Man, Li
VIAF ID: 120146936775913782226 (Personal)
Permalink: http://viaf.org/viaf/120146936775913782226
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- 100 0 _ ‡a Man Li
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4xx's: Alternate Name Forms (1)
Works
Title | Sources |
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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 | |
Advances in understanding the genetic basis of diabetic kidney disease | |
The association between APOL1 risk alleles and longitudinal kidney function differs by HIV viral suppression status | |
Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD. | |
A catalog of genetic loci associated with kidney function from analyses of a million individuals | |
Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval | |
Common genetic variants associate with serum phosphorus concentration | |
Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways | |
Common variants at ten loci modulate the QT interval duration in the QTSCD Study | |
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction | |
Comprehensive evaluation of imputation performance in African Americans | |
Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function | |
CUBN is a gene locus for albuminuria | |
Discovery of novel heart rate-associated loci using the Exome Chip | |
ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals | |
An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans | |
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function | |
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci | |
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge | |
Genetics of Plasma Soluble Receptor for Advanced Glycation End-Products and Cardiovascular Outcomes in a Community-based Population: Results from the Atherosclerosis Risk in Communities Study | |
Genome-wide association and functional follow-up reveals new loci for kidney function | |
Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND) | |
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria | |
Genome-wide association study of 1,5-anhydroglucitol identifies novel genetic loci linked to glucose metabolism | |
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility | |
Host APOL1 genotype is independently associated with proteinuria in HIV infection | |
Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals | |
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis. | |
Impact of repeated measures and sample selection on genome-wide association studies of fasting glucose | |
Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function | |
Laozi Benyi : a political philosophy for the last phase of time | |
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility | |
Machine Learning Based on MRI DWI Radiomics Features for Prognostic Prediction in Nasopharyngeal Carcinoma | |
Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program | |
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci | |
Modulation of genetic associations with serum urate levels by body-mass-index in humans | |
Multi-ethnic genome-wide association study for atrial fibrillation | |
Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors | |
The MYH9/APOL1 region and chronic kidney disease in European-Americans | |
MYH9 is associated with nondiabetic end-stage renal disease in African Americans | |
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk | |
NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality | |
Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study | |
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals | |
A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathy | |
Rare variants in SLC5A10 are associated with serum 1,5-anhydroglucitol (1,5-AG) in the Atherosclerosis Risk in Communities (ARIC) Study | |
Re-Sequencing of the APOL1-APOL4 and MYH9 Gene Regions in African Americans Does Not Identify Additional Risks for CKD Progression | |
Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene | |
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. | |
SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function | |
Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases | |
Strength of association for incident diabetes risk factors according to diabetes case definitions: the Atherosclerosis Risk in Communities Study | |
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels | |
Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin | |
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis | |
Urinary metabolites along with common and rare genetic variations are associated with incident chronic kidney disease. | |
The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization tool. | |
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry | |
VARPRISM: incorporating variant prioritization in tests of de novo mutation association | |
West African ancestry and nocturnal blood pressure in African Americans: the Jackson Heart Study. |