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A common variant of organic anion transporter 4 (OAT4/SLC22A11) gene is associated with renal underexcretion type gout

artículo científico publicado en 2013

ABCG2 dysfunction causes hyperuricemia due to both renal urate underexcretion and renal urate overload

artículo científico publicado en 2014

Common dysfunctional variants in ABCG2 are a major cause of early-onset gout

artículo científico publicado en 2013

Common dysfunctional variants of ABCG2 have stronger impact on hyperuricemia progression than typical environmental risk factors

artículo científico publicado en 2014

Common missense variant of monocarboxylate transporter 9 (MCT9/SLC16A9) gene is associated with renal overload gout, but not with all gout susceptibility

scientific article published on 29 August 2013

Common variant of leucine-rich repeat-containing 16A (LRRC16A) gene is associated with gout susceptibility

artículo científico publicado en 2014

GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes

artículo científico publicado en 2016

Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes

artículo científico publicado en 2015

Genome-wide association study revealed novel loci which aggravate asymptomatic hyperuricaemia into gout

scientific article published on 8 July 2019

Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals

artículo científico publicado en 2019

Identification of a hypouricemia patient with SLC2A9 R380W, a pathogenic mutation for renal hypouricemia type 2

artículo científico publicado en 2014

Independent effects of ADH1B and ALDH2 common dysfunctional variants on gout risk

artículo científico publicado en 2017

Subtype-specific gout susceptibility loci and enrichment of selection pressure on ABCG2 and ALDH2 identified by subtype genome-wide meta-analyses of clinically defined gout patients

artículo científico publicado en 2020

The effects of URAT1/SLC22A12 nonfunctional variants, R90H and W258X, on serum uric acid levels and gout/hyperuricemia progression.

artículo científico publicado en 2016

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