Adrian Dockery

10PUBLICATIONS
46CO-AUTHORS
NeurogeneticsOptical technologyEpigenetics (incl. genome methylation and epigenomics)Infant and child healthGene expression (incl. microarray and other genome-wide approaches)
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Publications (10)

|Jun 26, 2026
First Exonic Cryptic Branchpoint Variant in an Inherited Retinal Degeneration Detected in an Irish <i>RPGR</i> Pedigree with X-Linked Retinitis Pigmentosa.

|Dec 30, 2025
Secondary Ophthalmic Features Represent Diagnostic Clues and Potential Points of Intervention for Inherited Retinal Diseases (Target 5000 Report 3).

Kirk A J Stephenson, Julia Zhu, Marcus Conway

|Jan 25, 2025
Novel Splice-Altering Variants in the <i>CHM</i> and <i>CACNA1F</i> Genes Causative of X-Linked Choroideremia and Cone Dystrophy.

Anna R Ridgeway, Ciara Shortall, Laura K Finnegan

|Jan 23, 2024
The Role of the Ophthalmic Genetics Multidisciplinary Team in the Management of Inherited Retinal Degenerations-A Case-Based Review.

Marcus P Conway, Kirk A J Stephenson, Julia Zhu

|Apr 23, 2022
Electrophysiology-Guided Genetic Characterisation Maximises Molecular Diagnosis in an Irish Paediatric Inherited Retinal Degeneration Population.

Julia Zhu, Kirk A J Stephenson, Adrian Dockery

|Feb 28, 2022
Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants.

Hedwig M Velde, Janine Reurink, Sebastian Held

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Frequent Collaborators

5 joint publications

Laura Whelan

3 joint publications

Julia Zhu

3 joint publications

Kirk A J Stephenson

3 joint publications

Susanne Roosing