Eric A Pierce

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Kinga BujakowskaMassachusetts Eye and Ear Infirmary, Harvard Medical SchoolE-mail confirmado em meei.harvard.edu
Lois E. SmithProfessor of Ophthalmology, Harvard Medical School, Children's Hospital BostonE-mail confirmado em childrens.harvard.edu
Jean BennettUniversity of PennsylvaniaE-mail confirmado em pennmedicine.upenn.edu
Xiaowu GaiMedical College of WisconsinE-mail confirmado em mcw.edu
Michael H. FarkasAssociate Professor of Ophthalmology, State University of New York at BuffaloE-mail confirmado em buffalo.edu
Lloyd Paul Aiello, MD, PhDProfessor of Ophthalmology, Joslin Diabetes Center, Harvard Medical SchoolE-mail confirmado em joslin.harvard.edu
Rosario Fernández GodinoHead of Screening and Target Validation, Fundación MEDINAE-mail confirmado em meei.harvard.edu
Daniel Navarro-GomezOcular Genomics Institute, Massachusetts Eye and Ear Infirmary, Harvard Medical School, BostonE-mail confirmado em meei.harvard.edu
J Fraser WrightStanford UniversityE-mail confirmado em stanford.edu
Chris InglehearnProfessor of Molecular Ophthalmology, University of LeedsE-mail confirmado em leeds.ac.uk
David BirchChief Scientific and Executive Officer, Retina Foundation of the SouthwestE-mail confirmado em retinafoundation.org
Donald ZackWilmer institute, Johns Hopkins UniversityE-mail confirmado em jhmi.edu
Napoleone FerraraDistinguished Professor, Hildyard Endowed Chair in Eye Disease, UCSD Moores Cancer CenterE-mail confirmado em ucsd.edu
Joseph A. WhiteDana-Farber Cancer InstituteE-mail confirmado em jimmy.harvard.edu
Marni J. FalkDepartment of Pediatrics, The Children's Hospital of Philadelphia, University of PennsylvaniaE-mail confirmado em email.chop.edu
Sandro BanfiUniversita' della Campania "Luigi Vanvitelli" and TIGEM, ItalyE-mail confirmado em unina2.it
Edwin M. StoneUniversity of Iowa, Carver College of Medicine, Department of Ophthalmology and Visual SciencesE-mail confirmado em uiowa.edu

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Eric A Pierce

Ophthalmology, Harvard Medical School and Mass Eye and Ear

E-mail confirmado em broadinstitute.org - Página inicial

Inherited Retinal Degenerations Genomics Gene Therapy


Título Ordenar por citações Ordenar por ano Ordenar por título	Citado por Citado por	Ano
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	2630	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	1646	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	1300	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	1077	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	730	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	722	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	513	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	490	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	479	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	415*	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	414	2011
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	412	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	409	2013
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	391	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	387	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	257	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	244	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	225	2010
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	222	2012
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	211	2018

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