A citation-based method for searching scientific literature

Nalinda B Wasala, Shi-Jie Chen, Dongsheng Duan. Expert Opin Drug Discov 2020
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


Non-immunogenic utrophin gene therapy for the treatment of muscular dystrophy animal models.
Yafeng Song, Leon Morales, Alock S Malik, Andrew F Mead, Christopher D Greer, Marilyn A Mitchell, Mihail T Petrov, Leonard T Su, Margaret E Choi, Shira T Rosenblum,[...]. Nat Med 2019
32
22

Animal models are essential to biological research: issues and perspectives.
Françoise Barré-Sinoussi, Xavier Montagutelli. Future Sci OA 2015
88
22


Genome engineering using the CRISPR-Cas9 system.
F Ann Ran, Patrick D Hsu, Jason Wright, Vineeta Agarwala, David A Scott, Feng Zhang. Nat Protoc 2013
22



RNA-guided human genome engineering via Cas9.
Prashant Mali, Luhan Yang, Kevin M Esvelt, John Aach, Marc Guell, James E DiCarlo, Julie E Norville, George M Church. Science 2013
22


Long-term microdystrophin gene therapy is effective in a canine model of Duchenne muscular dystrophy.
Caroline Le Guiner, Laurent Servais, Marie Montus, Thibaut Larcher, Bodvaël Fraysse, Sophie Moullec, Marine Allais, Virginie François, Maeva Dutilleul, Alberto Malerba,[...]. Nat Commun 2017
98
22


Multiplex genome engineering using CRISPR/Cas systems.
Le Cong, F Ann Ran, David Cox, Shuailiang Lin, Robert Barretto, Naomi Habib, Patrick D Hsu, Xuebing Wu, Wenyan Jiang, Luciano A Marraffini,[...]. Science 2013
22

Correction of Three Prominent Mutations in Mouse and Human Models of Duchenne Muscular Dystrophy by Single-Cut Genome Editing.
Yi-Li Min, Francesco Chemello, Hui Li, Cristina Rodriguez-Caycedo, Efrain Sanchez-Ortiz, Alex A Mireault, John R McAnally, John M Shelton, Yu Zhang, Rhonda Bassel-Duby,[...]. Mol Ther 2020
14
22

X chromosome-linked muscular dystrophy (mdx) in the mouse.
G Bulfield, W G Siller, P A Wight, K J Moore. Proc Natl Acad Sci U S A 1984
22

Applications of CRISPR/Cas9 for the Treatment of Duchenne Muscular Dystrophy.
Kenji Rowel Q Lim, Chantal Yoon, Toshifumi Yokota. J Pers Med 2018
29
22

Engineering adeno-associated virus vectors for gene therapy.
Chengwen Li, R Jude Samulski. Nat Rev Genet 2020
177
22

Unified energetics analysis unravels SpCas9 cleavage activity for optimal gRNA design.
Dong Zhang, Travis Hurst, Dongsheng Duan, Shi-Jie Chen. Proc Natl Acad Sci U S A 2019
17
22

The Pathogenesis and Therapy of Muscular Dystrophies.
Simon Guiraud, Annemieke Aartsma-Rus, Natassia M Vieira, Kay E Davies, Gert-Jan B van Ommen, Louis M Kunkel. Annu Rev Genomics Hum Genet 2015
167
22

AAV Vector Immunogenicity in Humans: A Long Journey to Successful Gene Transfer.
Helena Costa Verdera, Klaudia Kuranda, Federico Mingozzi. Mol Ther 2020
97
22

Development of Novel Micro-dystrophins with Enhanced Functionality.
Julian N Ramos, Katrin Hollinger, Niclas E Bengtsson, James M Allen, Stephen D Hauschka, Jeffrey S Chamberlain. Mol Ther 2019
32
22

Surrogate gene therapy for muscular dystrophy.
Kay E Davies, Jeffrey S Chamberlain. Nat Med 2019
6
33

CRISPR-Induced Deletion with SaCas9 Restores Dystrophin Expression in Dystrophic Models In Vitro and In Vivo.
Benjamin L Duchêne, Khadija Cherif, Jean-Paul Iyombe-Engembe, Antoine Guyon, Joel Rousseau, Dominique L Ouellet, Xavier Barbeau, Patrick Lague, Jacques P Tremblay. Mol Ther 2018
30
22

Dystrophin and mutations: one gene, several proteins, multiple phenotypes.
Francesco Muntoni, Silvia Torelli, Alessandra Ferlini. Lancet Neurol 2003
582
22


A Five-Repeat Micro-Dystrophin Gene Ameliorated Dystrophic Phenotype in the Severe DBA/2J-mdx Model of Duchenne Muscular Dystrophy.
Chady H Hakim, Nalinda B Wasala, Xiufang Pan, Kasun Kodippili, Yongping Yue, Keqing Zhang, Gang Yao, Brittney Haffner, Sean X Duan, Julian Ramos,[...]. Mol Ther Methods Clin Dev 2017
42
22



Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies.
A H Beggs, E P Hoffman, J R Snyder, K Arahata, L Specht, F Shapiro, C Angelini, H Sugita, L M Kunkel. Am J Hum Genet 1991
355
11

CRISPR-Cas3 induces broad and unidirectional genome editing in human cells.
Hiroyuki Morisaka, Kazuto Yoshimi, Yuya Okuzaki, Peter Gee, Yayoi Kunihiro, Ekasit Sonpho, Huaigeng Xu, Noriko Sasakawa, Yuki Naito, Shinichiro Nakada,[...]. Nat Commun 2019
36
11

