{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T18:39:26Z","timestamp":1786991966409,"version":"build-2736575974"},"reference-count":10,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[2019,1,1]],"date-time":"2019-01-01T00:00:00Z","timestamp":1546300800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2019,1,1]],"date-time":"2019-01-01T00:00:00Z","timestamp":1546300800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2018,8,28]],"date-time":"2018-08-28T00:00:00Z","timestamp":1535414400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"DOI":"10.13039\/100000054","name":"National Cancer Institute","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100000054","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["K12CA138464"],"award-info":[{"award-number":["K12CA138464"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["jaadcasereports.org","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["JAAD Case Reports"],"published-print":{"date-parts":[[2019,1]]},"DOI":"10.1016\/j.jdcr.2018.08.024","type":"journal-article","created":{"date-parts":[[2018,12,5]],"date-time":"2018-12-05T06:59:49Z","timestamp":1543993189000},"page":"50-53","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":5,"title":["Vitiligo and melanocytic nevi: New findings in Coffin-Siris syndrome associated with ARID1 germline mutation"],"prefix":"10.1016","volume":"5","author":[{"given":"Catherine N.","family":"Tchanque-Fossuo","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sara E.","family":"Dahle","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maija","family":"Kiuru","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R. Rivkah","family":"Isseroff","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.jdcr.2018.08.024_bib1","author":"Vergano"},{"issue":"3","key":"10.1016\/j.jdcr.2018.08.024_bib2","first-page":"7","article-title":"Coffin Siris syndrome: a disorder of SWI|\/SNF pathway","volume":"9","author":"Mishra","year":"2016","journal-title":"Genet Clin"},{"issue":"4","key":"10.1016\/j.jdcr.2018.08.024_bib3","doi-asserted-by":"crossref","first-page":"376","DOI":"10.1038\/ng.2219","article-title":"Mutations affecting components of the SWI\/SNF complex cause Coffin-Siris syndrome","volume":"44","author":"Tsurusaki","year":"2012","journal-title":"Nat Genet"},{"key":"10.1016\/j.jdcr.2018.08.024_bib4","doi-asserted-by":"crossref","first-page":"276","DOI":"10.1002\/ajmg.c.31414","article-title":"The ARID1B phenotype: what we have learned so far","volume":"166C","author":"Santen","year":"2014","journal-title":"Am J Med Genet C Semin Med Genet"},{"issue":"12","key":"10.1016\/j.jdcr.2018.08.024_bib5","doi-asserted-by":"crossref","first-page":"3186","DOI":"10.1002\/ajmg.a.37356","article-title":"Report of a patient with a constitutional missense mutation in SMARCB1, Coffin\u2013Siris phenotype, and schwannomatosis","volume":"167","author":"Gossai","year":"2015","journal-title":"Am J Med Genet A"},{"key":"10.1016\/j.jdcr.2018.08.024_bib6","doi-asserted-by":"crossref","first-page":"101","DOI":"10.1016\/j.yjmcc.2015.09.010","article-title":"MITF interacts with the SWI\/SNF subunit, BRG1, to promote GATA4 expression in cardiac hypertrophy","volume":"88","author":"Mehta","year":"2015","journal-title":"J Mol Cell Cardiol"},{"issue":"4","key":"10.1016\/j.jdcr.2018.08.024_bib7","doi-asserted-by":"crossref","first-page":"195","DOI":"10.1159\/000476020","article-title":"A novel pathogenic variant in the MITF Gene segregating with a unique spectrum of ocular findings in an extended Iranian Waardenburg syndrome kindred","volume":"8","author":"Jalilian","year":"2017","journal-title":"Mol Syndromol"},{"issue":"1","key":"10.1016\/j.jdcr.2018.08.024_bib8","doi-asserted-by":"crossref","first-page":"59","DOI":"10.1186\/s13148-015-0091-3","article-title":"Targeted next-generation sequencing reveals high frequency of mutations in epigenetic regulators across treatment-na\u00efve patient melanomas","volume":"7","author":"Lee","year":"2015","journal-title":"Clin Epigenetics"},{"issue":"2","key":"10.1016\/j.jdcr.2018.08.024_bib9","doi-asserted-by":"crossref","first-page":"251","DOI":"10.1016\/j.cell.2012.06.024","article-title":"A landscape of driver mutations in melanoma","volume":"150","author":"Hodis","year":"2012","journal-title":"Cell"},{"issue":"20","key":"10.1016\/j.jdcr.2018.08.024_bib10","doi-asserted-by":"crossref","first-page":"1926","DOI":"10.1056\/NEJMoa1502583","article-title":"The genetic evolution of melanoma from precursor lesions","volume":"373","author":"Shain","year":"2015","journal-title":"N Engl J Med"}],"container-title":["JAAD Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2352512618302315?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2352512618302315?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,11,7]],"date-time":"2025-11-07T00:19:45Z","timestamp":1762474785000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S2352512618302315"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,1]]},"references-count":10,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2019,1]]}},"alternative-id":["S2352512618302315"],"URL":"https:\/\/doi.org\/10.1016\/j.jdcr.2018.08.024","relation":{},"ISSN":["2352-5126"],"issn-type":[{"value":"2352-5126","type":"print"}],"subject":[],"published":{"date-parts":[[2019,1]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Vitiligo and melanocytic nevi: New findings in Coffin-Siris syndrome associated with ARID1 germline mutation","name":"articletitle","label":"Article Title"},{"value":"JAAD Case Reports","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jdcr.2018.08.024","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2018 Elsevier Inc.","name":"copyright","label":"Copyright"}]}}