| Year |
Citation |
Score |
| 2020 |
Chen D, Chao DL, Rocha L, Kolar M, Nguyen Huu VA, Krawczyk M, Dasyani M, Wang T, Jafari M, Jabari M, Ross KD, Saghatelian A, Hamilton BA, Zhang K, Skowronska-Krawczyk D. The lipid elongation enzyme ELOVL2 is a molecular regulator of aging in the retina. Aging Cell. e13100. PMID 31943697 DOI: 10.1111/Acel.13100 |
0.361 |
|
| 2019 |
Laurent JM, Fu X, German S, Maurano MT, Zhang K, Boeke JD. Big DNA as a tool to dissect an age-related macular degeneration-associated haplotype. Precision Clinical Medicine. 2: 1-7. PMID 30944767 DOI: 10.1093/Pcmedi/Pby019 |
0.375 |
|
| 2019 |
Yuan P, Liang ZK, Liang H, Zheng LY, Li D, Li J, Zhang J, Tian J, Lai LH, Zhang K, He ZY, Zhang QX, Wang WJ. Expanding the phenotypic and genetic spectrum of Chinese patients with congenital absence of vas deferens bearing CFTR and ADGRG2 alleles. Andrology. PMID 30811104 DOI: 10.1111/andr.12592 |
0.338 |
|
| 2018 |
Wang P, Li X, Zhu W, Zhong Z, Moran A, Wang W, Zhang K, Shaochen Chen. 3D bioprinting of hydrogels for retina cell culturing. Bioprinting (Amsterdam, Netherlands). 11. PMID 31903439 DOI: 10.1016/J.Bprint.2018.E00029 |
0.303 |
|
| 2018 |
Stern JH, Tian Y, Funderburgh J, Pellegrini G, Zhang K, Goldberg JL, Ali RR, Young M, Xie Y, Temple S. Regenerating Eye Tissues to Preserve and Restore Vision. Cell Stem Cell. 22: 834-849. PMID 29859174 DOI: 10.1016/J.Stem.2018.05.013 |
0.332 |
|
| 2018 |
Moreno AM, Fu X, Zhu J, Katrekar D, Shih YV, Marlett J, Cabotaje J, Tat J, Naughton J, Lisowski L, Varghese S, Zhang K, Mali P. In Situ Gene Therapy via AAV-CRISPR-Cas9-Mediated Targeted Gene Regulation. Molecular Therapy : the Journal of the American Society of Gene Therapy. PMID 29754775 DOI: 10.1016/J.Ymthe.2018.04.017 |
0.324 |
|
| 2018 |
Lu Y, Zhang K. Cellular Reprogramming in the Retina - Seeing the Light. The New England Journal of Medicine. 378: 1059-1060. PMID 29539280 DOI: 10.1056/NEJMcibr1713887 |
0.331 |
|
| 2018 |
Fu X, Huu VAN, Duan Y, Kermany DS, Valentim CCS, Zhang R, Zhu J, Zhang CL, Sun X, Zhang K. Clinical applications of retinal gene therapies Precision Clinical Medicine. 1: 5-20. DOI: 10.1093/PCMEDI/PBY004 |
0.313 |
|
| 2017 |
Zhu J, Ming C, Fu X, Duan Y, Hoang DA, Rutgard J, Zhang R, Wang W, Hou R, Zhang D, Zhang E, Zhang C, Hao X, Xiong W, Zhang K. Gene and mutation independent therapy via CRISPR-Cas9 mediated cellular reprogramming in rod photoreceptors. Cell Research. PMID 28429769 DOI: 10.1038/Cr.2017.57 |
0.313 |
|
| 2016 |
Wang W, Gawlik K, Lopez J, Wen C, Zhu J, Wu F, Shi W, Scheibler S, Cai H, Vairavan R, Shi A, Haw W, Ferreyra H, Zhang M, Chang S, ... Zhang K, et al. Genetic and environmental factors strongly influence risk, severity and progression of age-related macular degeneration. Signal Transduction and Targeted Therapy. 1: 16016. PMID 29263899 DOI: 10.1038/sigtrans.2016.16 |
0.344 |
|
| 2016 |
Suzuki K, Tsunekawa Y, Hernandez-Benitez R, Wu J, Zhu J, Kim EJ, Hatanaka F, Yamamoto M, Araoka T, Li Z, Kurita M, Hishida T, Li M, Aizawa E, Guo S, ... ... Zhang K, ... ... Zhang K, et al. In vivo genome editing via CRISPR/Cas9 mediated homology-independent targeted integration. Nature. PMID 27851729 DOI: 10.1038/Nature20565 |
0.304 |
|
| 2016 |
Khawaja AP, Cooke Bailey JN, Kang JH, Allingham RR, Hauser MA, Brilliant M, Budenz DL, Christen WG, Fingert J, Gaasterland D, Gaasterland T, Kraft P, Lee RK, Lichter PR, Liu Y, ... ... Zhang K, et al. Assessing the Association of Mitochondrial Genetic Variation With Primary Open-Angle Glaucoma Using Gene-Set Analyses. Investigative Ophthalmology & Visual Science. 57: 5046-5052. PMID 27661856 DOI: 10.1167/Iovs.16-20017 |
0.506 |
|
| 2016 |
Liu Y, Bailey JC, Helwa I, Dismuke WM, Cai J, Drewry M, Brilliant MH, Budenz DL, Christen WG, Chasman DI, Fingert JH, Gaasterland D, Gaasterland T, Gordon MO, Igo RP, ... ... Zhang K, et al. A Common Variant in MIR182 Is Associated With Primary Open-Angle Glaucoma in the NEIGHBORHOOD Consortium. Investigative Ophthalmology & Visual Science. 57: 3974-3981. PMID 27537254 DOI: 10.1167/Iovs.16-19688 |
