A citation-based method for searching scientific literature

Michael J Ackerman, Silvia G Priori, Stephan Willems, Charles Berul, Ramon Brugada, Hugh Calkins, A John Camm, Patrick T Ellinor, Michael Gollob, Robert Hamilton, Ray E Hershberger, Daniel P Judge, Hervè Le Marec, William J McKenna, Eric Schulze-Bahr, Chris Semsarian, Jeffrey A Towbin, Hugh Watkins, Arthur Wilde, Christian Wolpert, Douglas P Zipes. Heart Rhythm 2011
Times Cited: 612







List of co-cited articles
2290 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
33

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
30


A Prospective Study of Sudden Cardiac Death among Children and Young Adults.
Richard D Bagnall, Robert G Weintraub, Jodie Ingles, Johan Duflou, Laura Yeates, Lien Lam, Andrew M Davis, Tina Thompson, Vanessa Connell, Jennie Wallace,[...]. N Engl J Med 2016
352
21

Genetic Evaluation of Cardiomyopathy-A Heart Failure Society of America Practice Guideline.
Ray E Hershberger, Michael M Givertz, Carolyn Y Ho, Daniel P Judge, Paul F Kantor, Kim L McBride, Ana Morales, Matthew R G Taylor, Matteo Vatta, Stephanie M Ware. J Card Fail 2018
126
19

Prevalence of the congenital long-QT syndrome.
Peter J Schwartz, Marco Stramba-Badiale, Lia Crotti, Matteo Pedrazzini, Alessandra Besana, Giuliano Bosi, Fulvio Gabbarini, Karine Goulene, Roberto Insolia, Savina Mannarino,[...]. Circulation 2009
530
16

Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada Syndrome.
S Mohsen Hosseini, Raymond Kim, Sharmila Udupa, Gregory Costain, Rebekah Jobling, Eriskay Liston, Seema M Jamal, Marta Szybowska, Chantal F Morel, Sarah Bowdin,[...]. Circulation 2018
129
16

2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC).
Perry M Elliott, Aris Anastasakis, Michael A Borger, Martin Borggrefe, Franco Cecchi, Philippe Charron, Albert Alain Hagege, Antoine Lafont, Giuseppe Limongelli, Heiko Mahrholdt,[...]. Eur Heart J 2014
16

Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases.
Philippe Charron, Michael Arad, Eloisa Arbustini, Cristina Basso, Zofia Bilinska, Perry Elliott, Tiina Helio, Andre Keren, William J McKenna, Lorenzo Monserrat,[...]. Eur Heart J 2010
250
14

Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes.
Jodie Ingles, Jennifer Goldstein, Courtney Thaxton, Colleen Caleshu, Edward W Corty, Stephanie B Crowley, Kristen Dougherty, Steven M Harrison, Jennifer McGlaughon, Laura V Milko,[...]. Circ Genom Precis Med 2019
91
14

2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy.
Jeffrey A Towbin, William J McKenna, Dominic J Abrams, Michael J Ackerman, Hugh Calkins, Francisco C C Darrieux, James P Daubert, Christian de Chillou, Eugene C DePasquale, Milind Y Desai,[...]. Heart Rhythm 2019
159
12

Truncations of titin causing dilated cardiomyopathy.
Daniel S Herman, Lien Lam, Matthew R G Taylor, Libin Wang, Polakit Teekakirikul, Danos Christodoulou, Lauren Conner, Steven R DePalma, Barbara McDonough, Elizabeth Sparks,[...]. N Engl J Med 2012
732
12


Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity.
Ahmed A Alfares, Melissa A Kelly, Gregory McDermott, Birgit H Funke, Matthew S Lebo, Samantha B Baxter, Jun Shen, Heather M McLaughlin, Eugene H Clark, Larry J Babb,[...]. Genet Med 2015
210
12

Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome.
Najim Lahrouchi, Hariharan Raju, Elisabeth M Lodder, Efstathios Papatheodorou, James S Ware, Michael Papadakis, Rafik Tadros, Della Cole, Jonathan R Skinner, Jackie Crawford,[...]. J Am Coll Cardiol 2017
113
11

2018 ESC Guidelines for the management of cardiovascular diseases during pregnancy.
Vera Regitz-Zagrosek, Jolien W Roos-Hesselink, Johann Bauersachs, Carina Blomström-Lundqvist, Renata Cífková, Michele De Bonis, Bernard Iung, Mark Richard Johnson, Ulrich Kintscher, Peter Kranke,[...]. Eur Heart J 2018
476
11

Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy.
Jaap I van Waning, Kadir Caliskan, Yvonne M Hoedemaekers, Karin Y van Spaendonck-Zwarts, Annette F Baas, S Matthijs Boekholdt, Joost P van Melle, Arco J Teske, Folkert W Asselbergs, Ad P C M Backx,[...]. J Am Coll Cardiol 2018
116
10

Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases.
Perry Elliott, Bert Andersson, Eloisa Arbustini, Zofia Bilinska, Franco Cecchi, Philippe Charron, Olivier Dubourg, Uwe Kühl, Bernhard Maisch, William J McKenna,[...]. Eur Heart J 2008
10

New perspectives on the prevalence of hypertrophic cardiomyopathy.
Christopher Semsarian, Jodie Ingles, Martin S Maron, Barry J Maron. J Am Coll Cardiol 2015
453
10

An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome.
Arnon Adler, Valeria Novelli, Ahmad S Amin, Emanuela Abiusi, Melanie Care, Eline A Nannenberg, Harriet Feilotter, Simona Amenta, Daniela Mazza, Hennie Bikker,[...]. Circulation 2020
67
14

The emerging role of the cardiac genetic counselor.
Jodie Ingles, Laura Yeates, Christopher Semsarian. Heart Rhythm 2011
72
12

Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy.
Richard D Bagnall, Jodie Ingles, Marcel E Dinger, Mark J Cowley, Samantha Barratt Ross, André E Minoche, Sean Lal, Christian Turner, Alison Colley, Sulekha Rajagopalan,[...]. J Am Coll Cardiol 2018
75
12

Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert Panel.
Melissa A Kelly, Colleen Caleshu, Ana Morales, Jillian Buchan, Zena Wolf, Steven M Harrison, Stuart Cook, Mitchell W Dillon, John Garcia, Eden Haverfield,[...]. Genet Med 2018
137
9

Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Ray E Hershberger, Michael M Givertz, Carolyn Y Ho, Daniel P Judge, Paul F Kantor, Kim L McBride, Ana Morales, Matthew R G Taylor, Matteo Vatta, Stephanie M Ware. Genet Med 2018
69
13

Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.
Roddy Walsh, Kate L Thomson, James S Ware, Birgit H Funke, Jessica Woodley, Karen J McGuire, Francesco Mazzarotto, Edward Blair, Anneke Seller, Jenny C Taylor,[...]. Genet Med 2017
336
9

Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria.
Frank I Marcus, William J McKenna, Duane Sherrill, Cristina Basso, Barbara Bauce, David A Bluemke, Hugh Calkins, Domenico Corrado, Moniek G P J Cox, James P Daubert,[...]. Circulation 2010
9

Genotype and Lifetime Burden of Disease in Hypertrophic Cardiomyopathy: Insights from the Sarcomeric Human Cardiomyopathy Registry (SHaRe).
Carolyn Y Ho, Sharlene M Day, Euan A Ashley, Michelle Michels, Alexandre C Pereira, Daniel Jacoby, Allison L Cirino, Jonathan C Fox, Neal K Lakdawala, James S Ware,[...]. Circulation 2018
176
9

Genetic Misdiagnoses and the Potential for Health Disparities.
Arjun K Manrai, Birgit H Funke, Heidi L Rehm, Morten S Olesen, Bradley A Maron, Peter Szolovits, David M Margulies, Joseph Loscalzo, Isaac S Kohane. N Engl J Med 2016
315
9

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
Connie R Bezzina, Julien Barc, Yuka Mizusawa, Carol Ann Remme, Jean-Baptiste Gourraud, Floriane Simonet, Arie O Verkerk, Peter J Schwartz, Lia Crotti, Federica Dagradi,[...]. Nat Genet 2013
305
8

Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing.
David J Tester, Argelia Medeiros-Domingo, Melissa L Will, Carla M Haglund, Michael J Ackerman. Mayo Clin Proc 2012
158
8

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
8

Nonfamilial Hypertrophic Cardiomyopathy: Prevalence, Natural History, and Clinical Implications.
Jodie Ingles, Charlotte Burns, Richard D Bagnall, Lien Lam, Laura Yeates, Tanya Sarina, Rajesh Puranik, Tom Briffa, John J Atherton, Tim Driscoll,[...]. Circ Cardiovasc Genet 2017
74
10


Arrhythmogenic Right Ventricular Cardiomyopathy.
Domenico Corrado, Mark S Link, Hugh Calkins. N Engl J Med 2017
249
8

