B. Keavney

P. Serruys, D. Rana, B. Keavney, 2016, EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology.

A Patient-Specific CFD Pipeline Using Doppler Echocardiography for Application in Coarctation of the Aorta in a Limited Resource Clinical Context

L. Zühlke, B. Keavney, A. Revell, 2020, Frontiers in Bioengineering and Biotechnology.

Defining the Normal Spectrum of Electrocardiographic and Left Ventricular Adaptations in Mixed-Race Male Adolescent Soccer Players.

B. Keavney, D. Oxborough, M. Papadakis, 2021, Circulation.

Local vessel injury following percutaneous coronary intervention does not promote early mobilisation of endothelial progenitor cells in the absence of myocardial necrosis

B. Keavney, A. Zaman, J. Ahmed, 2008, Heart.

Plasma fibrinogen and fibrinogen genotypes in 4685 cases of myocardial infarction and in 6002 controls: Test of causality by "Mendelian randomisation"

Sarah Parish, John Danesh, Marc Delepine, 2000 .

Large-scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls

Sarah Parish, Bernard Keavney, Sarah Clark, 1999, The Lancet.

Atrial fibrillation associated with ivabradine treatment: meta-analysis of randomised controlled trials

J. Bourke, B. Keavney, M. Teare, 2014, Heart.

Circulating endothelial progenitor cell numbers are not associated with donor organ age or allograft vasculopathy in cardiac transplant recipients.

B. Keavney, H. Arthur, G. Parry, 2009, Atherosclerosis.

Circulating endothelial progenitor cells exhibit diurnal variation.

B. Keavney, H. Arthur, P. Avery, 2008, Arteriosclerosis, thrombosis, and vascular biology.

Genetic Variants Associated With Myocardial Infarction Risk Factors in Over 8000 Individuals From Five Ethnic Groups: The INTERHEART Genetics Study

T. Hudson, S. Yusuf, A. Montpetit, 2009, Circulation. Cardiovascular genetics.

Impact of age on access site‐related outcomes in 469,983 percutaneous coronary intervention procedures: Insights from the British Cardiovascular Intervention Society

S. Anderson, B. Keavney, A. Zaman, 2015, Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions.

Seven haemostatic gene polymorphisms in coronary disease: meta-analysis of 66 155 cases and 91 307 controls

John Danesh, Bernard D Keavney, J. Danesh, 2006, The Lancet.

Significantly increased risk of chronic obstructive pulmonary disease amongst adults with predominantly mild congenital heart disease

J. Vestbo, B. Keavney, Stephanie L Baross, 2022, Scientific Reports.

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

P. O’Reilly, P. Elliott, D. Levy, 2017, Nature Genetics.

Data on cardiac lncRNA STX18-AS1 expression in developing human hearts and function during in vitro hESC-cardiomyocyte differentiation

B. Keavney, M. Choy, G. Black, 2022, Data in brief.

Fibrinogen and coronary heart disease: test of causality by 'Mendelian randomization'.

Sarah Parish, Bernard Keavney, John Danesh, 2006, International journal of epidemiology.

Toll the bell for another genetic association?

B. Keavney, 2006, European heart journal.

Exome sequencing identiﬁes GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deﬁciency

N. McGovern, M. Haniffa, B. Keavney, 2011 .

071 Concentric hypertrophic remodelling and subendocardial dysfunction in mitochondrial DNA point mutation carriers

Robert W. Taylor, D. Turnbull, A. Blamire, 2012, Heart.

Investigation of Copy Number Variation in South African Patients With Congenital Heart Defects

James M. Eales, L. Zühlke, B. Keavney, 2022, Circulation. Genomic and precision medicine.

Progress of 3D Organoid Technology for Preclinical Investigations: Towards Human In Vitro Models

X. Wang, B. Keavney, Yingjuan Liu, 2022, International Journal of Drug Discovery and Pharmacology.

Global prevalence of congenital heart disease in school-age children: a meta-analysis and systematic review

L. Zühlke, B. Keavney, M. Choy, 2020, BMC Cardiovascular Disorders.

J. Danesh, R. Collins, R. Peto, 2004, International journal of epidemiology.

Genetic epidemiological studies of coronary heart disease.

Bernard Keavney, B. Keavney, 2002, International journal of epidemiology.

The use of missing values in proteomic data-independent acquisition mass spectrometry to enable disease activity discrimination

Nophar Geifman, Arianna Dagliati, Davide Chiasserini, 2019, Bioinform..

