A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


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
100

Human embryonic stem cell-derived retinal pigment epithelium in patients with age-related macular degeneration and Stargardt's macular dystrophy: follow-up of two open-label phase 1/2 studies.
Steven D Schwartz, Carl D Regillo, Byron L Lam, Dean Eliott, Philip J Rosenfeld, Ninel Z Gregori, Jean-Pierre Hubschman, Janet L Davis, Gad Heilwell, Marc Spirn,[...]. Lancet 2015
674
100

Retinal AAV8-RS1 Gene Therapy for X-Linked Retinoschisis: Initial Findings from a Phase I/IIa Trial by Intravitreal Delivery.
Catherine Cukras, Henry E Wiley, Brett G Jeffrey, H Nida Sen, Amy Turriff, Yong Zeng, Camasamudram Vijayasarathy, Dario Marangoni, Lucia Ziccardi, Sten Kjellstrom,[...]. Mol Ther 2018
88
66

Genome editing with CRISPR-Cas nucleases, base editors, transposases and prime editors.
Andrew V Anzalone, Luke W Koblan, David R Liu. Nat Biotechnol 2020
285
66

Test-Retest Variability of Functional and Structural Parameters in Patients with Stargardt Disease Participating in the SAR422459 Gene Therapy Trial.
Maria A Parker, Dongseok Choi, Laura R Erker, Mark E Pennesi, Paul Yang, Elvira N Chegarnov, Peter N Steinkamp, Catherine L Schlechter, Claire-Marie Dhaenens, Saddek Mohand-Said,[...]. Transl Vis Sci Technol 2016
28
66

Search-and-replace genome editing without double-strand breaks or donor DNA.
Andrew V Anzalone, Peyton B Randolph, Jessie R Davis, Alexander A Sousa, Luke W Koblan, Jonathan M Levy, Peter J Chen, Christopher Wilson, Gregory A Newby, Aditya Raguram,[...]. Nature 2019
830
66

Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage.
Alexis C Komor, Yongjoo B Kim, Michael S Packer, John A Zuris, David R Liu. Nature 2016
66

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
66

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
66

Transduction of photoreceptors with equine infectious anemia virus lentiviral vectors: safety and biodistribution of StarGen for Stargardt disease.
Katie Binley, Peter Widdowson, Julie Loader, Michelle Kelleher, Sharifah Iqball, Georgina Ferrige, Jackie de Belin, Marie Carlucci, Diana Angell-Manning, Felicity Hurst,[...]. Invest Ophthalmol Vis Sci 2013
73
66


Dual adeno-associated virus vectors result in efficient in vitro and in vivo expression of an oversized gene, MYO7A.
Frank M Dyka, Sanford L Boye, Vince A Chiodo, William W Hauswirth, Shannon E Boye. Hum Gene Ther Methods 2014
74
66

DNA nanoparticle-mediated ABCA4 delivery rescues Stargardt dystrophy in mice.
Zongchao Han, Shannon M Conley, Rasha S Makkia, Mark J Cooper, Muna I Naash. J Clin Invest 2012
98
66

Rescue of the Stargardt phenotype in Abca4 knockout mice through inhibition of vitamin A dimerization.
Peter Charbel Issa, Alun R Barnard, Philipp Herrmann, Ilyas Washington, Robert E MacLaren. Proc Natl Acad Sci U S A 2015
68
66

Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations.
Frans P M Cremers, Winston Lee, Rob W J Collin, Rando Allikmets. Prog Retin Eye Res 2020
53
66

Effective delivery of large genes to the retina by dual AAV vectors.
Ivana Trapani, Pasqualina Colella, Andrea Sommella, Carolina Iodice, Giulia Cesi, Sonia de Simone, Elena Marrocco, Settimio Rossi, Massimo Giunti, Arpad Palfi,[...]. EMBO Mol Med 2014
131
66

Gene therapy and genome surgery in the retina.
James E DiCarlo, Vinit B Mahajan, Stephen H Tsang. J Clin Invest 2018
63
33

Lentiviral delivery of co-packaged Cas9 mRNA and a Vegfa-targeting guide RNA prevents wet age-related macular degeneration in mice.
Sikai Ling, Shiqi Yang, Xinde Hu, Di Yin, Yao Dai, Xiaoqing Qian, Dawei Wang, Xiaoyong Pan, Jiaxu Hong, Xiaodong Sun,[...]. Nat Biomed Eng 2021
7
33

