Bernard Keavney

2024

FLT4 causes developmental disorders of the cardiovascular and lymphovascular systems via pleiotropic molecular mechanisms

Monaghan, R. M., Naylor, R. W., Flatman, D., Kasher, P. R., Williams, S. G. & Keavney, B. D., 1 Jul 2024, In: Cardiovascular research. 120, 10, p. 1164-1176 13 p., cvae104.

Research output: Contribution to journal › Article › peer-review

Open Access

Genetic imputation of kidney transcriptome, proteome and multi-omics illuminates new blood pressure and hypertension targets

Human Kidney Tissue Resource Study Group, Xu, X., Khunsriraksakul, C., Eales, J. M., Rubin, S., Scannali, D., Saluja, S., Talavera, D., Markus, H., Wang, L., Drzal, M., Maan, A., Lay, A. C., Prestes, P. R., Regan, J., Diwadkar, A. R., Denniff, M., Rempega, G., Ryszawy, J. & Król, R. & 19 others, Dormer, J. P., Szulinska, M., Walczak, M., Antczak, A., Matías-García, P. R., Waldenberger, M., Woolf, A. S., Keavney, B., Zukowska-Szczechowska, E., Wystrychowski, W., Zywiec, J., Bogdanski, P., Danser, A. H. J., Samani, N. J., Guzik, T. J., Morris, A. P., Liu, D. J., Charchar, F. J. & Tomaszewski, M., 19 Mar 2024, In: Nature Communications. 15, 1, 2359.

Research output: Contribution to journal › Article › peer-review

Open Access

Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits

Morris, A., Keavney, B. & al, E., 11 Mar 2024, (Accepted/In press) In: Nature Genetics.

Research output: Contribution to journal › Article › peer-review

GET: a generic deep learning-based edge detection and optical tracking toolbox for 3D cardiac organoids and genetic investigations

Liu, Y., Teay, S. H. & Keavney, B., Jun 2024, In: Heart.

Research output: Contribution to journal › Article › peer-review

Interactive molecular causal networks of hypertension using a fast machine learning algorithm MRdualPC

Kelly, J., Xu, X., Eales, J. M., Keavney, B., Berzuini, C., Tomaszewski, M. & Guo, H., 2 Aug 2024, In: BMC Medical Research Methodology . 24, 1, 168.

Research output: Contribution to journal › Article › peer-review

Open Access

The impact of COVID-19 vaccination on patients with congenital heart disease in England: a case-control study

CVD-COVID-UK/COVID-IMPACT consortium , 11 Oct 2024, In: Heart. 9 p.

Research output: Contribution to journal › Article › peer-review

Open Access

Unsupervised ensemble-based phenotyping enhances discoverability of genes related to left-ventricular morphology

Bonazzola, R., Ferrante, E., Ravikumar, N., Xia, Y., Keavney, B., Plein, S., Syeda-Mahmood, T. & Frangi, A. F., Mar 2024, In: Nature Machine Intelligence. 6, 3, p. 291-306 16 p.

Research output: Contribution to journal › Article › peer-review

Open Access

2023

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

Bawamia, B., Spray, L., Wangsaputra, V. K., Bennaceur, K., Vahabi, S., Stellos, K., Kharatikoopaei, E., Ogundimu, E., Gale, C. P., Keavney, B., Maier, R., Hancock, H., Richardson, G., Austin, D. & Spyridopoulos, I., 1 Aug 2023, In: Geroscience. 45, 4, p. 2689-2705 17 p.

Research output: Contribution to journal › Article › peer-review

Open Access

Clinical risk associated with COVID-19 among 86000 patients with congenital heart disease

Williams, S. G., Frain, S., Guo, H., Carr, M. J., Ashcroft, D. M. & Keavney, B. D., 14 Dec 2023, In: Open Heart. 10, 2, e002415.

Research output: Contribution to journal › Article › peer-review

Open Access

Predicting congenital renal tract malformation genes using machine learning

Kabir, M., Stuart, H., Lopes, F., Fotiou, E., Keavney, B., Doig, A., Woolf, A. S. & Hentges, K., 14 Aug 2023, In: Scientific Reports. 13, 13204.

Research output: Contribution to journal › Article › peer-review

Open Access

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

RHDGen Network Consortium†, 1 Feb 2023, In: Circulation: Genomic and precision medicine. 16, 1, e003641.

