A citation-based method for searching scientific literature

S G Priori, C Napolitano, N Tiso, M Memmi, G Vignati, R Bloise, V Sorrentino, G A Danieli. Circulation 2001
Times Cited: 910







List of co-cited articles
2717 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia.
P J Laitinen, K M Brown, K Piippo, H Swan, J M Devaney, B Brahmbhatt, E A Donarum, M Marino, N Tiso, M Viitasalo,[...]. Circulation 2001
500
31

Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia.
Silvia G Priori, Carlo Napolitano, Mirella Memmi, Barbara Colombi, Fabrizio Drago, Maurizio Gasparini, Luciano DeSimone, Fernando Coltorti, Raffaella Bloise, Roberto Keegan,[...]. Circulation 2002
729
29

HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013.
Silvia G Priori, Arthur A Wilde, Minoru Horie, Yongkeun Cho, Elijah R Behr, Charles Berul, Nico Blom, Josep Brugada, Chern-En Chiang, Heikki Huikuri,[...]. Heart Rhythm 2013
29

A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel.
H Lahat, E Pras, T Olender, N Avidan, E Ben-Asher, O Man, E Levy-Nissenbaum, A Khoury, A Lorber, B Goldman,[...]. Am J Hum Genet 2001
440
28

Incidence and risk factors of arrhythmic events in catecholaminergic polymorphic ventricular tachycardia.
Meiso Hayashi, Isabelle Denjoy, Fabrice Extramiana, Alice Maltret, Nathalie Roux Buisson, Jean-Marc Lupoglazoff, Didier Klug, Miyuki Hayashi, Seiji Takatsuki, Elisabeth Villain,[...]. Circulation 2009
292
28

Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients.
A Leenhardt, V Lucet, I Denjoy, F Grau, D D Ngoc, P Coumel. Circulation 1995
603
27

Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death.
Mette Nyegaard, Michael T Overgaard, Mads T Søndergaard, Marta Vranas, Elijah R Behr, Lasse L Hildebrandt, Jacob Lund, Paula L Hedley, A John Camm, Göran Wettrell,[...]. Am J Hum Genet 2012
219
21



Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human.
Nathalie Roux-Buisson, Marine Cacheux, Anne Fourest-Lieuvin, Jeremy Fauconnier, Julie Brocard, Isabelle Denjoy, Philippe Durand, Pascale Guicheney, Florence Kyndt, Antoine Leenhardt,[...]. Hum Mol Genet 2012
154
19

Structural basis for the gating mechanism of the type 2 ryanodine receptor RyR2.
Wei Peng, Huaizong Shen, Jianping Wu, Wenting Guo, Xiaojing Pan, Ruiwu Wang, S R Wayne Chen, Nieng Yan. Science 2016
138
19


Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2).
N Tiso, D A Stephan, A Nava, A Bagattin, J M Devaney, F Stanchi, G Larderet, B Brahmbhatt, K Brown, B Bauce,[...]. Hum Mol Genet 2001
542
17

Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans.
Hiroshi Watanabe, Nagesh Chopra, Derek Laver, Hyun Seok Hwang, Sean S Davies, Daniel E Roach, Henry J Duff, Dan M Roden, Arthur A M Wilde, Björn C Knollmann. Nat Med 2009
372
16

RyR2 mutations linked to ventricular tachycardia and sudden death reduce the threshold for store-overload-induced Ca2+ release (SOICR).
Dawei Jiang, Bailong Xiao, Dongmei Yang, Ruiwu Wang, Philip Choi, Lin Zhang, Heping Cheng, S R Wayne Chen. Proc Natl Acad Sci U S A 2004
307
16

Catecholaminergic polymorphic ventricular tachycardia in children: analysis of therapeutic strategies and outcomes from an international multicenter registry.
Thomas M Roston, Jeffrey M Vinocur, Kathleen R Maginot, Saira Mohammed, Jack C Salerno, Susan P Etheridge, Mitchell Cohen, Robert M Hamilton, Andreas Pflaumer, Ronald J Kanter,[...]. Circ Arrhythm Electrophysiol 2015
124
16

Flecainide therapy reduces exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardia.
Christian van der Werf, Prince J Kannankeril, Frederic Sacher, Andrew D Krahn, Sami Viskin, Antoine Leenhardt, Wataru Shimizu, Naokata Sumitomo, Frank A Fish, Zahurul A Bhuiyan,[...]. J Am Coll Cardiol 2011
241
15


