A citation-based method for searching scientific literature

Daniela Rossi, Johanna Palmio, Anni Evilä, Lucia Galli, Virginia Barone, Tracy A Caldwell, Rachel A Policke, Esraa Aldkheil, Christopher E Berndsen, Nathan T Wright, Edoardo Malfatti, Guy Brochier, Enrico Pierantozzi, Albena Jordanova, Velina Guergueltcheva, Norma Beatriz Romero, Peter Hackman, Bruno Eymard, Bjarne Udd, Vincenzo Sorrentino. PLoS One 2017
Times Cited: 21







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



Times Cited
  Times     Co-cited
Similarity


Mutations in the N-terminal actin-binding domain of filamin C cause a distal myopathy.
Rachael M Duff, Valerie Tay, Peter Hackman, Gianina Ravenscroft, Catriona McLean, Paul Kennedy, Alina Steinbach, Wiebke Schöffler, Peter F M van der Ven, Dieter O Fürst,[...]. Am J Hum Genet 2011
88
42

Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency.
V Guergueltcheva, K Peeters, J Baets, C Ceuterick-de Groote, J J Martin, A Suls, E De Vriendt, V Mihaylova, T Chamova, L Almeida-Souza,[...]. Neurology 2011
38
38

Novel FLNC mutation in a patient with myofibrillar myopathy in combination with late-onset cerebellar ataxia.
Giorgio Tasca, Zagaa Odgerel, Mauro Monforte, Stefania Aurino, Nigel F Clarke, Leigh B Waddell, Bjarne Udd, Enzo Ricci, Lev G Goldfarb. Muscle Nerve 2012
22
33

Filamin C-related myopathies: pathology and mechanisms.
Dieter O Fürst, Lev G Goldfarb, Rudolf A Kley, Matthias Vorgerd, Montse Olivé, Peter F M van der Ven. Acta Neuropathol 2013
72
28

Exercise-induced alterations and loss of sarcomeric M-line organization in the diaphragm muscle of obscurin knockout mice.
D Randazzo, B Blaauw, C Paolini, E Pierantozzi, S Spinozzi, S Lange, J Chen, F Protasi, C Reggiani, V Sorrentino. Am J Physiol Cell Physiol 2017
17
29

A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy.
Matthias Vorgerd, Peter F M van der Ven, Vera Bruchertseifer, Thomas Löwe, Rudolf A Kley, Rolf Schröder, Hanns Lochmüller, Mirko Himmel, Katrin Koehler, Dieter O Fürst,[...]. Am J Hum Genet 2005
204
23

In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy.
Alexey Shatunov, Montse Olivé, Zagaa Odgerel, Christine Stadelmann-Nessler, Kerstin Irlbacher, Frank van Landeghem, Munkhuu Bayarsaikhan, Hee-Suk Lee, Bertrand Goudeau, Patrick F Chinnery,[...]. Eur J Hum Genet 2009
53
23

Muscle giants: molecular scaffolds in sarcomerogenesis.
Aikaterini Kontrogianni-Konstantopoulos, Maegen A Ackermann, Amber L Bowman, Solomon V Yap, Robert J Bloch. Physiol Rev 2009
158
23

Obscurin is a ligand for small ankyrin 1 in skeletal muscle.
Aikaterini Kontrogianni-Konstantopoulos, Ellene M Jones, Damian B Van Rossum, Robert J Bloch. Mol Biol Cell 2003
146
23

Widening the spectrum of filamin-C myopathy: Predominantly proximal myopathy due to the p.A193T mutation in the actin-binding domain of FLNC.
Fleur J A van den Bogaart, Kristl G Claeys, Rudolf A Kley, Benno Kusters, Simone Schrading, Erik J Kamsteeg, Nicol C Voermans. Neuromuscul Disord 2017
12
41

