Department of Pediatrics

Education

• BS, Honors in Neuroscience, Summa Cum Laude, The College of William and Mary, 2010
• MD, Washington University School of Medicine, 2015

Training

• Resident, St. Louis Children's Hospital, 2015 - 2018

Licensure and Board Certification

• 2018 - PresMO, Missouri Medical License, Missouri Board of Registration for the Healing Arts
• 2018 - PresIL, Illinois Medical License, Illinois Department of Financial and Professional Regulation
• 2018 - PresCertification in General Pediatrics, American Board of Pediatrics
• 2018 - PresAdvanced Trauma Life Support (ATLS)
• 2019 - PresPediatric Advanced Life Support (PALS)
• 2019 - PresNeonatal Resuscitation Program (NRP)
• 2019 - PresSexual Assault Forensic Examination - Child Abuse Resource and Education (SAFE-CARE)
• 2019 - PresNexplanon Insertion
• 2022 - PresCPI Nonviolent Crisis Intervention

Recent Publications view all (5)

Publication Co-Authors

Marwan Shinawi, M.D.

Cassandra M. Pruitt, M.D., FAAP

Mythili Srinivasan, M.D., Ph.D.

Linda Manwaring

David B. Wilson, M.D., Ph.D.

Washington University has a long tradition of collaboration amongst colleagues.The faculty above have co-authored publications with Cori Grant

1. Thompson E, Abdalla E, Superti-Furga A, McAlister W, Kratz L, Unger S, Royer-Bertrand B, Campos-Xavier B, Mittaz-Crettol L, Amin AK, DeSanto C, Wilson DB, Douglas G, Kozel B, Shinawi M. Lamin B receptor-related disorder is associated with a spectrum of skeletal dysplasia phenotypes. Bone. 2019;120:354-363. PMID:30448303 
2. Srinivasan M, Pruitt C, Casey E, Dhaliwal K, DeSanto C, Markus R, Rosen A. Quality Improvement Initiative to Increase the Use of Nasogastric Hydration in Infants With Bronchiolitis. Hosp Pediatr. 2017;7(8):436-443. PMCID:PMC5525377  PMID:28679563 
3. DeSanto C, D'Aco K, Araujo GC, Shannon N, DDD Study., Vernon H, Rahrig A, Monaghan KG, Niu Z, Vitazka P, Dodd J, Tang S, Manwaring L, Martir-Negron A, Schnur RE, Juusola J, Schroeder A, Pan V, Helbig KL, Friedman B, Shinawi M. WAC loss-of-function mutations cause a recognisable syndrome characterised by dysmorphic features, developmental delay and hypotonia and recapitulate 10p11.23 microdeletion syndrome. J Med Genet. 2015;52(11):754-61. PMID:26264232 
4. Safarpour D, Thibault DP, DeSanto CL, Boyd CM, Dorsey ER, Racette BA, Willis AW. Nursing home and end-of-life care in Parkinson disease. Neurology. 2015;85(5):413-9. PMCID:PMC4534080  PMID:26138947 
5. White JT, DeSanto CL, Gibbons C, Lardner CK, Panakos A, Rais S, Sharp K, Sullivan SD, Tidhar W, Wright L, Berrigan D, Heideman PD. Insulins, leptin and feeding in a population of Peromyscus leucopus (white-footed mouse) with variable fertility. Horm Behav. 2014;66(1):169-79. PMID:24583085