A citation-based method for searching scientific literature

Debra A Thompson, Robin R Ali, Eyal Banin, Kari E Branham, John G Flannery, David M Gamm, William W Hauswirth, John R Heckenlively, Alessandro Iannaccone, K Thiran Jayasundera, Naheed W Khan, Robert S Molday, Mark E Pennesi, Thomas A Reh, Richard G Weleber, David N Zacks. Invest Ophthalmol Vis Sci 2015
Times Cited: 61







List of co-cited articles
538 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Long-term effect of gene therapy on Leber's congenital amaurosis.
James W B Bainbridge, Manjit S Mehat, Venki Sundaram, Scott J Robbie, Susie E Barker, Caterina Ripamonti, Anastasios Georgiadis, Freya M Mowat, Stuart G Beattie, Peter J Gardner,[...]. N Engl J Med 2015
456
22

Efficacy and safety of voretigene neparvovec (AAV2-hRPE65v2) in patients with RPE65-mediated inherited retinal dystrophy: a randomised, controlled, open-label, phase 3 trial.
Stephen Russell, Jean Bennett, Jennifer A Wellman, Daniel C Chung, Zi-Fan Yu, Amy Tillman, Janet Wittes, Julie Pappas, Okan Elci, Sarah McCague,[...]. Lancet 2017
725
21

Effect of gene therapy on visual function in Leber's congenital amaurosis.
James W B Bainbridge, Alexander J Smith, Susie S Barker, Scott Robbie, Robert Henderson, Kamaljit Balaggan, Ananth Viswanathan, Graham E Holder, Andrew Stockman, Nick Tyler,[...]. N Engl J Med 2008
19

Gene therapy for leber congenital amaurosis caused by RPE65 mutations: safety and efficacy in 15 children and adults followed up to 3 years.
Samuel G Jacobson, Artur V Cideciyan, Ramakrishna Ratnakaram, Elise Heon, Sharon B Schwartz, Alejandro J Roman, Marc C Peden, Tomas S Aleman, Sanford L Boye, Alexander Sumaroka,[...]. Arch Ophthalmol 2012
440
19

Retinal gene therapy in patients with choroideremia: initial findings from a phase 1/2 clinical trial.
Robert E MacLaren, Markus Groppe, Alun R Barnard, Charles L Cottriall, Tanya Tolmachova, Len Seymour, K Reed Clark, Matthew J During, Frans P M Cremers, Graeme C M Black,[...]. Lancet 2014
522
18

Safety and efficacy of gene transfer for Leber's congenital amaurosis.
Albert M Maguire, Francesca Simonelli, Eric A Pierce, Edward N Pugh, Federico Mingozzi, Jeannette Bennicelli, Sandro Banfi, Kathleen A Marshall, Francesco Testa, Enrico M Surace,[...]. N Engl J Med 2008
18

Human embryonic stem cell-derived retinal pigment epithelium in patients with age-related macular degeneration and Stargardt's macular dystrophy: follow-up of two open-label phase 1/2 studies.
Steven D Schwartz, Carl D Regillo, Byron L Lam, Dean Eliott, Philip J Rosenfeld, Ninel Z Gregori, Jean-Pierre Hubschman, Janet L Davis, Gad Heilwell, Marc Spirn,[...]. Lancet 2015
720
18

Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvement.
Artur V Cideciyan, Samuel G Jacobson, William A Beltran, Alexander Sumaroka, Malgorzata Swider, Simone Iwabe, Alejandro J Roman, Melani B Olivares, Sharon B Schwartz, András M Komáromy,[...]. Proc Natl Acad Sci U S A 2013
301
14

Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics.
Artur V Cideciyan, Tomas S Aleman, Sanford L Boye, Sharon B Schwartz, Shalesh Kaushal, Alejandro J Roman, Ji-Jing Pang, Alexander Sumaroka, Elizabeth A M Windsor, James M Wilson,[...]. Proc Natl Acad Sci U S A 2008
538
14

Improvement and decline in vision with gene therapy in childhood blindness.
Samuel G Jacobson, Artur V Cideciyan, Alejandro J Roman, Alexander Sumaroka, Sharon B Schwartz, Elise Heon, William W Hauswirth. N Engl J Med 2015
243
14

The Natural History of the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Studies: Design and Baseline Characteristics: ProgStar Report No. 1.
Rupert W Strauss, Alex Ho, Beatriz Muñoz, Artur V Cideciyan, José-Alain Sahel, Janet S Sunness, David G Birch, Paul S Bernstein, Michel Michaelides, Elias I Traboulsi,[...]. Ophthalmology 2016
94
14

Retinitis pigmentosa.
Dyonne T Hartong, Eliot L Berson, Thaddeus P Dryja. Lancet 2006
13

Treatment of leber congenital amaurosis due to RPE65 mutations by ocular subretinal injection of adeno-associated virus gene vector: short-term results of a phase I trial.
William W Hauswirth, Tomas S Aleman, Shalesh Kaushal, Artur V Cideciyan, Sharon B Schwartz, Lili Wang, Thomas J Conlon, Sanford L Boye, Terence R Flotte, Barry J Byrne,[...]. Hum Gene Ther 2008
726
13

Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial.
Albert M Maguire, Katherine A High, Alberto Auricchio, J Fraser Wright, Eric A Pierce, Francesco Testa, Federico Mingozzi, Jeannette L Bennicelli, Gui-shuang Ying, Settimio Rossi,[...]. Lancet 2009
592
11

In vivo-directed evolution of a new adeno-associated virus for therapeutic outer retinal gene delivery from the vitreous.
Deniz Dalkara, Leah C Byrne, Ryan R Klimczak, Meike Visel, Lu Yin, William H Merigan, John G Flannery, David V Schaffer. Sci Transl Med 2013
401
11

Restoration of vision after transplantation of photoreceptors.
R A Pearson, A C Barber, M Rizzi, C Hippert, T Xue, E L West, Y Duran, A J Smith, J Z Chuang, S A Azam,[...]. Nature 2012
328
11

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy.
R Allikmets, N Singh, H Sun, N F Shroyer, A Hutchinson, A Chidambaram, B Gerrard, L Baird, D Stauffer, A Peiffer,[...]. Nat Genet 1997
991
11

Let There Be Light: Gene and Cell Therapy for Blindness.
Deniz Dalkara, Olivier Goureau, Katia Marazova, José-Alain Sahel. Hum Gene Ther 2016
78
11

Gene therapy for blindness.
José-Alain Sahel, Botond Roska. Annu Rev Neurosci 2013
95
9

Three-year follow-up after unilateral subretinal delivery of adeno-associated virus in patients with Leber congenital Amaurosis type 2.
Francesco Testa, Albert M Maguire, Settimio Rossi, Eric A Pierce, Paolo Melillo, Kathleen Marshall, Sandro Banfi, Enrico M Surace, Junwei Sun, Carmela Acerra,[...]. Ophthalmology 2013
225
9

Genetic reactivation of cone photoreceptors restores visual responses in retinitis pigmentosa.
Volker Busskamp, Jens Duebel, David Balya, Mathias Fradot, Tim James Viney, Sandra Siegert, Anna C Groner, Erik Cabuy, Valérie Forster, Mathias Seeliger,[...]. Science 2010
399
9

A randomized trial of vitamin A and vitamin E supplementation for retinitis pigmentosa.
E L Berson, B Rosner, M A Sandberg, K C Hayes, B W Nicholson, C Weigel-DiFranco, W Willett. Arch Ophthalmol 1993
391
9

Histopathology of the human retina in retinitis pigmentosa.
A H Milam, Z Y Li, R N Fariss. Prog Retin Eye Res 1998
457
9

Retinal repair by transplantation of photoreceptor precursors.
R E MacLaren, R A Pearson, A MacNeil, R H Douglas, T E Salt, M Akimoto, A Swaroop, J C Sowden, R R Ali. Nature 2006
754
9

Visual acuity as an outcome measure in clinical trials of retinal diseases.
Roy W Beck, Maureen G Maguire, Neil M Bressler, Adam R Glassman, Anne S Lindblad, Frederick L Ferris. Ophthalmology 2007
109
9

Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat.
P M D'Cruz, D Yasumura, J Weir, M T Matthes, H Abderrahim, M M LaVail, D Vollrath. Hum Mol Genet 2000
671
9

Emerging therapies for inherited retinal degeneration.
Hendrik P N Scholl, Rupert W Strauss, Mandeep S Singh, Deniz Dalkara, Botond Roska, Serge Picaud, José-Alain Sahel. Sci Transl Med 2016
125
9

Stargardt disease: clinical features, molecular genetics, animal models and therapeutic options.
Preena Tanna, Rupert W Strauss, Kaoru Fujinami, Michel Michaelides. Br J Ophthalmol 2017
152
9

Neural remodeling in retinal degeneration.
Robert E Marc, Bryan W Jones, Carl B Watt, Enrica Strettoi. Prog Retin Eye Res 2003
598
8


Gene therapy restores vision in a canine model of childhood blindness.
G M Acland, G D Aguirre, J Ray, Q Zhang, T S Aleman, A V Cideciyan, S E Pearce-Kelling, V Anand, Y Zeng, A M Maguire,[...]. Nat Genet 2001
862
8

AAV2 gene therapy readministration in three adults with congenital blindness.
Jean Bennett, Manzar Ashtari, Jennifer Wellman, Kathleen A Marshall, Laura L Cyckowski, Daniel C Chung, Sarah McCague, Eric A Pierce, Yifeng Chen, Jeannette L Bennicelli,[...]. Sci Transl Med 2012
282
8

Clinical trial of docosahexaenoic acid in patients with retinitis pigmentosa receiving vitamin A treatment.
Eliot L Berson, Bernard Rosner, Michael A Sandberg, Carol Weigel-DiFranco, Ann Moser, Robert J Brockhurst, K C Hayes, Chris A Johnson, Ellen J Anderson, Alexander R Gaudio,[...]. Arch Ophthalmol 2004
97
8