Genetic variants associated with risk of atrial fibrillation regulate expression of PITX2, CAV1, MYOZ1, C9orf3 and FANCC.

B. Keavney, M. Choy, N. Yonan, 2015, Journal of molecular and cellular cardiology.

Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression

Bernard Keavney, John Burn, Bongani M. Mayosi, 2010, PLoS genetics.

Correction of Population Stratification in Large Multi-Ethnic Association Studies

Thomas J. Hudson, Bernard Keavney, Salim Yusuf, 2008, PloS one.

Common Variation Neighbouring Micro-RNA 22 Is Associated with Increased Left Ventricular Mass

Antony Rodriguez, A. Harper, B. Keavney, 2013, PloS one.

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing

Tomas W. Fitzgerald, G. J. Swaminathan, J. Danesh, 2016, Nature Genetics.

Exploring Shared Susceptibility between Two Neural Crest Cells Originating Conditions: Neuroblastoma and Congenital Heart Disease

M. Devoto, H. Cordell, J. Maris, 2019, Genes.

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

Andrew D. Johnson, Lorna M. Lopez, P. O’Reilly, 2017, Hypertension.

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

He Gao, Andres Metspalu, Fotios Drenos, 2017, Nature Genetics.

Association of cholesteryl ester transfer protein genotypes with CETP mass and activity, lipid levels, and coronary risk.

J. Danesh, D. Saleheen, N. Sarwar, 2008, JAMA.

Association of Novel Locus With Rheumatic Heart Disease in Black African Individuals: Findings From the RHDGen Study.

A. Damasceno, L. Zühlke, H. Cordell, 2021, JAMA cardiology.

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

M Farrall, H Imrie, J. Connell, 2005, Journal of Medical Genetics.

STK39 polymorphisms and blood pressure: an association study in British Caucasians and assessment of cis-acting influences on gene expression

B. Keavney, B. Mayosi, P. Avery, 2009, BMC Medical Genetics.

Human Tra2 proteins jointly control a CHEK1 splicing switch among alternative and constitutive target exons

Anil Wipat, Tomaz Curk, Katherine James, 2014, Nature Communications.

Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot

Kathryn E. Hentges, Matthieu J. Miossec, G. Lathrop, 2019, Circulation research.

Deleterious genetic variants in NOTCH1 are a major contributor to the incidence of non-syndromic Tetralogy of Fallot

Kathryn E. Hentges, Matthieu J. Miossec, G. Bourque, 2018, bioRxiv.

Human Y Chromosome Exerts Pleiotropic Effects on Susceptibility to Atherosclerosis

James M. Eales, M. Jobling, N. Samani, 2019, Arteriosclerosis, thrombosis, and vascular biology.

Targeted Next‐Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability

Alessandra Renieri, Bernard Keavney, Michael Field, 2015, Human mutation.

Reproducibility of CRISPR-Cas9 methods for generation of conditional mouse alleles: a multi-center evaluation

Aidan R. O’Brien, W. R. Thompson, Kathryn E. Hentges, 2019, Genome Biology.

Re-Evaluating One-step Generation of Mice Carrying Conditional Alleles by CRISPR-Cas9-Mediated Genome Editing Technology

W. R. Thompson, Kathryn E. Hentges, A. Loudon, 2018, bioRxiv.

Response to correspondence on “Reproducibility of CRISPR-Cas9 methods for generation of conditional mouse alleles: a multi-center evaluation”

Aidan R. O’Brien, W. R. Thompson, A. Loudon, 2021, Genome biology.

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

J. Connell, M. Farrall, H. Watkins, 2005, Diabetes.

Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries

M. Nóbrega, T. Meitinger, M. Lathrop, 2021, Circulation research.

Positional mapping of PRKD1, NRP1 and PRDM1 as novel candidate disease genes in truncus arteriosus

F. Alkuraya, B. Keavney, J. Goodship, 2015, Journal of Medical Genetics.

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls

M. Hurles, K. Devriendt, M. Lathrop, 2011, Human molecular genetics.

Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults

Shu Ye, Frank Dudbridge, Harry Hemingway, 2018, Journal of the American College of Cardiology.

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

S. Heath, G. Lathrop, M. Farrall, 2013, Nature Genetics.

Left, right: a step forward in understanding transposition of the great arteries

B. Keavney, 2010, Heart.

A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.

