A citation-based method for searching scientific literature

Jodie Ingles, Laura Yeates, Christopher Semsarian. Heart Rhythm 2011
Times Cited: 72







List of co-cited articles
1285 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
612
54

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
34

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
31

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
25

A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report.
Robert Resta, Barbara Bowles Biesecker, Robin L Bennett, Sandra Blum, Susan Estabrooks Hahn, Michelle N Strecker, Janet L Williams. J Genet Couns 2006
367
23


Psychosocial impact of specialized cardiac genetic clinics for hypertrophic cardiomyopathy.
Jodie Ingles, Joanne M Lind, Philayrath Phongsavan, Christopher Semsarian. Genet Med 2008
72
20

Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families.
Elijah R Behr, Chrysoula Dalageorgou, Michael Christiansen, Petros Syrris, Sian Hughes, Maria T Tome Esteban, Edward Rowland, Steve Jeffery, William J McKenna. Eur Heart J 2008
251
20

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

Clinical predictors of genetic testing outcomes in hypertrophic cardiomyopathy.
Jodie Ingles, Tanya Sarina, Laura Yeates, Lauren Hunt, Ivan Macciocca, Louise McCormack, Ingrid Winship, Julie McGaughran, John Atherton, Christopher Semsarian. Genet Med 2013
70
21

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
25

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
44


Guidelines for genetic testing of inherited cardiac disorders.
Jodie Ingles, Poonam R Zodgekar, Laura Yeates, Ivan Macciocca, Christopher Semsarian, Diane Fatkin. Heart Lung Circ 2011
44
31

New perspectives on the prevalence of hypertrophic cardiomyopathy.
Christopher Semsarian, Jodie Ingles, Martin S Maron, Barry J Maron. J Am Coll Cardiol 2015
453
19

Quality of life and psychological distress in hypertrophic cardiomyopathy mutation carriers: a cross-sectional cohort study.
Imke Christiaans, Irene M van Langen, Erwin Birnie, Gouke J Bonsel, Arthur A M Wilde, Ellen M A Smets. Am J Med Genet A 2009
76
18

Sudden unexplained death: heritability and diagnostic yield of cardiological and genetic examination in surviving relatives.
Hanno L Tan, Nynke Hofman, Irene M van Langen, Allard C van der Wal, Arthur A M Wilde. Circulation 2005
270
18

Active cascade screening in primary inherited arrhythmia syndromes: does it lead to prophylactic treatment?
Nynke Hofman, Hanno L Tan, Marielle Alders, Irene M van Langen, Arthur A M Wilde. J Am Coll Cardiol 2010
69
18

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
18

Toronto hypertrophic cardiomyopathy genotype score for prediction of a positive genotype in hypertrophic cardiomyopathy.
Christiane Gruner, Joan Ivanov, Melanie Care, Lynne Williams, Gil Moravsky, Hua Yang, Balint Laczay, Katherine Siminovitch, Anna Woo, Harry Rakowski. Circ Cardiovasc Genet 2013
63
19

The value of cardiac genetic testing.
Jodie Ingles, Christopher Semsarian. Trends Cardiovasc Med 2014
31
38

Sudden cardiac death in the young: the molecular autopsy and a practical approach to surviving relatives.
Christopher Semsarian, Jodie Ingles, Arthur A M Wilde. Eur Heart J 2015
122
16

Natural history of genotype positive-phenotype negative patients with hypertrophic cardiomyopathy.
Belinda Gray, Jodie Ingles, Christopher Semsarian. Int J Cardiol 2011
47
23

Implantable cardioverter-defibrillators and prevention of sudden cardiac death in hypertrophic cardiomyopathy.
Barry J Maron, Paolo Spirito, Win-Kuang Shen, Tammy S Haas, Francesco Formisano, Mark S Link, Andrew E Epstein, Adrian K Almquist, James P Daubert, Thorsten Lawrenz,[...]. JAMA 2007
527
15

Cardiological assessment of first-degree relatives in sudden arrhythmic death syndrome.
E Behr, D A Wood, M Wright, P Syrris, M N Sheppard, A Casey, M J Davies, W McKenna. Lancet 2003
182
15

