Publications by Professor Bernard Keavney - ePrints

Browsing publications by Professor Bernard Keavney.

Newcastle Authors	Title	Year
Dr Carmen Martin-Ruiz Professor Thomas von Zglinicki Professor Gavin Richardson Lilia Draganova Dr Rachael Redgrave et al.	CMV-independent increase in CD27−CD28+ CD8+ EMRA T cells is inversely related to mortality in octogenarians	2020
Professor Heather Cordell Professor Bernard Keavney	Heritability of haemodynamics in the ascending aorta	2020
Professor Heather Cordell Professor Bernard Keavney	Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome	2020
Valentina Mamasoula Professor Heather Cordell Professor Bernard Keavney	Marked variation in heritability estimates of left ventricular mass depending on modality of measurement	2019
Matthieu Miossec Professor Heather Cordell Dr Lou Sutcliffe Dr Ana Topf Dr John O'Sullivan et al.	Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot	2018
Dr Jehill Parikh Jayant Kakarla Professor Bernard Keavney Dr John O'Sullivan Professor Gary Ford et al.	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	2017
Professor Bernard Keavney Dr Kristin Ayers Professor Heather Cordell Dr Lenore Launer Valentina Mamasoula et al.	Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk	2017
Dr Chunbo Yang Dr Yaobo Xu Dr Min Yu Dr David Lee Dr John O'Sullivan et al.	Induced pluripotent stem cell modelling of HLHS underlines the contribution of dysfunctional NOTCH signalling to impaired cardiogenesis	2017
Professor Heather Cordell Professor Bernard Keavney Professor Judith Goodship	Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valve	2017
Dr Kristin Ayers Professor Heather Cordell Valentina Mamasoula Professor Bernard Keavney	Genome-wide analysis identifies 12 loci influencing human reproductive behavior	2016
Dr Sarra Ryan Elizabeth Matheson Dr Paul Sinclair Dr Matthew Bashton Claire Schwab et al.	The role of the RAS pathway in iAMP21-ALL	2016
Dr Ruairidh Martin Dr Andrew Owens Professor Bernard Keavney	Genetic variants associated with risk of atrial fibrillation regulate expression of PITX2, CAV1, MYOZ1, C9orf3 and FANCC	2015
Professor Bernard Keavney Professor Azfar Zaman Dr Mark De Belder	Impact of age on access site-related outcomes in 469,983 percutaneous coronary intervention procedures: Insights from the British Cardiovascular Intervention Society	2015
Professor Bernard Keavney Professor Azfar Zaman Dr Mark De Belder	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	2015
Dr Richard Howey Valentina Mamasoula Dr Ana Topf Professor Judith Goodship Professor Bernard Keavney et al.	Increased Power for Detection of Parent-of-Origin Effects via the Use of Haplotype Estimation	2015
Dr Richard Howey Valentina Mamasoula Dr Ana Topf Professor Judith Goodship Professor Bernard Keavney et al.	Increased power for detection of parent-of-origin effects via the use of haplotype estimation	2015
Professor Azfar Zaman Professor Bernard Keavney Dr Mark De Belder	Stroke following percutaneous coronary intervention: type-specific incidence, outcomes and determinants seen by the British Cardiovascular Intervention Society 2007-12	2015
Dr Stephen Boag Dr Rajiv Das Dr Evgeniya Shmeleva Dr Alan Bagnall Dr Mohaned Egred et al.	T lymphocytes and fractalkine contribute to myocardial ischemia/reperfusion injury in patients	2015
Darren Houniet Dr Thahira Rahman Dr Yaobo Xu Professor Judith Goodship Professor Bernard Keavney et al.	Using population data for assessing next-generation sequencing performance	2015
Dr Jehill Parikh Jayant Kakarla Dr Kieren Hollingsworth Professor Bernard Keavney Dr John O'Sullivan et al.	Variations in right atrial flow patterns in the normal heart a potential contributor to cryptogenic stroke in the setting of patent foramen ovale	2015
Dr Stephen Boag Dr Rajiv Das Dr Mohaned Egred Professor Azfar Zaman Dr Alan Bagnall et al.	Dynamic Changes in T-Lymphocyte Counts Following Primary Percutaneous Coronary Intervention Predict Infarct Size and Microvascular Obstruction	2014
