Lista de obras - Daniel Rader - Dominio Público Uruguay

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

artículo científico publicado en 2015

A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes

scientific article published on 06 August 2019

A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex

artículo científico publicado en 2012

A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease

artículo científico publicado en 2011

A genome-wide association study reveals variants in ARL15 that influence adiponectin levels

artículo científico publicado en 2009

A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium

artículo científico publicado en 2009

A naturally occurring variant of endothelial lipase associated with elevated HDL exhibits impaired synthesis

scientific article published on 03 May 2009

ANGPTL3 Deficiency and Protection Against Coronary Artery Disease

artículo científico publicado en 2017

Abnormal lipoprotein particles and cholesterol efflux capacity in patients with psoriasis

artículo científico publicado en 2012

Adipose modulation of high-density lipoprotein cholesterol: implications for obesity, high-density lipoprotein metabolism, and cardiovascular disease.

scientific article published on October 2011

An inflammatory cascade leading to hyperresistinemia in humans

artículo científico publicado en 2004

Antisense oligonucleotides for atherosclerotic disease

scientific article published on 06 April 2020

Apolipoprotein E and coronary disease: a puzzling paradox

artículo científico publicado en 2006

Apolipoprotein(a) isoform size, lipoprotein(a) concentration, and coronary artery disease: a mendelian randomisation analysis

artículo científico publicado en 2017

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

Association of the vitamin D metabolism gene CYP24A1 with coronary artery calcification

artículo científico publicado en 2010

Biological, clinical and population relevance of 95 loci for blood lipids

artículo científico publicado en 2010

C-Reactive Protein and Coronary Artery Calcification

artículo científico publicado en 2003

CRISPR/Cas9-Mediated Gene Editing in Human iPSC-Derived Macrophage Reveals Lysosomal Acid Lipase Function in Human Macrophages-Brief Report

artículo científico publicado en 2017

CXCL12: a new player in coronary disease identified through human genetics

artículo científico

CXCL16 is a marker of inflammation, atherosclerosis, and acute coronary syndromes in humans

artículo científico publicado en 2007

Candidate gene association resource (CARe): design, methods, and proof of concept

artículo científico publicado en 2010

Candidate gene association study of coronary artery calcification in chronic kidney disease: findings from the CRIC study (Chronic Renal Insufficiency Cohort).

artículo científico publicado en 2013

Causal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization Study

artículo científico publicado en 2016

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

artículo científico publicado en 2016

Common variants associated with plasma triglycerides and risk for coronary artery disease

artículo científico publicado en 2013

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

artículo científico publicado en 2010

Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer

artículo científico publicado en 2009

Comparison of Coronary Artery Calcium Scores Between Patients With Psoriasis and Type 2 Diabetes

artículo científico publicado en 2016

Comparison of high-density lipoprotein cholesterol to apolipoprotein A-I and A-II to predict coronary calcium and the effect of insulin resistance

artículo científico publicado en 2011

Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies

artículo científico publicado en 2008

Coronary artery calcification and cardiovascular risk factors: impact of the analytic approach

artículo científico publicado en 2004

Correcting population stratification in genetic association studies using a phylogenetic approach

artículo científico publicado en 2010

Deep RNA Sequencing Uncovers a Repertoire of Human Macrophage Long Intergenic Noncoding RNAs Modulated by Macrophage Activation and Associated With Cardiometabolic Diseases

artículo científico publicado en 2017

Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol

artículo científico publicado en 2011

Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls

artículo científico publicado en 2010

Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia

artículo científico publicado en 2016

Differential association of plasma angiopoietin-like proteins 3 and 4 with lipid and metabolic traits

artículo científico publicado en 2014

Discovery and refinement of loci associated with lipid levels

artículo científico publicado en 2013

Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis

artículo científico publicado en 2020

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

article by Matthew B. Lanktree et al published June 2012 in American Journal of Human Genetics

Effects of Niacin, Statin, and Fenofibrate on Circulating Proprotein Convertase Subtilisin/Kexin Type 9 Levels in Patients With Dyslipidemia

artículo científico publicado en 2014

Effects of pioglitazone on lipoproteins, inflammatory markers, and adipokines in nondiabetic patients with metabolic syndrome

artículo científico publicado en 2005

Endothelial lipase concentrations are increased in metabolic syndrome and associated with coronary atherosclerosis

artículo científico publicado en 2005

Endothelial lipase is increased in vivo by inflammation in humans

artículo científico publicado en 2008

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

artículo científico publicado en 2017

Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia

artículo científico publicado en 2013

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

artículo científico publicado en 2014

Exome sequencing in suspected monogenic dyslipidemias

artículo científico publicado en 2015

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

artículo científico publicado en 2017

Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms

artículo científico publicado en 2017

From Loci to Biology: Functional Genomics of Genome-Wide Association for Coronary Disease

