Keavney, Bernard

Global birth prevalence of congenital heart defects 1970–2017: updated systematic review and meta-analysis of 260 studies

Liu, Y., Chen, S., Zühlke, L., Black, G. C., Choy, M.-K., Li, N., & Keavney, B. D. (2019) · International Journal of Epidemiology

Congenital Heart Disease StudiesCongenital heart defects research

Cited by 1,436

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

Program, T. M. V., Evangelou, E., Warren, H. R., Mosen-Ansorena, D., Mifsud, B., Pazoki, R., Gao, H., Ntritsos, G., Dimou, N., Cabrera, C. P., et al. (2018) · Nature Genetics

Genetic Associations and EpidemiologyBlood Pressure and Hypertension Studies

Cited by 1,381

Association of apolipoprotein E genotypes with lipid levels and coronary risk

Bennet, A. M., Di Angelantonio, E., Ye, Z., Wensley, F., Dahlin, A., Ahlbom, A., Keavney, B., Collins, R., Wiman, B., de Faire, U., et al. (2007) · JAMA

Lipoproteins and Cardiovascular HealthGenetic Associations and Epidemiology

Cited by 794

Enabling the genomic revolution in Africa

The H3Africa Consortium, Matovu, E., Bucheton, B., Chisi, J., Enyaru, J., Hertz-Fowler, C., Koffi, M., Macleod, A., Mumba, D., Sidibe, I., et al. (2014) · Science

Genetics, Bioinformatics, and Biomedical ResearchBiotechnology and Related Fields

Cited by 519

Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease

Soemedi, R., Wilson, I. J., Bentham, J., Darlay, R., Töpf, A., Zelenika, D., Cosgrove, C., Setchfield, K., Thornborough, C., Granados-Riveron, J., et al. (2012) · The American Journal of Human Genetics

Genomic variations and chromosomal abnormalitiesCongenital heart defects research

Cited by 315

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

Gupta, P., Patel, P., Štrauch, B., Lai, F. Y., Akbarov, A., Gulsin, G. S., Beech, A., Marešová, V., Topham, P. S., Stanley, A., et al. (2017) · Hypertension

Medication Adherence and ComplianceBlood Pressure and Hypertension Studies

Cited by 194

Whole exome sequencing reveals the major genetic contributors to nonsyndromic tetralogy of Fallot

Page, D. J., Miossec, M. J., Williams, S. G., Monaghan, R. M., Fotiou, E., Cordell, H. J., Sutcliffe, L., Topf, A., Bourgey, M., Bourque, G., et al. (2019) · Circulation Research

Congenital heart defects researchCongenital Heart Disease Studies

Cited by 189

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

Martin, R. I. R., Pogoryelova, O., Koref, M. S., Bourke, J. P., Teare, M. D., & Keavney, B. D. (2014) · Heart

Atrial Fibrillation Management and OutcomesHeart rate and cardiovascular health

Cited by 161

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

Bennaceur, K., Atwill, M., Al Zhrany, N., Hoffmann, J., Keavney, B., Breault, D., Richardson, G., von Zglinicki, T., Saretzki, G., & Spyridopoulos, I. (2014) · Atherosclerosis

Telomeres, Telomerase, and SenescenceAtherosclerosis and Cardiovascular Diseases

Cited by 51

A Common Variant in the PTPN11 Gene Contributes to the Risk of Tetralogy of Fallot

Goodship, J. A., Hall, D., Topf, A., Mamasoula, C., Griffin, H., Rahman, T. J., Glen, E., Tan, H., Palomino Doza, J., Relton, C. L., et al. (2012) · Circulation: Cardiovascular Genetics

Congenital Heart Disease StudiesCongenital heart defects research

Cited by 38

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

Palomino Doza, J., Topf, A., Bentham, J., Bhattacharya, S., Cosgrove, C., Brook, J. D., Granados-Riveron, J., Bu’Lock, F. A., O’Sullivan, J., Stuart, A. G., et al. (2013) · BMC Genetics

Congenital heart defects researchCongenital Heart Disease Studies

Cited by 14