Dr Ana Topf Dr Helen Griffin Dr Elise Glen Rachel Soemedi Dr Danielle Brown et al.	Functionally Significant, Rare Transcription Factor Variants in Tetralogy of Fallot	2014
Dr Ruairidh Martin Professor Bernard Keavney	Genetic Risk Markers for Atrial Fibrillation Influence Allelic Expression of Nearby Candidate Genes	2014
Professor Bernard Keavney	Human interleukin-27: wide individual variation in plasma levels and complex inter-relationships with interleukin-17A	2014
Andy Best Caroline Dalgliesh Elaine Hong Mahsa Kheirollahi Kouhestani Dr Yaobo Xu et al.	Human Tra2 proteins jointly control a CHEK1 splicing switch among alternative and constitutive target exons	2014
Professor Bernard Keavney Professor Azfar Zaman Dr Mark De Belder	Impact of left ventricular function in relation to procedural outcomes following percutaneous coronary intervention: insights from the British Cardiovascular Intervention Society	2014
Matthieu Miossec Raf Hussain Professor Judith Goodship Professor Bernard Keavney	Investigating the cause of transposition of great arteries	2014
Dr Joanna Collerton Dr Andrew Kingston Dr Fahad Yousaf Dr Karen Davies Dr Antoinette Kenny et al.	Utility of NT-proBNP as a rule-out test for left ventricular dysfunction in very old people with limiting dyspnoea: the Newcastle 85+Study	2014
Valentina Mamasoula Dr Tomasz Pierscionek Dr Darroch Hall Dr Ana Topf Dr Danielle Brown et al.	Association between C677T Polymorphism of Methylene Tetrahydrofolate Reductase and Congenital Heart Disease: Meta-Analysis of 7,697 Cases and 13,125 Controls	2013
Dr Thahira Rahman Valentina Mamasoula Dr Peter Avery Professor Bernard Keavney	Common Variation Neighbouring Micro-RNA 22 Is Associated with Increased Left Ventricular Mass	2013
Dr Matthew Bates Dr Kieren Hollingsworth Jane Newman Professor Djordje Jakovljevic Professor Andrew Blamire et al.	Concentric hypertrophic remodeling and subendocardial dysfunction in mitochondrial DNA point mutation carriers	2013
Dr Matthew Bates Jane Newman Professor Djordje Jakovljevic Dr Kieren Hollingsworth Professor Andrew Blamire et al.	Defining cardiac adaptations and safety of endurance training in patients with m.3243A>g-related mitochondrial disease	2013
Dr Thahira Rahman Professor Bernard Keavney Professor Judith Goodship	Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7	2013
Professor Heather Cordell Professor Bernard Keavney	Genetic Information and the Prediction of Incident Type 2 Diabetes in a High-Risk Multiethnic Population: The EpiDREAM genetic study	2013
Dr Ruairidh Martin Professor Bernard Keavney	Genetic Variation Associated with Low-Density Lipoprotein Cholesterol Levels Influences ZFHX3 Expression	2013
Professor Heather Cordell Dr Ana Topf Valentina Mamasoula Dr Rebecca Darlay Rachel Soemedi et al.	Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot	2013
Professor Heather Cordell Dr Ana Topf Valentina Mamasoula Rachel Soemedi Dr Ruairidh Martin et al.	Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16	2013
Dr Kelvin Lee Dr Mauro Santibanez Koref Dr Tuomo Polvikoski Dr Daniel Birchall Emeritus Professor David Mendelow et al.	Increased expression of fatty acid binding protein 4 and leptin in resident macrophages characterises atherosclerotic plaque rupture	2013
Addison Palomino Doza Dr Ana Topf Dr John O'Sullivan Professor Caroline Relton Professor Judith Goodship et al.	Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of Fallot	2013
Darren Houniet Dr Thahira Rahman Dr Mauro Santibanez Koref Professor Bernard Keavney	Mutations in FAM111B Cause Hereditary Fibrosing Poikiloderma with Tendon Contracture, Myopathy, and Pulmonary Fibrosis	2013
Professor Azfar Zaman Dr Javed Ahmed Dr Mohaned Egred Dr Richard Edwards Professor Ioakim Spyridopoulos et al.	Provision of Gastroprotective Medication and Bleeding Risk Following Acute Coronary Syndrome	2013