artículo científico publicado en 2016

From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus

artículo científico publicado en 2010

Functional analysis and transcriptomic profiling of iPSC-derived macrophages and their application in modeling Mendelian disease

artículo científico publicado en 2015

Gender differences in the association of C-reactive protein with coronary artery calcium in type-2 diabetes

artículo científico publicado en 2011

Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci

artículo científico publicado en 2014

Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations

artículo científico publicado en 2012

Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease

artículo científico publicado en 2016

Genetic analysis for a shared biological basis between migraine and coronary artery disease

artículo científico publicado en 2015

Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease

artículo científico publicado en 2017

Genetic basis of atherosclerosis: insights from mice and humans

artículo científico publicado en 2012

Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes.

artículo científico publicado en 2018

Genetic variants influencing circulating lipid levels and risk of coronary artery disease

artículo científico publicado en 2010

Genetically Determined Birthweight Associates with Atrial Fibrillation: A Mendelian Randomization Study

scientific article published on 27 April 2020

Genetics of height and risk of atrial fibrillation: A Mendelian randomization study

artículo científico publicado en 2020

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

scientific journal article

Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project

artículo científico publicado en 2011

Genomic profiling of human vascular cells identifies TWIST1 as a causal gene for common vascular diseases

scientific article published on 09 January 2020

GlycA Is a Novel Biomarker of Inflammation and Subclinical Cardiovascular Disease in Psoriasis.

artículo científico publicado en 2016

Hepatic protein phosphatase 1 regulatory subunit 3B (Ppp1r3b) promotes hepatic glycogen synthesis and thereby regulates fasting energy homeostasis.

artículo científico publicado en 2017

Higher order lipase gene association with plasma triglycerides

article

Higher plasma CXCL12 levels predict incident myocardial infarction and death in chronic kidney disease: findings from the Chronic Renal Insufficiency Cohort study

artículo científico publicado en 2013

Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity

artículo científico publicado en 2017

Human knockouts in a cohort with a high rate of consanguinity

Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies

artículo científico publicado en 2011

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

artículo científico publicado en 2017

Impact of natural selection on global patterns of genetic variation and association with clinical phenotypes at genes involved in SARS-CoV-2 infection

artículo científico publicado en 2022

Implementing Genomic Medicine in the Clinic

Implementing genomic medicine in the clinic: the future is here

artículo científico publicado en 2013

Inactivating mutations in NPC1L1 and protection from coronary heart disease

artículo científico publicado en 2014

Inflammation induces fibrinogen nitration in experimental human endotoxemia

artículo científico publicado en 2009

Interleukin-6 receptor pathways in coronary heart disease: a collaborative meta-analysis of 82 studies

artículo científico publicado en 2012

Knockout of Adamts7, a novel coronary artery disease locus in humans, reduces atherosclerosis in mice

artículo científico publicado en 2015

Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies

artículo científico publicado en 2010

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 identifies 13 new susceptibility loci for coronary artery disease

artículo científico publicado en 2011

Large-scale association analysis identifies new risk loci for coronary artery disease

artículo científico publicado en 2012

Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci

artículo científico publicado en 2012

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

artículo científico publicado en 2012

Limitations of Contemporary Guidelines for Managing Patients at High Genetic Risk of Coronary Artery Disease

scientific article published on 01 June 2020

Lipoprotein(a) and Risk of Myocardial Infarction and Death in Chronic Kidney Disease: Findings From the CRIC Study (Chronic Renal Insufficiency Cohort).

artículo científico

Loci influencing blood pressure identified using a cardiovascular gene-centric array

artículo científico publicado en 2013

Loci influencing blood pressure identified using a cardiovascular gene-centric array.

artículo científico publicado en 2013

Loss of Cardioprotective Effects at the ADAMTS7 Locus as a Result of Gene-Smoking Interactions

artículo científico publicado en 2017

Loss-of-function variants in endothelial lipase are a cause of elevated HDL cholesterol in humans

artículo científico publicado en 2009

Measurement of waist circumference predicts coronary atherosclerosis beyond plasma adipokines

article

Measures of insulin resistance add incremental value to the clinical diagnosis of metabolic syndrome in association with coronary atherosclerosis

artículo científico publicado en 2004

Meta-analysis and imputation refines the association of 15q25 with smoking quantity

artículo científico publicado en 2010

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

artículo científico publicado en 2010

Metabolic syndrome, components, and cardiovascular disease prevalence in chronic kidney disease: findings from the Chronic Renal Insufficiency Cohort (CRIC) Study

artículo científico publicado en 2011

Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project

artículo científico publicado en 2012

Multi-ethnic genome-wide association study for atrial fibrillation

article

Multiethnic Exome-Wide Association Study of Subclinical Atherosclerosis.

