| Year |
Citation |
Score |
| 2023 |
Boese EA, Drack AV, Roos BR, Alward WLM, Tollefson MR, Schnieders MJ, Scheetz TE, Boldt HC, Stone EM, Fingert JH. GJA3 Genetic Variation and Autosomal Dominant Congenital Cataracts and Glaucoma Following Cataract Surgery. Jama Ophthalmology. PMID 37589989 DOI: 10.1001/jamaophthalmol.2023.3535 |
0.462 |
|
| 2023 |
Fox AR, Fingert JH. Familial normal tension glaucoma genetics. Progress in Retinal and Eye Research. 96: 101191. PMID 37353142 DOI: 10.1016/j.preteyeres.2023.101191 |
0.391 |
|
| 2023 |
Boese EA, Alward WLM, Kwon YH, Roos BR, Stone EM, Scheetz TE, Fingert JH. Thrombospondin Mutations and Primary Congenital Glaucoma Patients in a United States Population. Journal of Glaucoma. PMID 37327471 DOI: 10.1097/IJG.0000000000002254 |
0.454 |
|
| 2023 |
Tejan-Kamara AZ, Boese EA, Pouw A, Sears NC, Roos BR, Stone EM, Scheetz TE, Fingert JH. Mutations in EFEMP1 in patients with juvenile open-angle glaucoma (JOAG). Ophthalmology. Glaucoma. PMID 37224920 DOI: 10.1016/j.ogla.2023.05.006 |
0.526 |
|
| 2022 |
Quigley HA, Stone EM, Fingert JH. Familial Glaucoma-A Pedigree Revisited With Genetic Testing After 70 Years. Jama Ophthalmology. PMID 35389460 DOI: 10.1001/jamaophthalmol.2022.0556 |
0.419 |
|
| 2021 |
Sohn EH, Han IC, Roos BR, Faga B, Luse MA, Binkley EM, Boldt HC, Folk JC, Russell SR, Mullins RF, Fingert JH, Stone EM, Scheetz TE. Genetic Association between and Choroidal Neovascularization in Age-Related Macular Degeneration. Ophthalmology Science. 1: 100002. PMID 37672224 DOI: 10.1016/j.xops.2020.100002 |
0.453 |
|
| 2021 |
Han IC, Burnight ER, Kaalberg EE, Boyce TM, Stone EM, Fingert JH, Mullins RF, Tucker BA, Wiley LA. Chimeric Helper-Dependent Adenoviruses Transduce Retinal Ganglion Cells and Müller Cells in Human Retinal Explants. Journal of Ocular Pharmacology and Therapeutics : the Official Journal of the Association For Ocular Pharmacology and Therapeutics. PMID 34597181 DOI: 10.1089/jop.2021.0057 |
0.432 |
|
| 2021 |
van der Heide C, Goar W, Meyer KJ, Alward WLM, Boese EA, Sears NC, Roos BR, Kwon YH, DeLuca AP, Siggs OM, Gonzaga-Jauregui C, Sheffield VC, Wang K, Stone EM, Mullins RF, ... ... Fingert JH, et al. Exome-based investigation of the genetic basis of human pigmentary glaucoma. Bmc Genomics. 22: 477. PMID 34174832 DOI: 10.1186/s12864-021-07782-0 |
0.485 |
|
| 2020 |
Hagedorn J, Avdic A, Schnieders MJ, Roos BR, Kwon YH, Drack AV, Boese EA, Fingert JH. Nanophthalmos patient with a THR518MET mutation in MYRF, a case report. Bmc Ophthalmology. 20: 388. PMID 33004036 DOI: 10.1186/s12886-020-01659-8 |
0.326 |
|
| 2020 |
Sears NC, Darbro BW, Alward WLM, Fingert JH. Progressive optic disc cupping over 20 years in a patient with -associated glaucoma. Ophthalmology. Glaucoma. 3: 167-168. PMID 32632409 DOI: 10.1016/J.Ogla.2019.11.003 |
0.319 |
|
| 2020 |
Quist TS, Johnson CA, Robin AL, Fingert JH. Long-Term Follow-Up of Normal Tension Glaucoma Patients With TBK1 Gene Mutations in One Large Pedigree. American Journal of Ophthalmology. PMID 31987900 DOI: 10.1016/J.Ajo.2020.01.017 |
0.431 |
|
| 2019 |
Hauser MA, Allingham RR, Aung T, Van Der Heide CJ, Taylor KD, Rotter JI, Wang SJ, Bonnemaijer PWM, Williams SE, Abdullahi SM, Abu-Amero KK, Anderson MG, Akafo S, Alhassan MB, ... ... Fingert JH, et al. Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry. Jama. 322: 1682-1691. PMID 31688885 DOI: 10.1001/Jama.2019.16161 |
0.347 |
|
| 2019 |
Fan BJ, Bailey JC, Igo RP, Kang JH, Boumenna T, Brilliant MH, Budenz DL, Fingert JH, Gaasterland T, Gaasterland D, Hauser MA, Kraft P, Lee RK, Lichter PR, Liu Y, et al. Association of a Primary Open-Angle Glaucoma Genetic Risk Score With Earlier Age at Diagnosis. Jama Ophthalmology. PMID 31436842 DOI: 10.1001/Jamaophthalmol.2019.3109 |
0.37 |
|
| 2019 |
Boese EA, Tollefson MR, Schnieders MJ, Darbro BW, Alward WLM, Fingert JH. Novel intragenic deletion in a pedigree with aniridia, morbid obesity, and diabetes. Current Eye Research. PMID 31361967 DOI: 10.1080/02713683.2019.1649704 |
0.355 |
|
| 2019 |
Sears NC, Boese EA, Miller MA, Fingert JH. Mendelian genes in primary open angle glaucoma. Experimental Eye Research. 107702. PMID 31238079 DOI: 10.1016/J.Exer.2019.107702 |