Mahshid S. Azamian, J. Lupski, S. Leal, 2016, Human molecular genetics.

Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development.

J. Rosenfeld, B. Keavney, J. Goodship, 2015, Congenital heart disease.

cell, monocyte, B and NK lymphoid deficiency Exome sequencing identifies GATA-2 mutation as the cause of dendritic

N. McGovern, B. Keavney, David McDonald, 2013 .

Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency.

Bernard Keavney, Patrick F Chinnery, John Loughlin, 2011, Blood.

Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot

S. Heath, G. Lathrop, A. Moorman, 2013, Human molecular genetics.

The genetics of congenital heart disease: The role of advanced genomic approaches

James M. Eales, L. Zühlke, B. Keavney, 2021, SA Heart.

Integration of Large-Scale Genomic Data Sources With Evolutionary History Reveals Novel Genetic Loci for Congenital Heart Disease

Kathryn E. Hentges, B. Keavney, K. Hentges, 2019, Circulation. Genomic and precision medicine.

Unsupervised ensemble-based phenotyping helps enhance the discoverability of genes related to heart morphology

Alejandro F Frangi, Alejandro F. Frangi, S. Plein, 2023, ArXiv.

Genetics of Coronary Heart Disease

B. Keavney, M. Cunnington, 2010 .

Circulating ceramides as biomarkers of cardiovascular disease: Evidence from phenotypic and genomic studies.

B. Keavney, A. Nicolaou, K. McGurk, 2021, Atherosclerosis.

Hypertension and renin-angiotensin system blockers are not associated with expression of angiotensin-converting enzyme 2 (ACE2) in the kidney

James M. Eales, N. Samani, B. Keavney, 2020, medRxiv.

Uncovering genetic mechanisms of hypertension through multi-omic analysis of the kidney

James M. Eales, A. Morris, N. Samani, 2021, Nature Genetics.

Coronary Artery Disease-Related Genetic Variant on Chromosome 10q11 Is Associated With Carotid Intima-Media Thickness and Atherosclerosis

T. Lehtimäki, N. Samani, Qingbo Xu, 2010, Arteriosclerosis, thrombosis, and vascular biology.

Rationale, Design, and the Baseline Characteristics of the RHDGen (The Genetics of Rheumatic Heart Disease) Network Study†

A. Damasceno, L. Zühlke, H. Cordell, 2022, Circulation. Genomic and precision medicine.

Measurement of blood pressure using the auscultatory and oscillometric methods in the same cuff deflation: validation and field trial of the A&D TM2421 monitor

B. Keavney, A. Caiazza, B. Casadei, 2000, Journal of Human Hypertension.

INSIG-2 promoter polymorphism and obesity related phenotypes: association study in 1428 members of 248 families

Bernard Keavney, B. Keavney, P. Avery, 2006, BMC Medical Genetics.

Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide lipidome reveal genetic influence over circulating lipids

M. Farrall, H. Cordell, H. Watkins, 2019, bioRxiv.

Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide lipidome reveal genetic influence over circulating lipids

M. Farrall, H. Cordell, H. Watkins, 2019, bioRxiv.

Mutations in the Sarcomere Gene MYH7 in Ebstein Anomaly

Bernard Keavney, Silke R. Sperling, Thomas Pickardt, 2011, Circulation. Cardiovascular genetics.

Targeted Next Generation Sequencing Analysis of 1000 individuals with Intellectual Disability

Roger E. Stevenson, Alessandra Renieri, Bernard Keavney, 2015 .

Ambulatory Blood Pressure Is Associated With Polymorphic Variation in P2X Receptor Genes

M. Farrall, H. Watkins, B. Keavney, 2008, Hypertension.

Ambulatory Blood Pressure Is Associated With Polymorphic Variation in P 2 X Receptor Genes

M. Farrall, H. Watkins, B. Keavney, 2008 .

Mutations in FAM111B cause hereditary fibrosing poikiloderma with tendon contracture, myopathy, and pulmonary fibrosis.

R. Redon, A. Munnich, B. Keavney, 2013, American journal of human genetics.

More Evidence Against a Causal Association between C-Reactive Protein and Diabetes

B. Keavney, 2008, PLoS medicine.

A novel RNA-mediated mechanism causing down-regulation of insulating promoter interactions in human embryonic stem cells

B. Keavney, M. Choy, S. Williams, 2021, Scientific Reports.

Author Correction: Promoter interactome of human embryonic stem cell-derived cardiomyocytes connects GWAS regions to cardiac gene networks

P. Freire-Pritchett, P. Fraser, B. Javierre, 2018, Nature Communications.

Identification of a POLG Variant in a Family with Arrhythmogenic Cardiomyopathy and Left Ventricular Fibrosis.