0.474 |
|
| 2016 |
Ouyang H, Goldberg JL, Chen S, Li W, Xu GT, Li W, Zhang K, Nussenblatt RB, Liu Y, Xie T, Chan CC, Zack DJ. Ocular Stem Cell Research from Basic Science to Clinical Application: A Report from Zhongshan Ophthalmic Center Ocular Stem Cell Symposium. International Journal of Molecular Sciences. 17. PMID 27102165 DOI: 10.3390/Ijms17030415 |
0.515 |
|
| 2016 |
Brandler WM, Antaki D, Gujral M, Noor A, Rosanio G, Chapman TR, Barrera DJ, Lin GN, Malhotra D, Watts AC, Wong LC, Estabillo JA, Gadomski TE, Hong O, Fajardo KV, ... ... Zhang K, et al. Frequency and Complexity of De Novo Structural Mutation in Autism. American Journal of Human Genetics. PMID 27018473 DOI: 10.1016/J.Ajhg.2016.02.018 |
0.308 |
|
| 2016 |
Bhisitkul RB, Desai SJ, Boyer DS, Sadda SR, Zhang K. Fellow Eye Comparisons for 7-Year Outcomes in Ranibizumab-Treated AMD Subjects from ANCHOR, MARINA, and HORIZON (SEVEN-UP Study). Ophthalmology. PMID 26996339 DOI: 10.1016/j.ophtha.2016.01.033 |
0.311 |
|
| 2016 |
Ghazi NG, Abboud EB, Nowilaty SR, Alkuraya H, Alhommadi A, Cai H, Hou R, Deng WT, Boye SL, Almaghamsi A, Al Saikhan F, Al-Dhibi H, Birch D, Chung C, Colak D, ... ... Zhang K, et al. Treatment of retinitis pigmentosa due to MERTK mutations by ocular subretinal injection of adeno-associated virus gene vector: results of a phase I trial. Human Genetics. PMID 26825853 DOI: 10.1007/S00439-016-1637-Y |
0.354 |
|
| 2016 |
Bailey JN, Loomis SJ, Kang JH, Allingham RR, Gharahkhani P, Khor CC, Burdon KP, Aschard H, Chasman DI, Igo RP, Hysi PG, Glastonbury CA, Ashley-Koch A, Brilliant M, Brown AA, ... ... Zhang K, et al. Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma. Nature Genetics. PMID 26752265 DOI: 10.1038/Ng.3482 |
0.548 |
|
| 2016 |
Fritsche LG, Igl W, Bailey JN, Grassmann F, Sengupta S, Bragg-Gresham JL, Burdon KP, Hebbring SJ, Wen C, Gorski M, Kim IK, Cho D, Zack D, Souied E, Scholl HP, ... ... Zhang K, et al. A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. Nature Genetics. 48: 134-43. PMID 26691988 DOI: 10.1038/Ng.3448 |
0.566 |
|
| 2015 |
Skowronska-Krawczyk D, Zhao L, Zhu J, Weinreb RN, Cao G, Luo J, Flagg K, Patel S, Wen C, Krupa M, Luo H, Ouyang H, Lin D, Wang W, Li G, ... ... Zhang K, et al. P16INK4a Upregulation Mediated by SIX6 Defines Retinal Ganglion Cell Pathogenesis in Glaucoma. Molecular Cell. PMID 26365380 DOI: 10.1016/J.Molcel.2015.07.027 |
0.39 |
|
| 2015 |
Cao G, Chen Y, Zhang J, Liu Y, Zhang M, Zhang K, Su Z. Effects of adiponectin polymorphisms on the risk of advanced age-related macular degeneration. Biomarkers : Biochemical Indicators of Exposure, Response, and Susceptibility to Chemicals. 20: 266-70. PMID 26301885 DOI: 10.3109/1354750X.2015.1068857 |
0.363 |
|
| 2015 |
Liu Y, Wu F, Lu L, Lin D, Zhang K. VIDEOS IN CLINICAL MEDICINE. Examination of the Retina. The New England Journal of Medicine. 373: e9. PMID 26287871 DOI: 10.1056/NEJMvcm1308125 |
0.349 |
|
| 2015 |
Zhao L, Chen XJ, Zhu J, Xi YB, Yang X, Hu LD, Ouyang H, Patel SH, Jin X, Lin D, Wu F, Flagg K, Cai H, Li G, Cao G, ... ... Zhang K, et al. Lanosterol reverses protein aggregation in cataracts. Nature. PMID 26200341 DOI: 10.1038/Nature14650 |
0.306 |
|
| 2015 |
Li G, Xu F, Zhu J, Krawczyk M, Zhang Y, Yuan J, Patel S, Wang Y, Lin Y, Zhang M, Cai H, Chen D, Zhang M, Cao G, Yeh E, ... ... Zhang K, et al. Transcription factor Paired Box 6 controls limbal stem cell lineage in development and disease. The Journal of Biological Chemistry. PMID 26045558 DOI: 10.1074/Jbc.M115.662940 |
0.322 |
|
| 2015 |
Huang LZ, Li YJ, Xie XF, Zhang JJ, Cheng CY, Yamashiro K, Chen LJ, Ma XY, Cheung CM, Wang YS, Zhang CF, Bai YJ, Hou J, Chen XL, Qi Y, ... ... Zhang K, et al. Whole-exome sequencing implicates UBE3D in age-related macular degeneration in East Asian populations. Nature Communications. 6: 6687. PMID 25872646 DOI: 10.1038/Ncomms7687 |
0.4 |
|
| 2015 |
