Barry A. Chioza
Barrack Road
Exeter, ENG, United Kingdom
Exeter, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 39 publications
Cell-type-specific DNA methylation dynamics in the prenatal and postnatal human cortex.
Journal: Cell genomics
Published: February 21, 2025
Guidance for the design and analysis of cell-type-specific DNA methylation epidemiology studies.
Journal: Briefings in bioinformatics
Published: November 06, 2024
Long-read transcript sequencing identifies differential isoform expression in the entorhinal cortex in a transgenic model of tau pathology.
Journal: Nature communications
Published: October 04, 2023
Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: June 21, 2022
DNA methylation signatures of Alzheimer's disease neuropathology in the cortex are primarily driven by variation in non-neuronal cell-types.
Journal: Nature communications
Published: April 01, 2022
Elucidating the clinical spectrum and molecular basis of HYAL2 deficiency.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 20, 2021
A biallelic SNIP1 Amish founder variant causes a recognizable neurodevelopmental disorder.
Journal: PLoS genetics
Published: June 14, 2021
A recurrent rare intronic variant in CAPN3 alters mRNA splicing and causes autosomal recessive limb-girdle muscular dystrophy-1 in three Pakistani pedigrees.
Journal: American journal of medical genetics. Part A
Published: April 27, 2021
Biallelic PI4KA variants cause neurological, intestinal and immunological disease.
Journal: Brain : a journal of neurology
Published: January 26, 2021
MNS1 variant associated with situs inversus and male infertility.
Journal: European journal of human genetics : EJHG
Published: March 27, 2019
Last Updated: 09/26/2026