Research output: Contribution to journal › Article

Open Access

2022

A review of causal discovery methods for molecular network analysis

Kelly, J., Berzuini, C., Keavney, B., Tomaszewski, M. & Guo, H., 1 Oct 2022, In: Molecular Genetics and Genomic Medicine. 10, 10, e2055.

Research output: Contribution to journal › Article › peer-review

Open Access

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

Liu, Y., Choy, M.-K., Abraham, S., Tenin, G., Black, G. C. & Keavney, B. D., 8 Aug 2022, In: Genes & Diseases.

Research output: Contribution to journal › Article › peer-review

Open Access

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

KORA-Study Group, 21 Jan 2022, In: Circulation research. 130, 2, p. 166-180 15 p.

Research output: Contribution to journal › Article › peer-review

Open Access

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

RHDGen Network Consortium, 22 Mar 2022, In: Clinical Proteomics. 19, 1, p. 7

Research output: Contribution to journal › Article › peer-review

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

Liu, Y., Choy, M.-K., Abraham, S., Tenin, G., Black, G. C. & Keavney, B. D., Dec 2022, In: Data in Brief. 45, p. 108770

Research output: Contribution to journal › Article › peer-review

Genetic analyses of circulating PUFA-derived mediators identifies heritable dihydroxyeicosatrienoic acid species

McGurk, K. A., Farrell, L., Kendall, A. C., Keavney, B. D. & Nicolaou, A., Jun 2022, In: Prostaglandins and Other Lipid Mediators. 160, p. 106638

Research output: Contribution to journal › Article › peer-review

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

Teekakirikul, P., Zhu, W., Xu, X., Young, C. B., Tan, T., Smith, A. M., Wang, C., Peterson, K. A., Gabriel, G. C., Ho, S., Sheng, Y., Moreau de Bellaing, A., Sonnenberg, D. A., Lin, J.-H., Fotiou, E., Tenin, G., Wang, M. X., Wu, Y. L., Feinstein, T. & Devine, W. & 17 others, Gou, H., Bais, A. S., Glennon, B. J., Zahid, M., Wong, T. C., Ahmad, F., Rynkiewicz, M. J., Lehman, W. J., Keavney, B., Alastalo, T.-P., Freckmann, M.-L., Orwig, K., Murray, S., Ware, S. M., Zhao, H., Feingold, B. & Lo, C. W., 15 Feb 2022, In: Cell reports. Medicine. 3, 2, p. 100501

Research output: Contribution to journal › Article

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

Saacks, N., Eales, J., Spracklen, T., Aldersley, T., Human, P., Verryn, M., Lawrenson, J. G., Cupido, B., Comitis, G., De Decker, R., Fourie, B., Swanson, L., Joachim, A., Brooks, A., Ramesar, R. S., Shaboodien, G., Keavney, B. & Zuhlke, L., 11 Mar 2022, (Accepted/In press) In: Circulation: Genomic and precision medicine.

Research output: Contribution to journal › Article › peer-review

Joint analysis of functionally related genes yields further candidates associated with Tetralogy of Fallot

Chelu, A., Williams, S., Keavney, B. D. & Talavera, D., 20 Jun 2022, In: Journal of Human Genetics.

Research output: Contribution to journal › Article › peer-review

Open Access

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

Byrne, D., Williams, S. G., Nakev, A., Frain, S., Baross, S., Vestbo, J., Keavney, B. & Talavera, D., 4 Nov 2022, In: Scientific Reports. 12, 1, 18703.

Research output: Contribution to journal › Article › peer-review

Open Access

2021

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

Liu, Y., Williams, S., Jones, H., Keavney, B. & Choy, M.-K., 1 Dec 2021, In: Scientific Reports. 11, 23233.

Research output: Contribution to journal › Article › peer-review

Open Access

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

Machipisa, T., Chong, M., Muhamed, B., Chishala, C., Shaboodien, G., Pandie, S., de Vries, J., Laing, N., Joachim, A., Daniels, R., Ntsekhe, M., Hugo-Hamman, C. T., Gitura, B., Ogendo, S., Lwabi, P., Okello, E., Damasceno, A., Novela, C., Mocumbi, A. O. & Madeira, G. & 15 others, Musuku, J., Mtaja, A., ElSayed, A., Elhassan, H. H. M., Bode-Thomas, F., Okeahialam, B. N., Zühlke, L. J., Mulder, N., Ramesar, R., Lesosky, M., Parks, T., Cordell, H. J., Keavney, B., Engel, M. E. & Paré, G., 1 Sept 2021, In: JAMA Cardiology. 6, 9, p. 1000-1011 12 p.