In Vivo CRISPR/Cas9-Mediated Genome Editing Mitigates Photoreceptor Degeneration in a Mouse Model of X-Linked Retinitis Pigmentosa.
Shuang Hu, Juan Du, Ningning Chen, Ruixuan Jia, Jinlu Zhang, Xiaozhen Liu, Liping Yang. Invest Ophthalmol Vis Sci 2020
7
33

Delivering CRISPR: a review of the challenges and approaches.
Christopher A Lino, Jason C Harper, James P Carney, Jerilyn A Timlin. Drug Deliv 2018
306
33

A multiplex CRISPR/Cas9 platform for fast and efficient editing of multiple genes in Arabidopsis.
Zhengjing Zhang, Yanfei Mao, Si Ha, Wenshan Liu, Jose Ramon Botella, Jian-Kang Zhu. Plant Cell Rep 2016
114
33

Development and applications of CRISPR-Cas9 for genome engineering.
Patrick D Hsu, Eric S Lander, Feng Zhang. Cell 2014
33

In Vivo Assessment of Potential Therapeutic Approaches for USH2A-Associated Diseases.
Nachiket D Pendse, Veronica Lamas, Basil S Pawlyk, Morgan L Maeder, Zheng-Yi Chen, Eric A Pierce, Qin Liu. Adv Exp Med Biol 2019
13
33

Francisella novicida Cas9 interrogates genomic DNA with very high specificity and can be used for mammalian genome editing.
Sundaram Acharya, Arpit Mishra, Deepanjan Paul, Asgar Hussain Ansari, Mohd Azhar, Manoj Kumar, Riya Rauthan, Namrata Sharma, Meghali Aich, Dipanjali Sinha,[...]. Proc Natl Acad Sci U S A 2019
21
33

RNA editing as a therapeutic approach for retinal gene therapy requiring long coding sequences.
Lewis E Fry, Caroline F Peddle, Alun R Barnard, Michelle E McClements, Robert E MacLaren. Int J Mol Sci 2020
19
33

CRISPR-LbCpf1 prevents choroidal neovascularization in a mouse model of age-related macular degeneration.
Taeyoung Koo, Sung Wook Park, Dong Hyun Jo, Daesik Kim, Jin Hyoung Kim, Hee-Yeon Cho, Jeungeun Kim, Jeong Hun Kim, Jin-Soo Kim. Nat Commun 2018
42
33

CRISPR-Cas9 DNA Base-Editing and Prime-Editing.
Ariel Kantor, Michelle E McClements, Robert E MacLaren. Int J Mol Sci 2020
34
33

Antisense Oligonucleotide- and CRISPR-Cas9-Mediated Rescue of mRNA Splicing for a Deep Intronic CLRN1 Mutation.
Anna-Lena Panagiotopoulos, Nina Karguth, Marina Pavlou, Sybille Böhm, Gilles Gasparoni, Jörn Walter, Alexander Graf, Helmut Blum, Martin Biel, Lisa Maria Riedmayr,[...]. Mol Ther Nucleic Acids 2020
4
33

One-step generation of mice carrying mutations in multiple genes by CRISPR/Cas-mediated genome engineering.
Haoyi Wang, Hui Yang, Chikdu S Shivalila, Meelad M Dawlaty, Albert W Cheng, Feng Zhang, Rudolf Jaenisch. Cell 2013
33

Development of a Pde6b Gene Knockout Rat Model for Studies of Degenerative Retinal Diseases.
Joon Hyung Yeo, Bok Kyoung Jung, Heuiran Lee, In-Jeoung Baek, Young Hoon Sung, Hae-Sol Shin, Hong Kyung Kim, Kyoung Yul Seo, Joo Yong Lee. Invest Ophthalmol Vis Sci 2019
7
33

Genome Editing as a Treatment for the Most Prevalent Causative Genes of Autosomal Dominant Retinitis Pigmentosa.
Michalitsa Diakatou, Gaël Manes, Beatrice Bocquet, Isabelle Meunier, Vasiliki Kalatzis. Int J Mol Sci 2019
20
33

CRISPR-Cas9-mediated therapeutic editing of Rpe65 ameliorates the disease phenotypes in a mouse model of Leber congenital amaurosis.
Dong Hyun Jo, Dong Woo Song, Chang Sik Cho, Un Gi Kim, Kyu Jun Lee, Kihwang Lee, Sung Wook Park, Daesik Kim, Jin Hyoung Kim, Jin-Soo Kim,[...]. Sci Adv 2019
27
33

