Barry Chioza
12PUBLICATIONS
57CO-AUTHORS

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Publications (12)
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|Aug 02, 2024
Long-read transcript sequencing identifies differential isoform expression in the entorhinal cortex in a transgenic model of tau pathology.Szi Kay Leung, Rosemary A Bamford, Aaron R Jeffries
|Sep 24, 2022
DNA methylation signatures of Alzheimer's disease neuropathology in the cortex are primarily driven by variation in non-neuronal cell-types.Gemma Shireby, Emma L Dempster, Stefania Policicchio
|Jun 21, 2022
Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice.Guney Bademci, María Lachgar-Ruiz, Mangesh Deokar
|Oct 26, 2021
A recurrent rare intronic variant in CAPN3 alters mRNA splicing and causes autosomal recessive limb-girdle muscular dystrophy-1 in three Pakistani pedigrees.Kamal Khan, Sarmad Mehmood, Chunyu Liu
|Sep 27, 2021
A biallelic SNIP1 Amish founder variant causes a recognizable neurodevelopmental disorder.Zineb Ammous, Lettie E Rawlins, Hannah Jones
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Frequent Collaborators
4 joint publications
Emma L Baple
3 joint publications
Jonathan Mill
3 joint publications
Emma L Dempster
3 joint publications
Eilis Hannon
2 joint publications
Harold E Cross
2 joint publications
Joseph S Leslie
2 joint publications
Aaron R Jeffries
2 joint publications
James Fasham
1 joint publications
Biswajit Chowdhury
1 joint publications
Fowzan S Alkuraya