Salvo J, Lyubasyuk V, Xu M, Wang H, Wang F, Nguyen D, Wang K, Luo H, Wen C, Shi C, Lin D, Zhang K, Chen R. Next-generation sequencing and novel variant determination in a cohort of 92 familial exudative vitreoretinopathy patients. Investigative Ophthalmology & Visual Science. 56: 1937-46. PMID 25711638 DOI: 10.1167/Iovs.14-16065 |
0.36 |
|
| 2014 |
Liu Y, Garrett ME, Yaspan BL, Bailey JC, Loomis SJ, Brilliant M, Budenz DL, Christen WG, Fingert JH, Gaasterland D, Gaasterland T, Kang JH, Lee RK, Lichter P, Moroi SE, ... ... Zhang K, et al. DNA copy number variants of known glaucoma genes in relation to primary open-angle glaucoma. Investigative Ophthalmology & Visual Science. 55: 8251-8. PMID 25414181 DOI: 10.1167/Iovs.14-15712 |
0.526 |
|
| 2014 |
Wang F, Wang Y, Zhang B, Zhao L, Lyubasyuk V, Wang K, Xu M, Li Y, Wu F, Wen C, Bernstein PS, Lin D, Zhu S, Wang H, Zhang K, et al. A missense mutation in HK1 leads to autosomal dominant retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 55: 7159-64. PMID 25316723 DOI: 10.1167/Iovs.14-15520 |
0.389 |
|
| 2014 |
Zhang T, Xie X, Cao G, Jiang H, Wu S, Su Z, Zhang K, Lu F. Malattia leventinese/Doyne honeycomb retinal dystrophy in a chinese family with mutation of the EFEMP1 gene. Retina (Philadelphia, Pa.). 34: 2462-71. PMID 25111685 DOI: 10.1097/IAE.0000000000000259 |
0.376 |
|
| 2014 |
Bailey JN, Yaspan BL, Pasquale LR, Hauser MA, Kang JH, Loomis SJ, Brilliant M, Budenz DL, Christen WG, Fingert J, Gaasterland D, Gaasterland T, Kraft P, Lee RK, Lichter PR, ... ... Zhang K, et al. Hypothesis-independent pathway analysis implicates GABA and acetyl-CoA metabolism in primary open-angle glaucoma and normal-pressure glaucoma. Human Genetics. 133: 1319-30. PMID 25037249 DOI: 10.1007/S00439-014-1468-7 |
0.523 |
|
| 2014 |
Ouyang H, Xue Y, Lin Y, Zhang X, Xi L, Patel S, Cai H, Luo J, Zhang M, Zhang M, Yang Y, Li G, Li H, Jiang W, Yeh E, ... ... Zhang K, et al. WNT7A and PAX6 define corneal epithelium homeostasis and pathogenesis. Nature. 511: 358-61. PMID 25030175 DOI: 10.1038/Nature13465 |
0.313 |
|
| 2014 |
Mandal NA, Tran JT, Zheng L, Wilkerson JL, Brush RS, McRae J, Agbaga MP, Zhang K, Petrukhin K, Ayyagari R, Anderson RE. In vivo effect of mutant ELOVL4 on the expression and function of wild-type ELOVL4. Investigative Ophthalmology & Visual Science. 55: 2705-13. PMID 24644051 DOI: 10.1167/Iovs.13-13198 |
0.332 |
|
| 2014 |
Kang JH, Loomis SJ, Yaspan BL, Bailey JC, Weinreb RN, Lee RK, Lichter PR, Budenz DL, Liu Y, Realini T, Gaasterland D, Gaasterland T, Friedman DS, McCarty CA, Moroi SE, ... ... Zhang K, et al. Vascular tone pathway polymorphisms in relation to primary open-angle glaucoma. Eye (London, England). 28: 662-71. PMID 24603425 DOI: 10.1038/Eye.2014.42 |
0.518 |
|
| 2014 |
Loomis SJ, Kang JH, Weinreb RN, Yaspan BL, Cooke Bailey JN, Gaasterland D, Gaasterland T, Lee RK, Lichter PR, Budenz DL, Liu Y, Realini T, Friedman DS, McCarty CA, Moroi SE, ... ... Zhang K, et al. Association of CAV1/CAV2 genomic variants with primary open-angle glaucoma overall and by gender and pattern of visual field loss. Ophthalmology. 121: 508-16. PMID 24572674 DOI: 10.1016/J.Ophtha.2013.09.012 |
0.548 |
|
| 2014 |
Zhao JJ, Ouyang H, Luo J, Patel S, Xue Y, Quach J, Sfeir N, Zhang M, Fu X, Ding S, Chen S, Zhang K. Induction of retinal progenitors and neurons from mammalian Müller glia under defined conditions. The Journal of Biological Chemistry. 289: 11945-51. PMID 24523410 DOI: 10.1074/Jbc.M113.532671 |
0.336 |
|
| 2014 |
Wang D, Zhou J, Hou X, Nguyen DH, Cao G, Li G, Qiu G, Zhang K, Zhang M, Su Z. CETP Gene may be Associated with Advanced Age-related Macular Degeneration in the Chinese Population. Ophthalmic Genetics. PMID 24498989 DOI: 10.3109/13816810.2014.881506 |
0.323 |
|
| 2014 |
Luo J, Baranov P, Patel S, Ouyang H, Quach J, Wu F, Qiu A, Luo H, Hicks C, Zeng J, Zhu J, Lu J, Sfeir N, Wen C, Zhang M, ... ... Zhang K, et al. Human retinal progenitor cell transplantation preserves vision. The Journal of Biological Chemistry. 289: 6362-71. PMID 24407289 DOI: 10.1074/Jbc.M113.513713 |
