A citation-based method for searching scientific literature

Joe W McGreevy, Chady H Hakim, Mark A McIntosh, Dongsheng Duan. Dis Model Mech 2015
Times Cited: 232







List of co-cited articles
1157 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity



The molecular basis of muscular dystrophy in the mdx mouse: a point mutation.
P Sicinski, Y Geng, A S Ryder-Cook, E A Barnard, M G Darlison, P J Barnard. Science 1989
985
21

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
20

The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations.
Catherine L Bladen, David Salgado, Soledad Monges, Maria E Foncuberta, Kyriaki Kekou, Konstantina Kosma, Hugh Dawkins, Leanne Lamont, Anna J Roy, Teodora Chamova,[...]. Hum Mutat 2015
293
16

Single-cut genome editing restores dystrophin expression in a new mouse model of muscular dystrophy.
Leonela Amoasii, Chengzu Long, Hui Li, Alex A Mireault, John M Shelton, Efrain Sanchez-Ortiz, John R McAnally, Samadrita Bhattacharyya, Florian Schmidt, Dirk Grimm,[...]. Sci Transl Med 2017
108
16


CRISPR-Cas9 corrects Duchenne muscular dystrophy exon 44 deletion mutations in mice and human cells.
Yi-Li Min, Hui Li, Cristina Rodriguez-Caycedo, Alex A Mireault, Jian Huang, John M Shelton, John R McAnally, Leonela Amoasii, Pradeep P A Mammen, Rhonda Bassel-Duby,[...]. Sci Adv 2019
93
17

Skeletal and cardiac myopathies in mice lacking utrophin and dystrophin: a model for Duchenne muscular dystrophy.
R M Grady, H Teng, M C Nichol, J C Cunningham, R S Wilkinson, J R Sanes. Cell 1997
499
15

Gene editing restores dystrophin expression in a canine model of Duchenne muscular dystrophy.
Leonela Amoasii, John C W Hildyard, Hui Li, Efrain Sanchez-Ortiz, Alex Mireault, Daniel Caballero, Rachel Harron, Thaleia-Rengina Stathopoulou, Claire Massey, John M Shelton,[...]. Science 2018
224
14

Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy.
A E Deconinck, J A Rafael, J A Skinner, S C Brown, A C Potter, L Metzinger, D J Watt, J G Dickson, J M Tinsley, K E Davies. Cell 1997
556
14

Somatic gene editing ameliorates skeletal and cardiac muscle failure in pig and human models of Duchenne muscular dystrophy.
A Moretti, L Fonteyne, F Giesert, P Hoppmann, A B Meier, T Bozoglu, A Baehr, C M Schneider, D Sinnecker, K Klett,[...]. Nat Med 2020
58
24

Characterization of dystrophin deficient rats: a new model for Duchenne muscular dystrophy.
Thibaut Larcher, Aude Lafoux, Laurent Tesson, Séverine Remy, Virginie Thepenier, Virginie François, Caroline Le Guiner, Helicia Goubin, Maéva Dutilleul, Lydie Guigand,[...]. PLoS One 2014
93
13

The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy.
H H Stedman, H L Sweeney, J B Shrager, H C Maguire, R A Panettieri, B Petrof, M Narusawa, J M Leferovich, J T Sladky, A M Kelly. Nature 1991
726
13

Therapeutic developments for Duchenne muscular dystrophy.
Ingrid E C Verhaart, Annemieke Aartsma-Rus. Nat Rev Neurol 2019
117
13

Canine X-linked muscular dystrophy. An animal model of Duchenne muscular dystrophy: clinical studies.
B A Valentine, B J Cooper, A de Lahunta, R O'Quinn, J T Blue. J Neurol Sci 1988
192
12

Humanizing the mdx mouse model of DMD: the long and the short of it.
Nora Yucel, Alex C Chang, John W Day, Nadia Rosenthal, Helen M Blau. NPJ Regen Med 2018
44
25


Generation of muscular dystrophy model rats with a CRISPR/Cas system.
Katsuyuki Nakamura, Wataru Fujii, Masaya Tsuboi, Jun Tanihata, Naomi Teramoto, Shiho Takeuchi, Kunihiko Naito, Keitaro Yamanouchi, Masugi Nishihara. Sci Rep 2014
85
11