Obscurin is required for ankyrinB-dependent dystrophin localization and sarcolemma integrity.
Davide Randazzo, Emiliana Giacomello, Stefania Lorenzini, Daniela Rossi, Enrico Pierantozzi, Bert Blaauw, Carlo Reggiani, Stephan Lange, Angela K Peter, Ju Chen,[...]. J Cell Biol 2013
39
19

Pathophysiology of protein aggregation and extended phenotyping in filaminopathy.
Rudolf A Kley, Piraye Serdaroglu-Oflazer, Yvonne Leber, Zagaa Odgerel, Peter F M van der Ven, Montse Olivé, Isidro Ferrer, Adekunle Onipe, Mariya Mihaylov, Juan M Bilbao,[...]. Brain 2012
57
19

Myofibrillar instability exacerbated by acute exercise in filaminopathy.
Frédéric Chevessier, Julia Schuld, Zacharias Orfanos, Anne-C Plank, Lucie Wolf, Alexandra Maerkens, Andreas Unger, Ursula Schlötzer-Schrehardt, Rudolf A Kley, Stephan Von Hörsten,[...]. Hum Mol Genet 2015
35
19


Structural analysis of obscurin gene in hypertrophic cardiomyopathy.
Takuro Arimura, Yuji Matsumoto, Osamu Okazaki, Takeharu Hayashi, Megumi Takahashi, Natsuko Inagaki, Kunihiko Hinohara, Naoto Ashizawa, Keisuke Yano, Akinori Kimura. Biochem Biophys Res Commun 2007
61
19

Binding of an ankyrin-1 isoform to obscurin suggests a molecular link between the sarcoplasmic reticulum and myofibrils in striated muscles.
Paola Bagnato, Virigina Barone, Emiliana Giacomello, Daniela Rossi, Vincenzo Sorrentino. J Cell Biol 2003
146
19

Deregulated Ca2+ cycling underlies the development of arrhythmia and heart disease due to mutant obscurin.
Li-Yen R Hu, Maegen A Ackermann, Peter A Hecker, Benjamin L Prosser, Brendan King, Kelly A O'Connell, Alyssa Grogan, Logan C Meyer, Christopher E Berndsen, Nathan T Wright,[...]. Sci Adv 2017
19
21

Obscurin determines the architecture of the longitudinal sarcoplasmic reticulum.
Stephan Lange, Kunfu Ouyang, Gretchen Meyer, Li Cui, Hongqiang Cheng, Richard L Lieber, Ju Chen. J Cell Sci 2009
86
19

Structural and functional aspects of filamins.
A van der Flier, A Sonnenberg. Biochim Biophys Acta 2001
311
19

Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients.
Rudolf A Kley, Yorck Hellenbroich, Peter F M van der Ven, Dieter O Fürst, Angela Huebner, Vera Bruchertseifer, Sören A Peters, Christoph M Heyer, Janbernd Kirschner, Rolf Schröder,[...]. Brain 2007
105
19

Filamin C Truncation Mutations Are Associated With Arrhythmogenic Dilated Cardiomyopathy and Changes in the Cell-Cell Adhesion Structures.
Rene L Begay, Sharon L Graw, Gianfranco Sinagra, Angeliki Asimaki, Teisha J Rowland, Dobromir B Slavov, Katherine Gowan, Kenneth L Jones, Francesca Brun, Marco Merlo,[...]. JACC Clin Electrophysiol 2018
67
19

Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNC.
D Avila-Smirnow, L Gueneau, S Batonnet-Pichon, F Delort, H-M Bécane, K Claeys, M Beuvin, B Goudeau, J-P Jais, I Nelson,[...]. Rev Neurol (Paris) 2016
14
21


Impairment of protein degradation in myofibrillar myopathy caused by FLNC/filamin C mutations.
Rudolf A Kley, Peter F M van der Ven, Montse Olivé, Jörg Höhfeld, Lev G Goldfarb, Dieter O Fürst, Matthias Vorgerd. Autophagy 2013
22
14

