A citation-based method for searching scientific literature

Dimitra Athanasiou, Monica Aguila, James Bellingham, Wenwen Li, Caroline McCulley, Philip J Reeves, Michael E Cheetham. Prog Retin Eye Res 2018
Times Cited: 123







List of co-cited articles
1223 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Retinitis pigmentosa.
Dyonne T Hartong, Eliot L Berson, Thaddeus P Dryja. Lancet 2006
37

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.
T P Dryja, T L McGee, E Reichel, L B Hahn, G S Cowley, D W Yandell, M A Sandberg, E L Berson. Nature 1990
792
27

Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy.
Hugo F Mendes, Jacqueline van der Spuy, J Paul Chapple, Michael E Cheetham. Trends Mol Med 2005
262
22

Restoration of visual function in P23H rhodopsin transgenic rats by gene delivery of BiP/Grp78.
Marina S Gorbatyuk, Tessa Knox, Matthew M LaVail, Oleg S Gorbatyuk, Syed M Noorwez, William W Hauswirth, Jonathan H Lin, Nicholas Muzyczka, Alfred S Lewin. Proc Natl Acad Sci U S A 2010
203
19

Probing mechanisms of photoreceptor degeneration in a new mouse model of the common form of autosomal dominant retinitis pigmentosa due to P23H opsin mutations.
Sanae Sakami, Tadao Maeda, Grzegorz Bereta, Kiichiro Okano, Marcin Golczak, Alexander Sumaroka, Alejandro J Roman, Artur V Cideciyan, Samuel G Jacobson, Krzysztof Palczewski. J Biol Chem 2011
148
19

Robust Endoplasmic Reticulum-Associated Degradation of Rhodopsin Precedes Retinal Degeneration.
Wei-Chieh Chiang, Heike Kroeger, Sanae Sakami, Carissa Messah, Douglas Yasumura, Michael T Matthes, Judith A Coppinger, Krzysztof Palczewski, Matthew M LaVail, Jonathan H Lin. Mol Neurobiol 2015
72
25

Non-syndromic retinitis pigmentosa.
Sanne K Verbakel, Ramon A C van Huet, Camiel J F Boon, Anneke I den Hollander, Rob W J Collin, Caroline C W Klaver, Carel B Hoyng, Ronald Roepman, B Jeroen Klevering. Prog Retin Eye Res 2018
233
17

Mutation-independent rhodopsin gene therapy by knockdown and replacement with a single AAV vector.
Artur V Cideciyan, Raghavi Sudharsan, Valérie L Dufour, Michael T Massengill, Simone Iwabe, Malgorzata Swider, Brianna Lisi, Alexander Sumaroka, Luis Felipe Marinho, Tatyana Appelbaum,[...]. Proc Natl Acad Sci U S A 2018
68
25

IRE1 signaling affects cell fate during the unfolded protein response.
Jonathan H Lin, Han Li, Douglas Yasumura, Hannah R Cohen, Chao Zhang, Barbara Panning, Kevan M Shokat, Matthew M Lavail, Peter Walter. Science 2007
961
16

Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa.
T P Dryja, T L McGee, L B Hahn, G S Cowley, J E Olsson, E Reichel, M A Sandberg, E L Berson. N Engl J Med 1990
343
16

Molecular mechanisms of rhodopsin retinitis pigmentosa and the efficacy of pharmacological rescue.
Mark P Krebs, David C Holden, Parth Joshi, Charles L Clark, Andrew H Lee, Shalesh Kaushal. J Mol Biol 2010
74
21

Crystal structure of rhodopsin: A G protein-coupled receptor.
K Palczewski, T Kumasaka, T Hori, C A Behnke, H Motoshima, B A Fox, I Le Trong, D C Teller, T Okada, R E Stenkamp,[...]. Science 2000
16



The cellular fate of mutant rhodopsin: quality control, degradation and aggresome formation.
Richard S Saliba, Peter M G Munro, Philip J Luthert, Michael E Cheetham. J Cell Sci 2002
256
14

Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in man.
A V Cideciyan, D C Hood, Y Huang, E Banin, Z Y Li, E M Stone, A H Milam, S G Jacobson. Proc Natl Acad Sci U S A 1998
214
13

Rhodopsin mutations in autosomal dominant retinitis pigmentosa.
C H Sung, C M Davenport, J C Hennessey, I H Maumenee, S G Jacobson, J R Heckenlively, R Nowakowski, G Fishman, P Gouras, J Nathans. Proc Natl Acad Sci U S A 1991
370
13