B. Keavney, G. Shaboodien, T. Spracklen, 2020, Circulation. Genomic and precision medicine.

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

M. Farrall, J. Francis, S. Neubauer, 2019, Scientific Reports.

Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1–BP2) deletion in the UK Biobank

J. Priest, B. Keavney, Priyanka Saha, 2020, European Journal of Human Genetics.

Large-scale examination of neuropsychiatric, cognitive and cardiovascular phenotypic associations with 15q11.2 BP1-BP2 deletion in ∼500,000 UK Biobank individuals

J. Priest, B. Keavney, Priyanka Saha, 2019, bioRxiv.

University of Huddersfield Repository Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization identify

S. Knight, P. Beales, B. Keavney, 2022 .

Atorvastatin induces T cell proliferation by a telomerase reverse transcriptase (TERT) mediated mechanism.

B. Keavney, G. Saretzki, I. Spyridopoulos, 2014, Atherosclerosis.

Human interleukin‐27: wide individual variation in plasma levels and complex inter‐relationships with interleukin‐17A

B. Keavney, R. Barker, M. Vickers, 2014, Clinical and experimental immunology.

Genetic Mechanisms Mediating Atherosclerosis Susceptibility at the Chromosome 9p21 Locus

B. Keavney, M. Cunnington, 2011, Current atherosclerosis reports.

Data-independent acquisition mass spectrometry in severe rheumatic heart disease (RHD) identifies a proteomic signature showing ongoing inflammation and effectively classifying RHD cases

A. Damasceno, L. Zühlke, B. Keavney, 2022, Clinical Proteomics.

High-Throughput 13-Parameter Immunophenotyping Identifies Shifts in the Circulating T-Cell Compartment Following Reperfusion in Patients with Acute Myocardial Infarction

Bernard Keavney, Carmen Martin-Ruiz, Murugapathy Veerasamy, 2012, PloS one.

Increased expression of fatty acid binding protein 4 and leptin in resident macrophages characterises atherosclerotic plaque rupture

D. Birchall, B. Keavney, M. Santibanez-Koref, 2013, Atherosclerosis.

Assessment of a large panel of candidate biomarkers of ageing in the Newcastle 85+ study

J. Bond, M. Eccles, M. Catt, 2011, Mechanisms of Ageing and Development.

Non-muscle myosin IIB (Myh10) is required for epicardial function and coronary vessel formation during mammalian development

Kathryn E. Hentges, S. Lovell, B. Keavney, 2017, PLoS genetics.

Fresh fields and pathways new: recent genetic insights into cardiac malformation

B. Keavney, L. J. Freeman, F. Leong, 2009, Heart.

C reactive protein and the risk of cardiovascular disease

Bernard Keavney, B. Keavney, 2011, BMJ : British Medical Journal.

Nonsynonymous variants in the SMAD6 gene predispose to congenital cardiovascular malformation

B. Keavney, J. Goodship, C. Wren, 2012, Human mutation.

Congenital heart disease risk loci identified by genome-wide association study in European patients.

R. Lange, J. Priest, T. Meitinger, 2020, The Journal of clinical investigation.

Left ventricular torsion, energetics, and diastolic function in normal human aging.

A. Blamire, G. MacGowan, B. Keavney, 2012, American journal of physiology. Heart and circulatory physiology.

Paraoxonase polymorphisms and coronary heart disease

J. Danesh, R. Collins, H. Watkins, 2004, The Lancet.

Chromosome 16q22 variants in a region associated with cardiovascular phenotypes correlate with ZFHX3 expression in a transcript-specific manner

B. Keavney, B. Mayosi, Ruairidh Martin, 2014, BMC Genetics.

STX18-AS1 is a Long Noncoding RNA predisposing to Atrial Septal Defect via downregulation of NKX2-5 in differentiating cardiomyocytes

B. Keavney, M. Choy, G. Black, 2020, bioRxiv.

Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot

H. Mefford, I. Thiffault, T. Pastinen, 2021, Genetics in Medicine.

Biochemical Screening for Nonadherence Is Associated With Blood Pressure Reduction and Improvement in Adherence

N. Samani, B. Williams, B. Keavney, 2017, Hypertension.

Common genetic variation in the type A endothelin-1 receptor is associated with ambulatory blood pressure: a family study

B. Keavney, P. Avery, T. Rahman, 2008, Journal of Human Hypertension.

Prediction of patient responses to antihypertensive drugs using genetic polymorphisms: investigation of renin-angiotensin system genes.

