Lista de obras -

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

artículo científico publicado en 2017

A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

artículo científico publicado en 2018

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

scientific article published on 31 May 2019

A collaborative approach to developing an electronic health record phenotyping algorithm for drug-induced liver injury

artículo científico publicado en 2013

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

artículo científico publicado en 2015

A conceptual model for translating omic data into clinical action

artículo científico publicado en 2015

A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry

artículo científico publicado en 2013

A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

scientific article published on 10 April 2019

AKI in hospitalized patients with COVID-19

artículo científico publicado en 2020

An Empirical Comparison of Joint and Stratified Frameworks for Studying G × E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene-Lifestyle Interactions Working Group

artículo científico publicado en 2016

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

artículo científico publicado en 2017

Analytical Validation of a Personalized Medicine APOL1 Genotyping Assay for Nondiabetic Chronic Kidney Disease Risk Assessment

artículo científico publicado en 2016

Apolipoprotein L1 Variants and Blood Pressure Traits in African Americans

artículo científico publicado en 2017

Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans

artículo científico publicado en 2013

Association analyses based on false discovery rate implicate new loci for coronary artery disease ⬇️

artículo científico

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records

artículo científico publicado en 2016

Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian Randomization

artículo científico publicado en 2020

Association of SARS-CoV-2 viral load at admission with in-hospital acute kidney injury: A retrospective cohort study

artículo científico publicado en 2021

Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks

artículo científico publicado en 2014

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

BAMBI Is Expressed in Endothelial Cells and Is Regulated by Lysosomal/Autolysosomal Degradation ⬇️

artículo científico publicado el 24 de septiembre de 2010

BAMBI regulates angiogenesis and endothelial homeostasis through modulation of alternative TGFβ signaling

artículo científico publicado en 2012

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

artículo científico publicado en 2017

Can genetic pleiotropy replicate common clinical constellations of cardiovascular disease and risk?

artículo científico publicado en 2012

Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease

artículo científico publicado en 2016

Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.

artículo científico publicado en 2018

Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

artículo científico publicado en 2016

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

artículo científico publicado en 2017

Crossing the omic chasm: a time for omic ancillary systems

artículo científico publicado en 2013

Defective fatty acid oxidation in renal tubular epithelial cells has a key role in kidney fibrosis development

artículo científico publicado en 2014

Defining the role of common variation in the genomic and biological architecture of adult human height

artículo científico publicado en 2014

Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public

artículo científico publicado en 2015

Development and validation of an electronic phenotyping algorithm for chronic kidney disease

artículo científico publicado en 2014

Digital Therapeutic Care Apps With Decision-Support Interventions for People With Low Back Pain in Germany: Cost-Effectiveness Analysis

artículo científico publicado en 2022

Digital Therapeutic Care and Decision Support Interventions for People With Low Back Pain: Systematic Review

artículo científico publicado en 2021

Directional dominance on stature and cognition in diverse human populations

artículo científico publicado en 2015

Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.

artículo científico publicado en 2017

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

artículo científico publicado en 2020

Disease progression subtype discovery from longitudinal EMR data with a majority of missing values and unknown initial time points

artículo científico publicado en 2014

Effect of Genetic African Ancestry on eGFR and Kidney Disease

artículo científico publicado en 2014

Endothelial mitochondrial oxidative stress determines podocyte depletion in segmental glomerulosclerosis

artículo científico

Epithelial Cell TGFβ Signaling Induces Acute Tubular Injury and Interstitial Inflammation ⬇️

artículo científico publicado el 28 de marzo de 2013

Erratum to: Genetic variation in APOL1 and MYH9 genes is associated with chronic kidney disease among Nigerians

artículo científico publicado en 2014

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

artículo científico publicado en 2017

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

artículo científico publicado en 2018

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

artículo científico publicado en 2016

Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

article by Jason Flannick et al published 22 May 2019 in Nature

Exome-wide association study of plasma lipids in >300,000 individuals

artículo científico publicado en 2017

Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci

artículo científico publicado en 2016

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

artículo científico publicado en 2018

Genetic Diversity Turns a New PAGE in Our Understanding of Complex Traits

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scientific article published on 17 September 2018

Genetic analysis of over one million people identifies 535 novel loci for blood pressure

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

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 background of patients from a university medical center in Manhattan: implications for personalized medicine

artículo científico publicado en 2011

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

artículo científico publicado en 2015

Genetic studies of body mass index yield new insights for obesity biology

artículo científico publicado en 2015

Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network

artículo científico publicado en 2016

Genetic variation in APOL1 and MYH9 genes is associated with chronic kidney disease among Nigerians

artículo científico publicado en 2012

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

artículo científico publicado en 2018

Genome-Wide Association of CKD Progression: The Chronic Renal Insufficiency Cohort Study

artículo científico publicado en 2016

Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development

artículo científico publicado en 2017

Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets

artículo científico publicado en 2017

Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations

artículo científico publicado en 2013

Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network

artículo científico publicado en 2013

Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.

