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Genetic loci influencing kidney function and chronic kidney disease
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-0177(199608)206:4<379::aid-aja4>3.0.co;2-fopenalex-snapshot
Expression of the T-box family genes,Tbx1-Tbx5, during early mouse development
inferredcites →https://doi.org/10.1002/jps.20536openalex-snapshot
Transport of drugs in the kidney by the human organic cation transporter, OCT2 and its genetic variants
inferredcites →https://doi.org/10.1016/j.molcel.2007.01.003openalex-snapshot
Identification of FAAP24, a Fanconi Anemia Core Complex Protein that Interacts with FANCM
inferredcites →https://doi.org/10.1038/clpt.2008.97openalex-snapshot
Adverse Drug Reactions With Halogenated Anesthetics
inferredcites →https://doi.org/10.1038/clpt.2009.139openalex-snapshot
Contribution of Organic Cation Transporter 2 (OCT2) to Cisplatin-Induced Nephrotoxicity
inferredcites →https://doi.org/10.1038/ng.226openalex-snapshot
MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis
inferredcites →https://doi.org/10.1038/ng.377openalex-snapshot
Multiple loci associated with indices of renal function and chronic kidney disease
inferredcites →https://doi.org/10.1038/ng1847openalex-snapshot
Principal components analysis corrects for stratification in genome-wide association studies
inferredcites →https://doi.org/10.1038/sj.ki.5002343openalex-snapshot
Chronic kidney disease as a global public health problem: Approaches and initiatives – a position statement from Kidney Disease Improving Global Outcomes
inferredcites →https://doi.org/10.1056/nejmra054415openalex-snapshot
Assessing Kidney Function — Measured and Estimated Glomerular Filtration Rate
inferredcites →https://doi.org/10.1146/annurev.biophys.29.1.81openalex-snapshot
GCN5-Related N-Acetyltransferases: A Structural Overview
inferredcites →https://doi.org/10.1146/annurev.genet.39.073003.105925openalex-snapshot
T-Box Genes in Vertebrate Development
inferredcites →https://doi.org/10.1289/ehp.00108177openalex-snapshot
Seasonal Influences on Childhood Lead Exposure
inferredcites →https://doi.org/10.1289/ehp.00108s2177openalex-snapshot
Metabolism of trichloroethylene.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9781118494073.ch3openalex-snapshot
Genetic Risk Factors for Diabetic Nephropathy
inferred← citeshttps://doi.org/10.1002/9781119739883.ch15openalex-snapshot
DRUG TRANSPORT IN THE KIDNEY
inferred← citeshttps://doi.org/10.1002/cpt.749openalex-snapshot
Endogenous Probes for Drug Transporters: Balancing Vision With Reality
inferred← citeshttps://doi.org/10.1002/gepi.21752openalex-snapshot
Genome‐Wide Association Study of a Heart Failure Related Metabolomic Profile Among African Americans in the Atherosclerosis Risk in Communities (ARIC) Study
inferred← citeshttps://doi.org/10.1002/mco2.70669openalex-snapshot
Trans‐Omics Integration Reveals That the Kidney Contributes to Systemic Aging via Sexually Dimorphic Accumulation of Glycosphingolipids
inferred← citeshttps://doi.org/10.1002/mgg3.925openalex-snapshot
Evolutionary history of disease‐susceptibility loci identified in longitudinal exome‐wide association studies
inferred← citeshttps://doi.org/10.1002/prca.201000136openalex-snapshot
Mapping of molecular pathways, biomarkers and drug targets for diabetic nephropathy
inferred← citeshttps://doi.org/10.1007/978-1-4614-1689-0_16openalex-snapshot
Genome-Wide Association Studies with Metabolomics
inferred← citeshttps://doi.org/10.1007/978-3-030-52719-8_120openalex-snapshot
Autosomal Dominant Tubulointerstitial Kidney Disease
inferred← citeshttps://doi.org/10.1007/978-3-030-63908-2_8openalex-snapshot
A Mechanistic-Based and Non-invasive Approach to Quantify the Capability of Kidney to Detoxify Cysteine-Disulfides
inferred← citeshttps://doi.org/10.1007/978-3-642-27843-3_120-1openalex-snapshot
Autosomal Dominant Tubulointerstitial Kidney Disease
inferred← citeshttps://doi.org/10.1007/978-94-007-7696-8_46openalex-snapshot
Biomarkers in Neonatology
inferred← citeshttps://doi.org/10.1007/978-94-007-7740-8_46-1openalex-snapshot
Biomarkers in Neonatology
inferred← citeshttps://doi.org/10.1007/s00018-012-0996-3openalex-snapshot
Genetic susceptibility to hypertensive renal disease
