EthylinWangJabsMD

PubMed

• Transcriptomic landscape of human induced pluripotent stem cell-derived osteogenic differentiation identifies a regulatory role of KLF16.
  Ru, Y., Ma, M., Zhou, X., Kriti, D., Cohen, N., D'Souza, S., Schaniel, C., Motch Perrine, S., Kuo, S., Pinto, D., Housman, G., Wu, M., Holmes, G., Schadt, E., van Bake...> ;Biorxiv. 2024 Feb 12
• Associations between maternal periconceptional alcohol consumption and risk of omphalocele among offspring, National Birth Defects Prevention Study, 1997-2011.
  Fisher, S., Romitti, P., Tracy, M., Howley, M., Browne, M., , Jabs, E.> ;Preventive Medicine. 2024 Mar 1
• Inability to move one's face dampens facial expression perception.
  Shruti Japee, Jessica Jordan, Judith Licht, Savannah Lokey, , Gang Chen, Joseph Snow, Ethylin Wang Jabs, Bryn D Webb, Elizabeth C Engle, Irini Manoli, Chris Baker, Les...> ;Cortex; a Journal Devoted to the Study of the Nervous System and Behavior. 2023 Dec 1
• Monozygotic twins discordant for a congenital cranial dysinnervation disorder with features of Moebius syndrome.
  Ryan W Gates, Bryn D Webb, David A Stevenson, Ethylin Wang Jabs, Colette DeFilippo, Maura R Z Ruzhnikov, Christina G Tise> ;American Journal of Medical Genetics. Part A. 2023 Nov 1
• 4 citations
  Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.
  Alan P Tenney, Silvio Alessandro Di Gioia, Bryn D Webb, Wai-Man Chan, Elke de Boer, Sarah J Garnai, Brenda J Barry, Tammy Ray, Michael Kosicki, Caroline D Robson, Zhon...> ;Nature Genetics. 2023 Jul 1
• Attitudes on pharmacogenomic results as secondary findings among medical geneticists.
  Meghan N Bartos, Stuart A Scott, Ethylin Wang Jabs, Hetanshi Naik> ;Pharmacogenetics and Genomics. 2022 Oct 1
• 4 citations
  Cleft Palate in Apert Syndrome.
  Delayna Willie, Greg Holmes, Ethylin Wang Jabs, Meng Wu> ;Journal of Developmental Biology. 2022 Aug 11
• 4 citations
  Maternal periconceptional alcohol consumption and gastroschisis in the National Birth Defects Prevention Study, 1997-2011.
  Sarah C Fisher, Meredith M Howley, Paul A Romitti, Tania A Desrosiers, Ethylin Wang Jabs, Marilyn L Browne> ;Paediatric and Perinatal Epidemiology. 2022 Nov 1
• 3 citations
  Meckel's Cartilage in Mandibular Development and Dysmorphogenesis.
  M Kathleen Pitirri, Emily L Durham, Natalie A Romano, Jacob I Santos, Abigail P Coupe, Hao Zheng, Danny Z Chen, Kazuhiko Kawasaki, Ethylin Wang Jabs, Joan T Richtsmeie...> ;Frontiers in Genetics. 2022 Jan 1
• 12 citations
  Single-cell analysis identifies a key role for Hhip in murine coronal suture development.
  Greg Holmes, Ana S Gonzalez-Reiche, Madrikha Saturne, Susan M Motch Perrine, Xianxiao Zhou, Ana C Borges, Bhavana Shewale, Joan T Richtsmeier, Bin Zhang, Harm van Bake...> ;Nature Communications. 2021 Dec 8
• 11 citations
  TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathy
  , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , > ;Human Genetics. 2021 Oct 15
• 2 citations
  Deletion of ERF and CIC causes abnormal skull morphology and global developmental delay.
  Ram Singh, Ana S. A. Cohen, Cathryn Poulton, Tina Duelund Hjortshøj, Moe Akahira-Azuma, Geetu Mendiratta, Wahab A. Khan, Dimitar N. Azmanov, Karen J. Woodward, Maria K...> ;Cold Spring Harbor Molecular Case Studies. 2021 Jun 11
• 1 citations
  A framework for the evaluation of patients with congenital facial weakness.