0.337 |
|
| 2014 |
Wang F, Wang H, Tuan HF, Nguyen DH, Sun V, Keser V, Bowne SJ, Sullivan LS, Luo H, Zhao L, Wang X, Zaneveld JE, Salvo JS, Siddiqui S, Mao L, ... ... Zhang K, et al. Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements. Human Genetics. 133: 331-45. PMID 24154662 DOI: 10.1007/S00439-013-1381-5 |
0.402 |
|
| 2013 |
Zhao L, Patel SH, Pei J, Zhang K. Antagonizing Wnt pathway in diabetic retinopathy. Diabetes. 62: 3993-5. PMID 24264398 DOI: 10.2337/db13-1309 |
0.304 |
|
| 2013 |
Helgason H, Sulem P, Duvvari MR, Luo H, Thorleifsson G, Stefansson H, Jonsdottir I, Masson G, Gudbjartsson DF, Walters GB, Magnusson OT, Kong A, Rafnar T, Kiemeney LA, Schoenmaker-Koller FE, ... ... Zhang K, et al. A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration. Nature Genetics. 45: 1371-4. PMID 24036950 DOI: 10.1038/ng.2740 |
0.338 |
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| 2013 |
Zhan X, Larson DE, Wang C, Koboldt DC, Sergeev YV, Fulton RS, Fulton LL, Fronick CC, Branham KE, Bragg-Gresham J, Jun G, Hu Y, Kang HM, Liu D, Othman M, ... ... Zhang K, et al. Identification of a rare coding variant in complement 3 associated with age-related macular degeneration. Nature Genetics. 45: 1375-9. PMID 24036949 DOI: 10.1038/Ng.2758 |
0.357 |
|
| 2013 |
Pasquale LR, Loomis SJ, Weinreb RN, Kang JH, Yaspan BL, Bailey JC, Gaasterland D, Gaasterland T, Lee RK, Scott WK, Lichter PR, Budenz DL, Liu Y, Realini T, Friedman DS, ... ... Zhang K, et al. Estrogen pathway polymorphisms in relation to primary open angle glaucoma: an analysis accounting for gender from the United States. Molecular Vision. 19: 1471-81. PMID 23869166 |
0.502 |
|
| 2013 |
Zhou J, Wang D, Zhang J, Zhang M, Lu F, Qiu G, Zhao L, Nguyen DH, Luo H, Cao G, Zhang W, Jiang W, Li G, Zhang K, Zhang M, et al. RAD51 gene is associated with advanced age-related macular degeneration in Chinese population. Clinical Biochemistry. 46: 1689-93. PMID 23868022 DOI: 10.1016/j.clinbiochem.2013.07.002 |
0.338 |
|
| 2013 |
Zhao L, Grob S, Avery R, Kimura A, Pieramici D, Lee J, Rabena M, Ortiz S, Quach J, Cao G, Luo H, Zhang M, Pei M, Song Y, Tornambe P, ... ... Zhang K, et al. Common variant in VEGFA and response to anti-VEGF therapy for neovascular age-related macular degeneration. Current Molecular Medicine. 13: 929-34. PMID 23745581 DOI: 10.2174/15665240113139990048 |
0.361 |
|
| 2013 |
Fritsche LG, Chen W, Schu M, Yaspan BL, Yu Y, Thorleifsson G, Zack DJ, Arakawa S, Cipriani V, Ripke S, Igo RP, Buitendijk GH, Sim X, Weeks DE, Guymer RH, ... ... Zhang K, et al. Seven new loci associated with age-related macular degeneration. Nature Genetics. 45: 433-9, 439e1-2. PMID 23455636 DOI: 10.1038/Ng.2578 |
0.576 |
|
| 2013 |
Luo J, Zhao L, Chen AY, Zhang X, Zhu J, Zhao J, Ouyang H, Luo H, Song Y, Lee J, Patel SH, Shaw PX, Sadda S, Zhuo Y, Rosenfeld MG, ... Zhang K, et al. TCF7L2 variation and proliferative diabetic retinopathy. Diabetes. 62: 2613-7. PMID 23434931 DOI: 10.2337/db12-1093 |
0.306 |
|
| 2013 |
Lee J, Zeng J, Hughes G, Chen Y, Grob S, Zhao L, Lee C, Krupa M, Quach J, Luo J, Zeng J, Wei X, Zhang X, Zhu J, Duan Y, ... ... Zhang K, et al. Association of LIPC and advanced age-related macular degeneration. Eye (London, England). 27: 265-70; quiz 271. PMID 23348725 DOI: 10.1038/eye.2012.276 |
0.32 |
|
| 2013 |
Du H, Sun X, Guma M, Luo J, Ouyang H, Zhang X, Zeng J, Quach J, Nguyen DH, Shaw PX, Karin M, Zhang K. JNK inhibition reduces apoptosis and neovascularization in a murine model of age-related macular degeneration. Proceedings of the National Academy of Sciences of the United States of America. 110: 2377-82. PMID 23341606 DOI: 10.1073/pnas.1221729110 |
0.31 |
|
| 2013 |
