A citation-based method for searching scientific literature

T M Redmond, S Yu, E Lee, D Bok, D Hamasaki, N Chen, P Goletz, J X Ma, R K Crouch, K Pfeifer. Nat Genet 1998
Times Cited: 751







List of co-cited articles
1189 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Mutation of key residues of RPE65 abolishes its enzymatic role as isomerohydrolase in the visual cycle.
T Michael Redmond, Eugenia Poliakov, Shirley Yu, Jen-Yue Tsai, Zhongjian Lu, Susan Gentleman. Proc Natl Acad Sci U S A 2005
315
29

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
783
29

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
28

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
27

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
474
25

RPE65 is the isomerohydrolase in the retinoid visual cycle.
Gennadiy Moiseyev, Ying Chen, Yusuke Takahashi, Bill X Wu, Jian-Xing Ma. Proc Natl Acad Sci U S A 2005
388
23

Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy.
S M Gu, D A Thompson, C R Srikumari, B Lorenz, U Finckh, A Nicoletti, K R Murthy, M Rathmann, G Kumaramanickavel, M J Denton,[...]. Nat Genet 1997
501
20

Rpe65 is the retinoid isomerase in bovine retinal pigment epithelium.
Minghao Jin, Songhua Li, Walid N Moghrabi, Hui Sun, Gabriel H Travis. Cell 2005
339
20

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
867
18

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
250
18

Mutations in RPE65 cause Leber's congenital amaurosis.
F Marlhens, C Bareil, J M Griffoin, E Zrenner, P Amalric, C Eliaou, S Y Liu, E Harris, T M Redmond, B Arnaud,[...]. Nat Genet 1997
495
17

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
310
16

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
733
16

Safety and durability of effect of contralateral-eye administration of AAV2 gene therapy in patients with childhood-onset blindness caused by RPE65 mutations: a follow-on phase 1 trial.
Jean Bennett, Jennifer Wellman, Kathleen A Marshall, Sarah McCague, Manzar Ashtari, Julie DiStefano-Pappas, Okan U Elci, Daniel C Chung, Junwei Sun, J Fraser Wright,[...]. Lancet 2016
268
16

Lecithin-retinol acyltransferase is essential for accumulation of all-trans-retinyl esters in the eye and in the liver.
Matthew L Batten, Yoshikazu Imanishi, Tadao Maeda, Daniel C Tu, Alexander R Moise, Darin Bronson, Daniel Possin, Russell N Van Gelder, Wolfgang Baehr, Krzysztof Palczewski. J Biol Chem 2004
276
15

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
445
14

Efficacy, Safety, and Durability of Voretigene Neparvovec-rzyl in RPE65 Mutation-Associated Inherited Retinal Dystrophy: Results of Phase 1 and 3 Trials.
Albert M Maguire, Stephen Russell, Jennifer A Wellman, Daniel C Chung, Zi-Fan Yu, Amy Tillman, Janet Wittes, Julie Pappas, Okan Elci, Kathleen A Marshall,[...]. Ophthalmology 2019
155
14

Chemistry of the retinoid (visual) cycle.
Philip D Kiser, Marcin Golczak, Krzysztof Palczewski. Chem Rev 2014
199
14

Rapid restoration of visual pigment and function with oral retinoid in a mouse model of childhood blindness.
J P Van Hooser, T S Aleman, Y G He, A V Cideciyan, V Kuksa, S J Pittler, E M Stone, S G Jacobson, K Palczewski. Proc Natl Acad Sci U S A 2000
210
13

Long-term restoration of rod and cone vision by single dose rAAV-mediated gene transfer to the retina in a canine model of childhood blindness.
Gregory M Acland, Gustavo D Aguirre, Jean Bennett, Tomas S Aleman, Artur V Cideciyan, Jeannette Bennicelli, Nadine S Dejneka, Susan E Pearce-Kelling, Albert M Maguire, Krzysztof Palczewski,[...]. Mol Ther 2005
339
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
601
13

Dark adaptation and the retinoid cycle of vision.
T D Lamb, E N Pugh. Prog Retin Eye Res 2004
466
13

Isorhodopsin rather than rhodopsin mediates rod function in RPE65 knock-out mice.
Jie Fan, Baerbel Rohrer, Gennadiy Moiseyev, Jian-Xing Ma, Rosalie K Crouch. Proc Natl Acad Sci U S A 2003
111
12

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
540
12

Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA).
Ji-Jing Pang, Bo Chang, Norman L Hawes, Ronald E Hurd, Muriel T Davisson, Jie Li, Syed M Noorwez, Ritu Malhotra, J Hugh McDowell, Shalesh Kaushal,[...]. Mol Vis 2005
167
12

Human cone photoreceptor dependence on RPE65 isomerase.
Samuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, Elise Heon, Marcin Golczak, William A Beltran, Alexander Sumaroka, Sharon B Schwartz, Alejandro J Roman, Elizabeth A M Windsor,[...]. Proc Natl Acad Sci U S A 2007
118
12