  Bryn D. Webb, Irini Manoli, Elizabeth C. Engle, Ethylin Wang Jabs> ;Orphanet Journal of Rare Diseases. 2021 Apr 7
• 11 citations
  Neonatal outcomes during the COVID-19 pandemic in New York City.
  Felix Richter, Arielle S. Strasser, Mayte Suárez-Fariñas, Shan Zhao, Girish N. Nadkarni, Ethylin Wang Jabs, Katherine Guttmann, Benjamin S. Glicksberg> ;Pediatric Research. 2021 Apr 7
• 4 citations
  Differentiating Moebius syndrome and other congenital facial weakness disorders with electrodiagnostic studies.
  Tanya J. Lehky, Reversa Joseph, Camilo Toro, Tianxia Wu, Carol Van Ryzin, Andrea L. Gropman, Flavia M. Facio, Bryn D. Webb, Ethylin Wang Jabs, Brenda S Barry, Elizabet...> ;Muscle & Nerve. 2021 Jan 19
• 9 citations
  Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex
  Susan M. Motch Perrine, Meng Wu, Greg Holmes, Bryan C. Bjork, Ethylin Wang Jabs, Joan T. Richtsmeier> ;Journal of Developmental Biology. 2020 Dec 5
• 18 citations
  FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research.
  Bridget Samuels, Robert Aho, James F. Brinkley, Alejandro Bugacov, Eleanor Feingold, Shannon Fisher, Ana S. Gonzalez-Reiche, Joseph G. Hacia, Benedikt Hallgrímsson, Ka...> ;Development. 2020 Sep 15
• 6 citations
  Genotype–Phenotype Correlation of Tracheal Cartilaginous Sleeves and Fgfr2 Mutations in Mice
  Austin S. Lam, Carrie C. Liu, Gail H. Deutsch, Joshua Rivera, Jonathan A. Perkins, Greg Holmes, Ethylin Wang Jabs, Michael L. Cunningham, John P. Dahl> ;The Laryngoscope. 2021 Mar 10
• 34 citations
  Integrated Transcriptome and Network Analysis Reveals Spatiotemporal Dynamics of Calvarial Suturogenesis
  Greg Holmes, Ana S. Gonzalez-Reiche, Na Lu, Xianxiao Zhou, Joshua Rivera, Divya Kriti, Robert Sebra, Anthony Williams, Michael J. Donovan, S. Steven Potter, Dalila Pin...> ;Cell Reports. 2020 Jul 7
• 2 citations
  Laser Capture Microdissection of Mouse Embryonic Cartilage and Bone for Gene Expression Analysis.
  Meng Wu, Divya Kriti, Harm van Bakel, Ethylin Wang Jabs, Greg Holmes> ;Journal of Visualized Experiments. 2019 Dec 18
• 6 citations
  Brain phenotyping in Moebius syndrome and other congenital facial weakness disorders by diffusion MRI morphometry.
  Neda Sadeghi, Elizabeth B. Hutchinson, Carol Van Ryzin, Edmond J. FitzGibbon, John A. Butman, Bryn D. Webb, Flavia M. Facio, Brian P. Brooks, Francis S. Collins, Ethyl...> ;Brain Communications. 2020 Jan 1
• 9 citations
  Nonsyndromic craniosynostosis: novel coding variants.
  Anshuman Sewda, Sierra R. White, Monica Erazo, Ke Hao, Gemma García-Fructuoso, Ivette Fernández-Rodriguez, Yann Heuzé, Joan T. Richtsmeier, Paul A. Romitti, Boris Reva...> ;Pediatric Research. 2019 Jan 14
• 17 citations
  Mandibular dysmorphology due to abnormal embryonic osteogenesis in FGFR2-related craniosynostosis mice
  Susan M. Motch Perrine, Meng Wu, Nicholas B. Stephens, Divya Kriti, Harm van Bakel, Ethylin Wang Jabs, Joan T. Richtsmeier> ;Disease Models & Mechanisms. 2019 Jan 1
• 21 citations
  Midface and upper airway dysgenesis in FGFR2-related craniosynostosis involves multiple tissue-specific and cell cycle effects.
  Greg Holmes, Courtney O'Rourke, Susan M. Motch Perrine, Na Lu, Harm van Bakel, Joan T. Richtsmeier, Ethylin Wang Jabs> ;Development. 2018 Oct 5
• Ten-year experience of more than 35,000 orofacial clefts in Africa.
  Conway, J. C.,Taub, P. J.,Kling, R.,Oberoi, K.,Doucette, J.,Jabs, E. W.> ;BMC Pediatr. 2015 Mar 18
• Join now to see all