inferred← citeshttps://doi.org/10.1007/s00216-020-03096-4openalex-snapshot
Glutathione conjugates of the mercapturic acid pathway and guanine adduct as biomarkers of exposure to CEES, a sulfur mustard analog
inferred← citeshttps://doi.org/10.1007/s00438-017-1394-1openalex-snapshot
Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population
inferred← citeshttps://doi.org/10.1007/s00726-015-1993-2openalex-snapshot
Homoarginine in the renal and cardiovascular systems
inferred← citeshttps://doi.org/10.1007/s00726-015-2000-7openalex-snapshot
Association of homoarginine and methylarginines with liver dysfunction and mortality in chronic liver disease
inferred← citeshttps://doi.org/10.1007/s10157-015-1083-5openalex-snapshot
Longitudinal relationships of metabolic syndrome and obesity with kidney function: Healthy Twin Study
inferred← citeshttps://doi.org/10.1007/s10157-016-1295-3openalex-snapshot
Genetic and environmental influences on the associations between change in kidney function and changes in cardiometabolic factors in Koreans
inferred← citeshttps://doi.org/10.1007/s12263-012-0313-7openalex-snapshot
Current status on genome–metabolome-wide associations: an opportunity in nutrition research
inferred← citeshttps://doi.org/10.1007/s13258-016-0411-9openalex-snapshot
Identification of genetic loci stratified by diabetic status and microRNA related SNPs influencing kidney function in Korean populations
inferred← citeshttps://doi.org/10.1007/s40620-017-0416-8openalex-snapshot
Predicting acute kidney injury: current status and future challenges
inferred← citeshttps://doi.org/10.1007/s44337-026-00674-wopenalex-snapshot
Genetic risk and telomere dynamics in chronic kidney disease associated with mitochondrial dysfunction and implications for Coenzyme Q10 therapy
inferred← citeshttps://doi.org/10.1016/b978-0-08-046884-6.00802-2openalex-snapshot
Renal Organic Cation and Anion Transport: From Physiology to Genes
inferred← citeshttps://doi.org/10.1016/b978-0-08-100601-6.02042-1openalex-snapshot
Renal Organic Cation and Anion Transport: From Physiology to Genes
inferred← citeshttps://doi.org/10.1016/b978-0-12-411602-3.00018-4openalex-snapshot
Genetics and Chronic Kidney Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.02042-0openalex-snapshot
Renal Organic Cation and Anion Transport: From Physiology to Genes☆
inferred← citeshttps://doi.org/10.1016/b978-1-4160-6193-9.10021-1openalex-snapshot
Risk Factors and Chronic Kidney Disease
inferred← citeshttps://doi.org/10.1016/j.abb.2015.07.018openalex-snapshot
Metabolic biomarkers for chronic kidney disease
inferred← citeshttps://doi.org/10.1016/j.ajhg.2012.04.023openalex-snapshot
Genetic Architecture of MicroRNA Expression: Implications for the Transcriptome and Complex Traits
inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2014.08.040openalex-snapshot
Creatinine, eGFR and association with myocardial infarction, ischemic heart disease and early death in the general population
inferred← citeshttps://doi.org/10.1016/j.beem.2011.09.001openalex-snapshot
Genetics for clinicians: From candidate genes to whole genome scans (technological advances)
inferred← citeshttps://doi.org/10.1016/j.cell.2023.01.016openalex-snapshot
Structures of LRP2 reveal a molecular machine for endocytosis
inferred← citeshttps://doi.org/10.1016/j.cmet.2010.05.009openalex-snapshot
Chronic Kidney Disease and GWAS: “The Proper Study of Mankind Is Man”
inferred← citeshttps://doi.org/10.1016/j.cmet.2013.06.013openalex-snapshot
A Genome-wide Association Study of the Human Metabolome in a Community-Based Cohort
inferred← citeshttps://doi.org/10.1016/j.diabres.2018.08.013openalex-snapshot
A renal genetic risk score (GRS) is associated with kidney dysfunction in people with type 2 diabetes
inferred← citeshttps://doi.org/10.1016/j.earlhumdev.2012.02.014openalex-snapshot
Genetic variants associated with adult blood pressure and kidney function do not affect fetal kidney volume. The Generation R Study
inferred← citeshttps://doi.org/10.1016/j.gene.2018.01.063openalex-snapshot
Identification of key microRNAs, transcription factors and genes associated with congenital obstructive nephropathy in a mouse model of megabladder
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e32063openalex-snapshot
