Julie S. Prendiville
Vancouver, BC, Canada
Last Updated: 09/26/2026
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Found 10 publications
Human germline biallelic loss-of-function OSMR variants cause severe allergic disease.
Journal: Journal of human immunity
Published: April 15, 2026
Human germline biallelic loss-of-function OSMR variants cause severe allergic disease.
Journal: medRxiv : the preprint server for health sciences
Published: September 19, 2025
ASXL1 deficiency causes epigenetic dysfunction, combined immunodeficiency, and EBV-associated lymphoma.
Journal: The Journal of experimental medicine
Published: June 01, 2024
Recurrent sterile abscesses in a case of X-linked neutropenia.
Journal: Pediatric dermatology
Published: March 24, 2020
Recessive Mutations in AP1B1 Cause Ichthyosis, Deafness, and Photophobia.
Journal: American journal of human genetics
Published: July 10, 2019
The importance of considering monogenic causes of autoimmunity: A somatic mutation in KRAS causing pediatric Rosai-Dorfman syndrome and systemic lupus erythematosus.
Journal: Clinical immunology (Orlando, Fla.)
Published: October 19, 2016
JAK1 gain-of-function causes an autosomal dominant immune dysregulatory and hypereosinophilic syndrome.
Journal: The Journal of allergy and clinical immunology
Published: June 28, 2016
Combined immunodeficiency associated with homozygous MALT1 mutations.
Journal: The Journal of allergy and clinical immunology
Published: July 10, 2013
Successful approach to treatment of Helicobacter bilis infection in X-linked agammaglobulinemia.
Journal: Journal of clinical immunology
Published: June 13, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026