W H Linda Kao


Ontology type: schema:Person     


Person Info

NAME

W H Linda

SURNAME

Kao

Publications in SciGraph latest 50 shown

  • 2017-01-09 Genetic evidence of assortative mating in humans in NATURE HUMAN BEHAVIOUR
  • 2016-10 Genetic variants in RBFOX3 are associated with sleep latency in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-01-21 Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function in NATURE COMMUNICATIONS
  • 2015-12 Genetic loci for serum magnesium among African-Americans and gene-environment interaction at MUC1 and TRPM6 in European-Americans: the Atherosclerosis Risk in Communities (ARIC) study in BMC GENETICS
  • 2015-12 Rationale and design for the Predictors of Arrhythmic and Cardiovascular Risk in End Stage Renal Disease (PACE) study in BMC NEPHROLOGY
  • 2015-12 Cross-sectional association of volume, blood pressures, and aortic stiffness with left ventricular mass in incident hemodialysis patients: the Predictors of Arrhythmic and Cardiovascular Risk in End-Stage Renal Disease (PACE) study in BMC NEPHROLOGY
  • 2015-12 Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci in NATURE GENETICS
  • 2015-12 Relative performance of gene- and pathway-level methods as secondary analyses for genome-wide association studies in BMC GENETICS
  • 2015-12 Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility in NATURE COMMUNICATIONS
  • 2015-04 Results from the Atherosclerosis Risk in Communities study suggest that low serum magnesium is associated with incident kidney disease in KIDNEY INTERNATIONAL
  • 2015-02 Effect of zinc supplementation on insulin secretion: interaction between zinc and SLC30A8 genotype in Old Order Amish in DIABETOLOGIA
  • 2014-12 Copy number polymorphisms near SLC2A9 are associated with serum uric acid concentrations in BMC GENETICS
  • 2014-12 Incidental findings on cardiac computed tomography in incident hemodialysis patients: the predictors of arrhythmic and cardiovascular events in end-stage renal disease (PACE) study in BMC NEPHROLOGY
  • 2014-12 Evaluation of microarray-based DNA methylation measurement using technical replicates: the Atherosclerosis Risk In Communities (ARIC) Study in BMC BIOINFORMATICS
  • 2014-08 Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization in NATURE GENETICS
  • 2014-03 Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility in NATURE GENETICS
  • 2013-10 Host APOL1 genotype is independently associated with proteinuria in HIV infection in KIDNEY INTERNATIONAL
  • 2013-10 Oral contraceptive pill use is associated with reduced odds of nonalcoholic fatty liver disease in menstruating women: results from NHANES III in JOURNAL OF GASTROENTEROLOGY
  • 2013-07 Using multiple measures for quantitative trait association analyses: application to estimated glomerular filtration rate in JOURNAL OF HUMAN GENETICS
  • 2013-06 Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin in HUMAN GENETICS
  • 2013-02 Genome-wide association analyses identify 18 new loci associated with serum urate concentrations in NATURE GENETICS
  • 2013-01 Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans in KIDNEY INTERNATIONAL
  • 2012-09 Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes in NATURE GENETICS
  • 2012-06 Meta-analysis identifies six new susceptibility loci for atrial fibrillation in NATURE GENETICS
  • 2012-05 A Community-Based Study of Nucleotide Excision Repair Polymorphisms in Relation to the Risk of Non-Melanoma Skin Cancer in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2011-11 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution in NATURE GENETICS
  • 2011-10 Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk in NATURE
  • 2011-08 The landscape of recombination in African Americans in NATURE
  • 2011-03-29 Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis in NATURE GENETICS
  • 2010-12 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction in NATURE GENETICS
  • 2010-12 Variation in the checkpoint kinase 2 gene is associated with type 2 diabetes in multiple populations in ACTA DIABETOLOGICA
  • 2010-11 Nicotinic acetylcholine receptor genes on chromosome 15q25.1 are associated with nicotine and opioid dependence severity in HUMAN GENETICS
  • 2010-11 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution in NATURE GENETICS
  • 2010-07 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis in NATURE GENETICS
  • 2010-05 Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk in NATURE GENETICS
  • 2010-05 New loci associated with kidney function and chronic kidney disease in NATURE GENETICS
  • 2010-03 Common variants in KCNN3 are associated with lone atrial fibrillation in NATURE GENETICS
  • 2010-02 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge in NATURE GENETICS
  • 2010-02 Genome-wide association study of PR interval in NATURE GENETICS
  • 2010-02 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk in NATURE GENETICS
  • 2009-12 Parental origin of sequence variants associated with complex diseases in NATURE
  • 2009-12 Association of APOEpolymorphism with chronic kidney disease in a nationally representative sample: a Third National Health and Nutrition Examination Survey (NHANES III) Genetic Study in BMC MEDICAL GENETICS
  • 2009-12 The INSIG2 rs7566605 genetic variant does not play a major role in obesity in a sample of 24,722 individuals from four cohorts in BMC MEDICAL GENETICS
  • 2009-08 Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry in NATURE GENETICS
  • 2009-06 Multiple loci associated with indices of renal function and chronic kidney disease in NATURE GENETICS
  • 2009-04 Common variants at ten loci modulate the QT interval duration in the QTSCD Study in NATURE GENETICS
  • 2008-12 Genome-wide association study for renal traits in the Framingham Heart and Atherosclerosis Risk in Communities Studies in BMC MEDICAL GENETICS
  • 2008-11 The association of sudden cardiac death with inflammation and other traditional risk factors in KIDNEY INTERNATIONAL
  • 2008-10 MYH9 is associated with nondiabetic end-stage renal disease in African Americans in NATURE GENETICS
  • 2008-09 Lack of association between uncoupling protein-2 Ala55Val polymorphism and incident diabetes in the atherosclerosis risk in communities study in ACTA DIABETOLOGICA
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