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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	Variants of the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in an African-American population enriched for nephropathy.
Academic Article	Relationship between genetic variants in myocardial sodium and potassium channel genes and QT interval duration in diabetics: the Diabetes Heart Study.
Academic Article	Human lipoxygenase pathway gene variation and association with markers of subclinical atherosclerosis in the diabetes heart study.
Academic Article	The new era of APOL1-associated glomerulosclerosis.
Academic Article	Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans.
Academic Article	Evaluation of genetic variation and association in the matrix metalloproteinase 9 (MMP9) gene in ESRD patients.
Academic Article	Nucleotide variation, haplotype structure, and association with end-stage renal disease of the human interleukin-1 gene cluster.
Academic Article	Variants of the CD40 gene but not of the CD40L gene are associated with coronary artery calcification in the Diabetes Heart Study (DHS).
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	Association of NOS1AP genetic variants with QT interval duration in families from the Diabetes Heart Study.
Academic Article	Hypertension-associated kidney disease: perhaps no more.
Academic Article	Susceptibility genes in common complex kidney disease.
Academic Article	Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant.
Academic Article	Association of APOL1 variants with mild kidney disease in the first-degree relatives of African American patients with non-diabetic end-stage renal disease.
Academic Article	Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk in Communities studies.
Concept	Genetic Variation
Academic Article	Association of SNPs in the UGT1A gene cluster with total bilirubin and mortality in the Diabetes Heart Study.
Academic Article	APOL1 and progression of nondiabetic nephropathy.
Academic Article	Common variants in Mendelian kidney disease genes and their association with renal function.
Academic Article	Analysis of common and coding variants with cardiovascular disease in the Diabetes Heart Study.
Academic Article	Gene-gene and gene-environment interactions in apolipoprotein L1 gene-associated nephropathy.
Academic Article	Apolipoprotein L1 gene variants associate with prevalent kidney but not prevalent cardiovascular disease in the Systolic Blood Pressure Intervention Trial.
Academic Article	Shroom3 contributes to the maintenance of the glomerular filtration barrier integrity.
Academic Article	Biogenesis and cytotoxicity of APOL1 renal risk variant proteins in hepatocytes and hepatoma cells.
Academic Article	Preferential association of a functional variant in complement receptor 2 with antibodies to double-stranded DNA.
Academic Article	Characterization of circulating APOL1 protein complexes in African Americans.
Academic Article	The genetic architecture of type 2 diabetes.
Grant	Subclinical CVD in African American Type 2 Diabetics
Academic Article	The Apolipoprotein L1 Gene and Cardiovascular Disease.
Academic Article	Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
Academic Article	Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance Imaging.
Academic Article	APOL1 Kidney Risk Variants and Cardiovascular Disease: An Individual Participant Data Meta-Analysis.
Academic Article	Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.

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Genetic Variation