| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Jasmin Divers | Q89813877 |
| Barry Freedman | Q67485116 | ||
| P2860 | cites work | Genome-wide associations of gene expression variation in humans | Q21145274 |
| Epistasis--the essential role of gene interactions in the structure and evolution of genetic systems | Q22122008 | ||
| Prospects for admixture mapping of complex traits | Q22337163 | ||
| Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome | Q24314612 | ||
| A High-Density Admixture Map for Disease Gene Discovery in African Americans | Q24533390 | ||
| MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis | Q24643421 | ||
| MYH9 is associated with nondiabetic end-stage renal disease in African Americans | Q24653027 | ||
| Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy | Q24672705 | ||
| PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 | ||
| Principal components analysis corrects for stratification in genome-wide association studies | Q27860975 | ||
| NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome | Q28116208 | ||
| Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis | Q28145757 | ||
| T-786-->C mutation in the 5'-flanking region of the endothelial nitric oxide synthase gene is associated with coronary spasm | Q28198949 | ||
| CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility | Q28206197 | ||
| Genetic variations in the gene encoding ELMO1 are associated with susceptibility to diabetic nephropathy | Q28241871 | ||
| Chromosomal assignment of the uromodulin gene (UMOD) to 16p13.11 | Q28262973 | ||
| Localization of the Tamm-Horsfall glycoprotein (uromodulin) gene to chromosome 16p12.3-16p13.11 | Q72411549 | ||
| Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases | Q73039878 | ||
| Association of a missense Glu298Asp mutation of the endothelial nitric oxide synthase gene with end stage renal disease | Q73162922 | ||
| Complete genomic screen for disease susceptibility loci in nuclear families | Q73271176 | ||
| Risk of advanced diabetic nephropathy in type 1 diabetes is associated with endothelial nitric oxide synthase gene polymorphism | Q73395910 | ||
| ELMO1 increases expression of extracellular matrix proteins and inhibits cell adhesion to ECMs | Q79190003 | ||
| Extensive genetic analysis of 10 candidate genes for hypertension in Japanese | Q80284413 | ||
| A genome scan for diabetic nephropathy in African Americans | Q80808525 | ||
| Donor variation in in vitro HIV-1 susceptibility of monocyte-derived macrophages | Q84079241 | ||
| Multiple loci associated with indices of renal function and chronic kidney disease | Q28943262 | ||
| GenABEL: an R library for genome-wide association analysis | Q29614587 | ||
| An integrative genomics approach to infer causal associations between gene expression and disease | Q29616385 | ||
| Confirmation of genetic associations at ELMO1 in the GoKinD collection supports its role as a susceptibility gene in diabetic nephropathy | Q30434280 | ||
| Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes | Q30435965 | ||
| Variants in intron 13 of the ELMO1 gene are associated with diabetic nephropathy in African Americans | Q30436877 | ||
| Engulfment of apoptotic cells: signals for a good meal | Q30445079 | ||
| Statistical tests for admixture mapping with case-control and cases-only data | Q30961723 | ||
| Overcoming the winner's curse: estimating penetrance parameters from case-control data | Q31105516 | ||
| Analysis and application of European genetic substructure using 300 K SNP information | Q33315564 | ||
| Podocyte-selective deletion of dicer induces proteinuria and glomerulosclerosis | Q33367473 | ||
| Megakaryocytes of patients with MYH9-related thrombocytopenia present an altered proplatelet formation | Q33385231 | ||
| The influence of carnosinase gene polymorphisms on diabetic nephropathy risk in African-Americans | Q33913749 | ||
| Non-muscle myosin heavy chain 9 gene MYH9 associations in African Americans with clinically diagnosed type 2 diabetes mellitus-associated ESRD | Q34021318 | ||
| A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis | Q34416768 | ||
| Carnosine as a protective factor in diabetic nephropathy: association with a leucine repeat of the carnosinase gene CNDP1. | Q34437314 | ||
| NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review | Q34495087 | ||
| Genomic control, a new approach to genetic-based association studies | Q34539204 | ||
| Methods for linkage analysis of quantitative trait loci in humans | Q34539211 | ||
| Case-control studies of association in structured or admixed populations. | Q34539216 | ||
| A leucine repeat in the carnosinase gene CNDP1 is associated with diabetic end-stage renal disease in European Americans | Q34598354 | ||
| A CTG polymorphism in the CNDP1 gene determines the secretion of serum carnosinase in Cos-7 transfected cells | Q34643805 | ||
| Variants in the plasmacytoma variant translocation gene (PVT1) are associated with end-stage renal disease attributed to type 1 diabetes | Q34691015 | ||
| Renal gene and protein expression signatures for prediction of kidney disease progression | Q34982782 | ||
| Mapping genes underlying ethnic differences in disease risk by linkage disequilibrium in recently admixed populations. | Q35239270 | ||
| Chronic blockade of nitric oxide synthesis in the rat produces systemic hypertension and glomerular damage | Q35604343 | ||
| A genomewide single-nucleotide-polymorphism panel for Mexican American admixture mapping | Q35788496 | ||
| Promoter polymorphism of the erythropoietin gene in severe diabetic eye and kidney complications | Q36657594 | ||
| Chromogranin A polymorphisms are associated with hypertensive renal disease. | Q36667220 | ||
