A citation-based method for searching scientific literature

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, Peter D Currie. Development 2009
Times Cited: 39







List of co-cited articles
317 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
125
56

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
172
43

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
74
30

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
30

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
483
25

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
55
25


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
25

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
160
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
124
23

Stages of embryonic development of the zebrafish.
C B Kimmel, W W Ballard, S R Kimmel, B Ullmann, T F Schilling. Dev Dyn 1995
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
46
23

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
173
20

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
20

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
59
20

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
20

Identification of a zebrafish model of muscular dystrophy.
David Bassett, Peter D Currie. Clin Exp Pharmacol Physiol 2004
55
17

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
17

Activity and distribution of paxillin, focal adhesion kinase, and cadherin indicate cooperative roles during zebrafish morphogenesis.
Bryan D Crawford, Clarissa A Henry, Todd A Clason, Amanda L Becker, Merrill B Hille. Mol Biol Cell 2003
100
17

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
17

Nrk2b-mediated NAD+ production regulates cell adhesion and is required for muscle morphogenesis in vivo: Nrk2b and NAD+ in muscle morphogenesis.
Michelle F Goody, Meghan W Kelly, Kevin N Lessard, Andre Khalil, Clarissa A Henry. Dev Biol 2010
43
17


Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice.
R A Williamson, M D Henry, K J Daniels, R F Hrstka, J C Lee, Y Sunada, O Ibraghimov-Beskrovnaya, K P Campbell. Hum Mol Genet 1997
422
15


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
18



Muscle development is disrupted in zebrafish embryos deficient for fibronectin.
Chelsi J Snow, Matthew T Peterson, Andre Khalil, Clarissa A Henry. Dev Dyn 2008
39
15

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
512
15

Characterization of the laminin gene family and evolution in zebrafish.
Tamar Sztal, Silke Berger, Peter D Currie, Thomas E Hall. Dev Dyn 2011
28
21

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
51
15

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
120
12

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
12

Animal models of human disease: zebrafish swim into view.
Graham J Lieschke, Peter D Currie. Nat Rev Genet 2007
12

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
12

The zebrafish as a model for muscular dystrophy and congenital myopathy.
David I Bassett, Peter D Currie. Hum Mol Genet 2003
94
12

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
12

Integrinalpha5-dependent fibronectin accumulation for maintenance of somite boundaries in zebrafish embryos.
Sumito Koshida, Yasuyuki Kishimoto, Hideko Ustumi, Toshihiro Shimizu, Makoto Furutani-Seiki, Hisato Kondoh, Shinji Takada. Dev Cell 2005
143
12



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

In vivo imaging of molecular interactions at damaged sarcolemma.
Urmas Roostalu, Uwe Strähle. Dev Cell 2012
100
12

Knockdown of col22a1 gene in zebrafish induces a muscular dystrophy by disruption of the myotendinous junction.
Benjamin Charvet, Alexandre Guiraud, Marilyne Malbouyres, Daniela Zwolanek, Emilie Guillon, Sandrine Bretaud, Catherine Monnot, Jörg Schulze, Hannah L Bader, Bruno Allard,[...]. Development 2013
51
12

Zebrafish models flex their muscles to shed light on muscular dystrophies.
Joachim Berger, Peter D Currie. Dis Model Mech 2012
43
12

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
12

Deletion of the laminin alpha4 chain leads to impaired microvessel maturation.
Jill Thyboll, Jarkko Kortesmaa, Renhai Cao, Raija Soininen, Ling Wang, Antti Iivanainen, Lydia Sorokin, Mårten Risling, Yihai Cao, Karl Tryggvason. Mol Cell Biol 2002
237
10

Zebrafish models for human FKRP muscular dystrophies.
Genri Kawahara, Jeffrey R Guyon, Yukio Nakamura, Louis M Kunkel. Hum Mol Genet 2010
60
10

Generality of vertebrate developmental patterns: evidence for a dermomyotome in fish.
S H Devoto, W Stoiber, C L Hammond, P Steinbacher, J R Haslett, M J F Barresi, S E Patterson, E G Adiarte, S M Hughes. Evol Dev 2006
100
10

Roles for zebrafish focal adhesion kinase in notochord and somite morphogenesis.
C A Henry, B D Crawford, Y L Yan, J Postlethwait, M S Cooper, M B Hille. Dev Biol 2001
49
10

Zebrafish collagen XII is present in embryonic connective tissue sheaths (fascia) and basement membranes.
Hannah L Bader, Douglas R Keene, Benjamin Charvet, Guido Veit, Wolfgang Driever, Manuel Koch, Florence Ruggiero. Matrix Biol 2009
44
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.