A citation-based method for searching scientific literature

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
Times Cited: 123







List of co-cited articles
1248 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
41

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
718
22

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).
Michael J Ackerman, Silvia G Priori, Stephan Willems, Charles Berul, Ramon Brugada, Hugh Calkins, A John Camm, Patrick T Ellinor, Michael Gollob, Robert Hamilton,[...]. Heart Rhythm 2011
605
22

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
21

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
68
30

Proposal for a revised definition of dilated cardiomyopathy, hypokinetic non-dilated cardiomyopathy, and its implications for clinical practice: a position statement of the ESC working group on myocardial and pericardial diseases.
Yigal M Pinto, Perry M Elliott, Eloisa Arbustini, Yehuda Adler, Aris Anastasakis, Michael Böhm, Denis Duboc, Juan Gimeno, Pascal de Groote, Massimo Imazio,[...]. Eur Heart J 2016
347
19

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
173
19


Dilated cardiomyopathy: the complexity of a diverse genetic architecture.
Ray E Hershberger, Dale J Hedges, Ana Morales. Nat Rev Cardiol 2013
440
17

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
249
17

Dilated Cardiomyopathy: Genetic Determinants and Mechanisms.
Elizabeth M McNally, Luisa Mestroni. Circ Res 2017
235
17

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
88
19

Atlas of the clinical genetics of human dilated cardiomyopathy.
Jan Haas, Karen S Frese, Barbara Peil, Wanda Kloos, Andreas Keller, Rouven Nietsch, Zhu Feng, Sabine Müller, Elham Kayvanpour, Britta Vogel,[...]. Eur Heart J 2015
290
17

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
149
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
15

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
333
15

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
235
14

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
208
14

The landscape of genetic variation in dilated cardiomyopathy as surveyed by clinical DNA sequencing.
Trevor J Pugh, Melissa A Kelly, Sivakumar Gowrisankar, Elizabeth Hynes, Michael A Seidman, Samantha M Baxter, Mark Bowser, Bryan Harrison, Daniel Aaron, Lisa M Mahanta,[...]. Genet Med 2014
180
14

Genetic Etiology for Alcohol-Induced Cardiac Toxicity.
James S Ware, Almudena Amor-Salamanca, Upasana Tayal, Risha Govind, Isabel Serrano, Joel Salazar-Mendiguchía, Jose Manuel García-Pinilla, Domingo A Pascual-Figal, Julio Nuñez, Gonzalo Guzzo-Merello,[...]. J Am Coll Cardiol 2018
77
16

ClinGen--the Clinical Genome Resource.
Heidi L Rehm, Jonathan S Berg, Lisa D Brooks, Carlos D Bustamante, James P Evans, Melissa J Landrum, David H Ledbetter, Donna R Maglott, Christa Lese Martin, Robert L Nussbaum,[...]. N Engl J Med 2015
492
13

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
344
13

Current Diagnostic and Treatment Strategies for Specific Dilated Cardiomyopathies: A Scientific Statement From the American Heart Association.
Biykem Bozkurt, Monica Colvin, Jennifer Cook, Leslie T Cooper, Anita Deswal, Gregg C Fonarow, Gary S Francis, Daniel Lenihan, Eldrin F Lewis, Dennis M McNamara,[...]. Circulation 2016
220
12

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
63
19

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).
Michael J Ackerman, Silvia G Priori, Stephan Willems, Charles Berul, Ramon Brugada, Hugh Calkins, A John Camm, Patrick T Ellinor, Michael Gollob, Robert Hamilton,[...]. Europace 2011
456
12

Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease.
Angharad M Roberts, James S Ware, Daniel S Herman, Sebastian Schafer, John Baksi, Alexander G Bick, Rachel J Buchan, Roddy Walsh, Shibu John, Samuel Wilkinson,[...]. Sci Transl Med 2015
235
12

Mutations in ribonucleic acid binding protein gene cause familial dilated cardiomyopathy.
Katharine M Brauch, Margaret L Karst, Kathleen J Herron, Mariza de Andrade, Patricia A Pellikka, Richard J Rodeheffer, Virginia V Michels, Timothy M Olson. J Am Coll Cardiol 2009
201
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
133
11

