X-Linked Retinoschisis in Females in a Consanguineous Family: A Rare Entity
Article Properties
-
DOI (url)
-
Publication Date2020/08/01
-
Journal
-
Indian UGC (journal)
-
Citations6
-
Mehmet Önen ORCID (unauthenticated)
-
Kürşat Zor ORCID (unauthenticated)
-
Erkut Küçük ORCID (unauthenticated)
-
Gamze Yıldırım ORCID (unauthenticated)
Cite
Önen, Mehmet, et al. “X-Linked Retinoschisis in Females in a Consanguineous Family: A Rare Entity”. Turkish Journal of Ophthalmology, vol. 50, no. 4, 2020, pp. 252-4, https://doi.org/10.4274/tjo.galenos.2020.42815.
Önen, M., Zor, K., Küçük, E., & Yıldırım, G. (2020). X-Linked Retinoschisis in Females in a Consanguineous Family: A Rare Entity. Turkish Journal of Ophthalmology, 50(4), 252-254. https://doi.org/10.4274/tjo.galenos.2020.42815
Önen M, Zor K, Küçük E, Yıldırım G. X-Linked Retinoschisis in Females in a Consanguineous Family: A Rare Entity. Turkish Journal of Ophthalmology. 2020;50(4):252-4.
Journal Category
Medicine
Ophthalmology
Citations
| Title | Journal | Journal Categories | Citations | Publication Date |
|---|---|---|---|---|
A Carrier Female Manifesting an Unusual X-Linked Retinoschisis Phenotype Associated with the Pathogenic Variant c.266delA, p.(Tyr89LeufsTer37) in RS1, and Skewed X-Inactivation | Genes |
| 1 | 2023 |
| Retinosquisis ligada al X en homocigosis: A propósito de un caso | Archivos de la Sociedad Española de Oftalmología | 2022 | ||
| X-linked retinoschisis: About a case | Archivos de la Sociedad Española de Oftalmología (English Edition) | 2022 | ||
| Cystoid macular oedema without leakage in fluorescein angiography: a literature review | Eye |
| 2 | 2022 |
| Clinical and genetic study of a pseudo-dominant retinoschisis pedigree: the first female patient reported in Chinese population | Ophthalmic Genetics |
| 2022 |
Citations Analysis
| Category | Category Repetition |
|---|---|
| Medicine: Medicine (General) | 2 |
| Medicine: Ophthalmology | 2 |
| Science: Biology (General): Genetics | 2 |
The category
Medicine: Medicine (General) 2
is the most commonly referenced area in studies that cite this article. The first research to cite this article was titled X-linked Retinoschisis Discovered after Congenital Cataract Surgery and was published in 2020. The most recent citation comes from a 2023 study titled A Carrier Female Manifesting an Unusual X-Linked Retinoschisis Phenotype Associated with the Pathogenic Variant c.266delA, p.(Tyr89LeufsTer37) in RS1, and Skewed X-Inactivation. This article reached its peak citation in 2022, with 4 citations. It has been cited in 6 different journals. Among related journals, the Genes cited this research the most, with 1 citations. The chart below illustrates the annual citation trends for this article.