Structural Basis for Gating and Activation of RyR1.
Amédée des Georges, Oliver B Clarke, Ran Zalk, Qi Yuan, Kendall J Condon, Robert A Grassucci, Wayne A Hendrickson, Andrew R Marks, Joachim Frank. Cell 2016
172
15

Familial evaluation in catecholaminergic polymorphic ventricular tachycardia: disease penetrance and expression in cardiac ryanodine receptor mutation-carrying relatives.
Christian van der Werf, Ineke Nederend, Nynke Hofman, Nan van Geloven, Corné Ebink, Ingrid M E Frohn-Mulder, A Marco W Alings, Hans A Bosker, Frank A Bracke, Freek van den Heuvel,[...]. Circ Arrhythm Electrophysiol 2012
92
15

Structure of the rabbit ryanodine receptor RyR1 at near-atomic resolution.
Zhen Yan, Xiaochen Bai, Chuangye Yan, Jianping Wu, Zhangqiang Li, Tian Xie, Wei Peng, Changcheng Yin, Xueming Li, Sjors H W Scheres,[...]. Nature 2015
281
14

FKBP12.6 deficiency and defective calcium release channel (ryanodine receptor) function linked to exercise-induced sudden cardiac death.
Xander H T Wehrens, Stephan E Lehnart, Fannie Huang, John A Vest, Steven R Reiken, Peter J Mohler, Jie Sun, Silvia Guatimosim, Long Sheng Song, Nora Rosemblit,[...]. Cell 2003
527
14

The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading frame mutational analysis.
Argelia Medeiros-Domingo, Zahurul A Bhuiyan, David J Tester, Nynke Hofman, Hennie Bikker, J Peter van Tintelen, Marcel M A M Mannens, Arthur A M Wilde, Michael J Ackerman. J Am Coll Cardiol 2009
198
14


Efficacy of Flecainide in the Treatment of Catecholaminergic Polymorphic Ventricular Tachycardia: A Randomized Clinical Trial.
Prince J Kannankeril, Jeremy P Moore, Marina Cerrone, Silvia G Priori, Naomi J Kertesz, Pamela S Ro, Anjan S Batra, Elizabeth S Kaufman, David L Fairbrother, Elizabeth V Saarel,[...]. JAMA Cardiol 2017
65
20

The clinical and genetic spectrum of catecholaminergic polymorphic ventricular tachycardia: findings from an international multicentre registry.
Thomas M Roston, Zhiguang Yuchi, Prince J Kannankeril, Julie Hathaway, Jeffrey M Vinocur, Susan P Etheridge, James E Potts, Kathleen R Maginot, Jack C Salerno, Mitchell I Cohen,[...]. Europace 2018
38
34

Absence of calsequestrin 2 causes severe forms of catecholaminergic polymorphic ventricular tachycardia.
Alex V Postma, Isabelle Denjoy, Theo M Hoorntje, Jean-Marc Lupoglazoff, Antoine Da Costa, Pascale Sebillon, Marcel M A M Mannens, Arthur A M Wilde, Pascale Guicheney. Circ Res 2002
285
13

Expanding spectrum of human RYR2-related disease: new electrocardiographic, structural, and genetic features.
Zahurul A Bhuiyan, Maarten P van den Berg, J Peter van Tintelen, Margreet T E Bink-Boelkens, Ans C P Wiesfeld, Marielle Alders, Alex V Postma, Irene van Langen, Marcel M A M Mannens, Arthur A M Wilde. Circulation 2007
152
12



Catecholaminergic polymorphic ventricular tachycardia: electrocardiographic characteristics and optimal therapeutic strategies to prevent sudden death.
N Sumitomo, K Harada, M Nagashima, T Yasuda, Y Nakamura, Y Aragaki, A Saito, K Kurosaki, K Jouo, M Koujiro,[...]. Heart 2003
238
12

Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts.
H Swan, K Piippo, M Viitasalo, P Heikkilä, T Paavonen, K Kainulainen, J Kere, P Keto, K Kontula, L Toivonen. J Am Coll Cardiol 1999
220
12

Catecholaminergic polymorphic ventricular tachycardia.
Antoine Leenhardt, Isabelle Denjoy, Pascale Guicheney. Circ Arrhythm Electrophysiol 2012
75
14