Biobanks in chronic disease management: A comprehensive review of strategies, challenges, and future directions
inferred← citeshttps://doi.org/10.1016/j.humpath.2012.01.023openalex-snapshot
Description of 2 angiogenic phenotypes in clear cell renal cell carcinoma
inferred← citeshttps://doi.org/10.1016/j.jacc.2016.05.092openalex-snapshot
Cystatin C and Cardiovascular Disease
inferred← citeshttps://doi.org/10.1016/j.jprot.2018.09.020openalex-snapshot
Proteomic and metabolomic approaches in the search for biomarkers in chronic kidney disease
inferred← citeshttps://doi.org/10.1016/j.kint.2020.02.034openalex-snapshot
Results from the German Chronic Kidney Disease (GCKD) study support association of relative telomere length with mortality in a large cohort of patients with moderate chronic kidney disease
inferred← citeshttps://doi.org/10.1016/j.kint.2022.05.021openalex-snapshot
Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies
inferred← citeshttps://doi.org/10.1016/j.mam.2018.06.002openalex-snapshot
Cellular and molecular mechanisms of kidney fibrosis
inferred← citeshttps://doi.org/10.1016/j.neulet.2016.12.001openalex-snapshot
Pharmacogenetics of lithium effects on glomerular function in bipolar disorder patients under chronic lithium treatment: a pilot study
inferred← citeshttps://doi.org/10.1016/j.redox.2021.101920openalex-snapshot
Protein glycation – biomarkers of metabolic dysfunction and early-stage decline in health in the era of precision medicine
inferred← citeshttps://doi.org/10.1016/j.redox.2024.103295openalex-snapshot
Withdrawn: Combinatorial lipidomics and proteomics underscore erythrocyte lipid membrane aberrations in the development of adverse cardio-cerebrovascular complications in maintenance hemodialysis patients
inferred← citeshttps://doi.org/10.1016/j.semnephrol.2013.05.008openalex-snapshot
Epigenetics of Progression of Chronic Kidney Disease: Fact or Fantasy?
inferred← citeshttps://doi.org/10.1016/j.semnephrol.2014.02.010openalex-snapshot
The Kidney and Uremic Toxin Removal: Glomerulus or Tubule?
inferred← citeshttps://doi.org/10.1016/j.semnephrol.2018.01.009openalex-snapshot
Genome-Wide Association Studies of Metabolite Concentrations (mGWAS): Relevance for Nephrology
inferred← citeshttps://doi.org/10.1016/j.tox.2021.152950openalex-snapshot
Evidence for the systemic diffusion of (2-chloroethyl)-ethyl-sulfide, a sulfur mustard analog, and its deleterious effects in brain
inferred← citeshttps://doi.org/10.1016/j.trim.2013.04.004openalex-snapshot
Association of chemokine gene variants with end stage renal disease in North Indian population
inferred← citeshttps://doi.org/10.1016/j.ymgme.2025.109710openalex-snapshot
A non-coding signature in SHROOM3 is associated with kidney disease progression in Fabry disease
inferred← citeshttps://doi.org/10.1016/s0140-6736(13)60439-0openalex-snapshot
Evolving importance of kidney disease: from subspecialty to global health burden
inferred← citeshttps://doi.org/10.1021/acs.jproteome.1c00585openalex-snapshot
Untargeted Metabolome- and Transcriptome-Wide Association Study Suggests Causal Genes Modulating Metabolite Concentrations in Urine
inferred← citeshttps://doi.org/10.1021/acs.jproteome.5c01053openalex-snapshot
Proximity Labeling Reveals How Lrp2 Interacts with the Endocytic Machine
inferred← citeshttps://doi.org/10.1021/acs.molpharmaceut.3c00700openalex-snapshot
Role of Transporters and Enzymes in Metabolism and Distribution of 4-Chlorokynurenine (AV-101)
inferred← citeshttps://doi.org/10.1038/ejhg.2017.50openalex-snapshot
Missing heritability: is the gap closing? An analysis of 32 complex traits in the Lifelines Cohort Study
inferred← citeshttps://doi.org/10.1038/hr.2012.77openalex-snapshot
Mapping genetic determinants of kidney damage in rat models
inferred← citeshttps://doi.org/10.1038/ki.2010.467openalex-snapshot
A genome-wide association study for diabetic nephropathy genes in African Americans
inferred← citeshttps://doi.org/10.1038/ki.2011.134openalex-snapshot
The rediscovery of uromodulin (Tamm–Horsfall protein): from tubulointerstitial nephropathy to chronic kidney disease
inferred← citeshttps://doi.org/10.1038/ki.2012.389openalex-snapshot
A family-based association study after genome-wide linkage analysis identified two genetic loci for renal function in a Mongolian population