Retinitis pigmentosa.
Christian Hamel. Orphanet J Rare Dis 2006
475
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
111
13

A Small Chaperone Improves Folding and Routing of Rhodopsin Mutants Linked to Inherited Blindness.
Petra Behnen, Angelo Felline, Antonella Comitato, Maria Teresa Di Salvo, Francesco Raimondi, Sahil Gulati, Shirin Kahremany, Krzysztof Palczewski, Valeria Marigo, Francesca Fanelli. iScience 2018
25
48

Allele-Specific Inhibition of Rhodopsin With an Antisense Oligonucleotide Slows Photoreceptor Cell Degeneration.
Susan F Murray, Ali Jazayeri, Michael T Matthes, Douglas Yasumura, Haidong Yang, Raechel Peralta, Andy Watt, Sue Freier, Gene Hung, Peter S Adamson,[...]. Invest Ophthalmol Vis Sci 2015
51
23


P23H opsin knock-in mice reveal a novel step in retinal rod disc morphogenesis.
Sanae Sakami, Alexander V Kolesnikov, Vladimir J Kefalov, Krzysztof Palczewski. Hum Mol Genet 2014
63
19

Clustered Regularly Interspaced Short Palindromic Repeats-Based Genome Surgery for the Treatment of Autosomal Dominant Retinitis Pigmentosa.
Yi-Ting Tsai, Wen-Hsuan Wu, Ting-Ting Lee, Wei-Pu Wu, Christine L Xu, Karen S Park, Xuan Cui, Sally Justus, Chyuan-Sheng Lin, Ruben Jauregui,[...]. Ophthalmology 2018
55
21


Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa.
C H Sung, B G Schneider, N Agarwal, D S Papermaster, J Nathans. Proc Natl Acad Sci U S A 1991
403
11

Retinoids assist the cellular folding of the autosomal dominant retinitis pigmentosa opsin mutant P23H.
Syed M Noorwez, Ritu Malhotra, J Hugh McDowell, Karen A Smith, Mark P Krebs, Shalesh Kaushal. J Biol Chem 2004
122
11

A novel small molecule chaperone of rod opsin and its potential therapy for retinal degeneration.
Yuanyuan Chen, Yu Chen, Beata Jastrzebska, Marcin Golczak, Sahil Gulati, Hong Tang, William Seibel, Xiaoyu Li, Hui Jin, Yong Han,[...]. Nat Commun 2018
28
39

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
617
11

Allele-Specific CRISPR-Cas9 Genome Editing of the Single-Base P23H Mutation for Rhodopsin-Associated Dominant Retinitis Pigmentosa.
Pingjuan Li, Benjamin P Kleinstiver, Mihoko Y Leon, Michelle S Prew, Daniel Navarro-Gomez, Scott H Greenwald, Eric A Pierce, J Keith Joung, Qin Liu. CRISPR J 2018
54
20

The role of the ER stress-response protein PERK in rhodopsin retinitis pigmentosa.
Dimitra Athanasiou, Monica Aguila, James Bellingham, Naheed Kanuga, Peter Adamson, Michael E Cheetham. Hum Mol Genet 2017
36
30

Pharmacological chaperone-mediated in vivo folding and stabilization of the P23H-opsin mutant associated with autosomal dominant retinitis pigmentosa.
Syed M Noorwez, Vladimir Kuksa, Yoshikazu Imanishi, Li Zhu, Sławomir Filipek, Krzysztof Palczewski, Shalesh Kaushal. J Biol Chem 2003
158
10

Molecular genetics and emerging therapies for retinitis pigmentosa: Basic research and clinical perspectives.
Marina França Dias, Kwangsic Joo, Jessica A Kemp, Silvia Ligório Fialho, Armando da Silva Cunha, Se Joon Woo, Young Jik Kwon. Prog Retin Eye Res 2018
157
10

In vivo Editing of the Human Mutant Rhodopsin Gene by Electroporation of Plasmid-based CRISPR/Cas9 in the Mouse Retina.
Maria Carmela Latella, Maria Teresa Di Salvo, Fabienne Cocchiarella, Daniela Benati, Giulia Grisendi, Antonella Comitato, Valeria Marigo, Alessandra Recchia. Mol Ther Nucleic Acids 2016
95
10

Retinitis pigmentosa mutants provide insight into the role of the N-terminal cap in rhodopsin folding, structure, and function.
Chikwado A Opefi, Kieron South, Christopher A Reynolds, Steven O Smith, Philip J Reeves. J Biol Chem 2013
28
32

