A citation-based method for searching scientific literature

C Bowes, T Li, M Danciger, L C Baxter, M L Applebury, D B Farber. Nature 1990
Times Cited: 682







List of co-cited articles
1029 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity



Retinitis pigmentosa.
Dyonne T Hartong, Eliot L Berson, Thaddeus P Dryja. Lancet 2006
25



Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene.
B Chang, N L Hawes, M T Pardue, A M German, R E Hurd, M T Davisson, S Nusinowitz, K Rengarajan, A P Boyd, S S Sidney,[...]. Vision Res 2007
244
17

Differential effect of the rd mutation on rods and cones in the mouse retina.
L D Carter-Dawson, M M LaVail, R L Sidman. Invest Ophthalmol Vis Sci 1978
435
15

Retinal degeneration mutants in the mouse.
B Chang, N L Hawes, R E Hurd, M T Davisson, S Nusinowitz, J R Heckenlively. Vision Res 2002
569
15

Retinal organization in the retinal degeneration 10 (rd10) mutant mouse: a morphological and ERG study.
Claudia Gargini, Eva Terzibasi, Francesca Mazzoni, Enrica Strettoi. J Comp Neurol 2007
336
13

Identification of a common non-apoptotic cell death mechanism in hereditary retinal degeneration.
Blanca Arango-Gonzalez, Dragana Trifunović, Ayse Sahaboglu, Katharina Kranz, Stylianos Michalakis, Pietro Farinelli, Susanne Koch, Fred Koch, Sandra Cottet, Ulrike Janssen-Bienhold,[...]. PLoS One 2014
119
13

The Inheritance of a Retinal Abnormality in White Mice.
C E Keeler. Proc Natl Acad Sci U S A 1924
132
13


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
290
11

PKG activity causes photoreceptor cell death in two retinitis pigmentosa models.
François Paquet-Durand, Stefanie M Hauck, Theo van Veen, Marius Ueffing, Per Ekström. J Neurochem 2009
77
12

A key role for cyclic nucleotide gated (CNG) channels in cGMP-related retinitis pigmentosa.
François Paquet-Durand, Susanne Beck, Stylianos Michalakis, Tobias Goldmann, Gesine Huber, Regine Mühlfriedel, Dragana Trifunović, M Dominik Fischer, Edda Fahl, Gabriele Duetsch,[...]. Hum Mol Genet 2011
78
12

Stimulation of the insulin/mTOR pathway delays cone death in a mouse model of retinitis pigmentosa.
Claudio Punzo, Karl Kornacker, Constance L Cepko. Nat Neurosci 2009
336
10

Photoreceptor degeneration: genetic and mechanistic dissection of a complex trait.
Alan F Wright, Christina F Chakarova, Mai M Abd El-Aziz, Shomi S Bhattacharya. Nat Rev Genet 2010
401
9

Activated mTORC1 promotes long-term cone survival in retinitis pigmentosa mice.
Aditya Venkatesh, Shan Ma, Yun Z Le, Michael N Hall, Markus A Rüegg, Claudio Punzo. J Clin Invest 2015
87
10

Antioxidants reduce cone cell death in a model of retinitis pigmentosa.
Keiichi Komeima, Brian S Rogers, Lili Lu, Peter A Campochiaro. Proc Natl Acad Sci U S A 2006
302
9

Excessive HDAC activation is critical for neurodegeneration in the rd1 mouse.
J Sancho-Pelluz, M V Alavi, A Sahaboglu, S Kustermann, P Farinelli, S Azadi, T van Veen, F J Romero, F Paquet-Durand, P Ekström. Cell Death Dis 2010
78
11

Leber congenital amaurosis linked to AIPL1: a mouse model reveals destabilization of cGMP phosphodiesterase.
Visvanathan Ramamurthy, Gregory A Niemi, Thomas A Reh, James B Hurley. Proc Natl Acad Sci U S A 2004
124
9

Two pathways of rod photoreceptor cell death induced by elevated cGMP.
Tian Wang, Stephen H Tsang, Jeannie Chen. Hum Mol Genet 2017
32
28

Calpain is activated in degenerating photoreceptors in the rd1 mouse.
Francois Paquet-Durand, Seifollah Azadi, Stefanie M Hauck, Marius Ueffing, Theo van Veen, Per Ekström. J Neurochem 2006
104
8

