Selected Publications
Korin Miller: Quoted in "Selma Blair on Living With Ehler-Danlos Syndrome: ‘I Hurt All the Time’" SELF Magazine : 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): 723-727,2023.
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.
Academic Contact Information
HUP - 5th Floor Silverstein, Suite 5100
3400 Spruce Street
Philadelphia,
PA
19104
Phone: 215-662-4740
Patient appointments: 800-789-7366