A citation-based method for searching scientific literature

Cinzia Bragato, Germano Gaudenzi, Flavia Blasevich, Giulio Pavesi, Lorenzo Maggi, Michele Giunta, Franco Cotelli, Marina Mora. Sci Rep 2016
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


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
25
44


Dynamin-2 mutations associated with centronuclear myopathy are hypermorphic and lead to T-tubule fragmentation.
Yu-Han Chin, Albert Lee, Hung-Wei Kan, Jessica Laiman, Mei-Chun Chuang, Sung-Tsang Hsieh, Ya-Wen Liu. Hum Mol Genet 2015
27
33

Dynamin 2 mutants linked to centronuclear myopathies form abnormally stable polymers.
Lei Wang, Barbara Barylko, Christopher Byers, Justin A Ross, David M Jameson, Joseph P Albanesi. J Biol Chem 2010
41
33

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
78
33

Dynamin, a membrane-remodelling GTPase.
Shawn M Ferguson, Pietro De Camilli. Nat Rev Mol Cell Biol 2012
549
33

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
78
33

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
54
33

Fiji: an open-source platform for biological-image analysis.
Johannes Schindelin, Ignacio Arganda-Carreras, Erwin Frise, Verena Kaynig, Mark Longair, Tobias Pietzsch, Stephan Preibisch, Curtis Rueden, Stephan Saalfeld, Benjamin Schmid,[...]. Nat Methods 2012
33

Amphiphysin (BIN1) negatively regulates dynamin 2 for normal muscle maturation.
Belinda S Cowling, Ivana Prokic, Hichem Tasfaout, Aymen Rabai, Frédéric Humbert, Bruno Rinaldi, Anne-Sophie Nicot, Christine Kretz, Sylvie Friant, Aurélien Roux,[...]. J Clin Invest 2017
28
33

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

In vivo characterization of human myofibrillar myopathy genes in zebrafish.
John B Bührdel, Sofia Hirth, Mirjam Kessler, Sören Westphal, Monika Forster, Linda Manta, Gerhard Wiche, Benedikt Schoser, Joachim Schessl, Rolf Schröder,[...]. Biochem Biophys Res Commun 2015
15
22

MYBPC1 mutations impair skeletal muscle function in zebrafish models of arthrogryposis.
Kyungsoo Ha, Jillian G Buchan, David M Alvarado, Kevin McCall, Anupama Vydyanath, Pradeep K Luther, Matthew I Goldsmith, Matthew B Dobbs, Christina A Gurnett. Hum Mol Genet 2013
34
22

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy.
J Liu, M Aoki, I Illa, C Wu, M Fardeau, C Angelini, C Serrano, J A Urtizberea, F Hentati, M B Hamida,[...]. Nat Genet 1998
645
22

Mild functional differences of dynamin 2 mutations associated to centronuclear myopathy and Charcot-Marie Tooth peripheral neuropathy.
Olga S Koutsopoulos, Catherine Koch, Valerie Tosch, Johann Böhm, Kathryn N North, Jocelyn Laporte. PLoS One 2011
29
22

Neuromuscular junction abnormalities in DNM2-related centronuclear myopathy.
Elizabeth M Gibbs, Nigel F Clarke, Kristy Rose, Emily C Oates, Richard Webster, Eva L Feldman, James J Dowling. J Mol Med (Berl) 2013
45
22


Dynamin 2 homozygous mutation in humans with a lethal congenital syndrome.
Olga S Koutsopoulos, Christine Kretz, Claudia M Weller, Aurelien Roux, Halina Mojzisova, Johann Böhm, Catherine Koch, Anne Toussaint, Emilie Heckel, Daphne Stemkens,[...]. Eur J Hum Genet 2013
38
22

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
68
22

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
246
22

Reducing dynamin 2 (DNM2) rescues DNM2-related dominant centronuclear myopathy.
Suzie Buono, Jacob A Ross, Hichem Tasfaout, Yotam Levy, Christine Kretz, Leighla Tayefeh, John Matson, Shuling Guo, Pascal Kessler, Brett P Monia,[...]. Proc Natl Acad Sci U S A 2018
16
22

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
283
22

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
154
22

Single Intramuscular Injection of AAV-shRNA Reduces DNM2 and Prevents Myotubular Myopathy in Mice.
Hichem Tasfaout, Valentina M Lionello, Christine Kretz, Pascale Koebel, Nadia Messaddeq, Deborah Bitz, Jocelyn Laporte, Belinda S Cowling. Mol Ther 2018
17
22

Centronuclear (myotubular) myopathy.
Heinz Jungbluth, Carina Wallgren-Pettersson, Jocelyn Laporte. Orphanet J Rare Dis 2008
181
22

Membrane fission by dynamin: what we know and what we need to know.
Bruno Antonny, Christopher Burd, Pietro De Camilli, Elizabeth Chen, Oliver Daumke, Katja Faelber, Marijn Ford, Vadim A Frolov, Adam Frost, Jenny E Hinshaw,[...]. EMBO J 2016
220
22

Crystal structure of nucleotide-free dynamin.
Katja Faelber, York Posor, Song Gao, Martin Held, Yvette Roske, Dennis Schulze, Volker Haucke, Frank Noé, Oliver Daumke. Nature 2011
202
22

