A citation-based method for searching scientific literature

Hualei Luo, Xueshan Xiao, Shiqiang Li, Wenmin Sun, Zhen Yi, Panfeng Wang, Qingjiong Zhang. Exp Eye Res 2021
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


An Ophthalmic Targeted Exome Sequencing Panel as a Powerful Tool to Identify Causative Mutations in Patients Suspected of Hereditary Eye Diseases.
Panfeng Wang, Shiqiang Li, Wenming Sun, Xueshan Xiao, Xiaoyun Jia, Mengchu Liu, Lieqiang Xu, Yuxi Long, Qingjiong Zhang. Transl Vis Sci Technol 2019
26
50

Modeling and Rescue of RP2 Retinitis Pigmentosa Using iPSC-Derived Retinal Organoids.
Amelia Lane, Katarina Jovanovic, Ciara Shortall, Daniele Ottaviani, Anna Brugulat Panes, Nele Schwarz, Rosellina Guarascio, Matthew J Hayes, Arpad Palfi, Naomi Chadderton,[...]. Stem Cell Reports 2020
41
50

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
50

Strategems in vitro for gene therapies directed to dominant mutations.
S Millington-Ward, B O'Neill, G Tuohy, N Al-Jandal, A S Kiang, P F Kenna, A Palfi, P Hayden, F Mansergh, A Kennan,[...]. Hum Mol Genet 1997
76
50

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
50

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
50

Optogenetic Strategies for Vision Restoration.
Qi Lu, Zhuo-Hua Pan. Adv Exp Med Biol 2021
3
100

In Situ Gene Therapy via AAV-CRISPR-Cas9-Mediated Targeted Gene Regulation.
Ana M Moreno, Xin Fu, Jie Zhu, Dhruva Katrekar, Yu-Ru V Shih, John Marlett, Jessica Cabotaje, Jasmine Tat, John Naughton, Leszek Lisowski,[...]. Mol Ther 2018
65
50

RNA targeting with CRISPR-Cas13.
Omar O Abudayyeh, Jonathan S Gootenberg, Patrick Essletzbichler, Shuo Han, Julia Joung, Joseph J Belanto, Vanessa Verdine, David B T Cox, Max J Kellner, Aviv Regev,[...]. Nature 2017
625
50

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
50

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
50

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
50

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
50

Zinc-finger-based transcriptional repression of rhodopsin in a model of dominant retinitis pigmentosa.
Claudio Mussolino, Daniela Sanges, Elena Marrocco, Ciro Bonetti, Umberto Di Vicino, Valeria Marigo, Alberto Auricchio, Germana Meroni, Enrico Maria Surace. EMBO Mol Med 2011
52
50

Hammerhead ribozymes designed to cleave all human rod opsin mRNAs which cause autosomal dominant retinitis pigmentosa.
Jack M Sullivan, Kathleen M Pietras, Bryant J Shin, John N Misasi. Mol Vis 2002
33
50

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
50

An AAV Dual Vector Strategy Ameliorates the Stargardt Phenotype in Adult Abca4-/- Mice.
Michelle E McClements, Alun R Barnard, Mandeep S Singh, Peter Charbel Issa, Zhichun Jiang, Roxana A Radu, Robert E MacLaren. Hum Gene Ther 2019
38
50

A new approach based on targeted pooled DNA sequencing identifies novel mutations in patients with Inherited Retinal Dystrophies.
Maitane Ezquerra-Inchausti, Ander Anasagasti, Olatz Barandika, Gonzaga Garay-Aramburu, Marta Galdós, Adolfo López de Munain, Cristina Irigoyen, Javier Ruiz-Ederra. Sci Rep 2018
10
33

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
33

Identification of a novel nonsense mutation in RP1 that causes autosomal recessive retinitis pigmentosa in an Indonesian family.
Anna M Siemiatkowska, Galuh D N Astuti, Kentar Arimadyo, Anneke I den Hollander, Sultana M H Faradz, Frans P M Cremers, Rob W J Collin. Mol Vis 2012
15
33

Novel association of RP1 gene mutations with autosomal recessive retinitis pigmentosa.
S Khaliq, A Abid, M Ismail, A Hameed, A Mohyuddin, P Lall, A Aziz, K Anwar, S Q Mehdi. J Med Genet 2005
53
33