Multiple Gene Variants in Hypertrophic Cardiomyopathy in the Era of Next-Generation Sequencing.
Charlotte Burns, Richard D Bagnall, Lien Lam, Christopher Semsarian, Jodie Ingles. Circ Cardiovasc Genet 2017
39
28

Outcome in phospholamban R14del carriers: results of a large multicentre cohort study.
Ingrid A W van Rijsingen, Paul A van der Zwaag, Judith A Groeneweg, Eline A Nannenberg, Jan D H Jongbloed, Aeilko H Zwinderman, Yigal M Pinto, Ronald H Lekanne Dit Deprez, Jan G Post, Hanno L Tan,[...]. Circ Cardiovasc Genet 2014
76
13

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,[...]. Eur Heart J 2010
719
10

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
348
10

Impact of genotype on clinical course in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated mutation carriers.
Aditya Bhonsale, Judith A Groeneweg, Cynthia A James, Dennis Dooijes, Crystal Tichnell, Jan D H Jongbloed, Brittney Murray, Anneline S J M te Riele, Maarten P van den Berg, Hennie Bikker,[...]. Eur Heart J 2015
198
10

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
10

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
814
10

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
995
10

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
74
13

Pediatric Cardiomyopathies.
Teresa M Lee, Daphne T Hsu, Paul Kantor, Jeffrey A Towbin, Stephanie M Ware, Steven D Colan, Wendy K Chung, John L Jefferies, Joseph W Rossano, Chesney D Castleberry,[...]. Circ Res 2017
88
11

Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy.
Francesco Mazzarotto, Upasana Tayal, Rachel J Buchan, William Midwinter, Alicja Wilk, Nicola Whiffin, Risha Govind, Erica Mazaika, Antonio de Marvao, Timothy J W Dawes,[...]. Circulation 2020
51
19

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
168
9

Defibrillator Implantation in Patients with Nonischemic Systolic Heart Failure.
Lars Køber, Jens J Thune, Jens C Nielsen, Jens Haarbo, Lars Videbæk, Eva Korup, Gunnar Jensen, Per Hildebrandt, Flemming H Steffensen, Niels E Bruun,[...]. N Engl J Med 2016
780
9

2013 ACCF/AHA guideline for the management of heart failure: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines.
Clyde W Yancy, Mariell Jessup, Biykem Bozkurt, Javed Butler, Donald E Casey, Mark H Drazner, Gregg C Fonarow, Stephen A Geraci, Tamara Horwich, James L Januzzi,[...]. J Am Coll Cardiol 2013
9

2016 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure: The Task Force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC)Developed with the special contribution of the Heart Failure Association (HFA) of the ESC.
Piotr Ponikowski, Adriaan A Voors, Stefan D Anker, Héctor Bueno, John G F Cleland, Andrew J S Coats, Volkmar Falk, José Ramón González-Juanatey, Veli-Pekka Harjola, Ewa A Jankowska,[...]. Eur Heart J 2016
9

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
126
9

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
9

The emerging role of the cardiac genetic counselor.
Jodie Ingles, Laura Yeates, Christopher Semsarian. Heart Rhythm 2011
71
12

Association of competitive and recreational sport participation with cardiac events in patients with arrhythmogenic right ventricular cardiomyopathy: results from the North American multidisciplinary study of arrhythmogenic right ventricular cardiomyopathy.
Anne-Christine Ruwald, Frank Marcus, N A Mark Estes, Mark Link, Scott McNitt, Bronislava Polonsky, Hugh Calkins, Jeffrey A Towbin, Arthur J Moss, Wojciech Zareba. Eur Heart J 2015
141
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,[...]. Heart Rhythm 2018
127
8

Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members.
Judith A Groeneweg, Aditya Bhonsale, Cynthia A James, Anneline S te Riele, Dennis Dooijes, Crystal Tichnell, Brittney Murray, Ans C P Wiesfeld, Abhishek C Sawant, Bina Kassamali,[...]. Circ Cardiovasc Genet 2015
222
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
69
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.