, PubMed 31144452
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 The novel HLA-A*03 variant, HLA-A*03:08:01:02, detected by sequencing-based typing
 HLA, 94 (1), 60-61
 DOI 10.1111/tan.13549, PubMed 30977308
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 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
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 Prenatal iron exposure and childhood type 1 diabetes
 Sci Rep, 8 (1), 9067
 DOI 10.1038/s41598-018-27391-4, PubMed 29899542
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 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
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 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
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 Plasma immunological markers in pregnancy and cord blood: A possible link between macrophage chemo-attractants and risk of childhood type 1 diabetes
 Am J Reprod Immunol, 79 (3)
 DOI 10.1111/aji.12802, PubMed 29266506
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 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
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 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
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 Unraveling the role of maternal anti-HLA class I antibodies in fetal and neonatal thrombocytopenia-Antibody specificity analysis using epitope data
 J Reprod Immunol, 122, 1-9
 DOI 10.1016/j.jri.2017.06.003, PubMed 28686909
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 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
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 Midpregnancy and cord blood immunologic biomarkers, HLA genotype, and pediatric celiac disease
 J Allergy Clin Immunol, 139 (5), 1696-1698
 DOI 10.1016/j.jaci.2016.10.016, PubMed 27865861
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 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
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 A Longitudinal Follow-up of Autoimmune Polyendocrine Syndrome Type 1
 J Clin Endocrinol Metab, 101 (8), 2975-83
 DOI 10.1210/jc.2016-1821, PubMed 27253668
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 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
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 High-throughput T-cell receptor sequencing across chronic liver diseases reveals distinct disease-associated repertoires
 Hepatology, 63 (5), 1608-19
 DOI 10.1002/hep.28116, PubMed 26257205
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 Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases
 Immunity, 42 (6), 1185-96
 DOI 10.1016/j.immuni.2015.04.021, PubMed 26084028
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 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
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 Resolution of HLA-B*44:02:01G, -DRB1*14:01:01G and -DQB1*03:01:01G reveals a high allelic variability among 12 European populations
 Tissue Antigens, 84 (5), 459-64
 DOI 10.1111/tan.12422, PubMed 25209151
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 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
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 Coeliac disease-associated polymorphisms influence thymic gene expression
 Genes Immun, 15 (6), 355-60
 DOI 10.1038/gene.2014.26, PubMed 24871462
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 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
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 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
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 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
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 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
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 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
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 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
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 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
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 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
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 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
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 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
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 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
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 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
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 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
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 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
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 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
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 ABI3 mediates expression of the peroxiredoxin antioxidant AtPER1 gene and induction by oxidative stress
 Plant Mol Biol, 53 (3), 313-26
 DOI 10.1023/b:plan.0000006937.21343.2a, PubMed 14750521
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 Seed 1-cysteine peroxiredoxin antioxidants are not involved in dormancy, but contribute to inhibition of germination during stress
 Plant Physiol, 133 (3), 1148-57
 DOI 10.1104/pp.103.025916, PubMed 14526116
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 OBITUARY Erik Thorsby (1938-2021)
 HLA, 98 (1), 3-4
 DOI 10.1111/tan.14290
