| Literature DB >> 35049169 |
Lujain Talaat Idriss1, Maryam Hussain2, Muhammad Khan2, Tauseef Ahmad3, Khushi Muhammad2, Mukhtiar Baig4, Muhammad Mumtaz Khan5.
Abstract
BACKGROUND AND AIM: Globally, congenital cataract remains one of the main causes of visual loss in children. This study was designed to plot the overall research output and evaluate some key bibliometric indicators in congenital cataracts research.Entities:
Mesh:
Year: 2021 PMID: 35049169 PMCID: PMC9191315 DOI: 10.1097/MD.0000000000027756
Source DB: PubMed Journal: Medicine (Baltimore) ISSN: 0025-7974 Impact factor: 1.817
Figure 1Current study flow chart.
Figure 2Frequency of publications and global citations from 1903 to July 27, 2021.
Figure 3Heat mapping of global research in congenital cataract.
Figure 4Document types.
Figure 5Top journals in congenital cataract research published at least 15 papers. (A) Publications; (B) Global citations; (C) Global citations per year; (D) Journals Impact Factor released in June 2021. Note: A: Investigative Ophthalmology & Visual Science; B: Molecular Vision; C: American Journal of Ophthalmology; D: Archives of Ophthalmology (it changed its name to JAMA Ophthalmology in 2013); E: Journal of Cataract and Refractive Surgery; F: Journal of AAPOS; G: British Journal of Ophthalmology; H: Acta Ophthalmologica; I: Journal of Pediatric Ophthalmology & Strabismus; J: American Journal of Human Genetics; K: PLoS One; L: Eye; M: Ophthalmology; N: International Journal of Ophthalmology; O: European Journal of Ophthalmology; P: Indian Journal of Ophthalmology; Q: European Journal of Human Genetics.
Figure 6(A) Top countries in congenital cataract research with more than 15 publications. A total of 232 publications were excluded from the above graph based on the missing country name. (B) Top institutes in congenital cataract research with at least 15 publications. A total of 192 publications were excluded from the above graph based on missing institution names.
Figure 7Top authors in congenital cataract with at least 15 publications.
Figure 8Most studied Web of Science categories in congenital cataract research.
Figure 9Most frequently used keywords in congenital cataract with at least 50 occurrences.
Top 10 most cited publications in congenital cataract research.
| Ranking | Study reference | Global citations |
| 1 | Gregg NM. Congenital cataract following German measles in the mother. Transactions of the Ophthalmological Society of Australia. 1941; 3: 35–46. | 1268 |
| 2 | Glaser T, Jepeal L, Edwards JG, Young SR, Favor J, et al. PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central-nervous-system defects. Nature Genetics. 1994; 7 (4): 463–471. | 545 |
| 3 | Litt M, Kramer P, LaMorticella DM, Murphey W, Lovrien EW, et al. Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA. Human Molecular Genetics. 1998; 7 (3): 471–474. | 378 |
| 4 | Li WC, Kuszak JR, Dunn K, Wang RR, Ma WC, et al. Lens epithelial-cell apoptosis appears to be a common cellular basis for non-congenital cataract development in humans and animals. Journal of Cell Biology. 1995; 130 (1): 169–181. | 294 |
| 5 | Hejtmancik JF. Congenital cataracts and their molecular genetics. Seminars in Cell & Developmental Biology. 2008; 19 (2): 134–149. | 252 |
| 6 | Mackay D, Ionides A, Kibar Z, Rouleau G, Berry V, et al. Connexin46 mutations in autosomal dominant congenital cataract. American Journal of Human Genetics. 1999; 64 (5): 1357–1364. | 228 |
| 7 | Beller R, Hoyt CS, Marg E, Odom JV. Good visual function after neonatal surgery for congenital monocular cataracts. American Journal of Ophthalmology. 1981; 91 (5): 559–565. | 200 |
| 8 | Berry V, Francis P, Reddy MA, Collyer D, Vithana E, et al. Alpha-b crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans. American Journal of Human Genetics. 2001; 69 (5): 1141–1145. | 197 |
| 9 | Birch EE, Stager DR. The critical period for surgical treatment of dense congenital unilateral cataract. Investigative Ophthalmology & Visual Science. 1996; 37 (8): 1532–1538. | 156 |
| 10 | Renwick JH, Lawler SD. Probable linkage between a congenital cataract locus and the duffy blood group locus. Annals of Human Genetics. 1963; 27 (1): 67–84. | 152 |
Figure 10Co-authorship countries visualization network mapping.
Figure 11Co-occurrence author keywords visualization network mapping.