Research output: Contribution to journal › Article

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

Trevino, C. E., Holleman, A. M., Corbitt, H., Maslen, C. L., Rosser, T. C., Cutler, D. J., Johnston, H. R., Rambo-Martin, B. L., Oberoi, J., Dooley, K. J., Capone, G. T., Reeves, R. H., Cordell, H. J., Keavney, B. D., Agopian, A. J., Goldmuntz, E., Gruber, P. J., O'Brien, J. E., Bittel, D. C. & Wadhwa, L. & 6 others, Cua, C. L., Moskowitz, I. P., Mulle, J. G., Epstein, M. P., Sherman, S. L. & Zwick, M. E., 20 Jul 2021, In: Scientific Reports. 11, 1, p. 15164

Research output: Contribution to journal › Article › peer-review

Open Access

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

McGurk, K., Keavney, B. & Nicolaou, A., 6 May 2021, In: Atherosclerosis. 327, p. 18-30 13 p.

Research output: Contribution to journal › Article › peer-review

Open Access

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

Reuter, M., Chaturvedi, R., Jobling, R., Pellecchia, G., Hamdan, O., Chung, W., Nalpathamkalam, T., Silversides, C., Wald, R., Marshall, C., Williams, S., Keavney, B., Thiruvahindrapuram, B., Scherer, S. & Bassett, A., Aug 2021, In: Circulation: Genomic and precision medicine. 14, 4, p. 476-484 e003410.

Research output: Contribution to journal › Article › peer-review

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

Lahm, H., Jia, M., Dreßen, M., Wirth, F., Puluca, N., Gilsbach, R., Keavney, B. D., Cleuziou, J., Beck, N., Bondareva, O., Dzilic, E., Burri, M., König, K. C., Ziegelmüller, J. A., Abou-Ajram, C., Neb, I., Zhang, Z., Doppler, S. A., Mastantuono, E. & Lichtner, P. & 10 others, Eckstein, G., Hörer, J., Ewert, P., Priest, J. R., Hein, L., Lange, R., Meitinger, T., Cordell, H. J., Müller-Myhsok, B. & Krane, M., 19 Jan 2021, In: The Journal of clinical investigation. 131, 2

Research output: Contribution to journal › Article › peer-review

Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

Audain, E., Wilsdon, A., Breckpot, J., Izarzugaza, J. M. G., Fitzgerald, T. W., Kahlert, A.-K., Sifrim, A., Wünnemann, F., Perez-Riverol, Y., Abdul-Khaliq, H., Bak, M., Bassett, A. S., Benson, D. W., Berger, F., Daehnert, I., Devriendt, K., Dittrich, S., Daubeney, P. E., Garg, V. & Hackmann, K. & 30 others, Hoff, K., Hofmann, P., Dombrowsky, G., Pickardt, T., Bauer, U., Keavney, B. D., Klaassen, S., Kramer, H.-H., Marshall, C. R., Milewicz, D. M., Lemaire, S., Coselli, J. S., Mitchell, M. E., Tomita-Mitchell, A., Prakash, S. K., Stamm, K., Stewart, A. F. R., Silversides, C. K., Siebert, R., Stiller, B., Rosenfeld, J. A., Vater, I., Postma, A. V., Caliebe, A., Brook, J. D., Andelfinger, G., Hurles, M. E., Thienpont, B., Larsen, L. A. & Hitz, M.-P., Sept 2021, In: PLoS Genetics. 17, 9, p. e1009809

Research output: Contribution to journal › Article › peer-review

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

German Competence Network for Congenital Heart Defects, Oct 2021, In: Genetics in medicine : official journal of the American College of Medical Genetics. 23, 10, p. 2013

Research output: Contribution to journal › Article › peer-review

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

Malhotra, A., Oxborough, D., Rao, P., Finocchiaro, G., Dhutia, H., Prasad, V., Miller, C., Keavney, B., Papadakis, M. & Sharma, S., 5 Jan 2021, In: Circulation. 143, 1, p. 94-96 3 p.

