| Year |
Citation |
Score |
| 2023 |
Voigt AP, Mullin NK, Navratil EM, Flamme-Wiese MJ, Lin LC, Scheetz TE, Han IC, Stone EM, Tucker BA, Mullins RF. Gene Expression Within a Human Choroidal Neovascular Membrane Using Spatial Transcriptomics. Investigative Ophthalmology & Visual Science. 64: 40. PMID 37878301 DOI: 10.1167/iovs.64.13.40 |
0.341 |
|
| 2023 |
Voigt AP, Mullin NK, Navratil EM, Flamme-Wiese MJ, Lin LC, Scheetz TE, Han IC, Stone EM, Tucker BA, Mullins RF. GENE EXPRESSION WITHIN A HUMAN CHOROIDAL NEOVASCULAR MEMBRANE USING SPATIAL TRANSCRIPTOMICS. Biorxiv : the Preprint Server For Biology. PMID 37398429 DOI: 10.1101/2023.06.16.544770 |
0.348 |
|
| 2023 |
Mullin NK, Voigt AP, Boese EA, Liu X, Stone EM, Tucker BA, Mullins RF. Transcriptomic and chromatin accessibility analysis of the human macular and peripheral retinal pigment epithelium at the single cell level. The American Journal of Pathology. PMID 36775060 DOI: 10.1016/j.ajpath.2023.01.012 |
0.372 |
|
| 2022 |
Lehmann GL, Ginsberg M, Nolan DJ, Rodríguez C, Martínez-González J, Zeng S, Voigt AP, Mullins RF, Rafii S, Rodriguez-Boulan E, Benedicto I. Retinal Pigment Epithelium-Secreted VEGF-A Induces Alpha-2-Macroglobulin Expression in Endothelial Cells. Cells. 11. PMID 36230937 DOI: 10.3390/cells11192975 |
0.351 |
|
| 2022 |
Mulfaul K, Russell JF, Voigt AP, Stone EM, Tucker BA, Mullins RF. The Essential Role of the Choriocapillaris in Vision: Novel Insights from Imaging and Molecular Biology. Annual Review of Vision Science. 8: 33-52. PMID 36108103 DOI: 10.1146/annurev-vision-100820-085958 |
0.333 |
|
| 2022 |
Fragiotta S, Parravano M, Sacconi R, Costanzo E, De Geronimo D, Prascina F, Capuano V, Souied EH, Han IC, Mullins R, Querques G. Sub-retinal pigment epithelium tubules in non-neovascular age-related macular degeneration. Scientific Reports. 12: 15198. PMID 36071082 DOI: 10.1038/s41598-022-19193-6 |
0.308 |
|
| 2022 |
Han IC, Bohrer LR, Gibson-Corley KN, Wiley LA, Shrestha A, Harman BE, Jiao C, Sohn EH, Wendland R, Allen BN, Worthington KS, Mullins RF, Stone EM, Tucker BA. Biocompatibility of Human Induced Pluripotent Stem Cell-Derived Retinal Progenitor Cell Grafts in Immunocompromised Rats. Cell Transplantation. 31: 9636897221104451. PMID 35758274 DOI: 10.1177/09636897221104451 |
0.312 |
|
| 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 |
0.329 |
|
| 2021 |
Tucker BA, Burnight ER, Cranston CM, Ulferts MJ, Luse MA, Westfall T, Scott CA, Marsden A, Gibson-Corley K, Wiley LA, Han IC, Slusarski DC, Mullins RF, Stone EM. Development and biological characterization of a clinical gene transfer vector for the treatment of MAK-associated retinitis pigmentosa. Gene Therapy. PMID 34518651 DOI: 10.1038/s41434-021-00291-5 |
0.31 |
|
| 2021 |
Voigt AP, Mullin NK, Whitmore SS, DeLuca AP, Burnight ER, Liu X, Tucker BA, Scheetz TE, Stone EM, Mullins RF. Human photoreceptor cells from different macular subregions have distinct transcriptional profiles. Human Molecular Genetics. PMID 34014299 DOI: 10.1093/hmg/ddab140 |
0.323 |
|
| 2021 |
Pouw AE, Greiner MA, Coussa RG, Jiao C, Han IC, Skeie JM, Fingert JH, Mullins RF, Sohn EH. Cell-Matrix Interactions in the Eye: From Cornea to Choroid. Cells. 10. PMID 33804633 DOI: 10.3390/cells10030687 |
0.693 |
|
| 2020 |
Voigt AP, Mullin NK, Stone EM, Tucker BA, Scheetz TE, Mullins RF. Single-cell RNA sequencing in vision research: Insights into human retinal health and disease. Progress in Retinal and Eye Research. 100934. PMID 33383180 DOI: 10.1016/j.preteyeres.2020.100934 |
0.324 |
|
| 2020 |
Han IC, Cheng JL, Burnight E, Ralston CL, Fick JL, Thomsen GJ, Tovar EF, Russell S, Sohn EH, Mullins RF, Stone E, Tucker BA, Wiley LA. Retinal Tropism and Transduction of Adeno-Associated Virus (AAV) Varies by Serotype and Route of Delivery (Intravitreal, Subretinal or Suprachoroidal) in Rats. Human Gene Therapy. PMID 32948113 DOI: 10.1089/Hum.2020.043 |
0.412 |
|
| 2020 |
Voigt AP, Whitmore SS, Lessing ND, DeLuca AP, Tucker BA, Stone EM, Mullins RF, Scheetz TE. Spectacle: An interactive resource for ocular single-cell RNA sequencing data analysis. Experimental Eye Research. 108204. PMID 32910939 DOI: 10.1016/J.Exer.2020.108204 |
0.308 |
|
| 2020 |
Stone NE, Voigt AP, Cooke JA, Giacalone JC, Hanasoge S, Mullins RF, Tucker BA, Sulchek T. Label-free microfluidic enrichment of photoreceptor cells. Experimental Eye Research. 108166. PMID 32771499 DOI: 10.1016/J.Exer.2020.108166 |
0.391 |
|
| 2020 |
Voigt AP, Whitmore SS, Mulfaul K, Chirco KR, Giacalone JC, Flamme-Wiese MJ, Stockman A, Stone EM, Tucker BA, Scheetz TE, Mullins RF. Bulk and single-cell gene expression analyses reveal aging human choriocapillaris has pro-inflammatory phenotype. Microvascular Research. 104031. PMID 32531351 DOI: 10.1016/J.Mvr.2020.104031 |
0.377 |
|
| 2020 |
Jiao C, Adler K, Liu X, Sun W, Mullins RF, Sohn EH. Visualization of Mouse Choroidal and Retinal Vasculature Using Fluorescent Tomato Lectin Perfusion. Translational Vision Science & Technology. 9: 1. PMID 32509436 DOI: 10.1167/Tvst.9.1.1 |
0.365 |
|
| 2020 |
Lehmann GL, Hanke-Gogokhia C, Hu Y, Bareja R, Salfati Z, Ginsberg M, Nolan DJ, Mendez-Huergo SP, Dalotto-Moreno T, Wojcinski A, Ochoa F, Zeng S, Cerliani JP, Panagis L, Zager PJ, ... Mullins RF, et al. Single-cell profiling reveals an endothelium-mediated immunomodulatory pathway in the eye choroid. The Journal of Experimental Medicine. 217. PMID 32196081 DOI: 10.1084/Jem.20190730 |
0.466 |
|
| 2020 |
Mulfaul K, Ozaki E, Fernando N, Brennan K, Chirco KR, Connolly E, Greene C, Maminishkis A, Salomon RG, Linetsky M, Natoli R, Mullins RF, Campbell M, Doyle SL. Toll-like Receptor 2 Facilitates Oxidative Damage-Induced Retinal Degeneration. Cell Reports. 30: 2209-2224.e5. PMID 32075760 DOI: 10.1016/J.Celrep.2020.01.064 |
0.364 |
|
| 2020 |
Voigt AP, Binkley E, Flamme-Wiese MJ, Zeng S, DeLuca AP, Scheetz TE, Tucker BA, Mullins RF, Stone EM. Single-Cell RNA Sequencing in Human Retinal Degeneration Reveals Distinct Glial Cell Populations. Cells. 9. PMID 32069977 DOI: 10.3390/Cells9020438 |