Journal Articles

• MAFs and haplotype frequencies for SNPs in ROR2 gene among parents of Han Chinese NSCL/P patients in China  
  Zhao, K.P., Huang, S., Wang, H., Hetmanski, J.B. Zhang, T. X., Schwender, H., Ye, X., Chen, Q., Jabs, E.W., Scott, A.F., and Beaty, T.H., Chin J Public Health, 1/1/2013
• HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- mice  
  Webb, B.D., Shaaban, S., Gaspar, H., Cunha, L.F., Schubert, C.R., Hao, K., Robson, C.D., Chan, W.-M., Andrews, C., MacKinnon, S., Oystreck, D.T., Hunter, D.G., Iacovel..., Am J Hum Genet, 1/1/2012
• Evidence for gene-environment interaction in a genome wide study of non-syndromic cleft palate  
  Beaty, T.H., Ruczinski, I., Murray, J.C., Marazita, M.L., Munger, R.G., Hetmanski, J.B., Murray, T., Redett, R.J., Fallin, M.D., Liang, K.Y., Wu, T., Patel, P.J., Jin,..., Genet Epidemiol, 1/1/2011
• Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: A focus group study  
  Streicher, S.A., Sanderson, S.C., Jabs, E.W., Diefenbach, M., Smirnoff, M., Peter, I., Horowitz, C.R., Brenner, B., and Richardson, L.D., J Community Genet, 1/1/2011
• Exome sequencing identifies the cause of a Mendelian disorder  
  Ng, S.B., Buckingham, K.J, Lee, C., Bigham, A.W., Tabor, H.K., Dent, K.M., Huff, C.D., Shannon, P.T., Jabs, E.W., Nickerson, D.A., Shendure, J., and Bamshad, M.J., Nat Genetics, 1/1/2010
• Association between genes on chromosome 4p16 and non-syndromic oral clefts in four populations  
  Ingersoll, R.G., Hetmanski, J., Park, J.W., Fallin, M.D., McIntosh, I., Wu-Chou, Y.H, Chen, P.K., Yeow, V., Chong, S.S., Cheah, F., Sull, J.W., Jee, S.H., Wang, H., Wu..., Eur J Hum Genet, 1/1/2010
• Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2+/P253R mice  
  Wang, Y, Sun, M., Uhlhorn,V.L., Zhou, X., Peter, I., Martinez-Abadias, N., Hill, C.A., Percival, C.J., Richtsmeier, J.T., Huso, D.L., and Jabs, E.W., BMC Dev Biol, 1/1/2010
• A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4  
  Beaty, T.H., Murray, J.C., Marazita, M.L., Munger, R.G., Ruczinski, I., Hetmanski, J.B., Liang, K.Y., Wu, T., Murray, T., Fallin, M.D., Redett, R.A., Raymond, G., Schw..., Nat Genetics, 1/1/2010
• Evidence of gene-environment interaction for IRF6 gene and maternal multivitamin supplementation in controlling risk of cleft lip with/without cleft palate  
  Wu, T., Liang, K.-Y., Hetmanski, J.B., Ruczinski, I., Fallin, M.D., Ingersoll, R.G., Wang, H., Huang, S., Ye, X., Wu-Chow, Y.-H., Chen, P.K., Jabs, E.W., Shi, B., Rede..., Hum Genet, 1/1/2010
• Maternal transmission effects of the PAX genes among cleft case-parent trios from four populations  
  Sull, J.W., Liang, K.Y., Hetmanski, J.B., Fallin, M.D., Ingersoll, R.G., Park, J., Wu-Chou, Y.H., Chen, P.K., Chong, S.S., Cheah, F., Yeow, V., Park, B.Y., Jee, S.H., ..., Eur J Hum Genet, 1/1/2009
• Evidence that TGFA influences risk for cleft lip with/without cleft palate through unconventional genetic mechanisms  
  Sull, J.W., Liang, K.Y., Hetmanski, J.B., Wu, T., Fallin, M.D., Ingersoll, R.G., Park, J.W., Wu-Chou, Y.H., Chen, P.K., Chong, S.S., Cheah, F., Yeow, V., Park, B.Y., J..., Hum Genet, 1/1/2009
• The ups and downs of mutation frequencies during aging can account for the Apert syndrome paternal age effect  
  Yoon, S.R., Qin, J., Glaser, R.L., Jabs, E.W., Wexler, N.S., Sokol, R., Arnheim, N., and Calabrese, P., PLOS Genetics, 1/1/2009
