Selected Publications
Korin Miller: Quoted in "Selma Blair on Living With Ehler-Danlos Syndrome: ‘I Hurt All the Time’" SELF Magazine : 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): 723-727,2023.
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 : 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 : 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 : 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 : 2023.
Kassabian B, Levy AM, Gardella E, Aledo-Serrano A, Ananth SL, Brea-Fernandez AJ, Caumes R, Chatron N, Dainelli A, De Wachter M, Denomme-Pichon AS, Dye TJ, Fazzi W, Felt R, Fernandez-Jaen A, Fernandez-Prieto M, Gantz E, Gasperowicz P, Gil-Nagel A, Gomez-Andres D, Greiner HM, Guerrini R, Haanpaa MK, Helin M, Hoyer J, Hurst ACE, Kallish S, Karkare SN, Khan A, Kleinendorst L, Koch J, Kothare SV, Koudijs SV, Lagae L, Lakeman P, Leppig KA, Lesca G, Lopergolo D, Lusk L, Mackenzie A, Mei D, Moller RS, Pereira EM, Platzer K, Quelin C, Revah-Politi A, Rheims S, Rodriguez-Palermo A, Rossi A, Santorelli F, Seinfeld S, van Haelst EM, Veenma DCM, Weber S, Weckhuysen S, Zacher P, Tumer Z, Rubboli G.: Developmental epileptic encephalopathy in DLG4-related synaptopathy Epilepsia : 2023.
Gold J, Elkaim Y, Asher A, Raper A, Bogus Z, Condit C, Elysee IF, Kennedy E, Hennessy L, Nathanson KL, Kallish S, Drivas TG: 5000 Adults in 5 years: a single adult genetic practice's experience reveals high testing yield across the lifespan and significant racial/socioeconomic disparities to access and testing Poster presentation at David W. Smith workshop : 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 : 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 : 2022.
Academic Contact Information
HUP - 5th Floor Silverstein, Suite 5100
3400 Spruce Street
Philadelphia,
PA
19104
Phone: 215-662-4740
Patient appointments: 800-789-7366