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For: Uyhazi KE, Binenbaum G, Carducci N, Zackai EH, Aleman TS. Early photoreceptor outer segment loss and retinoschisis in Cohen syndrome. Ophthalmic Genetics 2018;39:399-404. [DOI: 10.1080/13816810.2018.1459735] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 2.3] [Reference Citation Analysis]
Number Citing Articles
1 Pascoal C, Francisco R, Ferro T, Dos Reis Ferreira V, Jaeken J, Videira PA. CDG and immune response: From bedside to bench and back. J Inherit Metab Dis 2020;43:90-124. [PMID: 31095764 DOI: 10.1002/jimd.12126] [Cited by in Crossref: 17] [Cited by in F6Publishing: 18] [Article Influence: 5.7] [Reference Citation Analysis]
2 O’neil E, Serrano L, Scoles D, Cunningham KE, Han G, Chiang J, Bennett J, Aleman TS. Detailed retinal phenotype of Boucher-Neuhäuser syndrome associated with mutations in PNPLA6 mimicking choroideremia. Ophthalmic Genetics 2019;40:267-75. [DOI: 10.1080/13816810.2019.1605392] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
3 Rakusiewicz K, Kanigowska K, Hautz W, Wicher D, Młynek M, Wyszyńska M, Rogowska A, Jędrzejczak-Młodziejewska J, Danowska M, Czeszyk A. Coexistence of bilateral macular edema and pale optic disc in the patient with Cohen syndrome. Open Med (Wars) 2021;16:156-60. [PMID: 33542958 DOI: 10.1515/med-2021-0208] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
4 Daich Varela M, Motta FL, Webster AR, Arno G. A rare canonical splice-site variant in VPS13B causes attenuated Cohen syndrome. Ophthalmic Genet 2021;:1-6. [PMID: 34425733 DOI: 10.1080/13816810.2021.1970194] [Reference Citation Analysis]
5 Quinn MP, MacKeen LD, Vincent A, Strube YNJ. Early ocular findings in Cohen syndrome: case report and Canadian survey study. Can J Ophthalmol 2021;56:e26-8. [PMID: 32777201 DOI: 10.1016/j.jcjo.2020.07.011] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
6 Huang LC, Kelly JP, Cabrera MT, Olmos de Koo LC, Weiss AH, Herlihy EP. Optical coherence tomography findings in Cohen syndrome. J AAPOS 2020;24:306-9. [PMID: 32919079 DOI: 10.1016/j.jaapos.2020.07.004] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
7 Sevik MO, Aykut A, Şahin Ö. Resolution of cystoid macular edema with topical carbonic anhydrase inhibitor in a patient with retinal dystrophy associated with Cohen syndrome. Ophthalmic Genet 2021;:1-5. [PMID: 33974487 DOI: 10.1080/13816810.2021.1925928] [Reference Citation Analysis]
8 Gabrielle PH, Faivre L, Audo I, Zanlonghi X, Dollfus H, Thiadens AAHJ, Zeitz C, Mancini GMS, Perdomo Y, Mohand-Saïd S, Lizé E, Lhussiez V, Nandrot EF, Acar N, Creuzot-Garcher C, Sahel JA, Ansar M, Thauvin-Robinet C, Duplomb L, Da Costa R. Cystoid maculopathy is a frequent feature of Cohen syndrome-associated retinopathy. Sci Rep 2021;11:16412. [PMID: 34385517 DOI: 10.1038/s41598-021-95743-8] [Reference Citation Analysis]
9 Lhussiez V, Dubus E, Cesar Q, Acar N, Nandrot EF, Simonutti M, Audo I, Lizé E, Nguyen S, Geissler A, Bouchot A, Ansar M, Picaud S, Thauvin-Robinet C, Olivier-Faivre L, Duplomb L, Da Costa R. Cohen Syndrome-Associated Cataract Is Explained by VPS13B Functions in Lens Homeostasis and Is Modified by Additional Genetic Factors. Invest Ophthalmol Vis Sci 2020;61:18. [PMID: 32915983 DOI: 10.1167/iovs.61.11.18] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]