• Tyrosine- dependent basolateral targeting of human connexin43-eYFP in Madlin-Darby canine cells can be disrupted by the oculodentodigital dysplasia mutation L90V  
  Chtchetinin, J., Gifford, W.D., Li, S., Paznekas, W.A., Jabs, E.W., and Lai, A., FEBS Journal, 1/1/2009
• Excess maternal transmission of markers in TCOF1 among cleft palate case-parent trios from three populations  
  Sull, J.W., Liang, K.Y., Hetmanski, J.B., Fallin, M.D., Ingersoll, R.G., Park, J.W., Wu-Chou, Y.H., Chen, P.K., Chong, S.S., Cheah, F., Yeow, V., Park, B.Y., Jee, S.H...., Am J Med Genet, 1/1/2008
• Genetic analysis of non-syndromic craniosynostosis  
  Boyadjiev, S.A. and the International Craniosynostosis Consortium including Jabs, E.W., Orthod Craniofacial Res, 1/1/2007
• High throughput SNP and expression analyses of candidate genes for non-syndromic oral clefts  
  Park, J.W., Cai, J., McIntosh, I., Jabs, E.W., Fallin, M.D., Ingersoll, R., Hetmanski, J.B., Vekemans, M., Attie-Bitach, T., Lovett, M., Scott, A.F., and Beaty, T.H., J Med Genet, 1/1/2006
• Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, aneuploidies in sperm  
  Wyrobek, A.J., Eskenazi, B., Young, S., Arnheim, N., Tiemann-Boege, I., Jabs, E.W., Glaser, R.L., Pearson, F.S., and Evenson, D., Proc Natl Acad Sci, USA, 1/1/2006
• Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations  
  Beaty, T.H., Hetmanski, J.B., Fallin, M.D., Park, J.W., Sull, J.W., McIntosh, I., Liang, K.Y., Vander Kolk, C.A., Redett, R.J., Boyadjiev, S.A., Jabs., E.W., Chong, S...., Hum Genet, 1/1/2006
• Cleft lip/palate and CDH1/E-cadherin mutations in families with hereditary diffuse gastric cancer  
  Frebourg, T., Oliveira, C., Hochain, P., Karam, R., Manouvrier, S., Graziadio, C., Vekemans, M., Hartmann, A., Baert-Desurmont, S., Alexandre, C., Lejeune-Dumoulin, S...., J Med Genet, 1/1/2005
• Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene  
  Van Maldergem, L., Siitonen, H.A., Jalkh, N., Chouery, E., De Roy, M., Delague, V., Muenke, M., Jabs, E.W., Cai, J., Wang, L.L., Plon, S.E., Fourneau, C., Kestila, M.,..., J Med Genet, 1/1/2005
• The role of cathepsin C in Papillon-Lefevre syndrome, prepubertal periodontitis, and aggressive periodontitis  
  Hewitt, C., McCormick, D., Linden, G., Turk, D., Stern, I., Wallace, I., Southern, L., Zhang, L., Howard, R., Bullon, P., Wong, M., Widmer, R., Gaffar, K.A., Awawdeh, ..., Hum Mutat, 1/1/2004
• A novel mutation in the TWIST gene, implicated in Saethre-Chotzen syndrome, is found in the original case of ?Robinow-Sorauf syndrome?  
  Cai, J., Shoo, B.A., Sorauf, T., and Jabs, E.W., Clin Genet, 1/1/2003
• Screening of TCOF1 in patients from different populations: confirmation of mutational hot spots and identification of a novel missense mutation that suggests an import...  
  Splendore, A., Jabs, E.W., and Passos-Bueno, M.R., J Med Genet, 1/1/2002
• Physical mapping of the MEGF1 gene, human homologue of the Drosophila tumour suppressor gene fat, to the critical region of the 5q-syndrome  
  Fidler, C., Nakayama, M., Jabs, E.W., Cheng, J.-F., Strickson, A., Ohara, O., Wainscoat, J.S., and Boultwood, J., GeneScreen, 1/1/2001
• Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome  
  Glaser, R.L., Jiang, W., Boyadjiev, S.A., Tran, A.K., Zachary, A.A., Van Maldergem, L., Johnson, D., Walsh, S., Oldridge, M., Wall, S.A., Wilkie, A.O.M., and Jabs, E.W., Am J Hum Genet, 1/1/2000
• Join now to see all

