Lista de obras - Man Li - Dominio Público Uruguay

1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function

artículo científico publicado en 2017

A catalog of genetic loci associated with kidney function from analyses of a million individuals

scientific article published on 31 May 2019

A genome-wide association search for type 2 diabetes genes in African Americans

artículo científico publicado en 2012

A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathy

artículo científico publicado en 2017

APOL1 risk variants, race, and progression of chronic kidney disease

artículo científico publicado en 2013

Admixture mapping of obesity-related traits in African Americans: the Atherosclerosis Risk in Communities (ARIC) Study

artículo científico publicado en 2009

Admixture mapping scans identify a locus affecting retinal vascular caliber in hypertensive African Americans: the Atherosclerosis Risk in Communities (ARIC) study

artículo científico publicado en 2010

Advances in understanding the genetic basis of diabetic kidney disease

artículo científico publicado en 2018

An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

artículo científico publicado en 2017

Association of a fasting glucose genetic risk score with subclinical atherosclerosis: The Atherosclerosis Risk in Communities (ARIC) study ⬇️

artículo científico publicado en 2010

Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD.

artículo científico publicado en 2011

CUBN is a gene locus for albuminuria

artículo científico publicado en 2011

Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

Common genetic variants associate with serum phosphorus concentration

artículo científico publicado en 2010

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways ⬇️

artículo científico publicado en 2010

Common variants at ten loci modulate the QT interval duration in the QTSCD Study

artículo científico publicado en 2009

Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction

artículo científico publicado en 2010

Common variants in KCNN3 are associated with lone atrial fibrillation

artículo científico publicado en 2010

Common variants in Mendelian kidney disease genes and their association with renal function

artículo científico publicado en 2013

Comprehensive evaluation of imputation performance in African Americans

artículo científico publicado en 2012

Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function

artículo científico publicado en 2017

Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

scholarly article published in Nature Genetics

Discovery of novel heart rate-associated loci using the Exome Chip

artículo científico publicado en 2017

Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals

Genetic association and gene-gene interaction analyses in African American dialysis patients with nondiabetic nephropathy

artículo científico publicado en 2011

Genetic association for renal traits among participants of African ancestry reveals new loci for renal function

artículo científico publicado en 2011

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

artículo científico publicado en 2016

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

artículo científico publicado en 2015

Genetic variants in RBFOX3 are associated with sleep latency

artículo científico publicado en 2016

Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

scientific journal article

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

artículo científico publicado en 2015

Genome-Wide Association Study of Serum Fructosamine and Glycated Albumin in Adults Without Diagnosed Diabetes: Results From the Atherosclerosis Risk in Communities Study

article published in 2018

Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND)

artículo científico publicado en 2015

Genome-Wide Association of Copy Number Polymorphisms and Kidney Function

artículo científico publicado en 2017

Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes.

artículo científico publicado en 2015

Genome-wide association and functional follow-up reveals new loci for kidney function

artículo científico publicado en 2012

Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

artículo científico publicado en 2019

Genome-wide association study of 1,5-anhydroglucitol identifies novel genetic loci linked to glucose metabolism

artículo científico publicado en 2017

Genome-wide association study of PR interval

artículo científico publicado en 2010

Genome-wide association study of kidney function decline in individuals of European descent

artículo científico publicado en 2014

Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

artículo científico publicado en 2014

Host APOL1 genotype is independently associated with proteinuria in HIV infection

artículo científico publicado en 2013

Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals

artículo científico publicado en 2011

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.

