R01 HD042569/HD/NICHD NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2005	1
2006	4
2007	9
2008	8
2009	13
2010	11
2011	12
2012	12
2013	4
2014	8
2015	5
2016	3
2017	4
2018	13
2019	1
2025	0

1

Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.

Kapplinger JD, Tester DJ, Salisbury BA, Carr JL, Harris-Kerr C, Pollevick GD, Wilde AA, Ackerman MJ. Kapplinger JD, et al. Heart Rhythm. 2009 Sep;6(9):1297-303. doi: 10.1016/j.hrthm.2009.05.021. Epub 2009 Jun 23. Heart Rhythm. 2009. PMID: 19716085 Free PMC article.

2

Enhanced Classification of Brugada Syndrome-Associated and Long-QT Syndrome-Associated Genetic Variants in the SCN5A-Encoded Na(v)1.5 Cardiac Sodium Channel.

Kapplinger JD, Giudicessi JR, Ye D, Tester DJ, Callis TE, Valdivia CR, Makielski JC, Wilde AA, Ackerman MJ. Kapplinger JD, et al. Circ Cardiovasc Genet. 2015 Aug;8(4):582-95. doi: 10.1161/CIRCGENETICS.114.000831. Epub 2015 Apr 22. Circ Cardiovasc Genet. 2015. PMID: 25904541 Free PMC article.

3

Genetic testing for long-QT syndrome: distinguishing pathogenic mutations from benign variants.

Kapa S, Tester DJ, Salisbury BA, Harris-Kerr C, Pungliya MS, Alders M, Wilde AA, Ackerman MJ. Kapa S, et al. Circulation. 2009 Nov 3;120(18):1752-60. doi: 10.1161/CIRCULATIONAHA.109.863076. Epub 2009 Oct 19. Circulation. 2009. PMID: 19841300 Free PMC article.

4

QTc: how long is too long?

Johnson JN, Ackerman MJ. Johnson JN, et al. Br J Sports Med. 2009 Sep;43(9):657-62. doi: 10.1136/bjsm.2008.054734. Br J Sports Med. 2009. PMID: 19734499 Free PMC article. Review.

5

Characterization of a phenotype-based genetic test prediction score for unrelated patients with hypertrophic cardiomyopathy.

Bos JM, Will ML, Gersh BJ, Kruisselbrink TM, Ommen SR, Ackerman MJ. Bos JM, et al. Mayo Clin Proc. 2014 Jun;89(6):727-37. doi: 10.1016/j.mayocp.2014.01.025. Epub 2014 May 1. Mayo Clin Proc. 2014. PMID: 24793961 Free PMC article.

6

Calcium Revisited: New Insights Into the Molecular Basis of Long-QT Syndrome.

Giudicessi JR, Ackerman MJ. Giudicessi JR, et al. Circ Arrhythm Electrophysiol. 2016 Jul;9(7):e002480. doi: 10.1161/CIRCEP.116.002480. Circ Arrhythm Electrophysiol. 2016. PMID: 27390209 Free PMC article. Review. No abstract available.

7

Genotype- and phenotype-guided management of congenital long QT syndrome.

Giudicessi JR, Ackerman MJ. Giudicessi JR, et al. Curr Probl Cardiol. 2013 Oct;38(10):417-55. doi: 10.1016/j.cpcardiol.2013.08.001. Curr Probl Cardiol. 2013. PMID: 24093767 Free PMC article. Review.

8

Genetic testing in heritable cardiac arrhythmia syndromes: differentiating pathogenic mutations from background genetic noise.

Giudicessi JR, Ackerman MJ. Giudicessi JR, et al. Curr Opin Cardiol. 2013 Jan;28(1):63-71. doi: 10.1097/HCO.0b013e32835b0a41. Curr Opin Cardiol. 2013. PMID: 23128497 Free PMC article. Review.

9

Sudden infant death syndrome: do ion channels play a role?

Van Norstrand DW, Ackerman MJ. Van Norstrand DW, et al. Heart Rhythm. 2009 Feb;6(2):272-8. doi: 10.1016/j.hrthm.2008.07.028. Epub 2008 Jul 31. Heart Rhythm. 2009. PMID: 18823823 Free PMC article. Review. No abstract available.

10

Genetic testing for potentially lethal, highly treatable inherited cardiomyopathies/channelopathies in clinical practice.

Tester DJ, Ackerman MJ. Tester DJ, et al. Circulation. 2011 Mar 8;123(9):1021-37. doi: 10.1161/CIRCULATIONAHA.109.914838. Circulation. 2011. PMID: 21382904 Free PMC article. Review. No abstract available.

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