0.446 |
|
| 2020 |
Tucker BA, Mullins RF, Stone EM. Autologous cell replacement: a noninvasive AI approach to clinical release testing. The Journal of Clinical Investigation. PMID 31961338 DOI: 10.1172/Jci133821 |
0.342 |
|
| 2019 |
Wiley LA, Binkley EM, DeLuca AP, Workalemahu G, Tatro NJ, Luse MA, Kennedy EL, Folk JC, Scheetz TE, Ballas ZK, Tucker BA, Mullins RF, Han IC, Stone EM. AUTOIMMUNE RETINOPATHY MIMICKING HERITABLE RETINAL DEGENERATION IN A PATIENT WITH COMMON VARIABLE IMMUNE DEFICIENCY. Retinal Cases & Brief Reports. PMID 31764884 DOI: 10.1097/Icb.0000000000000941 |
0.314 |
|
| 2019 |
Voigt AP, Mulfaul K, Mullin NK, Flamme-Wiese MJ, Giacalone JC, Stone EM, Tucker BA, Scheetz TE, Mullins RF. Single-cell transcriptomics of the human retinal pigment epithelium and choroid in health and macular degeneration. Proceedings of the National Academy of Sciences of the United States of America. PMID 31712411 DOI: 10.1073/Pnas.1914143116 |
0.489 |
|
| 2019 |
Han IC, Burnight E, Ulferts MJ, Worthington KS, Russell SR, Sohn EH, Mullins RF, Stone E, Tucker BA, Wiley LA. Helper-Dependent Adenovirus Transduces the Human and Rat Retina but Elicits an Inflammatory Reaction When Delivered Subretinally in Rats. Human Gene Therapy. PMID 31456426 DOI: 10.1089/Hum.2019.159 |
0.406 |
|
| 2019 |
Giacalone JC, Andorf JL, Zhang Q, Burnight E, Ochoa D, Reutzel AJ, Collins MM, Sheffield V, Mullins RF, Han IC, Stone E, Tucker BA. Development of a Molecularly Stable Gene Therapy Vector for the Treatment of RPGR-associated X-linked Retinitis Pigmentosa. Human Gene Therapy. PMID 31106594 DOI: 10.1089/Hum.2018.244 |
0.336 |
|
| 2019 |
Voigt AP, Whitmore SS, Flamme-Wiese MJ, Riker M, Wiley LA, Tucker BA, Stone EM, Mullins RF, Scheetz TE. Molecular characterization of foveal versus peripheral human retina by single-cell RNA sequencing. Experimental Eye Research. PMID 31075224 DOI: 10.1016/J.Exer.2019.05.001 |
0.409 |
|
| 2019 |
Thompson JR, Worthington KS, Green BJ, Mullin NK, Jiao C, Kaalberg EE, Wiley LA, Han IC, Russell SR, Sohn EH, Guymon CA, Mullins RF, Stone EM, Tucker BA. Two-photon Polymerized Poly(caprolactone) Retinal Cell Delivery Scaffolds and their Systemic and Retinal Biocompatibility. Acta Biomaterialia. PMID 31055121 DOI: 10.1016/J.Actbio.2019.04.057 |
0.399 |
|
| 2019 |
Sohn EH, Flamme-Wiese MJ, Whitmore SS, Workalemahu G, Marneros AG, Boese EA, Kwon YH, Wang K, Abramoff MD, Tucker BA, Stone EM, Mullins RF. Choriocapillaris Degeneration in Geographic Atrophy. The American Journal of Pathology. PMID 31051169 DOI: 10.1016/J.Ajpath.2019.04.005 |
0.429 |
|
| 2019 |
Sacconi R, Mullins RF, Lutty GA, Borrelli E, Bandello F, Querques G. Subretinal pseudocyst: A novel optical coherence tomography finding in age-related macular degeneration. European Journal of Ophthalmology. 1120672119846437. PMID 31018677 DOI: 10.1177/1120672119846437 |
0.338 |
|
| 2019 |
Han IC, Whitmore SS, Critser DB, Lee SY, DeLuca AP, Daggett HT, Affatigato LM, Mullins RF, Tucker BA, Drack AV, Stone EM. Wide-Field Swept-Source OCT and Angiography in X-Linked Retinoschisis. Ophthalmology. Retina. 3: 178-185. PMID 31014769 DOI: 10.1016/J.Oret.2018.09.006 |
0.324 |
|
| 2019 |
Scruggs BA, Jiao C, Cranston CM, Kaalberg E, Wang K, Russell SR, Wiley LA, Mullins RF, Stone EM, Tucker BA, Sohn EH. Optimizing Donor Cellular Dissociation and Subretinal Injection Parameters for Stem Cell-Based Treatments. Stem Cells Translational Medicine. PMID 31004408 DOI: 10.1002/Sctm.18-0210 |
0.433 |
|
| 2019 |
Bohrer LR, Wiley LA, Burnight ER, Cooke JA, Giacalone JC, Anfinson KR, Andorf JL, Mullins RF, Stone EM, Tucker BA. Correction of NR2E3 Associated Enhanced S-cone Syndrome Patient-specific iPSCs using CRISPR-Cas9. Genes. 10. PMID 30959774 DOI: 10.3390/Genes10040278 |
0.378 |
|
| 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 |
0.379 |
|
| 2018 |
Giacalone JC, Miller MJ, Workalemahu G, Reutzel AJ, Ochoa D, Whitmore SS, Stone EM, Tucker BA, Mullins RF. Generation of an immortalized human choroid endothelial cell line (iChEC-1) using an endothelial cell specific promoter. Microvascular Research. 123: 50-57. PMID 30571950 DOI: 10.1016/J.Mvr.2018.12.002 |
0.371 |
|
| 2018 |
Cheng J, Sohn EH, Jiao C, Adler KL, Kaalberg EE, Russell SR, Mullins RF, Stone EM, Tucker BA, Han IC. Correlation of Optical Coherence Tomography and Retinal Histology in Normal and Pro23His Retinal Degeneration Pig. Translational Vision Science & Technology. 7: 18. PMID 30519502 DOI: 10.1167/Tvst.7.6.18 |
0.381 |
|
| 2018 |
Mullins RF, McGwin G, Searcey K, Clark ME, Kennedy EL, Curcio CA, Stone EM, Owsley C. The ARMS2 A69S Polymorphism Is Associated with Delayed Rod-Mediated Dark Adaptation in Eyes at Risk for Incident Age-Related Macular Degeneration. Ophthalmology. PMID 30389424 DOI: 10.1016/J.Ophtha.2018.10.037 |
0.385 |
|
| 2018 |
Spaide RF, Yannuzzi L, Freund KB, Mullins R, Stone E. EYES WITH SUBRETINAL DRUSENOID DEPOSITS AND NO DRUSEN: Progression of Macular Findings. Retina (Philadelphia, Pa.). PMID 30312263 DOI: 10.1097/Iae.0000000000002362 |
0.387 |
|
| 2018 |
Zeng S, Wen KK, Workalemahu G, Sohn EH, Wu M, Chirco KR, Flamme-Wiese MJ, Liu X, Stone EM, Tucker BA, Mullins RF. Imidazole Compounds for Protecting Choroidal Endothelial Cells from Complement Injury. Scientific Reports. 8: 13387. PMID 30190604 DOI: 10.1038/S41598-018-31846-Z |
0.397 |
|
| 2018 |
Chirco KR, Flamme-Wiese MJ, Wiley JS, Potempa LA, Stone EM, Tucker BA, Mullins RF. Evaluation of serum and ocular levels of membrane attack complex and C-reactive protein in CFH-genotyped human donors. Eye (London, England). PMID 30013157 DOI: 10.1038/S41433-018-0170-8 |
0.33 |
|
| 2018 |
Wagoner MD, Bohrer LR, Aldrich BT, Greiner MA, Mullins RF, Worthington KS, Tucker BA, Wiley LA. Feeder-free differentiation of cells exhibiting characteristics of corneal endothelium from human induced pluripotent stem cells. Biology Open. PMID 29685994 DOI: 10.1242/Bio.032102 |