Rpe65 is necessary for production of 11-cis-vitamin A in the retinal visual cycle.
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
739
8

Retinitis pigmentosa: rod photoreceptor rescue by a calcium-channel blocker in the rd mouse.
M Frasson, J A Sahel, M Fabre, M Simonutti, H Dreyfus, S Picaud. Nat Med 1999
181
8

Genes and mutations causing retinitis pigmentosa.
S P Daiger, L S Sullivan, S J Bowne. Clin Genet 2013
333
8


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
8

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
8

Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase.
S H Huang, S J Pittler, X Huang, L Oliveira, E L Berson, T P Dryja. Nat Genet 1995
208
8

Rod-derived cone viability factor promotes cone survival by stimulating aerobic glycolysis.
Najate Aït-Ali, Ram Fridlich, Géraldine Millet-Puel, Emmanuelle Clérin, François Delalande, Céline Jaillard, Frédéric Blond, Ludivine Perrocheau, Sacha Reichman, Leah C Byrne,[...]. Cell 2015
207
8

Excessive activation of poly(ADP-ribose) polymerase contributes to inherited photoreceptor degeneration in the retinal degeneration 1 mouse.
François Paquet-Durand, José Silva, Tanuja Talukdar, Leif E Johnson, Seifollah Azadi, Theo van Veen, Marius Ueffing, Stefanie M Hauck, Per A R Ekström. J Neurosci 2007
101
8

AIPL1, the protein that is defective in Leber congenital amaurosis, is essential for the biosynthesis of retinal rod cGMP phosphodiesterase.
Xiaoqing Liu, Oleg V Bulgakov, Xiao-Hong Wen, Michael L Woodruff, Basil Pawlyk, Jun Yang, Gordon L Fain, Michael A Sandberg, Clint L Makino, Tiansen Li. Proc Natl Acad Sci U S A 2004
82
9

Oxidative damage is a potential cause of cone cell death in retinitis pigmentosa.
Jikui Shen, Xiaoru Yang, Aling Dong, Robert M Petters, You-Wei Peng, Fulton Wong, Peter A Campochiaro. J Cell Physiol 2005
222
7

Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesterase.
C Bowes, T Li, W N Frankel, M Danciger, J M Coffin, M L Applebury, D B Farber. Proc Natl Acad Sci U S A 1993
152
7

Photoreceptor cell death mechanisms in inherited retinal degeneration.
Javier Sancho-Pelluz, Blanca Arango-Gonzalez, Stefan Kustermann, Francisco Javier Romero, Theo van Veen, Eberhart Zrenner, Per Ekström, François Paquet-Durand. Mol Neurobiol 2008
208
7

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
143
7


Retinitis pigmentosa: rapid neurodegeneration is governed by slow cell death mechanisms.
A Sahaboglu, O Paquet-Durand, J Dietter, K Dengler, S Bernhard-Kurz, P Ar Ekström, B Hitzmann, M Ueffing, F Paquet-Durand. Cell Death Dis 2013
52
13

A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene.
Bo Chang, Tanja Grau, Susann Dangel, Ron Hurd, Bernhard Jurklies, E Cumhur Sener, Sten Andreasson, Helene Dollfus, Britta Baumann, Sylvia Bolz,[...]. Proc Natl Acad Sci U S A 2009
134
7


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
517
7

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
387
7



Nrl is required for rod photoreceptor development.
A J Mears, M Kondo, P K Swain, Y Takada, R A Bush, T L Saunders, P A Sieving, A Swaroop. Nat Genet 2001
671
7

Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis.
M M Sohocki, S J Bowne, L S Sullivan, S Blackshaw, C L Cepko, A M Payne, S S Bhattacharya, S Khaliq, S Qasim Mehdi, D G Birch,[...]. Nat Genet 2000
213
7

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
857
7

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
682
7

Cellular mechanisms of hereditary photoreceptor degeneration - Focus on cGMP.
Michael Power, Soumyaparna Das, Karin Schütze, Valeria Marigo, Per Ekström, François Paquet-Durand. Prog Retin Eye Res 2020
47
14

Development and degeneration of retina in rds mutant mice: light microscopy.
S Sanyal, A De Ruiter, R K Hawkins. J Comp Neurol 1980
204
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.