Publications by Steffan Daniël Bos
41 publications found
Original articles
Serum neurofilament light chain associates with symptom burden in Lyme neuroborreliosis patients: a longitudinal cohort study from Norway
J Neurol (in press)
DOI 10.1007/s00415-024-12237-z, PubMed 38407594
Multiscale networks in multiple sclerosis
PLoS Comput Biol, 20 (2), e1010980
DOI 10.1371/journal.pcbi.1010980, PubMed 38329927
Predicting disease severity in multiple sclerosis using multimodal data and machine learning
J Neurol, 271 (3), 1133-1149
DOI 10.1007/s00415-023-12132-z, PubMed 38133801
Quantitative proteomics reveals protein dysregulation during T cell activation in multiple sclerosis patients compared to healthy controls
Clin Proteomics, 19 (1), 23
DOI 10.1186/s12014-022-09361-1, PubMed 35790914
Serum neurofilament light chain concentration predicts disease worsening in multiple sclerosis
Mult Scler, 28 (12), 1859-1870
DOI 10.1177/13524585221097296, PubMed 35658739
Brain disconnectome mapping derived from white matter lesions and serum neurofilament light levels in multiple sclerosis: A longitudinal multicenter study
Neuroimage Clin, 35, 103099
DOI 10.1016/j.nicl.2022.103099, PubMed 35772194
Exploring the role of the multiple sclerosis susceptibility gene CLEC16A in T cells
Scand J Immunol, 94 (1), e13050
DOI 10.1111/sji.13050, PubMed 34643957
Pregnancy does not modify the risk of MS in genetically susceptible women
Neurol Neuroimmunol Neuroinflamm, 7 (6)
DOI 10.1212/NXI.0000000000000898, PubMed 33037103
No differential gene expression for CD4+ T cells of MS patients and healthy controls
Mult Scler J Exp Transl Clin, 5 (2), 2055217319856903
DOI 10.1177/2055217319856903, PubMed 31223483
Quantitative proteomic analyses of CD4+ and CD8+ T cells reveal differentially expressed proteins in multiple sclerosis patients and healthy controls
Clin Proteomics, 16, 19
DOI 10.1186/s12014-019-9241-5, PubMed 31080378
Increased DNA methylation of SLFN12 in CD4+ and CD8+ T cells from multiple sclerosis patients
PLoS One, 13 (10), e0206511
DOI 10.1371/journal.pone.0206511, PubMed 30379917
SVM-based Tool to Detect Patients with Multiple Sclerosis Using a Commercial EMG Sensor
PR IEEE SEN ARRAY, 376-379
Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations
NPJ Genom Med, 2, 24
DOI 10.1038/s41525-017-0027-2, PubMed 29263835
Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies
Neurol Genet, 2 (4), e87
DOI 10.1212/NXG.0000000000000087, PubMed 27540591
Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies
Neurol.-Genet., 2 (4), eB7
DOI 10.1212/NXG.00000000000000B7
Allelic imbalance of multiple sclerosis susceptibility genes IKZF3 and IQGAP1 in human peripheral blood
BMC Genet, 17, 59
DOI 10.1186/s12863-016-0367-4, PubMed 27080863
Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors
Mult Scler, 22 (14), 1783-1793
DOI 10.1177/1352458516635873, PubMed 26920376
Assessing the Power of Exome Chips
PLoS One, 10 (10), e0139642
DOI 10.1371/journal.pone.0139642, PubMed 26437075
Multiple Sclerosis Risk Allele in CLEC16A Acts as an Expression Quantitative Trait Locus for CLEC16A and SOCS1 in CD4+ T Cells
PLoS One, 10 (7), e0132957
DOI 10.1371/journal.pone.0132957, PubMed 26203907
Transcriptional associations of osteoarthritis-mediated loss of epigenetic control in articular cartilage
Arthritis Rheumatol, 67 (8), 2108-16
DOI 10.1002/art.39162, PubMed 25892573
Genome-wide DNA methylation profiles indicate CD8+ T cell hypermethylation in multiple sclerosis
PLoS One, 10 (3), e0117403
DOI 10.1371/journal.pone.0117403, PubMed 25734800
