Item Type | Name |
Academic Article
|
Linkage heterogeneity of end-stage renal disease on human chromosome 10.
|
Academic Article
|
A genome-wide scan for type 2 diabetes in African-American families reveals evidence for a locus on chromosome 6q.
|
Academic Article
|
Association of protein tyrosine phosphatase 1B gene polymorphisms with measures of glucose homeostasis in Hispanic Americans: the insulin resistance atherosclerosis study (IRAS) family study.
|
Academic Article
|
Chronic and recurrent otitis media: a genome scan for susceptibility loci.
|
Academic Article
|
A genome scan for fasting insulin and fasting glucose identifies a quantitative trait locus on chromosome 17p: the insulin resistance atherosclerosis study (IRAS) family study.
|
Academic Article
|
Genetic mapping of disposition index and acute insulin response loci on chromosome 11q. The Insulin Resistance Atherosclerosis Study (IRAS) Family Study.
|
Academic Article
|
Heritability and expression of C-reactive protein in type 2 diabetes in the Diabetes Heart Study.
|
Academic Article
|
Genetic factors in diabetic nephropathy.
|
Academic Article
|
Evaluation of a SNP map of 6q24-27 confirms diabetic nephropathy loci and identifies novel associations in type 2 diabetes patients with nephropathy from an African-American population.
|
Academic Article
|
Polymorphisms near SOCS3 are associated with obesity and glucose homeostasis traits in Hispanic Americans from the Insulin Resistance Atherosclerosis Family Study.
|
Academic Article
|
Chromosome 7p linkage and association study for diabetes related traits and type 2 diabetes in an African-American population enriched for nephropathy.
|
Academic Article
|
Analysis of candidate genes on chromosome 20q12-13.1 reveals evidence for BMI mediated association of PREX1 with type 2 diabetes in European Americans.
|
Academic Article
|
Molecular basis of a linkage peak: exome sequencing and family-based analysis identify a rare genetic variant in the ADIPOQ gene in the IRAS Family Study.
|
Academic Article
|
Genomewide linkage scan for diabetic renal failure and albuminuria: the FIND study.
|
Academic Article
|
The impact of FADS genetic variants on ?6 polyunsaturated fatty acid metabolism in African Americans.
|
Academic Article
|
Informed conditioning on clinical covariates increases power in case-control association studies.
|
Academic Article
|
Evidence for a novel type 1 diabetes susceptibility locus on chromosome 8.
|
Academic Article
|
Association study of autoimmune thyroid disease at 5q23-q33 in Japanese patients.
|
Academic Article
|
Linkage of the metabolic syndrome to 1q23-q31 in Hispanic families: the Insulin Resistance Atherosclerosis Study Family Study.
|
Academic Article
|
Genome-wide linkage of plasma adiponectin reveals a major locus on chromosome 3q distinct from the adiponectin structural gene: the IRAS family study.
|
Academic Article
|
Genome-wide scans for diabetic nephropathy and albuminuria in multiethnic populations: the family investigation of nephropathy and diabetes (FIND).
|
Academic Article
|
Association of the distal region of the ectonucleotide pyrophosphatase/phosphodiesterase 1 gene with type 2 diabetes in an African-American population enriched for nephropathy.
|
Academic Article
|
MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis.
|
Academic Article
|
Genetic analysis of diabetic nephropathy on chromosome 18 in African Americans: linkage analysis and dense SNP mapping.
|
Academic Article
|
Genome-wide linkage scans for type 2 diabetes mellitus in four ethnically diverse populations-significant evidence for linkage on chromosome 4q in African Americans: the Family Investigation of Nephropathy and Diabetes Research Group.
|
Academic Article
|
Evaluation of DLG2 as a positional candidate for disposition index in African-Americans from the IRAS Family Study.
|
Academic Article
|
Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.
|
Academic Article
|
Genetic mapping of vascular calcified plaque loci on chromosome 16p in European Americans from the diabetes heart study.
|
Academic Article
|
Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans.
|
Concept
|
Chromosomes, Human, Pair 18
|
Concept
|
Chromosomes, Human, Pair 11
|
Concept
|
Chromosomes, Human, Pair 1
|
Concept
|
Chromosomes, Human, Pair 19
|
Concept
|
Chromosomes, Human, Pair 3
|
Concept
|
Chromosomes, Human, Pair 20
|
Concept
|
Chromosomes, Human, Pair 4
|
Concept
|
Chromosomes, Human, Pair 10
|
Concept
|
Chromosomes, Human, Pair 7
|
Concept
|
Chromosomes, Human, Pair 6
|
Concept
|
Chromosomes, Human, Pair 22
|
Concept
|
Chromosomes, Human, Pair 17
|
Concept
|
Chromosomes, Human, Pair 5
|
Concept
|
Chromosomes, Human, Pair 8
|
Concept
|
Chromosome Mapping
|
Academic Article
|
Diabetes: Unravelling the enigma of T2DM and cardiovascular disease.
|
Academic Article
|
Selecting SNPs informative for African, American Indian and European Ancestry: application to the Family Investigation of Nephropathy and Diabetes (FIND).
|
Academic Article
|
Mapping adipose and muscle tissue expression quantitative trait loci in African Americans to identify genes for type 2 diabetes and obesity.
|
Grant
|
Identification of diabetes genes on human chromosome 20
|
Grant
|
GENETIC MAPPING OF NONINSULIN DEPENDENT DIABETES
|
Grant
|
Intergration of Functional and Molecular Genetics to Identify Diabetes Genes
|
Academic Article
|
Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.
|
Academic Article
|
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.
|