0.484 |
|
| 2019 |
Hwang ES, Morgan DJ, Pennington KL, Owen LA, Fingert JH, Bernstein PS, DeAngelis MM. Progressive optic nerve changes in cavitary optic disc anomaly: integration of copy number alteration and cis-expression quantitative trait loci to assess disease etiology. Bmc Medical Genetics. 20: 63. PMID 31029096 DOI: 10.1186/S12881-019-0800-4 |
0.329 |
|
| 2019 |
Alward WLM, van der Heide C, Khanna CL, Roos BR, Sivaprasad S, Kam J, Ritch R, Lotery A, Igo RP, Cooke Bailey JN, Stone EM, Scheetz TE, Kwon YH, Pasquale LR, Wiggs JL, ... Fingert JH, et al. Myocilin Mutations in Patients With Normal-Tension Glaucoma. Jama Ophthalmology. PMID 30816940 DOI: 10.1001/Jamaophthalmol.2019.0005 |
0.584 |
|
| 2018 |
van der Heide CJ, Alward WLM, Flamme-Wiese M, Riker M, Syed NA, Anderson MG, Carter K, Kuehn MH, Stone EM, Mullins RF, Fingert JH. Histochemical Analysis of Glaucoma Caused by a Myocilin Mutation in a Human Donor Eye. Ophthalmology. Glaucoma. 1: 132-138. PMID 30906929 DOI: 10.1016/J.Ogla.2018.08.004 |
0.571 |
|
| 2018 |
Fingert JH. Penetrance of Myocilin Mutations-Who Gets Glaucoma? Jama Ophthalmology. PMID 30267050 DOI: 10.1001/Jamaophthalmol.2018.4470 |
0.386 |
|
| 2018 |
Burnight ER, Giacalone JC, Cooke JA, Thompson JR, Bohrer LR, Chirco KR, Drack AV, Fingert JH, Worthington KS, Wiley LA, Mullins RF, Stone EM, Tucker BA. CRISPR-Cas9 genome engineering: Treating inherited retinal degeneration. Progress in Retinal and Eye Research. PMID 29578069 DOI: 10.1016/J.Preteyeres.2018.03.003 |
0.564 |
|
| 2018 |
Anderson MG, Meyer KJ, Hedberg-Buenz A, Fingert JH. Update on Animal Models of Exfoliation Syndrome. Journal of Glaucoma. PMID 29419647 DOI: 10.1097/Ijg.0000000000000911 |
0.327 |
|
| 2018 |
Bailey JNC, Gharahkhani P, Kang JH, Butkiewicz M, Sullivan DA, Weinreb RN, Aschard H, Allingham RR, Ashley-Koch A, Lee RK, Moroi SE, Brilliant MH, Wollstein G, Schuman JS, Fingert JH, et al. Testosterone Pathway Genetic Polymorphisms in Relation to Primary Open-Angle Glaucoma: An Analysis in Two Large Datasets. Investigative Ophthalmology & Visual Science. 59: 629-636. PMID 29392307 DOI: 10.1167/Iovs.17-22708 |
0.371 |
|
| 2018 |
Schnieders MJ, Goar W, Griess M, Roos BR, Scheetz TE, Stone EM, Fingert JH. A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigree. Eye (London, England). PMID 29350691 DOI: 10.1038/Eye.2017.303 |
0.554 |
|
| 2017 |
Janson BJ, Alward WL, Kwon YH, Bettis DI, Fingert JH, Provencher LM, Goins KM, Wagoner MD, Greiner MA. Glaucoma-associated corneal endothelial cell damage: A review. Survey of Ophthalmology. PMID 29146208 DOI: 10.1016/J.Survophthal.2017.11.002 |
0.334 |
|
| 2017 |
DeLuca AP, Wallace LMA, Liebmann J, Ritch R, Kawase K, Kwon YH, Robin AL, Stone EM, Scheetz TE, Fingert JH. Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients. Journal of Glaucoma. PMID 28984711 DOI: 10.1097/Ijg.0000000000000792 |
0.535 |
|
| 2017 |
Jain A, Zode G, Kasetti RB, Ran FA, Yan W, Sharma TP, Bugge K, Searby CC, Fingert JH, Zhang F, Clark AF, Sheffield VC. CRISPR-Cas9-based treatment of myocilin-associated glaucoma. Proceedings of the National Academy of Sciences of the United States of America. PMID 28973933 DOI: 10.1073/Pnas.1706193114 |
0.391 |
|
| 2017 |
Chirco KR, Lewis CJ, Scheetz TE, Johnston RM, Tucker BA, Stone EM, Fingert JH, Mullins RF. Evaluation of sFLT1 protein levels in human eyes with the FLT1 rs9943922 polymorphism. Ophthalmic Genetics. 1-5. PMID 28949775 DOI: 10.1080/13816810.2017.1369550 |
0.536 |
|
| 2017 |
Aschard H, Kang JH, Iglesias AI, Hysi P, Cooke Bailey JN, Khawaja AP, Allingham RR, Ashley-Koch A, Lee RK, Moroi SE, Brilliant MH, Wollstein G, Schuman JS, Fingert JH, Budenz DL, et al. Genetic correlations between intraocular pressure, blood pressure and primary open-angle glaucoma: a multi-cohort analysis. European Journal of Human Genetics : Ejhg. PMID 28853718 DOI: 10.1038/Ejhg.2017.136 |
0.354 |
|
| 2017 |
Aung T, Ozaki M, Lee MC, Schlötzer-Schrehardt U, Thorleifsson G, Mizoguchi T, Igo RP, Haripriya A, Williams SE, Astakhov YS, Orr AC, Burdon KP, Nakano S, Mori K, Abu-Amero K, ... ... Fingert JH, et al. Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci. Nature Genetics. PMID 28553957 DOI: 10.1038/Ng.3875 |