Molecular findings from 537 individuals with inherited retinal disease.
Jamie M Ellingford, Stephanie Barton, Sanjeev Bhaskar, James O'Sullivan, Simon G Williams, Janine A Lamb, Binay Panda, Panagiotis I Sergouniotis, Rachel L Gillespie, Stephen P Daiger,[...]. J Med Genet 2016
85
33

Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa.
E A Pierce, T Quinn, T Meehan, T L McGee, E L Berson, T P Dryja. Nat Genet 1999
144
33

Genomic Landscape of Sporadic Retinitis Pigmentosa: Findings from 877 Spanish Cases.
Inmaculada Martin-Merida, Almudena Avila-Fernandez, Marta Del Pozo-Valero, Fiona Blanco-Kelly, Olga Zurita, Raquel Perez-Carro, Domingo Aguilera-Garcia, Rosa Riveiro-Alvarez, Ana Arteche, Maria Jose Trujillo-Tiebas,[...]. Ophthalmology 2019
22
33

Evaluation of 12 myopia-associated genes in Chinese patients with high myopia.
Jiali Li, Dan Jiang, Xueshan Xiao, Shiqiang Li, Xiaoyun Jia, Wenmin Sun, Xiangming Guo, Qingjiong Zhang. Invest Ophthalmol Vis Sci 2015
34
33

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.
S H Blanton, J R Heckenlively, A W Cottingham, J Friedman, L A Sadler, M Wagner, L H Friedman, S P Daiger. Genomics 1991
145
33

Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa.
L S Sullivan, J R Heckenlively, S J Bowne, J Zuo, W A Hide, A Gal, M Denton, C F Inglehearn, S H Blanton, S P Daiger. Nat Genet 1999
127
33

Pathogenicity discrimination and genetic test reference for CRX variants based on genotype-phenotype analysis.
Zhen Yi, Xueshan Xiao, Shiqiang Li, Wenmin Sun, Qingjiong Zhang. Exp Eye Res 2019
8
33

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
33

Genotype-functional-phenotype correlations in photoreceptor guanylate cyclase (GC-E) encoded by GUCY2D.
Dror Sharon, Hanna Wimberg, Yael Kinarty, Karl-Wilhelm Koch. Prog Retin Eye Res 2018
38
33

AAV-mediated photoreceptor transduction of the pig cone-enriched retina.
C Mussolino, M della Corte, S Rossi, F Viola, U Di Vicino, E Marrocco, S Neglia, M Doria, F Testa, R Giovannoni,[...]. Gene Ther 2011
62
33

Prevalence and pharmacological modulation of humoral immunity to AAV vectors in gene transfer to synovial tissue.
F Mingozzi, Y Chen, S C Edmonson, S Zhou, R M Thurlings, P P Tak, K A High, M J Vervoordeldonk. Gene Ther 2013
85
33

Changes in the photoreceptor mosaic of P23H-1 rats during retinal degeneration: implications for rod-cone dependent survival.
Diego García-Ayuso, Arturo Ortín-Martínez, Manuel Jiménez-López, Caridad Galindo-Romero, Nicolás Cuenca, Isabel Pinilla, Manuel Vidal-Sanz, Marta Agudo-Barriuso, María P Villegas-Pérez. Invest Ophthalmol Vis Sci 2013
38
33

Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutations.
Tomas S Aleman, Artur V Cideciyan, Alexander Sumaroka, Elizabeth A M Windsor, Waldo Herrera, D Alan White, Shalesh Kaushal, Anjani Naidu, Alejandro J Roman, Sharon B Schwartz,[...]. Invest Ophthalmol Vis Sci 2008
98
33

Clinical light exposure, photoreceptor degeneration, and AP-1 activation: a cell death or cell survival signal in the rhodopsin mutant retina?
Danian Gu, William A Beltran, Zexiao Li, Gregory M Acland, Gustavo D Aguirre. Invest Ophthalmol Vis Sci 2007
20
33


Antibody neutralization poses a barrier to intravitreal adeno-associated viral vector gene delivery to non-human primates.
M A Kotterman, L Yin, J M Strazzeri, J G Flannery, W H Merigan, D V Schaffer. Gene Ther 2015
93
33

