{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,8]],"date-time":"2026-07-08T05:09:59Z","timestamp":1783487399841,"version":"3.55.0"},"reference-count":40,"publisher":"The Endocrine Society","issue":"12","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2000,12,1]]},"DOI":"10.1210\/jcem.85.12.7038","type":"journal-article","created":{"date-parts":[[2014,1,8]],"date-time":"2014-01-08T17:05:05Z","timestamp":1389200705000},"page":"4639-4643","source":"Crossref","is-referenced-by-count":7,"title":["Vitamin D Receptor Gene Polymorphism Is Associated with Graves\u2019 Disease in the Japanese Population1"],"prefix":"10.1210","volume":"85","author":[{"given":"Yoshiyuki","family":"Ban","sequence":"first","affiliation":[{"name":"Third Department of Internal Medicine, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa, Tokyo 142-8666, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Matsuo","family":"Taniyama","sequence":"additional","affiliation":[{"name":"Third Department of Internal Medicine, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa, Tokyo 142-8666, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yoshio","family":"Ban","sequence":"additional","affiliation":[{"name":"Third Department of Internal Medicine, Showa University School of Medicine, 1-5-8 Hatanodai, Shinagawa, Tokyo 142-8666, Japan"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"80","reference":[{"key":"2019041117525850400_R1","doi-asserted-by":"crossref","first-page":"537","DOI":"10.1210\/edrv-10-4-537","article-title":"The causes of autoimmune thyroid disease.","volume":"10","author":"DeGroot","year":"1989","journal-title":"Endocr Rev"},{"key":"2019041117525850400_R2","author":"Mckenzie","year":"1988"},{"key":"2019041117525850400_R3","author":"Volpe","year":"1991"},{"key":"2019041117525850400_R4","first-page":"1569","article-title":"Human histocompatibility leukocyte antigen DQA1 *0501 allele associated with genetic susceptibility to Graves\u2019 disease in a Caucasian population.","volume":"76","author":"Yanagawa","year":"1993","journal-title":"J Clin Endocrinol Metab"},{"key":"2019041117525850400_R5","first-page":"2112","article-title":"Susceptibility and resistance alleles of human leukocyte antigen (HLA) DQA1 and HLA DQB1 are shared in endocrine autoimmune disease.","volume":"80","author":"Badenhoop","year":"1995","journal-title":"J Clin Endocrinol Metab"},{"key":"2019041117525850400_R6","doi-asserted-by":"crossref","first-page":"1195","DOI":"10.1093\/hmg\/8.7.1195","article-title":"The cytotoxic T lymphocyte antigen-4 is a major Graves\u2019 disease locus.","volume":"8","author":"Vaidya","year":"1999","journal-title":"Hum Mol Genet"},{"key":"2019041117525850400_R7","first-page":"41","article-title":"CTLA-4 gene polymorphism associated with Graves\u2019 disease in a Caucasian population.","volume":"80","author":"Yanagawa","year":"1995","journal-title":"J Clin Endocrinol Metab"},{"key":"2019041117525850400_R8","doi-asserted-by":"crossref","first-page":"1075","DOI":"10.1093\/hmg\/5.7.1075","article-title":"The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes.","volume":"5","author":"Nistico","year":"1996","journal-title":"Hum Mol Genet"},{"key":"2019041117525850400_R9","first-page":"143","article-title":"CTLA-4 alanine-17 confers genetic susceptibility to Graves\u2019 disease and to type 1 diabetes mellitus.","volume":"82","author":"Donner","year":"1997","journal-title":"J Clin Endocrinol Metab"},{"key":"2019041117525850400_R10","doi-asserted-by":"crossref","first-page":"843","DOI":"10.1089\/thy.1997.7.843","article-title":"CTLA-4 gene polymorphism confers susceptibility to Graves\u2019 disease in Japanese.","volume":"7","author":"Yanagawa","year":"1997","journal-title":"Thyroid"},{"key":"2019041117525850400_R11","doi-asserted-by":"crossref","first-page":"475","DOI":"10.1089\/thy.2000.10.475","article-title":"Vitamin D receptor initiation codon polymorphism in Japanese patients with Graves\u2019 disease.","volume":"10","author":"Ban","year":"2000","journal-title":"Thyroid"},{"key":"2019041117525850400_R12","doi-asserted-by":"crossref","first-page":"284","DOI":"10.1038\/367284a0","article-title":"Prediction of bone density from vitamin D receptor alleles.","volume":"367","author":"Morrison","year":"1994","journal-title":"Nature"},{"key":"2019041117525850400_R13","doi-asserted-by":"crossref","first-page":"841","DOI":"10.1016\/0092-8674(95)90200-7","article-title":"The RXR heterodimers and orphan