0.401 |
|
| 2017 |
Lewis C, Hedberg-Buenz A, DeLuca AP, Stone EM, Alward WLM, Fingert JH. Primary Congenital and Developmental Glaucomas. Human Molecular Genetics. PMID 28549150 DOI: 10.1093/Hmg/Ddx205 |
0.606 |
|
| 2017 |
Greiner MA, Terveen DC, Vislisel JM, Roos BR, Fingert JH. Assessment of a three-generation pedigree with Fuchs endothelial corneal dystrophy with anticipation for expansion of the triplet repeat in the TCF4 gene. Eye (London, England). 31: 1250-1252. PMID 28387761 DOI: 10.1038/Eye.2017.60 |
0.339 |
|
| 2017 |
Afshari NA, Igo RP, Morris NJ, Stambolian D, Sharma S, Pulagam VL, Dunn S, Stamler JF, Truitt BJ, Rimmler J, Kuot A, Croasdale CR, Qin X, Burdon KP, Riazuddin SA, ... ... Fingert JH, et al. Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy. Nature Communications. 8: 14898. PMID 28358029 DOI: 10.1038/Ncomms14898 |
0.361 |
|
| 2016 |
Fingert JH, Miller K, Hedberg-Buenz A, Roos BR, Lewis CJ, Mullins RF, Anderson MG. Transgenic TBK1 mice have features of normal tension glaucoma. Human Molecular Genetics. PMID 28025332 DOI: 10.1093/Hmg/Ddw372 |
0.333 |
|
| 2016 |
Miller MA, Fingert JH, Bettis DI. Genetics and genetic testing for glaucoma. Current Opinion in Ophthalmology. PMID 27898466 DOI: 10.1097/Icu.0000000000000344 |
0.345 |
|
| 2016 |
Pasquale LR, Aschard H, Kang JH, Bailey JN, Lindström S, Chasman DI, Christen WG, Allingham RR, Ashley-Koch A, Lee RK, Moroi SE, Brilliant MH, Wollstein G, Schuman JS, Fingert J, et al. Age at natural menopause genetic risk score in relation to age at natural menopause and primary open-angle glaucoma in a US-based sample. Menopause (New York, N.Y.). PMID 27760082 DOI: 10.1097/Gme.0000000000000741 |
0.342 |
|
| 2016 |
Scheetz TE, Faga B, Ortega L, Roos BR, Gordon MO, Kass MA, Wang K, Fingert JH. Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study. Ophthalmology. PMID 27707548 DOI: 10.1016/J.Ophtha.2016.08.036 |
0.351 |
|
| 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, 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 |
0.353 |
|
| 2016 |
Kader MA, Namburi P, Ramugade S, Ramakrishnan R, Krishnadas SR, Roos BR, Periasamy S, Robin AL, Fingert JH. Clinical and genetic characterization of a large primary open angle glaucoma pedigree. Ophthalmic Genetics. 1-4. PMID 27355837 DOI: 10.1080/13816810.2016.1193883 |
0.354 |
|
| 2016 |
Scheetz TE, Roos BR, Solivan-Timpe F, Miller K, DeLuca AP, Stone EM, Kwon YH, Alward WL, Wang K, Fingert JH. SQSTM1 Mutations and Glaucoma. Plos One. 11: e0156001. PMID 27275741 DOI: 10.1371/Journal.Pone.0156001 |
0.578 |
|
| 2016 |
Khor CC, Do T, Jia H, Nakano M, George R, Abu-Amero K, Duvesh R, Chen LJ, Li Z, Nongpiur ME, Perera SA, Qiao C, Wong HT, Sakai H, Barbosa de Melo M, ... ... Fingert JH, et al. Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma. Nature Genetics. PMID 27064256 DOI: 10.1038/Ng.3540 |
0.339 |
|
| 2016 |
Risma JM, Tehrani S, Wang K, Fingert JH, Alward WL, Kwon YH. The Utility of Diaton Tonometer Measurements in Patients With Ocular Hypertension, Glaucoma, and Glaucoma Tube Shunts: A Preliminary Study for its Potential Use in Keratoprosthesis Patients. Journal of Glaucoma. PMID 26950582 DOI: 10.1097/Ijg.0000000000000394 |
0.313 |
|
| 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, ... ... Fingert JH, 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 |
0.374 |
|
| 2015 |
Small KW, DeLuca AP, Whitmore SS, Rosenberg T, Silva-Garcia R, Udar N, Puech B, Garcia CA, Rice TA, Fishman GA, Héon E, Folk JC, Streb LM, Haas CM, Wiley LA, ... ... Fingert JH, et al. North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13. Ophthalmology. PMID 26507665 DOI: 10.1016/J.Ophtha.2015.10.006 |
0.553 |
|
| 2015 |
Khorram D, Choi M, Roos BR, Stone EM, Kopel T, Allen R, Alward WL, Scheetz TE, Fingert JH. Novel TMEM98 mutations in pedigrees with autosomal dominant nanophthalmos. Molecular Vision. 21: 1017-23. PMID 26392740 |
0.575 |
|
| 2015 |
Aung T, Ozaki M, Mizoguchi T, Allingham RR, Li Z, Haripriya A, Nakano S, Uebe S, Harder JM, Chan AS, Lee MC, Burdon KP, Astakhov YS, Abu-Amero KK, Zenteno JC, ... ... Fingert JH, et al. A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome. Nature Genetics. 47: 387-92. PMID 25706626 DOI: 10.1038/Ng.3226 |