inferred← citeshttps://doi.org/10.1038/ki.2013.45openalex-snapshot
Albuminuria is associated with too few glomeruli and too much testosterone
inferred← citeshttps://doi.org/10.1038/ki.2014.361openalex-snapshot
Genome-wide association study of kidney function decline in individuals of European descent
inferred← citeshttps://doi.org/10.1038/ki.2015.161openalex-snapshot
Genome-wide association study of acute kidney injury after coronary bypass graft surgery identifies susceptibility loci
inferred← citeshttps://doi.org/10.1038/nature10354openalex-snapshot
Human metabolic individuality in biomedical and pharmaceutical research
inferred← citeshttps://doi.org/10.1038/nature11632openalex-snapshot
An integrated map of genetic variation from 1,092 human genomes
inferred← citeshttps://doi.org/10.1038/ncomms10023openalex-snapshot
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
inferred← citeshttps://doi.org/10.1038/ncomms13357openalex-snapshot
A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape
inferred← citeshttps://doi.org/10.1038/ng.2352openalex-snapshot
Meta-analysis identifies multiple loci associated with kidney function–related traits in east Asian populations
inferred← citeshttps://doi.org/10.1038/ng.3405openalex-snapshot
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
inferred← citeshttps://doi.org/10.1038/ng.3607openalex-snapshot
Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits
inferred← citeshttps://doi.org/10.1038/ng.3660openalex-snapshot
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci
inferred← citeshttps://doi.org/10.1038/ng.837openalex-snapshot
A genome-wide association study of metabolic traits in human urine
inferred← citeshttps://doi.org/10.1038/ng.970openalex-snapshot
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma
inferred← citeshttps://doi.org/10.1038/nrg3314openalex-snapshot
Genetic variation in metabolic phenotypes: study designs and applications
inferred← citeshttps://doi.org/10.1038/nrneph.2011.189openalex-snapshot
Genome-wide association studies of chronic kidney disease: what have we learned?
inferred← citeshttps://doi.org/10.1038/nrneph.2011.85openalex-snapshot
The genetics of common kidney disease: a pathway toward clinical relevance
inferred← citeshttps://doi.org/10.1038/nrneph.2015.172openalex-snapshot
Hypertension-attributed nephropathy: what's in a name?
inferred← citeshttps://doi.org/10.1038/nrneph.2016.107openalex-snapshot
Insights into kidney diseases from genome-wide association studies
inferred← citeshttps://doi.org/10.1038/nrneph.2017.101openalex-snapshot
Uromodulin: from physiology to rare and complex kidney disorders
inferred← citeshttps://doi.org/10.1038/pr.2016.44openalex-snapshot
Influence of common genetic variants on childhood kidney outcomes
inferred← citeshttps://doi.org/10.1038/s10038-022-01118-wopenalex-snapshot
Association of MPPED2 gene variant rs10767873 with kidney function and risk of cardiovascular disease in patients with hypertension
inferred← citeshttps://doi.org/10.1038/s41431-021-00830-zopenalex-snapshot
Genetic correlations between traits associated with hyperuricemia, gout, and comorbidities
inferred← citeshttps://doi.org/10.1038/s41467-019-09861-zopenalex-snapshot
Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis
inferred← citeshttps://doi.org/10.1038/s41540-024-00350-8openalex-snapshot
Multivariate canonical correlation analysis identifies additional genetic variants for chronic kidney disease
inferred← citeshttps://doi.org/10.1038/s41581-024-00881-7openalex-snapshot
Advances in uromodulin biology and potential clinical applications
inferred← citeshttps://doi.org/10.1038/s41588-019-0407-xopenalex-snapshot
A catalog of genetic loci associated with kidney function from analyses of a million individuals
inferred← citeshttps://doi.org/10.1038/s41591-022-01869-1openalex-snapshot
Genome-wide polygenic score to predict chronic kidney disease across ancestries
inferred← citeshttps://doi.org/10.1038/s41598-017-16603-yopenalex-snapshot
RNA-seq of serial kidney biopsies obtained during progression of chronic kidney disease from dogs with X-linked hereditary nephropathy
inferred← citeshttps://doi.org/10.1038/s41598-019-56695-2openalex-snapshot