receptors.","volume":"83","author":"Mangelsdolf","year":"1995","journal-title":"Cell"},{"key":"2019041117525850400_R14","doi-asserted-by":"crossref","first-page":"915","DOI":"10.1359\/jbmr.1997.12.6.915","article-title":"A vitamin D receptor gene polymorphism in the translation initiation codon: effect on protein activity and relation to bone mineral density in Japanese women.","volume":"12","author":"Arai","year":"1997","journal-title":"J Bone Miner Res"},{"key":"2019041117525850400_R15","first-page":"1003","volume":"11","author":"Tokita","year":"1996","journal-title":"Vitamin D receptor alleles, bone mineral density and turnover in premenopausal Japanese women J Bone Miner Res"},{"key":"2019041117525850400_R16","first-page":"93","article-title":"Strength of linkage disequilibrium between two vitamin D receptor markers in five ethnic groups: implications for association studies.","volume":"6","author":"Ingles","year":"1997","journal-title":"Cancer Epidemiol Biomarkers Prev"},{"key":"2019041117525850400_R17","doi-asserted-by":"crossref","first-page":"166","DOI":"10.1093\/jnci\/89.2.166","article-title":"Association of prostate cancer risk with genetic polymorphisms in vitamin D receptor and androgen receptor.","volume":"89","author":"Ingles","year":"1997","journal-title":"J Natl Cancer Inst"},{"key":"2019041117525850400_R18","doi-asserted-by":"crossref","first-page":"1850","DOI":"10.1002\/jbmr.5650111204","article-title":"The presence of a polymorphism at the translation initiation site of the vitamin D receptor is associated with low bone mineral density in postmenopausal Mexican-American women.","volume":"11","author":"Gross","year":"1996","journal-title":"J Bone Miner Res"},{"key":"2019041117525850400_R19","doi-asserted-by":"crossref","first-page":"31","DOI":"10.1359\/jbmr.1998.13.1.31","article-title":"Lack of correlation between start codon polymorphism of the vitamin D receptor gene and bone mineral density in premenopausal French women: the OFELY study.","volume":"13","author":"Eccleshall","year":"1998","journal-title":"J Bone Miner Res"},{"key":"2019041117525850400_R20","doi-asserted-by":"crossref","first-page":"1043","DOI":"10.1359\/jbmr.1997.12.7.1043","article-title":"The vitamin D receptor start codon polymorphism (FokI) and bone mineral density in premenopausal American black and white women.","volume":"12","author":"Harris","year":"1997","journal-title":"J Bone Miner Res"},{"key":"2019041117525850400_R21","doi-asserted-by":"crossref","first-page":"1309","DOI":"10.1038\/nm1295-1309","article-title":"Vitamin D receptor genotypes in primary hyperparathyroidism.","volume":"1","author":"Carling","year":"1995","journal-title":"Nat Med"},{"key":"2019041117525850400_R22","first-page":"2255","article-title":"Vitamin D receptor (VDR) and parathyroid hormone mRNA levels correspond to polymorphic VDR alleles in human parathyroid tumors.","volume":"83","author":"Carling","year":"1998","journal-title":"J Clin Endocrinol Metab"},{"key":"2019041117525850400_R23","doi-asserted-by":"crossref","first-page":"971","DOI":"10.1007\/s001250050776","article-title":"Allelic variation in the vitamin D receptor influences susceptibility to IDDM in Indian Asians.","volume":"40","author":"McDermott","year":"1997","journal-title":"Diabetologia"},{"key":"2019041117525850400_R24","doi-asserted-by":"crossref","first-page":"47","DOI":"10.1016\/S0022-510X(99)00112-4","article-title":"Association of vitamin D receptor gene polymorphism with multiple sclerosis in Japanese.","volume":"166","author":"Fukazawa","year":"1999","journal-title":"J Neurol Sci"},{"key":"2019041117525850400_R25","first-page":"251","article-title":"On estimating the relation between blood group and disease.","volume":"19","year":"1995","journal-title":"Ann Hum Genet"},{"key":"2019041117525850400_R26","first-page":"2800","article-title":"Genetic influences on bone density: physiological correlates of vitamin D receptor gene alleles in premenopausal women.","volume":"80","author":"Howard","year":"1995","journal-title":"J Clin Endocrinol Metab"},{"key":"2019041117525850400_R27","doi-asserted-by":"crossref","first-page":"605","DOI":"10.1210\/jcem.77.3.8370683","article-title":"The genetic basis of autoimmune thyroid disease: time to focus on chromosomal loci other than the major histocompatibility complex.","volume":"77","year":"1993","journal-title":"J Clin Endocrinol Metab"},{"key":"2019041117525850400_R28","first-page":"496","article-title":"Genetics of autoimmune thyroid disease: lack of evidence for linkage to HLA within families.","volume":"74","author":"Roman","year":"1992","journal-title":"J