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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2018 3
2019 1
2020 7
2021 10
2022 8
2023 8
2024 2

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33 results

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Page 1
Photophobia in migraine: A symptom cluster?
Wilkins AJ, Haigh SM, Mahroo OA, Plant GT. Wilkins AJ, et al. Cephalalgia. 2021 Oct;41(11-12):1240-1248. doi: 10.1177/03331024211014633. Epub 2021 May 14. Cephalalgia. 2021. PMID: 33990148 Free PMC article. Review.
Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia.
Hysi PG, Choquet H, Khawaja AP, Wojciechowski R, Tedja MS, Yin J, Simcoe MJ, Patasova K, Mahroo OA, Thai KK, Cumberland PM, Melles RB, Verhoeven VJM, Vitart V, Segre A, Stone RA, Wareham N, Hewitt AW, Mackey DA, Klaver CCW, MacGregor S; Consortium for Refractive Error and Myopia; Khaw PT, Foster PJ; UK Eye and Vision Consortium; Guggenheim JA; 23andMe Inc.; Rahi JS, Jorgenson E, Hammond CJ. Hysi PG, et al. Nat Genet. 2020 Apr;52(4):401-407. doi: 10.1038/s41588-020-0599-0. Epub 2020 Mar 30. Nat Genet. 2020. PMID: 32231278 Free PMC article.
X-Linked Retinoschisis: Deep Phenotyping and Genetic Characterization.
Georgiou M, Finocchio L, Fujinami K, Fujinami-Yokokawa Y, Virgili G, Mahroo OA, Webster AR, Michaelides M. Georgiou M, et al. Ophthalmology. 2022 May;129(5):542-551. doi: 10.1016/j.ophtha.2021.11.019. Epub 2021 Nov 23. Ophthalmology. 2022. PMID: 34822951 Free article.
CNGB1-related rod-cone dystrophy: A mutation review and update.
Nassisi M, Smirnov VM, Solis Hernandez C, Mohand-Saïd S, Condroyer C, Antonio A, Kühlewein L, Kempf M, Kohl S, Wissinger B, Nasser F, Ragi SD, Wang NK, Sparrow JR, Greenstein VC, Michalakis S, Mahroo OA, Ba-Abbad R, Michaelides M, Webster AR, Degli Esposti S, Saffren B, Capasso J, Levin A, Hauswirth WW, Dhaenens CM, Defoort-Dhellemmes S, Tsang SH, Zrenner E, Sahel JA, Petersen-Jones SM, Zeitz C, Audo I. Nassisi M, et al. Hum Mutat. 2021 Jun;42(6):641-666. doi: 10.1002/humu.24205. Epub 2021 May 16. Hum Mutat. 2021. PMID: 33847019 Free PMC article. Review.
GWAS on retinal vasculometry phenotypes.
Jiang X, Hysi PG, Khawaja AP, Mahroo OA, Xu Z, Hammond CJ, Foster PJ, Welikala RA, Barman SA, Whincup PH, Rudnicka AR, Owen CG, Strachan DP; UK Biobank Eye and Vision Consortium. Jiang X, et al. PLoS Genet. 2023 Feb 9;19(2):e1010583. doi: 10.1371/journal.pgen.1010583. eCollection 2023 Feb. PLoS Genet. 2023. PMID: 36757925 Free PMC article.
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development.
Simcoe MJ, Shah A, Fan B, Choquet H, Weisschuh N, Waseem NH, Jiang C, Melles RB, Ritch R, Mahroo OA, Wissinger B, Jorgenson E, Wiggs JL, Garway-Heath DF, Hysi PG, Hammond CJ. Simcoe MJ, et al. Ophthalmology. 2022 Jun;129(6):626-636. doi: 10.1016/j.ophtha.2022.01.005. Epub 2022 Jan 11. Ophthalmology. 2022. PMID: 35031440 Free article.
CERKL-Associated Retinal Dystrophy: Genetics, Phenotype, and Natural History.
Daich Varela M, Duignan ES, De Silva SR, Ba-Abbad R, Fujinami-Yokokawa Y, Leo S, Fujinami K, Mahroo OA, Robson AG, Webster AR, Michaelides M. Daich Varela M, et al. Ophthalmol Retina. 2023 Oct;7(10):918-931. doi: 10.1016/j.oret.2023.06.007. Epub 2023 Jun 17. Ophthalmol Retina. 2023. PMID: 37331655 Free PMC article.
33 results