A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9
- 1 October 2010
- journal article
- Published by Elsevier in Kidney International
- Vol. 78 (7) , 698-704
- https://doi.org/10.1038/ki.2010.251
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- African ancestry allelic variation at the MYH9 gene contributes to increased susceptibility to non-diabetic end-stage kidney disease in Hispanic AmericansHuman Molecular Genetics, 2010
- Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15Human Molecular Genetics, 2010
- The association of the MYH9 gene and kidney outcomes in American Indians: the Strong Heart Family StudyHuman Genetics, 2009
- MYH9 is associated with nondiabetic end-stage renal disease in African AmericansNature Genetics, 2008
- MYH9 is a major-effect risk gene for focal segmental glomerulosclerosisNature Genetics, 2008
- A second generation human haplotype map of over 3.1 million SNPsNature, 2007
- PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage AnalysesAmerican Journal of Human Genetics, 2007
- Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversibleNature Genetics, 2006
- Principal components analysis corrects for stratification in genome-wide association studiesNature Genetics, 2006
- TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal functionNature Genetics, 2005