Books/Book Chapters

• Building Bones: Bone Development and Formation in Anthropology 
  Chapter: The contribution of angiogenesis to variation in bone development and evolution 
  Page 26 - 51Percival, C.J., Kawasaki, K., Huang, Y., Weiss, K., Jabs, E.W., Li, R., and Richtsmeier, J.T.Editors: Percival, C.J., Richtsmeier, J.T..Cambridge University Press, Cambridge, United Kingdom2017
• Human Microbiome: Ethical, Legal and Social Concerns 
  Chapter: Public Health and Research 
  Page 208 - 240Rhodes, R., Baumrin, S.B., Blaser, M.J., Earle, W.J., Indyk, D., Jabs E.W., Moros, D.A., Richardson, L.D., and Sacks, H.S.Oxford University Press2013
• Clinical Genomics: Practical Applications in Adult Patient Care 
  Chapter: Achondroplasia 
  Page 763 - 765Webb, B.D., Hoover-Fong, J.E., and Jabs, E.W.McGraw-Hill Education Medical, New York, NY2013
• Clinical Genomics: Practical Applications in Adult Patient Care 
  Chapter: Chromosomal Disorders in Adults 
  Page 816 - 821Manace-Brenman, K.P., Edelmann, L., and Jabs, E.W.McGraw-Hill Education Medical, New York, NY2013
• Emery & Rimoin's Principles and Practice of Medical Genetics 
  Chapter: Craniosynostosis 
  Page 1 - 34Jabs, E.W and Lewanda, A.F.Editors: Rimoin, D.L., Pyeritz, R.E., Korf, B.R..Elsevier2013
• Genetic Diseases of the Eye 
  Chapter: Ocular manifestations of syndromes with craniofacial abnormalities 
  Page 174 - 189Zein, M.W., Lewanda, A.F., Traboulsi, E.I., and Jabs, E.W.Editors: Traboulsi, E.I..Oxford University Press2012
• GeneReviews 
  Chapter: Roberts syndrome 
  Gordillo, M., Vega, H., and Jabs, E.WEditors: Pagon R.A., Bird T.C., Dolan C.R., Stephens K..University of Washington, Seattle2009
• Molecular Basis of Inborn Errors of Development 
  Chapter: ESCO2 and Roberts Syndrome 
  Page 1011 - 1019Gordillo, M., Vega H., and Jabs, E.W.Editors: Epstein, C.J., Erickson, R.P., and Wynshaw-Boris, A..Oxford University Press, New York, NYEdition 2nd,2008
• Molecular Basis of Inborn Errors of Development 
  Chapter: RECQL4 and Rothmund- Thomson, RAPADILINO, and Baller-Gerold 
  Page 1237 - 1245Van Maldergem, L., Siitonen, H.A., Jabs, E.W., and Gordillo, M.Editors: Epstein, C.J., Erickson, R.P., and Wynshaw-Boris, A..Oxford University Press, New York, NYEdition 2nd,2008
• Molecular Basis of Inborn Errors of Development 
  Chapter: TWIST and the Saethre-Chotzen syndrome 
  Page 474 - 481Jabs, E.W.Editors: Epstein, C.J., Erickson, R.P., and Wynshaw-Boris, A..Oxford University Press, New YorkEdition 2nd,2008
• Emery & Rimoin's Principles and Practice of Medical Genetics 
  Chapter: Craniosynostosis 
  Page 3359 - 3379Lewanda, A.F. and Jabs, E.W.Editors: Rimoin, D.L., Connor, J.M., Pyeritz, R.E., Korf, B.R..Churchill Livingstone, Philadelphia, PAEdition 5th,2007
• Oski's Pediatrics: Principles and Practice 
  Chapter: Dysmorphology: Genetic syndromes and associations 
  Page 2629 - 2670Lewanda, A.F., Boyadjiev, S.A., and Jabs E.W.Editors: McMillan, J.A., DeAngelis, C.D., Feigin, R.D., and Warshaw, J.P..Lippincott, Williams, & Wilkins Publishers, Philadelphia, PAEdition 4th,2006
• ASHG Code of Ethics 
  Chapter: ASHG Code of Ethics 