Dystrophin-deficient pigs provide new insights into the hierarchy of physiological derangements of dystrophic muscle.
Nikolai Klymiuk, Andreas Blutke, Alexander Graf, Sabine Krause, Katinka Burkhardt, Annegret Wuensch, Stefan Krebs, Barbara Kessler, Valeri Zakhartchenko, Mayuko Kurome,[...]. Hum Mol Genet 2013
85
11

Dystrophin-deficient mdx mice display a reduced life span and are susceptible to spontaneous rhabdomyosarcoma.
Jeffrey S Chamberlain, Joseph Metzger, Morayma Reyes, DeWayne Townsend, John A Faulkner. FASEB J 2007
226
10

Creation of a Novel Humanized Dystrophic Mouse Model of Duchenne Muscular Dystrophy and Application of a CRISPR/Cas9 Gene Editing Therapy.
Courtney S Young, Ekaterina Mokhonova, Marbella Quinonez, April D Pyle, Melissa J Spencer. J Neuromuscul Dis 2017
42
23

An error in dystrophin mRNA processing in golden retriever muscular dystrophy, an animal homologue of Duchenne muscular dystrophy.
N J Sharp, J N Kornegay, S D Van Camp, M H Herbstreith, S L Secore, S Kettle, W Y Hung, C D Constantinou, M J Dykstra, A D Roses. Genomics 1992
260
10

Pharmacological advances for treatment in Duchenne muscular dystrophy.
Simon Guiraud, Kay E Davies. Curr Opin Pharmacol 2017
80
12

Dystrophin and mutations: one gene, several proteins, multiple phenotypes.
Francesco Muntoni, Silvia Torelli, Alessandra Ferlini. Lancet Neurol 2003
591
10

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
170
10


Dystrophin protects the sarcolemma from stresses developed during muscle contraction.
B J Petrof, J B Shrager, H H Stedman, A M Kelly, H L Sweeney. Proc Natl Acad Sci U S A 1993
10

In vivo genome editing improves muscle function in a mouse model of Duchenne muscular dystrophy.
Christopher E Nelson, Chady H Hakim, David G Ousterout, Pratiksha I Thakore, Eirik A Moreb, Ruth M Castellanos Rivera, Sarina Madhavan, Xiufang Pan, F Ann Ran, Winston X Yan,[...]. Science 2016
648
9

Postnatal genome editing partially restores dystrophin expression in a mouse model of muscular dystrophy.
Chengzu Long, Leonela Amoasii, Alex A Mireault, John R McAnally, Hui Li, Efrain Sanchez-Ortiz, Samadrita Bhattacharyya, John M Shelton, Rhonda Bassel-Duby, Eric N Olson. Science 2016
557
9

Adenine base editing in mouse embryos and an adult mouse model of Duchenne muscular dystrophy.
Seuk-Min Ryu, Taeyoung Koo, Kyoungmi Kim, Kayeong Lim, Gayoung Baek, Sang-Tae Kim, Heon Seok Kim, Da-Eun Kim, Hyunji Lee, Eugene Chung,[...]. Nat Biotechnol 2018
183
9

An intronic LINE-1 element insertion in the dystrophin gene aborts dystrophin expression and results in Duchenne-like muscular dystrophy in the corgi breed.
Bruce F Smith, Yongping Yue, Philip R Woods, Joe N Kornegay, Jin-Hong Shin, Regina R Williams, Dongsheng Duan. Lab Invest 2011
66
13

Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy.
Niclas E Bengtsson, John K Hall, Guy L Odom, Michael P Phelps, Colin R Andrus, R David Hawkins, Stephen D Hauschka, Joel R Chamberlain, Jeffrey S Chamberlain. Nat Commun 2017
195
9

Entries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule.
Annemieke Aartsma-Rus, Judith C T Van Deutekom, Ivo F Fokkema, Gert-Jan B Van Ommen, Johan T Den Dunnen. Muscle Nerve 2006
390
9


