Allison M. Matthews
Vancouver, BC, Canada
Last Updated: 09/26/2026
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Found 19 publications
SCN3A-related neurodevelopmental disorder: Clinical case reports and biophysical characterization.
Journal: Channels (Austin, Tex.)
Published: October 30, 2025
Breaking rules: the complex relationship between DNA methylation and X-chromosome inactivation in the human placenta.
Journal: Biology of sex differences
Published: November 06, 2024
ASXL1 deficiency causes epigenetic dysfunction, combined immunodeficiency, and EBV-associated lymphoma.
Journal: The Journal of experimental medicine
Published: June 01, 2024
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease.
Journal: The Journal of experimental medicine
Published: October 14, 2022
Who's afraid of the X? Incorporating the X and Y chromosomes into the analysis of DNA methylation array data.
Journal: Epigenetics & chromatin
Published: September 02, 2022
Genome-wide sequencing and the clinical diagnosis of genetic disease: The CAUSES study.
Journal: HGG advances
Published: September 16, 2021
A cross-cohort analysis of autosomal DNA methylation sex differences in the term placenta.
Journal: Biology of sex differences
Published: March 05, 2021
Is the diagnostic rate for the common subtypes of A1AT deficiency consistent across two Canadian Provinces?
Journal: Clinical biochemistry
Published: February 18, 2021
Atypical cerebral palsy: genomics analysis enables precision medicine.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: August 29, 2018
Integration of genomics and metabolomics for prioritization of rare disease variants: a 2018 literature review.
Journal: Journal of inherited metabolic disease
Published: September 10, 2017
Last Updated: 09/26/2026