Genetic Variants Associated with Chronic Kidney Disease in a Spanish Population
inferred← citeshttps://doi.org/10.1038/s41598-020-69350-yopenalex-snapshot
High fractional excretion of glycation adducts is associated with subsequent early decline in renal function in type 1 diabetes
inferred← citeshttps://doi.org/10.1038/s41598-026-47877-wopenalex-snapshot
Rare variant optimized GWAS with functional validation identifies causal architecture of kidney function in East Asian population
inferred← citeshttps://doi.org/10.1038/srep11633openalex-snapshot
Functional annotation of HOT regions in the human genome: implications for human disease and cancer
inferred← citeshttps://doi.org/10.1038/srep23743openalex-snapshot
Conserved differences in protein sequence determine the human pathogenicity of Ebolaviruses
inferred← citeshttps://doi.org/10.1038/srep45040openalex-snapshot
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function
inferred← citeshttps://doi.org/10.1038/tpj.2017.14openalex-snapshot
Effect of UMOD genotype on long-term graft survival after kidney transplantation in patients treated with cyclosporine-based therapy
inferred← citeshttps://doi.org/10.1039/9781782627937-00310openalex-snapshot
Advances in Computational Analysis of Metabolomic NMR Data
inferred← citeshttps://doi.org/10.1053/j.ajkd.2010.05.018openalex-snapshot
Genome-Wide Association Studies in Nephrology Research
inferred← citeshttps://doi.org/10.1053/j.ajkd.2011.08.030openalex-snapshot
Performance of a Genetic Risk Score for CKD Stage 3 in the General Population
inferred← citeshttps://doi.org/10.1053/j.ajkd.2011.09.020openalex-snapshot
Genetic Association and Gene-Gene Interaction Analyses in African American Dialysis Patients With Nondiabetic Nephropathy
inferred← citeshttps://doi.org/10.1053/j.ajkd.2013.05.024openalex-snapshot
Population Ancestry and Genetic Risk for Diabetes and Kidney, Cardiovascular, and Bone Disease: Modifiable Environmental Factors May Produce the Cures
inferred← citeshttps://doi.org/10.1080/10408444.2019.1692191openalex-snapshot
The mercapturic acid pathway
inferred← citeshttps://doi.org/10.1093/hmg/dds369openalex-snapshot
Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function
inferred← citeshttps://doi.org/10.1093/hmg/ddu399openalex-snapshot
Rare mutations associating with serum creatinine and chronic kidney disease
inferred← citeshttps://doi.org/10.1093/hmg/ddv263openalex-snapshot
Genetics of human metabolism: an update
inferred← citeshttps://doi.org/10.1093/nar/gku483openalex-snapshot
VarMod: modelling the functional effects of non-synonymous variants
inferred← citeshttps://doi.org/10.1093/ndt/gfad209openalex-snapshot
Genome-wide association studies reconstructing chronic kidney disease
inferred← citeshttps://doi.org/10.1093/ndt/gfq753openalex-snapshot
APOL1 variants and kidney disease. There is no such thing as a free lunch
inferred← citeshttps://doi.org/10.1093/ndt/gfr764openalex-snapshot
The ERA-EDTA Working Group on inherited kidney disorders
inferred← citeshttps://doi.org/10.1093/ndt/gfs489openalex-snapshot
Systems biology building a useful model from multiple markers and profiles
inferred← citeshttps://doi.org/10.1093/ndt/gft307openalex-snapshot
The Biobank of Nephrological Diseases in the Netherlands cohort: the String of Pearls Initiative collaboration on chronic kidney disease in the university medical centers in the Netherlands
inferred← citeshttps://doi.org/10.1093/ndt/gft345openalex-snapshot
Determination of uromodulin in human urine: influence of storage and processing
inferred← citeshttps://doi.org/10.1093/ndt/gft428openalex-snapshot
Novel insights from genetic and epigenetic studies in understanding the complex uraemic phenotype
inferred← citeshttps://doi.org/10.1093/ndt/gft512openalex-snapshot
Homoarginine, kidney function and cardiovascular mortality risk
inferred← citeshttps://doi.org/10.1093/ndt/gfu300openalex-snapshot
Uromodulin: from monogenic to multifactorial diseases: FIGURE 1:
inferred← citeshttps://doi.org/10.1093/ndt/gfv342openalex-snapshot
Genetic loci associated with renal function measures and chronic kidney disease in children: the Pediatric Investigation for Genetic Factors Linked with Renal Progression Consortium
inferred← citeshttps://doi.org/10.1093/ndt/gfv356openalex-snapshot
