{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,18]],"date-time":"2025-11-18T05:54:35Z","timestamp":1763445275603,"version":"3.37.3"},"reference-count":22,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2017,11,21]],"date-time":"2017-11-21T00:00:00Z","timestamp":1511222400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/100009633","name":"Eunice Kennedy Shriver National Institute of Child Health and Human Development","doi-asserted-by":"publisher","award":["1R13HD089664\u201001"],"award-info":[{"award-number":["1R13HD089664\u201001"]}],"id":[{"id":"10.13039\/100009633","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100004374","name":"Medtronic","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100004374","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100003359","name":"Scoliosis Research Society","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100003359","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["American J of Med Genetics Pt A"],"published-print":{"date-parts":[[2018,1]]},"abstract":"<jats:sec><jats:label\/><jats:p>Scoliosis represents the most common musculoskeletal disorder in children and affects approximately 3% of the world population. Scoliosis is separated into two major phenotypic classifications: congenital and idiopathic. Idiopathic scoliosis is defined as a curvature of the spine of 10\u00b0 or greater visualized on plane radiograph and does not have associated vertebral malformations (VM). \u201cCongenital\u201d scoliosis (CS) due to malformations in vertebrae is frequently associated with other birth defects. Recently, significant advances have been made in understanding the genetic basis of both conditions. There is evidence that both conditions are etiologically related. A 2\u2010day conference entitled \u201cGenomic Approaches to Understanding and Treating Scoliosis\u201d was held at Scottish Rite Hospital for Children in Dallas, Texas, to synergize research in this field. This first combined, multidisciplinary conference featured international scoliosis researchers in basic and clinical sciences. A major outcome of the conference advancing scoliosis research was the proposal and subsequent vote in favor of merging the International Consortium for Vertebral Anomalies and Scoliosis (ICVAS) and International Consortium for Scoliosis Genetics (ICSG) into a single entity called International Consortium for Spinal Genetics, Development, and Disease (ICSGDD). The ICSGDD is proposed to meet annually as a forum to synergize multidisciplinary spine deformity research.<\/jats:p><\/jats:sec>","DOI":"10.1002\/ajmg.a.38550","type":"journal-article","created":{"date-parts":[[2017,11,21]],"date-time":"2017-11-21T05:40:33Z","timestamp":1511242833000},"page":"253-256","source":"Crossref","is-referenced-by-count":9,"title":["Summary of the first inaugural joint meeting of the International Consortium for scoliosis genetics and the International Consortium for vertebral anomalies and scoliosis, March 16\u201318, 2017, Dallas, Texas"],"prefix":"10.1002","volume":"176","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-2874-8064","authenticated-orcid":false,"given":"Philip F.","family":"Giampietro","sequence":"first","affiliation":[{"name":"Drexel University College of Medicine Philadelphia Pennsylvania"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Olivier","family":"Pourquie","sequence":"additional","affiliation":[{"name":"Harvard Medical School Boston Massachusetts"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Cathy","family":"Raggio","sequence":"additional","affiliation":[{"name":"Hospital for Special Surgery New York New York"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shiro","family":"Ikegawa","sequence":"additional","affiliation":[{"name":"RIKEN Center for Integrative Medical Sciences Tokyo Japan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Peter D.","family":"Turnpenny","sequence":"additional","affiliation":[{"name":"Royal Devon and Exeter Hospital Exeter United Kingdom"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ryan","family":"Gray","sequence":"additional","affiliation":[{"name":"University of Texas Austin Texas"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sally L.","family":"Dunwoodie","sequence":"additional","affiliation":[{"name":"Victor Chang Cardiac Research Institute Darlinghurst New South Wales Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Christina A.","family":"Gurnett","sequence":"additional","affiliation":[{"name":"Washington University in St Louis St. Louis Missouri"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Benjamin","family":"Alman","sequence":"additional","affiliation":[{"name":"Duke University Durham North Carolina"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kenneth","family":"Cheung","sequence":"additional","affiliation":[{"name":"The University of Hong Kong Hong Kong China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kenro","family":"Kusumi","sequence":"additional","affiliation":[{"name":"Arizona State University Tempe Arizona"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nancy","family":"Hadley\u2010Miller","sequence":"additional","affiliation":[{"name":"University of Colorado  Anschutz Medical Campus Aurora Colorado"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Carol A.","family":"Wise","sequence":"additional","affiliation":[{"name":"Texas Scottish Rite Hospital for Children Dallas Texas"},{"name":"University of Texas Southwestern Medical Center Dallas Texas"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2017,11,21]]},"reference":[{"key":"e_1_2_5_2_1","doi-asserted-by":"publisher","DOI":"10.1093\/hmg\/ddu224"},{"issue":"6","key":"e_1_2_5_3_1","first-page":"1334","article-title":"Mutations in the MESP2 gene cause spondylothoracic dysostosis\/Jarcho\u2013Levin syndrome","volume":"82","author":"Cornier A. 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