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: 123







List of co-cited articles
1062 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
165
48

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
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
78
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
508
23

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
421
23

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
37
59

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

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
36

Removal of dystroglycan causes severe muscular dystrophy in zebrafish embryos.
Michael J Parsons, Isabel Campos, Elizabeth M A Hirst, Derek L Stemple. Development 2002
126
20

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
26

Quantification of birefringence readily measures the level of muscle damage in zebrafish.
Joachim Berger, Tamar Sztal, Peter D Currie. Biochem Biophys Res Commun 2012
43
44

Zebrafish models for human FKRP muscular dystrophies.
Genri Kawahara, Jeffrey R Guyon, Yukio Nakamura, Louis M Kunkel. Hum Mol Genet 2010
58
31

Identification of a zebrafish model of muscular dystrophy.
David Bassett, Peter D Currie. Clin Exp Pharmacol Physiol 2004
54
31

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
53
32

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
75
21

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
34
47

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
489
15

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
34


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
49
30


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
17

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
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
44

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
39
33

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
177
12

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
100
12


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
52
23


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
66
18

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
175
11

Laminin-alpha4 and integrin-linked kinase mutations cause human cardiomyopathy via simultaneous defects in cardiomyocytes and endothelial cells.
Ralph Knöll, Ruben Postel, Jianming Wang, Ralph Krätzner, Gerrit Hennecke, Andrei M Vacaru, Padmanabhan Vakeel, Cornelia Schubert, Kenton Murthy, Brinda K Rana,[...]. Circulation 2007
157
11

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

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
99
11

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
269
11

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
18

Time-lapse analysis and mathematical characterization elucidate novel mechanisms underlying muscle morphogenesis.
Chelsi J Snow, Michelle Goody, Meghan W Kelly, Emma C Oster, Robert Jones, Andre Khalil, Clarissa A Henry. PLoS Genet 2008
33
33

In vivo drug discovery in the zebrafish.
Leonard I Zon, Randall T Peterson. Nat Rev Drug Discov 2005
866
11

Characterization of the laminin gene family and evolution in zebrafish.
Tamar Sztal, Silke Berger, Peter D Currie, Thomas E Hall. Dev Dyn 2011
27
40

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
42
26


Essential and overlapping roles for laminin alpha chains in notochord and blood vessel formation.
Steven M Pollard, Michael J Parsons, Makoto Kamei, Ross N W Kettleborough, Kevin A Thomas, Van N Pham, Moon-Kyoung Bae, Annabelle Scott, Brant M Weinstein, Derek L Stemple. Dev Biol 2006
78
12

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
118
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
46
21

The zebrafish as a model for muscular dystrophy and congenital myopathy.
David I Bassett, Peter D Currie. Hum Mol Genet 2003
92
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
93
10


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.