Professor Bernard Keavney	Quantitative Variation in Plasma Angiotensin-I Converting Enzyme Activity Shows Allelic Heterogeneity in the ABO Blood Group Locus	2013
Professor Judith Goodship Dr Darroch Hall Dr Ana Topf Valentina Mamasoula Dr Helen Griffin et al.	A Common Variant in the PTPN11 Gene Contributes to the Risk of Tetralogy of Fallot	2012
Professor Rita Horvath Vivienne Neeve Dr Angela Pyle Dr Helen Griffin Deepthi Ashok et al.	A new phenotype of brain iron accumulation with dystonia, optic atrophy, and peripheral neuropathy	2012
Valentina Mamasoula Dr Tomasz Pierscionek Dr Ana Topf Dr Thahira Rahman Dr John O'Sullivan et al.	Aetiological Role Of Folate Deficiency In Congenital Cardiovascular Malformation: Evidence From "Mendelian Randomisation" And Meta-Analysis	2012
Professor Bernard Keavney	Apolipoprotein(a) Genetic Sequence Variants Associated With Systemic Atherosclerosis and Coronary Atherosclerotic Burden But Not With Venous Thromboembolism	2012
Dr Joanna Collerton Dr Fahad Yousaf Dr Andrew Kingston Dr Antoinette Kenny Dr Karen Davies et al.	Cardiac dysfunction among the community dwelling very old	2012
Dr Rachael Redgrave Dr Benjamin Davison Dr Muhammad Amirrasouli Professor Bernard Keavney Professor Andrew Blamire et al.	Cardiosphere-Derived Cell Transplantation Rescues Cardiac Function Post-MI Independently of Endoglin Expression	2012
Dr Matt Bates Dr Kieren Hollingsworth Jane Newman Professor Djordje Jakovljevic Professor Bernard Keavney et al.	Concentric hypertrophic remodelling and subendocardial dysfunction in mitochondrial DNA point mutation carriers	2012
Rachel Soemedi Dr Ian Wilson Dr Rebecca Darlay Dr Ana Topf Dr Simon Zwolinski et al.	Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease	2012
Dr Matt Bates Dr Kieren Hollingsworth Jane Newman Professor Djordje Jakovljevic Professor Andrew Blamire et al.	Evidence of early cardiac impairment in m.3243A > G mutation carriers	2012
Dr Simon Bamforth Professor Bernard Keavney	Functional Significance of SRJ Domain Mutations in CITED2	2012
Jedrzej Hoffmann Dr Karel Fiser Dr Jolanta Weaver Ian Dimmick Monika Loeher et al.	High-Throughput 13-Parameter Immunophenotyping Identifies Shifts in the Circulating T-Cell Compartment Following Reperfusion in Patients with Acute Myocardial Infarction	2012
Dr Kieren Hollingsworth Professor Andrew Blamire Professor Bernard Keavney Dr Guy MacGowan	Left ventricular torsion, energetics, and diastolic function in normal human aging	2012
Dr Ana Topf Professor Judith Goodship Professor Deborah Henderson Dr John O'Sullivan Professor Bernard Keavney et al.	Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to congenital heart disease	2012
Professor Judith Goodship Professor Bernard Keavney	Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization	2012
Dr Elise Glen Dr Ana Topf Dr Darroch Hall Dr John O'Sullivan Linda Sneddon et al.	Nonsynonymous variants in the SMAD6 gene predispose to congenital cardiovascular malformation	2012
Rachel Soemedi Dr Ana Topf Dr Ian Wilson Dr Rebecca Darlay Dr Thahira Rahman et al.	Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls	2012
Dr Joanna Collerton Dr Andrew Kingston Dr Antoinette Kenny Dr Karen Davies Emerita Professor Carol Jagger et al.	Prevalence of left ventricular dysfunction in a UK community sample of very old people: the Newcastle 85+ study	2012
Valentina Mamasoula Dr Tomasz Pierscionek Addison Palomino Doza Dr Ana Topf Dr Thahira Rahman et al.	Aetiological role of folate deficiency in congenital heart disease: evidence from Mendelian randomisation and meta-analysis	2011
Dr Carmen Martin-Ruiz Emerita Professor Carol Jagger Dr Andrew Kingston Dr Joanna Collerton Professor Mike Catt et al.	Assessment of a large panel of candidate biomarkers of ageing in the Newcastle 85+ study	2011
Professor Judith Goodship Professor Bernard Keavney Dr Mauro Santibanez Koref	Bases adjacent to mononucleotide repeats show an increased single nucleotide polymorphism frequency in the human genome	2011
