Pediatric Genetics
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Pediatric Genetics
We are a leader in pediatric genetic research and education, with a strong commitment to advancing pediatric precision medicine and training the next generation of physician-scientists. Faculty contribute to cutting-edge research across a broad spectrum of genetic and metabolic disorders, including syndromic conditions such as Fragile X, Down, Williams, Kabuki, Rubinstein-Taybi and Smith-Lemli Opitz syndromes, as well as inborn errors of metabolism identified through newborn screening. Central to our academic mission is a strong foundation of multidisciplinary collaboration with partners in pediatric neurology, maternal-fetal medicine, ophthalmology, cardiology and other specialties.
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Explore Genetics
Through innovation, diagnostic expertise and educational outreach, we maintain state, local and national prominence while driving forward improvements in genetic care and outcomes for children and families. Our faculty engage with interdisciplinary partnerships on impactful research across a wide-ranging spectrum of genetic and metabolic disorders.
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