A citation-based method for searching scientific literature

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
Times Cited: 157







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



Times Cited
  Times     Co-cited
Similarity


Retinitis pigmentosa.
Dyonne T Hartong, Eliot L Berson, Thaddeus P Dryja. Lancet 2006
35

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
23

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
17

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
14

The mechanism of cone cell death in Retinitis Pigmentosa.
Peter A Campochiaro, Tahreem A Mir. Prog Retin Eye Res 2018
122
12

Comprehensive molecular diagnosis of a large cohort of Japanese retinitis pigmentosa and Usher syndrome patients by next-generation sequencing.
Maho Oishi, Akio Oishi, Norimoto Gotoh, Ken Ogino, Koichiro Higasa, Kei Iida, Yukiko Makiyama, Satoshi Morooka, Fumihiko Matsuda, Nagahisa Yoshimura. Invest Ophthalmol Vis Sci 2014
100
12

Retinitis pigmentosa.
Christian Hamel. Orphanet J Rare Dis 2006
475
11

Genes and mutations causing retinitis pigmentosa.
S P Daiger, L S Sullivan, S J Bowne. Clin Genet 2013
315
8

The molecular and cellular basis of rhodopsin retinitis pigmentosa reveals potential strategies for therapy.
Dimitra Athanasiou, Monica Aguila, James Bellingham, Wenwen Li, Caroline McCulley, Philip J Reeves, Michael E Cheetham. Prog Retin Eye Res 2018
123
8

Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease.
Keren J Carss, Gavin Arno, Marie Erwood, Jonathan Stephens, Alba Sanchis-Juan, Sarah Hull, Karyn Megy, Detelina Grozeva, Eleanor Dewhurst, Samantha Malka,[...]. Am J Hum Genet 2017
196
8

Neural remodeling in retinal degeneration.
Robert E Marc, Bryan W Jones, Carl B Watt, Enrica Strettoi. Prog Retin Eye Res 2003
578
7

Histopathology of the human retina in retinitis pigmentosa.
A H Milam, Z Y Li, R N Fariss. Prog Retin Eye Res 1998
443
7

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
107
7

Light-activated channels targeted to ON bipolar cells restore visual function in retinal degeneration.
Pamela S Lagali, David Balya, Gautam B Awatramani, Thomas A Münch, Douglas S Kim, Volker Busskamp, Constance L Cepko, Botond Roska. Nat Neurosci 2008
342
6

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
6

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
381
6

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
556
6

Genotype-phenotype correlation and mutation spectrum in a large cohort of patients with inherited retinal dystrophy revealed by next-generation sequencing.
Xiu-Feng Huang, Fang Huang, Kun-Chao Wu, Juan Wu, Jie Chen, Chi-Pui Pang, Fan Lu, Jia Qu, Zi-Bing Jin. Genet Med 2015
122
6

Pharmacological approaches to retinitis pigmentosa: A laboratory perspective.
Viviana Guadagni, Elena Novelli, Ilaria Piano, Claudia Gargini, Enrica Strettoi. Prog Retin Eye Res 2015
54
11

Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing.
Yan Xu, Liping Guan, Tao Shen, Jianguo Zhang, Xueshan Xiao, Hui Jiang, Shiqiang Li, Jianhua Yang, Xiaoyun Jia, Ye Yin,[...]. Hum Genet 2014
109
6

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
393
6

Retinitis Pigmentosa with EYS Mutations Is the Most Prevalent Inherited Retinal Dystrophy in Japanese Populations.
Yuuki Arai, Akiko Maeda, Yasuhiko Hirami, Chie Ishigami, Shinji Kosugi, Michiko Mandai, Yasuo Kurimoto, Masayo Takahashi. J Ophthalmol 2015
41
14

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
6

Two novel mutations in the EYS gene are possible major causes of autosomal recessive retinitis pigmentosa in the Japanese population.
Katsuhiro Hosono, Chie Ishigami, Masayo Takahashi, Dong Ho Park, Yasuhiko Hirami, Hiroshi Nakanishi, Shinji Ueno, Tadashi Yokoi, Akiko Hikoya, Taichi Fujita,[...]. PLoS One 2012
63
9

Genetic and Clinical Findings in a Large Cohort of Chinese Patients with Suspected Retinitis Pigmentosa.
Feng-Juan Gao, Jian-Kang Li, Han Chen, Fang-Yuan Hu, Sheng-Hai Zhang, Yu-He Qi, Ping Xu, Dan-Dan Wang, Lu-Sheng Wang, Qing Chang,[...]. Ophthalmology 2019
28
21