Dr Thahira Rahman Dr Peter Avery Professor Bernard Keavney	Common Variation at the 11-beta Hydroxysteroid Dehydrogenase Type 1 Gene Is Associated With Left Ventricular Mass	2011
Dr Peter Avery Dr Sheila Patel Dr Ibrahim Ibrahim Professor Mark Walker Professor Bernard Keavney et al.	Common variation in the adiponectin gene has an effect on systolic blood pressure	2011
Dr Darroch Hall Dr Thahira Rahman Dr Peter Avery Professor Bernard Keavney	Common variation in the CD36 (fatty acid translocase) gene is associated with left-ventricular mass	2011
Dr Rachel Dickinson Dr Helen Griffin Dr Venetia Bigley Dr Louise Reynard Raf Hussain et al.	Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency	2011
Dr Thahira Rahman Dr Darroch Hall Dr Peter Avery Professor Bernard Keavney	Genotype at the P554L Variant of the Hexose-6 Phosphate Dehydrogenase Gene Is Associated with Carotid Intima-Medial Thickness	2011
Jill Collerton Dr Fahad Yousaf Dr Andrew Kingston Dr Karen Davies Emerita Professor Carol Jagger et al.	High prevalence of undiagnosed cardiac dysfunction in the oldest old: Findings from the Newcastle 85+ Study	2011
Dr Fahad Yousaf Dr Joanna Collerton Dr Antoinette Kenny Emeritus Professor Thomas Kirkwood Emerita Professor Carol Jagger et al.	High prevalence of undiagnosed cardiac dysfunction in the oldest old: Findings from the Newcastle 85+ Study	2011
Dr Benjamin Davison Dr Rachael Redgrave Professor Bernard Keavney Professor Andrew Blamire Professor Helen Arthur et al.	In vivo depletion of endoglin results in significant left ventricular remodelling	2011
Dr Thahira Rahman Professor Bernard Keavney Professor Judith Goodship	Mutations in the sarcomere gene MYH7 in Ebstein anomaly	2011
Dr Elise Glen Dr Ana Topf Dr Darroch Hall Dr John O'Sullivan Linda Sneddon et al.	Non-synonymous SMAD6 mutations impaired inhibition of BMP signalling in patients with congenital cardiovascular malformation	2011
Dr Sarra Ryan Dr Vikki Rand Claire Schwab Heather Morrison Elizabeth Matheson et al.	Ras Signalling Pathway and Novel Target Genes Related to Down Syndrome Contribute to the Development of B-Cell Precursor Acute Lymphoblastic Leukemia (BCP-ALL) in iAMP21 Patients	2011
Dr Ana Topf Professor Bernard Keavney Professor Judith Goodship	22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresia	2010
Dr Michael Cunnington Dr Mauro Santibanez Koref Professor Sir John Burn Professor Bernard Keavney	Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression	2010
Hannah Watkins Professor Bernard Keavney	Coronary Artery Disease-Related Genetic Variant on Chromosome 10q11 Is Associated With Carotid Intima-Media Thickness and Atherosclerosis	2010
Dr Samir Gupta Professor Bernard Keavney	Elevated heart rate and cardiovascular outcomes in patients with coronary artery disease: Clinical evidence and pathophysiological mechanisms	2010
Professor Bernard Keavney	Left, right: A step forward in understanding transposition of the great arteries	2010
Dr Michael Cunnington Professor Sir John Burn Professor Bernard Keavney	Modulation of Anril Expression May Mediate the Association Between Chromosome 9P21 Variants and Coronary Atherosclerosis Risk	2010
Dr Michael Cunnington Professor Sir John Burn Professor Bernard Keavney	Modulation of ANRIL expression may mediate the association of chromosome 9P21 variants with coronary artery disease and stroke	2010
Dr Helen Griffin Dr Ana Topf Dr Elise Glen Dr John O'Sullivan Professor Sir John Burn et al.	Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants	2010
Professor Bernard Keavney	The interleukin-1 cluster, dyslipidaemia and risk of myocardial infarction	2010
Dr Ana Topf Professor Bernard Keavney Professor Judith Goodship	22q11 Deletions in Adults With Tetralogy of Fallot Are Highly Under Recognized	2009
Dr Thahira Rahman Dr Peter Avery Hannah Watkins Professor Bernard Keavney	Association between HSD11B1 polymorphism and left ventricular mass in families with hypertension	2009