Targeted next-generation sequencing assay for detection of mutations in primary myopathies.
Anni Evilä, Meharji Arumilli, Bjarne Udd, Peter Hackman. Neuromuscul Disord 2016
61
14

The pathomechanism of filaminopathy: altered biochemical properties explain the cellular phenotype of a protein aggregation myopathy.
Thomas Löwe, Rudolf A Kley, Peter F M van der Ven, Mirko Himmel, Angela Huebner, Matthias Vorgerd, Dieter O Fürst. Hum Mol Genet 2007
42
14

Obscurins: Goliaths and Davids take over non-muscle tissues.
Maegen A Ackermann, Marey Shriver, Nicole A Perry, Li-Yen R Hu, Aikaterini Kontrogianni-Konstantopoulos. PLoS One 2014
29
14


Obscurin modulates the assembly and organization of sarcomeres and the sarcoplasmic reticulum.
Aikaterini Kontrogianni-Konstantopoulos, Dawn H Catino, John C Strong, Sarah Sutter, Andrei B Borisov, David W Pumplin, Mark W Russell, Robert J Bloch. FASEB J 2006
79
14

The potential of obscurin as a therapeutic target in muscle disorders.
Davide Randazzo, Enrico Pierantozzi, Daniela Rossi, Vincenzo Sorrentino. Expert Opin Ther Targets 2017
6
50

Obscurin is required for the lateral alignment of striated myofibrils in zebrafish.
Maide O Raeker, Fengyun Su, Sarah B Geisler, Andrei B Borisov, Aikaterini Kontrogianni-Konstantopoulos, Susan E Lyons, Mark W Russell. Dev Dyn 2006
44
14

OBSCN Mutations Associated with Dilated Cardiomyopathy and Haploinsufficiency.
Steven Marston, Cecile Montgiraud, Alex B Munster, O'Neal Copeland, Onjee Choi, Cristobal Dos Remedios, Andrew E Messer, Elisabeth Ehler, Ralph Knöll. PLoS One 2015
47
14

Thick Filament Protein Network, Functions, and Disease Association.
Li Wang, Janelle Geist, Alyssa Grogan, Li-Yen R Hu, Aikaterini Kontrogianni-Konstantopoulos. Compr Physiol 2018
26
14

The kinase domains of obscurin interact with intercellular adhesion proteins.
Li-Yen R Hu, Aikaterini Kontrogianni-Konstantopoulos. FASEB J 2013
31
14

Organization of junctional sarcoplasmic reticulum proteins in skeletal muscle fibers.
Virginia Barone, Davide Randazzo, Valeria Del Re, Vincenzo Sorrentino, Daniela Rossi. J Muscle Res Cell Motil 2015
29
14

Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains.
Jonathan Janssens, Stéphanie Philtjens, Gernot Kleinberger, Sara Van Mossevelde, Julie van der Zee, Rita Cacace, Sebastiaan Engelborghs, Anne Sieben, Julia Banzhaf-Strathmann, Lubina Dillen,[...]. Acta Neuropathol Commun 2015
12
25


De novo mutations in FLNC leading to early-onset restrictive cardiomyopathy and congenital myopathy.
Artem Kiselev, Raquel Vaz, Anastasia Knyazeva, Aleksandr Khudiakov, Svetlana Tarnovskaya, Jiao Liu, Alexey Sergushichev, Sergey Kazakov, Dmitrij Frishman, Natalia Smolina,[...]. Hum Mutat 2018
26
14

Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy.
Rafael Valdés-Mas, Ana Gutiérrez-Fernández, Juan Gómez, Eliecer Coto, Aurora Astudillo, Diana A Puente, Julián R Reguero, Victoria Álvarez, César Morís, Diego León,[...]. Nat Commun 2014
94
14