The PediGFR consortium: studying the genetics of complex kidney traits in children
inferred← citeshttps://doi.org/10.1093/ndt/gfw066openalex-snapshot
Genotypic and phenotypic predictors of inflammation in patients with chronic kidney disease
inferred← citeshttps://doi.org/10.1093/ndt/gfw270openalex-snapshot
Genetic epidemiology in kidney disease
inferred← citeshttps://doi.org/10.1093/ndt/gfx337openalex-snapshot
Evaluation of a genetic risk score based on creatinine-estimated glomerular filtration rate and its association with kidney outcomes
inferred← citeshttps://doi.org/10.1093/ntr/ntu161openalex-snapshot
Organic Cation Transporter Variation and Response to Smoking Cessation Therapies
inferred← citeshttps://doi.org/10.1097/hjh.0000000000000151openalex-snapshot
Genetic variants in nicotinic acetylcholine receptor genes jointly contribute to kidney function in American Indians
inferred← citeshttps://doi.org/10.1097/hjh.0000000000001432openalex-snapshot
Uromodulin associates with cardiorenal function in patients with hypertension and cardiovascular disease
inferred← citeshttps://doi.org/10.1097/mcg.0b013e3182548df2openalex-snapshot
Biomarkers of Nutrient Bioactivity and Efficacy
inferred← citeshttps://doi.org/10.1097/mnh.0000000000000495openalex-snapshot
The kidney transcriptome, from single cells to whole organs and back
inferred← citeshttps://doi.org/10.1097/mnh.0000000000000522openalex-snapshot
Uromodulin in mineral metabolism
inferred← citeshttps://doi.org/10.1097/mnh.0b013e328354e78fopenalex-snapshot
Novel findings and future directions on the genetics of hypertension
inferred← citeshttps://doi.org/10.1097/qad.0000000000004504openalex-snapshot
Genome-wide association study of cardiovascular disease in people with HIV from the Million Veteran Program (MVP)
inferred← citeshttps://doi.org/10.1097/tp.0000000000000568openalex-snapshot
Homoarginine and Clinical Outcomes in Renal Transplant Recipients
inferred← citeshttps://doi.org/10.1101/2020.05.22.110197openalex-snapshot
Untargeted metabolome- and transcriptome-wide association study identifies causal genes modulating metabolite concentrations in urine
inferred← citeshttps://doi.org/10.1101/2023.07.14.548888openalex-snapshot
Role of transporters and enzymes in metabolism and distribution of 4 chlorokynurenine and metabolites
inferred← citeshttps://doi.org/10.1101/2024.09.22.614364openalex-snapshot
ALMS1 KO rat: a new model of metabolic syndrome with spontaneous hypertension
inferred← citeshttps://doi.org/10.1101/729715openalex-snapshot
Relationship between birth weight and chronic kidney disease: an integrative analysis of observational studies and causal inference through genetic approaches
inferred← citeshttps://doi.org/10.1108/qrj-04-2024-0097openalex-snapshot
A qualitative analysis of the impact of government schemes on chronic kidney disease patients in Uddanam, India
inferred← citeshttps://doi.org/10.1109/enbeng.2019.8692517openalex-snapshot
Changes in N-acetyltransferase 8 in kidney tubular cell: injury, recovery and mesenchymal stromal cell-based therapy
inferred← citeshttps://doi.org/10.1111/ajt.13180openalex-snapshot
Renal Allograft Fibrosis: Biology and Therapeutic Targets
inferred← citeshttps://doi.org/10.1111/apha.70174openalex-snapshot
Alms1 KO Rat: A New Model of Cardiometabolic Syndrome With Spontaneous Hypertension
inferred← citeshttps://doi.org/10.1111/bcp.16009openalex-snapshot
Determinants of early change in serum creatinine after initiation of dolutegravir‐based antiretroviral therapy in South Africa
inferred← citeshttps://doi.org/10.1111/ctr.12093openalex-snapshot
A genome‐wide association study of recipient genotype and medium‐term kidney allograft function
inferred← citeshttps://doi.org/10.1111/jdi.12391openalex-snapshot
Genetics of cardiovascular and renal complications in diabetes
inferred← citeshttps://doi.org/10.1134/s102279542212002xopenalex-snapshot
The Polymorphic Locus rs167479 of the RGL3 Gene Is Associated with the Risk of Severe Preeclampsia
inferred← citeshttps://doi.org/10.1136/bmjopen-2017-020759openalex-snapshot
Clinical and genetic associations of renal function and diabetic kidney disease in the United Arab Emirates: a cross-sectional study
inferred← citeshttps://doi.org/10.1136/hrt.2010.220731openalex-snapshot
