Staci Kallish, DO
Medical Genetics
Accepting new patients
Sees patients age 15 and up
Penn Translational Medicine and Human Genetics
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, School of Osteopathic Medicine
  • Residency: Cooper University Hospital
  • Fellowship: Children's Hospital of Philadelphia

What my patients think about me

Average Rating

164 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
pleasant, friendly and thorough
September 2025
it was an enjoyable visit.
August 2025
excellent work
July 2025
very nice doctor. obviously reviewed my record before our appointment

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, 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


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


Patel N, Liu Y, Thomas L, Kwok B, Kallish S, Spiller K, Petrie RJ, Han L Impact of Type V Collagen Haploinsufficiency on the Immuno-Mechanosensitive Transcriptomic Responses in Fibroblasts , Platform presentation at Biomedical Engineering Society Annual Meeting 2025: 2025


Gold JI, Elkaim Y, Gold NB, Asher S, Raper R, Condit C, Bogus Z, Elysee I, Hennessey L, Kennedy E, Chai T, Cohen S, Gehringer B, Gray SM, Streator A, Sweetser DA, Verma A, Salmasian H, Kripke C, Landry L, Nathanson KL, Rohanizadegan M, Kallish S, Drivas TG 8000 adults in 8 years: a single adult genetics practice's experience reveals high testing yield across the lifespan and significant racial and socioeconomic disparities in access to evaluation and testing , Poster presentation at American Society of Human Genetics 2025: 2025


Ocampo Mascaro J, Toder K, Kallish S, Al Mukaddam M Applying the Hypophosphatasia Diagnostic Criteria in a Patient Cohort at the Penn Bone Center , Poster presentation at Endocrine Society meeting: 2025


Ocampo Mascaro J, Toder K, Kallish S, Al Mukaddam M Applying the Hypophosphatasia Diagnostic Criteria in a Patient Cohort at the Penn Bone Center , Poster presentation at Endocrine Society meeting 2025: 2025


Kishnani P, Roberts M, Wenninger S, Kolbruck A, Kallish S Navigating treatment switch in Late-onset Pompe disease (LOPD) , Neurology, 13(Suppl 4): 2025,2-11


Safonov A, Nomakuchi TT, Chao E, Horton C, Dolinsky JS, Yussuf A, Richardson M, Speare V, Li S, Bogus ZC, Bonanni M, Raper A, Odia T, Wubbenhorst BS, Faulders E, Schuth EM, Loranger K, Zhang J, Scalise CB. ElNaggar A, Sha Y, Felker SA, Weiztel J, Kallish S, Ritchie MD, Penn Medicine Biobank, Nathanson KL, Drivas TG A genotype-first approach identified high incidence of NF1 pathogenic variants with distinct disease associations , Nature Communications, 16(3121): 2025,published electronically


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, epub ahead of print: 2025