A citation-based method for searching scientific literature

James J Dowling, Andrew P Vreede, Sean E Low, Elizabeth M Gibbs, John Y Kuwada, Carsten G Bonnemann, Eva L Feldman. PLoS Genet 2009
Times Cited: 157







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



Times Cited
  Times     Co-cited
Similarity


T-tubule disorganization and defective excitation-contraction coupling in muscle fibers lacking myotubularin lipid phosphatase.
Lama Al-Qusairi, Norbert Weiss, Anne Toussaint, Céline Berbey, Nadia Messaddeq, Christine Kretz, Despina Sanoudou, Alan H Beggs, Bruno Allard, Jean-Louis Mandel,[...]. Proc Natl Acad Sci U S A 2009
120
52

A gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast.
J Laporte, L J Hu, C Kretz, J L Mandel, P Kioschis, J F Coy, S M Klauck, A Poustka, N Dahl. Nat Genet 1996
465
45

The lipid phosphatase myotubularin is essential for skeletal muscle maintenance but not for myogenesis in mice.
Anna Buj-Bello, Vincent Laugel, Nadia Messaddeq, Hala Zahreddine, Jocelyn Laporte, Jean-Francois Pellissier, Jean-Louis Mandel. Proc Natl Acad Sci U S A 2002
154
38

MTM1 mutation associated with X-linked myotubular myopathy in Labrador Retrievers.
Alan H Beggs, Johann Böhm, Elizabeth Snead, Marek Kozlowski, Marie Maurer, Katie Minor, Martin K Childers, Susan M Taylor, Christophe Hitte, James R Mickelson,[...]. Proc Natl Acad Sci U S A 2010
90
33

Centronuclear (myotubular) myopathy.
Heinz Jungbluth, Carina Wallgren-Pettersson, Jocelyn Laporte. Orphanet J Rare Dis 2008
186
28

Mutations in dynamin 2 cause dominant centronuclear myopathy.
Marc Bitoun, Svetlana Maugenre, Pierre-Yves Jeannet, Emmanuelle Lacène, Xavier Ferrer, Pascal Laforêt, Jean-Jacques Martin, Jocelyn Laporte, Hanns Lochmüller, Alan H Beggs,[...]. Nat Genet 2005
289
28

Modeling the human MTM1 p.R69C mutation in murine Mtm1 results in exon 4 skipping and a less severe myotubular myopathy phenotype.
Christopher R Pierson, Ashley N Dulin-Smith, Ashley N Durban, Morgan L Marshall, Jordan T Marshall, Andrew D Snyder, Nada Naiyer, Jordan T Gladman, Dawn S Chandler, Michael W Lawlor,[...]. Hum Mol Genet 2012
43
62

Myotubularin controls desmin intermediate filament architecture and mitochondrial dynamics in human and mouse skeletal muscle.
Karim Hnia, Helene Tronchère, Kinga K Tomczak, Leonela Amoasii, Patrick Schultz, Alan H Beggs, Bernard Payrastre, Jean Louis Mandel, Jocelyn Laporte. J Clin Invest 2011
85
31

AAV-mediated intramuscular delivery of myotubularin corrects the myotubular myopathy phenotype in targeted murine muscle and suggests a function in plasma membrane homeostasis.
Anna Buj-Bello, Françoise Fougerousse, Yannick Schwab, Nadia Messaddeq, Danièle Spehner, Christopher R Pierson, Muriel Durand, Christine Kretz, Olivier Danos, Anne-Marie Douar,[...]. Hum Mol Genet 2008
82
31

Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.
Anne-Sophie Nicot, Anne Toussaint, Valérie Tosch, Christine Kretz, Carina Wallgren-Pettersson, Erik Iwarsson, Helen Kingston, Jean-Marie Garnier, Valérie Biancalana, Anders Oldfors,[...]. Nat Genet 2007
249
24

Reducing dynamin 2 expression rescues X-linked centronuclear myopathy.
Belinda S Cowling, Thierry Chevremont, Ivana Prokic, Christine Kretz, Arnaud Ferry, Catherine Coirault, Olga Koutsopoulos, Vincent Laugel, Norma B Romero, Jocelyn Laporte. J Clin Invest 2014
73
32

Gene therapy prolongs survival and restores function in murine and canine models of myotubular myopathy.
Martin K Childers, Romain Joubert, Karine Poulard, Christelle Moal, Robert W Grange, Jonathan A Doering, Michael W Lawlor, Branden E Rider, Thibaud Jamet, Nathalie Danièle,[...]. Sci Transl Med 2014
95
25

Defects in amphiphysin 2 (BIN1) and triads in several forms of centronuclear myopathies.
Anne Toussaint, Belinda Simone Cowling, Karim Hnia, Michel Mohr, Anders Oldfors, Yannick Schwab, Uluc Yis, Thierry Maisonobe, Tanya Stojkovic, Carina Wallgren-Pettersson,[...]. Acta Neuropathol 2011
85
27

