Items where authors include "Mahroo, O.A."

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. ISSN 2056-7944

Quinodoz, M., Rodenburg, K., Cvackova, Z. et al. (185 more authors) (2026) De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa. Nature Genetics, 58. pp. 169-179. ISSN 1061-4036

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