Dr Honey Thomas Professor John Dark Professor Helen Arthur Professor Bernard Keavney	Circulating endothelial progenitor cell numbers are not associated with donor organ age or allograft vasculopathy in cardiac transplant recipients	2009
Dr Peter Avery Professor Bernard Keavney	Familial and Phenotypic Associations of the Aldosterone Renin Ratio	2009
Professor Bernard Keavney	Fresh fields and pathways new: recent genetic insights into cardiac malformation	2009
Dr Michael Cunnington Dr Darroch Hall Dr Peter Avery Professor Bernard Keavney	Genetic Polymorphisms Linked to Coronary Artery Disease Are Not Associated With Carotid Artery Intima-Media Thickness, Less Ventricular Size or Intermediate Risk Phenotypes	2009
Professor Heather Cordell Professor Bernard Keavney	Genetic variants associated with myocardial infarction risk factors in over 8000 individuals from five ethnic groups: The INTERHEART Genetics Study	2009
Dr Helen Griffin Dr Darroch Hall Dr Ana Topf James Eden Professor Sir John Burn et al.	Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation	2009
Dr Honey Thomas Dr Peter Avery Dr Javed Ahmed Dr Richard Edwards Professor Azfar Zaman et al.	Local vessel injury following percutaneous coronary intervention does not promote early mobilisation of endothelial progenitor cells in the absence of myocardial necrosis	2009
Dr Michael Cunnington Dr Mauro Santibanez Koref Professor Sir John Burn Professor Bernard Keavney	Modulation of ANRIL Expression is a Possible Mechanism Mediating the Association Between Chromosome 9p21 Polymorphisms and Coronary Atherosclerosis Risk	2009
Dr Michael Cunnington Dr Darroch Hall Dr Peter Avery Hannah Watkins Professor Bernard Keavney et al.	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	2009
Angeline Tan Dr Ana Topf Dr Helen Griffin Raf Hussain James Eden et al.	Role of Genetic Variation in the Transcriptional Inhibitor Protein SMAD6 in the Predispoition to Congenital Cardiovascular Malformation	2009
Dr Michael Cunnington Dr Peter Avery Dr Mauro Santibanez Koref Professor Bernard Keavney	STK39 polymorphisms and blood pressure: an association study in British Caucasians and assessment of cis-acting influences on gene expression	2009
Addison Palomino Doza Dr Thahira Rahman Dr Peter Avery Professor Chris Edwards Professor Bernard Keavney et al.	Ambulatory blood pressure is associated with polymorphic variation in P2X receptor genes	2008
Professor Bernard Keavney	Association of cholesteryl ester transfer protein genotypes with CETP mass and activity, lipid levels, and coronary risk	2008
Dr Rachael Redgrave Dr Michael Cunnington Dr Peter Avery Professor Bernard Keavney Professor Helen Arthur et al.	Circulating endothelial progenitor cells exhibit diurnal variation	2008
Dr Rachael Redgrave Dr Michael Cunnington Professor Bernard Keavney Professor Helen Arthur	Circulating endothelial progenitor cells from healthy individuals exhibit diurnal variation	2008
Dr Thahira Rahman Michelle Baker Dr Darroch Hall Dr Peter Avery Professor Bernard Keavney et al.	Common genetic variation in the type A endothelin-1 receptor is associated with ambulatory blood pressure: A family study	2008
Professor Bernard Keavney	Correction of population stratification in large multi-ethnic association studies	2008
Dr Peter Avery Professor Bernard Keavney	Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension	2008
Professor Bernard Keavney	Genome-wide linkage analysis of electrocardiographic and echocardiographic left ventricular hypertrophy in families with hypertension	2008
Dr Honey Thomas Professor Helen Arthur Professor Bernard Keavney	Investigation of relationships between circulating endothelial progenitor cell numbers, cardiac allograft vasculopathy and donor heart age in cardiac transplant recipients	2008
Professor Bernard Keavney	More evidence against a causal association between C-reactive protein and diabetes	2008
