Gwyneth Jane Farrar

4PUBLICATIONS
179CO-AUTHORS
Neurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Neurogenetics
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Publications (4)

|Jan 20, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

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

Hedwig M Velde, Janine Reurink, Sebastian Held

|Jul 02, 2021
Molecular Inversion Probe-Based Sequencing of USH2A Exons and Splice Sites as a Cost-Effective Screening Tool in USH2 and arRP Cases.

Janine Reurink, Adrian Dockery, Dominika Oziębło

|Apr 29, 2021
BBS1 branchpoint variant is associated with non-syndromic retinitis pigmentosa.

Zeinab Fadaie, Laura Whelan, Adrian Dockery

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Frequent Collaborators

4 joint publications

Susanne Roosing

3 joint publications

Adrian Dockery

3 joint publications

Laura Whelan

3 joint publications

Frans P M Cremers