Staci M. Kallish

Staci M. Kallish, DO, serves as a Clinical Associate Professor of Medicine within the Division of Translational Medicine and Human Genetics at the Perelman School of Medicine, University of Pennsylvania. She practices as a Medical Geneticist across multiple institutions including the Hospital of the University of Pennsylvania, Penn Presbyterian Hospital, Children's Hospital of Philadelphia, and Lancaster General Hospital.

Education:

• Bachelor of Science in Biology, Emory University (1999)
• Doctor of Osteopathic Medicine, University of Medicine and Dentistry of New Jersey (2005)

Research Interests:

Dr. Kallish specializes in rare genetic disorders with clinical expertise in Lysosomal Storage Diseases, Inherited Connective Tissue Disorders, Neurofibromatosis type 1 (NF1), and Sex chromosome disorders. Her translational research integrates clinical genetics with therapeutic development for complex syndromes affecting bone metabolism, connective tissue, and neurodevelopment.

Publication Trends:

Her 2024-2025 publications reveal concentrated work on diagnostic criteria for hypophosphatasia, treatment protocols for Pompe disease, and genotype-phenotype correlations in NF1. She actively contributes to specialized clinical centers including the Penn Bone Center and Penn Aorta Center while collaborating on biobank initiatives for genomic medicine implementation.

Scientific Awards:

No scientific awards or honors were documented in the provided information.

Advising and Grants:

The source material contains no details regarding graduate student mentorship or research grant funding.

Labs and Teams:

Dr. Kallish is operationally integrated with the Penn Bone Center, Penn Aorta Center, and Penn Medicine Biobank, where she applies medical genetics expertise to multidisciplinary patient care, clinical education, and genomic research initiatives.