Theodore George Drivas, MD, PhD
Medical Genetics
Accepting new patients
Sees patients age 12 and up
Penn Translational Medicine and Human Genetics
Make an appointmentCall 800-789-7366
Penn Medicine Provider

About me

  • Co-Director, UPenn HHT Center of Excellence
  • Assistant Director of Scientific Outreach, Penn Medicine BioBank
  • Assistant Professor of Medicine (Translational Medicine and Human Genetics)
  • Assistant Professor of Medicine in Genetics

As a Clinical Geneticist at Penn Medicine, my goal is to provide diagnostic workup and medical management for any patient with a genetic or inherited condition. With my training in Medical Genetics and Internal Medicine, I see both adult and pediatric patients with any suspected genetic disorder, and have a special interest and expertise in the management of patients with ciliopathy conditions (disease affecting the primary cilium). When visiting our clinic, you can expect a detailed review of your medical and family history, a thorough physical exam, excellent genetic counseling from our team of Genetic Counselors, and a clear and comprehensive plan for diagnostic workup and management. 

Education and training

  • Medical School: University of Pennsylvania School of Medicine
  • Residency: NewYork-Presbyterian/Columbia University Medical Center
  • Residency: Children's Hospital of Philadelphia
  • Fellowship: Children's Hospital of Philadelphia

What my patients think about me

Average Rating

72 reviews

Comments are submitted by patients and reflect their views and opinions. The comments are not endorsed by and do not necessarily reflect the views of Penn Medicine.

October 2025
very thorough , in explaining the situation and what to do next
July 2025
he said he would help by providing information on some things that could help me with my problems
June 2025
very rare to get this level of caring and expertise.
May 2025
easy to talk to

Insurance accepted

My Locations

Penn Medicine hospital privileges

  • Hospital of the University of Pennsylvania: Has privileges to treat patients in the hospital.
  • Penn Presbyterian Medical Center: Has privileges to treat patients in the hospital.
Dr. Drivas is a Penn Medicine physician.

Qualifications and experience

Treatments and Conditions

My research

Zhang X, Lucas AM, Veturi Y, Drivas TG, Bone WP, Verma A, Chung WK, Crosslin D, Denny JC, Hebbring S, Jarvik GP, Kullo I, Larson EB, Rasmussen-Torvik LJ, Schaid DJ, Smoller JW, Stanaway IB, Wei WQ, Weng C, Ritchie MD. Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders , Nat Commun, 13(1): 2022,3428

Verma, A, Damrauer SM, Naseer N, Weaver J, Kripke CM, Guare L, Sirugo G, Kember RL, Drivas TG, Dudek SM, Bradford Y, Lucas A, Judy R, Verma SS, Meagher E, Nathanson KL, Feldman M, Ritchie MD, Rader DJ, and The Penn Medicine BioBank. The Penn Medicine BioBank: Towards a Genomics-Enabled Learning Healthcare System to Accelerate Precision Medicine in a Diverse Population , Journal of Personalized Medicine., 12(12): 2022,1974

Huffman JE, Butler-Laporte G, Khan A, Pairo-Castineira E, Drivas TG, Peloso GM, Nakanishi T; COVID-19 Host Genetics Initiative, Ganna A, Verma A, Baillie JK, Kiryluk K, Richards JB, Zeberg H. Multi-ancestry fine mapping implicates OAS1 splicing in risk of severe COVID-19 , Nat Genet, 54(2): 2022,125-127

Xiao B, Velez Edwards DR, Lucas A, Drivas TG, Gray K, Keating B, Weng C, Jarvik GP, Hakonarson H, Kottyan L, Elhadad N, Regeneron Genetics Center, Wei W, Luo Y, Kim D, Ritchie MD, Verma SS Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions , J Am Heart Assoc, 12(5): 2023,e026561

Butler-Laporte G, Povysil G, Kosmicki JA, Cirulli ET, Drivas TG, et al. (with 160 additional authors) Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative. , PLoS Genet., 18(11): 2022

Drivas TG, Lucas A, Zhang X, Ritchie MD. Mendelian pathway analysis of laboratory traits reveals distinct roles for ciliary subcompartments in common disease pathogenesis , Am J Hum Genet, 108(3): 2021,482-501

Drivas TG, Lucas A, Ritchie MD. eQTpLot: a user-friendly R package for the visualization of colocalization between eQTL and GWAS signals , BioData Min, 14(1): 2021,32

Drivas TG, Wojno AP, Tucker BA, Stone EM, Bennett J. Basal exon skipping and genetic pleiotropy: A predictive model of disease pathogenesis , Sci Transl Med, 7(291): 2015,291ra97

Drivas TG, Holzbaur EL, Bennett J. Disruption of CEP290 microtubule/membrane-binding domains causes retinal degeneration , J Clin Invest, 123(10): 2013,4525-39

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