0.334 |
|
| 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 |
0.431 |
|
| 2017 |
Jiao C, Eliott D, Spee C, He S, Wang K, Mullins RF, Hinton DR, Sohn EH. APOPTOSIS AND ANGIOFIBROSIS IN DIABETIC TRACTIONAL MEMBRANES AFTER VASCULAR ENDOTHELIAL GROWTH FACTOR INHIBITION: Results of a Prospective Trial. Report No. 2. Retina (Philadelphia, Pa.). PMID 29190236 DOI: 10.1097/Iae.0000000000001952 |
0.35 |
|
| 2017 |
Wiley LA, Burnight E, Kaalberg EE, Jiao C, Riker MJ, Halder JA, Luse MA, Han IC, Russell SR, Sohn EH, Stone E, Tucker BA, Mullins RF. ASSESSMENT OF AAV SEROTYPE TROPISM IN HUMAN RETINAL EXPLANTS. Human Gene Therapy. PMID 29160116 DOI: 10.1089/Hum.2017.179 |
0.434 |
|
| 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 |
0.428 |
|
| 2017 |
Wiley LA, Anfinson KR, Cranston CM, Kaalberg EE, Collins MM, Mullins RF, Stone EM, Tucker BA. Generation of Xeno-Free, cGMP-Compliant Patient-Specific iPSCs from Skin Biopsy. Current Protocols in Stem Cell Biology. 42: 4A.12.1-4A.12.14. PMID 28806854 DOI: 10.1002/Cpsc.30 |
0.394 |
|
| 2017 |
Zhao Z, Liang Y, Liu Y, Xu P, Flamme-Wiese MJ, Sun D, Sun J, Mullins RF, Chen Y, Cai J. Choroidal γδ T cells in protection against retinal pigment epithelium and retinal injury. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. PMID 28729290 DOI: 10.1096/Fj.201700533R |
0.354 |
|
| 2017 |
Burnight ER, Gupta M, Wiley LA, Anfinson KR, Tran A, Triboulet R, Hoffmann JM, Klaahsen DL, Andorf JL, Jiao C, Sohn EH, Adur MK, Ross JW, Mullins RF, Daley GQ, et al. Using CRISPR-Cas9 to Generate Gene-Corrected Autologous iPSCs for the Treatment of Inherited Retinal Degeneration. Molecular Therapy : the Journal of the American Society of Gene Therapy. PMID 28619647 DOI: 10.1016/J.Ymthe.2017.05.015 |
0.403 |
|
| 2017 |
Stone EM, Andorf JL, Whitmore SS, DeLuca AP, Giacalone JC, Streb LM, Braun TA, Mullins RF, Scheetz TE, Sheffield VC, Tucker BA. Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal Disease. Ophthalmology. PMID 28559085 DOI: 10.1016/J.Ophtha.2017.04.008 |
0.346 |
|
| 2017 |
Chirco KR, Worthington KS, Flamme-Wiese MJ, Riker MJ, Andrade JD, Ueberheide BM, Stone EM, Tucker BA, Mullins RF. Preparation and evaluation of human choroid extracellular matrix scaffolds for the study of cell replacement strategies. Acta Biomaterialia. PMID 28483697 DOI: 10.1016/J.Actbio.2017.05.011 |
0.365 |
|
| 2017 |
Mullins RF, Warwick AN, Sohn EH, Lotery AJ. From Compliment to Insult- Genetics of the Complement System in Physiology and Disease in the Human Retina. Human Molecular Genetics. PMID 28482029 DOI: 10.1093/Hmg/Ddx181 |
0.427 |
|
| 2017 |
Songstad AE, Worthington KS, Chirco KR, Giacalone JC, Whitmore SS, Anfinson KR, Ochoa D, Cranston CM, Riker MJ, Neiman M, Stone EM, Mullins RF, Tucker BA. Connective Tissue Growth Factor Promotes Efficient Generation of Human induced pluripotent stem cell-Derived Choroidal Endothelium. Stem Cells Translational Medicine. PMID 28474838 DOI: 10.1002/Sctm.16-0399 |
0.399 |
|
| 2017 |
Sharma TP, Wiley LA, Whitmore SS, Anfinson KR, Cranston CM, Oppedal DJ, Daggett HT, Mullins RF, Tucker BA, Stone EM. Patient-specific induced pluripotent stem cells to evaluate the pathophysiology of TRNT1-associated Retinitis pigmentosa. Stem Cell Research. 21: 58-70. PMID 28390992 DOI: 10.1016/J.Scr.2017.03.005 |
0.429 |
|
| 2017 |
Worthington KS, Wiley LA, Kaalberg EE, Collins MM, Mullins RF, Stone EM, Tucker BA. Two-photon polymerization for production of human iPSC-derived retinal cell grafts. Acta Biomaterialia. PMID 28351682 DOI: 10.1016/J.Actbio.2017.03.039 |
0.393 |
|
| 2017 |
Guziewicz KE, Sinha D, Gómez NM, Zorych K, Dutrow EV, Dhingra A, Mullins RF, Stone EM, Gamm DM, Boesze-Battaglia K, Aguirre GD. Bestrophinopathy: An RPE-photoreceptor interface disease. Progress in Retinal and Eye Research. PMID 28111324 DOI: 10.1016/J.Preteyeres.2017.01.005 |
0.432 |
|
| 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 |
0.345 |
|
| 2016 |
Lee WH, Higuchi H, Ikeda S, Macke EL, Takimoto T, Pattnaik BR, Liu C, Chu LF, Siepka SM, Krentz KJ, Rubinstein CD, Kalejta RF, Thomson JA, Mullins RF, Takahashi JS, et al. Mouse Tmem135 mutation reveals a mechanism involving mitochondrial dynamics that leads to age-dependent retinal pathologies. Elife. 5. PMID 27863209 DOI: 10.7554/Elife.19264 |
0.378 |
|
| 2016 |
Chirco KR, Sohn EH, Stone EM, Tucker BA, Mullins RF. Structural and molecular changes in the aging choroid: implications for age-related macular degeneration. Eye (London, England). PMID 27716746 DOI: 10.1038/Eye.2016.216 |
0.474 |
|
| 2016 |
Wiley LA, Burnight ER, DeLuca AP, Anfinson KR, Cranston CM, Kaalberg EE, Penticoff JA, Affatigato LM, Mullins RF, Stone EM, Tucker BA. cGMP production of patient-specific iPSCs and photoreceptor precursor cells to treat retinal degenerative blindness. Scientific Reports. 6: 30742. PMID 27471043 DOI: 10.1038/Srep30742 |
0.423 |
|
| 2016 |
Sohn EH, Chirco KR, Folk JC, Mullins RF. CLINICOPATHOLOGICAL CORRELATION IN A PATIENT WITH PREVIOUSLY TREATED BIRDSHOT CHORIORETINOPATHY. Retinal Cases & Brief Reports. PMID 27465484 DOI: 10.1097/Icb.0000000000000367 |
0.377 |
|
| 2016 |
Chirco KR, Scott Whitmore S, Wang K, Potempa LA, Halder JA, Stone EM, Tucker BA, Mullins RF. Monomeric C-reactive protein and inflammation in Age-related Macular Degeneration The role of monomeric C-reactive protein in AMD. The Journal of Pathology. PMID 27376713 DOI: 10.1002/Path.4766 |
0.433 |
|
| 2016 |
Sohn EH, van Dijk HW, Jiao C, Kok PH, Jeong W, Demirkaya N, Garmager A, Wit F, Kucukevcilioglu M, van Velthoven ME, DeVries JH, Mullins RF, Kuehn MH, Schlingemann RO, Sonka M, et al. Retinal neurodegeneration may precede microvascular changes characteristic of diabetic retinopathy in diabetes mellitus. Proceedings of the National Academy of Sciences of the United States of America. PMID 27114552 DOI: 10.1073/Pnas.1522014113 |
