Penn Medicine Provider
Medical Genetics
Staci Kallish, DO
4.7
(139)
Accepting new patients
Sees patients age 15 and up
Penn Translational Medicine and Human Genetics
Make an appointmentCall 800-789-7366

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
4.7

139 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.

May 2025
3.0
3.0
everyone was nice
April 2025
5.0
5.0
good service
April 2025
5.0
5.0
she's amazing
April 2025
5.0
5.0
very knowledgeable about the patient and condition

Insurance accepted

My Locations

Learn about location

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

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

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: 2025,in press

Kallish S, Cole M The role of Medical Genetics in the Penn Aorta Center , Penn Aorta center podcast: 2025

Kallish S, Wang G, Desai N Case study: connective tissue disorder , Penn Aorta Center video educational series: 2025

Zhu D, Patel NB, Pishko AM, Weinberg EM, Takako TI, Kallish S, Johnson FB, Babushok DV, Courtwright AM Evaluation of a screening protocol for telomere biology disorders in individuals with interstitial lung disease undergoing lung transplant evaluation , European Respiratory Journal Open Research: 2025

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, Youbao Sha Y, Felker SA, Weitzel J, Kallish S, Ritchie MD, Regeneron Genetics Center, Penn Medicine BioBank, Nathanson KL, Drivas TG A genotype-first approach identifies high incidence of NF1 pathogenic variants with distinct disease associations , Nature Communications: 2025

Ocampo Mascaro J, Tran R, Kallish S, Berman J, Mukaddam AM Clinical Features Of Adult Hypophosphatasia And Correlation Between Laboratory Findings And Patient’s Symptomatology: A Retrospective Review At The Penn Bone Center , Poster presentation at Endocrine Society meeting June 2024 : 2024

Korin Miller Quoted in "Selma Blair on Living With Ehler-Danlos Syndrome: ‘I Hurt All the Time’" , SELF Magazine: 2024

Bradbury A, Wood E, Phung L, Egleston B, Ofidis D, Mim R, Howe S, Hoffman-Andrews L, Owens A, Domchek S, Pyeritz R, Katona B, Kallish S, Sirugo G, Weaver J, Nathanson K, Rader D Facilitating return of genetic research results from a biobank repository: Participant uptake and utilization of digital interventions , Poster presentation at American College of Medical Genetics Annual Clinical Genetics meeting : 2024