Dustin Baldridge  baldridge_d@wustl.edu

Newborn Medicine

phone: (314) 454-6148

Education

  • BS, Summa Cum Laude, University of Dallas2002
  • PhD, Baylor College of Medicine2010
  • MD, Baylor College of Medicine2011

Training

  • Residency, St. Louis Children's Hospital and Washington University in St. Louis2011 - 2014
  • Chief Residency, St. Louis Children's Hospital and Washington University in St. Louis2014 - 2015

Licensure and Board Certification

  • American Board of Pediatrics 2014
  • MO, State Medical License 2014

Honors

  • Partners in Excellence Scholarship to the University of Dallas1998 - 2002
  • Honorable Mention, Barry M. Goldwater Scholarship Foundation2000
  • Barry M. Goldwater Scholar2001
  • Phi Beta Kappa Member2001
  • Sister Clodovia Lockett Endowed Scholarship in Pre-Medical Studies2001
  • Young Investigator Award from the American Society for Bone and Mineral Research2007
  • 3rd Place Oral Presentation, Baylor College of Medicine Genetics Department Retreat2009
  • American Society of Human Genetics Trainee Research Award Finalist2009
  • Certificate of Completion, Baylor College of Medicine Ethics Track2011

Recent Publications view all (12)


Publication Co-Authors

  1. Survival among children with "Lethal" congenital contracture syndrome 11 caused by novel mutations in the gliomedin gene (GLDN). Hum Mutat. 2017. PMID:28726266 
  2. The Exome Clinic and the role of medical genetics expertise in the interpretation of exome sequencing results. Genet Med. 2017. PMID:28252636 
  3. Digynic triploidy: utility and challenges of noninvasive prenatal testing. Clin Case Rep. 2015;3(6):406-10. PMCID:PMC4498852  PMID:26185638 
  4. Heterozygous de novo and inherited mutations in the smooth muscle actin (ACTG2) gene underlie megacystis-microcolon-intestinal hypoperistalsis syndrome. PLoS Genet. 2014;10(3):e1004258. PMCID:PMC3967950  PMID:24676022 
  5. Phenotypic variability of osteogenesis imperfecta type V caused by an IFITM5 mutation. J Bone Miner Res. 2013;28(7):1523-30. PMCID:PMC3688672  PMID:23408678 
  6. Mutations in FKBP10 cause recessive osteogenesis imperfecta and Bruck syndrome. J Bone Miner Res. 2011;26(3):666-72. PMCID:PMC3179293  PMID:20839288 
  7. Generalized connective tissue disease in Crtap-/- mouse. PLoS One. 2010;5(5):e10560. PMCID:PMC2868021  PMID:20485499 
  8. Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta. Am J Hum Genet. 2010;86(4):551-9. PMCID:PMC2850430  PMID:20362275 
  9. Signaling pathways in human skeletal dysplasias. Annu Rev Genomics Hum Genet. 2010;11:189-217. PMID:20690819 
  10. CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta. Hum Mutat. 2008;29(12):1435-42. PMCID:PMC2671575  PMID:18566967 
  11. The presence of germ line mosaicism in cleidocranial dysplasia. Clin Genet. 2007;71(6):589-91. PMID:17539909 
  12. Sequence and structure of the mouse connexin45 gene. Biosci Rep. 2001;21(5):683-9. PMID:12168774 
Last updated: 08/17/2017
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