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Cited by in F6Publishing
For: de Bruijn SE, Fadaie Z, Cremers FPM, Kremer H, Roosing S. The Impact of Modern Technologies on Molecular Diagnostic Success Rates, with a Focus on Inherited Retinal Dystrophy and Hearing Loss. Int J Mol Sci 2021;22:2943. [PMID: 33799353 DOI: 10.3390/ijms22062943] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Hendriks WJAJ, van Cruchten RTP, Pulido R. Hereditable variants of classical protein tyrosine phosphatase genes: Will they prove innocent or guilty? Front Cell Dev Biol 2023;10. [DOI: 10.3389/fcell.2022.1051311] [Reference Citation Analysis]
2 Ben-yosef T. Inherited Retinal Diseases. IJMS 2022;23:13467. [DOI: 10.3390/ijms232113467] [Reference Citation Analysis]
3 Matynia A, Wang J, Kim S, Li Y, Dimashkie A, Jiang Z, Hu J, Strom SP, Radu RA, Chen R, Gorin MB. Assessing Variant Causality and Severity Using Retinal Pigment Epithelial Cells Derived from Stargardt Disease Patients. Transl Vis Sci Technol 2022;11:33. [PMID: 35348597 DOI: 10.1167/tvst.11.3.33] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
4 Botto C, Dalkara D, El-Amraoui A. Progress in Gene Editing Tools and Their Potential for Correcting Mutations Underlying Hearing and Vision Loss. Front Genome Ed 2021;3:737632. [PMID: 34778871 DOI: 10.3389/fgeed.2021.737632] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
5 Kremer H. Novel gene discovery for hearing loss and other routes to increased diagnostic rates. Hum Genet 2021. [PMID: 34599370 DOI: 10.1007/s00439-021-02374-0] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]