Aciculin interacts with filamin C and Xin and is essential for myofibril assembly, remodeling and maintenance.
Sibylle Molt, John B Bührdel, Sergiy Yakovlev, Peter Schein, Zacharias Orfanos, Gregor Kirfel, Lilli Winter, Gerhard Wiche, Peter F M van der Ven, Wolfgang Rottbauer,[...]. J Cell Sci 2014
37
14

Congenital dilated cardiomyopathy caused by biallelic mutations in Filamin C.
Eyal Reinstein, Ana Gutierrez-Fernandez, Shay Tzur, Concetta Bormans, Shai Marcu, Einav Tayeb-Fligelman, Chana Vinkler, Annick Raas-Rothschild, Dana Irge, Meytal Landau,[...]. Eur J Hum Genet 2016
26
14

FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype-phenotype correlations.
Flavie Ader, Pascal De Groote, Patricia Réant, Caroline Rooryck-Thambo, Delphine Dupin-Deguine, Caroline Rambaud, Diala Khraiche, Claire Perret, Jean François Pruny, Michèle Mathieu-Dramard,[...]. Clin Genet 2019
21
14

Filamin C is a highly dynamic protein associated with fast repair of myofibrillar microdamage.
Yvonne Leber, Avnika A Ruparelia, Gregor Kirfel, Peter F M van der Ven, Bernd Hoffmann, Rudolf Merkel, Robert J Bryson-Richardson, Dieter O Fürst. Hum Mol Genet 2016
36
14

Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies.
Martín F Ortiz-Genga, Sofía Cuenca, Matteo Dal Ferro, Esther Zorio, Ricardo Salgado-Aranda, Vicente Climent, Laura Padrón-Barthe, Iria Duro-Aguado, Juan Jiménez-Jáimez, Víctor M Hidalgo-Olivares,[...]. J Am Coll Cardiol 2016
182
14

A combined laser microdissection and mass spectrometry approach reveals new disease relevant proteins accumulating in aggregates of filaminopathy patients.
Rudolf A Kley, Alexandra Maerkens, Yvonne Leber, Verena Theis, Anja Schreiner, Peter F M van der Ven, Julian Uszkoreit, Christian Stephan, Stefan Eulitz, Nicole Euler,[...]. Mol Cell Proteomics 2013
59
14

A novel mutation in the N-terminal acting-binding domain of Filamin C protein causing a distal myofibrillar myopathy.
Chiara Gemelli, Valeria Prada, Chiara Fiorillo, Sabrina Fabbri, Lorenzo Maggi, Alessandro Geroldi, Sara Gibertini, Paola Mandich, Lucia Trevisan, Paola Fossa,[...]. J Neurol Sci 2019
7
42

Filamin actin-binding and titin-binding fulfill distinct functions in Z-disc cohesion.
Nicanor González-Morales, Tristan K Holenka, Frieder Schöck. PLoS Genet 2017
24
14

FLNC Gene Splice Mutations Cause Dilated Cardiomyopathy.
Rene L Begay, Charles A Tharp, August Martin, Sharon L Graw, Gianfranco Sinagra, Daniela Miani, Mary E Sweet, Dobromir B Slavov, Neil Stafford, Molly J Zeller,[...]. JACC Basic Transl Sci 2016
57
14

The complete gene sequence of titin, expression of an unusual approximately 700-kDa titin isoform, and its interaction with obscurin identify a novel Z-line to I-band linking system.
M L Bang, T Centner, F Fornoff, A J Geach, M Gotthardt, M McNabb, C C Witt, D Labeit, C C Gregorio, H Granzier,[...]. Circ Res 2001
452
14

Atypical phenotypes in titinopathies explained by second titin mutations.
Anni Evilä, Anna Vihola, Jaakko Sarparanta, Olayinka Raheem, Johanna Palmio, Satu Sandell, Bruno Eymard, Isabel Illa, Ricard Rojas-Garcia, Karolina Hankiewicz,[...]. Ann Neurol 2014
48
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.