{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,15]],"date-time":"2026-01-15T03:00:23Z","timestamp":1768446023510,"version":"3.49.0"},"reference-count":19,"publisher":"Elsevier BV","issue":"8","license":[{"start":{"date-parts":[[2018,8,1]],"date-time":"2018-08-01T00:00:00Z","timestamp":1533081600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2019,8,1]],"date-time":"2019-08-01T00:00:00Z","timestamp":1564617600000},"content-version":"vor","delay-in-days":365,"URL":"http:\/\/www.elsevier.com\/open-access\/userlicense\/1.0\/"}],"funder":[{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"crossref","award":["R01 AR056292"],"award-info":[{"award-number":["R01 AR056292"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"crossref","award":["AR057212"],"award-info":[{"award-number":["AR057212"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"crossref"}]}],"content-domain":{"domain":["jidonline.org","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of Investigative Dermatology"],"published-print":{"date-parts":[[2018,8]]},"DOI":"10.1016\/j.jid.2018.02.025","type":"journal-article","created":{"date-parts":[[2018,3,2]],"date-time":"2018-03-02T13:19:11Z","timestamp":1519996751000},"page":"1884-1886","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":13,"title":["Genome-Wide Association of PVT1 with\u00a0Vitiligo"],"prefix":"10.1016","volume":"138","author":[{"given":"Songtao","family":"Ben","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ying","family":"Jin","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Stephanie A.","family":"Santorico","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Richard A.","family":"Spritz","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.jid.2018.02.025_bib1","doi-asserted-by":"crossref","first-page":"68","DOI":"10.1038\/nature15393","article-title":"A\u00a0global reference for human genetic variation","volume":"526","author":"Auton","year":"2015","journal-title":"Nature"},{"key":"10.1016\/j.jid.2018.02.025_bib2","doi-asserted-by":"crossref","first-page":"511","DOI":"10.1002\/jcp.21133","article-title":"The PVT-1 oncogene is a Myc protein target that is overexpressed in transformed cells","volume":"213","author":"Carramusa","year":"2007","journal-title":"J\u00a0Cell Physiol"},{"key":"10.1016\/j.jid.2018.02.025_bib3","doi-asserted-by":"crossref","first-page":"317","DOI":"10.2217\/epi.12.18","article-title":"The NIH Roadmap Epigenomics Program data resource","volume":"4","author":"Chadwick","year":"2012","journal-title":"Epigenomics"},{"key":"10.1016\/j.jid.2018.02.025_bib4","doi-asserted-by":"crossref","first-page":"304208","DOI":"10.1155\/2015\/304208","article-title":"PVT1: a rising star among oncogenic long noncoding RNAs","volume":"2015","author":"Colombo","year":"2015","journal-title":"Biomed Res Int"},{"key":"10.1016\/j.jid.2018.02.025_bib5","doi-asserted-by":"crossref","first-page":"675","DOI":"10.1002\/j.1460-2075.1985.tb03682.x","article-title":"Variant (6;15) translocations in murine plasmacytomas involve a chromosome 15 locus at least 72 kb from the c-myc oncogene","volume":"4","author":"Cory","year":"1985","journal-title":"EMBO J"},{"key":"10.1016\/j.jid.2018.02.025_bib6","doi-asserted-by":"crossref","first-page":"10","DOI":"10.1016\/j.bbrc.2015.12.101","article-title":"Long non-coding RNA PVT1 and cancer","volume":"471","author":"Cui","year":"2016","journal-title":"Biochem Biophys Res Commun"},{"key":"10.1016\/j.jid.2018.02.025_bib7","doi-asserted-by":"crossref","first-page":"57","DOI":"10.1038\/nature11247","article-title":"An integrated encyclopedia of DNA elements in the human genome","volume":"489","year":"2012","journal-title":"Nature"},{"key":"10.1016\/j.jid.2018.02.025_bib8","doi-asserted-by":"crossref","first-page":"2845","DOI":"10.1002\/j.1460-2075.1986.tb04578.x","article-title":"Chromosome 8 breakpoint far 3\u2032 of the c-myc oncogene in a Burkitt's lymphoma 2;8 variant translocation is equivalent to the murine pvt-1 locus","volume":"5","author":"Graham","year":"1986","journal-title":"EMBO