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For: Thomas MG, Papageorgiou E, Kuht HJ, Gottlob I. Normal and abnormal foveal development. Br J Ophthalmol 2020:bjophthalmol-2020-316348. [PMID: 33148537 DOI: 10.1136/bjophthalmol-2020-316348] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
Number Citing Articles
1 Rufai SR, Bowman R, Bunce C, Panteli V, McLean RJ, Teli S, Gottlob I, Thomas MG, Jeelani NUO, Proudlock FA. Feasibility and Repeatability of Handheld Optical Coherence Tomography in Children With Craniosynostosis. Transl Vis Sci Technol 2021;10:24. [PMID: 34313724 DOI: 10.1167/tvst.10.8.24] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Nicholson R, Osborne D, Fairhead L, Beed L, Hill CM, Lee H. Segmentation of the foveal and parafoveal retinal architecture using handheld spectral-domain optical coherence tomography in children with Down syndrome. Eye (Lond) 2022. [PMID: 35001092 DOI: 10.1038/s41433-021-01883-6] [Reference Citation Analysis]
3 Kuht HJ, Maconachie GD, Han J, Kessel L, Van Genderen MM, Mclean RJ, Hisaund M, Tu Z, Hertle RW, Gronskov K, Bai D, Wei A, Li W, Jiao Y, Smirnov V, Choi J, Tobin MD, Sheth Bmedsci V, Purohit R, Dawar B, Girach A, Strul S, May L, Chen FK, Heath Jeffery RC, Aamir A, Sano R, Jin J, Brooks BP, Kohl S, Arvelier B, Montoliu L, Engle EC, Proudlock FA, Nishad G, Pani P, Varma G, Gottlob I, Thomas MG. Genotypic and Phenotypic Spectrum of Foveal Hypoplasia: A Multi-centre Study. Ophthalmology 2022. [DOI: 10.1016/j.ophtha.2022.02.010] [Reference Citation Analysis]
4 Jiang Y, Li S, Xiao X, Sun W, Zhang Q. Genotype-Phenotype of Isolated Foveal Hypoplasia in a Large Cohort: Minor Iris Changes as an Indicator of PAX6 Involvement. Invest Ophthalmol Vis Sci 2021;62:23. [PMID: 34415986 DOI: 10.1167/iovs.62.10.23] [Reference Citation Analysis]
5 Hayashi T, Kondo H, Matsushita I, Mizobuchi K, Baba A, Iida K, Kubo H, Nakano T. Homozygous single nucleotide duplication of SLC38A8 in autosomal recessive foveal hypoplasia: The first Japanese case report. Doc Ophthalmol 2021. [PMID: 34037952 DOI: 10.1007/s10633-021-09842-y] [Reference Citation Analysis]
6 Iarossi G, Coppè AM, Passarelli C, Maltese PE, Sinibaldi L, Cappelli A, Cetola S, Novelli A, Buzzonetti L. Blue Cone Monochromatism with Foveal Hypoplasia Caused by the Concomitant Effect of Variants in OPN1LW/OPN1MW and GPR143 Genes. Int J Mol Sci 2021;22:8617. [PMID: 34445325 DOI: 10.3390/ijms22168617] [Reference Citation Analysis]
7 Aamir A, Kuht HJ, Grønskov K, Brooks BP, Thomas MG. Clinical utility gene card for oculocutaneous (OCA) and ocular albinism (OA)-an update. Eur J Hum Genet 2021;29:1577-83. [PMID: 33504991 DOI: 10.1038/s41431-021-00809-w] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
8 Knebel D, Rudolph G, Herold T, Priglinger S. [Waardenburg's Syndrome Type IIA with Partial Albinism]. Klin Monbl Augenheilkd 2021. [PMID: 34571549 DOI: 10.1055/a-1610-9690] [Reference Citation Analysis]
9 Levinsen M, Børresen ML, Roos L, Grønskov K, Kessel L. Causes of poor eye contact in infants: a population-based study. BMC Ophthalmol 2021;21:388. [PMID: 34743689 DOI: 10.1186/s12886-021-02151-7] [Reference Citation Analysis]
10 Jung SM, Valmaggia C, Türksever C, Todorova MG. Structural, Microvascular, and Functional Findings Associated with Fovea Plana. Klin Monbl Augenheilkd 2022;239:500-12. [PMID: 35472794 DOI: 10.1055/a-1766-7448] [Reference Citation Analysis]
11 Muns SM, Villegas VM, Schwartz SG. Clinical spectrum of blunted foveal contour. Ophthalmol Eye Dis 2022;14:251584142110708. [DOI: 10.1177/25158414211070864] [Reference Citation Analysis]