Risk factors for malignant ventricular arrhythmias in lamin a/c mutation carriers a European cohort study.
Ingrid A W van Rijsingen, Eloisa Arbustini, Perry M Elliott, Jens Mogensen, Johanna F Hermans-van Ast, Anneke J van der Kooi, J Peter van Tintelen, Maarten P van den Berg, Andrea Pilotto, Michele Pasotti,[...]. J Am Coll Cardiol 2012
281
8


2017 AHA/ACC/HRS Guideline for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines and the Heart Rhythm Society.
Sana M Al-Khatib, William G Stevenson, Michael J Ackerman, William J Bryant, David J Callans, Anne B Curtis, Barbara J Deal, Timm Dickfeld, Michael E Field, Gregg C Fonarow,[...]. J Am Coll Cardiol 2018
306
8

Guidelines for autopsy investigation of sudden cardiac death: 2017 update from the Association for European Cardiovascular Pathology.
Cristina Basso, Beatriz Aguilera, Jytte Banner, Stephan Cohle, Giulia d'Amati, Rosa Henriques de Gouveia, Cira di Gioia, Aurelie Fabre, Patrick J Gallagher, Ornella Leone,[...]. Virchows Arch 2017
134
7

Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene.
Arthur J Moss, Wataru Shimizu, Arthur A M Wilde, Jeffrey A Towbin, Wojciech Zareba, Jennifer L Robinson, Ming Qi, G Michael Vincent, Michael J Ackerman, Elizabeth S Kaufman,[...]. Circulation 2007
288
7

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.
D Fatkin, C MacRae, T Sasaki, M R Wolff, M Porcu, M Frenneaux, J Atherton, H J Vidaillet, S Spudich, U De Girolami,[...]. N Engl J Med 1999
899
7

Interdisciplinary psychosocial care for families with inherited cardiovascular diseases.
Colleen Caleshu, Nadine A Kasparian, Katharine S Edwards, Laura Yeates, Christopher Semsarian, Marco Perez, Euan Ashley, Christian J Turner, Joshua W Knowles, Jodie Ingles. Trends Cardiovasc Med 2016
34
20

Genetics of hypertrophic cardiomyopathy after 20 years: clinical perspectives.
Barry J Maron, Martin S Maron, Christopher Semsarian. J Am Coll Cardiol 2012
385
7

Left Ventricular Noncompaction: A Distinct Genetic Cardiomyopathy?
Eloisa Arbustini, Valentina Favalli, Nupoor Narula, Alessandra Serio, Maurizia Grasso. J Am Coll Cardiol 2016
108
7

Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource.
Natasha T Strande, Erin Rooney Riggs, Adam H Buchanan, Ozge Ceyhan-Birsoy, Marina DiStefano, Selina S Dwight, Jenny Goldstein, Rajarshi Ghosh, Bryce A Seifert, Tam P Sneddon,[...]. Am J Hum Genet 2017
190
7

Exercise increases age-related penetrance and arrhythmic risk in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated desmosomal mutation carriers.
Cynthia A James, Aditya Bhonsale, Crystal Tichnell, Brittney Murray, Stuart D Russell, Harikrishna Tandri, Ryan J Tedford, Daniel P Judge, Hugh Calkins. J Am Coll Cardiol 2013
346
7

Impact of genetics on the clinical management of channelopathies.
Peter J Schwartz, Michael J Ackerman, Alfred L George, Arthur A M Wilde. J Am Coll Cardiol 2013
186
7


Determining pathogenicity of genetic variants in hypertrophic cardiomyopathy: importance of periodic reassessment.
Jipin Das K, Jodie Ingles, Richard D Bagnall, Christopher Semsarian. Genet Med 2014
58
12

Shared Genetic Predisposition in Peripartum and Dilated Cardiomyopathies.
James S Ware, Jian Li, Erica Mazaika, Christopher M Yasso, Tiffany DeSouza, Thomas P Cappola, Emily J Tsai, Denise Hilfiker-Kleiner, Chizuko A Kamiya, Francesco Mazzarotto,[...]. N Engl J Med 2016
240
7

Establishment of Specialized Clinical Cardiovascular Genetics Programs: Recognizing the Need and Meeting Standards: A Scientific Statement From the American Heart Association.
Ferhaan Ahmad, Elizabeth M McNally, Michael J Ackerman, Linda C Baty, Sharlene M Day, Iftikhar J Kullo, Peace C Madueme, Martin S Maron, Matthew W Martinez, Lisa Salberg,[...]. Circ Genom Precis Med 2019
22
31


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.