Lesley Everett

7PUBLICATIONS
51CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesVision scienceInfant and child healthOptical technology
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Publications (7)

|Mar 04, 2026
Assessment of In-Frame Indel Variants in an Unsolved Cohort of Inherited Retinal Diseases Using Machine Learning.

David E Rauch, Meng Wang, Muhammad Jafar Hussain Hafiz

|Jan 21, 2026
Neuro-ophthalmic disorders resulting from defects in the gamma tubulin ring complex: a clinically oriented review.

Maya Helms, Emily S Levine, Lesley A Everett

|Apr 17, 2025
Variants in CFAP410 cause a range of retinal and skeletal phenotypes.

Ryan E Schmidt, Amy E Pohodich, David Birch

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

Ogul E Uner, Radwa Elsharawi, Margaret Reynolds

|Jul 30, 2024
Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study.

Austin D Igelman, Elizabeth White, Alaa Tayyib

|Aug 18, 2023
Expanding the phenotypic and genotypic spectrum of patients with HGSNAT-related retinopathy.

Mariana Matioli da Palma, Molly Marra, Austin D Igelman

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Frequent Collaborators

2 joint publications

Andrea Vincent

2 joint publications

Mark E Pennesi

2 joint publications

Katarina Stingl

2 joint publications

Elise Heon