Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndromeSolena Le Scouarnec, Richard Redon, Matilde Karakachoff et al.|Human Molecular Genetics|2015Cited by 136
Screening for Copy Number Variation in Genes Associated With the Long QT SyndromeJulien Barc, Jean‐Jacques Schott, François Briec et al.|Journal of the American College of Cardiology|2010Cited by 81
Risk estimation of uniparental disomy of chromosome 14 or 15 in a fetus with a parent carrying a non‐homologous Robertsonian translocation. Should we still perform prenatal diagnosis?Kamran Moradkhani, Cédric Le Caignec, Grégory Egea et al.|Prenatal Diagnosis|2019Cited by 17
Genotype-Phenotype Relationship in Patients and Relatives with <b><i>SHOX</i></b> Region Anomalies in the French PopulationJulie Auger, Myriam Rosilio, Amandine Baptiste et al.|Hormone Research in Paediatrics|2016Cited by 6
Supplementary Material for: Genotype-Phenotype Relationship in Patients and Relatives with SHOX Region Anomalies in the French PopulationJacques Auger, Myriam Rosilio, Amandine Baptiste et al.|INDIGO (University of Illinois at Chicago)|2016Cited by 0