A citation-based method for searching scientific literature

Elizabeth M Gibbs, Eric J Horstick, James J Dowling. FEBS J 2013
Times Cited: 43







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



Times Cited
  Times     Co-cited
Similarity


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
37

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
37

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
37

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
27

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
27

Stages of embryonic development of the zebrafish.
C B Kimmel, W W Ballard, S R Kimmel, B Ullmann, T F Schilling. Dev Dyn 1995
27

Animal models of human disease: zebrafish swim into view.
Graham J Lieschke, Peter D Currie. Nat Rev Genet 2007
27

Zebrafish models flex their muscles to shed light on muscular dystrophies.
Joachim Berger, Peter D Currie. Dis Model Mech 2012
43
27

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
25

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

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
18

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
18

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
18

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
26

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
18

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
18

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
18

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
157
16

In vivo drug discovery in the zebrafish.
Leonard I Zon, Randall T Peterson. Nat Rev Drug Discov 2005
888
16

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
39
17


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
79
16

Hooked! Modeling human disease in zebrafish.
Cristina Santoriello, Leonard I Zon. J Clin Invest 2012
258
16

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
86
16

In vivo imaging of molecular interactions at damaged sarcolemma.
Urmas Roostalu, Uwe Strähle. Dev Cell 2012
100
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
483
13

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





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
27

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
985
13

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
556
13

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
13

Structure and function of skeletal muscle in zebrafish early larvae.
Ying Dou, Monika Andersson-Lendahl, Anders Arner. J Gen Physiol 2008
38
15

Identification of a zebrafish model of muscular dystrophy.
David Bassett, Peter D Currie. Clin Exp Pharmacol Physiol 2004
55
13

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
11

Muscle diseases in the zebrafish.
Yung-Yao Lin. Neuromuscul Disord 2012
20
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
512
11

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
11

Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function.
Tamar E Sztal, Mo Zhao, Caitlin Williams, Viola Oorschot, Adam C Parslow, Aminah Giousoh, Michaela Yuen, Thomas E Hall, Adam Costin, Georg Ramm,[...]. Acta Neuropathol 2015
26
19

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

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
294
9

accordion, a zebrafish behavioral mutant, has a muscle relaxation defect due to a mutation in the ATPase Ca2+ pump SERCA1.
Hiromi Hirata, Louis Saint-Amant, Julie Waterbury, Wilson Cui, Weibin Zhou, Qin Li, Daniel Goldman, Michael Granato, John Y Kuwada. Development 2004
54
9

Targeted gene disruption in somatic zebrafish cells using engineered TALENs.
Jeffry D Sander, Lindsay Cade, Cyd Khayter, Deepak Reyon, Randall T Peterson, J Keith Joung, Jing-Ruey J Yeh. Nat Biotechnol 2011
416
9

Neuromuscular junction abnormalities in DNM2-related centronuclear myopathy.
Elizabeth M Gibbs, Nigel F Clarke, Kristy Rose, Emily C Oates, Richard Webster, Eva L Feldman, James J Dowling. J Mol Med (Berl) 2013
47
9


Modeling human muscle disease in zebrafish.
Jeffrey R Guyon, Leta S Steffen, Melanie H Howell, Timothy J Pusack, Christian Lawrence, Louis M Kunkel. Biochim Biophys Acta 2007
67
9

Notochord induction of zebrafish slow muscle mediated by Sonic hedgehog.
C S Blagden, P D Currie, P W Ingham, S M Hughes. Genes Dev 1997
277
9


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.