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Meta-analysis identifies multiple loci associated with kidney function–related traits in east Asian populations
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Outgoing claims: the papers this work cites, builds on, or argues with.
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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/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/gfw270openalex-snapshot
Genetic epidemiology in kidney disease
inferred← citeshttps://doi.org/10.1093/rheumatology/keae492openalex-snapshot
Genetic risk, lifestyle adherence, and risk of developing hyperuricaemia in a Japanese population
inferred← citeshttps://doi.org/10.1093/rheumatology/kex467openalex-snapshot
Association between ABCG2 rs2231142 and poor response to allopurinol: replication and meta-analysis
inferred← citeshttps://doi.org/10.1097/hjh.0000000000001241openalex-snapshot
PROX1 gene CC genotype as a major determinant of early onset of type 2 diabetes in slavic study participants from Action in Diabetes and Vascular Disease
inferred← citeshttps://doi.org/10.1097/md.0000000000018722openalex-snapshot
Non-diabetic end-stage renal disease in Saudis associated with polymorphism of MYH9 gene but not UMOD gene
inferred← citeshttps://doi.org/10.1097/mnh.0000000000000427openalex-snapshot
The systems biology of uric acid transporters
inferred← citeshttps://doi.org/10.1097/mnh.0b013e328363ffc8openalex-snapshot
Urate transporters in the genomic era
inferred← citeshttps://doi.org/10.1101/660506openalex-snapshot
Genetics of 38 blood and urine biomarkers in the UK Biobank
inferred← citeshttps://doi.org/10.1101/859959openalex-snapshot
Paracrine and autocrine R-spondin signalling is essential for the maintenance and differentiation of renal stem cells
inferred← citeshttps://doi.org/10.1101/gr.182881.114openalex-snapshot
Shroom3 contributes to the maintenance of the glomerular filtration barrier integrity
inferred← citeshttps://doi.org/10.1101/gr.261305.120openalex-snapshot
Alu insertion variants alter gene transcript levels
inferred← citeshttps://doi.org/10.1111/1753-0407.13393openalex-snapshot
Glomerular filtration rate estimated by differing measures and risk of all‐cause mortality among Chinese individuals without or with diabetes: A nationwide prospective study
inferred← citeshttps://doi.org/10.1111/1756-185x.13323openalex-snapshot
GLUT 9 influences uric acid concentration in patients with Lesch‐Nyhan disease
inferred← citeshttps://doi.org/10.1111/bcp.15792openalex-snapshot
Population pharmacokinetics, pharmacodynamics and pharmacogenetics modelling of oxypurinol in Hmong adults with gout and/or hyperuricemia
inferred← citeshttps://doi.org/10.1111/cge.14110openalex-snapshot
Genetic risk of hyperuricemia in hypertensive patients associated with antihypertensive drug therapy: A longitudinal study
inferred← citeshttps://doi.org/10.1111/jcmm.13176openalex-snapshot
Phloretin attenuates hyperuricemia‐induced endothelial dysfunction through co‐inhibiting inflammation and GLUT 9‐mediated uric acid uptake
inferred← citeshttps://doi.org/10.1111/jdi.12391openalex-snapshot
Genetics of cardiovascular and renal complications in diabetes
inferred← citeshttps://doi.org/10.1111/nep.13479openalex-snapshot
Association of genetic risk score and chronic kidney disease in a Japanese population
inferred← citeshttps://doi.org/10.1126/science.abg8289openalex-snapshot
Protein-coding repeat polymorphisms strongly shape diverse human phenotypes
inferred← citeshttps://doi.org/10.1126/science.aea6187openalex-snapshot
A cross-organ single-cell analysis of hypertension