0.376 |
|
| 2015 |
Hazlewood RJ, Roos BR, Solivan-Timpe F, Honkanen RA, Jampol LM, Gieser SC, Meyer KJ, Mullins RF, Kuehn MH, Scheetz TE, Kwon YH, Alward WL, Stone EM, Fingert JH. Heterozygous triplication of upstream regulatory sequences leads to dysregulation of matrix metalloproteinase 19 in patients with cavitary optic disc anomaly. Human Mutation. 36: 369-78. PMID 25581579 DOI: 10.1002/Humu.22754 |
0.545 |
|
| 2015 |
Awadalla MS, Fingert JH, Roos BE, Chen S, Holmes R, Graham SL, Chehade M, Galanopolous A, Ridge B, Souzeau E, Zhou T, Siggs OM, Hewitt AW, Mackey DA, Burdon KP, et al. Copy number variations of TBK1 in Australian patients with primary open-angle glaucoma. American Journal of Ophthalmology. 159: 124-30.e1. PMID 25284765 DOI: 10.1016/J.Ajo.2014.09.044 |
0.377 |
|
| 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, 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 |
0.388 |
|
| 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, 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 |
0.334 |
|
| 2014 |
Tucker BA, Solivan-Timpe F, Roos BR, Anfinson KR, Robin AL, Wiley LA, Mullins RF, Fingert JH. Duplication of TBK1 Stimulates Autophagy in iPSC-derived Retinal Cells from a Patient with Normal Tension Glaucoma. Journal of Stem Cell Research & Therapy. 3: 161. PMID 24883232 DOI: 10.4172/2157-7633.1000161 |
0.371 |
|
| 2014 |
Ritch R, Darbro B, Menon G, Khanna CL, Solivan-Timpe F, Roos BR, Sarfarzi M, Kawase K, Yamamoto T, Robin AL, Lotery AJ, Fingert JH. TBK1 gene duplication and normal-tension glaucoma. Jama Ophthalmology. 132: 544-8. PMID 24699864 DOI: 10.1001/Jamaophthalmol.2014.104 |
0.441 |
|
| 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, ... ... Fingert J, 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 |
0.323 |
|
| 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, ... ... Fingert J, 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 |
0.363 |
|
| 2014 |
Fingert JH, Darbro BW, Qian Q, Van Rheeden R, Miller K, Riker M, Solivan-Timpe F, Roos BR, Robin AL, Mullins RF. TBK1 and flanking genes in human retina. Ophthalmic Genetics. 35: 35-40. PMID 23421332 DOI: 10.3109/13816810.2013.768674 |
0.358 |
|
| 2014 |
Christopher M, Tang L, Fingert JH, Scheetz TE, Abramoff MD. Automated discovery of structural features of the optic nerve head on the basis of image and genetic data Progress in Biomedical Optics and Imaging - Proceedings of Spie. 9035. DOI: 10.1117/12.2043798 |
0.337 |
|
| 2013 |
Scheetz TE, Fingert JH, Wang K, Kuehn MH, Knudtson KL, Alward WL, Boldt HC, Russell SR, Folk JC, Casavant TL, Braun TA, Clark AF, Stone EM, Sheffield VC. A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel Loci. Plos One. 8: e58657. PMID 23536807 DOI: 10.1371/Journal.Pone.0058657 |
0.566 |
|
| 2013 |
Gupta V, Srivastava RM, Rao A, Mittal M, Fingert J. Clinical correlates to the goniodysgensis among juvenile-onset primary open-angle glaucoma patients. Graefe's Archive For Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fã¼R Klinische Und Experimentelle Ophthalmologie. 251: 1571-6. PMID 23358655 DOI: 10.1007/S00417-013-2262-2 |
0.318 |
|
| 2013 |
Seo S, Solivan-Timpe F, Roos BR, Robin AL, Stone EM, Kwon YH, Alward WL, Fingert JH. Identification of proteins that interact with TANK binding kinase 1 and testing for mutations associated with glaucoma. Current Eye Research. 38: 310-5. PMID 23286385 DOI: 10.3109/02713683.2012.754047 |
0.572 |
|
| 2013 |
Stamler JF, Roos BR, Wagoner MD, Goins KM, Kitzmann AS, Riley JB, Stone EM, Fingert JH. Confirmation of the association between the TCF4 risk allele and Fuchs endothelial corneal dystrophy in patients from the Midwestern United States. Ophthalmic Genetics. 34: 32-4. PMID 22998502 DOI: 10.3109/13816810.2012.726396 |
0.511 |
|
| 2013 |
Fingert JH, Burden JH, Wang K, Kwon YH, Alward WL, Anderson MG. Circumferential iris transillumination defects in exfoliation syndrome. Journal of Glaucoma. 22: 555-8. PMID 22525123 DOI: 10.1097/Ijg.0B013E318255Da16 |
0.324 |
|
| 2012 |
