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Office
8200 Dodge St
Omaha, NE 68114Phone+1 402-955-4140Fax+1 402-955-4100
Summary
- Danita Velasco, MD is a pediatrician based in Omaha, NE with a subspecialty in Medical Genetics. She completed both her residency in Pediatrics (2013-2016) and her fellowship in Medical Genetics and Genomics (2017-2019) at the University of Nebraska Medical Center College of Medicine. Dr. Velasco is currently a physician at Children's Nebraska, a position she has held since 2019. Her scholarly contributions include various publications in Journal of Medical Genetics, Clinical Genetics, Cytometry. Part B, Clinical Cytometry, and Human Mutation which have collectively been cited 35 times by other publications.
Education & Training
- University of Nebraska Medical Center College of MedicineFellowship, Medical Genetics and Genomics, 2017 - 2019
- University of Nebraska Medical Center College of MedicineResidency, Pediatrics, 2013 - 2016
- University of Nebraska College of MedicineClass of 2013
Certifications & Licensure
- GA State Medical License 2024 - 2026
- NE State Medical License 2016 - 2026
- IA State Medical License 2024 - 2025
- KS State Medical License 2024 - 2025
- American Board of Pediatrics Pediatrics
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Publications & Presentations
PubMed
- Genotype-phenotype correlations in 294 pediatric patients with osteogenesis imperfecta.Jay J Byrd, Andrew C White, Claire G Nissen, Makayla Schissel, Matthew Van Ormer
JBMR Plus. 2024-11-01 - 3 citationsExpanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals.Dana E Layo-Carris, Emily E Lubin, Annabel K Sangree, Kelly J Clark, Emily L Durham
European Journal of Human Genetics. 2024-08-01 - Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals.Dana E Layo-Carris, Emily E Lubin, Annabel K Sangree, Kelly J Clark, Emily L Durham
European Journal of Human Genetics. 2024-08-01
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