Genetics of Human Cardiovascular Disease
- 16 March 2012
- journal article
- review article
- Published by Elsevier BV in Cell
- Vol. 148 (6), 1242-1257
- https://doi.org/10.1016/j.cell.2012.03.001
Abstract
No abstract availableKeywords
This publication has 134 references indexed in Scilit:
- Mapping Rare and Common Causal Alleles for Complex Human DiseasesCell, 2011
- Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated CardiomyopathyAmerican Journal of Human Genetics, 2011
- Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studiesThe Lancet, 2011
- Direct Reprogramming of Fibroblasts into Functional Cardiomyocytes by Defined FactorsCell, 2010
- Pooled Association Tests for Rare Variants in Exon-Resequencing StudiesAmerican Journal of Human Genetics, 2010
- Genetic Heterogeneity in Human DiseaseCell, 2010
- Genetic Loci Associated With C-Reactive Protein Levels and Risk of Coronary Heart DiseaseJAMA, 2009
- Methods for Detecting Associations with Rare Variants for Common Diseases: Application to Analysis of Sequence DataAmerican Journal of Human Genetics, 2008
- Induction of Pluripotent Stem Cells from Adult Human Fibroblasts by Defined FactorsCell, 2007
- GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5Nature, 2003