PubRank

A A M Wilde

Author PubWeight™ 67.15‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Long-term prognosis of patients diagnosed with Brugada syndrome: Results from the FINGER Brugada Syndrome Registry. Circulation 2010 2.53
2 Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy. Neurology 2008 2.21
3 Is T-wave alternans testing feasible in candidates for prophylactic implantable defibrillators? Neth Heart J 2011 1.89
4 Bibliometric data in clinical cardiology revisited. The case of 37 Dutch professors. Neth Heart J 2011 1.79
5 Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients. J Med Genet 2005 1.78
6 Novel Brugada syndrome-causing mutation in ion-conducting pore of cardiac Na+ channel does not affect ion selectivity properties. Acta Physiol Scand 2005 1.67
7 [Initial diagnostic strategy in the case of transient losses of consciousness: the importance of the medical history]. Ned Tijdschr Geneeskd 2003 1.55
8 Genetic knowledge and counselling skills of Dutch cardiologists: sufficient for the genomics era? Eur Heart J 2003 1.52
9 [Genetic identification of patients and families with a long-QT syndrome: large regional differences in the result of 10 years]. Ned Tijdschr Geneeskd 2007 1.46
10 The works of Dirk Durrer (1918-1984). Neth Heart J 2012 1.39
11 [Medication for ADHD and the risk of cardiovascular mortality]. Ned Tijdschr Geneeskd 2006 1.39
12 The Hirsch-index: a simple, new tool for the assessment of scientific output of individual scientists: The case of Dutch professors in clinical cardiology. Neth Heart J 2009 1.30
13 The use of genotype-phenotype correlations in mutation analysis for the long QT syndrome. J Med Genet 2003 1.13
14 The cardiac sodium channel displays differential distribution in the conduction system and transmural heterogeneity in the murine ventricular myocardium. Basic Res Cardiol 2009 1.11
15 Impact of cardiac complications on outcome after aneurysmal subarachnoid hemorrhage: a meta-analysis. Neurology 2009 1.00
16 Family and population strategies for screening and counselling of inherited cardiac arrhythmias. Ann Med 2004 0.98
17 Fever-triggered ventricular arrhythmias in Brugada syndrome and type 2 long-QT syndrome. Neth Heart J 2010 0.94
18 First experience with the wearable cardioverter defibrillator in the Netherlands. Neth Heart J 2012 0.94
19 Recurrent and founder mutations in the Netherlands-Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathy. Neth Heart J 2013 0.94
20 Left cardiac sympathetic denervation in the Netherlands for the treatment of inherited arrhythmia syndromes. Neth Heart J 2014 0.93
21 Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands. Neth Heart J 2010 0.92
22 ECG determinants in adult patients with chronic right ventricular pressure overload caused by congenital heart disease: relation with plasma neurohormones and MRI parameters. Heart 2002 0.92
23 The sense and nonsense of direct-to-consumer genetic testing for cardiovascular disease. Neth Heart J 2011 0.91
24 Recurrent and founder mutations in the Netherlands : Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia. Neth Heart J 2010 0.91
25 Rationale and design of the CAREFUL study : The yield of CARdiogenetic scrEening in First degree relatives of sudden cardiac and UnexpLained death victims <45 years. Neth Heart J 2010 0.90
26 Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy. Neurology 2011 0.90
27 Can parents adjust to the idea that their child is at risk for a sudden death?: Psychological impact of risk for long QT syndrome. Am J Med Genet A 2005 0.88
28 High distress in parents whose children undergo predictive testing for long QT syndrome. Community Genet 2005 0.87
29 Prognostic value of microvolt T-wave alternans in a real-world ICD population. Twente ICD Cohort Studie (TICS). Neth Heart J 2014 0.87
30 Preferences of cardiologists and clinical geneticists for the future organization of genetic care in hypertrophic cardiomyopathy: a survey. Clin Genet 2005 0.85
31 Clinical implementation of guidelines for cardioverter defibrillator implantation: lost in translation? Neth Heart J 2007 0.84
32 Risk stratification for sudden cardiac death in hypertrophic cardiomyopathy: Dutch cardiologists and the care of mutation carriers. Neth Heart J 2009 0.84
33 Pregnancy and the risk of torsades de pointes in congenital long-QT syndrome. Neth Heart J 2008 0.83
34 Structural abnormalities of the left ventricle in hypertrophic cardiomyopathy mutation carriers detectable before the development of hypertrophy. Neth Heart J 2007 0.81
35 Netherlands Heart Journal: accepted into PubMed Central! Neth Heart J 2006 0.81