Mahajan VB, Skeie JM, Bassuk AG, Fingert JH, Braun TA, Daggett HT, Folk JC, Sheffield VC, Stone EM. Calpain-5 mutations cause autoimmune uveitis, retinal neovascularization, and photoreceptor degeneration. Plos Genetics. 8: e1003001. PMID 23055945 DOI: 10.1371/Journal.Pgen.1003001 |
0.576 |
|
| 2012 |
Fingert JH, Roos BR, Solivan-Timpe F, Miller KA, Oetting TA, Wang K, Kwon YH, Scheetz TE, Stone EM, Alward WL. Analysis of ASB10 variants in open angle glaucoma. Human Molecular Genetics. 21: 4543-8. PMID 22798626 DOI: 10.1093/Hmg/Dds288 |
0.583 |
|
| 2012 |
Mao M, Solivan-Timpe F, Roos BR, Mullins RF, Oetting TA, Kwon YH, Brzeskiewicz PM, Stone EM, Alward WL, Anderson MG, Fingert JH. Localization of SH3PXD2B in human eyes and detection of rare variants in patients with anterior segment diseases and glaucoma. Molecular Vision. 18: 705-13. PMID 22509100 |
0.514 |
|
| 2012 |
Kawase K, Allingham RR, Meguro A, Mizuki N, Roos B, Solivan-Timpe FM, Robin AL, Ritch R, Fingert JH. Confirmation of TBK1 duplication in normal tension glaucoma. Experimental Eye Research. 96: 178-80. PMID 22306015 DOI: 10.1016/J.Exer.2011.12.021 |
0.406 |
|
| 2011 |
Fingert JH. Primary open-angle glaucoma genes. Eye (London, England). 25: 587-95. PMID 21562585 DOI: 10.1038/Eye.2011.97 |
0.485 |
|
| 2011 |
Mullins RF, Skeie JM, Folk JC, Solivan-Timpe FM, Oetting TA, Huang J, Wang K, Stone EM, Fingert JH. Evaluation of variants in the selectin genes in age-related macular degeneration. Bmc Medical Genetics. 12: 58. PMID 21521525 DOI: 10.1186/1471-2350-12-58 |
0.584 |
|
| 2011 |
Fingert JH, Robin AL, Stone JL, Roos BR, Davis LK, Scheetz TE, Bennett SR, Wassink TH, Kwon YH, Alward WL, Mullins RF, Sheffield VC, Stone EM. Copy number variations on chromosome 12q14 in patients with normal tension glaucoma. Human Molecular Genetics. 20: 2482-94. PMID 21447600 DOI: 10.1093/Hmg/Ddr123 |
0.568 |
|
| 2011 |
Kuehn MH, Wang K, Roos B, Stone EM, Kwon YH, Alward WL, Mullins RF, Fingert JH. Chromosome 7q31 POAG locus: ocular expression of caveolins and lack of association with POAG in a US cohort. Molecular Vision. 17: 430-5. PMID 21321670 |
0.501 |
|
| 2011 |
Davis LK, Meyer KJ, Schindler EI, Beck JS, Rudd DS, Grundstad AJ, Scheetz TE, Braun TA, Fingert JH, Alward WL, Kwon YH, Folk JC, Russell SR, Wassink TH, Sheffield VC, et al. Copy number variations and primary open-angle glaucoma. Investigative Ophthalmology & Visual Science. 52: 7122-33. PMID 21310917 DOI: 10.1167/Iovs.10-5606 |
0.769 |
|
| 2011 |
Meyer KJ, Davis LK, Schindler EI, Beck JS, Rudd DS, Grundstad AJ, Scheetz TE, Braun TA, Fingert JH, Alward WL, Kwon YH, Folk JC, Russell SR, Wassink TH, Stone EM, et al. Genome-wide analysis of copy number variants in age-related macular degeneration. Human Genetics. 129: 91-100. PMID 20981449 DOI: 10.1007/S00439-010-0904-6 |
0.775 |
|
| 2011 |
Trantow CM, Cuffy TL, Fingert JH, Kuehn MH, Anderson MG. Microarray analysis of iris gene expression in mice with mutations influencing pigmentation. Investigative Ophthalmology & Visual Science. 52: 237-48. PMID 20739468 DOI: 10.1167/Iovs.10-5479 |
0.385 |
|
| 2010 |
Rosenberg T, Roos B, Johnsen T, Bech N, Scheetz TE, Larsen M, Stone EM, Fingert JH. Clinical and genetic characterization of a Danish family with North Carolina macular dystrophy. Molecular Vision. 16: 2659-68. PMID 21179233 |
0.508 |
|
| 2010 |
Sundaresan P, Kumar SM, Thompson S, Fingert JH. Reduced frequency of known mutations in a cohort of LHON patients from India. Ophthalmic Genetics. 31: 196-9. PMID 20809775 DOI: 10.3109/13816810.2010.510818 |
0.559 |
|
| 2010 |
Tang L, Scheetz TE, Mackey DA, Hewitt AW, Fingert JH, Kwon YH, Quellec G, Reinhardt JM, Abrà moff MD. Automated quantification of inherited phenotypes from color images: a twin study of the variability of optic nerve head shape. Investigative Ophthalmology & Visual Science. 51: 5870-7. PMID 20505201 DOI: 10.1167/Iovs.10-5527 |
0.356 |
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| 2010 |
Skeie JM, Fingert JH, Russell SR, Stone EM, Mullins RF. Complement component C5a activates ICAM-1 expression on human choroidal endothelial cells. Investigative Ophthalmology & Visual Science. 51: 5336-42. PMID 20484595 DOI: 10.1167/Iovs.10-5322 |
