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Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans.
Insights into the genetic architecture of diabetic nephropathy.
APOL1 and progression of nondiabetic nephropathy.
APOL1 associations with nephropathy, atherosclerosis, and all-cause mortality in African Americans with type 2 diabetes.
Genome-wide family-based linkage analysis of exome chip variants and cardiometabolic risk.
Gene-gene interactions in APOL1-associated nephropathy.
Analysis of coding variants identified from exome sequencing resources for association with diabetic and non-diabetic nephropathy in African Americans.
Evaluation of candidate nephropathy susceptibility genes in a genome-wide association study of African American diabetic kidney disease.
Coding variants in nephrin (NPHS1) and susceptibility to nephropathy in African Americans.
Lack of Association of the APOL1 G3 Haplotype in African Americans with ESRD.
Apolipoprotein L1 gene variants in deceased organ donors are associated with renal allograft failure.
Deceased donor multidrug resistance protein 1 and caveolin 1 gene variants may influence allograft survival in kidney transplantation.
APOL1 Genotype and Kidney Transplantation Outcomes From Deceased African American Donors.
APOL1 nephropathy risk variants are associated with altered high-density lipoprotein profiles in African Americans.
APOL1 renal-risk genotypes associate with longer hemodialysis survival in prevalent nondiabetic African American patients with end-stage renal disease.
APOL1 renal-risk variants associate with reduced cerebral white matter lesion volume and increased gray matter volume.
APOE Genotypes Associate With Cognitive Performance but Not Cerebral Structure: Diabetes Heart Study MIND.