中国学者近期发表的论文
1.	A novel causative mutation for congenital cataract and its underlying pathogenesis. Author: Xiu Y1, Fan Y2, Wu K3, Chen S1, Pan M1, Xu X4, Zhu Y2. Journal: Ophthalmic Genet. 2019 Feb;40(1):66-68. doi: 10.1080/13816810.2018.1558262. Epub 2018 Dec 26.    PubMed      DOI
2.	Novel mutations in the OPN1LW and NR2R3 genes in a patient with blue cone monochromacy. Author: Cai B1, Li Z1, Sun S1, Wang L1, Chen L1, Yang J1, Li X1. Journal: Ophthalmic Genet. 2019 Feb;40(1):43-48. doi: 10.1080/13816810.2018.1561902. Epub 2019 Jan 7.    PubMed      DOI
3.	Enhanced expression of son of sevenless homolog 1 is predictive of poor prognosis in uveal malignant melanoma patients. Author: Wang YS1, Wu L1. Journal: Ophthalmic Genet. 2019 Feb;40(1):22-28. doi: 10.1080/13816810.2019.1573904. Epub 2019 Feb 4.    PubMed      DOI
4.	Novel ocular findings in oculodentodigital dysplasia (ODDD): a case report and literature review. Author: Wang Z1, Sun L1, Wang P1, Chen C1, Zhang A1, Wang W1, Ding X1. Journal: Ophthalmic Genet. 2019 Feb;40(1):54-59. doi: 10.1080/13816810.2019.1571616. Epub 2019 Feb 15.    PubMed      DOI
5.	Phenotypic variability of SLC7A14 mutations in patients with inherited retinal dystrophy. Author: Guo LY1,2,3, Zheng SL4, Li J1,2,3, Zhu Q1,2,3, Duan WH1,2,3, Zhang Y5, Zhu YT5, Hu M1,2,3. Journal: Ophthalmic Genet. 2019 Apr;40(2):118-123. doi: 10.1080/13816810.2019.1586964. Epub 2019 Mar 29.    PubMed      DOI
6.	Association of genetic variants at MYP10 and MYP15 with high myopia in a Han Chinese population. Author: Jiang L1, Zheng R1, Luo D1, Wang T1, Zhai Y1, Ye Z2, Liu X1, Gong B1, Qu C2, Shi Y1,3. Journal: Ophthalmic Genet. 2019 May 28:1-5. doi: 10.1080/13816810.2019.1605388. [Epub ahead of print]    PubMed      DOI
7.	Additional Comments on "Ten SNPs of PAX6, Lumican, and MYOC Genes are not Associated with High Myopia in Han Chinese". Author: Liu L. Journal: Ophthalmic Genet. 2016;37(1):119-20. doi: 10.3109/13816810.2014.889170. Epub 2014 Feb 19. No abstract available.     PubMed
8.	A Novel Mutation of FOXC1 (R127L) in an Axenfeld-Rieger Syndrome Family with Glaucoma and Multiple Congenital Heart Diseases. Author: Du RF, Huang H, Fan LL, Li XP, Xia K, Xiang R. Journal: Ophthalmic Genet. 2016;37(1):111-5. doi: 10.3109/13816810.2014.924016. Epub 2014 Jun 10. No abstract available.     PubMed
9.	The TNF-α-308G/A Polymorphism is Not Associated with Ocular Chlamydia trachomatis Infection in Han Chinese Children. Author: Xue W, Wang Q, Li Z, Lu L, Zhu J, He X, Zhao R, Shi Y, Zou H. Journal: Ophthalmic Genet. 2016 Jun;37(2):245-7. doi: 10.3109/13816810.2015.1028650. Epub 2016 Jan 15.    PubMed
10.	Late-onset CORD in a patient with RDH12 mutations identified by whole exome sequencing. Author: Xin W, Xiao X, Li S, Zhang Q. Journal: Ophthalmic Genet. 2016 Sep;37(3):345-348. Epub 2016 Feb 5. No abstract available.     PubMed

同类著名期刊名称 h-index CiteScore PROGRESS IN RETINAL AND EYE RESEARCH 131 23.40 Ocular Surface 53 12.70 OPHTHALMOLOGY 217 14.80 SURVEY OF OPHTHALMOLOGY 120 7.50 AMERICAN JOURNAL OF OPHTHALMOLOGY 171 7.70 RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES 105 6.00 BRITISH JOURNAL OF OPHTHALMOLOGY 137 6.80 INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 196 6.50 ACTA OPHTHALMOLOGICA 77 4.80 EXPERIMENTAL EYE RESEARCH 112 4.80

中科院JCR同大类学科的热搜期刊 浏览次数 MEDICINE 302314 CANCER RESEARCH 166666 Molecular Medicine Reports 165593 International Journal of Nanomedicine 165206 CANCER LETTERS 160346 JOURNAL OF ETHNOPHARMACOLOGY 142631 BIOMEDICINE & PHARMACOTHERAPY 141962 Theranostics 136944 EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY 136744 International Journal of Environmental Research and Public Health 134408