artículo científico publicado en 2017

Impact of repeated measures and sample selection on genome-wide association studies of fasting glucose

artículo científico publicado en 2010

Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function

artículo científico publicado en 2012

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

artículo científico publicado en 2017

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

artículo científico publicado en 2012

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

artículo científico publicado en 2015

MYH9 is associated with nondiabetic end-stage renal disease in African Americans

artículo científico publicado en 2008

Machine Learning Based on MRI DWI Radiomics Features for Prognostic Prediction in Nasopharyngeal Carcinoma

artículo científico publicado en 2022

Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program

scientific article published on 26 August 2019

Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

artículo científico publicado en 2016

Modulation of genetic associations with serum urate levels by body-mass-index in humans

artículo científico publicado en 2015

Multi-ethnic genome-wide association study for atrial fibrillation

article

Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors

artículo científico publicado en 2010

Multiple loci associated with indices of renal function and chronic kidney disease

scientific journal article

NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality

artículo científico

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

New loci associated with kidney function and chronic kidney disease

artículo científico publicado en 2010

Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study

artículo científico publicado en 2014

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

artículo científico publicado en 2012

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

artículo científico publicado en 2015

Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene

artículo científico publicado en 2009

Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

artículo científico publicado en 2018

SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function

artículo científico publicado en 2016

Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases

artículo científico publicado en 2012

Strength of association for incident diabetes risk factors according to diabetes case definitions: the Atherosclerosis Risk in Communities Study

artículo científico publicado en 2012

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

artículo científico publicado en 2019

The MYH9/APOL1 region and chronic kidney disease in European-Americans

artículo científico publicado en 2011

The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization tool

artículo científico publicado en 2018

The association between APOL1 risk alleles and longitudinal kidney function differs by HIV viral suppression status

artículo científico publicado en 2014

Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin

artículo científico publicado en 2016

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

artículo científico publicado en 2010

Urinary metabolites along with common and rare genetic variations are associated with incident chronic kidney disease.

artículo científico publicado en 2017

VARPRISM: incorporating variant prioritization in tests of de novo mutation association

artículo científico publicado en 2016

Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry ⬇️

scientific article published on 13 July 2009

West African ancestry and nocturnal blood pressure in African Americans: the Jackson Heart Study

artículo científico publicado en 2018

Lista de obras de Man Li

1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function

A catalog of genetic loci associated with kidney function from analyses of a million individuals

A genome-wide association search for type 2 diabetes genes in African Americans

A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathy

APOL1 risk variants, race, and progression of chronic kidney disease

Admixture mapping of obesity-related traits in African Americans: the Atherosclerosis Risk in Communities (ARIC) Study

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

An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

Association of a fasting glucose genetic risk score with subclinical atherosclerosis: The Atherosclerosis Risk in Communities (ARIC) study ⬇️

Association of eGFR-Related Loci Identified by GWAS with Incident CKD and ESRD.

CUBN is a gene locus for albuminuria

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

Common variants in KCNN3 are associated with lone atrial fibrillation

Common variants in Mendelian kidney disease genes and their association with renal function

Comprehensive evaluation of imputation performance in African Americans

Corrigendum: 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function

Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

Discovery of novel heart rate-associated loci using the Exome Chip

Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6

ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals

Genetic association and gene-gene interaction analyses in African American dialysis patients with nondiabetic nephropathy

Genetic association for renal traits among participants of African ancestry reveals new loci for renal function

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 variants in RBFOX3 are associated with sleep latency

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 Study of Serum Fructosamine and Glycated Albumin in Adults Without Diagnosed Diabetes: Results From the Atherosclerosis Risk in Communities Study

Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND)

Genome-Wide Association of Copy Number Polymorphisms and Kidney Function

Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes.

Genome-wide association and functional follow-up reveals new loci for kidney function

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 association study of PR interval

Genome-wide association study of kidney function decline in individuals of European descent

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

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

MYH9 is associated with nondiabetic end-stage renal disease in African Americans

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

Multiple loci associated with indices of renal function and chronic kidney disease

NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

New loci associated with kidney function and chronic kidney disease

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

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

The MYH9/APOL1 region and chronic kidney disease in European-Americans

The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization tool

The association between APOL1 risk alleles and longitudinal kidney function differs by HIV viral suppression status

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.

VARPRISM: incorporating variant prioritization in tests of de novo mutation association