A citation-based method for searching scientific literature

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, Alan H Beggs. PLoS One 2012
Times Cited: 30







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



Times Cited
  Times     Co-cited
Similarity


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
127
46

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
81
40

Epistatic dissection of laminin-receptor interactions in dystrophic zebrafish muscle.
Tamar E Sztal, Carmen Sonntag, Thomas E Hall, Peter D Currie. Hum Mol Genet 2012
38
40

Stages of embryonic development of the zebrafish.
C B Kimmel, W W Ballard, S R Kimmel, B Ullmann, T F Schilling. Dev Dyn 1995
36

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
175
33

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
53
26


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
41
26

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
423
23

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
77
23

Quantification of birefringence readily measures the level of muscle damage in zebrafish.
Joachim Berger, Tamar Sztal, Peter D Currie. Biochem Biophys Res Commun 2012
52
23

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
119
23

Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy.
A Helbling-Leclerc, X Zhang, H Topaloglu, C Cruaud, F Tesson, J Weissenbach, F M Tomé, K Schwartz, M Fardeau, K Tryggvason. Nat Genet 1995
515
23

Removal of dystroglycan causes severe muscular dystrophy in zebrafish embryos.
Michael J Parsons, Isabel Campos, Elizabeth M A Hirst, Derek L Stemple. Development 2002
125
20

Animal models of human disease: zebrafish swim into view.
Graham J Lieschke, Peter D Currie. Nat Rev Genet 2007
20



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
19

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
79
16

Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin.
Jeffrey R Guyon, Julie Goswami, Susan J Jun, Marielle Thorne, Melanie Howell, Timothy Pusack, Genri Kawahara, Leta S Steffen, Michal Galdzicki, Louis M Kunkel. Hum Mol Genet 2009
48
16

Zebrafish models flex their muscles to shed light on muscular dystrophies.
Joachim Berger, Peter D Currie. Dis Model Mech 2012
44
16

Hooked! Modeling human disease in zebrafish.
Cristina Santoriello, Leonard I Zon. J Clin Invest 2012
265
16

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
60
16

Knockdown of desmin in zebrafish larvae affects interfilament spacing and mechanical properties of skeletal muscle.
Mei Li, Monika Andersson-Lendahl, Thomas Sejersen, Anders Arner. J Gen Physiol 2013
37
16

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
158
16


Identification of a zebrafish model of muscular dystrophy.
David Bassett, Peter D Currie. Clin Exp Pharmacol Physiol 2004
55
16

Laminin-111 protein therapy reduces muscle pathology and improves viability of a mouse model of merosin-deficient congenital muscular dystrophy.
Jachinta E Rooney, Jolie R Knapp, Bradley L Hodges, Ryan D Wuebbles, Dean J Burkin. Am J Pathol 2012
69
16

Dysregulation of matricellular proteins is an early signature of pathology in laminin-deficient muscular dystrophy.
Thomas Mehuron, Ajay Kumar, Lina Duarte, Jenny Yamauchi, Anthony Accorsi, Mahasweta Girgenrath. Skelet Muscle 2014
22
22

Severe muscular dystrophy in mice that lack dystrophin and alpha7 integrin.
Jachinta E Rooney, Jennifer V Welser, Melissa A Dechert, Nichole L Flintoff-Dye, Stephen J Kaufman, Dean J Burkin. J Cell Sci 2006
117
16

Whole-somite rotation generates muscle progenitor cell compartments in the developing zebrafish embryo.
Georgina E Hollway, Robert J Bryson-Richardson, Silke Berger, Nicholas J Cole, Thomas E Hall, Peter D Currie. Dev Cell 2007
123
16

Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan.
Tony Roscioli, Erik-Jan Kamsteeg, Karen Buysse, Isabelle Maystadt, Jeroen van Reeuwijk, Christa van den Elzen, Ellen van Beusekom, Moniek Riemersma, Rolph Pfundt, Lisenka E L M Vissers,[...]. Nat Genet 2012
143
13

Zebrafish models for human FKRP muscular dystrophies.
Genri Kawahara, Jeffrey R Guyon, Yukio Nakamura, Louis M Kunkel. Hum Mol Genet 2010
60
13

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
54
13

Abnormal vascular development in zebrafish models for fukutin and FKRP deficiency.
Alasdair J Wood, Juliane S Müller, Catherine D Jepson, Steve H Laval, Hanns Lochmüller, Kate Bushby, Rita Barresi, Volker Straub. Hum Mol Genet 2011
19
21

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
87
13

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
34
13

Structure and function of skeletal muscle in zebrafish early larvae.
Ying Dou, Monika Andersson-Lendahl, Anders Arner. J Gen Physiol 2008
39
13

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
78
13

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
56
13

The zebrafish as a model for muscular dystrophy and congenital myopathy.
David I Bassett, Peter D Currie. Hum Mol Genet 2003
96
13

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
486
13

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
41
13

Satellite cell of skeletal muscle fibers.
A MAURO. J Biophys Biochem Cytol 1961
13


The HDAC Inhibitor TSA Ameliorates a Zebrafish Model of Duchenne Muscular Dystrophy.
Nathan M Johnson, Gist H Farr, Lisa Maves. PLoS Curr 2013
16
25

Laminin-111 improves muscle repair in a mouse model of merosin-deficient congenital muscular dystrophy.
Pam M Van Ry, Priscilla Minogue, Bradley L Hodges, Dean J Burkin. Hum Mol Genet 2014
46
13

Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse.
H Xu, P Christmas, X R Wu, U M Wewer, E Engvall. Proc Natl Acad Sci U S A 1994
242
13

A common somitic origin for embryonic muscle progenitors and satellite cells.
Jérôme Gros, Marie Manceau, Virginie Thomé, Christophe Marcelle. Nature 2005
399
13



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.