Tanck MWT - Search Results

1

Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction.

Bezzina CR, Pazoki R, Bardai A, Marsman RF, de Jong JSSG, Blom MT, Scicluna BP, Jukema JW, Bindraban NR, Lichtner P, Pfeufer A, Bishopric NH, Roden DM, Meitinger T, Chugh SS, Myerburg RJ, Jouven X, Kääb S, Dekker LRC, Tan HL, Tanck MWT, Wilde AAM. Bezzina CR, et al. Among authors: tanck mwt. Nat Genet. 2010 Aug;42(8):688-691. doi: 10.1038/ng.623. Epub 2010 Jul 11. Nat Genet. 2010. PMID: 20622880 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. Hum Mol Genet. 2003 Jan 15;12(2):111-23. doi: 10.1093/hmg/ddg013. Hum Mol Genet. 2003. PMID: 12499392

3

Estimation of multilocus haplotype effects using weighted penalised log-likelihood: analysis of five sequence variations at the cholesteryl ester transfer protein gene locus.

Tanck MW, Klerkx AH, Jukema JW, De Knijff P, Kastelein JJ, Zwinderman AH. Tanck MW, et al. Ann Hum Genet. 2003 Mar;67(Pt 2):175-84. doi: 10.1046/j.1469-1809.2003.00021.x. Ann Hum Genet. 2003. PMID: 12675692

4

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

5

Functional interaction between -629C/A, -971G/A and -1337C/T polymorphisms in the CETP gene is a major determinant of promoter activity and plasma CETP concentration in the REGRESS Study.

Frisdal E, Klerkx AH, Le Goff W, Tanck MW, Lagarde JP, Jukema JW, Kastelein JJ, Chapman MJ, Guerin M. Frisdal E, et al. Hum Mol Genet. 2005 Sep 15;14(18):2607-18. doi: 10.1093/hmg/ddi291. Epub 2005 Jul 27. Hum Mol Genet. 2005. PMID: 16049032

6

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. Circulation. 2006 Jan 24;113(3):338-44. doi: 10.1161/CIRCULATIONAHA.105.580811. Epub 2006 Jan 16. Circulation. 2006. PMID: 16415376

7

Common variants of multiple genes that control reverse cholesterol transport together explain only a minor part of the variation of HDL cholesterol levels.

Boekholdt SM, Souverein OW, Tanck MW, Hovingh GK, Kuivenhoven JA, Peters RI, Jansen H, Schiffers PM, van der Wall EE, Doevendans PA, Reitsma PH, Zwinderman AH, Kastelein JJ, Jukema JW. Boekholdt SM, et al. Clin Genet. 2006 Mar;69(3):263-70. doi: 10.1111/j.1399-0004.2006.00578.x. Clin Genet. 2006. PMID: 16542392

8

Simultaneous estimation of gene-gene and gene-environment interactions for numerous loci using double penalized log-likelihood.

Tanck MW, Jukema JW, Zwinderman AH. Tanck MW, et al. Genet Epidemiol. 2006 Dec;30(8):645-51. doi: 10.1002/gepi.20176. Genet Epidemiol. 2006. PMID: 16917921

9

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. Circulation. 2006 Sep 12;114(11):1140-5. doi: 10.1161/CIRCULATIONAHA.105.606145. Epub 2006 Aug 28. Circulation. 2006. PMID: 16940195

10

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. Eur Heart J. 2007 Mar;28(5):575-80. doi: 10.1093/eurheartj/ehl355. Epub 2006 Nov 7. Eur Heart J. 2007. PMID: 17090615

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