Pasquale LR, Loomis SJ, Kang JH, Yaspan BL, Abdrabou W, Budenz DL, Chen TC, Delbono E, Friedman DS, Gaasterland D, Gaasterland T, Grosskreutz CL, Lee RK, Lichter PR, Liu Y, ... ... Zhang K, et al. CDKN2B-AS1 genotype-glaucoma feature correlations in primary open-angle glaucoma patients from the United States. American Journal of Ophthalmology. 155: 342-353.e5. PMID 23111177 DOI: 10.1016/J.Ajo.2012.07.023 |
0.553 |
|
| 2013 |
Wiggs JL, Hauser MA, Abdrabou W, Allingham RR, Budenz DL, Delbono E, Friedman DS, Kang JH, Gaasterland D, Gaasterland T, Lee RK, Lichter PR, Loomis S, Liu Y, McCarty C, ... ... Zhang K, et al. The NEIGHBOR consortium primary open-angle glaucoma genome-wide association study: rationale, study design, and clinical variables. Journal of Glaucoma. 22: 517-25. PMID 22828004 DOI: 10.1097/Ijg.0B013E31824D4Fd8 |
0.476 |
|
| 2012 |
Shaw PX, Zhang L, Zhang M, Du H, Zhao L, Lee C, Grob S, Lim SL, Hughes G, Lee J, Bedell M, Nelson MH, Lu F, Krupa M, Luo J, ... ... Zhang K, et al. Complement factor H genotypes impact risk of age-related macular degeneration by interaction with oxidized phospholipids. Proceedings of the National Academy of Sciences of the United States of America. 109: 13757-62. PMID 22875704 DOI: 10.1073/Pnas.1121309109 |
0.36 |
|
| 2012 |
Grob S, Luo J, Hughes G, Lee C, Zhou X, Lee J, Du H, Ferreyra H, Freeman WR, Kozak I, Zhang K. Genetic analysis of simultaneous geographic atrophy and choroidal neovascularization. Eye (London, England). 26: 1106-13. PMID 22699975 DOI: 10.1038/eye.2012.107 |
0.331 |
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| 2012 |
Zhang K, Zhang L, Weinreb RN. Ophthalmic drug discovery: novel targets and mechanisms for retinal diseases and glaucoma. Nature Reviews. Drug Discovery. 11: 541-59. PMID 22699774 DOI: 10.1038/Nrd3745 |
0.319 |
|
| 2012 |
Ulmer M, Li J, Yaspan BL, Ozel AB, Richards JE, Moroi SE, Hawthorne F, Budenz DL, Friedman DS, Gaasterland D, Haines J, Kang JH, Lee R, Lichter P, Liu Y, ... ... Zhang K, et al. Genome-wide analysis of central corneal thickness in primary open-angle glaucoma cases in the NEIGHBOR and GLAUGEN consortia. Investigative Ophthalmology & Visual Science. 53: 4468-74. PMID 22661486 DOI: 10.1167/Iovs.12-9784 |
0.549 |
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| 2012 |
Du H, Grob SR, Zhao L, Lee J, El-Sahn M, Hughes G, Luo J, Schaf K, Duan Y, Quach J, Wei X, Shaw P, Granet D, Zhang K. Myotonia congenita with strabismus in a large family with a mutation in the SCN4A gene. Eye. 26: 1039-1043. PMID 22653516 DOI: 10.1038/Eye.2012.80 |
0.34 |
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| 2012 |
Wiggs JL, Yaspan BL, Hauser MA, Kang JH, Allingham RR, Olson LM, Abdrabou W, Fan BJ, Wang DY, Brodeur W, Budenz DL, Caprioli J, Crenshaw A, Crooks K, Delbono E, ... ... Zhang K, et al. Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. Plos Genetics. 8: e1002654. PMID 22570617 DOI: 10.1371/Journal.Pgen.1002654 |
0.537 |
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| 2012 |
Zhao L, Grob S, Corey R, Krupa M, Luo J, Du H, Lee C, Hughes G, Lee J, Quach J, Zhu J, Shaw PX, Kozak I, Zhang K. A novel compound heterozygous mutation in the BEST1 gene causes autosomal recessive Best vitelliform macular dystrophy Eye. 26: 866-871. PMID 22422030 DOI: 10.1038/Eye.2012.27 |
0.322 |
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| 2012 |
Deng WT, Dinculescu A, Li Q, Boye SL, Li J, Gorbatyuk MS, Pang J, Chiodo VA, Matthes MT, Yasumura D, Liu L, Alkuraya FS, Zhang K, Vollrath D, LaVail MM, et al. Tyrosine-mutant AAV8 delivery of human MERTK provides long-term retinal preservation in RCS rats. Investigative Ophthalmology & Visual Science. 53: 1895-904. PMID 22408006 DOI: 10.1167/Iovs.11-8831 |
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| 2012 |
Tuo J, Grob S, Zhang K, Chan C. Genetics of Immunological and Inflammatory Components in Age-related Macular Degeneration Ocular Immunology and Inflammation. 20: 27-36. PMID 22324898 DOI: 10.3109/09273948.2011.628432 |
0.361 |
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| 2012 |