0.369 |
|
| 2016 |
Lee W, Higuchi H, Ikeda S, Macke EL, Takimoto T, Pattnaik BR, Liu C, Chu L, Siepka SM, Krentz KJ, Rubinstein CD, Kalejta RF, Thomson JA, Mullins RF, Takahashi JS, et al. Author response: Mouse Tmem135 mutation reveals a mechanism involving mitochondrial dynamics that leads to age-dependent retinal pathologies Elife. DOI: 10.7554/Elife.19264.020 |
0.344 |
|
| 2016 |
Wiley LA, Kaalberg EE, Penticoff JA, Mullins RF, Stone EM, Tucker BA. Expression of the retina-specific flippase, ABCA4, in epidermal keratinocytes F1000research. 5: 193. DOI: 10.12688/F1000Research.8089.1 |
0.429 |
|
| 2015 |
Tien T, Muto T, Zhang J, Sohn EH, Mullins RF, Roy S. Association of Reduced Connexin 43 Expression with Retinal Vascular Lesions in Human Diabetic Retinopathy. Experimental Eye Research. PMID 26738943 DOI: 10.1016/J.Exer.2015.12.011 |
0.368 |
|
| 2015 |
Songstad AE, Wiley LA, Duong K, Kaalberg E, Flamme-Wiese MJ, Cranston CM, Riker MJ, Levasseur D, Stone EM, Mullins RF, Tucker BA. Generating iPSC-Derived Choroidal Endothelial Cells to Study Age-Related Macular Degeneration. Investigative Ophthalmology & Visual Science. 56: 8258-67. PMID 26720480 DOI: 10.1167/Iovs.15-17073 |
0.408 |
|
| 2015 |
Giacalone JC, Wiley LA, Burnight ER, Songstad AE, Mullins RF, Stone EM, Tucker BA. Concise Review: Patient-Specific Stem Cells to Interrogate Inherited Eye Disease. Stem Cells Translational Medicine. PMID 26683869 DOI: 10.5966/Sctm.2015-0206 |
0.401 |
|
| 2015 |
Zeng S, Whitmore SS, Sohn EH, Riker MJ, Wiley LA, Scheetz TE, Stone EM, Tucker BA, Mullins RF. Molecular Response of Chorioretinal Endothelial Cells to Complement Injury: Implications for Macular Degeneration. The Journal of Pathology. PMID 26564985 DOI: 10.1002/Path.4669 |
0.407 |
|
| 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, ... ... Mullins RF, 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 |
0.387 |
|
| 2015 |
DeLuca AP, Whitmore SS, Barnes J, Sharma TP, Westfall TA, Scott CA, Weed MC, Wiley JS, Wiley LA, Johnston RM, Schnieders MJ, Lentz SR, Tucker BA, Mullins RF, Scheetz TE, et al. Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis. Human Molecular Genetics. PMID 26494905 DOI: 10.1093/Hmg/Ddv446 |
0.394 |
|
| 2015 |
Chirco KR, Tucker BA, Stone EM, Mullins RF. Selective accumulation of the complement membrane attack complex in aging choriocapillaris. Experimental Eye Research. PMID 26368849 DOI: 10.1016/J.Exer.2015.09.003 |
0.352 |
|
| 2015 |
Tucker BA, Cranston CM, Anfinson KA, Shrestha S, Streb LM, Leon A, Mullins RF, Stone EM. Using patient-specific induced pluripotent stem cells to interrogate the pathogenicity of a novel retinal pigment epithelium-specific 65 kDa cryptic splice site mutation and confirm eligibility for enrollment into a clinical gene augmentation trial. Translational Research : the Journal of Laboratory and Clinical Medicine. PMID 26364624 DOI: 10.1016/J.Trsl.2015.08.007 |
0.387 |
|
| 2015 |
Adhi M, Ferrara D, Mullins RF, Baumal CR, Mohler KJ, Kraus MF, Liu J, Badaro E, Alasil T, Hornegger J, Fujimoto JG, Duker JS, Waheed NK. Characterization of Choroidal Layers in Normal Aging Eyes Using Enface Swept-Source Optical Coherence Tomography. Plos One. 10: e0133080. PMID 26172550 DOI: 10.1371/Journal.Pone.0133080 |
0.374 |
|
| 2015 |
Sohn EH, Jiao C, Kaalberg E, Cranston C, Mullins RF, Stone EM, Tucker BA. Allogenic iPSC-derived RPE cell transplants induce immune response in pigs: a pilot study. Scientific Reports. 5: 11791. PMID 26138532 DOI: 10.1038/Srep11791 |
0.366 |
|
| 2015 |
Almeida DR, Chin EK, Tarantola RM, Folk JC, Boldt HC, Skeie JM, Mullins RF, Russell SR, Mahajan VB. Effect of internal limiting membrane abrasion on retinal tissues in macular holes. Investigative Ophthalmology & Visual Science. 56: 2783-9. PMID 26024069 DOI: 10.1167/Iovs.14-16355 |
0.685 |
|
| 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 |
0.302 |
|
| 2015 |
Almeida DR, Zhang L, Chin EK, Mullins RF, Kucukevcilioglu M, Critser DB, Sonka M, Stone EM, Folk JC, Abràmoff MD, Russell SR. Comparison of retinal and choriocapillaris thicknesses following sitting to supine transition in healthy individuals and patients with age-related macular degeneration. Jama Ophthalmology. 133: 297-303. PMID 25521616 DOI: 10.1001/Jamaophthalmol.2014.5168 |
0.428 |
|
| 2015 |
Wiley LA, Burnight ER, Mullins RF, Stone EM, Tucker BA. Stem cells as tools for studying the genetics of inherited retinal degenerations. Cold Spring Harbor Perspectives in Medicine. 5: a017160. PMID 25502747 DOI: 10.1101/Cshperspect.A017160 |
0.407 |
|
| 2015 |
Whitmore SS, Sohn EH, Chirco KR, Drack AV, Stone EM, Tucker BA, Mullins RF. Complement activation and choriocapillaris loss in early AMD: implications for pathophysiology and therapy. Progress in Retinal and Eye Research. 45: 1-29. PMID 25486088 DOI: 10.1016/J.Preteyeres.2014.11.005 |
0.434 |
|
| 2015 |
Wiley LA, Burnight ER, Songstad AE, Drack AV, Mullins RF, Stone EM, Tucker BA. Patient-specific induced pluripotent stem cells (iPSCs) for the study and treatment of retinal degenerative diseases. Progress in Retinal and Eye Research. 44: 15-35. PMID 25448922 DOI: 10.1016/J.Preteyeres.2014.10.002 |
0.437 |
|
| 2015 |
Burnight ER, Wiley LA, Mullins RF, Stone EM, Tucker BA. Gene therapy using stem cells. Cold Spring Harbor Perspectives in Medicine. 5. PMID 25395375 DOI: 10.1101/Cshperspect.A017434 |
0.412 |
|
| 2015 |
Stunkel M, Bhattarai S, Kemerley A, Stone EM, Wang K, Mullins RF, Drack AV. Vitritis in pediatric genetic retinal disorders. Ophthalmology. 122: 192-9. PMID 25217415 DOI: 10.1016/J.Ophtha.2014.07.037 |
0.399 |
|
| 2015 |
Sohn EH, Wang K, Thompson S, Riker MJ, Hoffmann JM, Stone EM, Mullins RF. Comparison of drusen and modifying genes in autosomal dominant radial drusen and age-related macular degeneration. Retina (Philadelphia, Pa.). 35: 48-57. PMID 25077532 DOI: 10.1097/Iae.0000000000000263 |
0.467 |
|
| 2014 |
