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Publications by Jeroen Breckpot

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

American Journal of Human Genetics

English

Repeat Genetic Testing With Targeted Capture Sequencing in Primary Arrhythmia Syndrome and Cardiomyopathy

European Journal of Human Genetics

English

Heterozygous Loss-Of-Function Variants of MEIS2 Cause a Triad of Palatal Defects, Congenital Heart Defects, and Intellectual Disability

European Journal of Human Genetics

English

Genotype-Phenotype Relationship and Risk Stratification in Loss-Of-Function SCN5A Mutation Carriers

Annals of Noninvasive Electrocardiology

Cardiovascular Medicine

English

An Ontology Describing Congenital Heart Defects Data

English

C Identification of the Major Genetic Contributors to Tetralogy of Fallot

English

Systems Genetics Analysis Identify Calcium Signalling Defects as Novel Cause of Congenital Heart Disease

English