Pariya Yousefi
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
Novel genotypes, phenotypes, and triggers in humans with OTULIN haploinsufficiency.
Journal: Journal of human immunity
Published: November 26, 2025
Human germline biallelic loss-of-function OSMR variants cause severe allergic disease.
Journal: medRxiv : the preprint server for health sciences
Published: September 19, 2025
Monogenic disorders of the IRF transcription factors.
Journal: The Journal of experimental medicine
Published: May 06, 2025
Primary atopic disorders: inborn errors of immunity causing severe allergic disease.
Journal: Current opinion in immunology
Published: August 14, 2024
A multimorphic variant in ThPOK causes an inborn error of immunity with T cell defects and fibrosis.
A multimorphic variant in ThPOK causes an inborn error of immunity with T cell defects and fibrosis.
Journal: The Journal of experimental medicine
Published: July 08, 2024
ASXL1 deficiency causes epigenetic dysfunction, combined immunodeficiency, and EBV-associated lymphoma.
Journal: The Journal of experimental medicine
Published: June 01, 2024
Antidepressant Exposure and DNA Methylation: Insights from a Methylome-Wide Association Study.
Journal: medRxiv : the preprint server for health sciences
Published: May 15, 2024
Expanding the molecular and phenotypic spectrum of CTLA-4 insufficiency.
Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology
Published: September 14, 2023
Transcription factor defects in inborn errors of immunity with atopy.
Journal: Frontiers in allergy
Published: June 10, 2023
Showing 1-10 of 10
Last Updated: 09/26/2026