K. Taylor Wild, MD

Medical School

MD - Georgetown University School of Medicine,Washington, DC

Residency

Pediatrics - Children's Hospital of Philadelphia, Philadelphia, PA

Fellowship

Neonatology - Children's Hospital of Philadelphia, Philadelphia, PA
Human Genetics - Children's Hospital of Philadelphia, PA

Papers

2020

Congenital diaphragmatic hernia as a prominent feature of a SPECC1L-related syndrome. Wild KT, Gordon T, Bhoj EJ, Du H, Jhangiani SN, Posey JE, Lupski JR, Scott DA, Zackai EH. Am J Med Genet A. 2020 Sep 21. doi: 10.1002/ajmg.a.61878. Online ahead of print. PMID: 32954677

Wild KT, Rintoul N, Kattan J, Gray B, Engle RW, Keene S, Best D, Davis C, DiGeronimo R, Raman L. Extracorporeal Life Support Organization (ELSO): Guidelines for Neonatal Respiratory Failure. ASAIO Journal: May 2020 - Volume 66 - Issue 5 - p 463-470. Read the abstract.

2018

Wild KT, Yudkoff M, Ierardi-Curto L, and Ganetzky R. Hyperornithinemia, Hyperammonemia, and Homocitrullinuria Causing Severe Neonatal Hyperammonemia. JIMD Rep. 2019;44:103-107. doi: 10.1007/8904_2018_132. Epub 2018 Sep 6.

2013

Wild KT, Betancourt LM, Brodsky NL, Hurt H. The effect of socioeconomic status on the language outcome of preterm infants at toddler age. Early Hum Dev. 2013;89(9):743-6.

Posters and Presentations

2018

Wild, K. Taylor & Batholomew, Dana & Edwards, Taryn & Froh, Elizabeth & Spatz, Diane & Villasis, Cynthia & Hedrick, Holly & Nawab, Ursula. (2018). Human Milk With a Cherry on Top: Achieving Adequate Growth for Infants with Congenital Diaphragmatic Hernia (CDH) Utilizing Human Milk. Poster presented at: Pediatric Academic Societies Annual Meeting; Toronto, ON CAN.

Wild, K. Taylor & Batholomew, Dana & Edwards, Taryn & Froh, Elizabeth & Spatz, Diane & Villasis, Cynthia & Hedrick, Holly & Nawab, Ursula. (2018). Human Milk With a Cherry on Top: Achieving Adequate Growth for Infants with Congenital Diaphragmatic Hernia (CDH) Utilizing Human Milk. Oral Presentation presented at: The Eastern Society for Pediatric Research; Philadelphia, PA.

Wild, K. Taylor & Bhoj, Elizabeth & Verloes, Alain & Zackai, Elaine, et al. (2018). Phenotypic spectrum of SPECC1L mutations encompasses Teebi hypertelorism syndrome but not Opitz BBBG syndrome: report of new families and critical review of the nosology Oral Presentation presented at: Annual David W Smith Workshop on Malformations and Morphogenesis; Banff, AB. CAN.

2017

Agawu, A & Argraves, M & Becker, A & Carroll, B & Christiano, J & Frosch, O & Karamessinis, L & Krass, P & Meadow, J & Mehta, S & Salazar, B, & Wild, T. (2017). PROJECT SPHERE: Shaping a Patient and Housestaff Engaged Rounding Environment. Poster presented at: ACGME Back to the Bedside Meeting; Chicago, IL.