Crystal structure of native RPE65, the retinoid isomerase of the visual cycle.
Philip D Kiser, Marcin Golczak, David T Lodowski, Mark R Chance, Krzysztof Palczewski. Proc Natl Acad Sci U S A 2009
114
12

Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis.
H Morimura, G A Fishman, S A Grover, A B Fulton, E L Berson, T P Dryja. Proc Natl Acad Sci U S A 1998
358
11

Cone opsin mislocalization in Rpe65-/- mice: a defect that can be corrected by 11-cis retinal.
Baerbel Rohrer, Heather R Lohr, Peter Humphries, T Michael Redmond, Mathias W Seeliger, Rosalie K Crouch. Invest Ophthalmol Vis Sci 2005
116
11

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
559
11

Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success.
Samuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, Alexander Sumaroka, Sharon B Schwartz, Elizabeth A M Windsor, Elias I Traboulsi, Elise Heon, Steven J Pittler, Ann H Milam,[...]. Proc Natl Acad Sci U S A 2005
213
11

Defining the residual vision in leber congenital amaurosis caused by RPE65 mutations.
Samuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, Alejandro J Roman, Alexander Sumaroka, Elizabeth A M Windsor, Sharon B Schwartz, Elise Heon, Edwin M Stone. Invest Ophthalmol Vis Sci 2009
97
11

Phototransduction in transgenic mice after targeted deletion of the rod transducin alpha -subunit.
P D Calvert, N V Krasnoperova, A L Lyubarsky, T Isayama, M Nicoló, B Kosaras, G Wong, K S Gannon, R F Margolskee, R L Sidman,[...]. Proc Natl Acad Sci U S A 2000
285
10

Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defect.
Artur V Cideciyan, Samuel G Jacobson, Arlene V Drack, Allen C Ho, Jason Charng, Alexandra V Garafalo, Alejandro J Roman, Alexander Sumaroka, Ian C Han, Maria D Hochstedler,[...]. Nat Med 2019
130
10

Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions.
Neruban Kumaran, Anthony T Moore, Richard G Weleber, Michel Michaelides. Br J Ophthalmol 2017
139
10


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
285
10

CRALBP supports the mammalian retinal visual cycle and cone vision.
Yunlu Xue, Susan Q Shen, Jonathan Jui, Alan C Rupp, Leah C Byrne, Samer Hattar, John G Flannery, Joseph C Corbo, Vladimir J Kefalov. J Clin Invest 2015
76
13

The cone-specific visual cycle.
Jin-Shan Wang, Vladimir J Kefalov. Prog Retin Eye Res 2011
198
10

A photic visual cycle of rhodopsin regeneration is dependent on Rgr.
P Chen, W Hao, L Rife, X P Wang, D Shen, J Chen, T Ogden, G B Van Boemel, L Wu, M Yang,[...]. Nat Genet 2001
140
10


A dominant mutation in RPE65 identified by whole-exome sequencing causes retinitis pigmentosa with choroidal involvement.
Sara J Bowne, Marian M Humphries, Lori S Sullivan, Paul F Kenna, Lawrence C S Tam, Anna S Kiang, Matthew Campbell, George M Weinstock, Daniel C Koboldt, Li Ding,[...]. Eur J Hum Genet 2011
106
9

Retinitis pigmentosa.
Dyonne T Hartong, Eliot L Berson, Thaddeus P Dryja. Lancet 2006
9

Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration.
D A Thompson, P Gyürüs, L L Fleischer, E L Bingham, C L McHenry, E Apfelstedt-Sylla, E Zrenner, B Lorenz, J E Richards, S G Jacobson,[...]. Invest Ophthalmol Vis Sci 2000
196
9

R91W mutation in Rpe65 leads to milder early-onset retinal dystrophy due to the generation of low levels of 11-cis-retinal.
Marijana Samardzija, Johannes von Lintig, Naoyuki Tanimoto, Vitus Oberhauser, Markus Thiersch, Charlotte E Remé, Mathias Seeliger, Christian Grimm, Andreas Wenzel. Hum Mol Genet 2008
79
11

Diseases caused by defects in the visual cycle: retinoids as potential therapeutic agents.
Gabriel H Travis, Marcin Golczak, Alexander R Moise, Krzysztof Palczewski. Annu Rev Pharmacol Toxicol 2007
292
9

Catalytic mechanism of a retinoid isomerase essential for vertebrate vision.
Philip D Kiser, Jianye Zhang, Mohsen Badiee, Qingjiang Li, Wuxian Shi, Xuewu Sui, Marcin Golczak, Gregory P Tochtrop, Krzysztof Palczewski. Nat Chem Biol 2015
53
16

Visual cycle impairment in cellular retinaldehyde binding protein (CRALBP) knockout mice results in delayed dark adaptation.
J C Saari, M Nawrot, B N Kennedy, G G Garwin, J B Hurley, J Huang, D E Possin, J W Crabb. Neuron 2001
182
9

Spontaneous activity of opsin apoprotein is a cause of Leber congenital amaurosis.
Michael L Woodruff, Zhongyan Wang, Hae Yun Chung, T Michael Redmond, Gordon L Fain, Janis Lem. Nat Genet 2003
152
9


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.