Items where authors include "Maconachie, G.D.E."

Article

Fassad, M.R., Vasudevan, P.C., Barwell, J. et al. (9 more authors) (2026) Whole-genome sequencing uncovers diverse genetic causes and phenotypic signatures in infantile nystagmus and albinism. npj Genomic Medicine, 11. 43. ISSN 2056-7944

Savant, R., Parida, S., Hunt, C. et al. (15 more authors) (2026) Artificial intelligence-driven virtual reality eye-tracking for the objective measurement of MRD1 and MRD2 in blepharoptosis. Scientific Reports, 16. 17430. ISSN 2045-2322

Shenoy, R., Samra, G.S., Sekhri, R. et al. (6 more authors) (2026) Clinician-led code-free deep learning for detecting papilledema and pseudopapilledema using optic disc imaging. Translational Vision Science & Technology, 15 (2). 25. ISSN 2164-2591

Hunt, C., Yoon, H.-J., Lirio, A. et al. (19 more authors) (2025) Genome-wide insights into the genes and pathways shaping human foveal development: redefining the genetic landscape of foveal hypoplasia. Investigative Ophthalmology & Visual Science, 66 (12). p. 22. ISSN 0146-0404

Sekhri, R., Kuht, H.J., Tu, Z. et al. (15 more authors) (2025) Identifying biomarkers for papilledema and pseudopapilledema. Scientific Reports, 15. 24847. ISSN 2045-2322

Shenoy, R. orcid.org/0000-0001-8118-9009, Maconachie, G.D.E. orcid.org/0000-0001-9131-3480, Parida, S. et al. (19 more authors) (2025) Foveal hypoplasia grading with optical coherence tomography: agreement and challenges across experience levels. Diagnostics, 15 (6). 763. ISSN 2075-4418

Kuht, H.J., Maconachie, G.D.E. orcid.org/0000-0001-9131-3480, Han, J. et al. (36 more authors) (2022) Genotypic and phenotypic spectrum of foveal hypoplasia : a multicenter study. Ophthalmology, 129 (6). pp. 708-718. ISSN 0161-6420

Thomas, M.G., Maconachie, G.D.E. orcid.org/0000-0001-9131-3480, Kuht, H.J. et al. (10 more authors) (2021) Optic nerve head and retinal abnormalities associated with congenital fibrosis of the extraocular muscles. International Journal of Molecular Sciences, 22 (5). 2575.

Kuht, H.J., Han, J., Maconachie, G.D.E. orcid.org/0000-0001-9131-3480 et al. (12 more authors) (2020) SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization. Human Molecular Genetics, 29 (18). pp. 2989-3002. ISSN 0964-6906

Maconachie, G.D.E. and Gottlob, I. (2015) The challenges of amblyopia treatment. Biomedical Journal, 38 (6). pp. 510-516. ISSN 2319-4170