A citation-based method for searching scientific literature

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
Times Cited: 127







List of co-cited articles
1021 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
51

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
27

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
33

Stages of embryonic development of the zebrafish.
C B Kimmel, W W Ballard, S R Kimmel, B Ullmann, T F Schilling. Dev Dyn 1995
25

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
24

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
56

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
38

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
21

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
43

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
40

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
25

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
19

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
50

Zebrafish models for human FKRP muscular dystrophies.
Genri Kawahara, Jeffrey R Guyon, Yukio Nakamura, Louis M Kunkel. Hum Mol Genet 2010
60
30

Identification of a zebrafish model of muscular dystrophy.
David Bassett, Peter D Currie. Clin Exp Pharmacol Physiol 2004
55
30

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
30

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
20



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
28

The zebrafish runzel muscular dystrophy is linked to the titin gene.
Leta S Steffen, Jeffrey R Guyon, Emily D Vogel, Melanie H Howell, Yi Zhou, Gerhard J Weber, Leonard I Zon, Louis M Kunkel. Dev Biol 2007
44
31


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
17

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
30
46

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

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
18


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
31

Laminin alpha1 chain reduces muscular dystrophy in laminin alpha2 chain deficient mice.
Kinga Gawlik, Yuko Miyagoe-Suzuki, Peter Ekblom, Shin'ichi Takeda, Madeleine Durbeej. Hum Mol Genet 2004
102
12

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


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
22

Basal lamina strengthens cell membrane integrity via the laminin G domain-binding motif of alpha-dystroglycan.
Renzhi Han, Motoi Kanagawa, Takako Yoshida-Moriguchi, Erik P Rader, Rainer A Ng, Daniel E Michele, David E Muirhead, Stefan Kunz, Steven A Moore, Susan T Iannaccone,[...]. Proc Natl Acad Sci U S A 2009
104
12

Mutations in the integrin alpha7 gene cause congenital myopathy.
Y K Hayashi, F L Chou, E Engvall, M Ogawa, C Matsuda, S Hirabayashi, K Yokochi, B L Ziober, R H Kramer, S J Kaufman,[...]. Nat Genet 1998
275
12


Animal models of human disease: zebrafish swim into view.
Graham J Lieschke, Peter D Currie. Nat Rev Genet 2007
11

In vivo drug discovery in the zebrafish.
Leonard I Zon, Randall T Peterson. Nat Rev Drug Discov 2005
905
11

Characterization of the laminin gene family and evolution in zebrafish.
Tamar Sztal, Silke Berger, Peter D Currie, Thomas E Hall. Dev Dyn 2011
30
36

Development of the zebrafish myoseptum with emphasis on the myotendinous junction.
Benjamin Charvet, Marilyne Malbouyres, Aurélie Pagnon-Minot, Florence Ruggiero, Dominique Le Guellec. Cell Tissue Res 2011
44
25


Zebrafish mutants identify an essential role for laminins in notochord formation.
Michael J Parsons, Steven M Pollard, Leonor Saúde, Benjamin Feldman, Pedro Coutinho, Elizabeth M A Hirst, Derek L Stemple. Development 2002
174
10

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
10

Zebrafish orthologs of human muscular dystrophy genes.
Leta S Steffen, Jeffrey R Guyon, Emily D Vogel, Rosanna Beltre, Timothy J Pusack, Yi Zhou, Leonard I Zon, Louis M Kunkel. BMC Genomics 2007
47
21

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix.
O Ibraghimov-Beskrovnaya, J M Ervasti, C J Leveille, C A Slaughter, S W Sernett, K P Campbell. Nature 1992
10

The zebrafish as a model for muscular dystrophy and congenital myopathy.
David I Bassett, Peter D Currie. Hum Mol Genet 2003
96
10

Laminin-111 protein therapy prevents muscle disease in the mdx mouse model for Duchenne muscular dystrophy.
Jachinta E Rooney, Praveen B Gurpur, Dean J Burkin. Proc Natl Acad Sci U S A 2009
96
10

The Tol2kit: a multisite gateway-based construction kit for Tol2 transposon transgenesis constructs.
Kristen M Kwan, Esther Fujimoto, Clemens Grabher, Benjamin D Mangum, Melissa E Hardy, Douglas S Campbell, John M Parant, H Joseph Yost, John P Kanki, Chi-Bin Chien. Dev Dyn 2007
10


An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy.
J Moll, P Barzaghi, S Lin, G Bezakova, H Lochmüller, E Engvall, U Müller, M A Ruegg. Nature 2001
176
10

Interactions between muscle fibers and segment boundaries in zebrafish.
Clarissa A Henry, Ian M McNulty, Wendy A Durst, Sarah E Munchel, Sharon L Amacher. Dev Biol 2005
59
16


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.