Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/17033
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dc.contributor.authorLee, Eric-
dc.contributor.authorLe, Trang-
dc.contributor.authorZhu, Ying-
dc.contributor.authorElakis, George-
dc.contributor.authorTurner, Anne-
dc.contributor.authorLo, William-
dc.contributor.authorVenselaar, Hanka-
dc.contributor.authorVerrenkamp, Carol-Ann-
dc.contributor.authorSnow, Nicole-
dc.contributor.authorMowat, David-
dc.contributor.authorKirk, Edwin Philip-
dc.contributor.authorSachdev, Rani-
dc.contributor.authorSmith, Janine-
dc.contributor.authorBrown, Natasha Jane-
dc.contributor.authorWallis, Mathew-
dc.contributor.authorBarnett, Chris-
dc.contributor.authorMcKenzie, Fiona-
dc.contributor.authorFreckmann, Mary-Louise-
dc.contributor.authorCollins, Felicity-
dc.contributor.authorChopra, Maya-
dc.contributor.authorGregersen, Nerine-
dc.contributor.authorHayes, Ian-
dc.contributor.authorRajagopalan, Sulekha-
dc.contributor.authorTan, Tiong Yang-
dc.contributor.authorStark, Zornitza-
dc.contributor.authorSavarirayan, Ravi-
dc.contributor.authorYeung, Alison-
dc.contributor.authorAdès, Lesley-
dc.contributor.authorGattas, Michael-
dc.contributor.authorGibson, Kate-
dc.contributor.authorGabbett, Michael-
dc.contributor.authorAmor, David John-
dc.contributor.authorLattanzi, Wanda-
dc.contributor.authorBoyd, Simeon-
dc.contributor.authorHaan, Eric-
dc.contributor.authorGianoutsos, Mark-
dc.contributor.authorCox, Timothy Chilton-
dc.contributor.authorBuckley, Michael Francis-
dc.contributor.authorRoscioli, Tony-
dc.date2017-12-07-
dc.date.accessioned2017-12-13T23:03:45Z-
dc.date.available2017-12-13T23:03:45Z-
dc.date.issued2018-
dc.identifier.citationGenetics in medicine : official journal of the American College of Medical Genetics 2018; 20(9): 1061-1068-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/17033-
dc.description.abstractPurposeThe craniosynostoses are characterized by premature fusion of one or more cranial sutures. The relative contribution of previously reported genes to craniosynostosis in large cohorts is unclear. Here we report on the use of a massively parallel sequencing panel in individuals with craniosynostosis without a prior molecular diagnosis.MethodsA 20-gene panel was designed based on the genes' association with craniosynostosis, and clinically validated through retrospective testing of an Australian and New Zealand cohort of 233 individuals with craniosynostosis in whom previous testing had not identified a causative variant within FGFR1-3 hot-spot regions or the TWIST1 gene. An additional 76 individuals were tested prospectively.ResultsPathogenic or likely pathogenic variants in non-FGFR genes were identified in 43 individuals, with diagnostic yields of 14% and 15% in retrospective and prospective cohorts, respectively. Variants were identified most frequently in TCF12 (N = 22) and EFNB1 (N = 8), typically in individuals with nonsyndromic coronal craniosynostosis or TWIST1-negative clinically suspected Saethre-Chotzen syndrome. Clinically significant variants were also identified in ALX4, EFNA4, ERF, and FGF10.ConclusionThese findings support the clinical utility of a massively parallel sequencing panel for craniosynostosis. TCF12 and EFNB1 should be included in genetic testing for nonsyndromic coronal craniosynostosis or clinically suspected Saethre-Chotzen syndrome.-
dc.language.isoeng-
dc.titleA craniosynostosis massively parallel sequencing panel study in 309 Australian and New Zealand patients: findings and recommendations-
dc.typeJournal Article-
dc.identifier.journaltitleGenetics in medicine : official journal of the American College of Medical Genetics-
dc.identifier.affiliationCraniofacial Unit, Sydney Children's Hospital, Randwick, Australiaen
dc.identifier.affiliationThe Children's Hospital at Westmead, Sydney, Australiaen
dc.identifier.affiliationDepartment of Clinical Genetics, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationSouth Australian Clinical Genetics Service, SA Pathology, Adelaide, Australiaen
dc.identifier.affiliationDepartment of Clinical Genetics, Royal North Shore Hospital, Sydney, Australiaen
dc.identifier.affiliationDepartment of Clinical Genetics, Liverpool Hospital, Sydney, Australiaen
dc.identifier.affiliationVictorian Clinical Genetics Services, Melbourne, Australiaen
dc.identifier.affiliationBrisbane Genetics, Brisbane, Australiaen
dc.identifier.affiliationRoyal Brisbane & Women's Hospital, Brisbane, Australiaen
dc.identifier.affiliationKing Edward Memorial Hospital, Perth, Australiaen
dc.identifier.affiliationDepartment of Pediatrics, School of Medicine UC Davis MIND Institute, Sacramento, California, USAen
dc.identifier.affiliationDivision of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, Washington, USAen
dc.identifier.affiliationGenetics Laboratory, NSW Health Pathology East, Sydney, Australiaen
dc.identifier.affiliationCentre for Clinical Genetics, Sydney Children's Hospital, Randwick, Australiaen
dc.identifier.affiliationCentre for Molecular and Biomolecular Informatics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.-
dc.identifier.affiliationImagine Institute of Genetic Diseases, Paris, France.-
dc.identifier.affiliationGenetic Health Service New Zealand, Auckland, New Zealand.-
dc.identifier.affiliationGenetic Health Service New Zealand, Christchurch Hospital, Christchurch, New Zealand.-
dc.identifier.affiliationInstitute of Anatomy and Cell Biology, Università Cattolica del Sacro Cuore, Rome, Italy.-
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/29215649-
dc.identifier.doi10.1038/gim.2017.214-
dc.identifier.pubmedid29215649-
dc.type.austinJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairetypeJournal Article-
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