{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,27]],"date-time":"2026-09-27T23:03:51Z","timestamp":1790550231886,"version":"4.1.0"},"reference-count":49,"publisher":"Wiley","issue":"12","license":[{"start":{"date-parts":[[2018,12,10]],"date-time":"2018-12-10T00:00:00Z","timestamp":1544400000000},"content-version":"vor","delay-in-days":9,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["American J of Med Genetics Pt A"],"published-print":{"date-parts":[[2018,12]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>\n                    The oculoauriculofrontonasal syndrome (OAFNS) is a rare disorder characterized by the association of frontonasal dysplasia (widely spaced eyes, facial cleft, and nose abnormalities) and oculo\u2010auriculo\u2010vertebral spectrum (OAVS)\u2010associated features, such as preauricular ear tags, ear dysplasia, mandibular asymmetry, epibulbar dermoids, eyelid coloboma, and costovertebral anomalies. The etiology is unknown so far. This work aimed to identify molecular bases for the OAFNS. Among a cohort of 130 patients with frontonasal dysplasia, accurate phenotyping identified 18 individuals with OAFNS. We describe their clinical spectrum, including the report of new features (micro\/anophtalmia, cataract, thyroid agenesis, polymicrogyria, olfactory bulb hypoplasia, and mandibular cleft), and emphasize the high frequency of nasal polyps in OAFNS (56%). We report the negative results of\n                    <jats:italic>ALX1, ALX3,<\/jats:italic>\n                    and\n                    <jats:italic>ALX4<\/jats:italic>\n                    genes sequencing and next\u2010generation sequencing strategy performed on blood\u2010derived DNA from respectively, four and four individuals. Exome sequencing was performed in four individuals, genome sequencing in one patient with negative exome sequencing result. Based on the data from this series and the literature, diverse hypotheses can be raised regarding the etiology of OAFNS: mosaic mutation, epigenetic anomaly, oligogenism, or nongenetic cause. In conclusion, this series represents further clinical delineation work of the rare OAFNS, and paves the way toward the identification of the causing mechanism.\n                  <\/jats:p>","DOI":"10.1002\/ajmg.a.40662","type":"journal-article","created":{"date-parts":[[2018,12,10]],"date-time":"2018-12-10T03:46:12Z","timestamp":1544413572000},"page":"2740-2750","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":10,"title":["The oculoauriculofrontonasal syndrome: Further clinical characterization and additional evidence suggesting a nontraditional mode of inheritance"],"prefix":"10.1002","volume":"176","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2193-8685","authenticated-orcid":false,"given":"Daphn\u00e9","family":"Lehalle","sequence":"first","affiliation":[{"name":"Centre de G\u00e9n\u00e9tique et Centre de R\u00e9f\u00e9rence Anomalies du D\u00e9veloppement et Syndromes Malformatifs de l'Interr\u00e9gion Est Centre Hospitalier Universitaire Dijon  Dijon France"},{"name":"Equipe GAD, INSERM LNC UMR 1231, Facult\u00e9 de M\u00e9decine Universit\u00e9 de Bourgogne Franche\u2010Comt\u00e9  Dijon France"},{"name":"Unit\u00e9 fonctionnelle de G\u00e9n\u00e9tique Clinique Centre Hospitalier Intercommunal de Cr\u00e9teil  Dijon France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Umut","family":"Altunoglu","sequence":"additional","affiliation":[{"name":"Medical Genetics Department, Istanbul Medical Faculty Istanbul University  Istanbul Turkey"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ange\u2010Line","family":"Bruel","sequence":"additional","affiliation":[{"name":"Equipe GAD, INSERM LNC UMR 1231, Facult\u00e9 de M\u00e9decine Universit\u00e9 de Bourgogne Franche\u2010Comt\u00e9  Dijon