Low homoarginine concentration is a novel risk factor for heart disease
inferred← citeshttps://doi.org/10.1136/jmedgenet-2013-101518openalex-snapshot
Identification of chromosome 3q28 and ALPK1 as susceptibility loci for chronic kidney disease in Japanese individuals by a genome-wide association study
inferred← citeshttps://doi.org/10.1152/ajprenal.00017.2023openalex-snapshot
Role of Alström syndrome 1 in the regulation of glomerular hemodynamics
inferred← citeshttps://doi.org/10.1152/ajprenal.00221.2013openalex-snapshot
Differential cystine and dibasic amino acid handling after loss of function of the amino acid transporter b 0,+ AT (Slc7a9) in mice
inferred← citeshttps://doi.org/10.1152/ajprenal.00306.2014openalex-snapshot
Genetic and epigenetic factors influencing chronic kidney disease
inferred← citeshttps://doi.org/10.1152/ajprenal.00334.2013openalex-snapshot
Genetics of hypertension: discoveries from the bench to human populations
inferred← citeshttps://doi.org/10.1152/ajprenal.00690.2011openalex-snapshot
Genetic analysis of albuminuria in collaborative cross and multiple mouse intercross populations
inferred← citeshttps://doi.org/10.1152/physiolgenomics.00087.2012openalex-snapshot
SLC22A2is associated with tubular creatinine secretion and bias of estimated GFR in renal transplantation
inferred← citeshttps://doi.org/10.1152/physiolgenomics.00089.2013openalex-snapshot
SORCS1 contributes to the development of renal disease in rats and humans
inferred← citeshttps://doi.org/10.1152/physrev.00008.2018openalex-snapshot
Learning Physiology from Inherited Kidney Disorders
inferred← citeshttps://doi.org/10.1155/2014/602526openalex-snapshot
Emerging Biomarkers and Metabolomics for Assessing Toxic Nephropathy and Acute Kidney Injury (AKI) in Neonatology
inferred← citeshttps://doi.org/10.1155/2019/1095215openalex-snapshot
Novel Haplotype Indicator for End-Stage Renal Disease Progression among Saudi Patients
inferred← citeshttps://doi.org/10.1158/1078-0432.ccr-11-2503openalex-snapshot
Proximal Tubular Secretion of Creatinine by Organic Cation Transporter OCT2 in Cancer Patients
inferred← citeshttps://doi.org/10.1159/000321013openalex-snapshot
Uromodulin Biology and Pathophysiology – An Update
inferred← citeshttps://doi.org/10.1159/000326685openalex-snapshot
Genetic Association Studies: Discovery of the Genetic Basis of Renal Disease
inferred← citeshttps://doi.org/10.1159/000326901openalex-snapshot
Chronic Kidney Disease: Novel Insights from Genome-Wide Association Studies
inferred← citeshttps://doi.org/10.1159/000481886openalex-snapshot
Genome-Wide Analysis Studies and Chronic Kidney Disease
inferred← citeshttps://doi.org/10.1159/000494390openalex-snapshot
Mercapturate Pathway in the Tubulocentric Perspective of Diabetic Kidney Disease
inferred← citeshttps://doi.org/10.1159/000496930openalex-snapshot
Genome-Wide Association Scan of Serum Urea in European Populations Identifies Two Novel Loci
inferred← citeshttps://doi.org/10.1161/atvbaha.112.247726openalex-snapshot
Endogenous Nitric Oxide Synthase Inhibitors in the Biology of Disease
inferred← citeshttps://doi.org/10.1161/strokeaha.113.003044openalex-snapshot
Predicting Stroke Through Genetic Risk Functions
inferred← citeshttps://doi.org/10.1172/jci.insight.95076openalex-snapshot
Role of Alström syndrome 1 in the regulation of blood pressure and renal function
inferred← citeshttps://doi.org/10.1177/0003319711418958openalex-snapshot
The Utility of Collaborative Biobanks for Cardiovascular Research
inferred← citeshttps://doi.org/10.1177/10742484211054620openalex-snapshot
Impact of Homoarginine on Myocardial Function and Remodeling in a Rat Model of Chronic Renal Failure
inferred← citeshttps://doi.org/10.1186/1471-2105-15-200openalex-snapshot
inPHAP: Interactive visualization of genotype and phased haplotype data
inferred← citeshttps://doi.org/10.1186/1471-2350-13-58openalex-snapshot
Genetic polymorphisms located in genes related to immune and inflammatory processes are associated with end-stage renal disease: a preliminary study
inferred← citeshttps://doi.org/10.1186/1471-2350-13-78openalex-snapshot
UMOD as a susceptibility gene for end-stage renal disease
inferred← citeshttps://doi.org/10.1186/1471-2369-14-95openalex-snapshot