Whitmore SS, Wagner AH, DeLuca AP, Drack AV, Stone EM, Tucker BA, Zeng S, Braun TA, Mullins RF, Scheetz TE. Transcriptomic analysis across nasal, temporal, and macular regions of human neural retina and RPE/choroid by RNA-Seq. Experimental Eye Research. 129: 93-106. PMID 25446321 DOI: 10.1016/J.Exer.2014.11.001 |
0.46 |
|
| 2014 |
Mullins RF, Schoo DP, Sohn EH, Flamme-Wiese MJ, Workamelahu G, Johnston RM, Wang K, Tucker BA, Stone EM. The membrane attack complex in aging human choriocapillaris: relationship to macular degeneration and choroidal thinning. The American Journal of Pathology. 184: 3142-53. PMID 25204844 DOI: 10.1016/J.Ajpath.2014.07.017 |
0.437 |
|
| 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 |
0.449 |
|
| 2014 |
Burnight ER, Wiley LA, Drack AV, Braun TA, Anfinson KR, Kaalberg EE, Halder JA, Affatigato LM, Mullins RF, Stone EM, Tucker BA. CEP290 gene transfer rescues Leber congenital amaurosis cellular phenotype. Gene Therapy. 21: 662-72. PMID 24807808 DOI: 10.1038/Gt.2014.39 |
0.39 |
|
| 2014 |
Ardeljan D, Wang Y, Park S, Shen D, Chu XK, Yu CR, Abu-Asab M, Tuo J, Eberhart CG, Olsen TW, Mullins RF, White G, Wadsworth S, Scaria A, Chan CC. Interleukin-17 retinotoxicity is prevented by gene transfer of a soluble interleukin-17 receptor acting as a cytokine blocker: implications for age-related macular degeneration. Plos One. 9: e95900. PMID 24780906 DOI: 10.1371/Journal.Pone.0095900 |
0.418 |
|
| 2014 |
Schubert C, Pryds A, Zeng S, Xie Y, Freund KB, Spaide RF, Merriam JC, Barbazetto I, Slakter JS, Chang S, Munch IC, Drack AV, Hernandez J, Yzer S, Merriam JE, ... ... Mullins RF, et al. Cadherin 5 is regulated by corticosteroids and associated with central serous chorioretinopathy. Human Mutation. 35: 859-67. PMID 24665005 DOI: 10.1002/Humu.22551 |
0.33 |
|
| 2014 |
Mullins RF, Khanna A, Schoo DP, Tucker BA, Sohn EH, Drack AV, Stone EM. Is age-related macular degeneration a microvascular disease? Advances in Experimental Medicine and Biology. 801: 283-9. PMID 24664709 DOI: 10.1007/978-1-4614-3209-8_36 |
0.416 |
|
| 2014 |
Tucker BA, Mullins RF, Stone EM. Stem cells for investigation and treatment of inherited retinal disease. Human Molecular Genetics. 23: R9-R16. PMID 24647603 DOI: 10.1093/Hmg/Ddu124 |
0.45 |
|
| 2014 |
Worthington KS, Wiley LA, Bartlett AM, Stone EM, Mullins RF, Salem AK, Guymon CA, Tucker BA. Mechanical properties of murine and porcine ocular tissues in compression. Experimental Eye Research. 121: 194-9. PMID 24613781 DOI: 10.1016/J.Exer.2014.02.020 |
0.404 |
|
| 2014 |
Thompson S, Blodi FR, Lee S, Welder CR, Mullins RF, Tucker BA, Stasheff SF, Stone EM. Photoreceptor cells with profound structural deficits can support useful vision in mice. Investigative Ophthalmology & Visual Science. 55: 1859-66. PMID 24569582 DOI: 10.1167/Iovs.13-13661 |
0.403 |
|
| 2014 |
Drack AV, Mullins RF, Pfeifer WL, Augustine EF, Stasheff SF, Hong SD. Immunosuppressive Treatment for Retinal Degeneration in Juvenile Neuronal Ceroid Lipofuscinosis (Juvenile Batten Disease). Ophthalmic Genetics. PMID 24547931 DOI: 10.3109/13816810.2014.886271 |
0.326 |
|
| 2014 |
Sohn EH, Khanna A, Tucker BA, Abrà moff MD, Stone EM, Mullins RF. Structural and biochemical analyses of choroidal thickness in human donor eyes. Investigative Ophthalmology & Visual Science. 55: 1352-60. PMID 24519422 DOI: 10.1167/Iovs.13-13754 |
0.442 |
|
| 2014 |
Sohn EH, Flamme-Wiese MJ, Whitmore SS, Wang K, Tucker BA, Mullins RF. Loss of CD34 expression in aging human choriocapillaris endothelial cells. Plos One. 9: e86538. PMID 24466138 DOI: 10.1371/Journal.Pone.0086538 |
0.38 |
|
| 2014 |
Murinello S, Mullins RF, Lotery AJ, Perry VH, Teeling JL. Fcγ receptor upregulation is associated with immune complex inflammation in the mouse retina and early age-related macular degeneration. Investigative Ophthalmology & Visual Science. 55: 247-58. PMID 24334446 DOI: 10.1167/Iovs.13-11821 |
0.359 |
|
| 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 |
0.324 |
|
| 2013 |
Whitmore SS, Braun TA, Skeie JM, Haas CM, Sohn EH, Stone EM, Scheetz TE, Mullins RF. Altered gene expression in dry age-related macular degeneration suggests early loss of choroidal endothelial cells. Molecular Vision. 19: 2274-97. PMID 24265543 |
0.696 |
|
| 2013 |
Tucker BA, Mullins RF, Streb LM, Anfinson K, Eyestone ME, Kaalberg E, Riker MJ, Drack AV, Braun TA, Stone EM. Patient-specific iPSC-derived photoreceptor precursor cells as a means to investigate retinitis pigmentosa. Elife. 2: e00824. PMID 23991284 DOI: 10.7554/Elife.00824 |
0.401 |
|
| 2013 |
Braun TA, Mullins RF, Wagner AH, Andorf JL, Johnston RM, Bakall BB, Deluca AP, Fishman GA, Lam BL, Weleber RG, Cideciyan AV, Jacobson SG, Sheffield VC, Tucker BA, Stone EM. Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease. Human Molecular Genetics. 22: 5136-45. PMID 23918662 DOI: 10.1093/Hmg/Ddt367 |
0.349 |
|
| 2013 |
Seo S, Mullins RF, Dumitrescu AV, Bhattarai S, Gratie D, Wang K, Stone EM, Sheffield V, Drack AV. Subretinal gene therapy of mice with Bardet-Biedl syndrome type 1. Investigative Ophthalmology & Visual Science. 54: 6118-32. PMID 23900607 DOI: 10.1167/Iovs.13-11673 |
0.43 |
|
| 2013 |
Abrà moff MD, Mullins RF, Lee K, Hoffmann JM, Sonka M, Critser DB, Stasheff SF, Stone EM. Human photoreceptor outer segments shorten during light adaptation. Investigative Ophthalmology & Visual Science. 54: 3721-8. PMID 23633665 DOI: 10.1167/Iovs.13-11812 |
0.327 |
|
| 2013 |
Wagner AH, Taylor KR, DeLuca AP, Casavant TL, Mullins RF, Stone EM, Scheetz TE, Braun TA. Prioritization of retinal disease genes: an integrative approach. Human Mutation. 34: 853-9. PMID 23508994 DOI: 10.1002/Humu.22317 |
0.373 |
|
| 2013 |
Wagner AH, Anand VN, Wang WH, Chatterton JE, Sun D, Shepard AR, Jacobson N, Pang IH, Deluca AP, Casavant TL, Scheetz TE, Mullins RF, Braun TA, Clark AF. Exon-level expression profiling of ocular tissues. Experimental Eye Research. 111: 105-11. PMID 23500522 DOI: 10.1016/J.Exer.2013.03.004 |