B. Keavney, P. Ratcliffe, B. Casadei, 1996, Journal of hypertension.

Evaluation of the angiotensinogen locus in human essential hypertension: a European study.

J. Connell, M. Caulfield, H. Schunkert, 1998, Hypertension.

Quantitative Variation in Plasma Angiotensin‐I Converting Enzyme Activity Shows Allelic Heterogeneity in the ABO Blood Group Locus

G. Lathrop, J. Connell, M. Farrall, 2013, Annals of human genetics.

Genetics of coronary heart disease: current knowledge and research principles.

W. Kraus, C. Granger, B. Keavney, 2000, American heart journal.

Fine-mapping of an ancestral recombination breakpoint in DCP1

G. Lathrop, M. Farrall, C. Mckenzie, 1999, Nature Genetics.

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

M. Farrall, H. Watkins, B. Keavney, 2008, European heart journal.

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

M. Farrall, H. Watkins, B. Keavney, 2002, European heart journal.

1044 Hypertension November 2017 Initially Nonadherent Hypertensive Patients Show Steeper Reduction in BP on Follow-Up Appointments Than Those Who Are Initially

N. Samani, B. Williams, B. Keavney, 2017 .

Renal denervation and blood pressure reduction in resistant hypertension: a systematic review and meta-analysis

B. Keavney, Y. Loke, C. Kwok, 2014, Open Heart.

Elevated heart rate and cardiovascular outcomes in patients with coronary artery disease: clinical evidence and pathophysiological mechanisms.

S. Padmanabhan, C. Lang, B. Keavney, 2010, Atherosclerosis.

Bariatric surgery and its impact on cardiovascular disease and mortality: a systematic review and meta-analysis.

S. Anderson, M. A. Khan, B. Keavney, 2014, International journal of cardiology.

Does rhythm matter in acute heart failure? An insight from the British Society for Heart Failure National Audit

S. Anderson, B. Keavney, J. Cleland, 2019, Clinical Research in Cardiology.

The role of the RAS pathway in iAMP21-ALL

A. Kohlmann, T. Haferlach, B. Keavney, 2016, Leukemia.

Impact of age on the prognostic value of left ventricular function in relation to procedural outcomes following percutaneous coronary intervention: Insights from the British cardiovascular intervention society

S. Anderson, I. Buchan, B. Keavney, 2015, Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions.

Prevalence of left ventricular dysfunction in a UK community sample of very old people: the Newcastle 85+ study

T. Kirkwood, C. Jagger, L. Robinson, 2012, Heart.

Angiotensin converting enzyme insertion or deletion polymorphism and coronary restenosis: meta-analysis of 16 studies

Bernard Keavney, John Danesh, J. Danesh, 2002, BMJ : British Medical Journal.

Title 1 Distinct genetic architectures for syndromic and nonsyndromic congenital 2 heart defects identified by exome sequencing 3

Tomas W. Fitzgerald, G. J. Swaminathan, J. Danesh, 2016 .

Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot.

S. Scherer, C. Marshall, A. Bassett, 2021, Circulation. Genomic and precision medicine.

Stroke Following Percutaneous Coronary Intervention: Type-specific incidence, outcomes and determinants seen by the British Cardiovascular Intervention Society 2007-2012

I. Buchan, C. Berry, B. Keavney, 2015 .

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

Andrew D. Johnson, Yan V. Sun, Sara M. Willems, 2018, Nature Genetics.

Genotype at a promoter polymorphism of the interleukin-6 gene is associated with baseline levels of plasma C-reactive protein.