Research output: Contribution to journal › Article › peer-review

Open Access

Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome

McGurk, K., Williams, S., Guo, H., Watkins, H., Farrall, M., Cordell, H. J., Nicolaou, A. & Keavney, B., 15 Mar 2021, In: Human Molecular Genetics.

Research output: Contribution to journal › Article › peer-review

Open Access

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

Audain, E., Wilsdon, A., Breckpot, J., Izarzugaza, J. M. G., Fitzgerald, T. W., Kahlert, A.-K., Sifrim, A., Wünnemann, F., Perez-Riverol, Y., Abdul-Khaliq, H., Bak, M., Bassett, A. S., Benson, D. W., Berger, F., Daehnert, I., Devriendt, K., Dittrich, S., Daubeney, P. E., Garg, V. & Hackmann, K. & 30 others, Hoff, K., Hofmann, P., Dombrowsky, G., Pickardt, T., Bauer, U., Keavney, B. D., Klaassen, S., Kramer, H.-H., Marshall, C. R., Milewicz, D. M., Lemaire, S., Coselli, J. S., Mitchell, M. E., Tomita-Mitchell, A., Prakash, S. K., Stamm, K., Stewart, A. F. R., Silversides, C. K., Siebert, R., Stiller, B., Rosenfeld, J. A., Vater, I., Postma, A. V., Caliebe, A., Brook, J. D., Andelfinger, G., Hurles, M. E., Thienpont, B., Larsen, L. A. & Hitz, M.-P., Jul 2021, In: PLoS Genetics. 17, 7, p. e1009679

Research output: Contribution to journal › Article › peer-review

PROTEA, A Southern African Multicenter Congenital Heart Disease Registry and Biorepository: Rationale, Design, and Initial Results

Aldersley, T., Lawrenson, J., Human, P., Shaboodien, G., Cupido, B., Comitis, G., De Decker, R., Fourie, B., Swanson, L., Joachim, A., Magadla, P., Ngoepe, M., Swanson, L., Revell, A., Ramesar, R., Brooks, A., Saacks, N., De Koning, B., Sliwa, K. & Anthony, J. & 3 others, Osman, A., Keavney, B. & Zühlke, L., 20 Oct 2021, In: Frontiers in pediatrics. 9

Research output: Contribution to journal › Article › peer-review

Open Access

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105 Downloads (Pure)

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

Williams, S., Byrne, D. & Keavney, B., 7 Sept 2021, In: Journal of Human Genetics. 66, p. 123 - 125 3 p.

Research output: Contribution to journal › Article › peer-review

Open Access

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

Škorić-Milosavljević, D., Lahrouchi, N., Bosada, F., Dombrowsky, G., Williams, S., Lesurf, R., Tjong, F., Walsh, R., El, B. I., Breckpot, J., Audain, E., Bezzina, C. & Keavney, B., 10 Jun 2021, In: Genetics in medicine : official journal of the American College of Medical Genetics.

Research output: Contribution to journal › Article › peer-review

Open Access

File

61 Downloads (Pure)

Rationale and design of the African Cardiomyopathy and Myocarditis Registry Program: The IMHOTEP study

IMHOTEP Investigators, 15 Jun 2021, In: International Journal of Cardiology. 333, p. 119-126 8 p.