0.459 |
|
| 2010 |
Fingert JH, Roos B, Eyestone ME, Pham JD, Mellot ML, Stone E. Novel intragenic FRMD7 deletion in a pedigree with congenital X-linked nystagmus. Ophthalmic Genetics. 31: 77-80. PMID 20450309 DOI: 10.3109/13816810903584989 |
0.567 |
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| 2009 |
Sundaresan P, Vijayalakshmi P, Thompson S, Ko AC, Fingert JH, Stone EM. Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in southern India. Molecular Vision. 15: 1781-7. PMID 19753312 |
0.641 |
|
| 2009 |
Kwon YH, Fingert JH, Kuehn MH, Alward WL. Primary open-angle glaucoma. The New England Journal of Medicine. 360: 1113-24. PMID 19279343 DOI: 10.1056/Nejmra0804630 |
0.355 |
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| 2009 |
Trantow CM, Mao M, Petersen GE, Alward EM, Alward WL, Fingert JH, Anderson MG. Lyst mutation in mice recapitulates iris defects of human exfoliation syndrome. Investigative Ophthalmology & Visual Science. 50: 1205-14. PMID 19029039 DOI: 10.1167/Iovs.08-2791 |
0.431 |
|
| 2008 |
Fingert JH, Oh K, Chung M, Scheetz TE, Andorf JL, Johnson RM, Sheffield VC, Stone EM. Association of a novel mutation in the retinol dehydrogenase 12 (RDH12) gene with autosomal dominant retinitis pigmentosa. Archives of Ophthalmology (Chicago, Ill. : 1960). 126: 1301-7. PMID 18779497 DOI: 10.1001/Archopht.126.9.1301 |
0.627 |
|
| 2008 |
Hayreh SS, Fingert JH, Stone E, Jacobson DM. Familial non-arteritic anterior ischemic optic neuropathy. Graefe's Archive For Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv FüR Klinische Und Experimentelle Ophthalmologie. 246: 1295-305. PMID 18587597 DOI: 10.1007/S00417-008-0853-0 |
0.498 |
|
| 2008 |
Shah SS, Al-Rajhi A, Brandt JD, Mannis MJ, Roos B, Sheffield VC, Syed NA, Stone EM, Fingert JH. Mutation in the SLC4A11 gene associated with autosomal recessive congenital hereditary endothelial dystrophy in a large Saudi family. Ophthalmic Genetics. 29: 41-5. PMID 18363173 DOI: 10.1080/13816810701850033 |
0.593 |
|
| 2008 |
Shankar SP, Fingert JH, Carelli V, Valentino ML, King TM, Daiger SP, Salomao SR, Berezovsky A, Belfort R, Braun TA, Sheffield VC, Sadun AA, Stone EM. Evidence for a novel x-linked modifier locus for leber hereditary optic neuropathy. Ophthalmic Genetics. 29: 17-24. PMID 18363168 DOI: 10.1080/13816810701867607 |
0.722 |
|
| 2008 |
Wang WH, McNatt LG, Pang IH, Millar JC, Hellberg PE, Hellberg MH, Steely HT, Rubin JS, Fingert JH, Sheffield VC, Stone EM, Clark AF. Increased expression of the WNT antagonist sFRP-1 in glaucoma elevates intraocular pressure. The Journal of Clinical Investigation. 118: 1056-64. PMID 18274669 DOI: 10.1172/Jci33871 |
0.495 |
|
| 2008 |
Wang WH, McNatt LG, Pang IH, Hellberg PE, Fingert JH, McCartney MD, Clark AF. Increased expression of serum amyloid A in glaucoma and its effect on intraocular pressure. Investigative Ophthalmology & Visual Science. 49: 1916-23. PMID 18223246 DOI: 10.1167/Iovs.07-1104 |
0.349 |
|
| 2007 |
Fingert JH, Alward WL, Kwon YH, Wang K, Streb LM, Sheffield VC, Stone EM. LOXL1 mutations are associated with exfoliation syndrome in patients from the midwestern United States. American Journal of Ophthalmology. 144: 974-975. PMID 18036875 DOI: 10.1016/J.Ajo.2007.09.034 |
0.515 |
|
| 2007 |
Fingert JH, Grassi MA, Janutka JC, East JS, Howard JG, Sheffield VC, Jacobson DM, Hayreh SS, Stone EM. Mitochondrial variant G4132A is associated with familial non-arteritic anterior ischemic optic neuropathy in one large pedigree. Ophthalmic Genetics. 28: 1-7. PMID 17454741 DOI: 10.1080/13816810701199399 |
0.532 |
|
| 2007 |
Fingert JH, Honkanen RA, Shankar SP, Affatigato LM, Ehlinger MA, Moore MD, Jampol LM, Sheffield VC, Stone EM, Alward WL. Familial cavitary optic disk anomalies: identification of a novel genetic locus. American Journal of Ophthalmology. 143: 795-800. PMID 17368552 DOI: 10.1016/J.Ajo.2007.01.042 |
0.719 |
|
| 2007 |
Honkanen RA, Jampol LM, Fingert JH, Moore MD, Taylor CM, Stone EM, Alward WL. Familial cavitary optic disk anomalies: clinical features of a large family with examples of progressive optic nerve head cupping. American Journal of Ophthalmology. 143: 788-794. PMID 17362864 DOI: 10.1016/J.Ajo.2007.01.029 |
