Cincinnati Children's Hospital Medical Center Medical Genetics and Genomics/Pediatrics

Program Director, Medical Genetics Residency Programs, Division of Human Genetics

Clinical genetics and genomics physician, Associate Professor at Cincinnati Children's Hospital Medical Center

Fabry disease; Robin sequence; 22q11 deletion; neurofibromatosis; craniofacial genetics; chromosomal anomalies, Fabry disease and other lysosomal storage diseases, craniofacial genetics, clinical intervention for genetic disease; neurofibromatosis; dysmorphology; prenatal diagnosis of genetic syndromes

Associate Program Director, Medical Genetics and Genomics Residencies

Clinical genetics and genomics physician, Assistant Professor of Clinical-Affiliate at University of Cincinnati Medical Center Inc.

Autism spectrum disorder; intellectual disability; neurodevelopmental disorders; psychiatric genetics, Mendelian neurodevelopmental disorders; neurodevelopmental new gene discovery; psychiatric genetics; catatonia; autism; intellectual disability

Director, Division of Human Genetics

Clinical genetics and genomics physician, Professor at Cincinnati Children's Hospital Medical Center

Developmental eye defects; genomics; multiple congenital anomaly syndromes, Medical genetics; dysmorphology, Human Genetics, Genomics

2nd Yr

Physician at Cincinnati Children's Hospital Medical Center

Human Genetics Residency Faculty

Clinical genetics physician, Professor at Cincinnati Children's Hospital Medical Center

History of bone complications of neurofibromatosis type 1 (NF1); learning and behavioral problems in NF1; and drug trials for plexiform..., Genetic disorders; congenital anomalies; neurofibromatosis; tuberous sclerosis; bone disease in neurofibromatosis; Ehlers-Danlos syndrome, Human Genetics

1st Yr

Human Genetics Residency Faculty

Clinical biochemical genetics physician, Professor at Cincinnati Children's Hospital Medical Center

Focus on inborn errors of metabolism, with an emphasis on long term outcome in PKU and in the molecular biology of galactosemia, Galactosemia; PKU; inborn errors; newborn screening; lysosomal storage disease, Human Genetics

Human Genetics Residency Faculty

Craniofacial surgery physician, Associate Professor at Cincinnati Children's Hospital Medical Center

Cardiovascular genetics, Craniofacial malformations, Stem Cell and Organoid Medicine (CuSTOM)