artículo científico publicado en 2017

Genome-wide molecular profiles of HCV-induced dysplasia and hepatocellular carcinoma

artículo científico publicado en 2007

Genome-wide study of resistant hypertension identified from electronic health records

artículo científico publicado en 2017

HGF upregulation contributes to angiogenesis in mice with keratinocyte-specific Smad2 deletion ⬇️

artículo científico publicado el 13 de septiembre de 2010

HGF upregulation contributes to angiogenesis in mice withkeratinocyte-specific Smad2 deletion

artículo científico publicado en 2013

Human and murine kidneys show gender- and species-specific gene expression differences in response to injury

artículo científico publicado en 2009

Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease

artículo científico publicado en 2017

Identification of type 2 diabetes subgroups through topological analysis of patient similarity

artículo científico publicado en 2015

Identification of unique venous thromboembolism-susceptibility variants in African-Americans

artículo científico publicado en 2017

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

Implementing Genomic Medicine in the Clinic

Implementing genomic medicine in the clinic: the future is here

artículo científico publicado en 2013

Incorporating temporal EHR data in predictive models for risk stratification of renal function deterioration

artículo científico publicado en 2014

Inducing and Recording Acute Stress Responses on a Large Scale With the Digital Stress Test (DST): Development and Evaluation Study

artículo científico publicado en 2022

Institutional profile: translational pharmacogenomics at the Icahn School of Medicine at Mount Sinai

artículo científico publicado en 2017

Keratinocyte-specific Smad2 ablation results in increased epithelial-mesenchymal transition during skin cancer formation and progression

artículo científico publicado en 2008

Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases

artículo científico publicado en 2016

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

artículo científico publicado en 2017

Loss-of-function mutations in APOC3, triglycerides, and coronary disease

artículo científico publicado en 2014

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

artículo científico publicado en 2015

Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci ⬇️

artículo científico publicado en 2016

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

artículo científico publicado en 2016

Meta-analysis of correlated traits via summary statistics from GWASs with an application in hypertension

artículo científico publicado en 2014

Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes

artículo científico publicado en 2014

Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs

artículo científico publicado en 2016

Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline

artículo científico publicado en 2020

Microvascular endothelial cells poised to take center stage in experimental renal fibrosis

artículo científico publicado en 2014

Mouse models of diabetic nephropathy

artículo científico publicado en 2009

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

scientific article published on 21 May 2020

Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids

article

Multi-ethnic genome-wide association study for atrial fibrillation

article

No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis ⬇️

scientific article published on 12 October 2016

Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney

artículo científico publicado en 2017

Opportunities for genomic clinical decision support interventions

artículo científico publicado en 2013

PROTEIN-CODING VARIANTS IMPLICATE NOVEL GENES RELATED TO LIPID HOMEOSTASIS CONTRIBUTING TO BODY FAT DISTRIBUTION

article

Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network

artículo científico publicado en 2015

Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index

artículo científico publicado en 2014

Physician Attitudes toward Adopting Genome-Guided Prescribing through Clinical Decision Support

artículo científico publicado en 2014

Plasma biomarkers are associated with renal outcomes in individuals with APOL1 risk variants

artículo científico publicado en 2018

Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

artículo científico publicado en 2016

Podocyte-selective deletion of dicer induces proteinuria and glomerulosclerosis

artículo científico publicado en 2008

Practical considerations in genomic decision support: The eMERGE experience

artículo científico publicado en 2015

Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valve

artículo científico publicado en 2017

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2017

Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution

article

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

scholarly article published in Nature Genetics

Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

erratum

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2018

Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

artículo científico publicado en 2019

Rare and low-frequency coding variants alter human adult height

artículo científico publicado en 2017

Refining The Accuracy Of Validated Target Identification Through Coding Variant Fine-Mapping In Type 2 Diabetes

article

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

artículo científico publicado en 2018

Return of results in the genomic medicine projects of the eMERGE network

artículo científico publicado en 2014

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

artículo científico publicado en 2016

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

artículo científico publicado en 2017

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

artículo científico publicado en 2016

Smad2-dependent downregulation of miR-30 is required for TGF-β-induced apoptosis in podocytes

artículo científico publicado en 2013

StudyU: A Platform for Designing and Conducting Innovative Digital N-of-1 Trials

scientific article published in 2022

Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease ⬇️

artículo científico publicado en 2017

TGFβ-Induced Actin Cytoskeleton Rearrangement in Podocytes Is Associated with Compensatory Adaptation of Mitochondrial Energy Metabolism

artículo científico publicado en 2015

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

artículo científico publicado en 2019

Testing the role of predicted gene knockouts in human anthropometric trait variation

artículo científico publicado en 2016

The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future ⬇️

artículo científico publicado el 6 de junio de 2013

The IGNITE network: a model for genomic medicine implementation and research

artículo científico publicado en 2016

The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

artículo científico publicado en 2015

The genetic architecture of type 2 diabetes

artículo científico publicado en 2016

The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis

artículo científico publicado en 2018

The phenotypic legacy of admixture between modern humans and Neandertals

artículo científico publicado en 2016

Trans-ethnic Evaluation Identifies Novel Low Frequency Loci Associated with 25-Hydroxyvitamin D Concentrations.