0.56 |
|
| 2007 |
Fingert JH, Alward WL, Kwon YH, Shankar SP, Andorf JL, Mackey DA, Sheffield VC, Stone EM. No association between variations in the WDR36 gene and primary open-angle glaucoma. Archives of Ophthalmology (Chicago, Ill. : 1960). 125: 434-6. PMID 17353431 DOI: 10.1001/Archopht.125.3.434-B |
0.693 |
|
| 2007 |
Hewitt AW, Bennett SL, Richards JE, Dimasi DP, Booth AP, Inglehearn C, Anwar R, Yamamoto T, Fingert JH, Héon E, Craig JE, Mackey DA. Myocilin Gly252Arg mutation and glaucoma of intermediate severity in Caucasian individuals. Archives of Ophthalmology (Chicago, Ill. : 1960). 125: 98-104. PMID 17210859 DOI: 10.1001/Archopht.125.1.98 |
0.462 |
|
| 2007 |
Hewitt AW, Bennett SL, Fingert JH, Cooper RL, Stone EM, Craig JE, Mackey DA. The optic nerve head in myocilin glaucoma. Investigative Ophthalmology & Visual Science. 48: 238-43. PMID 17197538 DOI: 10.1167/Iovs.06-0611 |
0.592 |
|
| 2006 |
Grassi MA, Fingert JH, Scheetz TE, Roos BR, Ritch R, West SK, Kawase K, Shire AM, Mullins RF, Stone EM. Ethnic variation in AMD-associated complement factor H polymorphism p.Tyr402His. Human Mutation. 27: 921-5. PMID 16865697 DOI: 10.1002/Humu.20359 |
0.514 |
|
| 2006 |
Fingert JH, Kwon YH, Moore PA, Johnston RM, Kim KY, Sheffield VC, Alward WL, Stone EM. The C677T variant in the methylenetetrahydrofolate reductase gene is not associated with disease in cohorts of pseudoexfoliation glaucoma and primary open-angle glaucoma patients from Iowa. Ophthalmic Genetics. 27: 39-41. PMID 16754204 DOI: 10.1080/13816810600677883 |
0.571 |
|
| 2006 |
Fingert JH, Eliason DA, Phillips NC, Lotery AJ, Sheffield VC, Stone EM. Case of Stargardt disease caused by uniparental isodisomy. Archives of Ophthalmology (Chicago, Ill. : 1960). 124: 744-5. PMID 16682602 DOI: 10.1001/Archopht.124.5.744 |
0.452 |
|
| 2003 |
Mackey DA, Healey DL, Fingert JH, Coote MA, Wong TL, Wilkinson CH, McCartney PJ, Rait JL, de Graaf AP, Stone EM, Craig JE. Glaucoma phenotype in pedigrees with the myocilin Thr377Met mutation. Archives of Ophthalmology (Chicago, Ill. : 1960). 121: 1172-80. PMID 12912696 DOI: 10.1001/Archopht.121.8.1172 |
0.585 |
|
| 2003 |
Mackey DA, Fingert JH, Luzhansky JZ, McCluskey PJ, Howell N, Hall AJ, Pierce AB, Hoy JF. Leber's hereditary optic neuropathy triggered by antiretroviral therapy for human immunodeficiency virus. Eye (London, England). 17: 312-7. PMID 12724691 DOI: 10.1038/Sj.Eye.6700362 |
0.305 |
|
| 2002 |
Fingert JH, Stone EM, Sheffield VC, Alward WL. Myocilin glaucoma. Survey of Ophthalmology. 47: 547-61. PMID 12504739 DOI: 10.1016/S0039-6257(02)00353-3 |
0.62 |
|
| 2002 |
Sale MM, Craig JE, Charlesworth JC, FitzGerald LM, Hanson IM, Dickinson JL, Matthews SJ, Heyningen Vv Vv, Fingert JH, Mackey DA. Broad phenotypic variability in a single pedigree with a novel 1410delC mutation in the PST domain of the PAX6 gene. Human Mutation. 20: 322. PMID 12325030 DOI: 10.1002/Humu.9066 |
0.435 |
|
| 2002 |
Alward WL, Kwon YH, Khanna CL, Johnson AT, Hayreh SS, Zimmerman MB, Narkiewicz J, Andorf JL, Moore PA, Fingert JH, Sheffield VC, Stone EM. Variations in the myocilin gene in patients with open-angle glaucoma. Archives of Ophthalmology (Chicago, Ill. : 1960). 120: 1189-97. PMID 12215093 DOI: 10.1001/Archopht.120.9.1189 |
0.566 |
|
| 2001 |
Shepard AR, Jacobson N, Fingert JH, Stone EM, Sheffield VC, Clark AF. Delayed secondary glucocorticoid responsiveness of MYOC in human trabecular meshwork cells. Investigative Ophthalmology & Visual Science. 42: 3173-81. PMID 11726619 |
0.415 |
|
| 2001 |
Craig JE, Baird PN, Healey DL, McNaught AI, McCartney PJ, Rait JL, Dickinson JL, Roe L, Fingert JH, Stone EM, Mackey DA. Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifier. Ophthalmology. 108: 1607-20. PMID 11535458 DOI: 10.1016/S0161-6420(01)00654-6 |
0.584 |
|
| 2001 |
Clark AF, Steely HT, Dickerson JE, English-Wright S, Stropki K, McCartney MD, Jacobson N, Shepard AR, Clark JI, Matsushima H, Peskind ER, Leverenz JB, Wilkinson CW, Swiderski RE, Fingert JH, et al. Glucocorticoid induction of the glaucoma gene MYOC in human and monkey trabecular meshwork cells and tissues. Investigative Ophthalmology & Visual Science. 42: 1769-80. PMID 11431441 |