0.367 |
|
| 2013 |
Tucker BA, Anfinson KR, Mullins RF, Stone EM, Young MJ. Use of a synthetic xeno-free culture substrate for induced pluripotent stem cell induction and retinal differentiation. Stem Cells Translational Medicine. 2: 16-24. PMID 23283489 DOI: 10.5966/Sctm.2012-0040 |
0.391 |
|
| 2013 |
Tucker BA, Mullins RF, Streb LM, Anfinson K, Eyestone ME, Kaalberg E, Riker MJ, Drack AV, Braun TA, Stone EM. Author response: Patient-specific iPSC-derived photoreceptor precursor cells as a means to investigate retinitis pigmentosa Elife. DOI: 10.7554/Elife.00824.015 |
0.406 |
|
| 2013 |
Tucker BA, Mullins RF, Streb LM, Anfnson K, Eyestone ME, Kaalberg E, Riker MJ, Drack AV, Braun TA, Stone EM. Patient-specifc iPSC-derived photoreceptor precursor cells as a means to investigate retinitis pigmentosa Elife. 2013. DOI: 10.7554/eLife.00824.001 |
0.301 |
|
| 2012 |
Zhang L, Lee K, Niemeijer M, Mullins RF, Sonka M, Abràmoff MD. Automated segmentation of the choroid from clinical SD-OCT. Investigative Ophthalmology & Visual Science. 53: 7510-9. PMID 23060139 DOI: 10.1167/Iovs.12-10311 |
0.325 |
|
| 2012 |
Mullins RF, Kuehn MH, Radu RA, Enriquez GS, East JS, Schindler EI, Travis GH, Stone EM. Autosomal recessive retinitis pigmentosa due to ABCA4 mutations: clinical, pathologic, and molecular characterization. Investigative Ophthalmology & Visual Science. 53: 1883-94. PMID 22395892 DOI: 10.1167/Iovs.12-9477 |
0.472 |
|
| 2012 |
Whitmore SS, Mullins RF. Transcriptome changes in age-related macular degeneration. Bmc Medicine. 10: 21. PMID 22369667 DOI: 10.1186/1741-7015-10-21 |
0.456 |
|
| 2012 |
Zeng S, Hernández J, Mullins RF. Effects of antioxidant components of AREDS vitamins and zinc ions on endothelial cell activation: implications for macular degeneration. Investigative Ophthalmology & Visual Science. 53: 1041-7. PMID 22247465 DOI: 10.1167/Iovs.11-8531 |
0.392 |
|
| 2012 |
Skeie JM, Hernandez J, Hinek A, Mullins RF. Molecular responses of choroidal endothelial cells to elastin derived peptides through the elastin-binding protein (GLB1). Matrix Biology : Journal of the International Society For Matrix Biology. 31: 113-9. PMID 22178079 DOI: 10.1016/J.Matbio.2011.11.003 |
0.709 |
|
| 2012 |
Drack AV, Dumitrescu AV, Bhattarai S, Gratie D, Stone EM, Mullins R, Sheffield VC. TUDCA slows retinal degeneration in two different mouse models of retinitis pigmentosa and prevents obesity in Bardet-Biedl syndrome type 1 mice. Investigative Ophthalmology & Visual Science. 53: 100-6. PMID 22110077 DOI: 10.1167/Iovs.11-8544 |
0.329 |
|
| 2012 |
Kay CN, Abramoff MD, Mullins RF, Kinnick TR, Lee K, Eyestone ME, Chung MM, Sohn EH, Stone EM. Three-dimensional distribution of the vitelliform lesion, photoreceptors, and retinal pigment epithelium in the macula of patients with best vitelliform macular dystrophy. Archives of Ophthalmology (Chicago, Ill. : 1960). 130: 357-64. PMID 22084158 DOI: 10.1001/Archophthalmol.2011.363 |
0.416 |
|
| 2012 |
Sohn EH, Mullins RF, Stone EM. Macular Dystrophies Retina Fifth Edition. 2: 852-890. DOI: 10.1016/B978-1-4557-0737-9.00042-4 |
0.329 |
|
| 2011 |
Tucker BA, Scheetz TE, Mullins RF, DeLuca AP, Hoffmann JM, Johnston RM, Jacobson SG, Sheffield VC, Stone EM. Exome sequencing and analysis of induced pluripotent stem cells identify the cilia-related gene male germ cell-associated kinase (MAK) as a cause of retinitis pigmentosa. Proceedings of the National Academy of Sciences of the United States of America. 108: E569-76. PMID 21825139 DOI: 10.1073/Pnas.1108918108 |
0.415 |
|
| 2011 |
Mullins RF, Dewald AD, Streb LM, Wang K, Kuehn MH, Stone EM. Elevated membrane attack complex in human choroid with high risk complement factor H genotypes. Experimental Eye Research. 93: 565-7. PMID 21729696 DOI: 10.1016/J.Exer.2011.06.015 |
0.365 |
|
| 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 |
0.707 |
|
| 2011 |
Ko AC, Brinton JP, Mahajan VB, Zimmerman B, Brinton GS, Stone EM, Folk JC, Mullins RF. Seroreactivity against aqueous-soluble and detergent-soluble retinal proteins in posterior uveitis. Archives of Ophthalmology (Chicago, Ill. : 1960). 129: 415-20. PMID 21482867 DOI: 10.1001/Archophthalmol.2011.65 |
0.409 |
|
| 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 |
0.342 |
|
| 2011 |
Mullins RF, Johnson MN, Faidley EA, Skeie JM, Huang J. Choriocapillaris vascular dropout related to density of drusen in human eyes with early age-related macular degeneration. Investigative Ophthalmology & Visual Science. 52: 1606-12. PMID 21398287 DOI: 10.1167/Iovs.10-6476 |
0.71 |
|
| 2011 |
Skeie JM, Zeng S, Faidley EA, Mullins RF. Angiogenin in age-related macular degeneration. Molecular Vision. 17: 576-82. PMID 21364907 |
0.732 |
|
| 2011 |
Kinnick TR, Mullins RF, Dev S, Leys M, Mackey DA, Kay CN, Lam BL, Fishman GA, Traboulsi E, Iezzi R, Stone EM. Autosomal recessive vitelliform macular dystrophy in a large cohort of vitelliform macular dystrophy patients. Retina (Philadelphia, Pa.). 31: 581-95. PMID 21273940 DOI: 10.1097/Iae.0B013E318203Ee60 |
0.354 |
|
| 2011 |
Stone EM, Cideciyan AV, Aleman TS, Scheetz TE, Sumaroka A, Ehlinger MA, Schwartz SB, Fishman GA, Traboulsi EI, Lam BL, Fulton AB, Mullins RF, Sheffield VC, Jacobson SG. Variations in NPHP5 in patients with nonsyndromic leber congenital amaurosis and Senior-Loken syndrome. Archives of Ophthalmology (Chicago, Ill. : 1960). 129: 81-7. PMID 21220633 DOI: 10.1001/Archophthalmol.2010.330 |
0.367 |
|
| 2011 |
Thompson S, Stasheff SF, Hernandez J, Nylen E, East JS, Kardon RH, Pinto LH, Mullins RF, Stone EM. Different inner retinal pathways mediate rod-cone input in irradiance detection for the pupillary light reflex and regulation of behavioral state in mice. Investigative Ophthalmology & Visual Science. 52: 618-23. PMID 20847113 DOI: 10.1167/Iovs.10-6146 |
0.384 |
|
| 2010 |
