| Safety and efficacy of gene transfer for Leber's congenital amaurosis AM Maguire, F Simonelli, EA Pierce, EN Pugh Jr, F Mingozzi, J Bennicelli, ... New England Journal of Medicine 358 (21), 2240-2248, 2008 | 2632 | 2008 |
| Suppression of retinal neovascularization in vivo by inhibition of vascular endothelial growth factor (VEGF) using soluble VEGF-receptor chimeric proteins LP Aiello, EA Pierce, ED Foley, H Takagi, H Chen, L Riddle, N Ferrara, ... Proceedings of the National Academy of Sciences 92 (23), 10457-10461, 1995 | 1649 | 1995 |
| Vascular endothelial growth factor/vascular permeability factor expression in a mouse model of retinal neovascularization EA Pierce, RL Avery, ED Foley, LP Aiello, LE Smith Proceedings of the National Academy of Sciences 92 (3), 905-909, 1995 | 1281 | 1995 |
| Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial AM Maguire, KA High, A Auricchio, JF Wright, EA Pierce, F Testa, ... The Lancet 374 (9701), 1597-1605, 2009 | 1083 | 2009 |
| Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administration F Simonelli, AM Maguire, F Testa, EA Pierce, F Mingozzi, JL Bennicelli, ... Molecular Therapy 18 (3), 643-650, 2010 | 736 | 2010 |
| Regulation of vascular endothelial growth factor by oxygen in a model of retinopathy of prematurity EA Pierce, ED Foley, LEH Smith Archives of ophthalmology 114 (10), 1219-1228, 1996 | 724 | 1996 |
| Safety and durability of effect of contralateral-eye administration of AAV2 gene therapy in patients with childhood-onset blindness caused by RPE65 mutations: a … J Bennett, J Wellman, KA Marshall, S McCague, M Ashtari, ... The Lancet 388 (10045), 661-672, 2016 | 519 | 2016 |
| Oligodeoxynucleotides inhibit retinal neovascularization in a murine model of proliferative retinopathy GS Robinson, EA Pierce, SL Rook, E Foley, R Webb, LE Smith Proceedings of the National Academy of Sciences 93 (10), 4851-4856, 1996 | 494 | 1996 |
| AAV2 gene therapy readministration in three adults with congenital blindness J Bennett, M Ashtari, J Wellman, KA Marshall, LL Cyckowski, DC Chung, ... Science translational medicine 4 (120), 120ra15-120ra15, 2012 | 483 | 2012 |
| TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum (vol 43, pg 189, 2011) EE Davis, Q Zhang, Q Liu, BH Diplas, LM Davey, J Hartley, C Stoetzel, ... NATURE GENETICS 43 (5), 499-499, 2011 | 422* | 2011 |
| TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum EE Davis, Q Zhang, Q Liu, BH Diplas, LM Davey, J Hartley, C Stoetzel, ... Nature genetics 43 (3), 189-196, 2011 | 421 | 2011 |
| Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with Leber congenital Amaurosis type 2 F Testa, AM Maguire, S Rossi, EA Pierce, P Melillo, K Marshall, S Banfi, ... Ophthalmology 120 (6), 1283-1291, 2013 | 410 | 2013 |
| Comparative analysis of RNA-Seq alignment algorithms and the RNA-Seq unified mapper (RUM) GR Grant, MH Farkas, AD Pizarro, NF Lahens, J Schug, BP Brunk, ... Bioinformatics 27 (18), 2518-2528, 2011 | 407 | 2011 |
| Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy EA Otto, TW Hurd, R Airik, M Chaki, W Zhou, C Stoetzel, SB Patil, S Levy, ... Nature genetics 42 (10), 840, 2010 | 394 | 2010 |
| The proteome of the mouse photoreceptor sensory cilium complex Q Liu, G Tan, N Levenkova, T Li, EN Pugh, JJ Rux, DW Speicher, ... Molecular & Cellular Proteomics 6 (8), 1299-1317, 2007 | 390 | 2007 |
| Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing MB Consugar, D Navarro-Gomez, EM Place, KM Bujakowska, ME Sousa, ... Genetics in Medicine 17 (4), 253-261, 2014 | 262 | 2014 |
| Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa EA Pierce, T Quinn, T Meehan, TL McGee, EL Berson, TP Dryja Nature genetics 22 (3), 248-254, 1999 | 250 | 1999 |
| Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy JA Poulter, M Ali, DF Gilmour, A Rice, H Kondo, K Hayashi, DA Mackey, ... The American Journal of Human Genetics 86 (2), 248-253, 2010 | 228 | 2010 |
| Inherited retinal degenerations: current landscape and knowledge gaps JL Duncan, EA Pierce, AM Laster, SP Daiger, DG Birch, JD Ash, ... Translational vision science & technology 7 (4), 6-6, 2018 | 227 | 2018 |
| NMNAT1 mutations cause Leber congenital amaurosis MJ Falk, Q Zhang, E Nakamaru-Ogiso, C Kannabiran, Z Fonseca-Kelly, ... Nature genetics 44 (9), 1040-1045, 2012 | 226 | 2012 |
Kinga BujakowskaMassachusetts Eye and Ear Infirmary, Harvard Medical Schoolยืนยันอีเมลแล้วที่ meei.harvard.edu