A citation-based method for searching scientific literature

Shigeru Sato, Yoshihiro Omori, Kimiko Katoh, Mineo Kondo, Motoi Kanagawa, Kentaro Miyata, Kazuo Funabiki, Toshiyuki Koyasu, Naoko Kajimura, Tomomitsu Miyoshi, Hajime Sawai, Kazuhiro Kobayashi, Akiko Tani, Tatsushi Toda, Jiro Usukura, Yasuo Tano, Takashi Fujikado, Takahisa Furukawa. Nat Neurosci 2008
Times Cited: 189







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



Times Cited
  Times     Co-cited
Similarity


Presynaptic dystroglycan-pikachurin complex regulates the proper synaptic connection between retinal photoreceptor and bipolar cells.
Yoshihiro Omori, Fumiyuki Araki, Taro Chaya, Naoko Kajimura, Shoichi Irie, Koji Terada, Yuki Muranishi, Toshinori Tsujii, Shinji Ueno, Toshiyuki Koyasu,[...]. J Neurosci 2012
57
50


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
322
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
25

Dystroglycan organizes axon guidance cue localization and axonal pathfinding.
Kevin M Wright, Krissy A Lyon, Haiwen Leung, Daniel J Leahy, Le Ma, David D Ginty. Neuron 2012
112
24

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
609
23

Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor.
S H Gee, F Montanaro, M H Lindenbaum, S Carbonetto. Cell 1994
446
22

Post-translational maturation of dystroglycan is necessary for pikachurin binding and ribbon synaptic localization.
Motoi Kanagawa, Yoshihiro Omori, Shigeru Sato, Kazuhiro Kobayashi, Yuko Miyagoe-Suzuki, Shin'ichi Takeda, Tamao Endo, Takahisa Furukawa, Tatsushi Toda. J Biol Chem 2010
36
58

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
179
19

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
518
18

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
303
18

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
234
17

Dystroglycan: from biosynthesis to pathogenesis of human disease.
Rita Barresi, Kevin P Campbell. J Cell Sci 2006
389
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
500
16

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
428
16

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
422
15

Matriglycan: a novel polysaccharide that links dystroglycan to the basement membrane.
Takako Yoshida-Moriguchi, Kevin P Campbell. Glycobiology 2015
97
15

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
288
14

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
158
14

The relationship between perlecan and dystroglycan and its implication in the formation of the neuromuscular junction.
H B Peng, A A Ali, D F Daggett, H Rauvala, J R Hassell, N R Smalheiser. Cell Adhes Commun 1998
129
14

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
594
14

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
129
14


Mechanism for Selective Synaptic Wiring of Rod Photoreceptors into the Retinal Circuitry and Its Role in Vision.
Yan Cao, Ignacio Sarria, Katherine E Fehlhaber, Naomi Kamasawa, Cesare Orlandi, Kiely N James, Jennifer L Hazen, Matthew R Gardner, Michael Farzan, Amy Lee,[...]. Neuron 2015
60
23

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
107
14

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
263
13

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
13

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
66
19

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
340
13

TRPM1 is a component of the retinal ON bipolar cell transduction channel in the mGluR6 cascade.
Chieko Koike, Takehisa Obara, Yoshitsugu Uriu, Tomohiro Numata, Rikako Sanuki, Kentarou Miyata, Toshiyuki Koyasu, Shinji Ueno, Kazuo Funabiki, Akiko Tani,[...]. Proc Natl Acad Sci U S A 2010
188
13

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
163
12

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
12

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
97
12

Dystroglycanopathies: coming into focus.
Caroline Godfrey, A Reghan Foley, Emma Clement, Francesco Muntoni. Curr Opin Genet Dev 2011
160
12

Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration.
Ronald D Cohn, Michael D Henry, Daniel E Michele, Rita Barresi, Fumiaki Saito, Steven A Moore, Jason D Flanagan, Mark W Skwarchuk, Michael E Robbins, Jerry R Mendell,[...]. Cell 2002
200
11

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
201
11

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
138
11

A role for dystrophin-associated glycoproteins and utrophin in agrin-induced AChR clustering.
J T Campanelli, S L Roberds, K P Campbell, R H Scheller. Cell 1994
346
11

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
58
18

Fukutin-related protein is essential for mouse muscle, brain and eye development and mutation recapitulates the wide clinical spectrums of dystroglycanopathies.
Yiumo Michael Chan, Elizabeth Keramaris-Vrantsis, Hart G Lidov, James H Norton, Natalia Zinchenko, Helen E Gruber, Randy Thresher, Derek J Blake, Jignya Ashar, Jeffrey Rosenfeld,[...]. Hum Mol Genet 2010
67
16

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
95
11


The presynaptic active zone protein bassoon is essential for photoreceptor ribbon synapse formation in the retina.
Oliver Dick, Susanne tom Dieck, Wilko Detlef Altrock, Josef Ammermüller, Reto Weiler, Craig Curtis Garner, Eckart Dieter Gundelfinger, Johann Helmut Brandstätter. Neuron 2003
299
10

Otx2 homeobox gene controls retinal photoreceptor cell fate and pineal gland development.
Akihiro Nishida, Akiko Furukawa, Chieko Koike, Yasuo Tano, Shinichi Aizawa, Isao Matsuo, Takahisa Furukawa. Nat Neurosci 2003
398
10

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
101
10


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
261
10

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
137
10


Visual impairment in the absence of dystroglycan.
Jakob S Satz, Alisdair R Philp, Huy Nguyen, Hajime Kusano, Jane Lee, Rolf Turk, Megan J Riker, Jasmine Hernández, Robert M Weiss, Michael G Anderson,[...]. J Neurosci 2009
43
23


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.