M. Lathrop, H. Watkins, C. Julier, 2002, Cardiovascular research.

Genotype at the P554L Variant of the Hexose-6 Phosphate Dehydrogenase Gene Is Associated with Carotid Intima-Medial Thickness

J. Connell, H. Watkins, B. Keavney, 2011, PloS one.

Association Between C677T Polymorphism of Methylene Tetrahydrofolate Reductase and Congenital Heart Disease: Meta-Analysis of 7697 Cases and 13 125 Controls

G. Lathrop, M. Farrall, A. Moorman, 2013, Circulation. Cardiovascular genetics.

Association between C 677 T Polymorphism of Methylene Tetrahydrofolate Reductase and Congenital Heart Disease : Meta-Analysis of 7 , 697 Cases and 13 , 125 Controls Running title : Mamasoula : MTHFR C 677 T polymorphism and congenital heart disease

Faith, G. Lathrop, D. Zélénika, 2013 .

Structural modelling of the cardiovascular system

B. Keavney, A. Revell, A. Jivkov, 2018, Biomechanics and modeling in mechanobiology.

Bases adjacent to mononucleotide repeats show an increased single nucleotide polymorphism frequency in the human genome

Bernard Keavney, Judith A. Goodship, K. J. Siddle, 2011, Bioinform..

Modern genomic techniques in the identification of genetic causes of cardiomyopathy

B. Keavney, G. Shaboodien, T. Spracklen, 2022, Heart.

Induced pluripotent stem cell modelling of HLHS underlines the contribution of dysfunctional NOTCH signalling to impaired cardiogenesis

Min Yu, Babajan Banaganapalli, Bernard Keavney, 2017, Human molecular genetics.

Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot

S. Scherer, C. Marshall, A. Bassett, 2021, medRxiv.

Impact of left ventricular function in relation to procedural outcomes following percutaneous coronary intervention: insights from the British Cardiovascular Intervention Society.

S. Anderson, B. Keavney, A. Zaman, 2014, European heart journal.

Functional Significance of SRJ Domain Mutations in CITED2

S. Bamforth, S. Bhattacharya, H. Watkins, 2012, PloS one.

Loss of Function of Parathyroid Hormone Receptor 1 Induces Notch-Dependent Aortic Defects During Zebrafish Vascular Development

H. Roehl, B. Keavney, P. Evans, 2013, Arteriosclerosis, thrombosis, and vascular biology.

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

M. Farrall, H. Watkins, B. Keavney, 2005, Stroke.

Genotype at the 174 G / C Polymorphism of the Interleukin-6 Gene Is Associated With Common Carotid Artery Intimal-Medial Thickness Family Study and Meta-Analysis

M. Farrall, H. Watkins, B. Keavney, 2005 .

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.

J. Connell, M. Farrall, H. Watkins, 2007, International journal of epidemiology.

Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome

A J Agopian, Cristina E. Trevino, D. Cutler, 2020, Scientific Reports.

Common variation in the CD36 (fatty acid translocase) gene is associated with left-ventricular mass

H. Watkins, B. Keavney, B. Mayosi, 2011, Journal of hypertension.

Common Variation at the 11-&bgr; Hydroxysteroid Dehydrogenase Type 1 Gene Is Associated With Left Ventricular Mass

J. Connell, H. Watkins, B. Keavney, 2011, Circulation. Cardiovascular genetics.

Large-scale evidence that the cardiotoxicity of smoking is not significantly modified by the apolipoprotein E ε2/ε3/ε4 genotype

J. Danesh, R. Collins, R. Peto, 2003, The Lancet.

Measured haplotype analysis of the aldosterone synthase gene and heart size

M. Farrall, H. Watkins, B. Keavney, 2005, European Journal of Human Genetics.

4D flow MRI assessment of right atrial flow patterns in the normal heart – influence of caval vein arrangement and implications for the patent foramen ovale

A. Blamire, B. Keavney, G. Ford, 2017, PloS one.

Provision of gastroprotective medication and bleeding risk following acute coronary syndrome.

B. Keavney, A. Yan, A. Zaman, 2013, The Journal of invasive cardiology.

CMV-independent increase in CD27−CD28+ CD8+ EMRA T cells is inversely related to mortality in octogenarians

B. Keavney, J. Collerton, T. Zglinicki, 2020, npj Aging and Mechanisms of Disease.

CMV-independent increase in CD27−CD28+ CD8+ EMRA T cells is inversely related to mortality in octogenarians

B. Keavney, J. Collerton, T. Zglinicki, 2020, npj Aging and Mechanisms of Disease.

Rare GATA6 variants associated with risk of congenital heart disease phenotypes in 200,000 UK Biobank exomes

B. Keavney, Dominic J. F. Byrne, Simon G. Williams, 2021, medRxiv.

Association analysis identifies new risk loci for congenital heart disease in Chinese populations

Hongbing Shen, Bixian Ni, Jiahao Sha, 2015, Nature Communications.

