Ethylin Wang Jabs

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