Kaylie Webb-Jones

Also affiliated with Retina Foundation of the Southwest

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 5 papers. Top paper: “A novel SVA retrotransposon insertion in the CHM gene results in loss of REP-1 causing choroideremia”.

A novel SVA retrotransposon insertion in the CHM gene results in loss of REP-1 causing choroideremia

Ophthalmic Genetics(2020)10.1080/13816810.2020.1768557

N/A

0.723DataRank · unranked

12 citations

Alina Radziwon, David G. Birch, Ian M. MacDonald, Kaylie Webb-Jones

Identification of Deep-Intronic Splice Mutations in a Large Cohort of Patients With Inherited Retinal Diseases

Frontiers in Genetics(2021)10.3389/fgene.2021.647400

N/A

0DataRank · unranked

69 citations

Jun Wang, Meng C. Wang, Austin D. Igelman, Kaylie Webb-Jones, Yumei Li +7 more

Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia

Human Mutation(2022)10.1002/humu.24371

N/A

0DataRank · unranked

20 citations

Britta Baumann, Peggy Reuter, Sten Andréasson, Isabelle Audo, Carmen Ayuso +46 more

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa

medRxiv(2025)10.1101/2025.01.06.24317169

N/A

0DataRank · unranked

15 citations

Kim Rodenburg, Zuzana Cvačková, Karolina Kamińska, Suzanne E. de Bruijn, Ana Belén Iglesias-Romero +95 more

Variants in CFAP410 cause a range of retinal and skeletal phenotypes

npj Genomic Medicine(2025)10.1038/s41525-025-00489-1

N/A

0DataRank · unranked

0 citations

Amy E. Pohodich, David G. Birch, Kaylie Webb-Jones, Byron L. Lam, Emily H. Jung +44 more