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Staci Kallish, DO

Staci Kallish, DO Physician

Assistant Professor of Clinical Medicine

Dr. Kallish is a Penn Medicine employed physician.

Clinical Specialties

Specialty:

  • Medicine
    • Medical Genetics

Programs & Centers:

Board Certification:

  • Medical Genetics - Clinical Biochemical Genetics, 2011
  • Pediatrics, 2008

Clinical Expertise:

  • Connective Tissue Disease
  • Genetic and Rare Diseases Treatments and Procedures
  • Genetic Testing
  • Metabolic Myopathies
  • Muscle Disease
  • Neurofibromatosis Type 1 (NF1)
  • Osteogenesis Imperfecta

Practice Locations and Appointments

Insurance Accepted

  • Aetna US Healthcare
  • Cigna
  • Cigna HealthSpring
  • Devon Health Services (Americare)
  • Gateway Health Plan
  • Geisinger Health Plan
  • HealthAmerica / HealthAssurance, a Coventry Plan
  • HealthPartners
  • HealthPartners Medicare
  • HealthSmart
  • Highmark Blue Shield
  • Horizon Blue Cross Blue Shield of New Jersey
  • Humana / Choicecare
  • Independence Blue Cross (Keystone East)
  • Intergroup
  • Keystone First
  • Multiplan
  • NJ Medicaid
  • NJ Qualcare
  • Oxford Health Plan
  • PA Medicaid
  • PA Medicare
  • Preferred Care
  • Preferred Health Care/LGH
  • Rail Road Medicare / Palmetto GBA
  • Tricare
  • United Healthcare
  • UnitedHealthcare Community Plan
  • US Family Health Plan

Education and Training

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

Memberships

American College of Medical Genetics, National American Medical Association, National National Tay-Sachs and Allied Diseases Association, National Society for Inherited Metabolic Disorders, National

Hospital Affiliation

Dr. Kallish is a Penn Medicine employed physician.

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.

Research

Selected Publications:

Kallish, SM: “Gaucher Disease and the Potential for Misdiagnosis”. The Jewish Ledger : 2015.

Kallish, SM: “Always Tired and Bruised? You May Have Gaucher Disease”. The Philadelphia Jewish Voice : 2015.

Staci Kallish: “Multiple Congenital Anomaly syndromes”. Recorded for Arcadia University Genetic Counseling Board Review : 2015.

Staci Kallish: “Cardiac Issues in Ehlers Danlos syndrome”. Online : 2014.

Kallish S, Kaplan P.: A severity scoring system for pediatric Gaucher disease. European Journal of Pediatrics 172 (1): 2013.

Palladino AA, Chen J, Kallish S, Stanley CA, Bennett MJ.: Measurement of tissue acyl-CoAs using flow-injection tandem mass spectrometry: acyl-CoA profiles in short chain fatty acid oxidation defects. Molecular Genetics and Metabolism, 107 (4): 679-683,2012.

Kallish S, McDonald-McGinn DM, van Haelst MM, Bartlett SP, Katowitz JA, Zackai EH.: Ablepharon Macrostomia syndrome: extension of the phenotype. , 155:3060-3062. American Journal of Medical Genetics Part A 155 : 3060-3062,2011.

Academic Contact Info

HUP - 5th Floor Silverstein, Suite 5100
3400 Spruce Street

Philadelphia, PA 19104
Fax: (215) 614-0298
Patient appointments: 800-789-PENN (7366)