Sofat R, Casas JP, Webster AR, Bird AC, Mann SS, Yates JR, Moore AT, Sepp T, Cipriani V, Bunce C, Khan JC, Shahid H, Swaroop A, Abecasis G, Branham KE, ... ... Zhang K, et al. Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype. International Journal of Epidemiology. 41: 250-62. PMID 22253316 DOI: 10.1093/Ije/Dyr204 |
0.359 |
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| 2012 |
Harkewicz R, Du H, Tong Z, Alkuraya H, Bedell M, Sun W, Wang X, Hsu YH, Esteve-Rudd J, Hughes G, Su Z, Zhang M, Lopes VS, Molday RS, Williams DS, ... ... Zhang K, et al. Essential role of ELOVL4 protein in very long chain fatty acid synthesis and retinal function. The Journal of Biological Chemistry. 287: 11469-80. PMID 22199362 DOI: 10.1074/Jbc.M111.256073 |
0.337 |
|
| 2012 |
Grob S, Kozak I, Zhang K. Retinal pigment epithelial tear resembling retinal tear Eye. 26: 333-334. PMID 22079970 DOI: 10.1038/Eye.2011.278 |
0.327 |
|
| 2012 |
Zhang L, Lim SL, Du H, Zhang M, Kozak I, Hannum G, Wang X, Ouyang H, Hughes G, Zhao L, Zhu X, Lee C, Su Z, Zhou X, Shaw R, ... ... Zhang K, et al. High temperature requirement factor A1 (HTRA1) gene regulates angiogenesis through transforming growth factor-β family member growth differentiation factor 6. The Journal of Biological Chemistry. 287: 1520-6. PMID 22049084 DOI: 10.1074/Jbc.M111.275990 |
0.398 |
|
| 2011 |
Sommer JR, Estrada JL, Collins EB, Bedell M, Alexander CA, Yang Z, Hughes G, Mir B, Gilger BC, Grob S, Wei X, Piedrahita JA, Shaw PX, Petters RM, Zhang K. Production of ELOVL4 transgenic pigs: a large animal model for Stargardt-like macular degeneration. The British Journal of Ophthalmology. 95: 1749-54. PMID 21873315 DOI: 10.1136/Bjophthalmol-2011-300417 |
0.365 |
|
| 2011 |
Jones A, Kumar S, Zhang N, Tong Z, Yang JH, Watt C, Anderson J, Amrita, Fillerup H, McCloskey M, Luo L, Yang Z, Ambati B, Marc R, Oka C, ... Zhang K, et al. Increased expression of multifunctional serine protease, HTRA1, in retinal pigment epithelium induces polypoidal choroidal vasculopathy in mice. Proceedings of the National Academy of Sciences of the United States of America. 108: 14578-83. PMID 21844367 DOI: 10.1073/Pnas.1102853108 |
0.389 |
|
| 2011 |
Carbone MA, Chen Y, Hughes GA, Weinreb RN, Zabriskie NA, Zhang K, Anholt RR. Genes of the unfolded protein response pathway harbor risk alleles for primary open angle glaucoma. Plos One. 6: e20649. PMID 21655191 DOI: 10.1371/journal.pone.0020649 |
0.372 |
|
| 2011 |
Du H, Lim SL, Grob S, Zhang K. Induced pluripotent stem cell therapies for geographic atrophy of age-related macular degeneration. Seminars in Ophthalmology. 26: 216-24. PMID 21609235 DOI: 10.3109/08820538.2011.577498 |
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Chen Y, Zeng J, Zhao C, Wang K, Trood E, Buehler J, Weed M, Kasuga D, Bernstein PS, Hughes G, Fu V, Chin J, Lee C, Crocker M, Bedell M, ... ... Zhang K, et al. Assessing susceptibility to age-related macular degeneration with genetic markers and environmental factors. Archives of Ophthalmology (Chicago, Ill. : 1960). 129: 344-51. PMID 21402993 DOI: 10.1001/archophthalmol.2011.10 |
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Zhang K, Harada Y, Wei X, Shukla D, Rajendran A, Tawansy K, Bedell M, Lim S, Shaw PX, He X, Yang Z. An Essential Role of the Cysteine-rich Domain of FZD4 in Norrin/Wnt Signaling and Familial Exudative Vitreoretinopathy Journal of Biological Chemistry. 286: 10210-10215. PMID 21177847 DOI: 10.1074/Jbc.M110.194399 |
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Chen Y, Bedell M, Zhang K. Age-related Macular Degeneration: Genetic and Environmental Factors of Disease Molecular Interventions. 10: 271-281. PMID 21045241 DOI: 10.1124/Mi.10.5.4 |
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Molday RS, Zhang K. Defective lipid transport and biosynthesis in recessive and dominant Stargardt macular degeneration. Progress in Lipid Research. 49: 476-92. PMID 20633576 DOI: 10.1016/J.Plipres.2010.07.002 |
