Bernard D Keavney
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Explore the profile of Bernard D Keavney including associated specialties, affiliations and a list of published articles.
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66
Citations
2959
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Recent Articles
1.
Saluja S, Myers D, Keavney B, Keshavarzi F, Anderson S
Glob Cardiol Sci Pract
. 2025 Feb;
2024(5):e202447.
PMID: 39931449
Background: Percutaneous pulmonary valve implantation (PPVI) has emerged as a promising treatment for congenital right ventricular outflow tract (RVOT) dysfunction and restoring conduit graft viability. Methods: This is a single-centre...
2.
Saluja S, Darlay R, Lennon R, Keavney B, Cordell H
J Hypertens
. 2024 Jul;
42(9):1647-1652.
PMID: 39011893
This study utilized UK Biobank data from 144 286 participants and employed whole-genome sequencing (WGS) data and time-to-event data over a 12-year follow-up period to identify susceptibility in genetic variants...
3.
Monaghan R, Naylor R, Flatman D, Kasher P, Williams S, Keavney B
Cardiovasc Res
. 2024 May;
120(10):1164-1176.
PMID: 38713105
Aims: Rare, deleterious genetic variants in FLT4 are associated with Tetralogy of Fallot (TOF), the most common cyanotic congenital heart disease. The distinct genetic variants in FLT4 are also an...
4.
Keaton J, Kamali Z, Xie T, Vaez A, Williams A, Goleva S, et al.
Nat Genet
. 2024 Apr;
56(5):778-791.
PMID: 38689001
Hypertension affects more than one billion people worldwide. Here we identify 113 novel loci, reporting a total of 2,103 independent genetic signals (P < 5 × 10) from the largest...
5.
Williams S, Frain S, Guo H, Carr M, Ashcroft D, Keavney B
Open Heart
. 2023 Dec;
10(2).
PMID: 38097365
Objective: To determine the magnitude of any excess risk of mortality and hospitalisation due to COVID-19 infection in patients with congenital heart disease (CHD) in the UK healthcare system. Methods:...
6.
Liu Y, Choy M, Abraham S, Tenin G, Black G, Keavney B
Genes Dis
. 2023 Jul;
10(4):1150-1153.
PMID: 37397526
No abstract available.
7.
Liu Y, Choy M, Abraham S, Tenin G, Black G, Keavney B
Data Brief
. 2022 Dec;
45:108770.
PMID: 36533287
This article presents data concerning , a long noncoding RNA gene identified from a Genome-wide association study of Atrial Septal Defect (ASD). The data describes its expression patterns in human...
8.
Byrne D, Williams S, Nakev A, Frain S, Baross S, Vestbo J, et al.
Sci Rep
. 2022 Nov;
12(1):18703.
PMID: 36333391
Adults with congenital heart disease (CHD) face increased risk of various comorbid diseases. Previous work on lung dysfunction in this population has mainly focused on restrictive lung disease, in patients...
9.
Saacks N, Eales J, Spracklen T, Aldersley T, Human P, Verryn M, et al.
Circ Genom Precis Med
. 2022 Oct;
15(6):e003510.
PMID: 36205932
Background: Congenital heart disease (CHD) is a leading non-infectious cause of pediatric morbidity and mortality worldwide. Although the etiology of CHD is poorly understood, genetic factors including copy number variants...
10.
Chelu A, Williams S, Keavney B, Talavera D
J Hum Genet
. 2022 Jun;
67(10):613-615.
PMID: 35718831
Although several genes involved in the development of Tetralogy of Fallot have been identified, no genetic diagnosis is available for the majority of patients. Low statistical power may have prevented...