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Resident, Division of Human Genetics

513-736-3652

About Me

Clinical Interests

TGF-β related syndromes; neuro-genetics; neurodevelopmental genetics; craniosynostosis and rare syndromic disorders

Research Interests

Translational modelling of rare syndromic disorders in particular the TGF-β related disorders; Shprintzen Goldberg Syndrome and Myhre syndrome; characterizing phenotypes in neurodevelopmental syndromes with a focus on neuroimaging; Okur-Chung Neurodevelopmental Syndrome

Clinical Divisions

Human Genetics

My Education

Residency: Combined Pediatric Medical Genetics, Cincinnati Children’s Hospital, Cincinnati, OH.

Residency Internship Year: Combined Pediatric Medical Genetics, University Hospitals, Rainbow Babies and Children's Hospital, Cleveland, OH.

Residency: Foundation Clinical Training year: Chelsea Westminster Hospital, London, United Kingdom.

MS: Human Genetics and Molecular Biology, Johns Hopkins University, Baltimore, MD.

MD: Imperial College London, School of Medicine, United Kingdom.

BSc: Cardiovascular Sciences, Imperial College London, United Kingdom.