Endoplasmic reticulum stress and the unfolded protein responses in retinal degeneration.
Sarah X Zhang, Emily Sanders, Steven J Fliesler, Joshua J Wang. Exp Eye Res 2014
89
5

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
5

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
5

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
5

Unravelling the genetics of inherited retinal dystrophies: Past, present and future.
Suzanne Broadgate, Jing Yu, Susan M Downes, Stephanie Halford. Prog Retin Eye Res 2017
54
9

Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal Disease.
Edwin M Stone, Jeaneen L Andorf, S Scott Whitmore, Adam P DeLuca, Joseph C Giacalone, Luan M Streb, Terry A Braun, Robert F Mullins, Todd E Scheetz, Val C Sheffield,[...]. Ophthalmology 2017
155
5

Cas9/sgRNA selective targeting of the P23H Rhodopsin mutant allele for treating retinitis pigmentosa by intravitreal AAV9.PHP.B-based delivery.
Serena G Giannelli, Mirko Luoni, Valerio Castoldi, Luca Massimino, Tommaso Cabassi, Debora Angeloni, Gian Carlo Demontis, Letizia Leocani, Massimiliano Andreazzoli, Vania Broccoli. Hum Mol Genet 2018
61
8

Retinal stimulation strategies to restore vision: Fundamentals and systems.
Lan Yue, James D Weiland, Botond Roska, Mark S Humayun. Prog Retin Eye Res 2016
87
5


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
223
5

Good epidemiologic practice in retinitis pigmentosa: from phenotyping to biobanking.
Marzio Chizzolini, Alessandro Galan, Elisabeth Milan, Adolfo Sebastiani, Ciro Costagliola, Francesco Parmeggiani. Curr Genomics 2011
76
6

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
333
5

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
190
5

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
113
5

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
283
5

A fully organic retinal prosthesis restores vision in a rat model of degenerative blindness.
José Fernando Maya-Vetencourt, Diego Ghezzi, Maria Rosa Antognazza, Elisabetta Colombo, Maurizio Mete, Paul Feyen, Andrea Desii, Ambra Buschiazzo, Mattia Di Paolo, Stefano Di Marco,[...]. Nat Mater 2017
98
5

A review of the mechanisms of cone degeneration in retinitis pigmentosa.
Daniel S Narayan, John P M Wood, Glyn Chidlow, Robert J Casson. Acta Ophthalmol 2016
92
5

ISCEV Standard for full-field clinical electroretinography (2015 update).
Daphne L McCulloch, Michael F Marmor, Mitchell G Brigell, Ruth Hamilton, Graham E Holder, Radouil Tzekov, Michael Bach. Doc Ophthalmol 2015
802
5

Retinitis pigmentosa: genes and disease mechanisms.
Stefano Ferrari, Enzo Di Iorio, Vanessa Barbaro, Diego Ponzin, Francesco S Sorrentino, Francesco Parmeggiani. Curr Genomics 2011
287
5

MutationTaster2: mutation prediction for the deep-sequencing age.
Jana Marie Schwarz, David N Cooper, Markus Schuelke, Dominik Seelow. Nat Methods 2014
5

Next-generation sequencing identifies unexpected genotype-phenotype correlations in patients with retinitis pigmentosa.
Johannes Birtel, Martin Gliem, Elisabeth Mangold, Philipp L Müller, Frank G Holz, Christine Neuhaus, Steffen Lenzner, Diana Zahnleiter, Christian Betz, Tobias Eisenberger,[...]. PLoS One 2018
40
12

Transplantation of photoreceptors into the degenerative retina: Current state and future perspectives.
Sylvia J Gasparini, Sílvia Llonch, Oliver Borsch, Marius Ader. Prog Retin Eye Res 2019
60
8

Generation of three-dimensional retinal tissue with functional photoreceptors from human iPSCs.
Xiufeng Zhong, Christian Gutierrez, Tian Xue, Christopher Hampton, M Natalia Vergara, Li-Hui Cao, Ann Peters, Tea Soon Park, Elias T Zambidis, Jason S Meyer,[...]. Nat Commun 2014
427
5

Age-related macular degeneration.
Paul Mitchell, Gerald Liew, Bamini Gopinath, Tien Y Wong. Lancet 2018
340
5



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.