John H. Fingert, Ph.D. - Publications

University of Iowa, Iowa City, IA 
Inherited eye disease

120 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
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  0.48
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  0.52
2019 Laville V, Kang JH, Cousins CC, Iglesias AI, Nagy R, Cooke Bailey JN, Igo RP, Song YE, Chasman DI, Christen WG, Kraft P, Rosner BA, Hu F, Wilson JF, Gharahkhani P, ... ... Fingert JH, et al. Genetic correlations between diabetes and glaucoma: an analysis of continuous and dichotomous phenotypes. American Journal of Ophthalmology. PMID 31121135 DOI: 10.1016/j.ajo.2019.05.015  0.36
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  0.52
2019 Tandon A, Zhang Z, Fingert JH, Kwon YH, Wang K, Alward WLM. The Heritability of Pigment Dispersion Syndrome and Pigmentary Glaucoma. American Journal of Ophthalmology. PMID 30796891 DOI: 10.1016/j.ajo.2019.02.017  0.52
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  0.52
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  0.52
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  0.32
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  0.36
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  0.36
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  0.52
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  0.52
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  0.52
2017 Guo Z, Kwon YH, Lee K, Wang K, Wahle A, Alward WLM, Fingert JH, Bettis DI, Johnson CA, Garvin MK, Sonka M, Abràmoff MD. Optical Coherence Tomography Analysis Based Prediction of Humphrey 24-2 Visual Field Thresholds in Patients With Glaucoma. Investigative Ophthalmology & Visual Science. 58: 3975-3985. PMID 28796875 DOI: 10.1167/iovs.17-21832  0.52
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  0.32
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  0.52
2017 Simpson A, Avdic A, Roos BR, DeLuca A, Miller K, Schnieders MJ, Scheetz TE, Alward WL, Fingert JH. LADD syndrome with glaucoma is caused by a novel gene. Molecular Vision. 23: 179-184. PMID 28400699  0.32
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  0.48
2016 Chirco KR, Hazlewood RJ, Miller K, Workalemahu G, Jampol LM, Lesser GR, Mullins RF, Kuehn MH, Fingert JH. MMP19 expression in the human optic nerve. Molecular Vision. 22: 1429-1436. PMID 28003733  0.48
2016 Fingert JH, Robin AL, Scheetz TE, Kwon YH, Liebmann JM, Ritch R, Alward WL. Tank-Binding Kinase 1 (TBK1) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis). Transactions of the American Ophthalmological Society. 114: T6. PMID 27881886  0.36
2016 Zarei K, Scheetz TE, Christopher M, Miller K, Hedberg-Buenz A, Tandon A, Anderson MG, Fingert JH, Abràmoff MD. Corrigendum: Automated Axon Counting in Rodent Optic Nerve Sections with AxonJ. Scientific Reports. 6: 34124. PMID 27759018 DOI: 10.1038/srep34124  0.32
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  0.36
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  0.52
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  0.52
2016 Zarei K, Scheetz TE, Christopher M, Miller K, Hedberg-Buenz A, Tandon A, Anderson MG, Fingert JH, Abràmoff MD. Automated Axon Counting in Rodent Optic Nerve Sections with AxonJ. Scientific Reports. 6: 26559. PMID 27226405 DOI: 10.1038/srep26559  0.52
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  0.36
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  0.52
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  0.52
2015 Pasquale LR, Borrás T, Fingert JH, Wiggs JL, Ritch R. Exfoliation syndrome: assembling the puzzle pieces. Acta Ophthalmologica. PMID 26648185 DOI: 10.1111/aos.12918  0.52
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  0.52
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  0.52
2015 Christopher M, Abràmoff MD, Tang L, Gordon MO, Kass MA, Budenz DL, Fingert JH, Scheetz TE. Stereo Photo Measured ONH Shape Predicts Development of POAG in Subjects With Ocular Hypertension. Investigative Ophthalmology & Visual Science. 56: 4470-9. PMID 26193923 DOI: 10.1167/iovs.14-16142  0.52
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. Corrigendum: A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome. Nature Genetics. 47: 689. PMID 26018902 DOI: 10.1038/ng0615-689c  0.36
2015 Springelkamp H, Mishra A, Hysi PG, Gharahkhani P, Höhn R, Khor CC, Cooke Bailey JN, Luo X, Ramdas WD, Vithana E, Koh V, Yazar S, Xu L, Forward H, Kearns LS, et al. Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology. Genetic Epidemiology. 39: 207-16. PMID 25631615 DOI: 10.1002/gepi.21886  0.52
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  0.52
2015 Munk MR, Simjanoski E, Fingert JH, Jampol LM. Enhanced depth imaging optical coherence tomography of congenital cavitary optic disc anomaly (CODA). The British Journal of Ophthalmology. 99: 549-55. PMID 25359902 DOI: 10.1136/bjophthalmol-2014-305722  0.52
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  0.52
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  0.52
2014 John SW, Harder JM, Fingert JH, Anderson MG. Animal models of exfoliation syndrome, now and future. Journal of Glaucoma. 23: S68-72. PMID 25275912 DOI: 10.1097/IJG.0000000000000121  0.52
