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The Canadian Journal of Cardiology|March 4, 2017
Familial Disease Is Not Always Genetic: A Family With Atrioventricular Block and Mitral RegurgitationAlexa M Vermeer, Elisabeth M Lodder, Imke Christiaans, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|May 6, 2017
Transthyretin amyloidosis: a phenocopy of hypertrophic cardiomyopathyAlexa M C Vermeer, Anneloes Janssen, Peter C Boorsma, et al.
Journal of Genetic Counseling|April 26, 2015
Feasibility of an Assessment Tool for Children's Competence to Consent to Predictive Genetic Testing: a Pilot StudyIrma M Hein, Pieter W Troost, Robert Lindeboom, et al.
BMJ Open|July 11, 2019
A tailored approach towards informing relatives at risk of inherited cardiac conditions: study protocol for a randomised controlled trialLieke M van den Heuvel, Yvonne M Hoedemaekers, Annette F Baas, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|February 2, 2010
Risk stratification for sudden cardiac death in hypertrophic cardiomyopathy: systematic review of clinical risk markersImke Christiaans, Klaartje van Engelen, Irene M van Langen, et al.
European Journal of Human Genetics : EJHG|March 27, 2023
Predicting personal cardiovascular disease risk based on family health history: Development of expert-based family criteria for the general populationTetske Dijkstra, Lieke M van den Heuvel, J Peter van Tintelen, et al.
American Journal of Medical Genetics. Part A|March 13, 2025
Presenting Clinical Information on Rare Chromosome 6 Disorders via a Parent-Centered Website: Parental and Professional ViewsEleana Rraku, Aafke Engwerda, Tyler D Medina, et al.
European Journal of Human Genetics : EJHG|November 6, 2022
Lymphedema as first clinical presentation of Cantu Syndrome: reversed phenotyping after identification of gain-of-function variant in ABCC9Jian Gao, Conor McClenaghan, Imke Christiaans, et al.
European Journal of Human Genetics : EJHG|August 13, 2009
Obtaining insurance after DNA diagnostics: a survey among hypertrophic cardiomyopathy mutation carriersImke Christiaans, Tjitske M Kok, Irene M van Langen, et al.
Nederlands Tijdschrift Voor Geneeskunde|February 6, 2010
[Hypertrophic cardiomyopathy: DNA diagnosis, genetic counselling and the risk of sudden cardiac death]Hubert F Baars, Imke Christiaans, Pim T A M de Nijs, et al.
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