Myotubular myopathy and the neuromuscular junction: a novel therapeutic approach from mouse models.
James J Dowling, Romain Joubert, Sean E Low, Ashley N Durban, Nadia Messaddeq, Xingli Li, Ashley N Dulin-Smith, Andrew D Snyder, Morgan L Marshall, Jordan T Marshall,[...]. Dis Model Mech 2012
37
59

Centronuclear myopathies: a widening concept.
Norma Beatriz Romero. Neuromuscul Disord 2010
161
21

Amphiphysin 2 (Bin1) and T-tubule biogenesis in muscle.
Eunkyung Lee, Melissa Marcucci, Laurie Daniell, Marc Pypaert, Ora A Weisz, Gian-Carlo Ochoa, Khashayar Farsad, Markus R Wenk, Pietro De Camilli. Science 2002
295
21


Enzyme replacement therapy rescues weakness and improves muscle pathology in mice with X-linked myotubular myopathy.
Michael W Lawlor, Dustin Armstrong, Marissa G Viola, Jeffrey J Widrick, Hui Meng, Robert W Grange, Martin K Childers, Cynthia P Hsu, Michael O'Callaghan, Christopher R Pierson,[...]. Hum Mol Genet 2013
50
38

MTM1 mutations in X-linked myotubular myopathy.
J Laporte, V Biancalana, S M Tanner, W Kress, V Schneider, C Wallgren-Pettersson, F Herger, A Buj-Bello, F Blondeau, S Liechti-Gallati,[...]. Hum Mutat 2000
144
18

A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice.
Anne-Cécile Durieux, Alban Vignaud, Bernard Prudhon, Mai Thao Viou, Maud Beuvin, Stéphane Vassilopoulos, Bodvaël Fraysse, Arnaud Ferry, Jeanne Lainé, Norma B Romero,[...]. Hum Mol Genet 2010
82
21

Defective autophagy and mTORC1 signaling in myotubularin null mice.
Kristina M Fetalvero, Yenyen Yu, Margaret Goetschkes, Guiqing Liang, Reginald A Valdez, Ty Gould, Ellen Triantafellow, Sebastian Bergling, Joseph Loureiro, John Eash,[...]. Mol Cell Biol 2013
57
31

RYR1 mutations are a common cause of congenital myopathies with central nuclei.
J M Wilmshurst, S Lillis, H Zhou, K Pillay, H Henderson, W Kress, C R Müller, A Ndondo, V Cloke, T Cullup,[...]. Ann Neurol 2010
177
17

Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy.
Johann Böhm, Valérie Biancalana, Elizabeth T Dechene, Marc Bitoun, Christopher R Pierson, Elise Schaefer, Hatice Karasoy, Melissa A Dempsey, Fabrice Klein, Nicolas Dondaine,[...]. Hum Mutat 2012
80
20

Increased expression of wild-type or a centronuclear myopathy mutant of dynamin 2 in skeletal muscle of adult mice leads to structural defects and muscle weakness.
Belinda S Cowling, Anne Toussaint, Leonela Amoasii, Pascale Koebel, Arnaud Ferry, Laurianne Davignon, Ichizo Nishino, Jean-Louis Mandel, Jocelyn Laporte. Am J Pathol 2011
57
28

Impaired neuromuscular transmission and response to acetylcholinesterase inhibitors in centronuclear myopathies.
Stephanie A Robb, Caroline A Sewry, James J Dowling, Lucy Feng, Tom Cullup, Sue Lillis, Stephen Abbs, Melissa M Lees, Jocelyn Laporte, Adnan Y Manzur,[...]. Neuromuscul Disord 2011
67
23

Myotubularin and PtdIns3P remodel the sarcoplasmic reticulum in muscle in vivo.
Leonela Amoasii, Karim Hnia, Gaëtan Chicanne, Andreas Brech, Belinda S Cowling, Martin Michael Müller, Yannick Schwab, Pascale Koebel, Arnaud Ferry, Bernard Payrastre,[...]. J Cell Sci 2013
38
42

Recessive truncating titin gene, TTN, mutations presenting as centronuclear myopathy.
Ozge Ceyhan-Birsoy, Pankaj B Agrawal, Carlos Hidalgo, Klaus Schmitz-Abe, Elizabeth T DeChene, Lindsay C Swanson, Rachel Soemedi, Nasim Vasli, Susan T Iannaccone, Perry B Shieh,[...]. Neurology 2013
120
16

Defective membrane remodeling in neuromuscular diseases: insights from animal models.
Belinda S Cowling, Anne Toussaint, Jean Muller, Jocelyn Laporte. PLoS Genet 2012
41
36

Phosphoinositides in cell regulation and membrane dynamics.
Gilbert Di Paolo, Pietro De Camilli. Nature 2006
15

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
47
31


X-linked myotubular and centronuclear myopathies.
Christopher R Pierson, Kinga Tomczak, Pankaj Agrawal, Behzad Moghadaszadeh, Alan H Beggs. J Neuropathol Exp Neurol 2005
75
18