2014 Springelkamp H, Höhn R, Mishra A, Hysi PG, Khor CC, Loomis SJ, Bailey JN, Gibson J, Thorleifsson G, Janssen SF, Luo X, Ramdas WD, Vithana E, Nongpiur ME, Montgomery GW, et al. Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process. Nature Communications. 5: 4883. PMID 25241763 DOI: 10.1038/ncomms5883  0.52
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  0.52
2014 Tandon A, Tehrani S, Greiner MA, Fingert JH, Alward WL. Thin central corneal thickness and early-onset glaucoma in lacrimo-auriculo-dento-digital syndrome. Jama Ophthalmology. 132: 782-4. PMID 24921174 DOI: 10.1001/jamaophthalmol.2014.306  0.52
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  0.48
2014 Carnes MU, Liu YP, Allingham RR, Whigham BT, Havens S, Garrett ME, Qiao C, Katsanis N, Wiggs JL, Pasquale LR, Ashley-Koch A, Oh EC, Hauser MA. Discovery and functional annotation of SIX6 variants in primary open-angle glaucoma. Plos Genetics. 10: e1004372. PMID 24875647 DOI: 10.1371/journal.pgen.1004372  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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, ... ... Fingert J, 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  0.52
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  0.52
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 FüR Klinische Und Experimentelle Ophthalmologie. 251: 1571-6. PMID 23358655 DOI: 10.1007/s00417-013-2262-2  0.52
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  0.52
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  0.52
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  0.52
2013 Christopher M, Tang L, Fingert JH, Scheetz TE, Abramoff MD. Changes in quantitative 3D shape features of the optic nerve head associated with age Proceedings of Spie - the International Society For Optical Engineering. 8670. DOI: 10.1117/12.2006908  0.52
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  0.52
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  0.52
2012 Wang K, Fingert JH. Statistical tests for detecting rare variants using variance-stabilising transformations. Annals of Human Genetics. 76: 402-9. PMID 22724536 DOI: 10.1111/j.1469-1809.2012.00718.x  0.52
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  0.52
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  0.52
2011 Fingert JH. Primary open-angle glaucoma genes. Eye (London, England). 25: 587-95. PMID 21562585 DOI: 10.1038/eye.2011.97  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
2010 Tang L, Scheetz TE, Mackey DA, Hewitt AW, Fingert JH, Kwon YH, Quellec G, Reinhardt JM, Abràmoff 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  0.52
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  0.52
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  0.52
2010 Fingert JH, Alward WL, Wang K, Yorio T, Clark AF. Assessment of SNPs associated with the human glucocorticoid receptor in primary open-angle glaucoma and steroid responders. Molecular Vision. 16: 596-601. PMID 20376328  0.52
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  0.52
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  0.36
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  0.52
2009 Kwon YH, Fingert JH, Kuehn MH. The authors reply New England Journal of Medicine. 360: 2679-2680. DOI: 10.1056/NEJMc090757  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
2007 Hewitt AW, Poulsen JP, Alward WL, Bennett SL, Budde WM, Cooper RL, Craig JE, Fingert JH, Foster PJ, Garway-Heath DF, Green CM, Hammond CJ, Hayreh SS, Jonas JB, Kaufman PL, et al. Heritable features of the optic disc: a novel twin method for determining genetic significance. Investigative Ophthalmology & Visual Science. 48: 2469-75. PMID 17525172 DOI: 10.1167/iovs.06-1470  0.52
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  0.52
2007 Abràmoff MD, Alward WL, Greenlee EC, Shuba L, Kim CY, Fingert JH, Kwon YH. Automated segmentation of the optic disc from stereo color photographs using physiologically plausible features. Investigative Ophthalmology & Visual Science. 48: 1665-73. PMID 17389498 DOI: 10.1167/iovs.06-1081  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
2005 Kuehn MH, Fingert JH, Kwon YH. Retinal ganglion cell death in glaucoma: mechanisms and neuroprotective strategies. Ophthalmology Clinics of North America. 18: 383-95, vi. PMID 16054996 DOI: 10.1016/j.ohc.2005.04.002  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
2000 Swiderski RE, Ross JL, Fingert JH, Clark AF, Alward WL, Stone EM, Sheffield VC. Localization of MYOC transcripts in human eye and optic nerve by in situ hybridization. Investigative Ophthalmology & Visual Science. 41: 3420-8. PMID 11006234  0.52
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.  0.52
1999 Simm RM, Fingert JH, Craig JE, McNaught AI, Mackey DA. Normal range of hearing associated with myocilin Thr377Met. Ophthalmic Genetics. 20: 205-7. PMID 10610189  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
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  0.52
1996 Fingert JH, Brown J, Taylor CM, Butler N, Lake M, Sheffield VC, Stone EM. Refinement of the dominant optic atrophy locus (3q) and clinical characterization of a large family Investigative Ophthalmology and Visual Science. 37: S656.  0.52
Show low-probability matches.