A citation-based method for searching scientific literature

Erin C Bailey, Sarah S Alrowaished, Elisabeth A Kilroy, Emma S Crooks, Daisy M Drinkert, Chaya M Karunasiri, Joseph J Belanger, Andre Khalil, Joshua B Kelley, Clarissa A Henry. Skelet Muscle 2019
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


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
50
57


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
67
42

PIK3C2B inhibition improves function and prolongs survival in myotubular myopathy animal models.
Nesrin Sabha, Jonathan R Volpatti, Hernan Gonorazky, Aaron Reifler, Ann E Davidson, Xingli Li, Nadine M Eltayeb, Claudia Dall'Armi, Gilbert Di Paolo, Susan V Brooks,[...]. J Clin Invest 2016
44
28

Muscular dystrophy modeling in zebrafish.
M Li, K J Hromowyk, S L Amacher, P D Currie. Methods Cell Biol 2017
15
28

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
57
28

Discovery of Novel Therapeutics for Muscular Dystrophies using Zebrafish Phenotypic Screens.
Jeffrey J Widrick, Genri Kawahara, Matthew S Alexander, Alan H Beggs, Louis M Kunkel. J Neuromuscul Dis 2019
13
28

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
155
28

Congenital myopathies: an update.
Jessica R Nance, James J Dowling, Elizabeth M Gibbs, Carsten G Bönnemann. Curr Neurol Neurosci Rep 2012
77
28

Time-lapse analysis and mathematical characterization elucidate novel mechanisms underlying muscle morphogenesis.
Chelsi J Snow, Michelle Goody, Meghan W Kelly, Emma C Oster, Robert Jones, Andre Khalil, Clarissa A Henry. PLoS Genet 2008
33
28

Nrk2b-mediated NAD+ production regulates cell adhesion and is required for muscle morphogenesis in vivo: Nrk2b and NAD+ in muscle morphogenesis.
Michelle F Goody, Meghan W Kelly, Kevin N Lessard, Andre Khalil, Clarissa A Henry. Dev Biol 2010
43
28

Muscle dysfunction in a zebrafish model of Duchenne muscular dystrophy.
Jeffrey J Widrick, Matthew S Alexander, Benjamin Sanchez, Devin E Gibbs, Genri Kawahara, Alan H Beggs, Louis M Kunkel. Physiol Genomics 2016
13
28


Genome engineering using the CRISPR-Cas9 system.
F Ann Ran, Patrick D Hsu, Jason Wright, Vineeta Agarwala, David A Scott, Feng Zhang. Nat Protoc 2013
28

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
52
28

Efficient engraftment of pluripotent stem cell-derived myogenic progenitors in a novel immunodeficient mouse model of limb girdle muscular dystrophy 2I.
Karim Azzag, Carolina Ortiz-Cordero, Nelio A J Oliveira, Alessandro Magli, Sridhar Selvaraj, Sudheer Tungtur, Weston Upchurch, Paul A Iaizzo, Qi Long Lu, Rita C R Perlingeiro. Skelet Muscle 2020
5
40

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
112
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
28

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
429
28

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
28

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
182
28


Human ES- and iPS-derived myogenic progenitors restore DYSTROPHIN and improve contractility upon transplantation in dystrophic mice.
Radbod Darabi, Robert W Arpke, Stefan Irion, John T Dimos, Marica Grskovic, Michael Kyba, Rita C R Perlingeiro. Cell Stem Cell 2012
257
28

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
131
28

Human embryoid bodies as a 3D tissue model of the extracellular matrix and α-dystroglycanopathies.
Alec R Nickolls, Michelle M Lee, Kristen Zukosky, Barbara S Mallon, Carsten G Bönnemann. Dis Model Mech 2020
3
66

AAV-mediated transfer of FKRP shows therapeutic efficacy in a murine model but requires control of gene expression.
Evelyne Gicquel, Natacha Maizonnier, Steven J Foltz, William J Martin, Nathalie Bourg, Fedor Svinartchouk, Karine Charton, Aaron M Beedle, Isabelle Richard. Hum Mol Genet 2017
22
28

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
342
28

Autologous intramuscular transplantation of engineered satellite cells induces exosome-mediated systemic expression of Fukutin-related protein and rescues disease phenotype in a murine model of limb-girdle muscular dystrophy type 2I.
Paola Frattini, Chiara Villa, Francesca De Santis, Mirella Meregalli, Marzia Belicchi, Silvia Erratico, Pamela Bella, Manuela Teresa Raimondi, Qilong Lu, Yvan Torrente. Hum Mol Genet 2017
14
28