The natural history of, and risk factors for, progressive Chronic Kidney Disease (CKD): the Renal Impairment in Secondary care (RIISC) study; rationale and protocol
inferred← citeshttps://doi.org/10.1186/1471-2369-15-138openalex-snapshot
UMODpolymorphism rs12917707 is not associated with severe or stable IgA nephropathy in a large Caucasian cohort
inferred← citeshttps://doi.org/10.1186/s12864-024-10449-1openalex-snapshot
Genetic variants affecting mitochondrial function provide further insights for kidney disease
inferred← citeshttps://doi.org/10.1186/s12881-016-0358-3openalex-snapshot
A single nucleotide polymorphism in the UMOD promoter is associated with end stage renal disease
inferred← citeshttps://doi.org/10.1186/s12881-016-0366-3openalex-snapshot
Genetic variation underlying renal uric acid excretion in Hispanic children: the Viva La Familia Study
inferred← citeshttps://doi.org/10.1186/s12882-016-0396-2openalex-snapshot
Familial aggregation of albuminuria and arterial hypertension in an Aboriginal Australian community and the contribution of variants in ACE and TP53
inferred← citeshttps://doi.org/10.1186/s12882-018-0890-9openalex-snapshot
Assessing known chronic kidney disease associated genetic variants in Saudi Arabian populations
inferred← citeshttps://doi.org/10.1186/s12967-018-1664-7openalex-snapshot
Genomic approaches in the search for molecular biomarkers in chronic kidney disease
inferred← citeshttps://doi.org/10.1242/dmm.035048openalex-snapshot
Modeling epigenetic modifications in renal development and disease with organoids and genome editing
inferred← citeshttps://doi.org/10.13130/rizzi-federica_phd2013-02-07openalex-snapshot
GENETIC BIOMARKERS OF RENAL FUNCTION
inferred← citeshttps://doi.org/10.1371/journal.pgen.1002264openalex-snapshot
Genetic Association for Renal Traits among Participants of African Ancestry Reveals New Loci for Renal Function
inferred← citeshttps://doi.org/10.1371/journal.pgen.1002270openalex-snapshot
A Genome-Wide Metabolic QTL Analysis in Europeans Implicates Two Loci Shaped by Recent Positive Selection
inferred← citeshttps://doi.org/10.1371/journal.pgen.1002292openalex-snapshot
Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD
inferred← citeshttps://doi.org/10.1371/journal.pgen.1002584openalex-snapshot
Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function
inferred← citeshttps://doi.org/10.1371/journal.pgen.1002921openalex-snapshot
New Susceptibility Loci Associated with Kidney Disease in Type 1 Diabetes
inferred← citeshttps://doi.org/10.1371/journal.pgen.1003005openalex-snapshot
Mining the Unknown: A Systems Approach to Metabolite Identification Combining Genetic and Metabolic Information
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004212openalex-snapshot
Genetic Determinants Influencing Human Serum Metabolome among African Americans
inferred← citeshttps://doi.org/10.1371/journal.pgen.1005487openalex-snapshot
Genome-Wide Association Study with Targeted and Non-targeted NMR Metabolomics Identifies 15 Novel Loci of Urinary Human Metabolic Individuality
inferred← citeshttps://doi.org/10.1371/journal.pgen.1005510openalex-snapshot
Integration of Genome-Wide SNP Data and Gene-Expression Profiles Reveals Six Novel Loci and Regulatory Mechanisms for Amino Acids and Acylcarnitines in Whole Blood
inferred← citeshttps://doi.org/10.1371/journal.pgen.1010599openalex-snapshot
Bayesian mixed model analysis uncovered 21 risk loci for chronic kidney disease in boxer dogs
inferred← citeshttps://doi.org/10.1371/journal.pone.0063560openalex-snapshot
Homoarginine and Progression of Chronic Kidney Disease: Results from the Mild to Moderate Kidney Disease Study
inferred← citeshttps://doi.org/10.1371/journal.pone.0093844openalex-snapshot
Mapping the Genetic Architecture of Gene Regulation in Whole Blood
inferred← citeshttps://doi.org/10.1371/journal.pone.0103355openalex-snapshot
The Role of N-Acetyltransferase 8 in Mesenchymal Stem Cell-Based Therapy for Liver Ischemia/Reperfusion Injury in Rats
inferred← citeshttps://doi.org/10.1371/journal.pone.0114240openalex-snapshot
Genome-Wide Association Study Reveals a Polymorphism in the Podocyte Receptor RANK for the Decline of Renal Function in Coronary Patients
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