List of works - Martin Farrall

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

scientific article

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

scientific article published on 6 October 2011

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 02 December 2012

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

scientific article (publication date: 26 July 2007)

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article published in December 2009

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

scientific article

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

scientific article published in June 2009

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

scientific article published on 18 June 2014

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

scientific journal article

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 5 October 2012

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

scientific article published on 16 October 2011

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

scientific article

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

scientific article

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

scientific article published on 17 August 2016

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

scientific article

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

scientific article

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

scholarly article

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

scientific article

Genetic loci influencing kidney function and chronic kidney disease

scientific article

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

scientific article published on 30 January 2017

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

scientific article published on 2 March 2016

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

scientific article

SLC2A9 is a high-capacity urate transporter in humans

scientific article

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

scientific article

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

scientific article published on 12 September 2016

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

scientific article

Inactivating mutations in NPC1L1 and protection from coronary heart disease

scientific article

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

scientific article

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

scientific article

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

scientific article published on 20 March 2009

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

scientific article

Genome-wide mapping of human loci for essential hypertension

scientific article

Genetically determined height and coronary artery disease

scientific article

Integrating case-control and TDT studies

scientific article published on 01 May 2005

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

scientific article published on 26 May 2013

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

scientific article

List of works by Martin Farrall

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Genetic loci influencing kidney function and chronic kidney disease

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

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

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

SLC2A9 is a high-capacity urate transporter in humans

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

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

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

Inactivating mutations in NPC1L1 and protection from coronary heart disease

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

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

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

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

Genome-wide mapping of human loci for essential hypertension

Genetically determined height and coronary artery disease

Integrating case-control and TDT studies

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

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