A citation-based method for searching scientific literature

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
Times Cited: 266







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



Times Cited
  Times     Co-cited
Similarity


Dystroglycan function requires xylosyl- and glucuronyltransferase activities of LARGE.
Kei-ichiro Inamori, Takako Yoshida-Moriguchi, Yuji Hara, Mary E Anderson, Liping Yu, Kevin P Campbell. Science 2012
185
54

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
46

SGK196 is a glycosylation-specific O-mannose kinase required for dystroglycan function.
Takako Yoshida-Moriguchi, Tobias Willer, Mary E Anderson, David Venzke, Tamieka Whyte, Francesco Muntoni, Hane Lee, Stanley F Nelson, Liping Yu, Kevin P Campbell. Science 2013
133
44

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
43

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
40

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
35

ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome.
Tobias Willer, Hane Lee, Mark Lommel, Takako Yoshida-Moriguchi, Daniel Beltran Valero de Bernabe, David Venzke, Sebahattin Cirak, Harry Schachter, Jiri Vajsar, Thomas Voit,[...]. Nat Genet 2012
159
34

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
34

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
32

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
32

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
31

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
30


Deciphering the glycosylome of dystroglycanopathies using haploid screens for lassa virus entry.
Lucas T Jae, Matthijs Raaben, Moniek Riemersma, Ellen van Beusekom, Vincent A Blomen, Arno Velds, Ron M Kerkhoven, Jan E Carette, Haluk Topaloglu, Peter Meinecke,[...]. Science 2013
205
28

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
26

Dystroglycan: from biosynthesis to pathogenesis of human disease.
Rita Barresi, Kevin P Campbell. J Cell Sci 2006
395
26

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
26

The glucuronyltransferase B4GAT1 is required for initiation of LARGE-mediated α-dystroglycan functional glycosylation.
Tobias Willer, Kei-Ichiro Inamori, David Venzke, Corinne Harvey, Greg Morgensen, Yuji Hara, Daniel Beltrán Valero de Bernabé, Liping Yu, Kevin M Wright, Kevin P Campbell. Elife 2014
63
41

Dystroglycanopathies: coming into focus.
Caroline Godfrey, A Reghan Foley, Emma Clement, Francesco Muntoni. Curr Opin Genet Dev 2011
166
24

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
23


Mining the O-mannose glycoproteome reveals cadherins as major O-mannosylated glycoproteins.
Malene B Vester-Christensen, Adnan Halim, Hiren Jitendra Joshi, Catharina Steentoft, Eric P Bennett, Steven B Levery, Sergey Y Vakhrushev, Henrik Clausen. Proc Natl Acad Sci U S A 2013
103
23

Matriglycan: a novel polysaccharide that links dystroglycan to the basement membrane.
Takako Yoshida-Moriguchi, Kevin P Campbell. Glycobiology 2015
105
23

B4GAT1 is the priming enzyme for the LARGE-dependent functional glycosylation of α-dystroglycan.
Jeremy L Praissman, David H Live, Shuo Wang, Annapoorani Ramiah, Zoeisha S Chinoy, Geert-Jan Boons, Kelley W Moremen, Lance Wells. Elife 2014
54
40

The functional O-mannose glycan on α-dystroglycan contains a phospho-ribitol primed for matriglycan addition.
Jeremy L Praissman, Tobias Willer, M Osman Sheikh, Ants Toi, David Chitayat, Yung-Yao Lin, Hane Lee, Stephanie H Stalnaker, Shuo Wang, Pradeep Kumar Prabhakar,[...]. Elife 2016
64
34

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
31

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
21

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
21

Like-acetylglucosaminyltransferase (LARGE)-dependent modification of dystroglycan at Thr-317/319 is required for laminin binding and arenavirus infection.
Yuji Hara, Motoi Kanagawa, Stefan Kunz, Takako Yoshida-Moriguchi, Jakob S Satz, Yvonne M Kobayashi, Zihan Zhu, Steven J Burden, Michael B A Oldstone, Kevin P Campbell. Proc Natl Acad Sci U S A 2011
76
26

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
20

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
20

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
20

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
20

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
19

Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation.
Shigeru Sato, Yoshihiro Omori, Kimiko Katoh, Mineo Kondo, Motoi Kanagawa, Kentaro Miyata, Kazuo Funabiki, Toshiyuki Koyasu, Naoko Kajimura, Tomomitsu Miyoshi,[...]. Nat Neurosci 2008
189
19

