Irene van Langen
Irene van Langen
Professor of Cinical Genetics, UMCG (MGE), University of Groningen
Geverifieerd e-mailadres voor umcg.nl - Homepage
Geciteerd door
Geciteerd door
A Single Na+ Channel Mutation Causing Both Long-QT and Brugada Syndromes
C Bezzina, MW Veldkamp, MP van den Berg, AV Postma, MB Rook, ...
Circulation research 85 (12), 1206-1213, 1999
Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases
P Charron, M Arad, E Arbustini, C Basso, Z Bilinska, P Elliott, T Helio, ...
European heart journal 31 (22), 2715-2726, 2010
Sudden unexplained death: heritability and diagnostic yield of cardiological and genetic examination in surviving relatives
HL Tan, N Hofman, IM Van Langen, AC Van Der Wal, AAM Wilde
Circulation 112 (2), 207-213, 2005
Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy
JP van Tintelen, MM Entius, ZA Bhuiyan, R Jongbloed, ACP Wiesfeld, ...
Circulation 113 (13), 1650-1658, 2006
A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill
WA Groenewegen, M Firouzi, CR Bezzina, S Vliex, IM Van Langen, ...
Circulation research 92 (1), 14-22, 2003
Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1)
AAM Wilde, RJE Jongbloed, PA Doevendans, DR Düren, RNW Hauer, ...
Journal of the American College of Cardiology 33 (2), 327-332, 1999
Arrhythmogenic right ventricular dysplasia/cardiomyopathy: pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right …
MGPJ Cox, PA van der Zwaag, C van der Werf, JJ van der Smagt, ...
Circulation 123 (23), 2690-2700, 2011
Expanding Spectrum of Human RYR2-Related Disease: New Electrocardiographic, Structural, and Genetic Features
ZA Bhuiyan, MP van den Berg, JP van Tintelen, MTE Bink-Boelkens, ...
Circulation 116 (14), 1569-1576, 2007
Risk stratification for sudden cardiac death in hypertrophic cardiomyopathy: systematic review of clinical risk markers
I Christiaans, K Van Engelen, IM Van Langen, E Birnie, GJ Bonsel, ...
Europace 12 (3), 313-321, 2010
Desmin‐related myopathy
KY van Spaendonck‐Zwarts, L van Hessem, JDH Jongbloed, ...
Clinical genetics 80 (4), 354-366, 2011
The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands
M Alders, R Jongbloed, W Deelen, A Van den Wijngaard, P Doevendans, ...
European Heart Journal 24 (20), 1848-1853, 2003
Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy
KY van Spaendonck-Zwarts, A Posafalvi, MP van den Berg, ...
European heart journal 35 (32), 2165-2173, 2014
Incidence, causes, and outcomes of out-of-hospital cardiac arrest in children: a comprehensive, prospective, population-based study in the Netherlands
A Bardai, J Berdowski, C Van Der Werf, MT Blom, M Ceelen, ...
Journal of the American College of Cardiology 57 (18), 1822-1828, 2011
Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience
KY van Spaendonck‐Zwarts, IAW van Rijsingen, MP van den Berg, ...
European journal of heart failure 15 (6), 628-636, 2013
TRIDENT-2: national implementation of genome-wide non-invasive prenatal testing as a first-tier screening test in the Netherlands
KRM van der Meij, EA Sistermans, MVE Macville, SJC Stevens, CJ Bax, ...
The American Journal of Human Genetics 105 (6), 1091-1101, 2019
Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?
N Hofman, AAM Wilde, S Kääb, IM Van Langen, MWT Tanck, ...
European heart journal 28 (5), 575-580, 2007
Diagnostic yield in sudden unexplained death and aborted cardiac arrest in the young: the experience of a tertiary referral center in The Netherlands
C van der Werf, N Hofman, HL Tan, PF van Dessel, M Alders, ...
Heart Rhythm 7 (10), 1383-1389, 2010
High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics
JP van Tintelen, RMW Hofstra, H Katerberg, T Rossenbacker, ...
American heart journal 154 (6), 1130-1139, 2007
Possible bradycardic mode of death and successful pacemaker treatment in a large family with features of long QT syndrome type 3 and Brugada syndrome
MP Van Den Berg, AAM Wilde, JW Viersma, JAN Brouwer, J Haaksma, ...
Journal of cardiovascular electrophysiology 12 (6), 630-636, 2001
Yield of molecular and clinical testing for arrhythmia syndromes: report of 15 years’ experience
N Hofman, HL Tan, M Alders, I Kolder, S De Haij, MMAM Mannens, ...
Circulation 128 (14), 1513-1521, 2013
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