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Barry Chioza

11PUBLICATIONS

52CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Central nervous systemCell and nuclear divisionGene mappingEpigenetics (incl. genome methylation and epigenomics)

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Publications (11)

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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 <i>MINAR2</i> 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

|Sep 20, 2019

MNS1 variant associated with situs inversus and male infertility.

Joseph S Leslie, Lettie E Rawlins, Barry A Chioza

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Frequent Collaborators

4 joint publications

Emma L Baple

2 joint publications

Harold E Cross

2 joint publications

Jonathan Mill

2 joint publications

Joseph S Leslie

2 joint publications

Emma L Dempster

2 joint publications

Eilis Hannon

2 joint publications

Aaron R Jeffries

2 joint publications

James Fasham

1 joint publications

Biswajit Chowdhury

1 joint publications

Fowzan S Alkuraya

Frequent Collaborators

4 joint publications

Emma L Baple

2 joint publications

Harold E Cross

2 joint publications

Jonathan Mill

2 joint publications

Joseph S Leslie

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