Ware JS - Search Results

1

Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples.

Walsh R, Thomson KL, Ware JS, Funke BH, Woodley J, McGuire KJ, Mazzarotto F, Blair E, Seller A, Taylor JC, Minikel EV, Exome Aggregation Consortium, MacArthur DG, Farrall M, Cook SA, Watkins H. Walsh R, et al. Among authors: ware js. Genet Med. 2017 Feb;19(2):192-203. doi: 10.1038/gim.2016.90. Epub 2016 Aug 17. Genet Med. 2017. PMID: 27532257 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

Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome).

Glover M, Ware JS, Henry A, Wolley M, Walsh R, Wain LV, Xu S, Van't Hoff WG, Tobin MD, Hall IP, Cook S, Gordon RD, Stowasser M, O'Shaughnessy KM. Glover M, et al. Among authors: ware js. Clin Sci (Lond). 2014 May;126(10):721-6. doi: 10.1042/CS20130326. Clin Sci (Lond). 2014. PMID: 24266877 Free PMC article.

10

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.

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

201 results

Search Page

Filters