Twenty-eight loci that influence serum urate levels: analysis of association with gout

Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

(2014) Leslie A. Lange et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Obesity-associated variants within FTO form long-range functional connections with IRX3

(2014) Scott Smemo et al.   NATURE

Sugar-sweetened beverage consumption: a risk factor for prevalent gout withSLC2A9genotype-specific effects on serum urate and risk of gout

(2013) Caitlin Batt et al.   ANNALS OF THE RHEUMATIC DISEASES

A sequence variant associated with sortilin-1 (SORT1) on 1p13.3 is independently associated with abdominal aortic aneurysm

(2013) Gregory T. Jones et al.   HUMAN MOLECULAR GENETICS

Effect of Genetic Polymorphisms on Development of Gout

(2013) W. Urano et al.   JOURNAL OF RHEUMATOLOGY

Gout-causing Q141K mutation in ABCG2 leads to instability of the nucleotide-binding domain and can be corrected with small molecules

(2013) O. M. Woodward et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Filipino Gout: A Review

(2013) Pooja Prasad et al.   ARTHRITIS CARE & RESEARCH

Association analysis of the SLC22A11 (organic anion transporter 4) and SLC22A12 (urate transporter 1) urate transporter locus with gout in New Zealand case-control sample sets reveals multiple ancestral-specific effects

(2013) Tanya J Flynn et al.   ARTHRITIS RESEARCH & THERAPY

Association of the lipoprotein receptor-related protein 2 gene with gout and non-additive interaction with alcohol consumption

(2013) Humaira Rasheed et al.   ARTHRITIS RESEARCH & THERAPY

Trans-Ethnic Fine-Mapping of Lipid Loci Identifies Population-Specific Signals and Allelic Heterogeneity That Increases the Trait Variance Explained

(2013) Ying Wu et al.   PLoS Genetics

A urate gene-by-diuretic interaction and gout risk in participants with hypertension: results from the ARIC study

(2012) Mara A McAdams-DeMarco et al.   ANNALS OF THE RHEUMATIC DISEASES

Association between gout and polymorphisms in GCKR in male Han Chinese

(2012) Jing Wang et al.   HUMAN GENETICS

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

(2012) Anna Köttgen et al.   NATURE GENETICS

National prevalence of gout derived from administrative health data in Aotearoa New Zealand

(2012) D. Winnard et al.   RHEUMATOLOGY

Systematic Localization of Common Disease-Associated Variation in Regulatory DNA

(2012) M. T. Maurano et al.   SCIENCE

The renal urate transporter SLC17A1 locus: confirmation of association with gout

(2012) Jade E Hollis-Moffatt et al.   ARTHRITIS RESEARCH & THERAPY

Interaction of the inflammasome genes CARD8 and NLRP3 in abdominal aortic aneurysms

(2011) Rebecca L. Roberts et al.   ATHEROSCLEROSIS

Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease

(2011) Manuel A Rivas et al.   NATURE GENETICS

Multiple Genetic Loci Influence Serum Urate Levels and Their Relationship With Gout and Cardiovascular Disease Risk Factors

(2010) Qiong Yang et al.   Circulation-Cardiovascular Genetics

A strong role for the ABCG2 gene in susceptibility to gout in New Zealand Pacific Island and Caucasian, but not Māori, case and control sample sets

(2010) Amanda J. Phipps-Green et al.   HUMAN MOLECULAR GENETICS

Role of the urate transporterSLC2A9gene in susceptibility to gout in New Zealand Māori, Pacific Island, and Caucasian case-control sample sets

(2009) Jade E. Hollis-Moffatt et al.   ARTHRITIS AND RHEUMATISM

Identification of a urate transporter, ABCG2, with a common functional polymorphism causing gout

(2009) O. M. Woodward et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Rare Variants of IFIH1, a Gene Implicated in Antiviral Responses, Protect Against Type 1 Diabetes

(2009) S. Nejentsev et al.   SCIENCE

Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations

(2009) Melanie Kolz et al.   PLoS Genetics