CRISPR/Cas9-Mediated Genome Editing as a Therapeutic Approach for Leber Congenital Amaurosis 10.
Guo-Xiang Ruan, Elizabeth Barry, Dan Yu, Michael Lukason, Seng H Cheng, Abraham Scaria. Mol Ther 2017
143
33

Strategies for In Vivo Genome Editing in Nondividing Cells.
Fatemeharefeh Nami, Mohsen Basiri, Leila Satarian, Cameron Curtiss, Hossein Baharvand, Catherine Verfaillie. Trends Biotechnol 2018
28
33

Correcting visual loss by genetics and prosthetics.
Kanmin Xue, Robert E MacLaren. Curr Opin Physiol 2020
1
100


CRISPR-SKIP: programmable gene splicing with single base editors.
Michael Gapinske, Alan Luu, Jackson Winter, Wendy S Woods, Kurt A Kostan, Nikhil Shiva, Jun S Song, Pablo Perez-Pinera. Genome Biol 2018
73
33

Somatic Gene Editing of GUCY2D by AAV-CRISPR/Cas9 Alters Retinal Structure and Function in Mouse and Macaque.
K Tyler McCullough, Sanford L Boye, Diego Fajardo, Kaitlyn Calabro, James J Peterson, Christianne E Strang, Dibyendu Chakraborty, Sebastian Gloskowski, Scott Haskett, Steven Samuelsson,[...]. Hum Gene Ther 2019
35
33

Optical Control of CRISPR/Cas9 Gene Editing.
James Hemphill, Erin K Borchardt, Kalyn Brown, Aravind Asokan, Alexander Deiters. J Am Chem Soc 2015
133
33

Progress in treating inherited retinal diseases: Early subretinal gene therapy clinical trials and candidates for future initiatives.
Alexandra V Garafalo, Artur V Cideciyan, Elise Héon, Rebecca Sheplock, Alexander Pearson, Caberry WeiYang Yu, Alexander Sumaroka, Gustavo D Aguirre, Samuel G Jacobson. Prog Retin Eye Res 2020
55
33

Molecular pathology of X linked retinoschisis: mutations interfere with retinoschisin secretion and oligomerisation.
T Wang, A Zhou, C T Waters, E O'Connor, R J Read, D Trump. Br J Ophthalmol 2006
56
33

Cytosine and adenine base editing of the brain, liver, retina, heart and skeletal muscle of mice via adeno-associated viruses.
Jonathan M Levy, Wei-Hsi Yeh, Nachiket Pendse, Jessie R Davis, Erin Hennessey, Rossano Butcher, Luke W Koblan, Jason Comander, Qin Liu, David R Liu. Nat Biomed Eng 2020
91
33


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
33

CRISPR/Cas9 system: a powerful technology for in vivo and ex vivo gene therapy.
Xiaohui Zhang, Liren Wang, Mingyao Liu, Dali Li. Sci China Life Sci 2017
16
33

Genome surgery using Cas9 ribonucleoproteins for the treatment of age-related macular degeneration.
Kyoungmi Kim, Sung Wook Park, Jin Hyoung Kim, Seung Hwan Lee, Daesik Kim, Taeyoung Koo, Kwang-Eun Kim, Jeong Hun Kim, Jin-Soo Kim. Genome Res 2017
82
33

Molecular Therapies for Choroideremia.
Jasmina Cehajic Kapetanovic, Alun R Barnard, Robert E MacLaren. Genes (Basel) 2019
6
33

Nucleic acid delivery to differentiated retinal pigment epithelial cells using cell-penetrating peptide as a carrier.
Bano Subia, Mika Reinisalo, Namit Dey, Shirin Tavakoli, Astrid Subrizi, Munia Ganguli, Marika Ruponen. Eur J Pharm Biopharm 2019
6
33


Nrl knockdown by AAV-delivered CRISPR/Cas9 prevents retinal degeneration in mice.
Wenhan Yu, Suddhasil Mookherjee, Vijender Chaitankar, Suja Hiriyanna, Jung-Woong Kim, Matthew Brooks, Yasaman Ataeijannati, Xun Sun, Lijin Dong, Tiansen Li,[...]. Nat Commun 2017
151
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.