Diagnostic yield in sudden unexplained death and aborted cardiac arrest in the young: the experience of a tertiary referral center in The Netherlands.
Christian van der Werf, Nynke Hofman, Hanno L Tan, Pascal F van Dessel, Marielle Alders, Allard C van der Wal, Irene M van Langen, Arthur A M Wilde. Heart Rhythm 2010
105
15


Poor psychological wellbeing particularly in mothers following sudden cardiac death in the young.
Laura Yeates, Lauren Hunt, Mona Saleh, Christopher Semsarian, Jodie Ingles. Eur J Cardiovasc Nurs 2013
21
52

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

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
15

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
15


A cost-effectiveness model of genetic testing for the evaluation of families with hypertrophic cardiomyopathy.
Jodie Ingles, Julie McGaughran, Paul A Scuffham, John Atherton, Christopher Semsarian. Heart 2012
76
13

Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.
P J Schwartz, S G Priori, C Spazzolini, A J Moss, G M Vincent, C Napolitano, I Denjoy, P Guicheney, G Breithardt, M T Keating,[...]. Circulation 2001
13

Risk stratification in the long-QT syndrome.
Silvia G Priori, Peter J Schwartz, Carlo Napolitano, Raffaella Bloise, Elena Ronchetti, Massimiliano Grillo, Alessandro Vicentini, Carla Spazzolini, Janni Nastoli, Georgia Bottelli,[...]. N Engl J Med 2003
903
13

Yield of molecular and clinical testing for arrhythmia syndromes: report of 15 years' experience.
Nynke Hofman, Hanno L Tan, MariĆ«lle Alders, Iris Kolder, Simone de Haij, Marcel M A M Mannens, Maria Paola Lombardi, Ronald H Lekanne Dit Deprez, Irene van Langen, Arthur A M Wilde. Circulation 2013
83
13

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
502
13

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
13

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
45

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
12

Key role of the molecular autopsy in sudden unexpected death.
Christopher Semsarian, Robert M Hamilton. Heart Rhythm 2012
38
23

Health status of cardiac genetic disease patients and their at-risk relatives.
Jodie Ingles, Laura Yeates, Lauren Hunt, Julie McGaughran, Paul A Scuffham, John Atherton, Christopher Semsarian. Int J Cardiol 2013
32
28

Genetic evaluation of cardiomyopathy--a Heart Failure Society of America practice guideline.
Ray E Hershberger, Joann Lindenfeld, Luisa Mestroni, Christine E Seidman, Matthew R G Taylor, Jeffrey A Towbin. J Card Fail 2009
306
12


Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals.
Ilan Goldenberg, Samuel Horr, Arthur J Moss, Coeli M Lopes, Alon Barsheshet, Scott McNitt, Wojciech Zareba, Mark L Andrews, Jennifer L Robinson, Emanuela H Locati,[...]. J Am Coll Cardiol 2011
158
12

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
12

Experiences, considerations and emotions relating to cardiogenetic evaluation in relatives of young sudden cardiac death victims.
Christian van der Werf, Astrid T Onderwater, Irene M van Langen, Ellen M A Smets. Eur J Hum Genet 2014
16
56

Exome analysis-based molecular autopsy in cases of sudden unexplained death in the young.
Richard D Bagnall, Jipin Das K, Johan Duflou, Christopher Semsarian. Heart Rhythm 2014
86
12

Safety of sports for athletes with implantable cardioverter-defibrillators: results of a prospective, multinational registry.
Rachel Lampert, Brian Olshansky, Hein Heidbuchel, Christine Lawless, Elizabeth Saarel, Michael Ackerman, Hugh Calkins, N A Mark Estes, Mark S Link, Barry J Maron,[...]. Circulation 2013
126
12

Posttraumatic Stress and Prolonged Grief After the Sudden Cardiac Death of a Young Relative.
Jodie Ingles, Catherine Spinks, Laura Yeates, Kevin McGeechan, Nadine Kasparian, Christopher Semsarian. JAMA Intern Med 2016
30
30


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.