Association between aldosterone production and variation in the 11beta-hydroxylase (CYP11B1) gene.

J. Connell, M. Farrall, H. Cordell, 2006, The Journal of clinical endocrinology and metabolism.

Plasma potassium level is associated with common genetic variation in the beta-subunit of the epithelial sodium channel.

B. Keavney, P. Avery, N. Gaukrodger, 2008, American journal of physiology. Regulatory, integrative and comparative physiology.

University of Dundee Genotype at the P554L Variant of the Hexose-6 Phosphate Dehydrogenase Gene Is Associated with Carotid Intima-Medial Thickness Rahman,

J. Connell, H. Watkins, B. Keavney, 2011 .

The interleukin-1 cluster, dyslipidaemia and risk of myocardial infarction

B. Keavney, 2010, BMC Medicine.

CommentaryThe interleukin-1 cluster , dyslipidaemia and risk of myocardial infarction

B. Keavney, 2015 .

Commentaryinterleukin-1 cluster, dyslipidaemia and risk of myocardial infarction

B. Keavney, 2010 .

Large-scale evidence that the cardiotoxicity of smoking is not significantly modified by the apolipoprotein E epsilon2/epsilon3/epsilon4 genotype.

J. Danesh, R. Collins, R. Peto, 2003, Lancet.

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

M. Farrall, H. Watkins, B. Keavney, 2009, Atherosclerosis.

Familial and phenotypic associations of the aldosterone Renin ratio.

J. Connell, H. Watkins, S. Padmanabhan, 2009, The Journal of clinical endocrinology and metabolism.

Chicken or Egg in the UK Biobank?

B. Keavney, 2019, Circulation research.

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

J. Connell, M. Farrall, H. Watkins, 2005, The Journal of clinical endocrinology and metabolism.

Evidence for a quantitative trait locus for plasma fibrinogen from a family–based association study

G. Lathrop, H. Watkins, C. Julier, 2001 .

Atrial Septal Defect (ASD) associated long non-coding RNA STX18-AS1 maintains time-course of in vitro cardiomyocyte differentiation

B. Keavney, M. Choy, G. Black, 2022, Genes & diseases.

Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1–BP2) deletion in the UK Biobank

Kathryn E. Hentges, J. Priest, B. Keavney, 2020, European Journal of Human Genetics.

Genetic association studies in complex diseases

B. Keavney, 2000, Journal of Human Hypertension.

Erratum: Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

P. O’Reilly, P. Elliott, D. Levy, 2017, Nature Genetics.

Utility of NT-proBNP as a rule-out test for left ventricular dysfunction in very old people with limiting dyspnoea: the Newcastle 85+ Study

G. MacGowan, T. Kirkwood, L. Robinson, 2014, BMC Cardiovascular Disorders.

Variation at the NFATC2 Locus Increases the Risk of Thiazolidinedione-Induced Edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) Study

Changchun Xie, Hertzel C. Gerstein, Bernard Keavney, 2010, Diabetes Care.

Exome sequencing reveals distinct genetic architectures for syndromic and nonsyndromic congenital heart defects

Tomas W. Fitzgerald, G. J. Swaminathan, M. Hurles, 2016 .

Evolution of genetic analysis strategies in coronary heart disease: a case of unnatural selection?

H. Watkins, B. Keavney, 2001, European Heart Journal.

Measured haplotype analysis of the angiotensin-I converting enzyme gene.

M Farrall, J. Connell, M. Farrall, 1998, Human molecular genetics.

Activation of telomerase by TA-65 enhances immunity and reduces inflammation post myocardial infarction

B. Keavney, C. Gale, I. Spyridopoulos, 2023, GeroScience.

Glypican-6 deficiency causes dose-dependent conotruncal congenital heart malformations through abnormal remodelling of the endocardial cushions

Kathryn E. Hentges, B. Keavney, K. Hentges, 2021, bioRxiv.

Association of Apolipoprotein E Genotypes With Lipid Levels and Coronary Risk

J. Danesh, R. Collins, A. Ahlbom, 2007 .

Genetic Information and the Prediction of Incident Type 2 Diabetes in a High-Risk Multiethnic Population

Swneke D. Bailey, S. Yusuf, J. Bosch, 2013, Diabetes Care.