Tumor suppressor function of laminin-binding alpha-dystroglycan requires a distinct beta3-N-acetylglucosaminyltransferase.
Xingfeng Bao, Motohiro Kobayashi, Shingo Hatakeyama, Kiyohiko Angata, Donald Gullberg, Jun Nakayama, Michiko N Fukuda, Minoru Fukuda. Proc Natl Acad Sci U S A 2009
74
25

DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy.
Rita Barone, Chiara Aiello, Valérie Race, Eva Morava, Francois Foulquier, Moniek Riemersma, Chiara Passarelli, Daniela Concolino, Massimo Carella, Filippo Santorelli,[...]. Ann Neurol 2012
93
20

Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly.
Sandrine Vuillaumier-Barrot, Céline Bouchet-Séraphin, Malika Chelbi, Louise Devisme, Samuel Quentin, Steven Gazal, Annie Laquerrière, Catherine Fallet-Bianco, Philippe Loget, Sylvie Odent,[...]. Am J Hum Genet 2012
87
21

Protein O-mannosylation is crucial for E-cadherin-mediated cell adhesion.
Mark Lommel, Patrick R Winterhalter, Tobias Willer, Maik Dahlhoff, Marlon R Schneider, Markus F Bartels, Ingrid Renner-Müller, Thomas Ruppert, Eckhard Wolf, Sabine Strahl. Proc Natl Acad Sci U S A 2013
55
34


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
18

A stoichiometric complex of neurexins and dystroglycan in brain.
S Sugita, F Saito, J Tang, J Satz, K Campbell, T C Südhof. J Cell Biol 2001
325
17

LARGE glycans on dystroglycan function as a tunable matrix scaffold to prevent dystrophy.
Matthew M Goddeeris, Biming Wu, David Venzke, Takako Yoshida-Moriguchi, Fumiaki Saito, Kiichiro Matsumura, Steven A Moore, Kevin P Campbell. Nature 2013
70
24

The Muscular Dystrophy Gene TMEM5 Encodes a Ribitol β1,4-Xylosyltransferase Required for the Functional Glycosylation of Dystroglycan.
Hiroshi Manya, Yoshiki Yamaguchi, Motoi Kanagawa, Kazuhiro Kobayashi, Michiko Tajiri, Keiko Akasaka-Manya, Hiroko Kawakami, Mamoru Mizuno, Yoshinao Wada, Tatsushi Toda,[...]. J Biol Chem 2016
35
48

Loss of alpha-dystroglycan laminin binding in epithelium-derived cancers is caused by silencing of LARGE.
Daniel Beltrán-Valero de Bernabé, Kei-Ichiro Inamori, Takako Yoshida-Moriguchi, Christine J Weydert, Hollie A Harper, Tobias Willer, Michael D Henry, Kevin P Campbell. J Biol Chem 2009
74
21

Xylosyl- and glucuronyltransferase functions of LARGE in α-dystroglycan modification are conserved in LARGE2.
Kei-ichiro Inamori, Yuji Hara, Tobias Willer, Mary E Anderson, Zihan Zhu, Takako Yoshida-Moriguchi, Kevin P Campbell. Glycobiology 2013
35
45

Human ISPD Is a Cytidyltransferase Required for Dystroglycan O-Mannosylation.
Moniek Riemersma, D Sean Froese, Walinka van Tol, Udo F Engelke, Jolanta Kopec, Monique van Scherpenzeel, Angel Ashikov, Tobias Krojer, Frank von Delft, Marco Tessari,[...]. Chem Biol 2015
46
34

Site mapping and characterization of O-glycan structures on alpha-dystroglycan isolated from rabbit skeletal muscle.
Stephanie H Stalnaker, Sana Hashmi, Jae-Min Lim, Kazuhiro Aoki, Mindy Porterfield, Gerardo Gutierrez-Sanchez, James Wheeler, James M Ervasti, Carl Bergmann, Michael Tiemeyer,[...]. J Biol Chem 2010
77
19

Molecular recognition by LARGE is essential for expression of functional dystroglycan.
Motoi Kanagawa, Fumiaki Saito, Stefan Kunz, Takako Yoshida-Moriguchi, Rita Barresi, Yvonne M Kobayashi, John Muschler, Jan P Dumanski, Daniel E Michele, Michael B A Oldstone,[...]. Cell 2004
196
15

Autosomal recessive dilated cardiomyopathy due to DOLK mutations results from abnormal dystroglycan O-mannosylation.
Dirk J Lefeber, Arjan P M de Brouwer, Eva Morava, Moniek Riemersma, Janneke H M Schuurs-Hoeijmakers, Birgit Absmanner, Kiek Verrijp, Willem M R van den Akker, Karin Huijben, Gerry Steenbergen,[...]. PLoS Genet 2011
102
15


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.