  Jabs, E.W., Knoppers, B.M, Van Dyke, D, Weinblatt, V., Toriello, H., and McGillivray, B.Editors: Boughman, J.A..2006
• Molecular Basis of Inborn Errors of Development 
  Chapter: TWIST and the Saethre-Chotzen Syndrome 
  Page 401 - 409Jabs, E.W.Editors: Epstein, C.J., Erickson, R.P., and Wynshaw-Boris, A..Oxford University Press, New York, NY2004
• Understanding Craniofacial Anomalies: The Etiopathogenesis of Craniosynostoses and Facial Clefting 
  Chapter: Genetic Etiologies of Craniosynostosis 
  Page 125 - 146Jabs, E.W.Editors: Mooney MP and Siegel MI.John W. Wiley and Sons2002
• Principles and Practice of Medical Genetics 
  Chapter: Craniosynostosis 
  Page 3673 - 3688Lewanda, A.F. and Jabs, E.W.Editors: Rimoin, D.L., Connor, J.M., Pyeritz, R.E., Korf, B.R..Churchill Livingstone, London, United KingdomEdition 4th,2002
• Current Protocols in Cell Biology 
  Chapter: SAGE analysis from 1microgram of total RNA. Unit 19.4 ?Serial Analysis of Gene Expression From 1 Microgram Total RNA? for Supplement 16 
  Cai, J., Ash, D., and Jabs, E.W.Editors: Bonifacino, J.S., Dasso, M., Harford, J.B., Lippincott-Schwartz, J., and Yamada, K.M..John D. Wiley & Sons, New York, NY2002
• Cleft Lip and Palate: From Origin to Treatment 
  Chapter: Genes implicated in lip and palate development 
  Page 25 - 39Chong, S.E. Cheah, F.S.H., and Jabs, E.W.Editors: Wyszynski, D.F..Oxford University Press2002
• Craniofacial Surgery: Science and Surgical Technique 
  Chapter: Genetics of mandibulofacial dysostosis 
  Page 55 - 63Jabs, E.W.Editors: Lin, K.Y., Ogle, R.C., and Jane, J.A..W.B. Saunders Company2001
• Plastic Surgery: Indications, Operations, and Outcomes 
  Page 619 - 636DeLeon, V.B., Jabs, E.W., and Richtsmeier, J.Editors: Achauer, B.M., Eriksson, E., Guyuron, B., Coleman, J.J. III, Russell, R.C., and Vander Kolk, C.A..Mosby-Year Book2000
• Developmental Biology: Frontiers for Clinical Genetics 
  Chapter: Online Mendelian Inheritance in Man (OMIM) as a knowledgebase for human developmental disorders 
  Boyadjiev, S.A. and Jabs, E.W.Editors: McInnes, R.R..2000
• Oski?s Pediatrics: Principles and Practice 
  Chapter: Dysmorphology: Genetic syndromes and associations 
  Page 2225 - 2259Lewanda, A.F. and Jabs, E.W.Editors: McMillan, J.A., DeAngelis, C.D., Feigin, R.D., and Warshaw, J.P..Lippincott, Williams, & Wilkins PublishersEdition 3rd,1999
• Principles of Molecular Medicine 
  Chapter: Fibroblast growth factor receptor-related skeletal disorders: Craniosynostosis and dwarfism syndromes. Section on Genetic Basis of Congenital Malformations (ed. Jabs, E.W.) 
  Page 1029 - 1038Muenke, M., Francomano, C. A., Cohen, M.M., Jr., and Jabs, E.W.Editors: Jameson, L..Humana Press1998
• Genetic Diseases of the Eye 
  Chapter: Syndromes with craniofacial anomalies. Section V. Ocular manifestations of inherited systemic diseases 
  Page 777 - 796Lewanda, A.F., Traboulsi, E.I., and Jabs, E.W.Editors: Traboulsi, E.I..Oxford University Press1998
• Methods in Molecular Biology, Vol. 68: Gene Isolation and Mapping Protocols 
  Chapter: Linkage analysis of genetic disorders 
  Page 11 - 25Taylor, E.W., Xu, J., Jabs, E.W., and Meyers, D.A.Editors: Boultwood, J.Humana Press, Totowa, NJ1997
• Join now to see all

