Background: Membranous nephropathy (MN) is a common cause of nephrotic syndrome in adults. Previous genome-wide association studies (GWAS) of 300 000 genotyped variants identified MN-associated loci at HLA-DQA1 and PLA2R1. Methods: We used a combined approach of genotype imputation, GWAS, human leucocyte antigen (HLA) imputation and extension to other aetiologies of chronic kidney disease (CKD) to investigate genetic MN risk variants more comprehensively. GWAS using 9 million high-quality imputed genotypes and classical HLA alleles were conducted for 323 MN European-ancestry cases and 345 controls. Additionally, 4960 patients with different CKD aetiologies in the German Chronic Kidney Disease (GCKD) study were genotyped for risk variants a...
Abstract The associations of single nucleotide polymorphisms (SNPs) in PLA2R1 and HLA-DQA1, as well ...
Risk alleles at genome loci containing phospholipase A2 receptor 1 (PLA2R1) and HLA-DQA1 closely ass...
Chronic kidney disease (CKD) is common, affecting about 10% of the general population, and causing s...
Background: Membranous nephropathy (MN) is a common cause of nephrotic syndrome in adults. Previou...
Membranous Nephropathy (MN) is a rare autoimmune cause of kidney failure. Here we report a genome-wi...
An HLA-DR3 association with membranous nephropathy (MN) was described in 1979 and additional evidenc...
Membranous Nephropathy (MN) is a rare autoimmune cause of kidney failure. Here we report a genome-wi...
BACKGROUND: Idiopathic membranous nephropathy is a major cause of the nephrotic syndrome in adults, ...
Background: Idiopathic membranous nephropathy is a major cause of the nephrotic syndrome in adults, ...
Membranous Nephropathy (MN) is one of the leading causes of end-stage renal disease (ESRD). MN is a...
Item does not contain fulltextRecurrence of primary membranous nephropathy after transplantation occ...
International audienceRecurrence of primary membranous nephropathy after transplantation occurs in u...
Puntuació de risc genètic; Glomerulonefritis; Nefropatia membranosaPuntuación de riesgo genético; Gl...
Chronic kidney disease (CKD) is common, affecting about 10% of the general population, and causing s...
Abstract The associations of single nucleotide polymorphisms (SNPs) in PLA2R1 and HLA-DQA1, as well ...
Risk alleles at genome loci containing phospholipase A2 receptor 1 (PLA2R1) and HLA-DQA1 closely ass...
Chronic kidney disease (CKD) is common, affecting about 10% of the general population, and causing s...
Background: Membranous nephropathy (MN) is a common cause of nephrotic syndrome in adults. Previou...
Membranous Nephropathy (MN) is a rare autoimmune cause of kidney failure. Here we report a genome-wi...
An HLA-DR3 association with membranous nephropathy (MN) was described in 1979 and additional evidenc...
Membranous Nephropathy (MN) is a rare autoimmune cause of kidney failure. Here we report a genome-wi...
BACKGROUND: Idiopathic membranous nephropathy is a major cause of the nephrotic syndrome in adults, ...
Background: Idiopathic membranous nephropathy is a major cause of the nephrotic syndrome in adults, ...
Membranous Nephropathy (MN) is one of the leading causes of end-stage renal disease (ESRD). MN is a...
Item does not contain fulltextRecurrence of primary membranous nephropathy after transplantation occ...
International audienceRecurrence of primary membranous nephropathy after transplantation occurs in u...
Puntuació de risc genètic; Glomerulonefritis; Nefropatia membranosaPuntuación de riesgo genético; Gl...
Chronic kidney disease (CKD) is common, affecting about 10% of the general population, and causing s...
Abstract The associations of single nucleotide polymorphisms (SNPs) in PLA2R1 and HLA-DQA1, as well ...
Risk alleles at genome loci containing phospholipase A2 receptor 1 (PLA2R1) and HLA-DQA1 closely ass...
Chronic kidney disease (CKD) is common, affecting about 10% of the general population, and causing s...