inferred← citeshttps://doi.org/10.1136/annrheumdis-2014-206191openalex-snapshot
Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes
inferred← citeshttps://doi.org/10.1136/annrheumdis-2016-209632openalex-snapshot
GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes
inferred← citeshttps://doi.org/10.1136/annrheumdis-2019-215521openalex-snapshot
Genome-wide association study revealed novel loci which aggravate asymptomatic hyperuricaemia into gout
inferred← citeshttps://doi.org/10.1136/bmjdrc-2019-000834openalex-snapshot
Mendelian randomization study of serum uric acid levels and diabetes risk: evidence from the Dongfeng-Tongji cohort
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/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/10.1136/rmdopen-2021-001623openalex-snapshot
Gout, Hyperuricaemia and Crystal-Associated Disease Network (G-CAN) common language definition of gout
inferred← citeshttps://doi.org/10.1146/annurev-physiol-031620-092817openalex-snapshot
Uromodulin: Roles in Health and Disease
inferred← citeshttps://doi.org/10.1152/ajprenal.00306.2014openalex-snapshot
Genetic and epigenetic factors influencing chronic kidney disease
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/10.1159/000488946openalex-snapshot
Genome-Wide Association Study of Renal Function Traits: Results from the Japan Multi-Institutional Collaborative Cohort Study
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/10.1159/000531783openalex-snapshot
Genome-Wide Association Studies for Albuminuria of Nondiabetic Taiwanese Population
inferred← citeshttps://doi.org/10.1161/cir.0000000000000558openalex-snapshot
Heart Disease and Stroke Statistics—2018 Update: A Report From the American Heart Association
inferred← citeshttps://doi.org/10.1161/strokeaha.114.006609openalex-snapshot
Polygenic Overlap Between Kidney Function and Large Artery Atherosclerotic Stroke
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/10.1186/1755-8794-7-10openalex-snapshot
A genome-wide association study identifies common variants influencing serum uric acid concentrations in a Chinese population
inferred← citeshttps://doi.org/10.1186/s12864-019-6363-0openalex-snapshot
A phenomics-based approach for the detection and interpretation of shared genetic influences on 29 biochemical indices in southern Chinese men
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/s12881-015-0208-8openalex-snapshot
Polymorphisms in GCKR, SLC17A1 and SLC22A12 were associated with phenotype gout in Han Chinese males: a case–control study
inferred← citeshttps://doi.org/10.1186/s12881-020-01147-2openalex-snapshot
The association between genetic polymorphisms in ABCG2 and SLC2A9 and urate: an updated systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1186/s12881-020-0987-4openalex-snapshot
ABCG2 rs2231142 variant in hyperuricemia is modified by SLC2A9 and SLC22A12 polymorphisms and cardiovascular risk factors in an elderly community-dwelling population
inferred← citeshttps://doi.org/10.1186/s12882-015-0207-1openalex-snapshot
Uric acid is associated with microalbuminuria and decreased glomerular filtration rate in the general population during 7 and 13 years of follow-up: The Tromsø Study
inferred← citeshttps://doi.org/10.1186/s12887-018-1272-yopenalex-snapshot
Long-term effects of the SLC2A9 G844A and SLC22A12 C246T variants on serum uric acid concentrations in children
inferred← citeshttps://doi.org/10.1186/s12902-020-00560-1openalex-snapshot
Association between serum vitamin D and uric acid in the eastern Chinese population: a population-based cross-sectional study
inferred← citeshttps://doi.org/10.1186/s12916-017-0878-5openalex-snapshot
The genetics of gout: towards personalised medicine?
