Richard Redon
Centre National de la Recherche Scientifique(FR)Inserm(FR)Institut du Thorax(FR)
Publications by Year
Research Areas
Cardiac electrophysiology and arrhythmias, Genomic variations and chromosomal abnormalities, Genomics and Rare Diseases, Ion channel regulation and function, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → Global variation in copy number in the human genome(2006)4,350 cited
- → Origins and functional impact of copy number variation in the human genome(2009)2,045 cited
- → Relative Impact of Nucleotide and Copy Number Variation on Gene Expression Phenotypes(2007)1,772 cited
- → Diet and the evolution of human amylase gene copy number variation(2007)1,484 cited
- → Copy number variation: New insights in genome diversity(2006)861 cited
- → Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls(2010)810 cited
- → Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death