Ware JS - Search Results

1

The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy.

Lahrouchi N, Raju H, Lodder EM, Papatheodorou S, Miles C, Ware JS, Papadakis M, Tadros R, Cole D, Skinner JR, Crawford J, Love DR, Pua CJ, Soh BY, Bhalshankar JD, Govind R, Tfelt-Hansen J, Winkel BG, van der Werf C, Wijeyeratne YD, Mellor G, Till J, Cohen M, Tome-Esteban M, Sharma S, Wilde AAM, Cook SA, Sheppard MN, Bezzina CR, Behr ER. Lahrouchi N, et al. Among authors: ware js. Eur J Hum Genet. 2020 Jan;28(1):17-22. doi: 10.1038/s41431-019-0500-8. Epub 2019 Sep 18. Eur J Hum Genet. 2020. PMID: 31534214 Free PMC article.

2

Next generation sequencing for clinical diagnostics and personalised medicine: implications for the next generation cardiologist.

Ware JS, Roberts AM, Cook SA. Ware JS, et al. Heart. 2012 Feb;98(4):276-81. doi: 10.1136/heartjnl-2011-300742. Epub 2011 Nov 29. Heart. 2012. PMID: 22128206 Review.

3

Republished review: Next generation sequencing for clinical diagnostics and personalised medicine: implications for the next generation cardiologist.

Ware JS, Roberts AM, Cook SA. Ware JS, et al. Postgrad Med J. 2012 Apr;88(1038):234-9. doi: 10.1136/pgmj.2011.300742rep. Postgrad Med J. 2012. PMID: 22441235

4

Paralogous annotation of disease-causing variants in long QT syndrome genes.

Ware JS, Walsh R, Cunningham F, Birney E, Cook SA. Ware JS, et al. Hum Mutat. 2012 Aug;33(8):1188-1191. doi: 10.1002/humu.22114. Epub 2012 Jun 7. Hum Mutat. 2012. PMID: 22581653 Free PMC article.

5

Next generation diagnostics in inherited arrhythmia syndromes : a comparison of two approaches.

Ware JS, John S, Roberts AM, Buchan R, Gong S, Peters NS, Robinson DO, Lucassen A, Behr ER, Cook SA. Ware JS, et al. J Cardiovasc Transl Res. 2013 Feb;6(1):94-103. doi: 10.1007/s12265-012-9401-8. Epub 2012 Sep 7. J Cardiovasc Transl Res. 2013. PMID: 22956155 Free PMC article.

6

Integrative genomics in cardiovascular medicine.

Ware JS, Petretto E, Cook SA. Ware JS, et al. Cardiovasc Res. 2013 Mar 15;97(4):623-30. doi: 10.1093/cvr/cvs303. Epub 2012 Sep 27. Cardiovasc Res. 2013. PMID: 23024270 Free PMC article. Review.

7

Towards clinical molecular diagnosis of inherited cardiac conditions: a comparison of bench-top genome DNA sequencers.

Li X, Buckton AJ, Wilkinson SL, John S, Walsh R, Novotny T, Valaskova I, Gupta M, Game L, Barton PJ, Cook SA, Ware JS. Li X, et al. Among authors: ware js. PLoS One. 2013 Jul 4;8(7):e67744. doi: 10.1371/journal.pone.0067744. Print 2013. PLoS One. 2013. PMID: 23861798 Free PMC article.

8

Paralogue annotation identifies novel pathogenic variants in patients with Brugada syndrome and catecholaminergic polymorphic ventricular tachycardia.

Walsh R, Peters NS, Cook SA, Ware JS. Walsh R, et al. Among authors: ware js. J Med Genet. 2014 Jan;51(1):35-44. doi: 10.1136/jmedgenet-2013-101917. Epub 2013 Oct 17. J Med Genet. 2014. PMID: 24136861 Free PMC article.

9

NECTAR: a database of codon-centric missense variant annotations.

Gong S, Ware JS, Walsh R, Cook SA. Gong S, et al. Among authors: ware js. Nucleic Acids Res. 2014 Jan;42(Database issue):D1013-9. doi: 10.1093/nar/gkt1245. Epub 2013 Dec 1. Nucleic Acids Res. 2014. PMID: 24297257 Free PMC article.

10

Bayesian models for syndrome- and gene-specific probabilities of novel variant pathogenicity.

Ruklisa D, Ware JS, Walsh R, Balding DJ, Cook SA. Ruklisa D, et al. Among authors: ware js. Genome Med. 2015 Jan 28;7(1):5. doi: 10.1186/s13073-014-0120-4. eCollection 2015. Genome Med. 2015. PMID: 25649125 Free PMC article.

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