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Riazuddin SA, Iqbal M, Wang Y, Masuda T, Chen Y, Bowne S, Sullivan LS, Waseem NH, Bhattacharya S, Daiger SP, Zhang K, Khan SN, Riazuddin S, Hejtmancik JF, Sieving PA, et al. A splice-site mutation in a retina-specific exon of BBS8 causes nonsyndromic retinitis pigmentosa. American Journal of Human Genetics. 86: 805-12. PMID 20451172 DOI: 10.1016/J.Ajhg.2010.04.001 |
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Michaelides M, Gaillard MC, Escher P, Tiab L, Bedell M, Borruat FX, Barthelmes D, Carmona R, Zhang K, White E, McClements M, Robson AG, Holder GE, Bradshaw K, Hunt DM, et al. The PROM1 mutation p.R373C causes an autosomal dominant bull's eye maculopathy associated with rod, rod-cone, and macular dystrophy. Investigative Ophthalmology & Visual Science. 51: 4771-80. PMID 20393116 DOI: 10.1167/iovs.09-4561 |
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Neale BM, Fagerness J, Reynolds R, Sobrin L, Parker M, Raychaudhuri S, Tan PL, Oh EC, Merriam JE, Souied E, Bernstein PS, Li B, Frederick JM, Zhang K, Brantley MA, et al. Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). Proceedings of the National Academy of Sciences of the United States of America. 107: 7395-400. PMID 20385826 DOI: 10.1073/Pnas.0912019107 |
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Yang Z, Tong Z, Chen Y, Zeng J, Lu F, Sun X, Zhao C, Wang K, Davey L, Chen H, London N, Muramatsu D, Salasar F, Carmona R, Kasuga D, ... ... Zhang K, et al. Genetic and functional dissection of HTRA1 and LOC387715 in age-related macular degeneration. Plos Genetics. 6: e1000836. PMID 20140183 DOI: 10.1371/Journal.Pgen.1000836 |
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Kuny S, Gaillard F, Mema SC, Freund PR, Zhang K, MacDonald IM, Sparrow JR, Sauvé Y. Inner retina remodeling in a mouse model of stargardt-like macular dystrophy (STGD3). Investigative Ophthalmology & Visual Science. 51: 2248-2262. PMID 19933199 DOI: 10.1167/Iovs.09-4718 |
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Takeuchi T, Hayashi T, Bedell M, Zhang K, Yamada H, Tsuneoka H. A novel haplotype with the R345W mutation in the EFEMP1 gene associated with autosomal dominant drusen in a Japanese family. Investigative Ophthalmology & Visual Science. 51: 1643-1650. PMID 19850834 DOI: 10.1167/Iovs.09-4497 |
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Zhang K, Jiao X, Chen Y, Yang Z, Hennis A, Nemesure B, Hoh J, Hejtmancik JF. Reply to Liu et al.: Differential effects of chromosome 2p16.3 variants on glaucoma in African derived populations Proceedings of the National Academy of Sciences of the United States of America. 107. DOI: 10.1073/Pnas.1000204107 |
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Yamashita T, Liu J, Gao J, LeNoue S, Wang C, Kaminoh J, Bowne SJ, Sullivan LS, Daiger SP, Zhang K, Fitzgerald ME, Kefalov VJ, Zuo J. Essential and synergistic roles of RP1 and RP1L1 in rod photoreceptor axoneme and retinitis pigmentosa. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 9748-60. PMID 19657028 DOI: 10.1523/Jneurosci.5854-08.2009 |
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Yang Z, Chen Y, Lillo C, Chien J, Yu Z, Michaelides M, Klein M, Howes KA, Li Y, Kaminoh Y, Chen H, Zhao C, Al-Sheikh YT, Karan G, Corbeil D, ... ... Zhang K, et al. Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice (Journal of Clinical Investigation (2008) 118, (2908-2916) DOI: 10.1172/JCI35891) Journal of Clinical Investigation. 119: 1396. DOI: 10.1172/Jci35891C1 |
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Chen Y, Jiang D, Yu L, Katz B, Zhang K, Wan B, Sun X. CYP1B1 and MYOC mutations in 116 Chinese patients with primary congenital glaucoma. Archives of Ophthalmology. 126: 1443-7. PMID 18852424 DOI: 10.1001/archopht.126.10.1443 |
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Jiang L, Wheaton D, Bereta G, Zhang K, Palczewski K, Birch DG, Baehr W. A novel GCAP1(N104K) mutation in EF-hand 3 (EF3) linked to autosomal dominant cone dystrophy. Vision Research. 48: 2425-32. PMID 18706439 DOI: 10.1016/J.Visres.2008.07.016 |