Genetic Information and the Prediction of Incident Type 2 Diabetes in a High-RiskMulti-Ethnic Population The EpiDREAM Genetic Study

Swneke D. Bailey, J. Bosch, A. Montpetit, 2013 .

An Induced Pluripotent Stem Cell Model of Hypoplastic Left Heart Syndrome (HLHS) Reveals Multiple Expression and Functional Differences in HLHS‐Derived Cardiac Myocytes

E. Sernagor, M. Stojkovic, M. Lako, 2014, Stem cells translational medicine.

Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of Fallot

S. Bhattacharya, B. Keavney, J. Goodship, 2013, BMC Genetics.

Discovery methods for systematic analysis of causal molecular networks in modern omics datasets

B. Keavney, C. Berzuini, M. Tomaszewski, 2022, 2201.12229.

Common Genetic Polymorphisms and Coronary Heart Disease

B. Keavney, 2002, Seminars in vascular medicine.

Association between HSD11B1 polymorphism and left ventricular mass in families with hypertension

H. Watkins, B. Keavney, B. Mayosi, 2009 .

Predicting congenital renal tract malformation genes using machine learning

Kathryn E. Hentges, A. Doig, B. Keavney, 2023, Scientific reports.

Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

Andrew D. Johnson, Lorna M. Lopez, Aude Saint Pierre, 2017, bioRxiv.

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

M. P. Concas, N. Eriksson, M. Nalls, 2016, Nature Genetics.

Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults

J. Danesh, P. Deloukas, M. Rutter, 2018, Journal of the American College of Cardiology.

Association of apolipoprotein E genotypes with lipid levels and coronary risk.

J. Danesh, R. Collins, A. Ahlbom, 2007, JAMA.

Association analyses based on false discovery rate implicate 243 susceptibility loci for coronary artery disease

J. Danesh, T. Assimes, I. Ntalla, 2017 .

P. Scambler, H. Cordell, B. Keavney, 2010, Heart.

Measured haplotype analysis of the aldosterone synthase gene and heart size

M. Farrall, H. Watkins, B. Keavney, 2003, European Journal of Human Genetics.

INSIG-2 promoter polymorphism and obesity related phenotypes: association study in 1428 members of 248 families

B. Keavney, P. Avery, T. Rahman, 2006, BMC Medical Genetics.

Rare GATA6 variants associated with risk of congenital heart disease phenotypes in 200,000 UK Biobank exomes

B. Keavney, Dominic J. F. Byrne, Simon G. Williams, 2021, Journal of Human Genetics.

Genetic resiliency associated with dominant lethal TPM1 mutation causing atrial septal defect with high heritability

Ferhaan Ahmad, T. Wong, B. Keavney, 2022, Cell Reports Medicine.

Bariatric surgery and its impact on cardiovascular disease and mortality: a systematic review and meta-analysis.

S. Anderson, M. A. Khan, B. Keavney, 2014, International journal of cardiology.

Structural modelling of the cardiovascular system

Alistair Revell, Nicholas Bojdo, Benjamin Owen, 2018, Biomechanics and Modeling in Mechanobiology.

Impact of left ventricular function in relation to procedural outcomes following percutaneous coronary intervention: insights from the British Cardiovascular Intervention Society.

S. Anderson, B. Keavney, A. Zaman, 2014, European heart journal.

Using population data for assessing next-generation sequencing performance

Saeed Al Turki, Judith A. Goodship, Mauro F. Santibanez-Koref, 2014, Bioinform..

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

Andrew D. Johnson, Sara M. Willems, Lorna M. Lopez, 2018, Nature Genetics.

Left ventricular torsion, energetics, and diastolic function in normal human aging.

A. Blamire, G. MacGowan, B. Keavney, 2012, American journal of physiology. Heart and circulatory physiology.

Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk (vol 49, pg 403, 2017)

P. O’Reilly, P. Elliott, L. Wain, 2017 .

Atorvastatin induces T cell proliferation by a telomerase reverse transcriptase (TERT) mediated mechanism.

B. Keavney, G. Saretzki, I. Spyridopoulos, 2014, Atherosclerosis.

Ebstein anomaly associated with left ventricular noncompaction: An autosomal dominant condition that can be caused by mutations in MYH7

B. Mulder, B. Keavney, A. Postma, 2013, American journal of medical genetics. Part C, Seminars in medical genetics.

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

Andrew D. Johnson, Sara M. Willems, Lorna M. Lopez, 2018, Nature Genetics.