Ethylin Wang Jabs Department of Genetics and Genomic Sciences Icahn School of Medicine at Mount Sinai Biography Publications Institution JoVE Articles Ethylin Wang Jabs has not added a biography. If you are Ethylin Wang Jabs and would like to personalize this page please email our Author Liaison for assistance. Publications Mandibular Dysmorphology Due to Abnormal Embryonic Osteogenesis in FGFR2-related Craniosynostosis Mice Disease Models & Mechanisms. 05, 2019 | Pubmed ID: 31064775 Nonsyndromic Craniosynostosis: Novel Coding Variants Pediatric Research. 03, 2019 | Pubmed ID: 30651579 Midface and Upper Airway Dysgenesis in FGFR2-related Craniosynostosis Involves Multiple Tissue-specific and Cell Cycle Effects Development (Cambridge, England). 10, 2018 | Pubmed ID: 30228104 C-type Natriuretic Peptide Analog Treatment of Craniosynostosis in a Crouzon Syndrome Mouse Model PloS One. 2018 | Pubmed ID: 30048539 Cytogenomic Identification and Long-read Single Molecule Real-time (SMRT) Sequencing of a () Deletion NPJ Genomic Medicine. 2018 | Pubmed ID: 29367880 Choanal Atresia and Craniosynostosis: Development and Disease Plastic and Reconstructive Surgery. 01, 2018 | Pubmed ID: 29280877 Identification of STAC3 Variants in Non-Native American Families with Overlapping Features of Carey-Fineman-Ziter Syndrome and Moebius Syndrome American Journal of Medical Genetics. Part A. Oct, 2017 | Pubmed ID: 28777491 A Defect in Myoblast Fusion Underlies Carey-Fineman-Ziter Syndrome Nature Communications. 07, 2017 | Pubmed ID: 28681861 Reconstructive Surgery in Times of Conflict The Journal of Craniofacial Surgery. Sep, 2016 | Pubmed ID: 27428908 The FaceBase Consortium: a Comprehensive Resource for Craniofacial Researchers Development (Cambridge, England). 07, 2016 | Pubmed ID: 27287806 Specific Functional Pathologies of Cx43 Mutations Associated with Oculodentodigital Dysplasia Molecular Biology of the Cell. 07, 2016 | Pubmed ID: 27226478 Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis Plastic and Reconstructive Surgery. Mar, 2016 | Pubmed ID: 26910679 Development and Preliminary Evaluation of an Online Educational Video About Whole-genome Sequencing for Research Participants, Patients, and the General Public Genetics in Medicine : Official Journal of the American College of Medical Genetics. 05, 2016 | Pubmed ID: 26334178 Novel Evidence of Association with Nonsyndromic Cleft Lip with or Without Cleft Palate Was Shown for Single Nucleotide Polymorphisms in FOXF2 Gene in an Asian Population Birth Defects Research. Part A, Clinical and Molecular Teratology. Oct, 2015 | Pubmed ID: 26278207 Ten-year Experience of More Than 35,000 Orofacial Clefts in Africa BMC Pediatrics. Feb, 2015 | Pubmed ID: 25884320 BCL11B Expression in Intramembranous Osteogenesis During Murine Craniofacial Suture Development Gene Expression Patterns : GEP. Jan, 2015 | Pubmed ID: 25511173 Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses Current Genetic Medicine Reports. Sep, 2014 | Pubmed ID: 26146596 Mirror Movements Identified in Patients with Moebius Syndrome Tremor and Other Hyperkinetic Movements (New York, N.Y.). 2014 | Pubmed ID: 25120946 Identification of an HMGB3 Frameshift Mutation in a Family with an X-linked Colobomatous Microphthalmia Syndrome Using Whole-genome and X-exome Sequencing JAMA Ophthalmology. Oct, 2014 | Pubmed ID: 24993872 A Novel ZRS Mutation Leads to Preaxial Polydactyly Type 2 in a Heterozygous Form and Werner Mesomelic Syndrome in a Homozygous Form Human Mutation. Aug, 2014 | Pubmed ID: 24777739 Craniofacial Divergence by Distinct Prenatal Growth Patterns in Fgfr2 Mutant Mice BMC Developmental Biology. Feb, 2014 | Pubmed ID: 24580805 Characterization of Ocular Motor Deficits in Congenital Facial Weakness: Moebius and Related Syndromes Brain : a Journal of Neurology. Apr, 2014 | Pubmed ID: 24561559 Embryonic Craniofacial Bone Volume and Bone Mineral Density in Fgfr2(+/P253R) and Nonmutant Mice Developmental Dynamics : an Official Publication of the American Association of Anatomists. Apr, 2014 | Pubmed ID: 24504751 Willingness to Participate in Genomics Research and Desire for Personal Results Among Underrepresented Minority Patients: a Structured Interview Study Journal of Community Genetics. Oct, 2013 | Pubmed ID: 23794263 The Study of Abnormal Bone Development in the Apert Syndrome Fgfr2+/S252W Mouse Using a 3D Hydrogel Culture Model Bone. Jul, 2008 | Pubmed ID: 18407821 Laser Capture Microdissection of Mouse Embryonic Cartilage and Bone for Gene Expression Analysis Meng Wu1, Divya Kriti1, Harm van Bakel1,2, Ethylin Wang Jabs1, Greg Holmes1 1Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, 2Icahn Institute for Data Science and Genomic Technology, Icahn School of Medicine at Mount Sinai JoVE 60503 Developmental Biology
Laser Capture Microdissection of Mouse Embryonic Cartilage and Bone for Gene Expression Analysis Meng Wu1, Divya Kriti1, Harm van Bakel1,2, Ethylin Wang Jabs1, Greg Holmes1 1Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, 2Icahn Institute for Data Science and Genomic Technology, Icahn School of Medicine at Mount Sinai JoVE 60503 Developmental Biology
