Selected Publications
Phung L, Wood E, Egleston B, Hoffman-Andrews L, Ofidis D, Howe S, Mim R, Griffin H, Fetzer D, Owens A, Domchek S, Pyeritz R, Katona B, Kallish S, Sirugo G, Weaver J, Nathanson KL, Rader DJ, Bradbury AR: Facilitating return of actionable genetic research results from a biobank repository: Participant uptake and utilization of digital interventions Human Genetics and Genomics Advances 5 : 2024.
Korin Miller: Quoted in "Selma Blair on Living With Ehler-Danlos Syndrome: ‘I Hurt All the Time’" SELF Magazine : 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.
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.
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.
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.
Academic Contact Information
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