artículo científico publicado en 2016

Myeloid Tribbles 1 induces early atherosclerosis via enhanced foam cell expansion

artículo científico publicado en 2019

NARC-1/PCSK9 and its natural mutants: zymogen cleavage and effects on the low density lipoprotein (LDL) receptor and LDL cholesterol

artículo científico publicado en 2004

NHLBI Working Group Recommendations to Reduce Lipoprotein(a)-Mediated Risk of Cardiovascular Disease and Aortic Stenosis

artículo científico publicado en 2018

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

Overexpression of apolipoprotein A-I promotes reverse transport of cholesterol from macrophages to feces in vivo

artículo científico publicado en 2003

Pathway-Wide Association Study Implicates Multiple Sterol Transport and Metabolism Genes in HDL Cholesterol Regulation.

artículo científico publicado en 2011

Pharmacological activation of liver X receptors promotes reverse cholesterol transport in vivo

artículo científico publicado en 2005

Phenome-wide association analysis suggests the APOL1 linked disease spectrum primarily drives kidney-specific pathways

scientific article published on 17 February 2020

Phenotypic extremes in rare variant study designs

artículo científico publicado en 2015

Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study

artículo científico publicado en 2012

Plasma Leptin Levels Are Associated with Coronary Atherosclerosis in Type 2 Diabetes

scientific article published on 01 August 2004

Plasma apolipoprotein C-III levels, triglycerides, and coronary artery calcification in type 2 diabetics

artículo científico publicado en 2015

Plasma cytokines, metabolic syndrome, and atherosclerosis in humans.

artículo científico publicado en 2007

Rare variant in scavenger receptor BI raises HDL cholesterol and increases risk of coronary heart disease

scientific journal article

Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution

article

Relationship of estimated GFR and coronary artery calcification in the CRIC (Chronic Renal Insufficiency Cohort) Study

artículo científico publicado en 2011

Resistin gene variation is associated with systemic inflammation but not plasma adipokine levels, metabolic syndrome or coronary atherosclerosis in nondiabetic Caucasians

artículo científico publicado en 2008

Resistin is an inflammatory marker of atherosclerosis in humans.

artículo científico publicado en 2005

Secretory phospholipase A(2)-IIA and cardiovascular disease: a mendelian randomization study

scientific article published on 31 July 2013

Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

artículo científico publicado en 2009

Serum Fractalkine (CX3CL1) and Cardiovascular Outcomes and Diabetes: Findings From the Chronic Renal Insufficiency Cohort (CRIC) Study

artículo científico publicado en 2015

Strong synaptic transmission impact by copy number variations in schizophrenia

artículo científico publicado en 2010

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

artículo científico publicado en 2017

Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarction

artículo científico publicado en 2015

The addition of niacin to statin therapy improves high-density lipoprotein cholesterol levels but not metrics of functionality

artículo científico publicado en 2013

The complexity of ABO in coronary heart disease – Authors' reply

artículo científico publicado en 2011

The influence of pravastatin and atorvastatin on markers of oxidative stress in hypercholesterolemic humans

artículo científico publicado en 2008

The metabolic syndrome: more than the sum of its parts?

artículo científico publicado en 2003

The novel atherosclerosis locus at 10q11 regulates plasma CXCL12 levels

artículo científico publicado en 2011

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

article

Transcriptome-Wide Analysis Reveals Modulation of Human Macrophage Inflammatory Phenotype Through Alternative Splicing

artículo científico publicado en 2016

Translational studies of lipoprotein-associated phospholipase A₂ in inflammation and atherosclerosis

artículo científico publicado en 2012

Two variants on chromosome 17 confer prostate cancer risk and the one in TCF2 protects against type 2 diabetes

article

Usefulness of insulin resistance estimation and the metabolic syndrome in predicting coronary atherosclerosis in type 2 diabetes mellitus

artículo científico publicado en 2011

Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease

artículo científico publicado en 2016

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

artículo científico publicado en 2006

Web of Science’s Citation Median Metrics Overcome the Major Constraints of the Journal Impact Factor

artículo científico publicado en 2022

Lista de obras de Daniel Rader

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

A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes

A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex

A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease

A genome-wide association study reveals variants in ARL15 that influence adiponectin levels

A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium

A naturally occurring variant of endothelial lipase associated with elevated HDL exhibits impaired synthesis

ANGPTL3 Deficiency and Protection Against Coronary Artery Disease

Abnormal lipoprotein particles and cholesterol efflux capacity in patients with psoriasis

Adipose modulation of high-density lipoprotein cholesterol: implications for obesity, high-density lipoprotein metabolism, and cardiovascular disease.

