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For: Mansfield BC, Yerxa BR, Branham KH. Implementation of a registry and open access genetic testing program for inherited retinal diseases within a non-profit foundation. Am J Med Genet C Semin Med Genet 2020;184:838-45. [PMID: 32783387 DOI: 10.1002/ajmg.c.31825] [Cited by in Crossref: 7] [Cited by in F6Publishing: 10] [Article Influence: 3.5] [Reference Citation Analysis]
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1 Abdul-Fatah A, Esmaeilisaraji L, Juan CM, Holcik M. Mitochondrial disease registries worldwide: A scoping review. PLoS One 2022;17:e0276883. [PMID: 36301904 DOI: 10.1371/journal.pone.0276883] [Reference Citation Analysis]
2 Britten‐jones AC, O'hare F, Edwards TL, Ayton LN, the VENTURE Study Consortium. Victorian evolution of inherited retinal diseases natural history registry ( VENTURE study): Rationale, methodology and initial participant characteristics. Clinical Exper Ophthalmology 2022. [DOI: 10.1111/ceo.14110] [Reference Citation Analysis]
3 Gocuk S, Jiao Y, Britten-jones AC, Kerr NM, Lim L, Skalicky S, Stawell R, Ayton LN, Mack HG. Genetic Testing of Inherited Retinal Disease in Australian Private Tertiary Ophthalmology Practice. OPTH 2022;Volume 16:1127-38. [DOI: 10.2147/opth.s353787] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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5 Sallum JMF, Kaur VP, Shaikh J, Banhazi J, Spera C, Aouadj C, Viriato D, Fischer MD. Epidemiology of Mutations in the 65-kDa Retinal Pigment Epithelium (RPE65) Gene-Mediated Inherited Retinal Dystrophies: A Systematic Literature Review. Adv Ther 2022;39:1179-98. [PMID: 35098484 DOI: 10.1007/s12325-021-02036-7] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Hunt H, Dittmer KE, Garrick DJ, Fairley RA, Heap SJ, Jolly RD. An inherited night blindness in Wiltshire sheep. Vet Pathol 2022;:3009858211067461. [PMID: 34974772 DOI: 10.1177/03009858211067461] [Reference Citation Analysis]
7 Lam BL, Leroy BP, Black G, Ong T, Yoon D, Trzupek K. Genetic testing and diagnosis of inherited retinal diseases. Orphanet J Rare Dis 2021;16:514. [PMID: 34906171 DOI: 10.1186/s13023-021-02145-0] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
8 Durham TA, Duncan JL, Ayala AR, Birch DG, Cheetham JK, Ferris FL 3rd, Hoyng CB, Pennesi ME, Sahel JA; Foundation Fighting Blindness Consortium Investigator Group. Tackling the Challenges of Product Development Through a Collaborative Rare Disease Network: The Foundation Fighting Blindness Consortium. Transl Vis Sci Technol 2021;10:23. [PMID: 34004001 DOI: 10.1167/tvst.10.4.23] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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10 Hufnagel RB, Walter MA, Arno G. Introduction to the special issue on Ophthalmic Genetics: Vision in 2020. Am J Med Genet C Semin Med Genet 2020;184:535-7. [PMID: 32864823 DOI: 10.1002/ajmg.c.31841] [Reference Citation Analysis]
11 Mansfield BC, Yerxa BR, Branham KH. Implementation of a registry and open access genetic testing program for inherited retinal diseases within a non-profit foundation. Am J Med Genet C Semin Med Genet 2020;184:838-45. [PMID: 32783387 DOI: 10.1002/ajmg.c.31825] [Cited by in Crossref: 7] [Cited by in F6Publishing: 10] [Article Influence: 3.5] [Reference Citation Analysis]