Phosphatase-dead myotubularin ameliorates X-linked centronuclear myopathy phenotypes in mice.
Leonela Amoasii, Dimitri L Bertazzi, Hélène Tronchère, Karim Hnia, Gaëtan Chicanne, Bruno Rinaldi, Belinda S Cowling, Arnaud Ferry, Bruno Klaholz, Bernard Payrastre,[...]. PLoS Genet 2012
32
43

The myopathy-causing mutation DNM2-S619L leads to defective tubulation in vitro and in developing zebrafish.
Elizabeth M Gibbs, Ann E Davidson, William R Telfer, Eva L Feldman, James J Dowling. Dis Model Mech 2014
28
50

SPEG interacts with myotubularin, and its deficiency causes centronuclear myopathy with dilated cardiomyopathy.
Pankaj B Agrawal, Christopher R Pierson, Mugdha Joshi, Xiaoli Liu, Gianina Ravenscroft, Behzad Moghadaszadeh, Tiffany Talabere, Marissa Viola, Lindsay C Swanson, Göknur Haliloğlu,[...]. Am J Hum Genet 2014
95
14

Antisense oligonucleotide-mediated Dnm2 knockdown prevents and reverts myotubular myopathy in mice.
Hichem Tasfaout, Suzie Buono, Shuling Guo, Christine Kretz, Nadia Messaddeq, Sheri Booten, Sarah Greenlee, Brett P Monia, Belinda S Cowling, Jocelyn Laporte. Nat Commun 2017
47
29

Genotype-phenotype correlations in X-linked myotubular myopathy.
Meriel McEntagart, Gretchen Parsons, Anna Buj-Bello, Valérie Biancalana, Iain Fenton, Mark Little, Michael Krawczak, Nick Thomas, Gail Herman, Angus Clarke,[...]. Neuromuscul Disord 2002
91
14


Oxidative stress and successful antioxidant treatment in models of RYR1-related myopathy.
James J Dowling, Sandrine Arbogast, Junguk Hur, Darcee D Nelson, Anna McEvoy, Trent Waugh, Isabelle Marty, Joel Lunardi, Susan V Brooks, John Y Kuwada,[...]. Brain 2012
79
16

Myotubularin phosphatases: policing 3-phosphoinositides.
Fred L Robinson, Jack E Dixon. Trends Cell Biol 2006
170
13

Characterisation of mutations in 77 patients with X-linked myotubular myopathy, including a family with a very mild phenotype.
Valérie Biancalana, Olivier Caron, Sabina Gallati, Frank Baas, Wolfram Kress, Giuseppe Novelli, Maria Rosaria D'Apice, Clotilde Lagier-Tourenne, Anna Buj-Bello, Norma B Romero,[...]. Hum Genet 2003
89
14

The myotubularin-amphiphysin 2 complex in membrane tubulation and centronuclear myopathies.
Barbara Royer, Karim Hnia, Christos Gavriilidis, Hélène Tronchère, Valérie Tosch, Jocelyn Laporte. EMBO Rep 2013
38
34

Lack of myotubularin (MTM1) leads to muscle hypotrophy through unbalanced regulation of the autophagy and ubiquitin-proteasome pathways.
Lama Al-Qusairi, Ivana Prokic, Leonela Amoasii, Christine Kretz, Nadia Messaddeq, Jean-Louis Mandel, Jocelyn Laporte. FASEB J 2013
44
29

Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutations.
Johann Böhm, Valérie Biancalana, Edoardo Malfatti, Nicolas Dondaine, Catherine Koch, Nasim Vasli, Wolfram Kress, Matthias Strittmatter, Ana Lia Taratuto, Hernan Gonorazky,[...]. Brain 2014
58
22

A phosphoinositide conversion mechanism for exit from endosomes.
Katharina Ketel, Michael Krauss, Anne-Sophie Nicot, Dmytro Puchkov, Marnix Wieffer, Rainer Müller, Devaraj Subramanian, Carsten Schultz, Jocelyn Laporte, Volker Haucke. Nature 2016
100
13

A natural history study of X-linked myotubular myopathy.
Kimberly Amburgey, Etsuko Tsuchiya, Sabine de Chastonay, Michael Glueck, Rachel Alverez, Cam-Tu Nguyen, Anne Rutkowski, Joseph Hornyak, Alan H Beggs, James J Dowling. Neurology 2017
42
30

Myotubularin-deficient myoblasts display increased apoptosis, delayed proliferation, and poor cell engraftment.
Michael W Lawlor, Matthew S Alexander, Marissa G Viola, Hui Meng, Romain Joubert, Vandana Gupta, Norio Motohashi, Richard A Manfready, Cynthia P Hsu, Ping Huang,[...]. Am J Pathol 2012
30
40

Medical complications in long-term survivors with X-linked myotubular myopathy.
G E Herman, M Finegold, W Zhao, B de Gouyon, A Metzenberg. J Pediatr 1999
127
12

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