Staci M. Kallish, DO

faculty photo
Assistant Professor of Clinical Medicine
Department: Medicine

Contact information
HUP - 5th Floor Silverstein, Suite 5100
3400 Spruce Street
Philadelphia, PA 19104
Office: 215-662-4740
Fax: 215-614-0298
BS (Biology)
Emory University, 1999.
DO (Medicine)
University of Medicine and Dentistry of New Jersey, 2005.
Permanent link
> Perelman School of Medicine   > Faculty   > Details

Description of Clinical Expertise

Lysosomal Storage Diseases
Inherited Connective Tissue disorders
Neurofibromatosis type 1 (NF1)

Selected Publications

Al Mukaddam M, Kallish S, Raper A, Asher S, Khan AN.: Heterozygous mutation in WNT1 gene in brothers with early-onset osteoporosis. Poster presentation at American Society for Bone and Mineral Research meeting September 2019.

Abdallah S. Geara, Staci Kallish, and Jonathan J. Hogan: The Impact of Whole-Exome Sequencing on Kidney Disease Ontology: The Tip of the Iceberg? New England Journal of Medicine 74(2): 281-283, 2019 Notes: Epub 2019 Apr 23.

Theodore G. Drivas, Stephanie B. Asher, Maria Bonanni, Staci Kallish: Identification of lysosomal storage disease by expanded carrier screening. Poster presentation at WORLD Symposium lysosomal storage disease research and conference 2019.

Agarwal R, Kallish S, Al Mukaddam M. : Hypoparathyroidism due to 22q11.2 deletion syndrome presenting as acute cardiomyopathy. American Association of Clinical Endocrinologists 4(6): e467-e471, November/December 2018.

Asher SB, Chen R, Kallish S. : Mitral valve prolapse and aortic root dilation in adults with hypermobile Ehlers-Danlos syndrome and related disorders. American Journal of Medical Genetics 176A(9): 1838-1844, September 2018.

Ian M. Campbell, Sarah E. Sheppard, T. Blaine Crowley, Daniel E. McGinn, Alice Bailey, Michael J. McGinn, Marta Unolt, Jelle F. Homans, Erin Y. Chen, Harold I. Salmons, J. William Gaynor, Elizabeth Goldmuntz, Oksana A. Jackson, Lorraine E. Katz, Maria R. Mascarenhas, Vincent F. X. Deeney, René M. Castelein, Karen B. Zur, Lisa Elden, Staci Kallish, Thomas F. Kolon, Sarah E. Hopkins, Madeline A. Chadehumbe, Michele P. Lambert, Brian J. Forbes, Julie S. Moldenhauer, Erica M. Schindewolf, Cynthia B. Solot, Edward M. Moss, Raquel E. Gur, Kathleen E. Sullivan, Beverly S. Emanuel, Elaine H. Zackai1, Donna M. McDonald-McGinn: What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia. American Journal of Medical Genetics 176A: 2058–2069, 2018.

Stephanie B. Asher, Rensa Chen, Staci Kallish: Mitral Valve Prolapse and Aortic Root Dilation in Adults with Hypermobile Ehlers-Danlos Syndrome and Related Disorders Poster presentation at American College of Medical Genetics annual meeting 2018.

Rahul Agarwal, Staci Kallish, Mona Al Mukaddam : Hypoparathyroidism Presenting as Acute Cardiomyopathy in Undiagnosed 22q11.2 Deletion syndrome Poster presentation at 11th Biennial 22q11.2 Conference, Whistler, British Columbia 2018.

Stephanie B. Asher, Rensa Chen, Staci Kallish : Mitral Valve Prolapse and Aortic Root Dilation in Adults with Hypermobile Ehlers-Danlos Syndrome and Related Disorders. Poster presentation at Penn DOM Research Day 2018.

Unolt M, Barry J, Digilio MC, Marino B, Bassett A, Oechslin E, Low DL, Belasco JL, Kallish S, Sullivan K, Zackai EH, McDonald-McGinn DM. : Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome. European Journal of Medical Genetics 61(7): 411-415, 2018.

back to top
Last updated: 12/02/2020
The Trustees of the University of Pennsylvania