inferred← citeshttps://doi.org/10.1186/s12986-016-0096-8openalex-snapshot
Interactions with the MC4R rs17782313 variant, mental stress and energy intake and the risk of obesity in Genome Epidemiology Study
inferred← citeshttps://doi.org/10.1186/s13069-015-0033-xopenalex-snapshot
Precision renal medicine: a roadmap towards targeted kidney fibrosis therapies
inferred← citeshttps://doi.org/10.1186/s13073-016-0383-zopenalex-snapshot
Alternate-locus aware variant calling in whole genome sequencing
inferred← citeshttps://doi.org/10.1186/s13073-026-01642-wopenalex-snapshot
African ancestry-enriched variants in the GATM gene are associated with elevated serum creatinine levels
inferred← citeshttps://doi.org/10.1186/s13075-015-0609-2openalex-snapshot
An update on the genetic architecture of hyperuricemia and gout
inferred← citeshttps://doi.org/10.1186/s13075-020-2136-zopenalex-snapshot
Pleiotropic effect of the ABCG2 gene in gout: involvement in serum urate levels and progression from hyperuricemia to gout
inferred← citeshttps://doi.org/10.1186/s13075-022-02917-4openalex-snapshot
Polygenic risk score trend and new variants on chromosome 1 are associated with male gout in genome-wide association study
inferred← citeshttps://doi.org/10.1186/s40101-025-00394-7openalex-snapshot
Anthropometric and metabolic differences and distribution of ABCG2 rs2231142 variant between lowland and highland Papuans in West Papua, Indonesia
inferred← citeshttps://doi.org/10.1186/s40168-020-00923-9openalex-snapshot
The interplay between host genetics and the gut microbiome reveals common and distinct microbiome features for complex human diseases
inferred← citeshttps://doi.org/10.1186/s41065-019-0103-yopenalex-snapshot
ABCG2 gene polymorphism rs2231142 is associated with gout comorbidities but not allopurinol response in primary gout patients of a Chinese Han male population
inferred← citeshttps://doi.org/10.1186/s41927-021-00239-7openalex-snapshot
Genetic assessment of hyperuricemia and gout in Asian, Native Hawaiian, and Pacific Islander subgroups of pregnant women: biospecimens repository cross-sectional study
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/10.12688/f1000research.6970.1openalex-snapshot
Recent advances in understanding of chronic kidney disease
inferred← citeshttps://doi.org/10.1371/annotation/1238450b-9ba4-4afb-aee3-a3c11b4f5ea1openalex-snapshot
Correction: Genome Wide Association Study of Age at Menarche in the Japanese Population
inferred← citeshttps://doi.org/10.1371/journal.pbio.3000152openalex-snapshot
Single-cell transcriptomics reveals gene expression dynamics of human fetal kidney development
inferred← citeshttps://doi.org/10.1371/journal.pgen.1005352openalex-snapshot
Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND)
inferred← citeshttps://doi.org/10.1371/journal.pone.0063821openalex-snapshot
Genome Wide Association Study of Age at Menarche in the Japanese Population
inferred← citeshttps://doi.org/10.1371/journal.pone.0081888openalex-snapshot
A Genome-Wide Search for Linkage of Estimated Glomerular Filtration Rate (eGFR) in the Family Investigation of Nephropathy and Diabetes (FIND)
inferred← citeshttps://doi.org/10.1371/journal.pone.0087645openalex-snapshot
Integration of Sequence Data from a Consanguineous Family with Genetic Data from an Outbred Population Identifies PLB1 as a Candidate Rheumatoid Arthritis Risk Gene
inferred← citeshttps://doi.org/10.1371/journal.pone.0092468openalex-snapshot
Variation in Genes that Regulate Blood Pressure Are Associated with Glomerular Filtration Rate in Chinese
inferred← citeshttps://doi.org/10.1371/journal.pone.0148270openalex-snapshot
Association of RAC1 Gene Polymorphisms with Primary End-Stage Renal Disease in Chinese Renal Recipients
inferred← citeshttps://doi.org/10.1371/journal.pone.0165893openalex-snapshot
Extensive Association of Common Disease Variants with Regulatory Sequence
inferred← citeshttps://doi.org/10.1371/journal.pone.0170222openalex-snapshot
Targeted Sequencing of Lung Function Loci in Chronic Obstructive Pulmonary Disease Cases and Controls
inferred← citeshttps://doi.org/10.1371/journal.pone.0185476openalex-snapshot
Association between kidney function and genetic polymorphisms in atherosclerotic and chronic kidney diseases: A cross-sectional study in Japanese male workers
inferred← citeshttps://doi.org/10.1371/journal.pone.0194044openalex-snapshot
Genome-wide association analysis identifies multiple loci associated with kidney disease-related traits in Korean populations
inferred← citeshttps://doi.org/10.1371/journal.pone.0206174openalex-snapshot
Association of common gene variants in glucokinase regulatory protein with cardiorenal disease: A systematic review and meta-analysis
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