| P50 | author | Hanne F Harbo | Q90089338 |
| P2093 | author name string | Tone Berge | |
| | Ingvild Sørum Leikfoss | |
| P2860 | cites work | Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS | Q21563317 |
| | APCs express DCIR, a novel C-type lectin surface receptor containing an immunoreceptor tyrosine-based inhibitory motif | Q22003753 |
| | An integrated encyclopedia of DNA elements in the human genome | Q22122150 |
| | Temporal trends in the incidence of multiple sclerosis: a systematic review | Q22241655 |
| | Specific association of a CLEC16A/KIAA0350 polymorphism with NOD2/CARD15(-) Crohn's disease patients | Q24600432 |
| | A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis | Q24609382 |
| | Phospho.ELM: a database of phosphorylation sites--update 2011 | Q24613280 |
| | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis | Q24635370 |
| | The expanding genetic overlap between multiple sclerosis and type I diabetes | Q24642348 |
| | MS prevalence in New Zealand, an ethnically and latitudinally diverse country | Q57231209 |
| | Multiple sclerosis-associated single-nucleotide polymorphisms in CLEC16A correlate with reduced SOCS1 and DEXI expression in the thymus | Q60445325 |
| | Dcir deficiency causes development of autoimmune diseases in mice due to excess expansion of dendritic cells | Q62735693 |
| | HLA-DRB101 subtyping by allele-specific PCR amplification: A sensitive, specific and rapid technique | Q68330025 |
| | Mice lacking the MHC class II transactivator (CIITA) show tissue-specific impairment of MHC class II expression | Q71066478 |
| | Genetic susceptibility to multiple sclerosis: detection of polymorphic nucleotides and an intron in the 3' untranslated region of the major histocompatibility complex class II transactivator gene | Q73734459 |
| | MHC2TA single nucleotide polymorphism and genetic risk for autoimmune adrenal insufficiency | Q79929416 |
| | Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus | Q83000727 |
| | More CLEC16A gene variants associated with multiple sclerosis | Q85044989 |
| | CIITA gene variants are associated with rheumatoid arthritis in Scandinavian populations | Q57224319 |
| | Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants | Q24646663 |
| | The role of the CD58 locus in multiple sclerosis | Q24649291 |
| | Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes | Q24652324 |
| | CDD: specific functional annotation with the Conserved Domain Database | Q24655481 |
| | Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci | Q24656799 |
| | Identification of Rab11 as a small GTPase binding protein for the Evi5 oncogene | Q24670211 |
| | Role of autophagy in immunity and autoimmunity, with a special focus on systemic lupus erythematosus | Q26859557 |
| | Environmental risk factors for multiple sclerosis: a review with a focus on molecular mechanisms | Q27006548 |
| | Haploview: analysis and visualization of LD and haplotype maps | Q27860955 |
| | Multiple sclerosis: a modifying influence of HLA class I genes in an HLA class II associated autoimmune disease | Q28140475 |
| | Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro | Q28242551 |
| | Astrocytes in multiple sclerosis: a product of their environment | Q28282324 |
| | The CD40-autophagy pathway is needed for host protection despite IFN-Γ-dependent immunity and CD40 induces autophagy via control of P21 levels | Q28476673 |
| | MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction | Q28581447 |
| | Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis | Q28943261 |
| | Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis | Q28943369 |
| | Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis | Q28943396 |
| | Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis | Q29417041 |
| | Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci | Q29417047 |
| | Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles | Q29417120 |
| | Multiple sequence alignment using ClustalW and ClustalX | Q29547698 |
| | Risk alleles for multiple sclerosis identified by a genomewide study | Q29614890 |
| | Systematic localization of common disease-associated variation in regulatory DNA | Q29614895 |
| | High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis | Q30419111 |
| | Seven newly identified loci for autoimmune thyroid disease | Q30424090 |
| | HLA-A confers an HLA-DRB1 independent influence on the risk of multiple sclerosis | Q33291761 |
| | Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms | Q33378475 |
| | Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations | Q33549716 |
| | Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci | Q33630669 |
| | Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene | Q33645905 |
| | The novel endosomal membrane protein Ema interacts with the class C Vps-HOPS complex to promote endosomal maturation. | Q33717079 |
| | Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility | Q33790356 |
| | CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis | Q33832877 |
| | Multiple sclerosis susceptibility alleles in African Americans. | Q33892035 |
| | Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals | Q34184766 |
| | Mycobacterial lipoprotein activates autophagy via TLR2/1/CD14 and a functional vitamin D receptor signalling | Q34268455 |
| | The STAT3 beacon: IL-6 recurrently activates STAT 3 from endosomal structures | Q42054710 |
