Staci Kallish, DO
Medical Genetics
Accepting new patients
Sees patients age 15 and up
Penn Translational Medicine and Human Genetics
Headshot of Staci Kallish, DO
Penn Medicine Provider

About me

  • Associate Professor of Clinical Medicine (Translational Medicine and Human Genetics)
  • Associate Professor of Medicine in Pediatrics

Education and training

  • Medical School: University of Medicine and Dentistry of New Jersey
  • Residency: Cooper University Hospital
  • Fellowship: Children's Hospital of Philadelphia

What my patients think about me

Average Rating

177 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.

Anonymous
February 2026
very supportive and knowledgeable. i didn't feel rushed at all and left feeling very reassured i was in good hands.
Anonymous
February 2026
support received and information learned on appointment made it worthwhile
Anonymous
February 2026
i was seeking guidance from experts in the area of my rather unusual condition. i feel assured that my case is being handled by a team that has the skills needed here.
Anonymous
January 2026
process is smooth.

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.
  • Lancaster General Hospital: Has privileges to treat patients in the hospital.
Dr. Kallish is a Penn Medicine physician.

Qualifications and experience

Treatments and Conditions

My research

Kallish S, Nelson M, Ostrovsky Y, Zabinski J, Hennessy L, Veleva-Rotse BO, Guiliano JD Can artificial intelligence reduce racial and ethnic disparities in Fabry disease diagnosis? , Poster presentation at American College of Medical Genetics meeting 2026: 2026


Schaefer L, Christensen S, Carlson E, Bamba V, Kanakatti Shankar R, Brickman W, Law JH, Prakash S, Gutmark Little I, Flechner P, Klein K, Ladd J, Crenshaw ML, Kallish S, Davis S, Pinnaro C, Strong A Prevalence of congenital anomalies of the kidney and urinary tract in a national database of patients with Turner syndrome , Poster presentation at American College of Medical Genetics meeting 2026 : 2026


Gilmartin AA, Blout Zawatsky C, Somanchi H, Yeo J, Hickey RE, Kallish S, Pritchard AB, Madry A, Quadri A, Chase CL, Shelkowitz E, Chang I, Baker J, Swanson K, Anderson K, Duque Lasio ML, Gold NB Actionable parental diagnoses from expanded carrier screening , Poster presentation at American College of Medical Genetics meeting 2026 : 2026


Cohen E, Hennessy L, Mazzella A, Kessler LJ, Hartman TR, Testa L, Kallish S Optimizing Diagnostic Referrals for Marfan Syndrome: Phenotypic Risk Stratification in the Pediatric Population , Poster presentation at American College of Medical Genetics meeting 2026 : 2026


Elysee I, Hennessy L, Kallish S Evaluation for A-gal syndrome leading to diagnoses of late-onset Fabry disease , Poster presentation at WORLD symposium: 2026


Gold JI, Elkaim Y, Gold NB, Asher S, Raper A, Condit C, Bogus Z, Elysee I, Hennessy L, Kennedy E, Briere LC, Sweetser DA, Kripke C, Verma A, Salmasian H, Landry L, Nathanson KL, Kallish S, Drivas TG Racial and socioeconomic disparities in genetic evaluation and testing in the adult patient population , American Journal of Human Genetics, 13(1): 2026,29-40


Kallish S, Camporeale A, Hopkin RJ, Jovanovic A, Nordbeck P, Veleva-Rotse BO, Krusinska E, Torra R. Long-term efficacy of migalastat in females with Fabry disease , Journal of Medical Genetics, 62(12): 2025,798-807


Kallish S, Nelson M, Ostrovsky Y, Zabinski J, Hennessey L, Veleva-Rotse BO, Guiliano JD Can artifical intelligence reduce racial and ethnic disparities in Fabry disease diagnosis? , Poster presentation as American Society of Nephrology Kidney week 2025: 2025


Cocchella G, Phung L, Wood E, Egleston B, Hoffman-Andrews L, Brown S, Ofidis D, Mim R, Griffin H, Fetzer D, Owens A, Domchek S, Pyeritz R, Katona BW, Kallish S, Sirugo G, Weaver J, Nathanson KL, Rader DL, Bradbury AR An electronic review of clinical outcomes after return of actionable genetic research results from a health system research biobank , European Journal Medical Genetics: 2025,105061


Bradbury AR, Wood EM, Godbole AR, Shastri S, Brian Egleston B, Hoffman-Andrews L, Brown S, Ofidis D, Feng J, Owens A, Domchek S, Katona B, Kallish S, Sirugo G, Weaver J, Fleisher L, Wen KY, Elkin E, Nathanson K, Rader D RESPECT3: A randomized study evaluating return of actionable genetic research results from the Penn Medicine Biobank , Platform presentation to American Society of Human Genetics meeting 2025: 2025