Lista de obras - Martin Farrall - Dominio Público Uruguay

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 QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.

artículo científico publicado en 2007

A common LPA null allele associates with lower lipoprotein(a) levels and coronary artery disease risk.

artículo científico publicado en 2014

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

artículo científico publicado en 2015

A large-scale, consortium-based genomewide association study of asthma

artículo científico publicado en 2010

A mouse-to-man candidate gene study identifies association of chronic otitis media with the loci TGIF1 and FBXO11

artículo científico publicado en 2017

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

A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

artículo científico publicado en 2016

A quantitative trait locus for SBP maps near KCNB1 and PTGIS in a population isolate

artículo científico publicado en 2009

A rare variant of the leptin gene has large effects on blood pressure and carotid intima-medial thickness: a study of 1428 individuals in 248 families.

artículo científico publicado en 2005

Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis

artículo científico publicado en 2016

Ambulatory blood pressure is associated with polymorphic variation in P2X receptor genes.

artículo científico publicado en 2008

Analysis of 14 Candidate Genes for Diabetic Nephropathy on Chromosome 3q in European Populations: Strongest Evidence for Association With a Variant in the Promoter Region of the Adiponectin Gene

article

Analysis of 51 proposed hypertrophic cardiomyopathy genes from genome sequencing data in sarcomere negative cases has negligible diagnostic yield

article

Angiotensin-1-converting enzyme (ACE) plasma concentration is influenced by multiple ACE-linked quantitative trait nucleotides

artículo científico publicado en 2002

Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism

artículo científico publicado en 2012

Aryl hydrocarbon receptor nuclear translocator-like (BMAL1) is associated with susceptibility to hypertension and type 2 diabetes

artículo científico publicado en 2007

Association between Aldosterone Production and Variation in the 11β-Hydroxylase (CYP11B1) Gene

article

Association between Angiotensin-Converting Enzyme Gene Polymorphisms and Diabetic Nephropathy: Case-Control, Haplotype, and Family-Based Study in Three European Populations

article

Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls

scientific article published on 22 July 2013

Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data

artículo científico publicado en 2014

Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: a family study.

artículo científico publicado en 2005

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 scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

artículo científico publicado en 2007

Blood pressure loci identified with a gene-centric array

artículo científico publicado en 2011

Cardiovascular twist to the rapidly evolving apolipoprotein L1 story.

artículo científico publicado en 2014

Chromosome 2p Shows Significant Linkage to Antihypertensive Response in the British Genetics of Hypertension Study

article

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

artículo científico publicado en 2016

Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies

artículo científico publicado en 2009

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

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

artículo científico publicado en 2014

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

artículo científico publicado en 2016

Differential Gene Expression in Macrophages From Human Atherosclerotic Plaques Shows Convergence on Pathways Implicated by Genome-Wide Association Study Risk Variants

article

Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals

artículo científico publicado en 2017

Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family

scientific article published on 27 March 2019

Distribution and medical impact of loss-of-function variants in the Finnish founder population

artículo científico publicado en 2014

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

Electrocardiographic measures of left ventricular hypertrophy show greater heritability than echocardiographic left ventricular mass

artículo científico publicado en 2002

Epistasis Between Type 2 Diabetes Susceptibility Loci on Chromosomes 1q21-25 and 10q23-26 in Northern Europeans

artículo científico publicado en 2006

Erratum: Measured haplotype analysis of the aldosterone synthase gene and heart size

artículo científico publicado en 2005

European rational approach for the genetics of diabetic complications--EURAGEDIC: patient populations and strategy

artículo científico publicado en 2008

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

Functional annotations of diabetes nephropathy susceptibility loci through analysis of genome-wide renal gene expression in rat models of diabetes mellitus

artículo científico publicado en 2009

G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetes

artículo científico publicado en 2008

Gearing up for genome-wide gene-association studies.

artículo científico publicado en 2005

Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia

artículo científico publicado en 2014

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

artículo científico publicado en 2014

Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease

artículo científico publicado en 2009

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 analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension

artículo científico publicado en 2007

Genetic evidence of assortative mating in humans

article

Genetic loci influencing kidney function and chronic kidney disease

artículo científico publicado en 2010

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies

artículo científico publicado en 2012

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

artículo científico publicado en 2015

Genetic susceptibility to coronary artery disease: from promise to progress.

artículo científico publicado en 2006

Genetic variants associated with Lp(a) lipoprotein level and coronary disease

artículo científico publicado en 2009

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

artículo científico publicado en 2011

Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma

artículo científico publicado en 2007

Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion.

artículo científico publicado en 2004

Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation

artículo científico publicado en 2009

Genetically determined height and coronary artery disease

artículo científico publicado en 2015

Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.

