Dr. Gerard Vockley MD

Dr. Gerard Vockley is a medical genetics doctor in Pittsburgh, Pennsylvania. He is affiliated with multiple hospitals in the area, including Children's Hospital of Pittsburgh of UPMC and Magee-Womens Hospital of UPMC. He received his medical degree from Perelman School of Medicine at the University of Pennsylvania and has been in practice for 30 years. He is one of 3 doctors at Children's Hospital of Pittsburgh of UPMC and one of 5 at Magee-Womens Hospital of UPMC who specialize in Medical Genetics.

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Office Location

See Contact Information

Specialty & Clinical Interests

Clinical Biochemical/Molecular Genetics

Education & Medical Training

University of Colorado
Residency, Pediatrics, 1984 - 1986

Perelman School of Medicine at the University of Pennsylvania
Class of 1984

Certifications & Licensure

American Board of Medical Genetics
Certified in Clinical Biochemical/Molecular Genetics

American Board of Medical Genetics
Certified in Clinical Genetics

American Board of Pediatrics
Certified in Pediatrics

PA State Medical License

Awards, Honors & Recognition

Elected Member, The American Society for Clinical Investigation
2000

Publications & Presentations

Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples.
Talkowski, M. E., McClain, L., Allen, T., Bradford, L. D., Calkins, M., Edwards, N., Georgieva, L., Go, R., Gur, R., Gur, R., Kirov, G., Chowdari, K., Kwentus, J., Lyons, P., Mansour, H., McEvoy, J., O'Donovan, M. C., O'Jile, J., Owen, M. J., Santos, A., Savage, R., Toncheva, D., Vockley, G., Wood, J., Devlin, B., Nimgaonkar, V. L.

The response of patients with phenylketonuria and elevated serum phenylalanine to treatment with oral sapropterin dihydrochloride (6R-tetrahydrobiopterin): a phase II, multicentre, open-label, screening study.
Burton, B. K., Grange, D. K., Milanowski, A., Vockley, G., Feillet, F., Crombez, E. A., Abadie, V., Harding, C. O., Cederbaum, S., Dobbelaere, D., Smith, A., Dorenbaum, A.

2-methylbutyryl-CoA dehydrogenase deficiency in Hmong infants identified by expanded newborn screen.
van Calcar, S. C., Gleason, L. A., Lindh, H., Hoffman, G., Rhead, W., Vockley, G., Wolff, J. A., Durkin, M. S.

See all 5 publications

Insurances Accepted

  • Aetna Choice POS II
  • Aetna HMO
  • BCBS Blue Card PPO
  • CIGNA HMO
  • CIGNA Open Access
  • CIGNA PPO
  • Great West PPO
  • HealthAmerica HealthAssurance PPO
  • Highmark BCBS ClassicBlue
  • Highmark BCBS PPOBlue
  • Humana ChoiceCare Network PPO
  • Multiplan PHCS PPO
  • Multiplan PPO
  • United Healthcare - Direct Choice Plus POS
  • United Healthcare - Direct Options PPO
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