Staci M. Kallish, DO

faculty photo
Associate Professor of Clinical Medicine (Translational Medicine and Human Genetics)
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.
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Description of Clinical Expertise

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

Selected Publications

Korin Miller: Quoted in "Selma Blair on Living With Ehler-Danlos Syndrome: ‘I Hurt All the Time’" SELF Magazine February 2024.

Lima Martinez B, Hennessy L, Asher SB, Kessler LJ, Testa L, Hartman TR, Kallish S: Comparing Parental Perspectives of Raising Children Affected with Inherited vs. De Novo Marfan Syndrome. Poster presentation at American College of Medical Genetics Annual Clinical Genetics meeting 2024.

Bradbury A, Wood E, Phung L, Egleston B, Ofidis D, Mim R, Howe S, Hoffman-Andrews L, Owens A, Domchek S, Pyeritz R, Katona B, Kallish S, Sirugo G, Weaver J, Nathanson K, Rader D: Facilitating Return of Genetic Research Results from a Biobank Repository: Participant Uptake and Utilization of Digital Interventions. Poster presentation at American College of Medical Genetics Annual Clinical Genetics meeting 2024.

Mazzella A, Asher S, Elysee I, Hennessy L, Raper A, Drivas T, Kallish S: Variants of Uncertain Significance in Genes Associated with Inherited Connective Tissue Disorders Pose Unique Challenges. Poster presentation at American College of Medical Genetics Annual Clinical Genetics meeting 2024.

Crane HM, Asher S, Conway L, Drivas TG, Kallish S: Unraveling a history of overlap: A phenotypic comparison ofRBCK1-related disease and glycogen storage disease type IV. American Journal of Medical Genetics 2024.

Morganroth J, Ljungberg L, Goldstein A, Kallish S, Asher S, Quinn C, Price RS, Karam C: Pearls & Oy-sters: Case Report of a Patient With Adult-Onset Thymidine Kinase 2 Gene Deficiency. Neurology 101(16): 723-727, October 2023.

Bichet DG, Hopkin RJ, Aguiar P, Allam SR, Chien YH, Giugliani R, Kallish S, Kineen S, Lidove O, Niu DM, Olivotto I, Politei J, Rakoski P, Torra R, Tondel C, Hughes DA: Consensus recommendations for the treatment and management of patients with Fabry disease on migalastat: a modified Delphi study. Frontiers in Medicine September 2023.

Priestley JRC, Rippert AL, Condit C, Izumi K, Kallish S, Drivas TG.: Unmasking the challenges of Kabuki syndrome in adulthood: a case series. American Journal of Medical Genetics June 2023.

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.

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Last updated: 05/28/2024
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