artículo científico publicado en 2018

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

artículo científico publicado en 2016

Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI.

artículo científico publicado en 2017

Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci

artículo científico publicado en 2017

Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies

artículo científico publicado en 2019

Transforming Growth Factor-β, Bioenergetics, and Mitochondria in Renal Disease ⬇️

artículo científico publicado el 1 de mayo de 2012

Utility of endogenous creatinine clearance as a measure of renal function in mice

artículo científico publicado en 2004

Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans

artículo científico publicado en 2016

Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol

artículo científico publicado en 2014

X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome

artículo científico publicado en 2015

iGAS: A framework for using electronic intraoperative medical records for genomic discovery

artículo científico publicado en 2017

Lista de obras de

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

A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure

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

A collaborative approach to developing an electronic health record phenotyping algorithm for drug-induced liver injury

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

A conceptual model for translating omic data into clinical action

A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry

A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

AKI in hospitalized patients with COVID-19

An Empirical Comparison of Joint and Stratified Frameworks for Studying G × E Interactions: Systolic Blood Pressure and Smoking in the CHARGE Gene-Lifestyle Interactions Working Group

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

Analytical Validation of a Personalized Medicine APOL1 Genotyping Assay for Nondiabetic Chronic Kidney Disease Risk Assessment

Apolipoprotein L1 Variants and Blood Pressure Traits in African Americans

Apolipoprotein L1 gene variants associate with hypertension-attributed nephropathy and the rate of kidney function decline in African Americans

Association analyses based on false discovery rate implicate new loci for coronary artery disease ⬇️

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records

Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian Randomization

Association of SARS-CoV-2 viral load at admission with in-hospital acute kidney injury: A retrospective cohort study

Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks

Associations of autozygosity with a broad range of human phenotypes

BAMBI Is Expressed in Endothelial Cells and Is Regulated by Lysosomal/Autolysosomal Degradation ⬇️

BAMBI regulates angiogenesis and endothelial homeostasis through modulation of alternative TGFβ signaling

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

Can genetic pleiotropy replicate common clinical constellations of cardiovascular disease and risk?

Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease

Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.

Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study

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

Crossing the omic chasm: a time for omic ancillary systems

Defective fatty acid oxidation in renal tubular epithelial cells has a key role in kidney fibrosis development

Defining the role of common variation in the genomic and biological architecture of adult human height

Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public

Development and validation of an electronic phenotyping algorithm for chronic kidney disease

Digital Therapeutic Care Apps With Decision-Support Interventions for People With Low Back Pain in Germany: Cost-Effectiveness Analysis

Digital Therapeutic Care and Decision Support Interventions for People With Low Back Pain: Systematic Review

Directional dominance on stature and cognition in diverse human populations

Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

Disease progression subtype discovery from longitudinal EMR data with a majority of missing values and unknown initial time points

Effect of Genetic African Ancestry on eGFR and Kidney Disease

Endothelial mitochondrial oxidative stress determines podocyte depletion in segmental glomerulosclerosis

Epithelial Cell TGFβ Signaling Induces Acute Tubular Injury and Interstitial Inflammation ⬇️

Erratum to: Genetic variation in APOL1 and MYH9 genes is associated with chronic kidney disease among Nigerians

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

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

Exome-wide association study of plasma lipids in >300,000 individuals

Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

Genetic Diversity Turns a New PAGE in Our Understanding of Complex Traits

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

Genetic analysis of over one million people identifies 535 novel loci for blood pressure

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

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

Genetic background of patients from a university medical center in Manhattan: implications for personalized medicine

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

Genetic studies of body mass index yield new insights for obesity biology

Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network

Genetic variation in APOL1 and MYH9 genes is associated with chronic kidney disease among Nigerians

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

Genome-Wide Association of CKD Progression: The Chronic Renal Insufficiency Cohort Study

Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development

Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets

Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations

Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network

Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.

Genome-wide molecular profiles of HCV-induced dysplasia and hepatocellular carcinoma

Genome-wide study of resistant hypertension identified from electronic health records

HGF upregulation contributes to angiogenesis in mice with keratinocyte-specific Smad2 deletion ⬇️

HGF upregulation contributes to angiogenesis in mice withkeratinocyte-specific Smad2 deletion

Human and murine kidneys show gender- and species-specific gene expression differences in response to injury

Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease

Identification of type 2 diabetes subgroups through topological analysis of patient similarity

Identification of unique venous thromboembolism-susceptibility variants in African-Americans

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.

Implementing Genomic Medicine in the Clinic

Implementing genomic medicine in the clinic: the future is here