France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mirna","family":"Assoum","sequence":"additional","affiliation":[{"name":"Equipe GAD, INSERM LNC UMR 1231, Facult\u00e9 de M\u00e9decine Universit\u00e9 de Bourgogne Franche\u2010Comt\u00e9  Dijon France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yannis","family":"Duffourd","sequence":"additional","affiliation":[{"name":"Equipe GAD, INSERM LNC UMR 1231, Facult\u00e9 de M\u00e9decine Universit\u00e9 de Bourgogne Franche\u2010Comt\u00e9  Dijon France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alice","family":"Masurel","sequence":"additional","affiliation":[{"name":"Centre de G\u00e9n\u00e9tique et Centre de R\u00e9f\u00e9rence Anomalies du D\u00e9veloppement et Syndromes Malformatifs de l'Interr\u00e9gion Est Centre Hospitalier Universitaire Dijon  Dijon France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Genevi\u00e8ve","family":"Baujat","sequence":"additional","affiliation":[{"name":"Service de G\u00e9n\u00e9tique, INSERM U781, H\u00f4pital Necker\u2010Enfants Malades Institut Imagine, University Sorbonne\u2010Paris\u2010Cit\u00e9  Paris France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bettina","family":"Bessieres","sequence":"additional","affiliation":[{"name":"Unite d'embryofoetopathologie, Service d'Histologie\u2010Embryologie\u2010Cytog\u00e9n\u00e9tique H\u00f4pital Necker \u2013 Enfants Malades, APHP  Paris France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Guillaume","family":"Captier","sequence":"additional","affiliation":[{"name":"Service de chirurgie orthop\u00e9dique et plastique p\u00e9diatrique, H\u00f4pital Lapeyronie CHU Montpellier  Montpellier France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Patrick","family":"Edery","sequence":"additional","affiliation":[{"name":"Service de g\u00e9n\u00e9tique et Centre de R\u00e9f\u00e9rence des Anomalies du d\u00e9veloppement de la r\u00e9gion Auvergne\u2010Rh\u00f4ne\u2010Alpes CHU de Lyon  Lyon France"},{"name":"Centre de Recherche en Neurosciences de Lyon INSERM U1028 CNRS UMR 5292, UCB Lyon 1  Lyon France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nursel H.","family":"El\u00e7io\u011flu","sequence":"additional","affiliation":[{"name":"Department of Pediatric Genetics Marmara University Medical School  Istanbul Turkey"},{"name":"Eastern Mediterranean University Medical School  Mersin Turkey"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David","family":"Genevi\u00e8ve","sequence":"additional","affiliation":[{"name":"Genetic Department for Rare Disease and Personalised Medicine, Clinical Division Montpellier University, Inserm U1183  Montpellier France"},{"name":"Centre de r\u00e9f\u00e9rence des anomalies du d\u00e9veloppement et syndromes malformatifs  Sud\u2010Ouest Occitanie France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alice","family":"Goldenberg","sequence":"additional","affiliation":[{"name":"Department of Genetics Rouen University Hospital, Normandy Centre for Genomic and Personalized Medicine  Rouen France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Delphine","family":"H\u00e9ron","sequence":"additional","affiliation":[{"name":"AP\u2010HP, H\u00f4pital de la Piti\u00e9\u2010Salp\u00eatri\u00e8re, D\u00e9partement de G\u00e9n\u00e9tique  Paris France"},{"name":"Centre de R\u00e9f\u00e9rence \"d\u00e9ficiences intellectuelles de causes rares\"  Paris France"},{"name":"Groupe de Recherche Clinique (GRC) \"d\u00e9ficience intellectuelle et autisme\" UPMC  Paris France"},{"name":"INSERM, U 1127, CNRS UMR 7225, Sorbonne Universit\u00e9s, UPMC Univ Paris 06 UMR S 1127  Paris France"},{"name":"Institut du Cerveau et de la Moelle \u00e9pini\u00e8re, ICM  Paris France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sarah","family":"Grotto","sequence":"additional","affiliation":[{"name":"Department of