Staci M. Kallish

faculty photo
Assistant Professor of Clinical Medicine
Medical Geneticist, Hospital of the University of Pennsylvania, Philadelphia, PA, University of Pennsylvania
Medical Geneticist, Penn Presbyterian Hospital, Philadelphia, Pennsylvania
Medical Geneticist, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania
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.
Permanent link
 

Description of Itmat Expertise

Lysosomal storage diseases

Selected Publications

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

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: 1838-1844, 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. 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.

Agarwal R, Kallish S, Al Mukaddam M. : Hypoparathyroidism due to 22q11.2 deletion syndrome presenting as acute cardiomyopathy. American Association of Clinical Endocrinologists 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 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.

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.

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

back to top
Last updated: 12/03/2018
The Trustees of the University of Pennsylvania