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.
Stephan Züchner, Irina V Mersiyanova, Maria Muglia, Nisrine Bissar-Tadmouri, Julie Rochelle, Elena L Dadali, Mario Zappia, Eva Nelis, Alessandra Patitucci, Jan Senderek,[...]. Nat Genet 2004
22

Thyroxine suppresses thrombocytopoiesis and stimulates erythropoiesis in mice.
P S Sullivan, T P McDonald. Proc Soc Exp Biol Med 1992
21
11

Stimulatory effects of thyroid hormone on brain angiogenesis in vivo and in vitro.
Liqun Zhang, Christiana Marie Cooper-Kuhn, Ulf Nannmark, Klas Blomgren, Hans Georg Kuhn. J Cereb Blood Flow Metab 2010
38
11

TSH receptor function is required for normal thyroid differentiation in zebrafish.
Robert Opitz, Emilie Maquet, Maxime Zoenen, Rajesh Dadhich, Sabine Costagliola. Mol Endocrinol 2011
50
11


Role of Thyroid Hormones in Skeletal Development and Bone Maintenance.
J H Duncan Bassett, Graham R Williams. Endocr Rev 2016
156
11

A Novel Mutation in THRA Gene Associated With an Atypical Phenotype of Resistance to Thyroid Hormone.
Stéphanie Espiard, Frédérique Savagner, Frédéric Flamant, Virginie Vlaeminck-Guillem, Romain Guyot, Mathilde Munier, Michele d'Herbomez, William Bourguet, Graziella Pinto, Christian Rose,[...]. J Clin Endocrinol Metab 2015
34
11

Thyroid-hormone-dependent negative regulation of thyrotropin beta gene by thyroid hormone receptors: study with a new experimental system using CV1 cells.
Keiko Nakano, Akio Matsushita, Shigekazu Sasaki, Hiroko Misawa, Kozo Nishiyama, Yumiko Kashiwabara, Hirotoshi Nakamura. Biochem J 2004
35
11

Thyroid gland development and function in the zebrafish model.
P Porazzi, D Calebiro, F Benato, N Tiso, L Persani. Mol Cell Endocrinol 2009
122
11

Erythroid defects in TRalpha-/- mice.
Tulene S Kendrick, Christine J Payne, Michael R Epis, Jessica R Schneider, Peter J Leedman, S Peter Klinken, Evan Ingley. Blood 2008
39
11

Endothelial cell self-fusion during vascular pruning.
Anna Lenard, Stephan Daetwyler, Charles Betz, Elin Ellertsdottir, Heinz-Georg Belting, Jan Huisken, Markus Affolter. PLoS Biol 2015
80
11

Intrinsic expression of a multiexon type 3 deiodinase gene controls zebrafish embryo size.
Cuicui Guo, Xia Chen, Huaidong Song, Michelle A Maynard, Yi Zhou, Alexei V Lobanov, Vadim N Gladyshev, Jared J Ganis, David Wiley, Rebecca H Jugo,[...]. Endocrinology 2014
19
11

Thyroid hormone receptor α and regulation of type 3 deiodinase.
Olga Barca-Mayo, Xiao-Hui Liao, Manuela Alonso, Caterina Di Cosmo, Arturo Hernandez, Samuel Refetoff, Roy E Weiss. Mol Endocrinol 2011
44
11




Brain glucose utilization in mice with a targeted mutation in the thyroid hormone alpha or beta receptor gene.
Y Itoh, T Esaki, M Kaneshige, H Suzuki, M Cook, L Sokoloff, S Y Cheng, J Nunez. Proc Natl Acad Sci U S A 2001
63
11


Type 2 iodothyronine deiodinase is essential for thyroid hormone-dependent embryonic development and pigmentation in zebrafish.
Chaminda N Walpita, Alexander D Crawford, Els D R Janssens, Serge Van der Geyten, Veerle M Darras. Endocrinology 2009
80
11

Disruptions of global and JAGGED1-mediated notch signaling affect thyroid morphogenesis in the zebrafish.
Patrizia Porazzi, Federica Marelli, Francesca Benato, Tiziana de Filippis, Davide Calebiro, Francesco Argenton, Natascia Tiso, Luca Persani. Endocrinology 2012
27
11

Thyroid hormone resistance syndrome due to mutations in the thyroid hormone receptor α gene (THRA).
Anna Tylki-Szymańska, Rocio Acuna-Hidalgo, Małgorzata Krajewska-Walasek, Agnieszka Lecka-Ambroziak, Marloes Steehouwer, Christian Gilissen, Han G Brunner, Agnieszka Jurecka, Agnieszka Różdżyńska-Świątkowska, Alexander Hoischen,[...]. J Med Genet 2015
46
11

Clinical phenotype and mutant TRα1.
Alies van Mullem, Ramona van Heerebeek, Dionisios Chrysis, Edward Visser, Marco Medici, Maria Andrikoula, Agathocles Tsatsoulis, Robin Peeters, Theo J Visser. N Engl J Med 2012
129
11

A two-color acid-free cartilage and bone stain for zebrafish larvae.
M B Walker, C B Kimmel. Biotech Histochem 2007
368
11


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.