artículo científico publicado en 2017

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

artículo científico publicado en 2012

Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia

artículo científico publicado en 2008

Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

artículo científico publicado en 2011

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

artículo científico publicado en 2011

Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis

artículo científico publicado en 2012

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

artículo científico publicado en 2010

Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension

artículo científico publicado en 2010

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.

artículo científico publicado en 2013

Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension

artículo científico publicado en 2008

Genome-wide mapping of human loci for essential hypertension

artículo científico publicado en 2003

Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17

artículo científico publicado en 2006

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

scientific journal article

Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations

artículo científico publicado en 2009

Genotype at the -174G/C polymorphism of the interleukin-6 gene is associated with common carotid artery intimal-medial thickness: family study and meta-analysis.

artículo científico publicado en 2005

Global genetic architecture of an erythroid quantitative trait locus, HMIP-2

artículo científico publicado en 2014

Glutathione S-transferase polymorphisms may be associated with risk of oedematous severe childhood malnutrition.

artículo científico publicado en 2006

HLA has strongest association with IgA nephropathy in genome-wide analysis

artículo científico publicado en 2010

Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study

article

High-resolution genetic mapping of the ACE-linked QTL influencing circulating ACE activity

scientific article published on 01 September 2002

Hundreds of variants clustered in genomic loci and biological pathways affect human height

artículo científico publicado en 2010

Identification of the BCAR1-CFDP1-TMEM170A locus as a determinant of carotid intima-media thickness and coronary artery disease risk

artículo científico publicado en 2012

Identifying small-effect genetic associations overlooked by the conventional fixed-effect model in a large-scale meta-analysis of coronary artery disease

scientific article published on 01 January 2020

Identifying systematic heterogeneity patterns in genetic association meta-analysis studies.

artículo científico publicado en 2017

Impact of lipoprotein(a) levels and apolipoprotein(a) isoform size on risk of coronary heart disease

artículo científico publicado en 2014

Inactivating mutations in NPC1L1 and protection from coronary heart disease

artículo científico publicado en 2014

Increased Support for Linkage of a Novel Locus on Chromosome 5q13 for Essential Hypertension in the British Genetics of Hypertension Study

article

Integrating case-control and TDT studies

artículo científico publicado en 2005

Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults

artículo científico publicado en 2007

Interpreting gene-association studies

artículo científico publicado en 2005

Ischemic stroke is associated with the ABO locus: the EuroCLOT study

artículo científico publicado en 2013

Lack of genetic support for shared aetiology of Coronary Artery Disease and Late-onset Alzheimer's disease.

artículo científico publicado en 2018

Large scale association analysis identifies three susceptibility loci for coronary artery disease

artículo científico publicado en 2011

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

artículo científico publicado en 2012

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

artículo científico publicado en 2012

Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension

artículo científico publicado en 2006

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 mutations in APOC3, triglycerides, and coronary disease

artículo científico publicado en 2014

Marked variation in heritability estimates of left ventricular mass depending on modality of measurement

artículo científico publicado en 2019

Measured haplotype analysis of the aldosterone synthase gene and heart size.

artículo científico publicado en 2003

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

artículo científico publicado en 2010

Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations

artículo científico publicado en 2009

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

artículo científico publicado en 2010

Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions

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

article

Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.

artículo científico publicado en 2017

New genetic loci link adipose and insulin biology to body fat distribution

artículo científico publicado en 2015

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

Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.

artículo científico publicado en 2018

Novel genetic variants linked to coronary artery disease by genome-wide association are not associated with carotid artery intima-media thickness or intermediate risk phenotypes.

artículo científico publicado en 2008

Phenotypic consequences of variation across the aldosterone synthase and 11-beta hydroxylase locus in a hypertensive cohort: data from the MRC BRIGHT Study.

artículo científico publicado en 2007

Polymorphisms in genes involved in folate metabolism as risk factors for oedematous severe childhood malnutrition: a hypothesis-generating study.

artículo científico publicado en 2006

Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion

artículo científico publicado en 2009

Polymorphisms in type II SH2 domain-containing inositol 5-phosphatase (INPPL1, SHIP2) are associated with physiological abnormalities of the metabolic syndrome

artículo científico publicado en 2004

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

Quantitative Trait Genetic Linkage Analysis of Body Mass Index in Familial Coronary Artery Disease

artículo científico publicado en 2008

Quantitative variation in plasma angiotensin-I converting enzyme activity shows allelic heterogeneity in the ABO blood group locus

artículo científico publicado en 2013

Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.

artículo científico publicado en 2016

Reports of the death of the epistasis model are greatly exaggerated.