Ko AC, Hernández J, Brinton JP, Faidley EA, Mugge SA, Mets MB, Kardon RH, Folk JC, Mullins RF, Stone EM. Anti-γ-enolase autoimmune retinopathy manifesting in early childhood. Archives of Ophthalmology (Chicago, Ill. : 1960). 128: 1590-5. PMID 21149784 DOI: 10.1001/Archophthalmol.2010.295 |
0.423 |
|
| 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 |
0.675 |
|
| 2010 |
Pretorius PR, Baye LM, Nishimura DY, Searby CC, Bugge K, Yang B, Mullins RF, Stone EM, Sheffield VC, Slusarski DC. Identification and functional analysis of the vision-specific BBS3 (ARL6) long isoform. Plos Genetics. 6: e1000884. PMID 20333246 DOI: 10.1371/Journal.Pgen.1000884 |
0.387 |
|
| 2010 |
Mullins RF, Skeie JM. Essentials of retinal morphology Neuromethods. 46: 1-11. DOI: 10.1007/978-1-60761-541-5_1 |
0.661 |
|
| 2009 |
Mullins RF, Faidley EA, Daggett HT, Jomary C, Lotery AJ, Stone EM. Localization of complement 1 inhibitor (C1INH/SERPING1) in human eyes with age-related macular degeneration. Experimental Eye Research. 89: 767-73. PMID 19607829 DOI: 10.1016/J.Exer.2009.07.001 |
0.481 |
|
| 2009 |
Skeie JM, Mullins RF. Macrophages in neovascular age-related macular degeneration: friends or foes? Eye (London, England). 23: 747-55. PMID 18600240 DOI: 10.1038/Eye.2008.206 |
0.711 |
|
| 2008 |
Ennis S, Jomary C, Mullins R, Cree A, Chen X, MacLeod A, Jones S, Collins A, Stone E, Lotery A. Association between the SERPING1 gene and age-related macular degeneration: a two-stage case-control study The Lancet. 372: 1828-1834. PMID 18842294 DOI: 10.1016/S0140-6736(08)61348-3 |
0.372 |
|
| 2008 |
Skeie JM, Mullins RF. Elastin-mediated choroidal endothelial cell migration: possible role in age-related macular degeneration. Investigative Ophthalmology & Visual Science. 49: 5574-80. PMID 18708613 DOI: 10.1167/Iovs.08-1984 |
0.714 |
|
| 2008 |
Thompson S, Mullins RF, Philp AR, Stone EM, Mrosovsky N. Divergent phenotypes of vision and accessory visual function in mice with visual cycle dysfunction (Rpe65 rd12) or retinal degeneration (rd/rd). Investigative Ophthalmology & Visual Science. 49: 2737-42. PMID 18515598 DOI: 10.1167/Iovs.07-1546 |
0.364 |
|
| 2008 |
Jones YJ, Goins KM, Sutphin JE, Mullins R, Skeie JM. Comparison of the femtosecond laser (IntraLase) versus manual microkeratome (Moria ALTK) in dissection of the donor in endothelial keratoplasty: initial study in eye bank eyes. Cornea. 27: 88-93. PMID 18245973 DOI: 10.1097/Ico.0B013E31815771F5 |
0.676 |
|
| 2007 |
Davis RE, Swiderski RE, Rahmouni K, Nishimura DY, Mullins RF, Agassandian K, Philp AR, Searby CC, Andrews MP, Thompson S, Berry CJ, Thedens DR, Yang B, Weiss RM, Cassell MD, et al. A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity. Proceedings of the National Academy of Sciences of the United States of America. 104: 19422-7. PMID 18032602 DOI: 10.1073/Pnas.0708571104 |
0.303 |
|
| 2007 |
Ismail AR, Cates CA, Mullins RF, Manners RM, Lotery AJ. Autosomal dominant early onset aponeurotic ptosis and corneal limbal vascularization in a three-generation family. Ophthalmic Plastic and Reconstructive Surgery. 23: 484-6. PMID 18030124 DOI: 10.1097/Iop.0B013E318157D3F9 |
0.309 |
|
| 2007 |
Mullins RF, Kuehn MH, Faidley EA, Syed NA, Stone EM. Differential macular and peripheral expression of bestrophin in human eyes and its implication for best disease. Investigative Ophthalmology & Visual Science. 48: 3372-80. PMID 17591911 DOI: 10.1167/Iovs.06-0868 |
0.433 |
|
| 2007 |
Swiderski RE, Nishimura DY, Mullins RF, Olvera MA, Ross JL, Huang J, Stone EM, Sheffield VC. Gene expression analysis of photoreceptor cell loss in bbs4-knockout mice reveals an early stress gene response and photoreceptor cell damage. Investigative Ophthalmology & Visual Science. 48: 3329-40. PMID 17591906 DOI: 10.1167/Iovs.06-1477 |
0.45 |
|
| 2007 |
Bakall B, Radu RA, Stanton JB, Burke JM, McKay BS, Wadelius C, Mullins RF, Stone EM, Travis GH, Marmorstein AD. Enhanced accumulation of A2E in individuals homozygous or heterozygous for mutations in BEST1 (VMD2). Experimental Eye Research. 85: 34-43. PMID 17477921 DOI: 10.1016/J.Exer.2007.02.018 |
0.415 |
|
| 2007 |
Guziewicz KE, Zangerl B, Lindauer SJ, Mullins RF, Sandmeyer LS, Grahn BH, Stone EM, Acland GM, Aguirre GD. Bestrophin gene mutations cause canine multifocal retinopathy: a novel animal model for best disease. Investigative Ophthalmology & Visual Science. 48: 1959-67. PMID 17460247 DOI: 10.1167/Iovs.06-1374 |
0.35 |
|
| 2007 |
Pinto LH, Vitaterna MH, Shimomura K, Siepka SM, Balannik V, McDearmon EL, Omura C, Lumayag S, Invergo BM, Glawe B, Cantrell DR, Inayat S, Olvera MA, Vessey KA, McCall MA, ... ... Mullins RF, et al. Generation, identification and functional characterization of the nob4 mutation of Grm6 in the mouse. Visual Neuroscience. 24: 111-23. PMID 17430614 DOI: 10.1017/S0952523807070149 |
0.381 |
|
| 2007 |
Mullins RF. Genetic insights into the pathobiology of age-related macular degeneration. International Ophthalmology Clinics. 47: 1-14. PMID 17237671 DOI: 10.1097/Iio.0B013E31802Bd3E6 |
0.325 |
|
| 2007 |
Mullins RF, Olvera MA, Clark AF, Stone EM. Fibulin-5 distribution in human eyes: relevance to age-related macular degeneration. Experimental Eye Research. 84: 378-80. PMID 17109857 DOI: 10.1016/J.Exer.2006.09.021 |
0.464 |
|
| 2007 |
Clapper JD, Skeie JM, Mullins RF, Guymon CA. Development and characterization of photopolymerizable biodegradable materials from PEG-PLA-PEG block macromonomers Polymer. 48: 6554-6564. DOI: 10.1016/J.Polymer.2007.08.023 |
0.622 |
|
| 2006 |
Zangerl B, Goldstein O, Philp AR, Lindauer SJ, Pearce-Kelling SE, Mullins RF, Graphodatsky AS, Ripoll D, Felix JS, Stone EM, Acland GM, Aguirre GD. Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humans. Genomics. 88: 551-63. PMID 16938425 DOI: 10.1016/J.Ygeno.2006.07.007 |
0.427 |
|
| 2006 |
Mullins RF, Skeie JM, Malone EA, Kuehn MH. Macular and peripheral distribution of ICAM-1 in the human choriocapillaris and retina. Molecular Vision. 12: 224-35. PMID 16604055 |
0.713 |
|
| 2005 |