Research output: Contribution to journal › Article › peer-review

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

Gurumurthy, C. B., O'Brien, A. R., Quadros, R. M., Adams, J., Alcaide, P., Ayabe, S., Ballard, J., Batra, S. K., Beauchamp, M.-C., Becker, K. A., Bernas, G., Brough, D., Carrillo-Salinas, F., Chan, W., Chen, H., Dawson, R., DeMambro, V., D'Hont, J., Dibb, K. & Eudy, J. D. & 93 others, Gan, L., Gao, J., Gonzales, A., Guntur, A., Guo, H., Harms, D. W., Harrington, A., Hentges, K. E., Humphreys, N., Imai, S., Ishii, H., Iwama, M., Jonasch, E., Karolak, M., Keavney, B., Khin, N.-C., Konno, M., Kotani, Y., Kunihiro, Y., Lakshmanan, I., Larochelle, C., Lawrence, C. B., Li, L., Lindner, V., Liu, X.-D., Lopez-Castejon, G., Loudon, A., Lowe, J., Jerome-Majeweska, L., Matsusaka, T., Miura, H., Miyasaka, Y., Morpurgo, B., Motyl, K., Nabeshima, Y.-I., Nakade, K., Nakashiba, T., Nakashima, K., Obata, Y., Ogiwara, S., Ouellet, M., Oxburgh, L., Piltz, S., Pinz, I., Ponnusamy, M. P., Ray, D., Redder, R. J., Rosen, C. J., Ross, N., Ruhe, M. T., Ryzhova, L., Salvador, A. M., Alam, S. S., Sedlacek, R., Sharma, K., Smith, C., Staes, K., Starrs, L., Sugiyama, F., Takahashi, S., Tanaka, T., Trafford, A., Uno, Y., Vanhoutte, L., Vanrockeghem, F., Willis, B. J., Wright, C. S., Yamauchi, Y., Yi, X., Yoshimi, K., Zhang, X., Zhang, Y., Ohtsuka, M., Das, S., Garry, D. J., Hochepied, T., Thomas, P., Parker-Thornburg, J., Adamson, A. D., Yoshiki, A., Schmouth, J.-F., Golovko, A., Thompson, W. R., Lloyd, K. C. K., Wood, J. A., Cowan, M., Mashimo, T., Mizuno, S., Zhu, H., Kasparek, P., Liaw, L., Miano, J. M. & Burgio, G., 7 Apr 2021, In: Genome Biology. 22, 1, p. 99

Research output: Contribution to journal › Article › peer-review

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

Eales, J., Jiang, X., Xu, X., Saluja, S., Akbarov, A., Cano-Gomez, E., McNulty, M. T., Finan, C., Guo, H., Wystrychowski, W., Szulinska, M., Thomas, H., Pramanik, S., Chopade, S., Prestes, P. R., Wise, I., Evangelou, E., Salehi, M., Shakanti, Y. & Ekholm, M. & 30 others, Denniff, M., Nazgiewicz, A., Eichinger, F., Godfrey, B., Antczak, A., Glyda, M., Król, R., Eyre, S., Brown, J., Berzuini, C., Bowes, J., Caulfield, M., Zukowska-Szczechowska, E., Zywiec, J., Bogdanski, P., Kretzler, M., Woolf, A. S., Talavera, D., Keavney, B., Maffia, P., Guzik, T. J., O'Keefe, R., Trynka, G., Samani, N. J., Hingorani, A. D., Sampson, M. G., Morris, A. P., Charchar, F. J., Tomaszewski, M. & Morris, A., 6 May 2021, In: Nature Genetics. 53, 5, p. 630–637 8 p.

Research output: Contribution to journal › Article › peer-review

Open Access

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2020

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

Swanson, L., Owen, B., Keshmiri, A., Deyranlou, A., Aldersley, T., Lawrenson, J., Human, P., De Decker, R., Fourie, B., Comitis, G., Engel, M. E., Keavney, B., Zühlke, L., Ngoepe, M. & Revell, A., 3 Jun 2020, In: Frontiers in Bioengineering and Biotechnology. 8, 409.

Research output: Contribution to journal › Article › peer-review

Open Access

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

Williams, S., Nakev, A., Guo, H., Frain, S., Tenin, G., Liakhovitskaia, A., Priest, J., Hentges, K. & Keavney, B., 1 Sept 2020, In: European Journal of Human Genetics. 28, p. 1265–1273

Research output: Contribution to journal › Article › peer-review

Open Access

Cardiac Imaging of Aortic Valve Area From 34 287 UK Biobank Participants Reveals Novel Genetic Associations and Shared Genetic Comorbidity With Multiple Disease Phenotypes

Córdova-Palomera, A., Tcheandjieu, C., Fries, J. A., Varma, P., Chen, V. S., Fiterau, M., Xiao, K., Tejeda, H., Keavney, B. D., Cordell, H. J., Tanigawa, Y., Venkataraman, G., Rivas, M. A., Ré, C., Ashley, E. & Priest, J. R., Dec 2020, In: Circulation: Genomic and precision medicine. 13, 6, p. 609-617 9 p., e003014.

Research output: Contribution to journal › Article › peer-review

Open Access

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

Martin-Ruiz, C., Hoffmann, J., Shmeleva, E., Zglinicki, T. V., Richardson, G., Draganova, L., Redgrave, R., Collerton, J., Arthur, H., Keavney, B. & Spyridopoulos, I., 21 Jan 2020, (E-pub ahead of print) In: npj Aging and Mechanisms of Disease. 6, 1, 3.

