A citation-based method for searching scientific literature

Christopher J Moore, Huey Tse Goh, Jane E Hewitt. Genomics 2008
Times Cited: 31







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



Times Cited
  Times     Co-cited
Similarity


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
70

Zebrafish models for human FKRP muscular dystrophies.
Genri Kawahara, Jeffrey R Guyon, Yukio Nakamura, Louis M Kunkel. Hum Mol Genet 2010
60
51

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
48

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
41

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
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
35

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
35

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
35

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
35

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
32

Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C.
M Brockington, Y Yuva, P Prandini, S C Brown, S Torelli, M A Benson, R Herrmann, L V Anderson, R Bashir, J M Burgunder,[...]. Hum Mol Genet 2001
345
32

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
32

Dystroglycan: from biosynthesis to pathogenesis of human disease.
Rita Barresi, Kevin P Campbell. J Cell Sci 2006
395
32

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
32

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
29

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
29

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
29

Demonstration of mammalian protein O-mannosyltransferase activity: coexpression of POMT1 and POMT2 required for enzymatic activity.
Hiroshi Manya, Atsuro Chiba, Aruto Yoshida, Xiaohui Wang, Yasunori Chiba, Yoshifumi Jigami, Richard U Margolis, Tamao Endo. Proc Natl Acad Sci U S A 2004
266
29

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
29

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy.
K Kobayashi, Y Nakahori, M Miyake, K Matsumura, E Kondo-Iida, Y Nomura, M Segawa, M Yoshioka, K Saito, M Osawa,[...]. Nature 1998
600
29

Targeted disruption of the Walker-Warburg syndrome gene Pomt1 in mouse results in embryonic lethality.
Tobias Willer, Belén Prados, Juan Manuel Falcón-Pérez, Ingrid Renner-Müller, Gerhard K H Przemeck, Mark Lommel, Antonio Coloma, M Carmen Valero, Martin Hrabé de Angelis, Widmar Tanner,[...]. Proc Natl Acad Sci U S A 2004
114
29

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
29

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
37

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
25


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
25

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
25

Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies.
Prabhjit K Grewal, Jennifer M McLaughlan, Christopher J Moore, Claudia A Browning, Jane E Hewitt. Glycobiology 2005
68
25

The zebrafish as a model for muscular dystrophy and congenital myopathy.
David I Bassett, Peter D Currie. Hum Mol Genet 2003
94
25

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
25

Abnormal vascular development in zebrafish models for fukutin and FKRP deficiency.
Alasdair J Wood, Juliane S Müller, Catherine D Jepson, Steve H Laval, Hanns Lochmüller, Kate Bushby, Rita Barresi, Volker Straub. Hum Mol Genet 2011
18
44

Localization and functional analysis of the LARGE family of glycosyltransferases: significance for muscular dystrophy.
Martin Brockington, Silvia Torelli, Paola Prandini, Chiara Boito, Nazanin F Dolatshad, Cheryl Longman, Susan C Brown, Francesco Muntoni. Hum Mol Genet 2005
76
22



A genetic model for muscle-eye-brain disease in mice lacking protein O-mannose 1,2-N-acetylglucosaminyltransferase (POMGnT1).
Jianmin Liu, Sherry L Ball, Yuan Yang, Pinchao Mei, Lei Zhang, Haining Shi, Henry J Kaminski, Vance P Lemmon, Huaiyu Hu. Mech Dev 2006
98
22

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
22

Delta-sarcoglycan is required for early zebrafish muscle organization.
Jeffrey R Guyon, Alycia N Mosley, Susan J Jun, Federica Montanaro, Leta S Steffen, Yi Zhou, Vincenzo Nigro, Len I Zon, Louis M Kunkel. Exp Cell Res 2005
38
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

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
22

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
22


Fukutin gene mutations in steroid-responsive limb girdle muscular dystrophy.
Caroline Godfrey, Diana Escolar, Martin Brockington, Emma M Clement, Rachael Mein, Cecilia Jimenez-Mallebrera, Silvia Torelli, Lucy Feng, Susan C Brown, Caroline A Sewry,[...]. Ann Neurol 2006
100
19

LARGE2 facilitates the maturation of alpha-dystroglycan more effectively than LARGE.
Katsuya Fujimura, Hiromichi Sawaki, Tokiko Sakai, Toru Hiruma, Nobuo Nakanishi, Takashi Sato, Takashi Ohkura, Hisashi Narimatsu. Biochem Biophys Res Commun 2005
44
19

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.
Steven A Moore, Fumiaki Saito, Jianguo Chen, Daniel E Michele, Michael D Henry, Albee Messing, Ronald D Cohn, Susan E Ross-Barta, Steve Westra, Roger A Williamson,[...]. Nature 2002
424
19


The twisted abdomen phenotype of Drosophila POMT1 and POMT2 mutants coincides with their heterophilic protein O-mannosyltransferase activity.
Tomomi Ichimiya, Hiroshi Manya, Yoshiko Ohmae, Hideki Yoshida, Kuniaki Takahashi, Ryu Ueda, Tamao Endo, Shoko Nishihara. J Biol Chem 2004
71
19

Functional requirements for fukutin-related protein in the Golgi apparatus.
Chris T Esapa, Matthew A Benson, Jörn E Schröder, Enca Martin-Rendon, Martin Brockington, Susan C Brown, Francesco Muntoni, Stephan Kröger, Derek J Blake. Hum Mol Genet 2002
103
19

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
19

O-mannosyl phosphorylation of alpha-dystroglycan is required for laminin binding.
Takako Yoshida-Moriguchi, Liping Yu, Stephanie H Stalnaker, Sarah Davis, Stefan Kunz, Michael Madson, Michael B A Oldstone, Harry Schachter, Lance Wells, Kevin P Campbell. Science 2010
237
19

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
19


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.