Rescue of photoreceptor degeneration by curcumin in transgenic rats with P23H rhodopsin mutation.
Vidyullatha Vasireddy, Venkata R M Chavali, Victory T Joseph, Rajendra Kadam, Jonathan H Lin, Jeffrey A Jamison, Uday B Kompella, Geereddy Bhanuprakash Reddy, Radha Ayyagari. PLoS One 2011
57
15

The cell stress machinery and retinal degeneration.
Dimitra Athanasiou, Monica Aguilà, Dalila Bevilacqua, Sergey S Novoselov, David A Parfitt, Michael E Cheetham. FEBS Lett 2013
88
10

Effect of vitamin A supplementation on rhodopsin mutants threonine-17 --> methionine and proline-347 --> serine in transgenic mice and in cell cultures.
T Li, M A Sandberg, B S Pawlyk, B Rosner, K C Hayes, T P Dryja, E L Berson. Proc Natl Acad Sci U S A 1998
139
9

Genes and mutations causing retinitis pigmentosa.
S P Daiger, L S Sullivan, S J Bowne. Clin Genet 2013
315
9

Retinitis pigmentosa associated with rhodopsin mutations: Correlation between phenotypic variability and molecular effects.
Alessandro Iannaccone, David Man, Naushin Waseem, Barbara J Jennings, Madhavi Ganapathiraju, Kevin Gallaher, Elisheva Reese, Shomi S Bhattacharya, Judith Klein-Seetharaman. Vision Res 2006
55
16

G protein-coupled receptor rhodopsin.
Krzysztof Palczewski. Annu Rev Biochem 2006
476
9

Development of a gene-editing approach to restore vision loss in Leber congenital amaurosis type 10.
Morgan L Maeder, Michael Stefanidakis, Christopher J Wilson, Reshica Baral, Luis Alberto Barrera, George S Bounoutas, David Bumcrot, Hoson Chao, Dawn M Ciulla, Jennifer A DaSilva,[...]. Nat Med 2019
214
9

AAV delivery of wild-type rhodopsin preserves retinal function in a mouse model of autosomal dominant retinitis pigmentosa.
Haoyu Mao, Thomas James, Alison Schwein, Arseniy E Shabashvili, William W Hauswirth, Marina S Gorbatyuk, Alfred S Lewin. Hum Gene Ther 2011
87
10

In Vivo CRISPR/Cas9 Gene Editing Corrects Retinal Dystrophy in the S334ter-3 Rat Model of Autosomal Dominant Retinitis Pigmentosa.
Benjamin Bakondi, Wenjian Lv, Bin Lu, Melissa K Jones, Yuchun Tsai, Kevin J Kim, Rachelle Levy, Aslam Abbasi Akhtar, Joshua J Breunig, Clive N Svendsen,[...]. Mol Ther 2016
180
9

Suppression and replacement gene therapy for autosomal dominant disease in a murine model of dominant retinitis pigmentosa.
Sophia Millington-Ward, Naomi Chadderton, Mary O'Reilly, Arpad Palfi, Tobias Goldmann, Claire Kilty, Marian Humphries, Uwe Wolfrum, Jean Bennett, Peter Humphries,[...]. Mol Ther 2011
102
9

The mechanism of cone cell death in Retinitis Pigmentosa.
Peter A Campochiaro, Tahreem A Mir. Prog Retin Eye Res 2018
122
9


NLRP3 inflammasome activation drives bystander cone photoreceptor cell death in a P23H rhodopsin model of retinal degeneration.
Ishaq A Viringipurampeer, Andrew L Metcalfe, Abu E Bashar, Olena Sivak, Anat Yanai, Zeinabsadat Mohammadi, Orson L Moritz, Cheryl Y Gregory-Evans, Kevin Gregory-Evans. Hum Mol Genet 2016
40
22

Retinitis pigmentosa: genes and disease mechanisms.
Stefano Ferrari, Enzo Di Iorio, Vanessa Barbaro, Diego Ponzin, Francesco S Sorrentino, Francesco Parmeggiani. Curr Genomics 2011
287
9

Microglial phagocytosis of living photoreceptors contributes to inherited retinal degeneration.
Lian Zhao, Matthew K Zabel, Xu Wang, Wenxin Ma, Parth Shah, Robert N Fariss, Haohua Qian, Christopher N Parkhurst, Wen-Biao Gan, Wai T Wong. EMBO Mol Med 2015
207
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.