A citation-based method for searching scientific literature

I M van Langen, E Birnie, N J Leschot, G J Bonsel, A A M Wilde. Eur Heart J 2003
Times Cited: 35







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



Times Cited
  Times     Co-cited
Similarity


Educating health-care professionals about genetics and genomics.
Alan E Guttmacher, Mary E Porteous, Joseph D McInerney. Nat Rev Genet 2007
195
20

The emerging role of the cardiac genetic counselor.
Jodie Ingles, Laura Yeates, Christopher Semsarian. Heart Rhythm 2011
71
20


Genetic counseling and cardiac care in predictively tested hypertrophic cardiomyopathy mutation carriers: the patients' perspective.
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
41
17

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
17


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
17

Low penetrance in the long-QT syndrome: clinical impact.
S G Priori, C Napolitano, P J Schwartz. Circulation 1999
560
14


The 'new genetics' and primary care: GPs' views on their role and their educational needs.
E K Watson, D Shickle, N Qureshi, J Emery, J Austoker. Fam Pract 1999
136
14

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
901
14

Preferences of cardiologists and clinical geneticists for the future organization of genetic care in hypertrophic cardiomyopathy: a survey.
I M van Langen, E Birnie, E Schuurman, H L Tan, N Hofman, G J Bonsel, A A M Wilde. Clin Genet 2005
16
31

Uptake of genetic counselling and predictive DNA testing in hypertrophic cardiomyopathy.
Imke Christiaans, Erwin Birnie, Gouke J Bonsel, Arthur Am Wilde, Irene M van Langen. Eur J Hum Genet 2008
69
14

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
14

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
526
14

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
439
14

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
14

Idiopathic short QT interval: a new clinical syndrome?
I Gussak, P Brugada, J Brugada, R S Wright, S L Kopecky, B R Chaitman, P Bjerregaard. Cardiology 2000
396
14

Long-term follow-up of patients with short QT syndrome.
Carla Giustetto, Rainer Schimpf, Andrea Mazzanti, Chiara Scrocco, Philippe Maury, Olli Anttonen, Vincent Probst, Jean-Jacques Blanc, Pascal Sbragia, Paola Dalmasso,[...]. J Am Coll Cardiol 2011
170
14

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
14

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia.
S G Priori, C Napolitano, N Tiso, M Memmi, G Vignati, R Bloise, V Sorrentino, G A Danieli. Circulation 2001
907
14

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
725
14

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
14

Yield of genetic screening in inherited cardiac channelopathies: how to prioritize access to genetic testing.
Rong Bai, Carlo Napolitano, Raffaella Bloise, Nicola Monteforte, Silvia G Priori. Circ Arrhythm Electrophysiol 2009
94
14

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
291
14


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
43
14

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
14

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
499
14

Atrial fibrillation in patients with Brugada syndrome relationships of gene mutation, electrophysiology, and clinical backgrounds.
Kengo F Kusano, Makiko Taniyama, Kazufumi Nakamura, Daiji Miura, Kimikazu Banba, Satoshi Nagase, Hiroshi Morita, Nobuhiro Nishii, Atsuyuki Watanabe, Takeshi Tada,[...]. J Am Coll Cardiol 2008
112
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
894
14

Psychological consequences of predictive genetic testing: a systematic review.
M Broadstock, S Michie, T Marteau. Eur J Hum Genet 2000
235
11

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.
Q Wang, M E Curran, I Splawski, T C Burn, J M Millholland, T J VanRaay, J Shen, K W Timothy, G M Vincent, T de Jager,[...]. Nat Genet 1996
11

Natural history of dilated cardiomyopathy due to lamin A/C gene mutations.
Matthew R G Taylor, Pamela R Fain, Gianfranco Sinagra, Misi L Robinson, Alastair D Robertson, Elisa Carniel, Andrea Di Lenarda, Teresa J Bohlmeyer, Debra A Ferguson, Gary L Brodsky,[...]. J Am Coll Cardiol 2003
286
11

Family history and colorectal cancer screening: a survey of physician knowledge and practice patterns.
Paul C Schroy, Adam F Barrison, Bruce S Ling, Sheila Wilson, Adam C Geller. Am J Gastroenterol 2002
111
11

Comparison of activities and attitudes of general practitioners concerning genetic counseling over a 10-year time-span.
Marieke J H Baars, Denhard J de Smit, Miranda W Langendam, Herman J Adèr, Leo P ten Kate. Patient Educ Couns 2003
11
36

Awareness of genetic testing for colorectal cancer predisposition among specialists in gastroenterology.
Shivani Batra, Heiddis Valdimarsdottir, Margaret McGovern, Steven Itzkowitz, Karen Brown. Am J Gastroenterol 2002
56
11


Genomic medicine: who will practice it? A call to open arms.
A E Guttmacher, J Jenkins, W R Uhlmann. Am J Med Genet 2001
71
11


Will the learners be learned?
Susan J Hayflick, M Patrice Eiff. Genet Med 2002
13
30

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
11

Inferolateral early repolarization in athletes.
M Juhani Junttila, Solomon J Sager, Monika Freiser, Scott McGonagle, Agustin Castellanos, Robert J Myerburg. J Interv Card Electrophysiol 2011
47
11

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
11

Incidence and prognostic value of early repolarization pattern in the 12-lead electrocardiogram.
Daisuke Haruta, Kiyotaka Matsuo, Akira Tsuneto, Shinichiro Ichimaru, Ayumi Hida, Nobuko Sera, Misa Imaizumi, Eiji Nakashima, Koji Maemura, Masazumi Akahoshi. Circulation 2011
150
11

Risk of fatal arrhythmic events in long QT syndrome patients after syncope.
Christian Jons, Arthur J Moss, Ilan Goldenberg, Judy Liu, Scott McNitt, Wojciech Zareba, Ming Qi, Jennifer L Robinson. J Am Coll Cardiol 2010
72
11

Prevalence and characteristics of early repolarization in the CASPER registry: cardiac arrest survivors with preserved ejection fraction registry.
Nicolas Derval, Christopher S Simpson, David H Birnie, Jeffrey S Healey, Vijay Chauhan, Jean Champagne, Martin Gardner, Shubhayan Sanatani, Raymond Yee, Allan C Skanes,[...]. J Am Coll Cardiol 2011
95
11

Calcium channel blockers and beta-blockers versus beta-blockers alone for preventing exercise-induced arrhythmias in catecholaminergic polymorphic ventricular tachycardia.
Rafael Rosso, Jonathan M Kalman, Ori Rogowski, Shmuel Diamant, Amir Birger, Simon Biner, Bernard Belhassen, Sami Viskin. Heart Rhythm 2007
108
11

ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome.
A J Moss, W Zareba, J Benhorin, E H Locati, W J Hall, J L Robinson, P J Schwartz, J A Towbin, G M Vincent, M H Lehmann. Circulation 1995
423
11

Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: clinical features and assignment of the disease gene to chromosome 1p13-21.
H Lahat, M Eldar, E Levy-Nissenbaum, T Bahan, E Friedman, A Khoury, A Lorber, D L Kastner, B Goldman, E Pras. Circulation 2001
179
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.