Jeroen Breckpot
Rambam Health Care Campus(IL)Center for Human Genetics(US)KU Leuven(BE)
Publications by Year
Research Areas
Congenital heart defects research, Genomic variations and chromosomal abnormalities, Congenital Heart Disease Studies, Genomics and Rare Diseases, Cardiomyopathy and Myosin Studies
Most-Cited Works
- → Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing(2016)464 cited
- → European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases(2022)338 cited
- → Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease(2012)337 cited
- → Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot(2019)193 cited
- → Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans(2014)185 cited
- → Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16(2013)165 cited