BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Li J, Chen X, Yan Y, Yao K. Molecular genetics of congenital cataracts. Exp Eye Res 2020;191:107872. [PMID: 31770519 DOI: 10.1016/j.exer.2019.107872] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 2.7] [Reference Citation Analysis]
Number Citing Articles
1 Yu Y, Qiao Y, Ye Y, Li J, Yao K. Identification and characterization of six β-crystallin gene mutations associated with congenital cataract in Chinese families. Mol Genet Genomic Med 2021;9:e1617. [PMID: 33594837 DOI: 10.1002/mgg3.1617] [Reference Citation Analysis]
2 Jia ZK, Fu CX, Wang AL, Yao K, Chen XJ. Cataract-causing allele in CRYAA (Y118D) proceeds through endoplasmic reticulum stress in mouse model. Zool Res 2021;42:300-9. [PMID: 33929105 DOI: 10.24272/j.issn.2095-8137.2020.354] [Reference Citation Analysis]
3 Yang D, Zhou H, Lin J, Zhao S, Zhou H, Yin Z, Ni B, Chen Y, Xie W. Case Report: A Novel Missense Variant in the SIPA1L3 Gene Associated With Cataracts in a Chinese Family. Front Genet 2021;12:715599. [PMID: 34603379 DOI: 10.3389/fgene.2021.715599] [Reference Citation Analysis]
4 Wang X, Wang D, Wang Q, Huang W, Dongye M, Zhang X, Lin D, Lin Z, Li J, Hu W, Li X, Lin X, Zhong Q, Chen W, Lin H. Broadening the Mutation Spectrum in GJA8 and CHMP4B: Novel Missense Variants and the Associated Phenotypes in Six Chinese Han Congenital Cataracts Families. Front Med (Lausanne) 2021;8:713284. [PMID: 34722561 DOI: 10.3389/fmed.2021.713284] [Reference Citation Analysis]
5 Chen D, Zhu S. Whole-exome sequencing identification of a recurrent CRYBB2 variant in a four-generation Chinese family with congenital nuclear cataracts. Exp Ther Med 2021;22:1375. [PMID: 34650623 DOI: 10.3892/etm.2021.10810] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Zin OA, Neves LM, Motta FL, Horovitz DDG, Guida L, Gomes LHF, Cunha DP, Rodrigues APS, Zin AA, Sallum JMF, Vasconcelos ZFM. Novel Mutation in CRYBB3 Causing Pediatric Cataract and Microphthalmia. Genes (Basel) 2021;12:1069. [PMID: 34356085 DOI: 10.3390/genes12071069] [Reference Citation Analysis]
7 Mei S, Wu Y, Wang Y, Cui Y, Zhang M, Zhang T, Huang X, Yu S, Yu T, Zhao J. Disruption of PIKFYVE causes congenital cataract in human and zebrafish. Elife 2022;11:e71256. [PMID: 35023829 DOI: 10.7554/eLife.71256] [Reference Citation Analysis]
8 Ding N, Chen Z, Song X, Tang X. Novel mutation of GJA8 in autosomal dominant congenital cataracts. Ann Transl Med 2020;8:1127. [PMID: 33240976 DOI: 10.21037/atm-20-4663] [Reference Citation Analysis]
9 Li X, Si N, Song Z, Ren Y, Xiao W. Clinical and genetic findings in patients with congenital cataract and heart diseases. Orphanet J Rare Dis 2021;16:242. [PMID: 34059112 DOI: 10.1186/s13023-021-01873-7] [Reference Citation Analysis]
10 Ni SH, Zhang JM, Zhao J. A novel missense mutation of CRYBA1 in a northern Chinese family with inherited coronary cataract with blue punctate opacities. Eur J Ophthalmol 2021;:11206721211008355. [PMID: 33827296 DOI: 10.1177/11206721211008355] [Reference Citation Analysis]
11 Li H, Jiang H, Rong R, Jiang J, Ji D, Song W, Xia X. Identification of GJA3 p.S50P Mutation in a Chinese Family with Autosomal Dominant Congenital Cataract and Its Underlying Pathogenesis. DNA Cell Biol 2020;39:1760-6. [PMID: 32808810 DOI: 10.1089/dna.2020.5605] [Reference Citation Analysis]
12 Harding P, Toms M, Schiff E, Owen N, Bell S, Lloyd IC, Moosajee M. EPHA2 Segregates with Microphthalmia and Congenital Cataracts in Two Unrelated Families. Int J Mol Sci 2021;22:2190. [PMID: 33671840 DOI: 10.3390/ijms22042190] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Pandey B, Belnap N, Balak C, Huentelman M, Ramsey K, Narayanan V, Plotnik J. Progressive bilateral nuclear cataracts associated with cerebellar-facial-dental syndrome: case report, literature review, and identification of a new genetic variant. J AAPOS 2021:S1091-8531(21)00544-9. [PMID: 34628026 DOI: 10.1016/j.jaapos.2021.07.006] [Reference Citation Analysis]