A citation-based method for searching scientific literature

Joachim Berger, Peter D Currie. Dis Model Mech 2012
Times Cited: 42







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



Times Cited
  Times     Co-cited
Similarity


Dystrophin-deficient zebrafish feature aspects of the Duchenne muscular dystrophy pathology.
Joachim Berger, Silke Berger, Thomas E Hall, Graham J Lieschke, Peter D Currie. Neuromuscul Disord 2010
54
28


Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo.
David I Bassett, Robert J Bryson-Richardson, David F Daggett, Philippe Gautier, David G Keenan, Peter D Currie. Development 2003
168
26

Animal models of human disease: zebrafish swim into view.
Graham J Lieschke, Peter D Currie. Nat Rev Genet 2007
21

The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin alpha2-deficient congenital muscular dystrophy.
Thomas E Hall, Robert J Bryson-Richardson, Silke Berger, Arie S Jacoby, Nicholas J Cole, Georgina E Hollway, Joachim Berger, Peter D Currie. Proc Natl Acad Sci U S A 2007
123
21

Genes controlling and mediating locomotion behavior of the zebrafish embryo and larva.
M Granato, F J van Eeden, U Schach, T Trowe, M Brand, M Furutani-Seiki, P Haffter, M Hammerschmidt, C P Heisenberg, Y J Jiang,[...]. Development 1996
417
21

Zebrafish models of collagen VI-related myopathies.
W R Telfer, A S Busta, C G Bonnemann, E L Feldman, J J Dowling. Hum Mol Genet 2010
76
21

Quantification of birefringence readily measures the level of muscle damage in zebrafish.
Joachim Berger, Tamar Sztal, Peter D Currie. Biochem Biophys Res Commun 2012
45
21

Drug screening in a zebrafish model of Duchenne muscular dystrophy.
Genri Kawahara, Jeremy A Karpf, Jennifer A Myers, Matthew S Alexander, Jeffrey R Guyon, Louis M Kunkel. Proc Natl Acad Sci U S A 2011
117
21

The dystrophin associated protein complex in zebrafish.
J R Guyon, A N Mosley, Y Zhou, K F O'Brien, X Sheng, K Chiang, A J Davidson, J M Volinski, L I Zon, L M Kunkel. Hum Mol Genet 2003
78
19

NAD+ biosynthesis ameliorates a zebrafish model of muscular dystrophy.
Michelle F Goody, Meghan W Kelly, Christine J Reynolds, Andre Khalil, Bryan D Crawford, Clarissa A Henry. PLoS Biol 2012
50
19

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
553
19

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
19

Evaluation of exon-skipping strategies for Duchenne muscular dystrophy utilizing dystrophin-deficient zebrafish.
Joachim Berger, Silke Berger, Arie S Jacoby, Steve D Wilton, Peter D Currie. J Cell Mol Med 2011
26
26

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
983
16



Fluoxetine prevents dystrophic changes in a zebrafish model of Duchenne muscular dystrophy.
Trent A Waugh, Eric Horstick, Junguk Hur, Samuel W Jackson, Ann E Davidson, Xingli Li, James J Dowling. Hum Mol Genet 2014
40
17

Identification of separate slow and fast muscle precursor cells in vivo, prior to somite formation.
S H Devoto, E Melançon, J S Eisen, M Westerfield. Development 1996
485
14

Zebrafish models for human FKRP muscular dystrophies.
Genri Kawahara, Jeffrey R Guyon, Yukio Nakamura, Louis M Kunkel. Hum Mol Genet 2010
59
14

The zebrafish dag1 mutant: a novel genetic model for dystroglycanopathies.
Vandana Gupta, Genri Kawahara, Stacey R Gundry, Aye T Chen, Wayne I Lencer, Yi Zhou, Leonard I Zon, Louis M Kunkel, Alan H Beggs. Hum Mol Genet 2011
79
14


Flightless flies: Drosophila models of neuromuscular disease.
Thomas E Lloyd, J Paul Taylor. Ann N Y Acad Sci 2010
83
14

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
80
14

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
497
14

In vivo imaging of molecular interactions at damaged sarcolemma.
Urmas Roostalu, Uwe Strähle. Dev Cell 2012
100
11

Developmental defects in a zebrafish model for muscular dystrophies associated with the loss of fukutin-related protein (FKRP).
Paul Thornhill, David Bassett, Hanns Lochmüller, Kate Bushby, Volker Straub. Brain 2008
53
11

Expression of DUX4 in zebrafish development recapitulates facioscapulohumeral muscular dystrophy.
Hiroaki Mitsuhashi, Satomi Mitsuhashi, Taylor Lynn-Jones, Genri Kawahara, Louis M Kunkel. Hum Mol Genet 2013
51
11