Nicole Gaukrodger Dr Peter Avery Professor Bernard Keavney	Plasma potassium level is associated with common genetic variation in the β-subunit of the epithelial sodium channel	2008
Dr Helen Imrie Dr Rachael Fraser Professor Heather Cordell Professor Bernard Keavney	Association between aldosterone production and variation in the gene encoding 11-beta hydroxylase (CYP11B1)	2007
Dr Thahira Rahman Professor Bernard Keavney	Association between polymorphic variation in the endothelin-1 type a receptor gene and ambulatory blood pressure	2007
Professor Bernard Keavney Dr Thahira Rahman James Eden Raf Hussain	Association between the purinergic receptors P2X4, P2X6 and P2X7 genetic variation and blood pressure in a British population	2007
Professor Bernard Keavney	Association of apolipoprotein e genotypes with lipid levels and coronary risk	2007
Dr Kelvin Lee Dr Tuomo Polvikoski Dr Daniel Birchall Dr Mauro Santibanez Koref Emeritus Professor David Mendelow et al.	Genome-wide cell-specific gene expression analysis identifies the involvement of the adipocytokine signalling pathway in atherosclerotic plaque rupture	2007
Dr Helen Griffin Professor Bernard Keavney Professor Judith Goodship	Mutations in the cardiac transcription factor TBX1 may contribute to susceptibility to tetralogy of fallot in patients without 22q11 deletion	2007
Dr Joanna Collerton Dr Carmen Martin-Ruiz Dr Antoinette Kenny Dr Karen Davies Professor Thomas von Zglinicki et al.	Telomere length is associated with left ventricular function in the oldest old: The Newcastle 85+ study	2007
Michelle Baker Dr Thahira Rahman Dr Darroch Hall Dr Peter Avery Hannah Watkins et al.	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	2007
Jill Collerton Dr Carmen Martin-Ruiz Dr Karen Davies Professor Thomas von Zglinicki Emeritus Professor Thomas Kirkwood et al.	White blood cell telomere length is associated with left ventricular function in the oldest old: The newcastle 85+study	2007
Dr Helen Imrie Professor Heather Cordell Dr Peter Avery Professor Bernard Keavney	Association between aldosterone production and variation in the 11β-hydroxylase (CYP11B1) gene	2006
Dr Simon Bamforth Professor Bernard Keavney	Cited2 haploinsufficiency is associated with congenital heart defects in mouse and man: Introducing the GO-CHD Study	2006
Professor Bernard Keavney	Fibrinogen and coronary heart disease: Test of causality by 'Mendelian randomization'	2006
Professor Bernard Keavney Dr Peter Avery Nicole Gaukrodger Dr Helen Imrie Michelle Baker et al.	Genetic variation at the CYP11B locus accounts for heritabilities of aldosterone metabolite (THAIdo) excretion and 11beta-hydroxylase activity	2006
Professor Bernard Keavney	Genome wide linkage analysis of von Willebrand factor antigen levels	2006
Dr Kelvin Lee Dr Tuomo Polvikoski Dr Daniel Birchall Dr Mauro Santibanez Koref Emeritus Professor David Mendelow et al.	Genome-wide cell-specific approach to atherosclerotic plaque rupture identifies the involvement of the adipocytokine signaling pathway	2006
Dr Darroch Hall Dr Thahira Rahman Dr Peter Avery Professor Bernard Keavney	INSIG-2 promoter polymorphism and obesity related phenotypes: Association study in 1428 members of 248 families	2006
Professor Bernard Keavney	Seven haemostatic gene polymorphisms in coronary disease: Meta-analysis of 66 155 cases and 91 307 controls	2006
Professor Bernard Keavney	Toll the bell for another genetic association?	2006
Dr Helen Imrie Nicole Gaukrodger Dr Peter Avery Michelle Baker Judith Connell et al.	A rare variant of the leptin (LEP) gene has large effects on blood pressure (BP) and carotid intima-medial thickness (CIMT): Study of 1428 individuals in 248 families	2005
Nicole Gaukrodger Dr Helen Imrie Dr Peter Avery Michelle Baker Hannah Watkins et al.	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	2005
Michelle Baker Nicole Gaukrodger Dr Helen Imrie Hannah Watkins Judith Connell et al.	Association between common polymorphisms of the pro-opiomelanocortin (POMC) gene and body fat distribution: A family study	2005