Genetic variants are major determinants of CSF antibody levels in multiple sclerosis
Brain, 138 (Pt 3), 632-43
DOI 10.1093/brain/awu405, PubMed 25616667
Retinoic acid enhances the levels of IL-10 in TLR-stimulated B cells from patients with relapsing-remitting multiple sclerosis
J Neuroimmunol, 278, 11-8
DOI 10.1016/j.jneuroim.2014.11.019, PubMed 25595247
Genes involved in the osteoarthritis process identified through genome wide expression analysis in articular cartilage; the RAAK study
PLoS One, 9 (7), e103056
DOI 10.1371/journal.pone.0103056, PubMed 25054223
A gain of function mutation in TNFRSF11B encoding osteoprotegerin causes osteoarthritis with chondrocalcinosis
Ann Rheum Dis, 74 (9), 1756-62
DOI 10.1136/annrheumdis-2013-205149, PubMed 24743232
Underlying molecular mechanisms of DIO2 susceptibility in symptomatic osteoarthritis
Ann Rheum Dis, 74 (8), 1571-9
DOI 10.1136/annrheumdis-2013-204739, PubMed 24695009
Oligoclonal bands and age at onset correlate with genetic risk score in multiple sclerosis
Mult Scler, 20 (6), 660-8
DOI 10.1177/1352458513506503, PubMed 24099750
GREM1, FRZB and DKK1 mRNA levels correlate with osteoarthritis and are regulated by osteoarthritis-associated factors
Arthritis Res Ther, 15 (5), R126
DOI 10.1186/ar4306, PubMed 24286177
Identification and systematic annotation of tissue-specific differentially methylated regions using the Illumina 450k array
Epigenetics Chromatin, 6 (1), 26
DOI 10.1186/1756-8935-6-26, PubMed 23919675
Genes expressed in blood link osteoarthritis with apoptotic pathways
Ann Rheum Dis, 73 (10), 1844-53
DOI 10.1136/annrheumdis-2013-203405, PubMed 23864235
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function
PLoS Genet, 9 (2), e1003266
DOI 10.1371/journal.pgen.1003266, PubMed 23408906
Metabolic health in families enriched for longevity is associated with low prevalence of hand osteoarthritis and influences OA biomarker profiles
Ann Rheum Dis, 72 (10), 1669-74
DOI 10.1136/annrheumdis-2012-202013, PubMed 23104762
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study
Lancet, 380 (9844), 815-23
DOI 10.1016/S0140-6736(12)60681-3, PubMed 22763110
Increased type II deiodinase protein in OA-affected cartilage and allelic imbalance of OA risk polymorphism rs225014 at DIO2 in human OA joint tissues
Ann Rheum Dis, 71 (7), 1254-8
DOI 10.1136/annrheumdis-2011-200981, PubMed 22492780
Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22
Ann Rheum Dis, 70 (2), 349-55
DOI 10.1136/ard.2010.132787, PubMed 21068099
Meta-analyses of genes modulating intracellular T3 bio-availability reveal a possible role for the DIO3 gene in osteoarthritis susceptibility
Ann Rheum Dis, 70 (1), 164-7
DOI 10.1136/ard.2010.133660, PubMed 20724312
A genome-wide linkage scan reveals CD53 as an important regulator of innate TNF-alpha levels
Eur J Hum Genet, 18 (8), 953-9
DOI 10.1038/ejhg.2010.52, PubMed 20407468
Interleukin-1 gene cluster variants with innate cytokine production profiles and osteoarthritis in subjects from the Genetics, Osteoarthritis and Progression Study
Arthritis Rheum, 62 (4), 1119-26
DOI 10.1002/art.27325, PubMed 20131253
Incidence of gastrointestinal stromal tumours is underestimated: results of a nation-wide study
Eur J Cancer, 41 (18), 2868-72
DOI 10.1016/j.ejca.2005.09.009, PubMed 16293410
Review articles
A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip
Ann Rheum Dis, 73 (12), 2130-6
DOI 10.1136/annrheumdis-2012-203114, PubMed 23989986
New insights into osteoarthritis: early developmental features of an ageing-related disease
Curr Opin Rheumatol, 20 (5), 553-9
DOI 10.1097/BOR.0b013e32830aba48, PubMed 18698177