J"},{"key":"10.1016\/j.jid.2018.02.025_bib9","doi-asserted-by":"crossref","first-page":"69","DOI":"10.3389\/fgene.2012.00069","article-title":"The 8q24 gene desert: an oasis of non-coding transcriptional activity","volume":"3","author":"Huppi","year":"2012","journal-title":"Front Genet"},{"key":"10.1016\/j.jid.2018.02.025_bib10","doi-asserted-by":"crossref","first-page":"1418","DOI":"10.1038\/ng.3680","article-title":"Genome-wide association studies of autoimmune vitiligo identify 23 new risk generalized loci and highlight key pathways and regulatory variants","volume":"48","author":"Jin","year":"2016","journal-title":"Nat Genet"},{"key":"10.1016\/j.jid.2018.02.025_bib11","doi-asserted-by":"crossref","first-page":"1686","DOI":"10.1056\/NEJMoa0908547","article-title":"Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo","volume":"362","author":"Jin","year":"2010","journal-title":"N\u00a0Engl J Med"},{"key":"10.1016\/j.jid.2018.02.025_bib12","doi-asserted-by":"crossref","first-page":"576","DOI":"10.1038\/ng.602","article-title":"Common variants in FOXP1 are associated with generalized vitiligo","volume":"42","author":"Jin","year":"2010","journal-title":"Nat Genet"},{"key":"10.1016\/j.jid.2018.02.025_bib13","doi-asserted-by":"crossref","first-page":"676","DOI":"10.1038\/ng.2272","article-title":"Genome-wide association analyses identify 13 new susceptibility loci for vitiligo","volume":"44","author":"Jin","year":"2012","journal-title":"Nat Genet"},{"key":"10.1016\/j.jid.2018.02.025_bib14","series-title":"Vitiligo","author":"Picardo","year":"2018"},{"key":"10.1016\/j.jid.2018.02.025_bib15","doi-asserted-by":"crossref","first-page":"245","DOI":"10.1016\/j.det.2016.11.013","article-title":"Genetics of vitiligo","volume":"35","author":"Spritz","year":"2017","journal-title":"Dermatol Clin"},{"key":"10.1016\/j.jid.2018.02.025_bib16","doi-asserted-by":"crossref","first-page":"e974467","DOI":"10.4161\/23723556.2014.974467","article-title":"The PVT1-MYC duet in cancer","volume":"2","author":"Tseng","year":"2015","journal-title":"Mol Cell Oncol"},{"key":"10.1016\/j.jid.2018.02.025_bib17","doi-asserted-by":"crossref","first-page":"1834","DOI":"10.1128\/MCB.6.5.1834","article-title":"Proviral integration site Mis-1 in rat thymomas corresponds to the pvt-1 translocation breakpoint in murine plasmacytomas","volume":"6","author":"Villeneuve","year":"1986","journal-title":"Mol Cell Biol"},{"key":"10.1016\/j.jid.2018.02.025_bib18","doi-asserted-by":"crossref","first-page":"D930","DOI":"10.1093\/nar\/gkr917","article-title":"HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants","volume":"40","author":"Ward","year":"2012","journal-title":"Nucleic Acids Res"},{"key":"10.1016\/j.jid.2018.02.025_bib19","doi-asserted-by":"crossref","first-page":"713","DOI":"10.1038\/nature08979","article-title":"Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls","volume":"464","author":"Craddock","year":"2010","journal-title":"Nature"}],"container-title":["Journal of Investigative Dermatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022202X18301519?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022202X18301519?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,7,31]],"date-time":"2019-07-31T21:24:43Z","timestamp":1564608283000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0022202X18301519"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,8]]},"references-count":19,"journal-issue":{"issue":"8","published-print":{"date-parts":[[2018,8]]}},"alternative-id":["S0022202X18301519"],"URL":"https:\/\/doi.org\/10.1016\/j.jid.2018.02.025","relation":{},"ISSN":["0022-202X"],"issn-type":[{"value":"0022-202X","type":"print"}],"subject":[],"published":{"date-parts":[[2018,8]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Genome-Wide Association of PVT1 with\u00a0Vitiligo","name":"articletitle","label":"Article Title"},{"value":"Journal of Investigative Dermatology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jid.2018.02.025","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2018 The Authors. Published by Elsevier, Inc. on behalf of the Society for Investigative Dermatology.","name":"copyright","label":"Copyright"}]}}