Will ML - Search Results

1

Homozygous/Compound Heterozygous Triadin Mutations Associated With Autosomal-Recessive Long-QT Syndrome and Pediatric Sudden Cardiac Arrest: Elucidation of the Triadin Knockout Syndrome.

Altmann HM, Tester DJ, Will ML, Middha S, Evans JM, Eckloff BW, Ackerman MJ. Altmann HM, et al. Among authors: will ml. Circulation. 2015 Jun 9;131(23):2051-60. doi: 10.1161/CIRCULATIONAHA.115.015397. Epub 2015 Apr 28. Circulation. 2015. PMID: 25922419

2

Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndrome.

Ackerman MJ, Tester DJ, Jones GS, Will ML, Burrow CR, Curran ME. Ackerman MJ, et al. Among authors: will ml. Mayo Clin Proc. 2003 Dec;78(12):1479-87. doi: 10.4065/78.12.1479. Mayo Clin Proc. 2003. PMID: 14661677

3

Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromes.

Choi G, Kopplin LJ, Tester DJ, Will ML, Haglund CM, Ackerman MJ. Choi G, et al. Among authors: will ml. Circulation. 2004 Oct 12;110(15):2119-24. doi: 10.1161/01.CIR.0000144471.98080.CA. Epub 2004 Oct 4. Circulation. 2004. PMID: 15466642

4

Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing.

Tester DJ, Will ML, Haglund CM, Ackerman MJ. Tester DJ, et al. Among authors: will ml. Heart Rhythm. 2005 May;2(5):507-17. doi: 10.1016/j.hrthm.2005.01.020. Heart Rhythm. 2005. PMID: 15840476

5

Identification of a common genetic substrate underlying postpartum cardiac events in congenital long QT syndrome.

Khositseth A, Tester DJ, Will ML, Bell CM, Ackerman MJ. Khositseth A, et al. Among authors: will ml. Heart Rhythm. 2004 May;1(1):60-4. doi: 10.1016/j.hrthm.2004.01.006. Heart Rhythm. 2004. PMID: 15851119

6

Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testing.

Tester DJ, Kopplin LJ, Will ML, Ackerman MJ. Tester DJ, et al. Among authors: will ml. Heart Rhythm. 2005 Oct;2(10):1099-105. doi: 10.1016/j.hrthm.2005.07.012. Heart Rhythm. 2005. PMID: 16188589

7

Effect of clinical phenotype on yield of long QT syndrome genetic testing.

Tester DJ, Will ML, Haglund CM, Ackerman MJ. Tester DJ, et al. Among authors: will ml. J Am Coll Cardiol. 2006 Feb 21;47(4):764-8. doi: 10.1016/j.jacc.2005.09.056. Epub 2006 Jan 26. J Am Coll Cardiol. 2006. PMID: 16487842 Free article.

8

Mutation detection in congenital long QT syndrome: cardiac channel gene screen using PCR, dHPLC, and direct DNA sequencing.

Tester DJ, Will ML, Ackerman MJ. Tester DJ, et al. Among authors: will ml. Methods Mol Med. 2006;128:181-207. doi: 10.1385/1-59745-159-2:181. Methods Mol Med. 2006. PMID: 17071997

9

Repeat long QT syndrome genetic testing of phenotype-positive cases: prevalence and etiology of detection misses.

Medlock MM, Tester DJ, Will ML, Bos JM, Ackerman MJ. Medlock MM, et al. Among authors: will ml. Heart Rhythm. 2012 Dec;9(12):1977-82. doi: 10.1016/j.hrthm.2012.08.010. Epub 2012 Aug 8. Heart Rhythm. 2012. PMID: 22885918

10

Whole-Exome Molecular Autopsy After Exertion-Related Sudden Unexplained Death in the Young.

Anderson JH, Tester DJ, Will ML, Ackerman MJ. Anderson JH, et al. Among authors: will ml. Circ Cardiovasc Genet. 2016 Jun;9(3):259-65. doi: 10.1161/CIRCGENETICS.115.001370. Epub 2016 Apr 25. Circ Cardiovasc Genet. 2016. PMID: 27114410

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