{"id":3,"date":"2016-05-26T14:47:05","date_gmt":"2016-05-26T14:47:05","guid":{"rendered":"http:\/\/labs.icahn.mssm.edu\/jabslab\/calendar\/"},"modified":"2022-01-10T04:56:04","modified_gmt":"2022-01-10T04:56:04","slug":"aboutus","status":"publish","type":"page","link":"https:\/\/labs.icahn.mssm.edu\/jabslab\/aboutus\/","title":{"rendered":"Our Research"},"content":{"rendered":"<p>[et_pb_section fb_built=&#8221;1&#8243; admin_label=&#8221;Section&#8221; _builder_version=&#8221;4.9.0&#8243; custom_padding=&#8221;10px||10px||false|false&#8221;][et_pb_row admin_label=&#8221;Row&#8221; _builder_version=&#8221;4.9.0&#8243; background_size=&#8221;initial&#8221; background_position=&#8221;top_left&#8221; background_repeat=&#8221;repeat&#8221;][et_pb_column type=&#8221;4_4&#8243; _builder_version=&#8221;3.25&#8243; custom_padding=&#8221;|||&#8221; custom_padding__hover=&#8221;|||&#8221;][et_pb_text _builder_version=&#8221;4.9.0&#8243; _module_preset=&#8221;default&#8221;]<\/p>\n<h1>Our Research<\/h1>\n<p>[\/et_pb_text][et_pb_text admin_label=&#8221;Text&#8221; _builder_version=&#8221;3.27.4&#8243; background_size=&#8221;initial&#8221; background_position=&#8221;top_left&#8221; background_repeat=&#8221;repeat&#8221;]<\/p>\n<p><span style=\"font-weight: 400\">Our research centers on elucidating the pathogenesis of<strong> pediatric human malformation disorders<\/strong> and <strong>genetic birth defects<\/strong>, including:\u00a0<\/span><\/p>\n<ul>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Craniosynostosis<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Cleft lip and palate\u00a0<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Mandibular dysgenesis\u00a0<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Limb dysplasias<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Neural tube defects<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Crouzon syndrome\u00a0<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Apert syndrome<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Treacher Collins syndrome\u00a0<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Goldenhar syndrome\u00a0<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Moebius syndrome\u00a0<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Pierre-Robin complex<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Roberts syndrome<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Bear-Stevenson syndrome<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">Oculodentodigital dysplasia\u00a0<\/span><\/li>\n<li style=\"font-weight: 400\"><span style=\"font-weight: 400\">&amp; other phenotypes related to craniofacial and limb disorders!\u00a0<\/span><\/li>\n<\/ul>\n<p><span style=\"font-weight: 400\">To dissect these phenotypes we apply a combination of genetic, genomic, cellular and molecular biology approaches, genetic engineering, next generation sequencing, bioinformatics, systems biology, and clinical tools.\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400\">We are also involved in GWASs being conducted on non-syndromic congenital anomalies for isolated craniosynostosis and cleft lip with or without cleft palate.\u00a0<\/span><\/p>\n<p><span style=\"font-weight: 400\">Our projects have a direct <strong>clinical impact<\/strong> for patients with malformation disorders and for the support and management they may require.<\/span><\/p>\n<p>&nbsp;<\/p>\n<h1><a href=\"https:\/\/labs.icahn.mssm.edu\/jabslab\/wp-content\/uploads\/sites\/181\/2021\/04\/Combined-Figure-2-Figure-5_v2.jpg\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter size-full wp-image-308\" src=\"https:\/\/labs.icahn.mssm.edu\/jabslab\/wp-content\/uploads\/sites\/181\/2021\/04\/Combined-Figure-2-Figure-5_v2.jpg\" alt=\"\" width=\"2000\" height=\"1141\" srcset=\"https:\/\/labs.icahn.mssm.edu\/jabslab\/wp-content\/uploads\/sites\/181\/2021\/04\/Combined-Figure-2-Figure-5_v2.jpg 2000w, https:\/\/labs.icahn.mssm.edu\/jabslab\/wp-content\/uploads\/sites\/181\/2021\/04\/Combined-Figure-2-Figure-5_v2-300x171.jpg 300w, https:\/\/labs.icahn.mssm.edu\/jabslab\/wp-content\/uploads\/sites\/181\/2021\/04\/Combined-Figure-2-Figure-5_v2-1024x584.jpg 1024w, https:\/\/labs.icahn.mssm.edu\/jabslab\/wp-content\/uploads\/sites\/181\/2021\/04\/Combined-Figure-2-Figure-5_v2-768x438.jpg 768w, https:\/\/labs.icahn.mssm.edu\/jabslab\/wp-content\/uploads\/sites\/181\/2021\/04\/Combined-Figure-2-Figure-5_v2-1536x876.jpg 1536w\" sizes=\"(max-width: 2000px) 100vw, 2000px\" \/><\/a><\/h1>\n<p>[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section]<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Our Research<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"<p><span style=\"font-weight: 400;\">Our research centers on elucidating the pathogenesis of pediatric human malformation disorders and genetic birth defects, including:\u00a0<\/span><\/p><ul><li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Craniosynostosis<\/span><\/li><li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Cleft lip and palate\u00a0<\/span><\/li><li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Mandibular dysgenesis\u00a0<\/span><\/li><li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Limb dysplasias<\/span><\/li><li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Neural tube defects<\/span><\/li><li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Crouzon syndrome\u00a0<\/span><\/li><li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Apert syndrome<\/span><\/li><li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Treacher Collins syndrome\u00a0<\/span><\/li><li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Goldenhar syndrome\u00a0<\/span><\/li><li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Moebius syndrome\u00a0<\/span><\/li><li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Pierre-Robin complex<\/span><\/li><li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Roberts syndrome<\/span><\/li><li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Bear-Stevenson syndrome<\/span><\/li><li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Oculodentodigital dysplasia\u00a0<\/span><\/li><li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">& other phenotypes related to craniofacial and limb disorders!\u00a0<\/span><\/li><\/ul><p><span style=\"font-weight: 400;\">To dissect these phenotypes we apply a combination of genetic, genomic, cellular and molecular biology approaches, genetic engineering, next generation sequencing, bioinformatics, systems biology, and clinical tools.\u00a0<\/span><\/p><p><span style=\"font-weight: 400;\">We are also involved in GWASs being conducted on non-syndromic congenital anomalies for isolated craniosynostosis and cleft lip with or without cleft palate.\u00a0<\/span><\/p><p><span style=\"font-weight: 400;\">Our projects have a direct clinical impact for patients with malformation disorders and for the support and management they may require.<\/span><\/p><p>\u00a0<\/p><h1><a href=\"https:\/\/labs.icahn.mssm.edu\/jabslab\/wp-content\/uploads\/sites\/181\/2021\/04\/Combined-Figure-2-Figure-5_v2.jpg\"><img class=\"aligncenter size-full wp-image-308\" src=\"https:\/\/labs.icahn.mssm.edu\/jabslab\/wp-content\/uploads\/sites\/181\/2021\/04\/Combined-Figure-2-Figure-5_v2.jpg\" alt=\"\" width=\"2000\" height=\"1141\" 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