to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
Return to Top
Search Result Details
Back to Search Results
This page shows the details of why an item matched the keywords from your search.
One or more keywords matched the following items that are connected to
A genome-wide scan for type 2 diabetes in African-American families reveals evidence for a locus on chromosome 6q.
Linkage analysis of diabetes status among hypertensive families: the Hypertension Genetic Epidemiology Network study.
Genome scan of glomerular filtration rate and albuminuria: the HyperGEN study.
Genome-wide association scan for survival on dialysis in African-Americans with type 2 diabetes.
A genome-wide scan for urinary albumin excretion in hypertensive families.
A genome scan for diabetic nephropathy in African Americans.
A genome scan for all-cause end-stage renal disease in African Americans.
Quantitative trait loci on chromosome 8q24 for pancreatic beta-cell function and 7q11 for insulin sensitivity in obese nondiabetic white and black families: evidence from genome-wide linkage scans in the NHLBI Hypertension Genetic Epidemiology Network (HyperGEN) study.
Coincident linkage of type 2 diabetes, metabolic syndrome, and measures of cardiovascular disease in a genome scan of the diabetes heart study.
Genome-wide scans for diabetic nephropathy and albuminuria in multiethnic populations: the family investigation of nephropathy and diabetes (FIND).
Mining the genome for susceptibility to diabetic nephropathy: the role of large-scale studies and consortia.
Genome-wide scan for estimated glomerular filtration rate in multi-ethnic diabetic populations: the Family Investigation of Nephropathy and Diabetes (FIND).
Association analysis in african americans of European-derived type 2 diabetes single nucleotide polymorphisms from whole-genome association studies.
MYH9 is associated with nondiabetic end-stage renal disease in African Americans.
MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis.
Admixture mapping in lupus identifies multiple functional variants within IFIH1 associated with apoptosis, inflammation, and autoantibody production.
Inherited causes of clonal haematopoiesis in 97,691 whole genomes.