Pinto LH, Vitaterna MH, Shimomura K, Siepka SM, McDearmon EL, Fenner D, Lumayag SL, Omura C, Andrews AW, Baker M, Invergo BM, Olvera MA, Heffron E, Mullins RF, Sheffield VC, et al. Generation, characterization, and molecular cloning of the Noerg-1 mutation of rhodopsin in the mouse. Visual Neuroscience. 22: 619-29. PMID 16332273 DOI: 10.1017/S0952523805225117 |
0.402 |
|
| 2005 |
Mullins RF, Oh KT, Heffron E, Hageman GS, Stone EM. Late development of vitelliform lesions and flecks in a patient with best disease: clinicopathologic correlation. Archives of Ophthalmology (Chicago, Ill. : 1960). 123: 1588-94. PMID 16286623 DOI: 10.1001/Archopht.123.11.1588 |
0.422 |
|
| 2005 |
Mullins RF, Grassi MA, Skeie JM. Glycoconjugates of choroidal neovascular membranes in age-related macular degeneration. Molecular Vision. 11: 509-17. PMID 16052166 |
0.719 |
|
| 2005 |
Goverdhan SV, Howell MW, Mullins RF, Osmond C, Hodgkins PR, Self J, Avery K, Lotery AJ. Association of HLA class I and class II polymorphisms with age-related macular degeneration. Investigative Ophthalmology & Visual Science. 46: 1726-34. PMID 15851575 DOI: 10.1167/Iovs.04-0928 |
0.312 |
|
| 2005 |
Chong NH, Keonin J, Luthert PJ, Frennesson CI, Weingeist DM, Wolf RL, Mullins RF, Hageman GS. Decreased thickness and integrity of the macular elastic layer of Bruch's membrane correspond to the distribution of lesions associated with age-related macular degeneration. The American Journal of Pathology. 166: 241-51. PMID 15632016 DOI: 10.1016/S0002-9440(10)62248-1 |
0.405 |
|
| 2004 |
Nishimura DY, Fath M, Mullins RF, Searby C, Andrews M, Davis R, Andorf JL, Mykytyn K, Swiderski RE, Yang B, Carmi R, Stone EM, Sheffield VC. Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin. Proceedings of the National Academy of Sciences of the United States of America. 101: 16588-93. PMID 15539463 DOI: 10.1073/Pnas.0405496101 |
0.32 |
|
| 2004 |
Mykytyn K, Mullins RF, Andrews M, Chiang AP, Swiderski RE, Yang B, Braun T, Casavant T, Stone EM, Sheffield VC. Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assembly. Proceedings of the National Academy of Sciences of the United States of America. 101: 8664-9. PMID 15173597 DOI: 10.1073/Pnas.0402354101 |
0.327 |
|
| 2003 |
Lotery AJ, Yang GS, Mullins RF, Russell SR, Schmidt M, Stone EM, Lindbloom JD, Chiorini JA, Kotin RM, Davidson BL. Adeno-associated virus type 5: transduction efficiency and cell-type specificity in the primate retina. Human Gene Therapy. 14: 1663-71. PMID 14633408 DOI: 10.1089/104303403322542301 |
0.434 |
|
| 2002 |
Anderson DH, Mullins RF, Hageman GS, Johnson LV. A role for local inflammation in the formation of drusen in the aging eye. American Journal of Ophthalmology. 134: 411-31. PMID 12208254 DOI: 10.1016/S0002-9394(02)01624-0 |
0.375 |
|
| 2002 |
Lotery AJ, Derksen TA, Russell SR, Mullins RF, Sauter S, Affatigato LM, Stone EM, Davidson BL. Gene transfer to the nonhuman primate retina with recombinant feline immunodeficiency virus vectors. Human Gene Therapy. 13: 689-96. PMID 11936968 DOI: 10.1089/104303402317322258 |
0.42 |
|
| 2001 |
Hageman GS, Luthert PJ, Victor Chong NH, Johnson LV, Anderson DH, Mullins RF. An integrated hypothesis that considers drusen as biomarkers of immune-mediated processes at the RPE-Bruch's membrane interface in aging and age-related macular degeneration. Progress in Retinal and Eye Research. 20: 705-32. PMID 11587915 DOI: 10.1016/S1350-9462(01)00010-6 |
0.421 |
|
| 2001 |
Mullins RF, Aptsiauri N, Hageman GS. Structure and composition of drusen associated with glomerulonephritis: Implications for the role of complement activation in drusen biogenesis Eye. 15: 390-395. PMID 11450763 DOI: 10.1038/Eye.2001.142 |
0.395 |
|
| 2001 |
Anderson DH, Ozaki S, Nealon M, Neitz J, Mullins RF, Hageman GS, Johnson LV. Local cellular sources of apolipoprotein E in the human retina and retinal pigmented epithelium: implications for the process of drusen formation. American Journal of Ophthalmology. 131: 767-81. PMID 11384575 DOI: 10.1016/S0002-9394(00)00961-2 |
0.418 |
|
| 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 |
0.322 |
|
| 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 |
0.378 |
|
| 2000 |
Mullins RF, Russell SR, Anderson DH, Hageman GS. Drusen associated with aging and age-related macular degeneration contain proteins common to extracellular deposits associated with atherosclerosis, elastosis, amyloidosis, and dense deposit disease. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 14: 835-46. PMID 10783137 DOI: 10.1096/Fasebj.14.7.835 |
0.425 |
|
| 2000 |
Russell SR, Mullins RF, Schneider BL, Hageman GS. Location, substructure, and composition of basal laminar drusen compared with drusen associated with aging and age-related macular degeneration. American Journal of Ophthalmology. 129: 205-14. PMID 10682974 DOI: 10.1016/S0002-9394(99)00345-1 |
0.32 |
|
| 1999 |
Mullins RF, Hageman GS. Human ocular drusen possess novel core domains with a distinct carbohydrate composition Journal of Histochemistry and Cytochemistry. 47: 1533-1539. PMID 10567437 DOI: 10.1177/002215549904701205 |
0.362 |
|
| 1999 |
Ozaki S, Johnson LV, Mullins RF, Hageman GS, Anderson DH. The human retina and retinal pigment epithelium are abundant sources of vitronectin mRNA. Biochemical and Biophysical Research Communications. 258: 524-9. PMID 10329419 DOI: 10.1006/Bbrc.1999.0672 |
0.35 |
|
| 1999 |
Hageman GS, Mullins RF, Russell SR, Johnson LV, Anderson DH. Vitronectin is a constituent of ocular drusen and the vitronectin gene is expressed in human retinal pigmented epithelial cells. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 13: 477-84. PMID 10064614 DOI: 10.1096/Fasebj.13.3.477 |
0.47 |
|
| 1997 |
Mullins RF, Johnson LV, Anderson DH, Hageman GS. Characterization of drusen-associated glycoconjugates. Ophthalmology. 104: 288-94. PMID 9052634 DOI: 10.1016/S0161-6420(97)30322-4 |
0.417 |
|
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