artículo científico publicado en 2003

SLC2A9 is a high-capacity urate transporter in humans

artículo científico publicado en 2008

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

scientific article published on 31 July 2013

Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies

artículo científico publicado en 2009

Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits

artículo científico publicado en 2013

Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants

artículo científico publicado en 2014

Sporadic—but Not Variant—Creutzfeldt-Jakob Disease Is Associated with Polymorphisms Upstream of PRNP Exon 1 ⬇️

artículo científico publicado el 5 de noviembre de 2001

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.

artículo científico publicado en 2007

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

artículo científico publicado en 2017

Targeting 160 candidate genes for blood pressure regulation with a genome-wide genotyping array

artículo científico publicado en 2009

The C-532T polymorphism of the angiotensinogen gene is associated with pulse pressure: a possible explanation for heterogeneity in genetic association studies of AGT and hypertension

artículo científico publicado en 2007

The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humans.

artículo científico publicado en 2007

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 genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

artículo científico publicado en 2016

Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour ⬇️

artículo científico publicado el 29 de agosto de 2011

Trans-ethnic association study of blood pressure determinants in over 750,000 individuals

scientific article published on 21 December 2018

Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension

article

Using eQTL weights to improve power for genome-wide association studies: a genetic study of childhood asthma.

artículo científico publicado en 2013

Vitamin D levels and susceptibility to asthma, elevated immunoglobulin E levels, and atopic dermatitis: A Mendelian randomization study.

artículo científico publicado en 2017

Lista de obras de Martin Farrall

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

A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.

A common LPA null allele associates with lower lipoprotein(a) levels and coronary artery disease risk.

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

A large-scale, consortium-based genomewide association study of asthma

A mouse-to-man candidate gene study identifies association of chronic otitis media with the loci TGIF1 and FBXO11

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

A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape

A quantitative trait locus for SBP maps near KCNB1 and PTGIS in a population isolate

A rare variant of the leptin gene has large effects on blood pressure and carotid intima-medial thickness: a study of 1428 individuals in 248 families.

Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis

Ambulatory blood pressure is associated with polymorphic variation in P2X receptor genes.

Analysis of 14 Candidate Genes for Diabetic Nephropathy on Chromosome 3q in European Populations: Strongest Evidence for Association With a Variant in the Promoter Region of the Adiponectin Gene

Analysis of 51 proposed hypertrophic cardiomyopathy genes from genome sequencing data in sarcomere negative cases has negligible diagnostic yield

Angiotensin-1-converting enzyme (ACE) plasma concentration is influenced by multiple ACE-linked quantitative trait nucleotides

Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism

Aryl hydrocarbon receptor nuclear translocator-like (BMAL1) is associated with susceptibility to hypertension and type 2 diabetes

Association between Aldosterone Production and Variation in the 11β-Hydroxylase (CYP11B1) Gene

Association between Angiotensin-Converting Enzyme Gene Polymorphisms and Diabetic Nephropathy: Case-Control, Haplotype, and Family-Based Study in Three European Populations

Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls

Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data

Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: a family study.

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

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

Blood pressure loci identified with a gene-centric array

Cardiovascular twist to the rapidly evolving apolipoprotein L1 story.

Chromosome 2p Shows Significant Linkage to Antihypertensive Response in the British Genetics of Hypertension Study

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

Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies

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

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

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

Differential Gene Expression in Macrophages From Human Atherosclerotic Plaques Shows Convergence on Pathways Implicated by Genome-Wide Association Study Risk Variants

Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals

Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family

Distribution and medical impact of loss-of-function variants in the Finnish founder population

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

Electrocardiographic measures of left ventricular hypertrophy show greater heritability than echocardiographic left ventricular mass

Epistasis Between Type 2 Diabetes Susceptibility Loci on Chromosomes 1q21-25 and 10q23-26 in Northern Europeans

Erratum: Measured haplotype analysis of the aldosterone synthase gene and heart size

European rational approach for the genetics of diabetic complications--EURAGEDIC: patient populations and strategy

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

Functional annotations of diabetes nephropathy susceptibility loci through analysis of genome-wide renal gene expression in rat models of diabetes mellitus

G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetes

Gearing up for genome-wide gene-association studies.

Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia

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

Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease

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 analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension

Genetic evidence of assortative mating in humans

Genetic loci influencing kidney function and chronic kidney disease

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies

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

Genetic susceptibility to coronary artery disease: from promise to progress.

Genetic variants associated with Lp(a) lipoprotein level and coronary disease

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma

Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion.

Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation

Genetically determined height and coronary artery disease

Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia

Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure

Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.

Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension

Genome-wide mapping of human loci for essential hypertension

Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations

Genotype at the -174G/C polymorphism of the interleukin-6 gene is associated with common carotid artery intimal-medial thickness: family study and meta-analysis.

Global genetic architecture of an erythroid quantitative trait locus, HMIP-2