Interim results from the international trial of Second Sight's visual prosthesis.
Mark S Humayun, Jessy D Dorn, Lyndon da Cruz, Gislin Dagnelie, José-Alain Sahel, Paulo E Stanga, Artur V Cideciyan, Jacque L Duncan, Dean Eliott, Eugene Filley,[...]. Ophthalmology 2012
383
8

Viral-mediated RdCVF and RdCVFL expression protects cone and rod photoreceptors in retinal degeneration.
Leah C Byrne, Deniz Dalkara, Gabriel Luna, Steven K Fisher, Emmanuelle Clérin, Jose-Alain Sahel, Thierry Léveillard, John G Flannery. J Clin Invest 2015
108
8

A longitudinal study of Stargardt disease: quantitative assessment of fundus autofluorescence, progression, and genotype correlations.
Kaoru Fujinami, Noemi Lois, Rajarshi Mukherjee, Vikki A McBain, Kazushige Tsunoda, Kazuo Tsubota, Edwin M Stone, Fred W Fitzke, Catey Bunce, Anthony T Moore,[...]. Invest Ophthalmol Vis Sci 2013
87
8

Visual acuity loss and clinical observations in a large series of patients with Stargardt disease.
Ygal Rotenstreich, Gerald A Fishman, Robert J Anderson. Ophthalmology 2003
149
8

Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing.
Mark B Consugar, Daniel Navarro-Gomez, Emily M Place, Kinga M Bujakowska, Maria E Sousa, Zoë D Fonseca-Kelly, Daniel G Taub, Maria Janessian, Dan Yi Wang, Elizabeth D Au,[...]. Genet Med 2015
157
8

Biology and therapy of inherited retinal degenerative disease: insights from mouse models.
Shobi Veleri, Csilla H Lazar, Bo Chang, Paul A Sieving, Eyal Banin, Anand Swaroop. Dis Model Mech 2015
145
8

Results at 2 Years after Gene Therapy for RPE65-Deficient Leber Congenital Amaurosis and Severe Early-Childhood-Onset Retinal Dystrophy.
Richard G Weleber, Mark E Pennesi, David J Wilson, Shalesh Kaushal, Laura R Erker, Lauren Jensen, Maureen T McBride, Terence R Flotte, Margaret Humphries, Roberto Calcedo,[...]. Ophthalmology 2016
115
8

Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa.
A Gal, Y Li, D A Thompson, J Weir, U Orth, S G Jacobson, E Apfelstedt-Sylla, D Vollrath. Nat Genet 2000
511
8

Visual Acuity Loss and Associated Risk Factors in the Retrospective Progression of Stargardt Disease Study (ProgStar Report No. 2).
Xiangrong Kong, Rupert W Strauss, Michel Michaelides, Artur V Cideciyan, José-Alain Sahel, Beatriz Muñoz, Sheila West, Hendrik P N Scholl. Ophthalmology 2016
48
10

Progression of Stargardt Disease as Determined by Fundus Autofluorescence in the Retrospective Progression of Stargardt Disease Study (ProgStar Report No. 9).
Rupert W Strauss, Beatriz Muñoz, Alexander Ho, Anamika Jha, Michel Michaelides, Artur V Cideciyan, Isabelle Audo, David G Birch, Amir H Hariri, Muneeswar G Nittala,[...]. JAMA Ophthalmol 2017
53
9

Inherited Retinal Degenerations: Current Landscape and Knowledge Gaps.
Jacque L Duncan, Eric A Pierce, Amy M Laster, Stephen P Daiger, David G Birch, John D Ash, Alessandro Iannaccone, John G Flannery, José A Sahel, Donald J Zack,[...]. Transl Vis Sci Technol 2018
79
8

Leber congenital amaurosis: genes, proteins and disease mechanisms.
Anneke I den Hollander, Ronald Roepman, Robert K Koenekoop, Frans P M Cremers. Prog Retin Eye Res 2008
544
6

Cellular responses following retinal injuries and therapeutic approaches for neurodegenerative diseases.
Nicolás Cuenca, Laura Fernández-Sánchez, Laura Campello, Victoria Maneu, Pedro De la Villa, Pedro Lax, Isabel Pinilla. Prog Retin Eye Res 2014
244
6


A comprehensive review of retinal gene therapy.
Shannon E Boye, Sanford L Boye, Alfred S Lewin, William W Hauswirth. Mol Ther 2013
194
6

Identification and characterization of rod-derived cone viability factor.
Thierry Léveillard, Saddek Mohand-Saïd, Olivier Lorentz, David Hicks, Anne-Claire Fintz, Emmanuelle Clérin, Manuel Simonutti, Valérie Forster, Nükhet Cavusoglu, Frédéric Chalmel,[...]. Nat Genet 2004
295
6

Protection of mouse photoreceptors by survival factors in retinal degenerations.
M M LaVail, D Yasumura, M T Matthes, C Lau-Villacorta, K Unoki, C H Sung, R H Steinberg. Invest Ophthalmol Vis Sci 1998
420
6


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.