Sudden cardiac arrest associated with early repolarization.
Michel Haïssaguerre, Nicolas Derval, Frederic Sacher, Laurence Jesel, Isabel Deisenhofer, Luc de Roy, Jean-Luc Pasquié, Akihiko Nogami, Dominique Babuty, Sinikka Yli-Mayry,[...]. N Engl J Med 2008
903
11

TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT.
Harsha D Devalla, Roselle Gélinas, Elhadi H Aburawi, Abdelaziz Beqqali, Philippe Goyette, Christian Freund, Marie-A Chaix, Rafik Tadros, Hui Jiang, Antony Le Béchec,[...]. EMBO Mol Med 2016
46
23

Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients.
A V Postma, I Denjoy, J Kamblock, M Alders, J-M Lupoglazoff, G Vaksmann, L Dubosq-Bidot, P Sebillon, M M A M Mannens, P Guicheney,[...]. J Med Genet 2005
183
11

Efficacy of implantable cardioverter defibrillators in young patients with catecholaminergic polymorphic ventricular tachycardia: success depends on substrate.
Christina Y Miyake, Gregory Webster, Richard J Czosek, Michal J Kantoch, Anne M Dubin, Kishor Avasarala, Joseph Atallah. Circ Arrhythm Electrophysiol 2013
63
17

Clinical Management of Catecholaminergic Polymorphic Ventricular Tachycardia: The Role of Left Cardiac Sympathetic Denervation.
Gaetano M De Ferrari, Veronica Dusi, Carla Spazzolini, J Martijn Bos, Dominic J Abrams, Charles I Berul, Lia Crotti, Andrew M Davis, Michael Eldar, Maria Kharlap,[...]. Circulation 2015
143
11

Arrhythmogenesis in catecholaminergic polymorphic ventricular tachycardia: insights from a RyR2 R4496C knock-in mouse model.
Nian Liu, Barbara Colombi, Mirella Memmi, Spyros Zissimopoulos, Nicoletta Rizzi, Sara Negri, Marcello Imbriani, Carlo Napolitano, F Anthony Lai, Silvia G Priori. Circ Res 2006
222
11

Structure of a mammalian ryanodine receptor.
Ran Zalk, Oliver B Clarke, Amédée des Georges, Robert A Grassucci, Steven Reiken, Filippo Mancia, Wayne A Hendrickson, Joachim Frank, Andrew R Marks. Nature 2015
244
11

Genotypic heterogeneity and phenotypic mimicry among unrelated patients referred for catecholaminergic polymorphic ventricular tachycardia genetic testing.
David J Tester, Puneeta Arya, Melissa Will, Carla M Haglund, Amanda L Farley, Jonathan C Makielski, Michael J Ackerman. Heart Rhythm 2006
82
12

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
10

Implantable cardioverter-defibrillator use in catecholaminergic polymorphic ventricular tachycardia: A systematic review.
Thomas M Roston, Karolina Jones, Nathaniel M Hawkins, J Martijn Bos, Peter J Schwartz, Frances Perry, Michael J Ackerman, Zachary W M Laksman, Padma Kaul, Krystien V V Lieve,[...]. Heart Rhythm 2018
35
28

Architecture and conformational switch mechanism of the ryanodine receptor.
Rouslan G Efremov, Alexander Leitner, Ruedi Aebersold, Stefan Raunser. Nature 2015
201
10


Inherited calcium channelopathies in the pathophysiology of arrhythmias.
Luigi Venetucci, Marco Denegri, Carlo Napolitano, Silvia G Priori. Nat Rev Cardiol 2012
120
10

Modulation of cardiac ryanodine receptor 2 by calmodulin.
Deshun Gong, Ximin Chi, Jinhong Wei, Gewei Zhou, Gaoxingyu Huang, Lin Zhang, Ruiwu Wang, Jianlin Lei, S R Wayne Chen, Nieng Yan. Nature 2019
45
22

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism.
Igor Splawski, Katherine W Timothy, Leah M Sharpe, Niels Decher, Pradeep Kumar, Raffaella Bloise, Carlo Napolitano, Peter J Schwartz, Robert M Joseph, Karen Condouris,[...]. Cell 2004
986
9

Arrhythmogenic Right Ventricular Cardiomyopathy.
Domenico Corrado, Mark S Link, Hugh Calkins. N Engl J Med 2017
249
9



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.