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
Education:
BS (Biology)
Emory University, 1999.
DO (Medicine)
University of Medicine and Dentistry of New Jersey, 2005.
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Selected Publications

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 epub ahead of print, 2019.

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.

Xu M, Horrell J, Snitow M, Cui J, Gochnauer H, Syrett CM, Kallish S, Seykora JT, Liu F, Gaillard D, Katz JP, Kaestner KH, Levin B, Mansfield C, Douglas JE, Cowart BJ, Tordoff M, Liu F, Zhu X, Barlow LA, Rubin AL, McGrath JA, Morrisey EE, Chu EY, Millar SE. : WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation. Nature Communications 8(15397), 2017.

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Last updated: 06/05/2019
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