0.401 |
|
| 2001 |
Clark AF, Kawase K, English-Wright S, Lane D, Steely HT, Yamamoto T, Kitazawa Y, Kwon YH, Fingert JH, Swiderski RE, Mullins RF, Hageman GS, Alward WL, Sheffield VC, Stone EM. Expression of the glaucoma gene myocilin (MYOC) in the human optic nerve head. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 15: 1251-3. PMID 11344104 DOI: 10.1096/Fj.00-0663Fje |
0.535 |
|
| 2001 |
Jacobson N, Andrews M, Shepard AR, Nishimura D, Searby C, Fingert JH, Hageman G, Mullins R, Davidson BL, Kwon YH, Alward WL, Stone EM, Clark AF, Sheffield VC. Non-secretion of mutant proteins of the glaucoma gene myocilin in cultured trabecular meshwork cells and in aqueous humor. Human Molecular Genetics. 10: 117-25. PMID 11152659 DOI: 10.1093/Hmg/10.2.117 |
0.549 |
|
| 2001 |
Fingert JH, Clark AF, Craig JE, Alward WL, Snibson GR, McLaughlin M, Tuttle L, Mackey DA, Sheffield VC, Stone EM. Evaluation of the myocilin (MYOC) glaucoma gene in monkey and human steroid-induced ocular hypertension. Investigative Ophthalmology & Visual Science. 42: 145-52. PMID 11133859 |
0.32 |
|
| 2000 |
Williams-Lyn D, Flanagan J, Buys Y, Trope GE, Fingert J, Stone EM, Héon E. The genetic aspects of adult-onset glaucoma: a perspective from the Greater Toronto area. Canadian Journal of Ophthalmology-Journal Canadien D Ophtalmologie. 35: 12-17. PMID 10711378 DOI: 10.1016/S0008-4182(00)80103-9 |
0.628 |
|
| 2000 |
Williams-Lyn D, Flanagan J, Buys Y, Trope GE, Fingert J, Stone EM, Heon E. The genetic aspects of adult-onset glaucoma: A perspective from the Greater Toronto area Canadian Journal of Ophthalmology. 35: 12-17. |
0.392 |
|
| 1999 |
Mellott ML, Brown J, Fingert JH, Taylor CM, Keech RV, Sheffield VC, Stone EM. Clinical characterization and linkage analysis of a family with congenital X-linked nystagmus and deuteranomaly. Archives of Ophthalmology (Chicago, Ill. : 1960). 117: 1630-3. PMID 10604668 DOI: 10.1001/Archopht.117.12.1630 |
0.584 |
|
| 1999 |
Fingert JH, Héon E, Liebmann JM, Yamamoto T, Craig JE, Rait J, Kawase K, Hoh ST, Buys YM, Dickinson J, Hockey RR, Williams-Lyn D, Trope G, Kitazawa Y, Ritch R, et al. Analysis of myocilin mutations in 1703 glaucoma patients from five different populations. Human Molecular Genetics. 8: 899-905. PMID 10196380 DOI: 10.1093/Hmg/8.5.899 |
0.569 |
|
| 1998 |
Kennan AM, Mansergh FC, Fingert JH, Clark T, Ayuso C, Kenna PF, Humphries P, Farrar GJ. A novel Asp380Ala mutation in the GLC1A/myocilin gene in a family with juvenile onset primary open angle glaucoma. Journal of Medical Genetics. 35: 957-60. PMID 9832047 DOI: 10.1136/Jmg.35.11.957 |
0.479 |
|
| 1998 |
Fingert JH, Ying L, Swiderski RE, Nystuen AM, Arbour NC, Alward WL, Sheffield VC, Stone EM. Characterization and comparison of the human and mouse GLC1A glaucoma genes. Genome Research. 8: 377-84. PMID 9548973 DOI: 10.1101/Gr.8.4.377 |
0.521 |
|
| 1998 |
Alward WL, Fingert JH, Coote MA, Johnson AT, Lerner SF, Junqua D, Durcan FJ, McCartney PJ, Mackey DA, Sheffield VC, Stone EM. Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A) The New England Journal of Medicine. 338: 1022-7. PMID 9535666 DOI: 10.1056/Nejm199804093381503 |
0.625 |
|
| 1997 |
Lam BL, Fingert JH, Shutt BC, Singleton EM, Merin LM, Brown HH, Sheffield VC, Stone EM. Clinical and molecular characterization of a family affected with X-linked ocular albinism (OA1) Ophthalmic Genetics. 18: 175-84. PMID 9457748 DOI: 10.3109/13816819709041432 |
0.526 |
|
| 1997 |
Brown J, Fingert JH, Taylor CM, Lake M, Sheffield VC, Stone EM. Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1) Archives of Ophthalmology (Chicago, Ill. : 1960). 115: 95-9. PMID 9006432 DOI: 10.1001/Archopht.1997.01100150097016 |
0.563 |
|
| 1997 |
Stone EM, Fingert JH, Alward WL, Nguyen TD, Polansky JR, Sunden SL, Nishimura D, Clark AF, Nystuen A, Nichols BE, Mackey DA, Ritch R, Kalenak JW, Craven ER, Sheffield VC. Identification of a gene that causes primary open angle glaucoma. Science (New York, N.Y.). 275: 668-70. PMID 9005853 DOI: 10.1126/Science.275.5300.668 |
0.619 |
|
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