I’m a resident physician specializing in pediatrics and medical genetics. My job is to diagnose rare genetic disorders and to assist patients, families and other care team members in understanding how these diagnoses influence their medical care and lives.
As someone with a rare genetic disorder, I am incredibly motivated to translate my personal experiences with chronic medical issues into better outcomes for my patients and their families. With my research, I am interested in better understanding the causes and mechanisms underlying rare genetic disorders.
I have had the privilege of caring for many individuals requiring complex, often lifelong, medical care. Geneticists are uniquely suited to assist patients, families and medical professionals in accessing and coordinating this care. I also learn from patients and their families, as every family has a unique story and lived experience. Families impacted by rare diseases have a powerful perspective on the many challenges of modern medical care.
When I'm not meeting with children and their families in the clinic and hospital, you can find me working on my car, riding my motorcycle (with a helmet, of course!), or studying military history. I am also a classically trained cellist!
Residency: Combined Program in Pediatrics and Medical Genetics, Cincinnati Children's Hospital Medical Center.
MD: University of Michigan, Ann Arbor, 2022.
PhD: Human Genetics, University of Michigan, Ann Arbor, 2022.
BS: Biology, Indiana University, Bloomington, 2010.
BA: Chemistry, Indiana University, Bloomington, 2010.
Medical genetics and genomics
Human Genetics
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