Michelle Baker Nicole Gaukrodger Dr Helen Imrie Hannah Watkins Dr Peter Avery et al.	Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: A family study	2005
Dr Peter Avery Michelle Baker Nicole Gaukrodger Dr Helen Imrie Hannah Watkins et al.	Association between the-174G/C polymorphism of the interleukin-6 gene and carotid atherosclerosis: Family study and meta-analysis	2005
Professor Bernard Keavney	Common genetic polymorphisms and coronary artery disease	2005
Professor Bernard Keavney Nicole Gaukrodger Dr Helen Imrie Michelle Baker Dr Rachael Fraser et al.	Genetic variation at the locus encompassing 11-β hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion	2005
Dr Peter Avery Michelle Baker Nicole Gaukrodger Dr Helen Imrie Hannah Watkins et al.	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	2005
Professor Bernard Keavney	Commentary: Katan's remarkable foresight: Genes and causality 18 years on	2004
Professor Bernard Keavney	Four paraoxonase gene polymorphisms in 11 212 cases of coronary heart disease and 12 786 controls: Meta-analysis of 43 studies	2004
Professor Bernard Keavney	Lipid-related genes and myocardial infarction in 4685 cases and 3460 controls: Discrepancies between genotype, blood lipid concentrations, and coronary disease risk	2004
Dr Janice Wheeler Professor Bernard Keavney Hannah Watkins	Paraoxonase polymorphisms and coronary heart disease - Reply	2004
Professor Bernard Keavney	In search of genetic precision	2003
Professor Bernard Keavney	In search of genetic precision - Reply	2003
Professor Bernard Keavney	Large-scale evidence that the cardiotoxicity of smoking is not significantly modified by the apolipoprotein E ε2/ε3/ε4 genotype	2003
Professor Bernard Keavney	Measured haplotype analysis of the aldosterone synthase gene and heart size	2003
Professor Bernard Keavney	Outcome following percutaneous coronary intervention: Not, so far, in our genes	2003
Professor Bernard Keavney	Angiotensin converting enzyme insertion or deletion polymorphism and coronary restenosis: meta-analysis of 16 studies	2002
Professor Bernard Keavney Hannah Watkins	Electrocardiographic measures of left ventricular hypertrophy show greater heritability than echocardiographic left ventricular mass	2002
Professor Bernard Keavney	Genetic epidemiological studies of coronary heart disease	2002
Professor Bernard Keavney	Genotype at a promoter polymorphism of the interleukin-6 gene is associated with baseline levels of plasma C-reactive protein	2002
Professor Bernard Keavney Hannah Watkins	Measured haplotype analysis of the aldosterone synthase gene and cardiac hypertrophy	2002
Hannah Watkins Professor Bernard Keavney	Evidence for a quantitative trait locus for plasma fibrinogen from a family-based association study	2001
Professor Bernard Keavney Hannah Watkins	Evolution of genetic analysis strategies in coronary heart disease: a case of unnatural selection?	2001
Professor Bernard Keavney	SNPs and snails and puppy dogs' tails: analysis of SNP haplotype data using the gamete competition model	2001
Professor Bernard Keavney	Trans-ethnic fine mapping of a quantitative trait locus for circulating angiotensin I-converting enzyme (ACE)	2001
Professor Bernard Keavney	Genetic association studies in complex diseases	2000
Professor Bernard Keavney	Genetics of coronary heart disease: Current knowledge and research principles	2000
Professor Bernard Keavney Dr Adrian Palmer	Large scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls	2000
Professor Bernard Keavney Stephen Clark	Large-scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls. International Studies of Infarct Survival (ISIS) Collaborators.	2000
Professor Bernard Keavney	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	2000
Professor Bernard Keavney	Recommendations for national and local regulatory authorities concerning research in genetic markers of disease	2000
Professor Bernard Keavney	Screening for the GRA mutation in Jamaica	2000