Research output: Contribution to journal › Article › peer-review

Open Access

Global prevalence of Congenital Heart Disease in school-age children: a meta-analysis and systematic review

Liu, Y., Chen, S., Zuhlke, L., Babu-Narayan, S. V., Black, G., Choy, M.-K., Li, N. & Keavney, B., 19 Nov 2020, In: B M C Cardiovascular Disorders. 20

Research output: Contribution to journal › Article › peer-review

Open Access

Heritability of haemodynamics in the ascending aorta

McGurk, K., Owen, B., Watson, W., Nethononda, R., Cordell, H. J., Farrall, M., Rider, O. J., Watkins, H., Revell, A. & Keavney, B., 1 Sept 2020, In: Scientific Reports. 10, 14356.

Research output: Contribution to journal › Article › peer-review

Open Access

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

Jiang, X., Eales, J. M., Scannali, D., Nazgiewicz, A., Prestes, P., Maier, M., Denniff, M., Xu, X., Saluja, S., Cano-Gamez, E., Wystrychowski, W., Szulinska, M., Antczak, A., Byars, S., Skrypnik, D., Glyda, M., Król, R., Zywiec, J., Zukowska-Szczechowska, E. & Burrell, L. M. & 13 others, Woolf, A. S., Greenstein, A., Bogdanski, P., Keavney, B., Morris, A. P., Heagerty, A., Williams, B., Harrap, S. B., Trynka, G., Samani, N. J., Guzik, T. J., Charchar, F. J. & Tomaszewski, M., 27 Oct 2020, In: European Heart Journal . 41, 48, p. 4580-4588 9 p.

Research output: Contribution to journal › Article › peer-review

Open Access

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

Trevino, C. E., Holleman, A. M., Corbitt, H., Maslen, C. L., Rosser, T. C., Cutler, D. J., Johnston, H. R., Rambo-Martin, B. L., Oberoi, J., Dooley, K. J., Capone, G. T., Reeves, R. H., Cordell, H. J., Keavney, B. D., Agopian, A. J., Goldmuntz, E., Gruber, P. J., O'Brien, J. E., Bittel, D. C. & Wadhwa, L. & 6 others, Cua, C. L., Moskowitz, I. P., Mulle, J. G., Epstein, M. P., Sherman, S. L. & Zwick, M. E., 22 Oct 2020, In: Scientific Reports. 10, 1, p. 18051

Research output: Contribution to journal › Article › peer-review

Open Access

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

McGurk, K., Dagliati, A., Chiasserini, D., Lee, D., Plant, D., Baricevic-Jones, I., Kelsall, J., Eineman, R., Reed, R., Geary, B., Unwin, R., Nicolaou, A., Keavney, B., Barton, A., Whetton, A. & Geifman, N., 1 Apr 2020, In: Bioinformatics. 36, 7, p. 2217-2223 7 p.

Research output: Contribution to journal › Article › peer-review

Open Access

Vector-based discrete element method for solid elastic materials

Owen, B., Nasar, A., Harwood, A., Hewitt, S., Bojdo, N., Keavney, B., Rogers, B. D. & Revell, A., 4 May 2020, (Accepted/In press) In: Computer Physics Communications.

Research output: Contribution to journal › Article › peer-review

2019

Does rhythm matter in Acute Heart Failure? an insight from the British Society for Heart Failure National Audit

Anderson, S., Shoaib, A., Myint, P. K., Cleland, J., Hardman, S. M., McDonagh, T., Dargie, H., Keavney, B., Garratt, C. & Mamas, M., 2019, In: Clinical Research in Cardiology.

Research output: Contribution to journal › Article › peer-review

Open Access

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

Testori, A., Lasorsa, V. A., Cimmino, F., Cantalupo, S., Cardinale, A., Avitabile, M., Limongelli, G., Russo, M. G., Diskin, S., Maris, J., Devoto, M., Keavney, B., Cordell, H. J., Iolascon, A. & Capasso, M., 30 Aug 2019, In: Genes. 10, 9

Research output: Contribution to journal › Article › peer-review

Open Access

Bernard Keavney, BSc BM BCh DM FRCP

Research output

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