A duchenne muscular dystrophy gene hot spot mutation in dystrophin-deficient cavalier king charles spaniels is amenable to exon 51 skipping.
Gemma L Walmsley, Virginia Arechavala-Gomeza, Marta Fernandez-Fuente, Margaret M Burke, Nicole Nagel, Angela Holder, Rachael Stanley, Kate Chandler, Stanley L Marks, Francesco Muntoni,[...]. PLoS One 2010
71
12

Role of telomere dysfunction in cardiac failure in Duchenne muscular dystrophy.
Foteini Mourkioti, Jackie Kustan, Peggy Kraft, John W Day, Ming-Ming Zhao, Maria Kost-Alimova, Alexei Protopopov, Ronald A DePinho, Daniel Bernstein, Alan K Meeker,[...]. Nat Cell Biol 2013
89
10

Effect of genetic background on the dystrophic phenotype in mdx mice.
William D Coley, Laurent Bogdanik, Maria Candida Vila, Qing Yu, Jack H Van Der Meulen, Sree Rayavarapu, James S Novak, Marie Nearing, James L Quinn, Allison Saunders,[...]. Hum Mol Genet 2016
96
9

A novel rabbit model of Duchenne muscular dystrophy generated by CRISPR/Cas9.
Tingting Sui, Yeh Siang Lau, Di Liu, Tingjun Liu, Li Xu, Yandi Gao, Liangxue Lai, Zhanjun Li, Renzhi Han. Dis Model Mech 2018
40
22

Canine models of Duchenne muscular dystrophy and their use in therapeutic strategies.
Joe N Kornegay, Janet R Bogan, Daniel J Bogan, Martin K Childers, Juan Li, Peter Nghiem, David A Detwiler, C Aaron Larsen, Robert W Grange, Ratna K Bhavaraju-Sanka,[...]. Mamm Genome 2012
96
9



Progress toward Gene Therapy for Duchenne Muscular Dystrophy.
Joel R Chamberlain, Jeffrey S Chamberlain. Mol Ther 2017
100
8

Short telomeres and stem cell exhaustion model Duchenne muscular dystrophy in mdx/mTR mice.
Alessandra Sacco, Foteini Mourkioti, Rose Tran, Jinkuk Choi, Michael Llewellyn, Peggy Kraft, Marina Shkreli, Scott Delp, Jason H Pomerantz, Steven E Artandi,[...]. Cell 2010
301
8

The Dystrophin Complex: Structure, Function, and Implications for Therapy.
Quan Q Gao, Elizabeth M McNally. Compr Physiol 2015
123
8

Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.
V M Chapman, D R Miller, D Armstrong, C T Caskey. Proc Natl Acad Sci U S A 1989
175
8

A Single CRISPR-Cas9 Deletion Strategy that Targets the Majority of DMD Patients Restores Dystrophin Function in hiPSC-Derived Muscle Cells.
Courtney S Young, Michael R Hicks, Natalia V Ermolova, Haruko Nakano, Majib Jan, Shahab Younesi, Saravanan Karumbayaram, Chino Kumagai-Cresse, Derek Wang, Jerome A Zack,[...]. Cell Stem Cell 2016
202
8

In vivo gene editing in dystrophic mouse muscle and muscle stem cells.
Mohammadsharif Tabebordbar, Kexian Zhu, Jason K W Cheng, Wei Leong Chew, Jeffrey J Widrick, Winston X Yan, Claire Maesner, Elizabeth Y Wu, Ru Xiao, F Ann Ran,[...]. Science 2016
604
8

A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity.
Martin Jinek, Krzysztof Chylinski, Ines Fonfara, Michael Hauer, Jennifer A Doudna, Emmanuelle Charpentier. Science 2012
8


Early myopathy in Duchenne muscular dystrophy is associated with elevated mitochondrial H2 O2 emission during impaired oxidative phosphorylation.
Meghan C Hughes, Sofhia V Ramos, Patrick C Turnbull, Irena A Rebalka, Andrew Cao, Cynthia M F Monaco, Nina E Varah, Brittany A Edgett, Jason S Huber, Peyman Tadi,[...]. J Cachexia Sarcopenia Muscle 2019
40
20


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.