36 GENCOR: a national registry for patients and families suffering from a familial heart disease in the Netherlands. Neth Heart J 2006 0.81
37 Recurrent and founder mutations in inherited cardiac diseases in the Netherlands. Neth Heart J 2009 0.80
38 Letter regarding article by McNair et al, "SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia". Circulation 2005 0.80
39 Recurrent and Founder Mutations in the Netherlands: the Long-QT Syndrome. Neth Heart J 2010 0.80
40 Founder mutations in the Netherlands: familial idiopathic ventricular fibrillation and DPP6. Neth Heart J 2011 0.80
41 Percutaneous pulmonary valve replacement: a new development in the lifetime strategy for patients with congenital heart disease. Neth Heart J 2007 0.79
42 [Hypertrophic cardiomyopathy: a genetically-carried heart disease]. Ned Tijdschr Geneeskd 2002 0.79
43 Flush after syncope: not always an arrhythmia. J Cardiovasc Electrophysiol 2006 0.77
44 A large family characterised by nocturnal sudden death. Neth Heart J 2002 0.77
45 Towards a better risk stratification for sudden cardiac death in patients with structural heart disease. Neth Heart J 2009 0.77
46 T-wave alternans in a patient with long-QT syndrome type 3. Neth Heart J 2006 0.77
47 Arrhythmogenic right ventricular cardiomyopathy: asymptomatic to life threatening as illustrated by the cases of two sisters. Neth Heart J 2007 0.77
48 De novo mutation in the KCNQ1 gene causal to Jervell and Lange-Nielsen syndrome. Clin Genet 2013 0.76
49 Genetic predisposition for sudden cardiac death in myocardial ischaemia: the Arrhythmia Genetics in the NEtherlandS study. Neth Heart J 2011 0.76
50 Palpitations and dizziness in a 65-year-old man. Neth Heart J 2006 0.75
51 TDI-echocardiography: a new screening tool for long QT syndrome? Eur J Echocardiogr 2003 0.75
52 COMPANION - a friend indeed. Neth Heart J 2003 0.75
53 Primary prevention: prime time?: ICD trials (and tribulations). Neth Heart J 2004 0.75
54 Brugada syndrome. Eur Heart J 2002 0.75
55 Not just any ICD device in patients with long-QT syndrome. Neth Heart J 2007 0.75
56 One more time: bibliometric analysis of scientific output remains complicated. Neth Heart J 2011 0.75
57 An extended family suddenly confronted with a life-threatening hereditary arrhythmia. Neth Heart J 2005 0.75
58 Case histories: increasing role for major journals. Neth Heart J 2009 0.75
59 Diversity in cardiac sodium channel disease phenotype in transgenic mice carrying a single SCN5A mutation. Neth Heart J 2007 0.75
60 Recent breakthroughs in the genetics of atrial fibrillation. Neth Heart J 2003 0.75
61 The ECG of a (cardio)myopathy? Neth Heart J 2005 0.75
62 'Brugada ECG' elicited by imipramine overdose. Neth Heart J 2004 0.75
63 Cardiogenetic counselling in a non-university hospital. Neth Heart J 2007 0.75
64 Rationale of the SEAS study: Serial Echocardiography After Subarachnoid haemorrhage, a prospective national, multicentre, multidisciplinary, cohort study to evaluate cardiac abnormalities following intracranial haemorrhage. Neth Heart J 2006 0.75
65 Right you are. Neth Heart J 2005 0.75
66 Should I be worried? Neth Heart J 2006 0.75
67 ECG screening of newborns to avoid sudden infant death syndrome? Neth Heart J 2006 0.75
68 Recommendations and cardiological evaluation of athletes with arrhythmias: Part 2. Neth Heart J 2004 0.75
69 Recommendations and cardiological evaluation of athletes with arrhythmias: Part 1. Neth Heart J 2004 0.75
70 It's not what you think it is. Neth Heart J 2005 0.75
71 Primary ventricular fibrillation in acute myocardial infarction: an inherited disease? Neth Heart J 2001 0.75
72 Nightly phenomena, day time work? Neth Heart J 2004 0.75
73 A fainting lady with some extrasystoles. Neth Heart J 2004 0.75
74 Familial primary arrhythmia syndromes: Nice to know or need to know. Neth Heart J 2002 0.75
75 Should you be worried? Neth Heart J 2014 0.75
76 Reversed remodelling of dilated left sided cardiomyopathy after upgrading from VVIR to VVIR biventricular pacing. Europace 2002 0.75
77 Should you be worried? Neth Heart J 2014 0.75
78 A patient with recurrent syncope and ST-elevation on the electrocardiogram. Europace 2004 0.75
79 [Congenital long QT-syndrome: the cause of recurrent syncope and sudden death at a young age]. Ned Tijdschr Geneeskd 2007 0.75
80 Genotype-phenotype analysis of Jervell and Lange-Nielsen syndrome in six families from Saudi Arabia. Clin Genet 2013 0.75
81 [The optimal treatment of chronic heart failure with beta-blockers may be dependent upon the genetic background of the patient]. Ned Tijdschr Geneeskd 2007 0.75