Lectures

• Integration of Systems and Developmental Biology in Skull Morphogenesis 
  1/14/2018
• Birth Defects Webinar 
  1/19/2017
• How to get aHEAD with omics 
  1/12/2017
• Craniosynostosis: Genomic and Systems Approach 
  1/9/2017
• Genome-wide DNA methylation profiling and transcriptome in neural tubes of Folr1 knockout mice 
  1/2/2017
• Craniosynostosis: Pfeiffer Syndrome 
  1/14/2016
• The Face of Fibroblast Growth Factor Signaling 
  1/13/2016
• Transcriptome Atlases of Craniofacial Sutures 
  1/8/2015
• Birth Defects: Moebius Syndrome and Related Facial Weakness Disorders 
  1/23/2014
• Spoke Project 
  1/8/2014
• Craniosynostosis Network 
  1/8/2014
• Impact of Genomics on Craniofacial Disorders 
  1/7/2014
• Genetic Epidemiology and Prevention of Oral Clefting 
  1/6/2014
• Gorlin Syndrome and General Medical Genetic Approaches 
  1/25/2012
• Twenty Years Later What Have We Learned about the Molecular Basis of Craniofacial Disorders? 
  1/16/2012
• Craniosynostosis Syndromes and Molecular Therapeutic Strategies 
  1/29/2011
• Genomic Approach to Prenatal Diagnosis 
  The First Bethune Hospital, Jinlin University, Changchun, China - 1/20/2011
• Personal Genomic Sequencing in Medical Care: Rare and Common Disorders 
  1/15/2011
• FGFR Related Craniosynostosis Syndromes and Potential Therapeutic Strategies 
  1/12/2011
• Genetic Epidemiology of Oral Clefting in Africa 
  1/11/2011
• Developmental Genetics 
  1/1/2011
• Molecular Basis of Human Congenital Anomalies, Human Developmental Syndromes 
  1/28/2010
• The Impact of Whole Genome Sequencing on Pediatric Care Starting with Congenital Anomalies 
  1/2/2010
• Genetic Update 
  1/14/2009
• The Human Face: Reflections through Genetic Diseases 
  1/13/2009
• Join now to see all