Clin Endocrinol Metab"},{"key":"2019041117525850400_R29","doi-asserted-by":"crossref","first-page":"331","DOI":"10.1046\/j.1365-2265.1998.00542.x","article-title":"No evidence for allelic association of human CTLA-4 promoter polymorphism with autoimmune thyroid disease in either population-based case-control or family-based studies.","volume":"49","author":"Heward","year":"1998","journal-title":"Clin Endocrinol (Oxf)"},{"key":"2019041117525850400_R30","doi-asserted-by":"crossref","first-page":"599","DOI":"10.1016\/0960-0760(95)00106-A","article-title":"Immunomodulatory actions of 1,25-dihydroxyvitamin D3.","volume":"53","year":"1995","journal-title":"J Steroid Biochem Mol Biol"},{"key":"2019041117525850400_R31","doi-asserted-by":"crossref","first-page":"383","DOI":"10.1016\/0167-5699(95)80006-9","article-title":"The role of IL-12 in the induction of organ-specific autoimmune diseases.","volume":"16","author":"Trembleau","year":"1995","journal-title":"Immunol Today"},{"key":"2019041117525850400_R32","doi-asserted-by":"crossref","first-page":"1184","DOI":"10.1016\/S0026-0495(97)90214-6","article-title":"Effect of 1\u03b1-hydroxyvitamin D3 on serum levels of thyroid hormones in hyperthyroid patients with untreated Graves\u2019 disease.","volume":"46","author":"Kawakami-Tani","year":"1997","journal-title":"Metabolism"},{"key":"2019041117525850400_R33","doi-asserted-by":"crossref","first-page":"6665","DOI":"10.1073\/pnas.89.15.6665","article-title":"Contribution of trans-acting factor alleles to normal physiological variability: vitamin D receptor gene polymorphism and circulating osteocalcin.","volume":"89","author":"Morrison","year":"1992","journal-title":"Proc Natl Acad Sci USA"},{"key":"2019041117525850400_R34","doi-asserted-by":"crossref","first-page":"1238","DOI":"10.1016\/S0140-6736(95)92019-6","article-title":"Vitamin D receptor genotypes and bone mineral density.","volume":"345","author":"Kroger","year":"1995","journal-title":"Lancet"},{"key":"2019041117525850400_R35","doi-asserted-by":"crossref","first-page":"1027","DOI":"10.1016\/S0140-6736(94)91690-X","article-title":"Vitamin D receptor gene polymorphism and bone mineral density in healthy Japanese women.","volume":"344","author":"Yamagata","year":"1994","journal-title":"Lancet"},{"key":"2019041117525850400_R36","first-page":"4656","article-title":"Mapping the major susceptibility loci for familial Graves\u2019 and Hashimoto\u2019s diseases: evidence for genetic heterogeneity and gene interactions.","volume":"84","author":"Tomer","year":"1999","journal-title":"J Clin Endocrinol Metab"},{"key":"2019041117525850400_R37","first-page":"4321","article-title":"Linkage analysis of candidate genes in autoimmune thyroid disease. III. Detailed analysis of chromosome 14 localizes GD-1 close to MNG-1.","volume":"83","author":"Tomer","year":"1998","journal-title":"J Clin Endocrinol Metab"},{"key":"2019041117525850400_R38","doi-asserted-by":"crossref","first-page":"1749","DOI":"10.1086\/302146","article-title":"A Graves\u2019 disease-susceptibility locus maps to chromosome 20q11.2.","volume":"63","author":"Tomer","year":"1998","journal-title":"Am J Hum Genet"},{"key":"2019041117525850400_R39","first-page":"3290","article-title":"Linkage analysis of candidate genes in autoimmune thyroid disease. II. Selected gender-related genes and the X-chromosome.","volume":"83","author":"Barbesino","year":"1998","journal-title":"J Clin Endocrinol Metab"},{"key":"2019041117525850400_R40","first-page":"1580","article-title":"Linkage analysis of candidate genes in autoimmune thyroid disease. I. Selected immunoregulatory genes.","volume":"83","author":"Barbesino","year":"1998","journal-title":"J Clin Endocrinol Metab"}],"container-title":["The Journal of Clinical Endocrinology &amp; Metabolism"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/academic.oup.com\/jcem\/article-pdf\/85\/12\/4639\/9181830\/jcem4639.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,4,12]],"date-time":"2019-04-12T06:16:47Z","timestamp":1555049807000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/jcem\/article\/85\/12\/4639\/2853972"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2000,12,1]]},"references-count":40,"journal-issue":{"issue":"12","published-print":{"date-parts":[[2000,12,1]]}},"URL":"https:\/\/doi.org\/10.1210\/jcem.85.12.7038","relation":{},"ISSN":["0021-972X","1945-7197"],"issn-type":[{"value":"0021-972X","type":"print"},{"value":"1945-7197","type":"electronic"}],"subject":[],"published":{"date-parts":[[2000,12,1]]}}}