Roberts JD - Search Results

1

Detection of genomic deletions of PKP2 in arrhythmogenic right ventricular cardiomyopathy.

Roberts JD, Herkert JC, Rutberg J, Nikkel SM, Wiesfeld AC, Dooijes D, Gow RM, van Tintelen JP, Gollob MH. Roberts JD, et al. Clin Genet. 2013 May;83(5):452-6. doi: 10.1111/j.1399-0004.2012.01950.x. Epub 2012 Sep 10. Clin Genet. 2013. PMID: 22889254

2

Inherited cardiomyopathies mimicking arrhythmogenic right ventricular cardiomyopathy.

Roberts JD, Veinot JP, Rutberg J, Gollob MH. Roberts JD, et al. Cardiovasc Pathol. 2010 Sep-Oct;19(5):316-20. doi: 10.1016/j.carpath.2009.06.003. Epub 2009 Jul 24. Cardiovasc Pathol. 2010. PMID: 19632136

3

Impact of genetic discoveries on the classification of lone atrial fibrillation.

Roberts JD, Gollob MH. Roberts JD, et al. J Am Coll Cardiol. 2010 Feb 23;55(8):705-12. doi: 10.1016/j.jacc.2009.12.005. J Am Coll Cardiol. 2010. PMID: 20170805 Free article. Review.

4

Evaluation of non-synonymous NPPA single nucleotide polymorphisms in atrial fibrillation.

Roberts JD, Davies RW, Lubitz SA, Thibodeau IL, Nery PB, Birnie DH, Benjamin EJ, Lemery R, Ellinor PT, Gollob MH. Roberts JD, et al. Europace. 2010 Aug;12(8):1078-83. doi: 10.1093/europace/euq161. Epub 2010 Jun 12. Europace. 2010. PMID: 20543198 Free PMC article.

5

The genetic and clinical features of cardiac channelopathies.

Roberts JD, Gollob MH. Roberts JD, et al. Future Cardiol. 2010 Jul;6(4):491-506. doi: 10.2217/fca.10.27. Future Cardiol. 2010. PMID: 20608822 Review.

6

The short QT syndrome: proposed diagnostic criteria.

Gollob MH, Redpath CJ, Roberts JD. Gollob MH, et al. Among authors: roberts jd. J Am Coll Cardiol. 2011 Feb 15;57(7):802-12. doi: 10.1016/j.jacc.2010.09.048. J Am Coll Cardiol. 2011. PMID: 21310316 Free article.

7

Distinguishing pathogenic mutations from innocuous rare variants in gene discovery for Brugada syndrome.

Roberts JD, Gollob MH. Roberts JD, et al. Can J Cardiol. 2012 Mar-Apr;28(2):160-1. doi: 10.1016/j.cjca.2012.01.016. Epub 2012 Feb 14. Can J Cardiol. 2012. PMID: 22336521 No abstract available.

8

Point-of-care genetic testing for personalisation of antiplatelet treatment (RAPID GENE): a prospective, randomised, proof-of-concept trial.

Roberts JD, Wells GA, Le May MR, Labinaz M, Glover C, Froeschl M, Dick A, Marquis JF, O'Brien E, Goncalves S, Druce I, Stewart A, Gollob MH, So DY. Roberts JD, et al. Lancet. 2012 May 5;379(9827):1705-11. doi: 10.1016/S0140-6736(12)60161-5. Epub 2012 Mar 29. Lancet. 2012. PMID: 22464343 Clinical Trial.

9

Early repolarization: a rare primary arrhythmic syndrome and common modifier of arrhythmic risk.

Roberts JD, Gollob MH. Roberts JD, et al. J Cardiovasc Electrophysiol. 2013 Jul;24(7):837-43. doi: 10.1111/jce.12156. Epub 2013 Apr 30. J Cardiovasc Electrophysiol. 2013. PMID: 23631702

10

A contemporary review on the genetic basis of atrial fibrillation.

Roberts JD, Gollob MH. Roberts JD, et al. Methodist Debakey Cardiovasc J. 2014 Jan-Mar;10(1):18-24. doi: 10.14797/mdcj-10-1-18. Methodist Debakey Cardiovasc J. 2014. PMID: 24932358 Free PMC article. Review.

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