Search Results - "KAO, W. H. LINDA"
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APOL1 Risk Variants, Race, and Progression of Chronic Kidney Disease
Published in The New England journal of medicine (05-12-2013)“…In this study, APOL1 variants were associated with an increased risk of progression of chronic kidney disease in black patients, as compared with white…”
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Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study
Published in The Lancet (British edition) (06-12-2008)“…Summary Background Hyperuricaemia, a highly heritable trait, is a key risk factor for gout. We aimed to identify novel genes associated with serum uric acid…”
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3
Effect of zinc supplementation on insulin secretion: interaction between zinc and SLC30A8 genotype in Old Order Amish
Published in Diabetologia (01-02-2015)“…Aims/hypothesis SLC30A8 encodes a zinc transporter in the beta cell; individuals with a common missense variant (rs13266634; R325W) in SLC30A8 demonstrate a…”
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Risk of type 2 diabetes and obesity is differentially associated with variation in FTO in whites and African-Americans in the ARIC study
Published in PloS one (20-05-2010)“…Single nucleotide polymorphisms (SNPs) in the fat mass and obesity associated (FTO) gene are associated with body mass index (BMI) in populations of European…”
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A pseudolikelihood approach for assessing genetic association in case–control studies with unmeasured population structure
Published in Statistical methods in medical research (01-11-2020)“…The case–control study design is one of the main tools for detecting associations between genetic markers and diseases. It is well known that population…”
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Nicotinic acetylcholine receptor genes on chromosome 15q25.1 are associated with nicotine and opioid dependence severity
Published in Human genetics (01-11-2010)“…A locus on chromosome 15q25.1 previously implicated in nicotine, alcohol, and cocaine dependence, smoking, and lung cancer encodes subunits of the nicotinic…”
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Single-nucleotide polymorphisms in LPA explain most of the ancestry-specific variation in Lp(a) levels in African Americans
Published in PloS one (24-01-2011)“…Lipoprotein(a) (Lp(a)) is an important causal cardiovascular risk factor, with serum Lp(a) levels predicting atherosclerotic heart disease and genetic…”
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Oral contraceptive pill use is associated with reduced odds of nonalcoholic fatty liver disease in menstruating women: results from NHANES III
Published in Journal of gastroenterology (01-10-2013)“…Background Higher prevalence of nonalcoholic fatty liver disease (NAFLD) in men and postmenopausal women than in premenopausal women has suggested a potential…”
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Association of estimated glomerular filtration rate and urinary uromodulin concentrations with rare variants identified by UMOD gene region sequencing
Published in PloS one (31-05-2012)“…Recent genome-wide association studies (GWAS) have identified common variants in the UMOD region associated with kidney function and disease in the general…”
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Association of Scavenger Receptor Class B Type I Polymorphisms With Subclinical Atherosclerosis: The Multi-Ethnic Study of Atherosclerosis
Published in Circulation. Cardiovascular genetics (01-02-2010)“…BACKGROUND—Little is known about the association of scavenger receptor class B type I (SCARB1) single-nucleotide polymorphisms (SNPs) and subclinical…”
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Admixture mapping scans identify a locus affecting retinal vascular caliber in hypertensive African Americans: the Atherosclerosis Risk in Communities (ARIC) study
Published in PLoS genetics (01-04-2010)“…Retinal vascular caliber provides information about the structure and health of the microvascular system and is associated with cardiovascular and…”
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Biomarkers of vascular calcification and mortality in patients with ESRD
Published in Clinical journal of the American Society of Nephrology (01-04-2014)“…Vascular calcification is common among patients undergoing dialysis and is associated with mortality. Factors such as osteoprotegerin (OPG), osteopontin (OPN),…”
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The Pharmacogenetics of Type 2 Diabetes: A Systematic Review
Published in Diabetes care (01-03-2014)“…We performed a systematic review to identify which genetic variants predict response to diabetes medications. We performed a search of electronic databases…”
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Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene
Published in PLoS genetics (01-01-2009)“…Persistently low white blood cell count (WBC) and neutrophil count is a well-described phenomenon in persons of African ancestry, whose etiology remains…”
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A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization
Published in Nature genetics (01-06-2006)“…Extremes of the electrocardiographic QT interval, a measure of cardiac repolarization, are associated with increased cardiovascular mortality. We identified a…”
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Uromodulin Levels Associate with a Common UMOD Variant and Risk for Incident CKD
Published in Journal of the American Society of Nephrology (01-02-2010)“…Common variants in the region of the UMOD gene, which encodes uromodulin (Tamm-Horsfall protein), associate with chronic kidney disease (CKD) and estimated GFR…”
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Multiple Genetic Loci Influence Serum Urate Levels and Their Relationship With Gout and Cardiovascular Disease Risk Factors
Published in Circulation. Cardiovascular genetics (01-12-2010)“…BACKGROUND—Elevated serum urate levels can lead to gout and are associated with cardiovascular risk factors. We performed a genome-wide association study to…”
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The MYH9/APOL1 region and chronic kidney disease in European-Americans
Published in Human molecular genetics (15-06-2011)“…Polymorphisms in the MYH9 and adjacent APOL1 gene region demonstrate a strong association with non-diabetic kidney disease in African-Americans. However, it is…”
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Association of Functional Polymorphism rs2231142 (Q141K) in the ABCG2 Gene With Serum Uric Acid and Gout in 4 US Populations The PAGE Study
Published in American journal of epidemiology (01-05-2013)“…A loss-of-function mutation (Q141K, rs2231142) in the ATP-binding cassette, subfamily G, member 2 gene (ABCG2) has been shown to be associated with serum uric…”
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Common Genetic Variants Associate with Serum Phosphorus Concentration
Published in Journal of the American Society of Nephrology (01-07-2010)“…Phosphorus is an essential mineral that maintains cellular energy and mineralizes the skeleton. Because complex actions of ion transporters and regulatory…”
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