| High-density single nucleotide polymorphism genome-wide linkage scan for susceptibility genes for diabetic nephropathy in type 1 diabetes: discordant sibpair approach | Q36842660 | ||
| Exclusion of polymorphisms in carnosinase genes (CNDP1 and CNDP2) as a cause of diabetic nephropathy in type 1 diabetes: results of large case-control and follow-up studies | Q36842676 | ||
| Patients with ACTN4 mutations demonstrate distinctive features of glomerular injury. | Q36855889 | ||
| TCF7L2 variants associate with CKD progression and renal function in population-based cohorts | Q36906045 | ||
| Genetic susceptibility, HIV infection, and the kidney | Q36910656 | ||
| MicroRNA-377 is up-regulated and can lead to increased fibronectin production in diabetic nephropathy | Q37039063 | ||
| Focal segmental glomerulosclerosis: recent advances | Q37085401 | ||
| Multiple superoxide dismutase 1/splicing factor serine alanine 15 variants are associated with the development and progression of diabetic nephropathy: the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complicat | Q37127488 | ||
| Association of genetic variants at 3q22 with nephropathy in patients with type 1 diabetes mellitus | Q37156204 | ||
| Susceptibility loci for murine HIV-associated nephropathy encode trans-regulators of podocyte gene expression | Q37170764 | ||
| Association of genetic variants with chronic kidney disease in Japanese individuals | Q37176806 | ||
| HIV-associated nephropathy: epidemiology, pathogenesis, diagnosis and management | Q37202856 | ||
| Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans | Q37232156 | ||
| CCR5 deletion protects against inflammation-associated mortality in dialysis patients | Q37259261 | ||
| Chromogranin A regulates renal function by triggering Weibel-Palade body exocytosis | Q37259309 | ||
| Using gene expression to investigate the genetic basis of complex disorders | Q37292880 | ||
| Hypertension-associated kidney disease: perhaps no more | Q37299028 | ||
| Gene-environment interactions in the etiology of obesity: defining the fundamentals | Q37335845 | ||
| Polymorphisms in the nonmuscle myosin heavy chain 9 gene (MYH9) are associated with albuminuria in hypertensive African Americans: the HyperGEN study | Q37359254 | ||
| The emerging role of structural variations in common disorders: initial findings and discovery challenges | Q37415148 | ||
| Association of eNOS Glu298Asp polymorphism with end-stage renal disease | Q44167947 | ||
| NPHS2 mutation associated with recurrence of proteinuria after transplantation | Q44795813 | ||
| Genome-wide scans for diabetic nephropathy and albuminuria in multiethnic populations: the family investigation of nephropathy and diabetes (FIND). | Q45014719 | ||
| T-786C polymorphism of the endothelial nitric oxide synthase gene is associated with albuminuria in the diabetes heart study | Q45295878 | ||
| Genetic interactions between the donor and the recipient for susceptibility to acute rejection in kidney transplantation: polymorphisms of CCR5. | Q45949356 | ||
| Genome-wide linkage analysis of serum creatinine in three isolated European populations. | Q46040078 | ||
| Regulation and consequences of differential gene expression in diabetic kidney disease | Q46366801 | ||
| Glu298Asp and NOS4ab polymorphisms in diabetic nephropathy. | Q50774440 | ||
| NPHS1 gene mutation in Japanese patients with congenital nephrotic syndrome. | Q51750860 | ||
| Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS) | Q57740824 | ||
| Immature Renal Structures Associated With a Novel UMOD Sequence Variant | Q57980322 | ||
| A Search for Variants Associated With Young-Onset Type 2 Diabetes in American Indians in a 100K Genotyping Array | Q59150454 | ||
| Gene for susceptibility to diabetic nephropathy in type 2 diabetes maps to 18q22.3-23 | Q59150735 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 79-84 | |
| P577 | publication date | 2010-01-01 | |
| P1433 | published in | Current Opinion in Nephrology and Hypertension | Q15756282 |
| P1476 | title | Susceptibility genes in common complex kidney disease | |
| P478 | volume | 19 |
| Q42809598 | A knowledge-driven interaction analysis reveals potential neurodegenerative mechanism of multiple sclerosis susceptibility. |
| Q87393485 | Chapter 8: Future directions and controversies |
| Q44761644 | Differences in the quality of diabetes care caused by social inequalities disappear after treatment and education in a tertiary care centre |
| Q21144945 | Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans |
| Q34556186 | Etiopathology of chronic tubular, glomerular and renovascular nephropathies: clinical implications |
| Q36250613 | Genetic and environmental factors associated with type 2 diabetes and diabetic vascular complications |
| Q33968487 | Genetic kidney diseases |
| Q45106409 | Genetic locus on MWF rat chromosome 6 affects kidney damage in response to L-NAME treatment in spontaneously hypertensive rats. |
| Q40834847 | Genetic predisposition to albuminuria is associated with increased arterial stiffness: role of elastin |
| Q35187084 | Genetics of kidney failure and the evolving story of APOL1. |
| Q37781545 | Genome-Wide Association Studies in Nephrology Research |
| Q45814770 | Induction of albuminuria and kidney damage in SHR by transfer of chromosome 8 from Munich Wistar Frömter rats |
| Q38014678 | Mapping genetic determinants of kidney damage in rat models. |
| Q93609101 | References |
| Q37093820 | SORCS1 contributes to the development of renal disease in rats and humans |
| Q34182007 | The population genetics of chronic kidney disease: insights from the MYH9-APOL1 locus |
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