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
182
28

Crystal structures of fukutin-related protein (FKRP), a ribitol-phosphate transferase related to muscular dystrophy.
Naoyuki Kuwabara, Rieko Imae, Hiroshi Manya, Tomohiro Tanaka, Mamoru Mizuno, Hiroki Tsumoto, Motoi Kanagawa, Kazuhiro Kobayashi, Tatsushi Toda, Toshiya Senda,[...]. Nat Commun 2020
10
28

Gene Correction of LGMD2A Patient-Specific iPSCs for the Development of Targeted Autologous Cell Therapy.
Sridhar Selvaraj, Neha R Dhoke, James Kiley, Alba Judith Mateos-Aierdi, Sudheer Tungtur, Ricardo Mondragon-Gonzalez, Grace Killeen, Vanessa K P Oliveira, Adolfo López de Munain, Rita C R Perlingeiro. Mol Ther 2019
20
28

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
264
28

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
60
28

Adeno-associated virus 9 mediated FKRP gene therapy restores functional glycosylation of α-dystroglycan and improves muscle functions.
Lei Xu, Pei Juan Lu, Chi-Hsien Wang, Elizabeth Keramaris, Chunping Qiao, Bin Xiao, Derek J Blake, Xiao Xiao, Qi Long Lu. Mol Ther 2013
45
28

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
60
28

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
32
28

Apoptosis inhibitors and mini-agrin have additive benefits in congenital muscular dystrophy mice.
Sarina Meinen, Shuo Lin, Raphael Thurnherr, Michael Erb, Thomas Meier, Markus A Rüegg. EMBO Mol Med 2011
35
14

Genetic modifiers of muscular dystrophy act on sarcolemmal resealing and recovery from injury.
Mattia Quattrocelli, Joanna Capote, Joyce C Ohiri, James L Warner, Andy H Vo, Judy U Earley, Michele Hadhazy, Alexis R Demonbreun, Melissa J Spencer, Elizabeth M McNally. PLoS Genet 2017
14
14

Analysis of Zebrafish Larvae Skeletal Muscle Integrity with Evans Blue Dye.
Sarah J Smith, Eric J Horstick, Ann E Davidson, James Dowling. J Vis Exp 2015
8
14

Applying genome-wide CRISPR-Cas9 screens for therapeutic discovery in facioscapulohumeral muscular dystrophy.
Angela Lek, Yuanfan Zhang, Keryn G Woodman, Shushu Huang, Alec M DeSimone, Justin Cohen, Vincent Ho, James Conner, Lillian Mead, Andrew Kodani,[...]. Sci Transl Med 2020
15
14


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
40
14

Congenital muscular dystrophies in the UK population: Clinical and molecular spectrum of a large cohort diagnosed over a 12-year period.
Maria Sframeli, Anna Sarkozy, Marta Bertoli, Guja Astrea, Judith Hudson, Mariacristina Scoto, Rachael Mein, Michael Yau, Rahul Phadke, Lucy Feng,[...]. Neuromuscul Disord 2017
45
14

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
25
14


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
14

COL6A and LAMA2 Mutation Congenital Muscular Dystrophy: A Clinical and Electrophysiological Study.
Sumit Verma, Parul Goyal, Lokesh Guglani, Charlotte Peinhardt, Diane Pelzek, Paul E Barkhaus. J Clin Neuromuscul Dis 2018
5
20

RGD inhibition of itgb1 ameliorates laminin-α2-deficient zebrafish fibre pathology.
Alasdair J Wood, Naomi Cohen, Veronica Joshi, Mei Li, Adam Costin, Lucy Hersey, Emily A McKaige, Jessica D Manneken, Carmen Sonntag, Lee B Miles,[...]. Hum Mol Genet 2019
5
20

Cellular rescue in a zebrafish model of congenital muscular dystrophy type 1A.
T E Hall, A J Wood, O Ehrlich, M Li, C S Sonntag, N J Cole, I G Huttner, T E Sztal, P D Currie. NPJ Regen Med 2019
8
14

Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype.
Karen K McKee, Stephanie C Crosson, Sarina Meinen, Judith R Reinhard, Markus A Rüegg, Peter D Yurchenco. J Clin Invest 2017
32
14


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.