Tanck M - Search Results

1

The role of renin-angiotensin-aldosterone system polymorphisms in phenotypic expression of MYBPC3-related hypertrophic cardiomyopathy.

Kolder IC, Michels M, Christiaans I, Ten Cate FJ, Majoor-Krakauer D, Danser AH, Lekanne Deprez RH, Tanck M, Wilde AA, Bezzina CR, Dooijes D. Kolder IC, et al. Among authors: tanck m. Eur J Hum Genet. 2012 Oct;20(10):1071-7. doi: 10.1038/ejhg.2012.48. Epub 2012 May 9. Eur J Hum Genet. 2012. PMID: 22569109 Free PMC article.

2

Haplotype analysis of the CETP gene: not TaqIB, but the closely linked -629C-->A polymorphism and a novel promoter variant are independently associated with CETP concentration.

Klerkx AH, Tanck MW, Kastelein JJ, Molhuizen HO, Jukema JW, Zwinderman AH, Kuivenhoven JA. Klerkx AH, et al. Among authors: tanck mw. Hum Mol Genet. 2003 Jan 15;12(2):111-23. doi: 10.1093/hmg/ddg013. Hum Mol Genet. 2003. PMID: 12499392

3

Polymorphisms in APOA1 and LPL genes are statistically independently associated with fasting TG in men with CAD.

Souverein OW, Jukema JW, Boekholdt SM, Zwinderman AH, Tanck MW. Souverein OW, et al. Eur J Hum Genet. 2005 Apr;13(4):445-51. doi: 10.1038/sj.ejhg.5201362. Eur J Hum Genet. 2005. PMID: 15657615

4

Genetic determinants of plasma HDL-cholesterol levels in familial hypercholesterolemia.

van Aalst-Cohen ES, Jansen AC, Boekholdt SM, Tanck MW, Fontecha MR, Cheng S, Li J, Defesche JC, Kuivenhoven JA, Kastelein JJ. van Aalst-Cohen ES, et al. Among authors: tanck mw. Eur J Hum Genet. 2005 Oct;13(10):1137-42. doi: 10.1038/sj.ejhg.5201467. Eur J Hum Genet. 2005. PMID: 16030523

5

Common sodium channel promoter haplotype in asian subjects underlies variability in cardiac conduction.

Bezzina CR, Shimizu W, Yang P, Koopmann TT, Tanck MW, Miyamoto Y, Kamakura S, Roden DM, Wilde AA. Bezzina CR, et al. Among authors: tanck mw. Circulation. 2006 Jan 24;113(3):338-44. doi: 10.1161/CIRCULATIONAHA.105.580811. Epub 2006 Jan 16. Circulation. 2006. PMID: 16415376

6

Familial sudden death is an important risk factor for primary ventricular fibrillation: a case-control study in acute myocardial infarction patients.

Dekker LR, Bezzina CR, Henriques JP, Tanck MW, Koch KT, Alings MW, Arnold AE, de Boer MJ, Gorgels AP, Michels HR, Verkerk A, Verheugt FW, Zijlstra F, Wilde AA. Dekker LR, et al. Among authors: tanck mw. Circulation. 2006 Sep 12;114(11):1140-5. doi: 10.1161/CIRCULATIONAHA.105.606145. Epub 2006 Aug 28. Circulation. 2006. PMID: 16940195

7

Diagnostic criteria for congenital long QT syndrome in the era of molecular genetics: do we need a scoring system?

Hofman N, Wilde AA, Kääb S, van Langen IM, Tanck MW, Mannens MM, Hinterseer M, Beckmann BM, Tan HL. Hofman N, et al. Among authors: tanck mw. Eur Heart J. 2007 Mar;28(5):575-80. doi: 10.1093/eurheartj/ehl355. Epub 2006 Nov 7. Eur Heart J. 2007. PMID: 17090615

8

Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies.

Meregalli PG, Tan HL, Probst V, Koopmann TT, Tanck MW, Bhuiyan ZA, Sacher F, Kyndt F, Schott JJ, Albuisson J, Mabo P, Bezzina CR, Le Marec H, Wilde AA. Meregalli PG, et al. Among authors: tanck mw. Heart Rhythm. 2009 Mar;6(3):341-8. doi: 10.1016/j.hrthm.2008.11.009. Epub 2008 Nov 11. Heart Rhythm. 2009. PMID: 19251209

9

Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillation.

Alders M, Koopmann TT, Christiaans I, Postema PG, Beekman L, Tanck MW, Zeppenfeld K, Loh P, Koch KT, Demolombe S, Mannens MM, Bezzina CR, Wilde AA. Alders M, et al. Among authors: tanck mw. Am J Hum Genet. 2009 Apr;84(4):468-76. doi: 10.1016/j.ajhg.2009.02.009. Epub 2009 Mar 12. Am J Hum Genet. 2009. PMID: 19285295 Free PMC article.

10

Prognosis among survivors of primary ventricular fibrillation in the percutaneous coronary intervention era.

de Jong JS, Marsman RF, Henriques JP, Koch KT, de Winter RJ, Tanck MW, Wilde AA, Dekker LR. de Jong JS, et al. Among authors: tanck mw. Am Heart J. 2009 Sep;158(3):467-72. doi: 10.1016/j.ahj.2009.06.028. Am Heart J. 2009. PMID: 19699872 Free article.

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