PubRank

Florence Kyndt

Author PubWeight™ 29.21‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death. Nature 2003 5.94
2 An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing. Heart Rhythm 2009 4.99
3 Identification of a strong genetic background for progressive cardiac conduction defect by epidemiological approach. Heart 2012 2.39
4 Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutation. Europace 2013 2.14
5 Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. Nat Genet 2013 1.86
6 Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance. J Am Coll Cardiol 2011 1.82
7 Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human. Hum Mol Genet 2012 1.64
8 SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome. Circ Cardiovasc Genet 2009 1.64
9 Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies. Heart Rhythm 2008 1.56
10 Response to intravenous ajmaline: a retrospective analysis of 677 ajmaline challenges. Europace 2009 1.47
11 Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease. J Am Coll Cardiol 2003 1.34
12 Multifocal ectopic Purkinje-related premature contractions: a new SCN5A-related cardiac channelopathy. J Am Coll Cardiol 2012 1.01
13 Filamin-a-related myxomatous mitral valve dystrophy: genetic, echocardiographic and functional aspects. J Cardiovasc Transl Res 2011 0.83
14 Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations. Basic Res Cardiol 2014 0.78
15 Cardiac Phenotype and Long-Term Follow-Up of Patients With Mutations in NKX2-5 Gene. J Am Coll Cardiol 2016 0.76
16 Cosegregation of the Marfan syndrome and the long QT syndrome in the same family leads to a severe cardiac phenotype. Am J Cardiol 2003 0.75
17 Familial Catecholamine-Induced QT Prolongation in Unexplained Sudden Cardiac Death. J Am Coll Cardiol 2017 0.75