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Freedman, Barry
One or more keywords matched the following items that are connected to
Freedman, Barry
Item Type
Name
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.
Search Criteria
Genome Human