Other

• Ethylin Wang Jabs Lab 
  Icahn School of Medicine at Mount Sinai
  http://www.mssm.edu/research/labs/ethylin-wang-jabs-laboratory
• Treacher Collins syndrome 
  Katsanis, S.H. and Jabs, E.W., Adam M.P., Ardinger H.H., Pagon R.A., Wallace S.E., Bean L.J.H., Stephens K., Amemiya A..
  GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle - 8/20/2020
• ESCO2 spectrum disorder 
  Vega, H., Gordillo, M., and Jabs, E.W., Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors
  https://www.ncbi.nlm.nih.gov/pubmed/20301332
  GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle - 3/26/2020
• STAC3 disorder. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. 
  Webb, B.D., Manoli, I., and Jabs, E.W., Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors.
  GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle - 6/20/2019
• Treacher Collins syndrome. 
  Katsanis, S.H. and Jabs, E.W, Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors.
  http://www.genetests.org
  GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle - 9/27/2018
• Roberts Syndrome. Pagon RA, Adam MP, Bird TD, et al., editors 
  Gordillo, M., Vega, H., and Jabs, E.W., GeneReviews
  http://www.ncbi.nlm.nih.gov/books/NBK1153/
  1/14/2013
• Clinical Delineation of KID Syndrome, an Ectodermal Dysplasia 
  Jabs, E.W., NFED Research Report, NFED 30th Anniversary
  1/1/2011
• Treacher Collins Syndrome 
  Katsanis, S.H. and Jabs, E.W., GeneReviews at GeneTests: Medical Genetics Information Resource
  http://www.genetests.org
  1/1/2011
• Roberts Syndrome. Pagon RA, Bird TC, Dolan CR, Stephens K, editors 
  Gordillo, M., Vega, H., and Jabs, E.W., GeneReviews
  1/1/2009
• Roberts syndrome 
  Gordillo, M., Vega, H., and Jabs, E.W., GeneReviews
  1/1/2006
• FaceBase: An Online Resource for Craniofacial Research 
  Brinkley, J.F., Fisher, S., Harris, M.P., Holmes, G., Hooper, J.E., Jabs, E.W., Jones, K.L., Kesselman, C., Klein, O.D., Maas, R.L., Marazita, M.L., Selleri, L., Sprit..., The Node
• Ethylin Wang Jabs 
  
  https://en.wikipedia.org/wiki/Ethylin_Wang_Jabs
• Interdisciplinary Training in Systems and Developmental Biology and Birth Defects 
  
  http://icahn.mssm.edu/research/genomics/education/nih-training
• Craniosynostosis Network 
  
  https://clinicaltrials.gov/ct2/show/NCT03025763?term=ethylin&rank=1
• Study of Moebius Syndrome and Other Congenital Facial Weakness Disorders 
  
  https://clinicaltrials.gov/ct2/show/NCT02055248?term=ethylin&rank=2
• MSSM Residencies and Fellowships 
  
  http://www.mssm.edu/departments-and-institutes/genetics-and-genomic-sciences/programs-and-training/medical-genetics-residency-and-fellowship-programs
• Whole genome sequencing and you 
  
  http://www.youtube.com/watch?v=IXamRS85hXU
• Power of the Smile Interview 
  
  https://www.youtube.com/watch?v=XGkzyiJaMOQ
• Improving Life for Kids with Facial Deformities 
  
  http://krieger.jhu.edu/magazine/2015/05/improving-life-for-kids-with-facial-deformities/
• Countdown to Life ? The Extraordinary Making of You - 1. The First 8 Weeks British Broadcasting Corporation 
  
  https://www.youtube.com/watch?v=Y3D8UMEpqok
• Collaboration for Craniofacial Development and Disorders 
  
  http://www.hopkinsmedicine.org/craniofacial
• COGENE: The Craniofacial and Oral Gene Expression Network 
  
  http://hg.wustl.edu/COGENE
• International Collaborative Genetic Research Training Program 
  
  http://www.hopkinsmedicine.org/ICGRTP/traininggrant/
• Mentored Master of Science Thesis of Nicholas Heitman 
  
  http://search.proquest.com/index
• Facebook Live at Mount Sinai Dr. Ethylin Jabs in honor of #DownSyndromeAwarenessMonth #LiveAtMountSinai 
• Join now to see all