Staci M. Kallish, DO
Associate 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
3400 Spruce Street
Philadelphia, PA 19104
Office: 215-662-4740
Fax: 215-614-0298
Fax: 215-614-0298
Education:
BS (Biology)
Emory University, 1999.
DO (Medicine)
University of Medicine and Dentistry of New Jersey, 2005.
Permanent linkBS (Biology)
Emory University, 1999.
DO (Medicine)
University of Medicine and Dentistry of New Jersey, 2005.
Description of Clinical Expertise
Lysosomal Storage DiseasesInherited Connective Tissue disorders
Neurofibromatosis type 1 (NF1)
Selected Publications
Aguiar P, Biondetti GP, Warnock D, Kallish S, Nelson MN, Giuliano JD, Zabinski JW, Boussios C, Curhan G, Bandaria JN, Gliklich RE, Jefferies JL.: Estimation of arrhythmia risk in patients with Fabry disease using a machine learning model. Poster presentation to WORLD Symposium February 2023.Kallish S, Biondetti GP, Jefferies JL, Aguiar P, Nelson MN, Giuliano JD, Zabinski JW, Boussios C, Curhan G, Bandaria JN, Gliklich RE, Warnock D.: Estimation of stroke risk in patients with Fabry disease using a machine learning model. Poster presentation at WORLD Symposium February 2023.
Crane H, Asher S, Conway L, Drivas T, Kallish, S : Characterizing the Natural History of RBCK1-Related Disease: A Phenotypic Comparison of Rare Disease Diagnoses Poster presentation at National Society of Genetic Counselors meeting October 2022.
Patel N, Li T, Duggan J, Kallish S, Spiller KL, Petrie RJ, Han L.: Impact of type V collagen deficiency on fibroblast mechanosensing under inflammatory stimulation. Summer Biomechanics, Bioengineering and Biotransport conference June 2022.
Reinhart MB and Kallish S: Musculoskeletal and connective tissue disorders. Netter's Pediatrics 2022.
Kaplan FS, Groppe JC, Xu M, Towler OW, Grunvald E, Kalunuian K, Kallish S, Al Mukaddam M, Pignolo RJ, Shore EM.: An ACVR1 R375P pathogenic variant in two families with mild fibrodysplasia ossificans progressiva. American Journal of Medical Genetics 2022.
Kahn B, Apostolidis SA, Bhatt V, Greenplate AR, Kallish S, LaCava A, Lucas A, Meyer NJ, Negoianu D, Ogdie AR, Shashaty MGS, Takach PA, Zuroff L, Wherry EJ, Anesi GL: Multisystem inflammation and organ dysfunction after BNT162b2 messenger RNA coronavirus disease 2019 vaccination. Critical Care Explorations 3(11), November 2021.
Sheppard SE, Campbell IM, Harr MH, Gold N, Li D, Bjornsson HT, Cohen J, Fahrner JA, Fatemi A, Harris JR, Nowak C, Stevens CA, Grand K, Au M, Graham Jr JM, Sanchez-Lara PA, Del Campo M, Jones MC, Abdul-Rahman O, Alkuraya FS, Bassetti JA, Bergstrom K, Bhoj E, Dugan S, Kaplan JD, Derar N, Gripp KW, Hauser N, Innes AM, Keena B, Kodra N, Miller R, Nelson B, Nowaczyk MJ, Rahbeeni Z, Ben-Shachar S, Shieh JT, Slavotinek A, Sobering AK, Abbott MA, Allain DC, Amlie-Wolf L, Ay PYB, Bedoukian E, Beek G, Barry J, Berg J, Bernstein JA, Cytrynbaum C, Chung BHY, Donoghue S, Dorrani N, Eaton A, Flores-Daboub JA, Dubbs H, Felix CA, Fong CT, Fung JLF, Gangaram B, Goldstein A, Greenberg R, Ha TK, Hersh J, Izumi K, Kallish S, Kravets E, Kwok PY, Jobling RK, Knight Johnson AE, Kushner J, Lee BH, Levin B, Lindstrom K, Manickam K, Mardach R, McCormick E, McLeod DR, Mentch FD, Minks K, Muraresku C, Nelson SF, Porazzi P, Pichurin PN, Powell-Hamilton NN, Powis Z, Ritter A, Rogers C, Rohena L, Ronspies C, Schroeder A, Stark Z, Starr L, Stoler J, Suwannarat P, Velinov M, Weksberg R, Wilnai Y, Zadeh N, Zand DJ, Falk MJ, Hakonarson H, Zackai EH, Quintero-Rivera F.: Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome. American Journal of Medical Genetics 2021.
Turin CG, Joeng KS, Kallish S, Raper A, Asher S, Campeau PM, Khan AN, Al Mukaddam M.: Heterozygous variant in WNT1 gene in two brothers with early onset osteoporosis. Bone Reports 15, 2021.
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.