A citation-based method for searching scientific literature

Alasdair J Wood, Juliane S Müller, Catherine D Jepson, Steve H Laval, Hanns Lochmüller, Kate Bushby, Rita Barresi, Volker Straub. Hum Mol Genet 2011
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


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
66

Zebrafish models for human FKRP muscular dystrophies.
Genri Kawahara, Jeffrey R Guyon, Yukio Nakamura, Louis M Kunkel. Hum Mol Genet 2010
60
61

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
53
55

Genes required for functional glycosylation of dystroglycan are conserved in zebrafish.
Christopher J Moore, Huey Tse Goh, Jane E Hewitt. Genomics 2008
31
44

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
38

Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan.
M Brockington, D J Blake, P Prandini, S C Brown, S Torelli, M A Benson, C P Ponting, B Estournet, N B Romero, E Mercuri,[...]. Am J Hum Genet 2001
433
33

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
33

Protein O-mannosylation is necessary for normal embryonic development in zebrafish.
Eriko Avsar-Ban, Hisayoshi Ishikawa, Hiroshi Manya, Masatoki Watanabe, Shinichi Akiyama, Hideo Miyake, Tamao Endo, Yutaka Tamaru. Glycobiology 2010
24
33

Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan.
Caroline Godfrey, Emma Clement, Rachael Mein, Martin Brockington, Janine Smith, Beril Talim, Volker Straub, Stephanie Robb, Ros Quinlivan, Lucy Feng,[...]. Brain 2007
268
27

Dystroglycan: from biosynthesis to pathogenesis of human disease.
Rita Barresi, Kevin P Campbell. J Cell Sci 2006
395
27

A dystroglycan mutation associated with limb-girdle muscular dystrophy.
Yuji Hara, Burcu Balci-Hayta, Takako Yoshida-Moriguchi, Motoi Kanagawa, Daniel Beltrán-Valero de Bernabé, Hülya Gündeşli, Tobias Willer, Jakob S Satz, Robert W Crawford, Steven J Burden,[...]. N Engl J Med 2011
166
27

Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker-Warburg syndrome.
D Beltran-Valero de Bernabé, T Voit, C Longman, A Steinbrecher, V Straub, Y Yuva, R Herrmann, J Sperner, C Korenke, C Diesen,[...]. J Med Genet 2004
184
27

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
27

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
139
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
79
27

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
27

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
27

LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies.
Rita Barresi, Daniel E Michele, Motoi Kanagawa, Hollie A Harper, Sherri A Dovico, Jakob S Satz, Steven A Moore, Wenli Zhang, Harry Schachter, Jan P Dumanski,[...]. Nat Med 2004
188
27

ISPD produces CDP-ribitol used by FKTN and FKRP to transfer ribitol phosphate onto α-dystroglycan.
Isabelle Gerin, Benoît Ury, Isabelle Breloy, Céline Bouchet-Seraphin, Jennifer Bolsée, Mathias Halbout, Julie Graff, Didier Vertommen, Giulio G Muccioli, Nathalie Seta,[...]. Nat Commun 2016
70
27

A comparative study of alpha-dystroglycan glycosylation in dystroglycanopathies suggests that the hypoglycosylation of alpha-dystroglycan does not consistently correlate with clinical severity.
Cecilia Jimenez-Mallebrera, Silvia Torelli, Lucy Feng, Jihee Kim, Caroline Godfrey, Emma Clement, Rachael Mein, Stephen Abbs, Susan C Brown, Kevin P Campbell,[...]. Brain Pathol 2009
83
22

Dystroglycanopathies: coming into focus.
Caroline Godfrey, A Reghan Foley, Emma Clement, Francesco Muntoni. Curr Opin Genet Dev 2011
166
22

Animal models of human disease: zebrafish swim into view.
Graham J Lieschke, Peter D Currie. Nat Rev Genet 2007
22

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
22

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
22

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
22

Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker-Warburg syndrome.
Karen Buysse, Moniek Riemersma, Gareth Powell, Jeroen van Reeuwijk, David Chitayat, Tony Roscioli, Erik-Jan Kamsteeg, Christa van den Elzen, Ellen van Beusekom, Susan Blaser,[...]. Hum Mol Genet 2013
98
22

Zebrafish based small molecule screens for novel DMD drugs.
Genri Kawahara, Louis M Kunkel. Drug Discov Today Technol 2013
15
26

Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan.
Elizabeth Stevens, Keren J Carss, Sebahattin Cirak, A Reghan Foley, Silvia Torelli, Tobias Willer, Dimira E Tambunan, Shu Yau, Lina Brodd, Caroline A Sewry,[...]. Am J Hum Genet 2013
105
22

Stages of embryonic development of the zebrafish.
C B Kimmel, W W Ballard, S R Kimmel, B Ullmann, T F Schilling. Dev Dyn 1995
22

Identification of a Post-translational Modification with Ribitol-Phosphate and Its Defect in Muscular Dystrophy.
Motoi Kanagawa, Kazuhiro Kobayashi, Michiko Tajiri, Hiroshi Manya, Atsushi Kuga, Yoshiki Yamaguchi, Keiko Akasaka-Manya, Jun-Ichi Furukawa, Mamoru Mizuno, Hiroko Kawakami,[...]. Cell Rep 2016
117
22

Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan.
Cheryl Longman, Martin Brockington, Silvia Torelli, Cecilia Jimenez-Mallebrera, Colin Kennedy, Nofal Khalil, Lucy Feng, Ravindra K Saran, Thomas Voit, Luciano Merlini,[...]. Hum Mol Genet 2003
304
16

Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1.
A Yoshida, K Kobayashi, H Manya, K Taniguchi, H Kano, M Mizuno, T Inazu, H Mitsuhashi, S Takahashi, M Takeuchi,[...]. Dev Cell 2001
521
16

Abnormalities in alpha-dystroglycan expression in MDC1C and LGMD2I muscular dystrophies.
Susan C Brown, Silvia Torelli, Martin Brockington, Yeliz Yuva, Cecilia Jimenez, Lucy Feng, Louise Anderson, Isabella Ugo, Stephan Kroger, Kate Bushby,[...]. Am J Pathol 2004
124
16

POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome.
J van Reeuwijk, M Janssen, C van den Elzen, D Beltran-Valero de Bernabé, P Sabatelli, L Merlini, M Boon, H Scheffer, M Brockington, F Muntoni,[...]. J Med Genet 2005
291
16

The proteasomal inhibitor MG132 prevents muscular dystrophy in zebrafish.
Steve J Winder, Leanne Lipscomb, Caroline Angela Parkin, Mikko Juusola. PLoS Curr 2011
21
16

Intragenic deletion in the LARGE gene causes Walker-Warburg syndrome.
Jeroen van Reeuwijk, Prabhjit K Grewal, Mustafa A M Salih, Daniel Beltrán-Valero de Bernabé, Jenny M McLaughlan, Caroline B Michielse, Ralf Herrmann, Jane E Hewitt, Alice Steinbrecher, Mohamed Z Seidahmed,[...]. Hum Genet 2007
94
16

Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome.
Daniel Beltrán-Valero de Bernabé, Sophie Currier, Alice Steinbrecher, Jacopo Celli, Ellen van Beusekom, Bert van der Zwaag, Hülya Kayserili, Luciano Merlini, David Chitayat, William B Dobyns,[...]. Am J Hum Genet 2002
503
16

Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies.
Daniel E Michele, Rita Barresi, Motoi Kanagawa, Fumiaki Saito, Ronald D Cohn, Jakob S Satz, James Dollar, Ichizo Nishino, Richard I Kelley, Hannu Somer,[...]. Nature 2002
616
16

Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies.
Dirk J Lefeber, Johannes Schönberger, Eva Morava, Mailys Guillard, Karin M Huyben, Kiek Verrijp, Olga Grafakou, Athanasios Evangeliou, Frank W Preijers, Panagiota Manta,[...]. Am J Hum Genet 2009
140
16

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
16

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
16

Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome.
M Chiara Manzini, Dimira E Tambunan, R Sean Hill, Tim W Yu, Thomas M Maynard, Erin L Heinzen, Kevin V Shianna, Christine R Stevens, Jennifer N Partlow, Brenda J Barry,[...]. Am J Hum Genet 2012
119
16

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
16

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
16

Zebrafish models flex their muscles to shed light on muscular dystrophies.
Joachim Berger, Peter D Currie. Dis Model Mech 2012
43
16

Hooked! Modeling human disease in zebrafish.
Cristina Santoriello, Leonard I Zon. J Clin Invest 2012
258
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
35
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
157
16

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
16

The HDAC Inhibitor TSA Ameliorates a Zebrafish Model of Duchenne Muscular Dystrophy.
Nathan M Johnson, Gist H Farr, Lisa Maves. PLoS Curr 2013
15
20


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.