Kaylie Jones

5PUBLICATIONS
192CO-AUTHORS
Neurology and neuromuscular diseasesInfant and child healthEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (5)

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

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Jan 07, 2025
Phosphoribosyl pyrophosphate synthetase 1 (PRPS1) associated retinal degeneration: an international study.

Ogul E Uner, Radwa Elsharawi, Margaret Reynolds

|Mar 25, 2022
Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia.

Maria Solaki, Britta Baumann, Peggy Reuter

|Jan 19, 2021
Variable expressivity in patients with autosomal recessive retinitis pigmentosa associated with the gene CNGB1.

Bojana Radojevic, Kaylie Jones, Martin Klein

|May 23, 2020
A novel SVA retrotransposon insertion in the CHM gene results in loss of REP-1 causing choroideremia.

Kaylie D Jones, Alina Radziwon, David G Birch

Pageof 1