A citation-based method for searching scientific literature

I M van Langen, E Birnie, E Schuurman, H L Tan, N Hofman, G J Bonsel, A A M Wilde. Clin Genet 2005
Times Cited: 16







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



Times Cited
  Times     Co-cited
Similarity


Genetic knowledge and counselling skills of Dutch cardiologists: sufficient for the genomics era?
I M van Langen, E Birnie, N J Leschot, G J Bonsel, A A M Wilde. Eur Heart J 2003
35
31

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
31

Clinical and genetic issues in familial dilated cardiomyopathy.
Emily L Burkett, Ray E Hershberger. J Am Coll Cardiol 2005
233
25

Educating health-care professionals about genetics and genomics.
Alan E Guttmacher, Mary E Porteous, Joseph D McInerney. Nat Rev Genet 2007
195
25

Genetic testing and genetic counseling in cardiovascular genetic medicine: overview and preliminary recommendations.
Jason Cowan, Ana Morales, Jimena Dagua, Ray E Hershberger. Congest Heart Fail 2008
25
25

Yield of genetic testing in hypertrophic cardiomyopathy.
Sara L Van Driest, Steve R Ommen, A Jamil Tajik, Bernard J Gersh, Michael J Ackerman. Mayo Clin Proc 2005
112
25

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
25


Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.
Sharie B Parks, Jessica D Kushner, Deirdre Nauman, Donna Burgess, Susan Ludwigsen, Amanda Peterson, Duanxiang Li, Petra Jakobs, Michael Litt, Charles B Porter,[...]. Am Heart J 2008
157
18


Proposal for contemporary screening strategies in families with hypertrophic cardiomyopathy.
Barry J Maron, J G Seidman, Christine E Seidman. J Am Coll Cardiol 2004
121
18

American College of Cardiology/European Society of Cardiology clinical expert consensus document on hypertrophic cardiomyopathy. A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the European Society of Cardiology Committee for Practice Guidelines.
Barry J Maron, William J McKenna, Gordon K Danielson, Lukas J Kappenberger, Horst J Kuhn, Christine E Seidman, Pravin M Shah, William H Spencer, Paolo Spirito, Folkert J Ten Cate,[...]. J Am Coll Cardiol 2003
958
18


Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy.
Pascale Richard, Philippe Charron, Lucie Carrier, Céline Ledeuil, Theary Cheav, Claire Pichereau, Abdelaziz Benaiche, Richard Isnard, Olivier Dubourg, Marc Burban,[...]. Circulation 2003
820
18

Genetic basis of hypertrophic cardiomyopathy: from bench to the clinics.
Ronny Alcalai, Jonathan G Seidman, Christine E Seidman. J Cardiovasc Electrophysiol 2008
231
18

Psychosocial impact of specialized cardiac genetic clinics for hypertrophic cardiomyopathy.
Jodie Ingles, Joanne M Lind, Philayrath Phongsavan, Christopher Semsarian. Genet Med 2008
72
18

Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience.
P Charron, D Héron, M Gargiulo, P Richard, O Dubourg, M Desnos, J B Bouhour, J Feingold, L Carrier, B Hainque,[...]. J Med Genet 2002
49
18

Familial screening and genetic counselling in hypertrophic cardiomyopathy: the Rotterdam experience.
M Michels, Y M Hoedemaekers, M J Kofflard, I Frohn-Mulder, D Dooijes, D Majoor-Krakauer, F J Ten Cate. Neth Heart J 2007
32
18


New insights into the pathology of inherited cardiomyopathy.
Siân E Hughes, William J McKenna. Heart 2005
88
12



Psychological consequences of predictive genetic testing: a systematic review.
M Broadstock, S Michie, T Marteau. Eur J Hum Genet 2000
236
12


Genetic counseling.
F C Fraser. Am J Hum Genet 1974
183
12

Provision of genetic services in Europe: current practices and issues.
Béatrice Godard, Helena Kääriäinen, Ulf Kristoffersson, Lisbeth Tranebjaerg, Domenico Coviello, Ségolène Aymé. Eur J Hum Genet 2003
61
12


Recurrence risks in offspring of adults with major heart defects: results from first cohort of British collaborative study.
J Burn, P Brennan, J Little, S Holloway, R Coffey, J Somerville, N R Dennis, L Allan, R Arnold, J E Deanfield,[...]. Lancet 1998
223
12

Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect.
Kayoko Hirayama-Yamada, Mitsuhiro Kamisago, Kaoru Akimoto, Hiroyuki Aotsuka, Yoshihide Nakamura, Hideshi Tomita, Michiko Furutani, Shin-ichiro Imamura, Atsuyoshi Takao, Makoto Nakazawa,[...]. Am J Med Genet A 2005
150
12

Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies.
Luc M Beauchesne, Carole A Warnes, Heidi M Connolly, Naser M Ammash, Martha Grogan, Syed M Jalal, Virginia V Michels. J Am Coll Cardiol 2005
55
12

Role of TBX1 in human del22q11.2 syndrome.
Hisato Yagi, Yoshiyuki Furutani, Hiromichi Hamada, Takashi Sasaki, Shuichi Asakawa, Shinsei Minoshima, Fukiko Ichida, Kunitaka Joo, Misa Kimura, Shin-ichiro Imamura,[...]. Lancet 2003
524
12

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome.
S Merscher, B Funke, J A Epstein, J Heyer, A Puech, M M Lu, R J Xavier, M B Demay, R G Russell, S Factor,[...]. Cell 2001
654
12

Congenital heart disease caused by mutations in the transcription factor NKX2-5.
J J Schott, D W Benson, C T Basson, W Pease, G M Silberbach, J P Moak, B J Maron, C E Seidman, J G Seidman. Science 1998
894
12

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.
Vidu Garg, Irfan S Kathiriya, Robert Barnes, Marie K Schluterman, Isabelle N King, Cheryl A Butler, Caryn R Rothrock, Reenu S Eapen, Kayoko Hirayama-Yamada, Kunitaka Joo,[...]. Nature 2003
800
12


New developments in genetics-knowledge, attitudes and information needs of practice nurses.
C Bankhead, J Emery, N Qureshi, H Campbell, J Austoker, E Watson. Fam Pract 2001
35
12


Can parents adjust to the idea that their child is at risk for a sudden death?: Psychological impact of risk for long QT syndrome.
Karin S W H Hendriks, F J M Grosfeld, J P van Tintelen, I M van Langen, A A M Wilde, J van den Bout, H F J ten Kroode. Am J Med Genet A 2005
38
12

Integrating genetics as practices of primary care.
Rosemary Robins, Sylvia Metcalfe. Soc Sci Med 2004
37
12


Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy.
Sara L Van Driest, Vlad C Vasile, Steve R Ommen, Melissa L Will, A Jamil Tajik, Bernard J Gersh, Michael J Ackerman. J Am Coll Cardiol 2004
300
12

Family history: an essential tool for cardiovascular genetic medicine.
Ana Morales, Jason Cowan, Jimena Dagua, Ray E Hershberger. Congest Heart Fail 2008
31
12

Primary prevention of sudden death in patients with lamin A/C gene mutations.
Christophe Meune, Jop H Van Berlo, Frédéric Anselme, Gisèle Bonne, Yigal M Pinto, Denis Duboc. N Engl J Med 2006
252
12

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
12

Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.
Ray E Hershberger, Sharie B Parks, Jessica D Kushner, Duanxiang Li, Susan Ludwigsen, Petra Jakobs, Deirdre Nauman, Donna Burgess, Julie Partain, Michael Litt. Clin Transl Sci 2008
133
12

Cardiac beta-myosin heavy chain defects in two families with non-compaction cardiomyopathy: linking non-compaction to hypertrophic, restrictive, and dilated cardiomyopathies.
Yvonne M Hoedemaekers, Kadir Caliskan, Danielle Majoor-Krakauer, Ingrid van de Laar, Michelle Michels, Maarten Witsenburg, Folkert J ten Cate, Maarten L Simoons, Dennis Dooijes. Eur Heart J 2007
89
12

Penetrance of mutations in plakophilin-2 among families with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Darshan Dalal, Cynthia James, Rajiv Devanagondi, Crystal Tichnell, April Tucker, Kalpana Prakasa, Philip J Spevak, David A Bluemke, Theodore Abraham, Stuart D Russell,[...]. J Am Coll Cardiol 2006
89
12

Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype.
Toru Kubo, Juan R Gimeno, Ajay Bahl, Ulla Steffensen, Morten Steffensen, Eyman Osman, Rajesh Thaman, Jens Mogensen, Perry M Elliott, Yoshinori Doi,[...]. J Am Coll Cardiol 2007
116
12

Arrhythmogenic right ventricular dysplasia: a United States experience.
Darshan Dalal, Khurram Nasir, Chandra Bomma, Kalpana Prakasa, Harikrishna Tandri, Jonathan Piccini, Ariel Roguin, Crystal Tichnell, Cynthia James, Stuart D Russell,[...]. Circulation 2005
313
12

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation.
A A Geisterfer-Lowrance, S Kass, G Tanigawa, H P Vosberg, W McKenna, C E Seidman, J G Seidman. Cell 1990
961
12


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.