| P50 | author | Maria Swanberg | Q58034743 |
| | Kaisa Ivaska | Q43095042 |
| | Paul Gerdhem | Q43170324 |
| P2093 | author name string | Kristina Åkesson | |
| | Fiona E McGuigan | |
| P2860 | cites work | Genome-wide association with bone mass and geometry in the Framingham Heart Study | Q21093326 |
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| | Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American women | Q24595779 |
| | Specific association of a CLEC16A/KIAA0350 polymorphism with NOD2/CARD15(-) Crohn's disease patients | Q24600432 |
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| | Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males | Q28943355 |
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| | Identification of a gene module associated with BMD through the integration of network analysis and genome-wide association data | Q30450935 |
| | Bone mineral density assessed by quantitative ultrasound and dual energy X-ray absorptiometry. Normative data in Malmö, Sweden | Q32062700 |
| | Polymorphism in the MHC2TA gene is associated with features of the metabolic syndrome and cardiovascular mortality | Q33267324 |
| | New sequence variants in HLA class II/III region associated with susceptibility to knee osteoarthritis identified by genome-wide association study | Q33543752 |
| | HLA-A, B antigens and alpha 1-antitrypsin phenotypes in nodal generalised osteoarthritis and erosive osteoarthritis | Q33561757 |
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| | Genome-wide association meta-analysis of cortical bone mineral density unravels allelic heterogeneity at the RANKL locus and potential pleiotropic effects on bone | Q33761251 |
| | CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis | Q33832877 |
| | Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk | Q33885943 |
| | Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese | Q33900611 |
| | HLA class II association with rheumatoid arthritis: facts and interpretations | Q34132727 |
| | A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene | Q34651283 |
| | Epidemiology and outcomes of osteoporotic fractures | Q34671295 |
| | 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 |
| | Prediction of bone loss using biochemical markers of bone turnover. | Q50802939 |
| | Association of interleukin-6 promoter variant with bone mineral density in pre-menopausal women. | Q53655230 |
| | A functional polymorphic variant in the interleukin-6 gene promoter associated with low bone resorption in postmenopausal women | Q57243105 |
| | Interferon-gamma gene polymorphisms associated with susceptibility to systemic lupus erythematosus | Q57330700 |
| | T-cell-mediated regulation of osteoclastogenesis by signalling cross-talk between RANKL and IFN-γ | Q59064307 |
| | Purification and partial sequence of human osteoclast-activating factor: identity with interleukin 1 beta | Q69872300 |
| | Association of susceptibility to multiple sclerosis in Sweden with HLA class II DRB1 and DQB1 alleles | Q72417150 |
| | A single nucleotide polymorphism in the first intron of the human IFN-gamma gene: absolute correlation with a polymorphic CA microsatellite marker of high IFN-gamma production | Q73128640 |
| | Polymorphisms of the interleukin-6 gene are associated with bone mineral density | Q73488372 |
| | Postmenopausal changes in production of type 1 and type 2 cytokines and the effects of hormone replacement therapy | Q74186553 |
| | Clinical evaluation of the Elecsys beta-CrossLaps serum assay, a new assay for degradation products of type I collagen C-tlopeptides | Q74250206 |
| | Association of the collagen type 1 (COL1A 1) Sp1 binding site polymorphism to femoral neck bone mineral density and wrist fracture in 1044 elderly Swedish women | Q79243370 |
| | Environment-gene interaction in multiple sclerosis: human herpesvirus 6 and MHC2TA | Q80747633 |
| | Variation in the BMP2 gene: bone mineral density and ultrasound in young adult and elderly women | Q80861257 |
| | Serial assessment of serum bone metabolism markers identifies women with the highest rate of bone loss and osteoporosis risk | Q81226222 |
| | Bone turnover markers and prediction of fracture: a prospective follow-up study of 1040 elderly women for a mean of 9 years | Q84979796 |
| | 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 |
| | Signalling through C-type lectin receptors: shaping immune responses | Q34986405 |
| | Biochemical markers of bone turnover part II: clinical applications in the management of osteoporosis | Q35053491 |
| | Polymorphisms in the macrophage migration inhibitory factor gene and bone loss in postmenopausal women. | Q35078681 |
| | Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex | Q35155990 |
| | IL21R and PTH may underlie variation of femoral neck bone mineral density as revealed by a genome-wide association study | Q35156181 |
| | Genome-wide association study for femoral neck bone geometry | Q35156251 |
| | Mixed lymphocyte cultures in rheumatoid arthritis | Q35200536 |
| | Estrogen deficiency induces bone loss by increasing T cell proliferation and lifespan through IFN-gamma-induced class II transactivator. | Q35918333 |
| | The rs4774 CIITA missense variant is associated with risk of systemic lupus erythematosus. | Q36070941 |
| | Vascular calcification and osteoporosis--from clinical observation towards molecular understanding | Q36676122 |
| | Common variants in the region around Osterix are associated with bone mineral density and growth in childhood | Q37147155 |
| | Genome-wide association and follow-up replication studies identified ADAMTS18 and TGFBR3 as bone mass candidate genes in different ethnic groups | Q37156037 |
| | Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study. | Q37185215 |
| | Human genetics of osteoporosis | Q37333057 |
| | Effect of precision on longitudinal follow-up of bone mineral density measurements in elderly women and men. | Q38483721 |
| | Multiple sclerosis risk markers in HLA-DRA, HLA-C, and IFNG genes are associated with sex-specific childhood leukemia risk | Q39633649 |
| | Cardiovascular diseases and future risk of hip fracture in women | Q40214496 |
| | Modulation of gene expression by the MHC class II transactivator | Q40695550 |
| | Presence of oestrogen receptors in human blood mononuclear cells and thymocytes | Q41446896 |
| | Multiple genetic loci for bone mineral density and fractures | Q43870049 |
| | Two promoter polymorphisms regulating interleukin-6 gene expression are associated with circulating levels of C-reactive protein and markers of bone resorption in postmenopausal women | Q44273290 |
| | Rates of fracture in participants and non-participants in the Osteoporosis Prospective Risk Assessment study | Q44626304 |
| | Major histocompatibility complex class II transactivator gene polymorphism: associations with Löfgren's syndrome | Q45203112 |
| | Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians | Q46466235 |
| | A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits | Q47936547 |
| | MHC class II transactivator negatively regulates RANKL-mediated osteoclast differentiation by downregulating NFATc1 and OSCAR. | Q48199749 |
| | Risk factors for fragility fracture in middle age. A prospective population-based study of 33,000 men and women | Q48498089 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 10 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | bone fracture | Q68833 |
| P304 | page(s) | e47964 | |
| P577 | publication date | 2012-10-25 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | Polymorphisms in the inflammatory genes CIITA, CLEC16A and IFNG influence BMD, bone loss and fracture in elderly women | |
| P478 | volume | 7 | |