Genes and Mutations Causing Autosomal Dominant Retinitis Pigmentosa.
Stephen P Daiger, Sara J Bowne, Lori S Sullivan. Cold Spring Harb Perspect Med 2014
68
33

In contrast to AAV-mediated Cntf expression, AAV-mediated Gdnf expression enhances gene replacement therapy in rodent models of retinal degeneration.
Prateek K Buch, Robert E MacLaren, Yanaí Durán, Kamaljit S Balaggan, Angus MacNeil, Frank C Schlichtenbrede, Alexander J Smith, Robin R Ali. Mol Ther 2006
76
33

Rod function deficit in retained photoreceptors of patients with class B Rhodopsin mutations.
Artur V Cideciyan, Samuel G Jacobson, Alejandro J Roman, Alexander Sumaroka, Vivian Wu, Jason Charng, Brianna Lisi, Malgorzata Swider, Gustavo D Aguirre, William A Beltran. Sci Rep 2020
4
50

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
33

Ectopic expression of a microbial-type rhodopsin restores visual responses in mice with photoreceptor degeneration.
Anding Bi, Jinjuan Cui, Yu-Ping Ma, Elena Olshevskaya, Mingliang Pu, Alexander M Dizhoor, Zhuo-Hua Pan. Neuron 2006
419
33

Gene-based therapy for alpha-1 antitrypsin deficiency.
Christian Mueller, Terence R Flotte. COPD 2013
32
33

Restoring visual function to blind mice with a photoswitch that exploits electrophysiological remodeling of retinal ganglion cells.
Ivan Tochitsky, Aleksandra Polosukhina, Vadim E Degtyar, Nicholas Gallerani, Caleb M Smith, Aaron Friedman, Russell N Van Gelder, Dirk Trauner, Daniela Kaufer, Richard H Kramer. Neuron 2014
98
33

Photochemical restoration of visual responses in blind mice.
Aleksandra Polosukhina, Jeffrey Litt, Ivan Tochitsky, Joseph Nemargut, Yivgeny Sychev, Ivan De Kouchkovsky, Tracy Huang, Katharine Borges, Dirk Trauner, Russell N Van Gelder,[...]. Neuron 2012
136
33

Long-term protection of retinal structure but not function using RAAV.CNTF in animal models of retinitis pigmentosa.
F Q Liang, T S Aleman, N S Dejneka, L Dudus, K J Fisher, A M Maguire, S G Jacobson, J Bennett. Mol Ther 2001
180
33

High-resolution homozygosity mapping is a powerful tool to detect novel mutations causative of autosomal recessive RP in the Dutch population.
Rob W J Collin, L Ingeborgh van den Born, B Jeroen Klevering, Marta de Castro-Miró, Karin W Littink, Kentar Arimadyo, Maleeha Azam, Volkan Yazar, Marijke N Zonneveld, Codrut C Paun,[...]. Invest Ophthalmol Vis Sci 2011
55
33

A CEP290 C-Terminal Domain Complements the Mutant CEP290 of Rd16 Mice In Trans and Rescues Retinal Degeneration.
Suddhasil Mookherjee, Holly Yu Chen, Kevin Isgrig, Wenhan Yu, Suja Hiriyanna, Rivka Levron, Tiansen Li, Peter Colosi, Wade Chien, Anand Swaroop,[...]. Cell Rep 2018
21
33

Assessment of AAV Vector Tropisms for Mouse and Human Pluripotent Stem Cell-Derived RPE and Photoreceptor Cells.
Anai Gonzalez-Cordero, Debbie Goh, Kamil Kruczek, Arifa Naeem, Milan Fernando, Sophia-Martha Kleine Holthaus, Matsuki Takaaki, Samuel J I Blackford, Magdalena Kloc, Leticia Agundez,[...]. Hum Gene Ther 2018
29
33

Next generation of adeno-associated virus 2 vectors: point mutations in tyrosines lead to high-efficiency transduction at lower doses.
Li Zhong, Baozheng Li, Cathryn S Mah, Lakshmanan Govindasamy, Mavis Agbandje-McKenna, Mario Cooper, Roland W Herzog, Irene Zolotukhin, Kenneth H Warrington, Kirsten A Weigel-Van Aken,[...]. Proc Natl Acad Sci U S A 2008
388
33


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.