Genetics Rouen University Hospital, Normandy Centre for Genomic and Personalized Medicine  Rouen France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sandrine","family":"Marlin","sequence":"additional","affiliation":[{"name":"Service de G\u00e9n\u00e9tique, INSERM U781, H\u00f4pital Necker\u2010Enfants Malades Institut Imagine, University Sorbonne\u2010Paris\u2010Cit\u00e9  Paris France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Audrey","family":"Putoux","sequence":"additional","affiliation":[{"name":"Service de g\u00e9n\u00e9tique et Centre de R\u00e9f\u00e9rence des Anomalies du d\u00e9veloppement de la r\u00e9gion Auvergne\u2010Rh\u00f4ne\u2010Alpes CHU de Lyon  Lyon France"},{"name":"Centre de Recherche en Neurosciences de Lyon INSERM U1028 CNRS UMR 5292, UCB Lyon 1  Lyon France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5797-8152","authenticated-orcid":false,"given":"Massimiliano","family":"Rossi","sequence":"additional","affiliation":[{"name":"Service de g\u00e9n\u00e9tique et Centre de R\u00e9f\u00e9rence des Anomalies du d\u00e9veloppement de la r\u00e9gion Auvergne\u2010Rh\u00f4ne\u2010Alpes CHU de Lyon  Lyon France"},{"name":"Centre de Recherche en Neurosciences de Lyon INSERM U1028 CNRS UMR 5292, UCB Lyon 1  Lyon France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pascale","family":"Saugier\u2010Veber","sequence":"additional","affiliation":[{"name":"Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics Normandy Centre for Genomic and Personalized Medicine  Rouen France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"St\u00e9phane","family":"Triau","sequence":"additional","affiliation":[{"name":"Service de Foetopathologie CHU Angers  Angers France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Christelle","family":"Cabrol","sequence":"additional","affiliation":[{"name":"Centre de G\u00e9n\u00e9tique humaine CHU Besan\u00e7on  Besan\u00e7on France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Myriam","family":"V\u00e9zain","sequence":"additional","affiliation":[{"name":"Normandie Univ, UNIROUEN, Inserm U1245 and Rouen University Hospital, Department of Genetics Normandy Centre for Genomic and Personalized Medicine  Rouen France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Catherine","family":"Vincent\u2010Delorme","sequence":"additional","affiliation":[{"name":"Department of Clinical Genetics CHU Lille  Lille France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Christel","family":"Thauvin\u2010Robinet","sequence":"additional","affiliation":[{"name":"Centre de G\u00e9n\u00e9tique et Centre de R\u00e9f\u00e9rence Anomalies du D\u00e9veloppement et Syndromes Malformatifs de l'Interr\u00e9gion Est Centre Hospitalier Universitaire Dijon  Dijon France"},{"name":"Equipe GAD, INSERM LNC UMR 1231, Facult\u00e9 de M\u00e9decine Universit\u00e9 de Bourgogne Franche\u2010Comt\u00e9  Dijon France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Julien","family":"Thevenon","sequence":"additional","affiliation":[{"name":"Centre de G\u00e9n\u00e9tique et Centre de R\u00e9f\u00e9rence Anomalies du D\u00e9veloppement et Syndromes Malformatifs de l'Interr\u00e9gion Est Centre Hospitalier Universitaire Dijon  Dijon France"},{"name":"Equipe GAD, INSERM LNC UMR 1231, Facult\u00e9 de M\u00e9decine Universit\u00e9 de Bourgogne Franche\u2010Comt\u00e9  Dijon France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Pierre","family":"Vabres","sequence":"additional","affiliation":[{"name":"Equipe GAD, INSERM LNC UMR 1231, Facult\u00e9 de M\u00e9decine Universit\u00e9 de Bourgogne Franche\u2010Comt\u00e9  Dijon France"},{"name":"Service de Dermatologie CHU Dijon  Dijon France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Patrick","family":"Callier","sequence":"additional","affiliation":[{"name":"Equipe GAD, INSERM LNC UMR 