| | Follow-up study of the first genome-wide association scan in alopecia areata: IL13 and KIAA0350 as susceptibility loci supported with genome-wide significance | Q42645680 |
| | Cloning of dexamethasone-induced transcript: a novel glucocorticoid-induced gene that is upregulated in emphysema | Q42655512 |
| | Evaluation of the established non-MHC multiple sclerosis loci in an Indian population | Q43561912 |
| | A cytokine gene screen uncovers SOCS1 as genetic risk factor for multiple sclerosis | Q44596853 |
| | Suppressor of cytokine signaling 1 regulates the immune response to infection by a unique inhibition of type I interferon activity | Q45345628 |
| | Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians | Q46466235 |
| | Genetic association of PRDM1-ATG5 intergenic region and autophagy with systemic lupus erythematosus in a Chinese population | Q46869773 |
| | A role for the membrane Golgi protein Ema in autophagy. | Q52739371 |
| | HL-A antigens and multiple sclerosis. | Q53892212 |
| | Involvement of CLEC16A in activation of astrocytes after LPS treated. | Q54343733 |
| | Genetic variation in the autophagy gene ULK1 and risk of Crohn's disease. | Q55054234 |
| | Variation in interleukin 7 receptor α chain (IL7R) influences risk of multiple sclerosis | Q56681076 |
| | Analysis of the HLA and non-HLA susceptibility loci in Japanese type 1 diabetes | Q56898479 |
| | Age-dependent variation of genotypes in MHC II transactivator gene (CIITA) in controls and association to type 1 diabetes | Q57224275 |
| | Linking disease associations with regulatory information in the human genome | Q34298038 |
| | CD226 Gly307Ser association with multiple autoimmune diseases: a meta-analysis | Q34448788 |
| | The C-type lectin-like domain superfamily | Q34473873 |
| | Splicing in disease: disruption of the splicing code and the decoding machinery | Q34582131 |
| | A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene | Q34651283 |
| | Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis | Q34657157 |
| | When cell biology meets development: endocytic regulation of signaling pathways | Q34671656 |
| | Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency | Q34790983 |
| | Association of type 1 diabetes with two Loci on 12q13 and 16p13 and the influence coexisting thyroid autoimmunity in Japanese | Q34862116 |
| | Variation within the CLEC16A gene shows consistent disease association with both multiple sclerosis and type 1 diabetes in Sardinia. | Q34863892 |
| | Intron polymorphism in the KIAA0350 gene is reproducibly associated with susceptibility to type 1 diabetes (T1D) in the Han Chinese population | Q34932373 |
| | Chromosomal region 16p13: further evidence of increased predisposition to immune diseases. | Q34946418 |
| | Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus. | Q34976409 |
| | Risk alleles for multiple sclerosis in multiplex families. | Q34985640 |
| | Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. | Q34986752 |
| | Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis | Q35008221 |
| | Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex | Q35155990 |
| | Genetic analysis of adult-onset autoimmune diabetes | Q35227229 |
| | Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene | Q35747169 |
| | Divergent roles for C-type lectins expressed by cells of the innate immune system | Q35914429 |
| | SOCS, Inflammation, and Autoimmunity | Q35927538 |
| | Association of primary biliary cirrhosis with variants in the CLEC16A, SOCS1, SPIB and SIAE immunomodulatory genes. | Q35990216 |
| | Mapping complex disease traits with global gene expression | Q35997212 |
| | The rs4774 CIITA missense variant is associated with risk of systemic lupus erythematosus. | Q36070941 |
| | The Correlation between the CLEC16A Gene and Genetic Susceptibility to Type 1 Diabetes in Chinese Children | Q36072137 |
| | MHC II molecules in inflammatory diseases: interplay of qualities and quantities | Q36247807 |
| | C-type lectin receptor-induced NF-κB activation in innate immune and inflammatory responses | Q37728922 |
| | Genome-wide association studies in multiple sclerosis: lessons and future prospects | Q37839499 |
| | Promise and pitfalls of the Immunochip | Q37846258 |
| | Latitude is significantly associated with the prevalence of multiple sclerosis: a meta-analysis | Q37863350 |
| | Systematic review of disease-modifying therapies to assess unmet needs in multiple sclerosis: tolerability and adherence | Q37976344 |
| | The genetics of multiple sclerosis: an up-to-date review | Q38020959 |
| | The centrosome regulates the Rab11- dependent recycling endosome pathway at appendages of the mother centriole. | Q39278282 |
| | Biochemical monitoring of the early endocytic traffic of the type I interferon receptor | Q39760199 |
| | Class II transactivator regulates the expression of multiple genes involved in antigen presentation | Q41944761 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | multiple sclerosis | Q8277 |
| P304 | page(s) | 4476-4497 | |
| P577 | publication date | 2013-02-25 | |
| P1433 | published in | International Journal of Molecular Sciences | Q3153277 |
| P1476 | title | From Identification to Characterization of the Multiple Sclerosis Susceptibility Gene CLEC16A. | |
| P478 | volume | 14 | |