Author details

Full Name

Bernard Keavney

Affiliation

ORCID

Career Start Year

1995

Papers

198

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36548480	Rationale, Design, and the Baseline Characteristics of the RHDGen (The Genetics of Rheumatic Heart Disease) Network Studyâ¿ .	Circ Genom Precis Med	2023
37580336	Predicting congenital renal tract malformation genes using machine learning.	Sci Rep	2023
37086366	Activation of telomerase by TA-65 enhances immunity and reduces inflammation post myocardial infarction.		2023
35140110	Modern genomic techniques in the identification of genetic causes of cardiomyopathy.	Heart	2022
36087049	A review of causal discovery methods for molecular network analysis.	Molecular genetics & genomic medicine	2022
36333391	Significantly increased risk of chronic obstructive pulmonary disease amongst adults with predominantly mild congenital heart disease.	Scientific Reports	2022
36205932	Investigation of Copy Number Variation in South African Patients With Congenital Heart Defects.	Circulation. Genomic and precision medicine	2022
35472599	Genetic analyses of circulating PUFA-derived mediators identifies heritable dihydroxyeicosatrienoic acid species.	Prostaglandins and Other Lipid Mediators	2022
35718831	Joint analysis of functionally related genes yields further candidates associated with Tetralogy of Fallot.	Journal of Human Genetics	2022
37397526	Atrial Septal Defect (ASD) associated long non-coding RNA <i>STX18-AS1</i> maintains time-course of <i>in vitro</i> cardiomyocyte differentiation.	Genes Dis	2022
36533287	Data on cardiac lncRNA <i>STX18-AS1</i> expression in developing human hearts and function during <i>in vitro</i> hESC-cardiomyocyte differentiation.	Data Brief	2022
34493817	Rare GATA6 variants associated with risk of congenital heart disease phenotypes in 200,000 UK Biobank exomes.	Journal of Human Genetics	2022
34886679	Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries.	Circ Res	2022
34547032	Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.	PLoS Genet	2021
34285246	Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.	Sci Rep	2021
33958779	Uncovering genetic mechanisms of hypertension through multi-omic analysis of the kidney.	Nat Genet	2021
34004484	Circulating ceramides as biomarkers of cardiovascular disease: Evidence from phenotypic and genomic studies.	Atherosclerosis	2021
34106200	Association of Novel Locus With Rheumatic Heart Disease in Black African Individuals: Findings From the RHDGen Study.	JAMA Cardiol	2021
33607192	Rationale and design of the African Cardiomyopathy and Myocarditis Registry Program: The IMHOTEP study.	Int J Cardiol	2021
33827648	Response to correspondence on "Reproducibility of CRISPR-Cas9 methods for generation of conditional mouse alleles: a multi-center evaluation".	Genome Biol	2021
33437986	Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome.	Hum Mol Genet	2021
34328347	Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot.	Circ Genom Precis Med	2021
33378235	Defining the Normal Spectrum of Electrocardiographic and Left Ventricular Adaptations in Mixed-Race Male Adolescent Soccer Players.	Circulation	2021
33201861	Congenital heart disease risk loci identified by genome-wide association study in European patients.	J Clin Invest	2021
33067626	The physiological and pathological functions of VEGFR3 in cardiac and lymphatic development and related diseases.	Cardiovascular Research	2021
33276707	Identification of a Variant in a Family With Arrhythmogenic Cardiomyopathy and Left Ventricular Fibrosis.	Circulation. Genomic and precision medicine	2021
34746065	PROTEA, A Southern African Multicenter Congenital Heart Disease Registry and Biorepository: Rationale, Design, and Initial Results.	Frontiers in Pediatrics	2021
34853328	A novel RNA-mediated mechanism causing down-regulation of insulating promoter interactions in human embryonic stem cells.	Scientific Reports	2021
33213369	Global prevalence of congenital heart disease in school-age children: a meta-analysis and systematic review.	BMC Cardiovasc Disord	2020
31790148	The use of missing values in proteomic data-independent acquisition mass spectrometry to enable disease activity discrimination.	Bioinformatics	2020
31944917	The Open Science of Atrial Fibrillation.	Circulation Research	2020
31993214	CMV-independent increase in CD27-CD28+ CD8+ EMRA T cells is inversely related to mortality in octogenarians.	npj Aging and Mechanisms of Disease	2020
32327713	Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1-BP2) deletion in the UK Biobank.	Eur J Hum Genet	2020
33206176	Hypertension and renin-angiotensin system blockers are not associated with expression of angiotensin-converting enzyme 2 (ACE2) in the kidney.	Eur Heart J	2020
32873833	Heritability of haemodynamics in the ascending aorta.	Sci Rep	2020
32582648	A Patient-Specific CFD Pipeline Using Doppler Echocardiography for Application in Coarctation of the Aorta in a Limited Resource Clinical Context.	Frontiers in Bioengineering and Biotechnology	2020
33125279	Cardiac Imaging of Aortic Valve Area From 34 287 UK Biobank Participants Reveals Novel Genetic Associations and Shared Genetic Comorbidity With Multiple Disease Phenotypes.	Circ Genom Precis Med	2020
31480262	Exploring Shared Susceptibility between Two Neural Crest Cells Originating Conditions: Neuroblastoma and Congenital Heart Disease.	Genes (Basel)	2019
31613678	Integration of Large-Scale Genomic Data Sources With Evolutionary History Reveals Novel Genetic Loci for Congenital Heart Disease.	Circulation. Genomic and precision medicine	2019
30582441	Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot.	Circ Res	2019
31537879	Marked variation in heritability estimates of left ventricular mass depending on modality of measurement.	Sci Rep	2019
31505685	Scientific Business Abstracts of the 113th Annual Meeting of the Association of Physicians of Great Britain and Ireland.	QJM	2019
31505685	Scientific Business Abstracts of the 113th Annual Meeting of the Association of Physicians of Great Britain and Ireland.	QJM	2019
31505685	Scientific Business Abstracts of the 113th Annual Meeting of the Association of Physicians of Great Britain and Ireland.	QJM	2019
30870123	Chicken or Egg in the UK Biobank?	Circulation Research	2019
30963233	Does rhythm matter in acute heart failure? An insight from the British Society for Heart Failure National Audit.	Clin Res Cardiol	2019
30783674	Global birth prevalence of congenital heart defects 1970-2017: updated systematic review and meta-analysis of 260 studies.	Int J Epidemiol	2019
29307480	Corrigendum to "Cardiovascular, obstetric and neonatal outcomes in women with a previous Fontan repair'' [Eur. J. Obstet. Gynaecol. Reprod. Biol. 219 (2017) 53-56].	European Journal of Obstetrics, Gynecology and Reproductive Biology	2018
30309464	Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults: Implications for Primary Prevention.	J Am Coll Cardiol	2018
30429575	Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.	Nat Genet	2018