1231, Facult\u00e9 de M\u00e9decine Universit\u00e9 de Bourgogne Franche\u2010Comt\u00e9  Dijon France"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0376-499X","authenticated-orcid":false,"given":"Hulya","family":"Kayserili","sequence":"additional","affiliation":[{"name":"Medical Genetics Department, Istanbul Medical Faculty Istanbul University  Istanbul Turkey"},{"name":"Ko\u00e7 University School of Medicine (KUSoM) Medical Genetics Department  \u0130stanbul Turkey"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9770-444X","authenticated-orcid":false,"given":"Laurence","family":"Faivre","sequence":"additional","affiliation":[{"name":"Centre de G\u00e9n\u00e9tique et Centre de R\u00e9f\u00e9rence Anomalies du D\u00e9veloppement et Syndromes Malformatifs de l'Interr\u00e9gion Est Centre Hospitalier Universitaire Dijon  Dijon France"},{"name":"Equipe GAD, INSERM LNC UMR 1231, Facult\u00e9 de M\u00e9decine Universit\u00e9 de Bourgogne Franche\u2010Comt\u00e9  Dijon France"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2018,12,10]]},"reference":[{"key":"e_1_2_8_2_1","doi-asserted-by":"publisher","DOI":"10.1136\/bcr-02-2012-5940"},{"key":"e_1_2_8_3_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.jcms.2011.11.003"},{"key":"e_1_2_8_4_1","first-page":"285","article-title":"Intracranial lipomas, hydrocephalus and other CNS anomalies in oculoauriculo\u2010vertebral dysplasia (Goldenhar\u2010Gorlin syndrome)","volume":"11","author":"Aleksic S.","year":"1984","journal-title":"Child's Brain"},{"key":"e_1_2_8_5_1","doi-asserted-by":"publisher","DOI":"10.1002\/(SICI)1096-8628(19960517)63:2<346::AID-AJMG4>3.0.CO;2-R"},{"key":"e_1_2_8_6_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0165-5876(01)00555-9"},{"key":"e_1_2_8_7_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ajhg.2016.02.006"},{"key":"e_1_2_8_8_1","doi-asserted-by":"publisher","DOI":"10.1038\/ejhg.2017.101"},{"key":"e_1_2_8_9_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.37217"},{"key":"e_1_2_8_10_1","doi-asserted-by":"publisher","DOI":"10.1111\/cge.12775"},{"key":"e_1_2_8_11_1","doi-asserted-by":"publisher","DOI":"10.1597\/14-108"},{"key":"e_1_2_8_12_1","unstructured":"CareyJ YongS.1981.Frontonasal dysplasia and the Goldenhar syndrome: The oculo\u2010auriculo\u2010frontonasal syndrome. Conference on malformations and morphogenesis Hanover. Dartmouth College New Hampshire."},{"key":"e_1_2_8_13_1","doi-asserted-by":"publisher","DOI":"10.1597\/1545-1569_1996_033_0519_fmatos_2.3.co_2"},{"key":"e_1_2_8_14_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.35926"},{"key":"e_1_2_8_15_1","doi-asserted-by":"publisher","DOI":"10.1097\/MCD.0b013e3282f449c8"},{"key":"e_1_2_8_16_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.jcms.2011.10.010"},{"key":"e_1_2_8_17_1","doi-asserted-by":"publisher","DOI":"10.1597\/08-167.1"},{"key":"e_1_2_8_18_1","first-page":"183","article-title":"A new syndrome of oculoauriculovertebral dysplasia and midline craniofacial defect: The oculoauriculofrontonasal syndrome: Two new cases in sibs","volume":"19","author":"Golabi M.","year":"1983","journal-title":"Birth Defects Original Article Series"},{"key":"e_1_2_8_19_1","first-page":"400","article-title":"Goldenhar syndrome. Discordance in monozygotic twins","volume":"20","author":"Gomez Garcia A.","year":"1984","journal-title":"Anales Espa\u00f1oles de