Keavney BD - Search Results

1

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

Williams SG, Frain S, Guo H, Carr MJ, Ashcroft DM, Keavney BD. Williams SG, et al. Among authors: keavney bd. Open Heart. 2023 Dec 14;10(2):e002415. doi: 10.1136/openhrt-2023-002415. Open Heart. 2023. PMID: 38097365 Free PMC article.

2

Induced pluripotent stem cell modelling of HLHS underlines the contribution of dysfunctional NOTCH signalling to impaired cardiogenesis.

Yang C, Xu Y, Yu M, Lee D, Alharti S, Hellen N, Ahmad Shaik N, Banaganapalli B, Sheikh Ali Mohamoud H, Elango R, Przyborski S, Tenin G, Williams S, O'Sullivan J, Al-Radi OO, Atta J, Harding SE, Keavney B, Lako M, Armstrong L. Yang C, et al. Hum Mol Genet. 2017 Aug 15;26(16):3031-3045. doi: 10.1093/hmg/ddx140. Hum Mol Genet. 2017. PMID: 28521042 Free PMC article.

3

Promoter interactome of human embryonic stem cell-derived cardiomyocytes connects GWAS regions to cardiac gene networks.

Choy MK, Javierre BM, Williams SG, Baross SL, Liu Y, Wingett SW, Akbarov A, Wallace C, Freire-Pritchett P, Rugg-Gunn PJ, Spivakov M, Fraser P, Keavney BD. Choy MK, et al. Among authors: keavney bd. Nat Commun. 2018 Jun 28;9(1):2526. doi: 10.1038/s41467-018-04931-0. Nat Commun. 2018. PMID: 29955040 Free PMC article.

4

Author Correction: Promoter interactome of human embryonic stem cell-derived cardiomyocytes connects GWAS regions to cardiac gene networks.

Choy MK, Javierre BM, Williams SG, Baross SL, Liu Y, Wingett SW, Akbarov A, Wallace C, Freire-Pritchett P, Rugg-Gunn PJ, Spivakov M, Fraser P, Keavney BD. Choy MK, et al. Among authors: keavney bd. Nat Commun. 2018 Nov 12;9(1):4792. doi: 10.1038/s41467-018-07399-0. Nat Commun. 2018. PMID: 30420621 Free PMC article.

5

Integration of Large-Scale Genomic Data Sources With Evolutionary History Reveals Novel Genetic Loci for Congenital Heart Disease.

Fotiou E, Williams S, Martin-Geary A, Robertson DL, Tenin G, Hentges KE, Keavney B. Fotiou E, et al. Circ Genom Precis Med. 2019 Oct;12(10):442-451. doi: 10.1161/CIRCGEN.119.002694. Epub 2019 Oct 15. Circ Genom Precis Med. 2019. PMID: 31613678 Free PMC article.

6

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

Williams SG, Nakev A, Guo H, Frain S, Tenin G, Liakhovitskaia A, Saha P, Priest JR, Hentges KE, Keavney BD. Williams SG, et al. Among authors: keavney bd. Eur J Hum Genet. 2020 Sep;28(9):1265-1273. doi: 10.1038/s41431-020-0626-8. Epub 2020 Apr 23. Eur J Hum Genet. 2020. PMID: 32327713 Free PMC article.

7

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

Eales JM, Jiang X, Xu X, Saluja S, Akbarov A, Cano-Gamez E, McNulty MT, Finan C, Guo H, Wystrychowski W, Szulinska M, Thomas HB, Pramanik S, Chopade S, Prestes PR, Wise I, Evangelou E, Salehi M, Shakanti Y, Ekholm M, 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 AS, Talavera D, Keavney B, Maffia P, Guzik TJ, O'Keefe RT, Trynka G, Samani NJ, Hingorani A, Sampson MG, Morris AP, Charchar FJ, Tomaszewski M. Eales JM, et al. Nat Genet. 2021 May;53(5):630-637. doi: 10.1038/s41588-021-00835-w. Epub 2021 May 6. Nat Genet. 2021. PMID: 33958779

8

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

Williams SG, Byrne DJF, Keavney BD. Williams SG, et al. Among authors: keavney bd. J Hum Genet. 2022 Feb;67(2):123-125. doi: 10.1038/s10038-021-00976-0. Epub 2021 Sep 7. J Hum Genet. 2022. PMID: 34493817 Free PMC article.

9

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

Salie MT, Yang J, Ramírez Medina CR, Zühlke LJ, Chishala C, Ntsekhe M, Gitura B, Ogendo S, Okello E, Lwabi P, Musuku J, Mtaja A, Hugo-Hamman C, El-Sayed A, Damasceno A, Mocumbi A, Bode-Thomas F, Yilgwan C, Amusa GA, Nkereuwem E, Shaboodien G, Da Silva R, Lee DCH, Frain S, Geifman N, Whetton AD, Keavney B, Engel ME; RHDGen Network Consortium. Salie MT, et al. Clin Proteomics. 2022 Mar 22;19(1):7. doi: 10.1186/s12014-022-09345-1. Clin Proteomics. 2022. PMID: 35317720 Free PMC article.

10

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

Chelu A, Williams SG, Keavney BD, Talavera D. Chelu A, et al. Among authors: keavney bd. J Hum Genet. 2022 Oct;67(10):613-615. doi: 10.1038/s10038-022-01051-y. Epub 2022 Jun 20. J Hum Genet. 2022. PMID: 35718831 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

139 results

Search Page