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One or more keywords matched the following items that are connected to Freedman, Barry
Item TypeName
Academic Article A genome-wide scan for type 2 diabetes in African-American families reveals evidence for a locus on chromosome 6q.
Academic Article Linkage analysis of diabetes status among hypertensive families: the Hypertension Genetic Epidemiology Network study.
Academic Article Genome scan of glomerular filtration rate and albuminuria: the HyperGEN study.
Academic Article Genome-wide association scan for survival on dialysis in African-Americans with type 2 diabetes.
Academic Article A genome-wide scan for urinary albumin excretion in hypertensive families.
Academic Article A genome scan for diabetic nephropathy in African Americans.
Academic Article A genome scan for all-cause end-stage renal disease in African Americans.
Academic Article 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.
Academic Article Coincident linkage of type 2 diabetes, metabolic syndrome, and measures of cardiovascular disease in a genome scan of the diabetes heart study.
Academic Article Genome-wide scans for diabetic nephropathy and albuminuria in multiethnic populations: the family investigation of nephropathy and diabetes (FIND).
Academic Article Mining the genome for susceptibility to diabetic nephropathy: the role of large-scale studies and consortia.
Academic Article Genome-wide scan for estimated glomerular filtration rate in multi-ethnic diabetic populations: the Family Investigation of Nephropathy and Diabetes (FIND).
Academic Article Association analysis in african americans of European-derived type 2 diabetes single nucleotide polymorphisms from whole-genome association studies.
Academic Article MYH9 is associated with nondiabetic end-stage renal disease in African Americans.
Academic Article MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis.
Academic Article Admixture mapping in lupus identifies multiple functional variants within IFIH1 associated with apoptosis, inflammation, and autoantibody production.
Concept Genome, Human
Academic Article Inherited causes of clonal haematopoiesis in 97,691 whole genomes.
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  • Genome Human