Genome-wide association study identifies risk loci within the major histocompatibility complex region for Hunner-type interstitial cystitis

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

Trans-ethnic Mendelian-randomization study reveals causal relationships between cardiometabolic factors and chronic kidney disease

All-cause and cardiovascular disease mortality in underweight patients with diabetic nephropathy: BioBank Japan cohort

An X chromosome-wide meta-analysis based on Japanese cohorts revealed that non-autosomal variations are associated with serum urate

SHROOM3, the gene associated with chronic kidney disease, affects the podocyte structure

Claudin-2 deficiency associates with hypercalciuria in mice and human kidney stone disease

Single Nucleotide Polymorphisms of HAAO and IRX6 Genes as Risk Factors for Hypospadias

Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies

Genome-Wide Association Study of Renal Function Traits: Results from the Japan Multi-Institutional Collaborative Cohort Study

A variant within the FTO confers susceptibility to diabetic nephropathy in Japanese patients with type 2 diabetes

A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes.

Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity

A replication study for three nephrolithiasis loci at 5q35.3, 7p14.3 and 13q14.1 in the Japanese population

A genome-wide association study of nephrolithiasis in the Japanese population identifies novel susceptible Loci at 5q35.3, 7p14.3, and 13q14.1

Common variation in GPC5 is associated with acquired nephrotic syndrome

KEAP1–NRF2 system regulates age-related spermatogenesis dysfunction