Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypesHirotaka Matsuo, Nariyoshi Shinomiya, Toshinori Chiba et al.|Annals of the Rheumatic Diseases|2015Cited by 183
GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genesAkiyoshi Nakayama, Hirotaka Matsuo, Toshihide Higashino et al.|Annals of the Rheumatic Diseases|2016Cited by 173
ABCG2 dysfunction causes hyperuricemia due to both renal urate underexcretion and renal urate overloadHirotaka Matsuo, Nariyoshi Shinomiya, Hirofumi Nakaoka et al.|Scientific Reports|2014Cited by 163
Common dysfunctional variants in ABCG2 are a major cause of early-onset goutHirotaka Matsuo, Nariyoshi Shinomiya, Toshinori Chiba et al.|Scientific Reports|2013Cited by 132
Genome-wide association study revealed novel loci which aggravate asymptomatic hyperuricaemia into goutYusuke Kawamura, Toshihide Higashino, Mariko Naito et al.|Annals of the Rheumatic Diseases|2019Cited by 103