Danita Velasco, MD, FACMG - Assistant Professor
Genetic Medicine - Pediatrics
University of Nebraska Medical Center, Children's Nebraska
Full Member
Area(s) of Emphasis:
Heart Diseases, Genetics Development Exposures & Injuries, Lifespan Diseases
Research Interests:
Genetic Syndromes, Skeletal Dysplasia, Hypophosphatasia, Osteogenesis Imperfecta
Current Research Summary:
As a clinical geneticist, I am interested in delineation of rare and emerging syndromes and the recommended care and treatment as available. This includes interest in facilitating diagnosis as well as connection to appropriate support for families when a diagnosis has been made. I have a special interest in rare bone disorders and the emerging therapeutic options available for these conditions. Currently, I am involved in research to connect individuals with undiagnosed genetic disorders to Whole Genome Sequencing (Genomic Answers for Kids). I am also involved in the Brittle Bone Disease Osteogenesis Imperfecta patient registry for natural history (BBD7701) and the clinical trial for a randomized, double blind active control study for the safety and efficacy of setrusumab, an anti-sclerostin monoclonal antibody as treatment for osteogenesis imperfecta (UX143-CL301).