An inflammatory cascade leading to hyperresistinemia in humans

Antisense oligonucleotides for atherosclerotic disease

Apolipoprotein E and coronary disease: a puzzling paradox

Apolipoprotein(a) isoform size, lipoprotein(a) concentration, and coronary artery disease: a mendelian randomisation analysis

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

Association of the vitamin D metabolism gene CYP24A1 with coronary artery calcification

Biological, clinical and population relevance of 95 loci for blood lipids

C-Reactive Protein and Coronary Artery Calcification

CRISPR/Cas9-Mediated Gene Editing in Human iPSC-Derived Macrophage Reveals Lysosomal Acid Lipase Function in Human Macrophages-Brief Report

CXCL12: a new player in coronary disease identified through human genetics

CXCL16 is a marker of inflammation, atherosclerosis, and acute coronary syndromes in humans

Candidate gene association resource (CARe): design, methods, and proof of concept

Candidate gene association study of coronary artery calcification in chronic kidney disease: findings from the CRIC study (Chronic Renal Insufficiency Cohort).

Causal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization Study

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

Common variants associated with plasma triglycerides and risk for coronary artery disease

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

Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer

Comparison of Coronary Artery Calcium Scores Between Patients With Psoriasis and Type 2 Diabetes

Comparison of high-density lipoprotein cholesterol to apolipoprotein A-I and A-II to predict coronary calcium and the effect of insulin resistance

Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies

Coronary artery calcification and cardiovascular risk factors: impact of the analytic approach

Correcting population stratification in genetic association studies using a phylogenetic approach

Deep RNA Sequencing Uncovers a Repertoire of Human Macrophage Long Intergenic Noncoding RNAs Modulated by Macrophage Activation and Associated With Cardiometabolic Diseases

Dense genotyping of candidate gene loci identifies variants associated with high-density lipoprotein cholesterol

Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls

Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia

Differential association of plasma angiopoietin-like proteins 3 and 4 with lipid and metabolic traits

Discovery and refinement of loci associated with lipid levels

Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

Effects of Niacin, Statin, and Fenofibrate on Circulating Proprotein Convertase Subtilisin/Kexin Type 9 Levels in Patients With Dyslipidemia

Effects of pioglitazone on lipoproteins, inflammatory markers, and adipokines in nondiabetic patients with metabolic syndrome

Endothelial lipase concentrations are increased in metabolic syndrome and associated with coronary atherosclerosis

Endothelial lipase is increased in vivo by inflammation in humans

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

Exome sequencing and directed clinical phenotyping diagnose cholesterol ester storage disease presenting as autosomal recessive hypercholesterolemia

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

Exome sequencing in suspected monogenic dyslipidemias

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

Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms

From Loci to Biology: Functional Genomics of Genome-Wide Association for Coronary Disease

From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus

Functional analysis and transcriptomic profiling of iPSC-derived macrophages and their application in modeling Mendelian disease

Gender differences in the association of C-reactive protein with coronary artery calcium in type-2 diabetes

Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci

Gene-centric meta-analysis of lipid traits in African, East Asian and Hispanic populations

Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease

Genetic analysis for a shared biological basis between migraine and coronary artery disease

Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease

Genetic basis of atherosclerosis: insights from mice and humans

Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes.

Genetic variants influencing circulating lipid levels and risk of coronary artery disease

Genetically Determined Birthweight Associates with Atrial Fibrillation: A Mendelian Randomization Study

Genetics of height and risk of atrial fibrillation: A Mendelian randomization study

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project

Genomic profiling of human vascular cells identifies TWIST1 as a causal gene for common vascular diseases

GlycA Is a Novel Biomarker of Inflammation and Subclinical Cardiovascular Disease in Psoriasis.

Hepatic protein phosphatase 1 regulatory subunit 3B (Ppp1r3b) promotes hepatic glycogen synthesis and thereby regulates fasting energy homeostasis.

Higher order lipase gene association with plasma triglycerides

Higher plasma CXCL12 levels predict incident myocardial infarction and death in chronic kidney disease: findings from the Chronic Renal Insufficiency Cohort study

Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity

Human knockouts in a cohort with a high rate of consanguinity

Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies

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

Impact of natural selection on global patterns of genetic variation and association with clinical phenotypes at genes involved in SARS-CoV-2 infection

Implementing Genomic Medicine in the Clinic

Implementing genomic medicine in the clinic: the future is here