Bhavi P. Modi
Vancouver, BC, Canada
Last Updated: 09/26/2026
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Found 29 publications
Human germline biallelic loss-of-function OSMR variants cause severe allergic disease.
Journal: Journal of human immunity
Published: April 15, 2026
Primary atopic disorders: Monogenic insights into immunity.
Journal: Journal of human immunity
Published: January 16, 2026
Combined Long-Read Genome and Transcriptome Sequencing Establishes Novel Variants in MEGF8 as the Cause for Carpenter Syndrome Type 2.
Journal: American journal of medical genetics. Part A
Published: November 24, 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
ASXL1 deficiency causes epigenetic dysfunction, combined immunodeficiency, and EBV-associated lymphoma.
Journal: The Journal of experimental medicine
Published: June 01, 2024
HostSeq: a Canadian whole genome sequencing and clinical data resource.
Journal: BMC genomic data
Published: June 15, 2022
Inborn Errors of Immunity Associated With Type 2 Inflammation in the USIDNET Registry.
Journal: Frontiers in immunology
Published: December 08, 2021
Can leaky splicing and evasion of premature termination codon surveillance contribute to the phenotypic variability in Alkuraya-Kucinskas syndrome?
Journal: European journal of medical genetics
Published: June 14, 2021
Inborn errors of immunity manifesting as atopic disorders.
Journal: The Journal of allergy and clinical immunology
Published: June 03, 2021
Adult GAMT deficiency: A literature review and report of two siblings.
Journal: Molecular genetics and metabolism reports
Published: April 17, 2021
Last Updated: 09/26/2026