Pediatr\u00eda"},{"key":"e_1_2_8_20_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.32859"},{"key":"e_1_2_8_21_1","doi-asserted-by":"publisher","DOI":"10.1097\/00019605-199707000-00009"},{"key":"e_1_2_8_22_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.31962"},{"key":"e_1_2_8_23_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.a.33485"},{"key":"e_1_2_8_24_1","doi-asserted-by":"publisher","DOI":"10.1136\/bjo.52.4.346"},{"key":"e_1_2_8_25_1","doi-asserted-by":"publisher","DOI":"10.1002\/tera.1420320103"},{"key":"e_1_2_8_26_1","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pgen.1002999"},{"key":"e_1_2_8_27_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.10120"},{"key":"e_1_2_8_28_1","doi-asserted-by":"publisher","DOI":"10.1002\/uog.1792"},{"key":"e_1_2_8_29_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0278-2391(98)90121-5"},{"key":"e_1_2_8_30_1","doi-asserted-by":"publisher","DOI":"10.1093\/hmg\/ddp391"},{"key":"e_1_2_8_31_1","doi-asserted-by":"publisher","DOI":"10.1093\/hmg\/ddx107"},{"key":"e_1_2_8_32_1","first-page":"125","article-title":"Mesenchymal derivatives of the neural crest: Analysis of chimaeric quail and chick embryos","volume":"34","author":"Le Lievre C. S.","year":"1975","journal-title":"Journal of Embryology and Experimental Morphology"},{"key":"e_1_2_8_33_1","doi-asserted-by":"publisher","DOI":"10.1136\/jmedgenet-2016-103774"},{"key":"e_1_2_8_34_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.earlhumdev.2011.07.009"},{"key":"e_1_2_8_35_1","doi-asserted-by":"publisher","DOI":"10.1111\/cge.12722"},{"key":"e_1_2_8_36_1","doi-asserted-by":"publisher","DOI":"10.1002\/ajmg.1320250617"},{"key":"e_1_2_8_37_1","doi-asserted-by":"publisher","DOI":"10.1002\/wdev.161"},{"key":"e_1_2_8_38_1","doi-asserted-by":"publisher","DOI":"10.1097\/MCD.0b013e328010d402"},{"key":"e_1_2_8_39_1","doi-asserted-by":"publisher","DOI":"10.1016\/0030-4220(88)90014-X"},{"key":"e_1_2_8_40_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ajhg.2014.07.008"},{"key":"e_1_2_8_41_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ajhg.2014.06.006"},{"key":"e_1_2_8_42_1","doi-asserted-by":"publisher","DOI":"10.1097\/00019605-199510000-00010"},{"key":"e_1_2_8_43_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ejmg.2017.01.008"},{"key":"e_1_2_8_44_1","doi-asserted-by":"publisher","DOI":"10.1597\/15-078"},{"key":"e_1_2_8_45_1","doi-asserted-by":"publisher","DOI":"10.1073\/pnas.0402819101"},{"key":"e_1_2_8_46_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ajhg.2009.04.009"},{"key":"e_1_2_8_47_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.ajhg.2010.04.002"},{"key":"e_1_2_8_48_1","doi-asserted-by":"publisher","DOI":"10.1097\/MCD.0000000000000085"},{"key":"e_1_2_8_49_1","doi-asserted-by":"publisher","DOI":"10.1007\/s00439-007-0336-0"},{"key":"e_1_2_8_50_1","doi-asserted-by":"publisher","DOI":"10.1086\/421532"}],"container-title":["American Journal of Medical Genetics Part A"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajmg.a.40662","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/full-xml\/10.1002\/ajmg.a.40662","content-type":"application\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1002\/ajmg.a.40662","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,9,14]],"date-time":"2023-09-14T05:47:54Z","timestamp":1694670474000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajmg.a.40662"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2018,12]]},"references-count":49,"journal-issue":{"issue":"12","published-print":{"date-parts":[[2018,12]]}},"alternative-id":["10.1002\/ajmg.a.40662"],"URL":"https:\/\/doi.org\/10.1002\/ajmg.a.40662","archive":["Portico"],"relation":{},"ISSN":["1552-4825","1552-4833"],"issn-type":[{"value":"1552-4825","type":"print"},{"value":"1552-4833","type":"electronic"}],"subject":[],"published":{"date-parts":[[2018,12]]},"assertion":[{"value":"2018-04-04","order":0,"name":"received","label":"Received","group":{"name":"publication_history","label":"Publication History"}},{"value":"2018-08-23","order":1,"name":"accepted","label":"Accepted","group":{"name":"publication_history","label":"Publication History"}},{"value":"2018-12-10","order":2,"name":"published","label":"Published","group":{"name":"publication_history","label":"Publication History"}}]}}