CRISPR/Cas9-Mediated Genome Editing Corrects Dystrophin Mutation in Skeletal Muscle Stem Cells in a Mouse Model of Muscle Dystrophy.
Pei Zhu, Furen Wu, Jeffrey Mosenson, Hongmei Zhang, Tong-Chuan He, Wen-Shu Wu. Mol Ther Nucleic Acids 2017
40
11

Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells.
Majid Fardaei, Mark T Rogers, Helena M Thorpe, Kenneth Larkin, Marion G Hamshere, Peter S Harper, J David Brook. Hum Mol Genet 2002
323
11

Muscle wasting in disease: molecular mechanisms and promising therapies.
Shenhav Cohen, James A Nathan, Alfred L Goldberg. Nat Rev Drug Discov 2015
496
11

Precise Correction of Disease Mutations in Induced Pluripotent Stem Cells Derived From Patients With Limb Girdle Muscular Dystrophy.
Soeren Turan, Alfonso P Farruggio, Waracharee Srifa, John W Day, Michele P Calos. Mol Ther 2016
52
11

Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy.
Thai H Ho, Rajesh S Savkur, Michael G Poulos, Michael A Mancini, Maurice S Swanson, Thomas A Cooper. J Cell Sci 2005
141
11

Transcriptome-wide off-target RNA editing induced by CRISPR-guided DNA base editors.
Julian Grünewald, Ronghao Zhou, Sara P Garcia, Sowmya Iyer, Caleb A Lareau, Martin J Aryee, J Keith Joung. Nature 2019
204
11

Engineering of high-precision base editors for site-specific single nucleotide replacement.
Junjie Tan, Fei Zhang, Daniel Karcher, Ralph Bock. Nat Commun 2019
59
11

Massively parallel profiling and predictive modeling of the outcomes of CRISPR/Cas9-mediated double-strand break repair.
Wei Chen, Aaron McKenna, Jacob Schreiber, Maximilian Haeussler, Yi Yin, Vikram Agarwal, William Stafford Noble, Jay Shendure. Nucleic Acids Res 2019
47
11

A highly specific SpCas9 variant is identified by in vivo screening in yeast.
Antonio Casini, Michele Olivieri, Gianluca Petris, Claudia Montagna, Giordano Reginato, Giulia Maule, Francesca Lorenzin, Davide Prandi, Alessandro Romanel, Francesca Demichelis,[...]. Nat Biotechnol 2018
170
11

Immunogenicity of Cas9 Protein.
Aditi Mehta, Olivia M Merkel. J Pharm Sci 2020
23
11

Concordant but Varied Phenotypes among Duchenne Muscular Dystrophy Patient-Specific Myoblasts Derived using a Human iPSC-Based Model.
In Young Choi, HoTae Lim, Kenneth Estrellas, Jyothi Mula, Tatiana V Cohen, Yuanfan Zhang, Christopher J Donnelly, Jean-Philippe Richard, Yong Jun Kim, Hyesoo Kim,[...]. Cell Rep 2016
85
11

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
69
11

Efficient recovery of dysferlin deficiency by dual adeno-associated vector-mediated gene transfer.
William Lostal, Marc Bartoli, Nathalie Bourg, Carinne Roudaut, Azeddine Bentaïb, Katsuya Miyake, Nicolas Guerchet, Françoise Fougerousse, Paul McNeil, Isabelle Richard. Hum Mol Genet 2010
94
11

CRISPR provides acquired resistance against viruses in prokaryotes.
Rodolphe Barrangou, Christophe Fremaux, Hélène Deveau, Melissa Richards, Patrick Boyaval, Sylvain Moineau, Dennis A Romero, Philippe Horvath. Science 2007
11

Rationally engineered Cas9 nucleases with improved specificity.
Ian M Slaymaker, Linyi Gao, Bernd Zetsche, David A Scott, Winston X Yan, Feng Zhang. Science 2016
11

Genome editing. The new frontier of genome engineering with CRISPR-Cas9.
Jennifer A Doudna, Emmanuelle Charpentier. Science 2014
11

Genome Editing of Expanded CTG Repeats within the Human DMPK Gene Reduces Nuclear RNA Foci in the Muscle of DM1 Mice.
Mirella Lo Scrudato, Karine Poulard, Célia Sourd, Stéphanie Tomé, Arnaud F Klein, Guillaume Corre, Aline Huguet, Denis Furling, Geneviève Gourdon, Ana Buj-Bello. Mol Ther 2019
17
11

CIRCLE-seq: a highly sensitive in vitro screen for genome-wide CRISPR-Cas9 nuclease off-targets.
Shengdar Q Tsai, Nhu T Nguyen, Jose Malagon-Lopez, Ved V Topkar, Martin J Aryee, J Keith Joung. Nat Methods 2017
290
11

Analysis and minimization of cellular RNA editing by DNA adenine base editors.
Holly A Rees, Christopher Wilson, Jordan L Doman, David R Liu. Sci Adv 2019
86
11

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
88
11

CRISPR/Cas9-Mediated Deletion of CTG Expansions Recovers Normal Phenotype in Myogenic Cells Derived from Myotonic Dystrophy 1 Patients.
Claudia Provenzano, Marisa Cappella, Rea Valaperta, Rosanna Cardani, Giovanni Meola, Fabio Martelli, Beatrice Cardinali, Germana Falcone. Mol Ther Nucleic Acids 2017
33
11

Cytosine base editor generates substantial off-target single-nucleotide variants in mouse embryos.
Erwei Zuo, Yidi Sun, Wu Wei, Tanglong Yuan, Wenqin Ying, Hao Sun, Liyun Yuan, Lars M Steinmetz, Yixue Li, Hui Yang. Science 2019
296
11


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.