Hooked! Modeling human disease in zebrafish.
Cristina Santoriello, Leonard I Zon. J Clin Invest 2012
250
11

Zebrafish Fukutin family proteins link the unfolded protein response with dystroglycanopathies.
Yung-Yao Lin, Richard J White, Silvia Torelli, Sebahattin Cirak, Francesco Muntoni, Derek L Stemple. Hum Mol Genet 2011
57
11

Zebrafish relatively relaxed mutants have a ryanodine receptor defect, show slow swimming and provide a model of multi-minicore disease.
Hiromi Hirata, Takaki Watanabe, Jun Hatakeyama, Shawn M Sprague, Louis Saint-Amant, Ayako Nagashima, Wilson W Cui, Weibin Zhou, John Y Kuwada. Development 2007
85
11

Neb: a zebrafish model of nemaline myopathy due to nebulin mutation.
William R Telfer, Darcee D Nelson, Trent Waugh, Susan V Brooks, James J Dowling. Dis Model Mech 2012
33
15

A splice site mutation in laminin-α2 results in a severe muscular dystrophy and growth abnormalities in zebrafish.
Vandana A Gupta, Genri Kawahara, Jennifer A Myers, Aye T Chen, Thomas E Hall, M Chiara Manzini, Peter D Currie, Yi Zhou, Leonard I Zon, Louis M Kunkel,[...]. PLoS One 2012
29
17

Loss of myotubularin function results in T-tubule disorganization in zebrafish and human myotubular myopathy.
James J Dowling, Andrew P Vreede, Sean E Low, Elizabeth M Gibbs, John Y Kuwada, Carsten G Bonnemann, Eva L Feldman. PLoS Genet 2009
155
11

Zebrafish integrin-linked kinase is required in skeletal muscles for strengthening the integrin-ECM adhesion complex.
Ruben Postel, Padmanabhan Vakeel, Jacek Topczewski, Ralph Knöll, Jeroen Bakkers. Dev Biol 2008
73
11

The zebrafish reference genome sequence and its relationship to the human genome.
Kerstin Howe, Matthew D Clark, Carlos F Torroja, James Torrance, Camille Berthelot, Matthieu Muffato, John E Collins, Sean Humphray, Karen McLaren, Lucy Matthews,[...]. Nature 2013
11



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
384
11

Dystrophic muscle improvement in zebrafish via increased heme oxygenase signaling.
Genri Kawahara, Molly J Gasperini, Jennifer A Myers, Jeffrey J Widrick, Alal Eran, Peter R Serafini, Matthew S Alexander, Mathew T Pletcher, Carl A Morris, Louis M Kunkel. Hum Mol Genet 2014
22
22

The zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachment.
Arie S Jacoby, Elisabeth Busch-Nentwich, Robert J Bryson-Richardson, Thomas E Hall, Joachim Berger, Silke Berger, Carmen Sonntag, Caroline Sachs, Robert Geisler, Derek L Stemple,[...]. Development 2009
38
13

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
81
11

Dissecting muscle and neuronal disorders in a Drosophila model of muscular dystrophy.
Halyna R Shcherbata, Andriy S Yatsenko, Larissa Patterson, Vanita D Sood, Uri Nudel, David Yaffe, David Baker, Hannele Ruohola-Baker. EMBO J 2007
98
11

Identification of a zebrafish model of muscular dystrophy.
David Bassett, Peter D Currie. Clin Exp Pharmacol Physiol 2004
55
11


Animal models of Duchenne muscular dystrophy: from basic mechanisms to gene therapy.
Joe W McGreevy, Chady H Hakim, Mark A McIntosh, Dongsheng Duan. Dis Model Mech 2015
221
11

DHODH modulates transcriptional elongation in the neural crest and melanoma.
Richard Mark White, Jennifer Cech, Sutheera Ratanasirintrawoot, Charles Y Lin, Peter B Rahl, Christopher J Burke, Erin Langdon, Matthew L Tomlinson, Jack Mosher, Charles Kaufman,[...]. Nature 2011
290
9

Efficient genome editing in zebrafish using a CRISPR-Cas system.
Woong Y Hwang, Yanfang Fu, Deepak Reyon, Morgan L Maeder, Shengdar Q Tsai, Jeffry D Sander, Randall T Peterson, J-R Joanna Yeh, J Keith Joung. Nat Biotechnol 2013
9

Oxidative stress and successful antioxidant treatment in models of RYR1-related myopathy.
James J Dowling, Sandrine Arbogast, Junguk Hur, Darcee D Nelson, Anna McEvoy, Trent Waugh, Isabelle Marty, Joel Lunardi, Susan V Brooks, John Y Kuwada,[...]. Brain 2012
76
9

Muscle diseases in the zebrafish.
Yung-Yao Lin. Neuromuscul Disord 2012
19
21


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.