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Tonna S, Dandapani SV, Uscinski A, Appel GB, Schlöndorff JS, Zhang K, Denker BM, Pollak MR. Functional genetic variation in aminopeptidase A (ENPEP): lack of clear association with focal and segmental glomerulosclerosis (FSGS). Gene. 410: 44-52. PMID 18206321 DOI: 10.1016/J.Gene.2007.11.014 |
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Li C, Kosmorsky G, Zhang K, Katz BJ, Ge J, Traboulsi EI. Optic atrophy and sensorineural hearing loss in a family caused by an R445H OPA1 mutation. American Journal of Medical Genetics. Part A. 208-11. PMID 16158427 DOI: 10.1002/ajmg.a.30794 |
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Kaiser PK, Brown DM, Zhang K, Hudson HL, Holz FG, Shapiro H, Schneider S, Acharya NR. Ranibizumab for predominantly classic neovascular age-related macular degeneration: subgroup analysis of first-year ANCHOR results. American Journal of Ophthalmology. 144: 850-857. PMID 17949673 DOI: 10.1016/J.Ajo.2007.08.012 |
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Lu F, Hu J, Zhao P, Lin Y, Yang Y, Liu X, Fan Y, Chen B, Liao S, Du Q, Lei C, Cameron DJ, Zhang K, Yang Z. HTRA1 variant increases risk to neovascular age-related macular degeneration in Chinese population. Vision Research. 47: 3120-3. PMID 17904186 DOI: 10.1016/j.visres.2007.08.010 |
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Fu L, Garland D, Yang Z, Shukla D, Rajendran A, Pearson E, Stone EM, Zhang K, Pierce EA. The R345W mutation in EFEMP1 is pathogenic and causes AMD-like deposits in mice. Human Molecular Genetics. 16: 2411-22. PMID 17666404 DOI: 10.1093/Hmg/Ddm198 |
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Tuo J, Bojanowski CM, Zhou M, Shen D, Ross RJ, Rosenberg KI, Cameron DJ, Yin C, Kowalak JA, Zhuang Z, Zhang K, Chan CC. Murine ccl2/cx3cr1 deficiency results in retinal lesions mimicking human age-related macular degeneration. Investigative Ophthalmology & Visual Science. 48: 3827-36. PMID 17652758 DOI: 10.1167/iovs.07-0051 |
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Alvarez BV, Vithana EN, Yang Z, Koh AH, Yeung K, Yong V, Shandro HJ, Chen Y, Kolatkar P, Palasingam P, Zhang K, Aung T, Casey JR. Identification and characterization of a novel mutation in the carbonic anhydrase IV gene that causes retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 48: 3459-68. PMID 17652713 DOI: 10.1167/iovs.06-1515 |
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Cameron DJ, Tong Z, Yang Z, Kaminoh J, Kamiyah S, Chen H, Zeng J, Chen Y, Luo L, Zhang K. Essential role of Elovl4 in very long chain fatty acid synthesis, skin permeability barrier function, and neonatal survival. International Journal of Biological Sciences. 3: 111-9. PMID 17304340 |
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Wang C, Hu J, Bernstein PS, Teske MP, Payne M, Yang Z, Li C, Adams D, Baird JH, Zhang K. Intravitreal injection of triamcinolone acetonide for macular edema due to retinitis pigmentosa and other retinal diseases. Advances in Experimental Medicine and Biology. 572: 309-14. PMID 17249589 DOI: 10.1007/0-387-32442-9_43 |
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Moshfeghi DM, Yang Z, Faulkner ND, Karan G, Thirumalaichary S, Pearson E, Zhao Y, Tsai T, Zhang K. Choroidal neovascularization in patients with adult-onset foveomacular dystrophy caused by mutations in the RDS/peripherin gene. Advances in Experimental Medicine and Biology. 572: 35-40. PMID 17249552 DOI: 10.1007/0-387-32442-9_6 |
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Pauer GJT, Xi Q, Zhang K, Traboulsi EI, Hagstrom SA. Mutation screen of the membrane-type frizzled-related protein (MFRP) gene in patients with inherited retinal degenerations. Ophthalmic Genetics. 26: 157-161. PMID 16352475 DOI: 10.1080/13816810500374425 |
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