Witteman JC - Search Results

1

Common variation in the NOS1AP gene is associated with reduced glucose-lowering effect and with increased mortality in users of sulfonylurea.

Becker ML, Aarnoudse AJ, Newton-Cheh C, Hofman A, Witteman JC, Uitterlinden AG, Visser LE, Stricker BH. Becker ML, et al. Among authors: witteman jc. Pharmacogenet Genomics. 2008 Jul;18(7):591-7. doi: 10.1097/FPC.0b013e328300e8c5. Pharmacogenet Genomics. 2008. PMID: 18551039

2

Mortality in patients with hypertension on angiotensin-I converting enzyme (ACE)-inhibitor treatment is influenced by the ACE insertion/deletion polymorphism.

Bleumink GS, Schut AF, Sturkenboom MC, van Duijn CM, Deckers JW, Hofman A, Kingma JH, Witteman JC, Stricker BH. Bleumink GS, et al. Among authors: witteman jc. Pharmacogenet Genomics. 2005 Feb;15(2):75-81. doi: 10.1097/01213011-200502000-00003. Pharmacogenet Genomics. 2005. PMID: 15861031

3

C-reactive protein levels, variation in the C-reactive protein gene, and cancer risk: the Rotterdam Study.

Siemes C, Visser LE, Coebergh JW, Splinter TA, Witteman JC, Uitterlinden AG, Hofman A, Pols HA, Stricker BH. Siemes C, et al. Among authors: witteman jc. J Clin Oncol. 2006 Nov 20;24(33):5216-22. doi: 10.1200/JCO.2006.07.1381. J Clin Oncol. 2006. PMID: 17114654

4

The risk of myocardial infarction in patients with reduced activity of cytochrome P450 2C9.

Visser LE, van Schaik RH, Jan Danser AH, Hofman A, Witteman JC, van Duijn CM, Uitterlinden AG, Pols HA, Stricker BH. Visser LE, et al. Among authors: witteman jc. Pharmacogenet Genomics. 2007 Jul;17(7):473-9. doi: 10.1097/01.fpc.0000236335.57046.c8. Pharmacogenet Genomics. 2007. PMID: 17558303

5

Common NOS1AP variants are associated with a prolonged QTc interval in the Rotterdam Study.

Aarnoudse AJ, Newton-Cheh C, de Bakker PI, Straus SM, Kors JA, Hofman A, Uitterlinden AG, Witteman JC, Stricker BH. Aarnoudse AJ, et al. Among authors: witteman jc. Circulation. 2007 Jul 3;116(1):10-6. doi: 10.1161/CIRCULATIONAHA.106.676783. Epub 2007 Jun 18. Circulation. 2007. PMID: 17576865

6

Identification of a common variant at the NOS1AP locus strongly associated to QT-interval duration.

Eijgelsheim M, Aarnoudse AL, Rivadeneira F, Kors JA, Witteman JC, Hofman A, van Duijn CM, Uitterlinden AG, Stricker BH. Eijgelsheim M, et al. Among authors: witteman jc. Hum Mol Genet. 2009 Jan 15;18(2):347-57. doi: 10.1093/hmg/ddn341. Epub 2008 Oct 16. Hum Mol Genet. 2009. PMID: 18927126

7

A common NOS1AP genetic polymorphism is associated with increased cardiovascular mortality in users of dihydropyridine calcium channel blockers.

Becker ML, Visser LE, Newton-Cheh C, Hofman A, Uitterlinden AG, Witteman JC, Stricker BH. Becker ML, et al. Among authors: witteman jc. Br J Clin Pharmacol. 2009 Jan;67(1):61-7. doi: 10.1111/j.1365-2125.2008.03325.x. Epub 2008 Nov 17. Br J Clin Pharmacol. 2009. PMID: 19076153 Free PMC article.

8

Calcium channel blockers, NOS1AP, and heart-rate-corrected QT prolongation.

van Noord C, Aarnoudse AJ, Eijgelsheim M, Sturkenboom MC, Straus SM, Hofman A, Kors JA, Newton-Cheh C, Witteman JC, Stricker BH. van Noord C, et al. Among authors: witteman jc. Pharmacogenet Genomics. 2009 Apr;19(4):260-6. doi: 10.1097/FPC.0b013e328324e556. Pharmacogenet Genomics. 2009. PMID: 19247217

9

Genetic variation in NOS1AP is associated with sudden cardiac death: evidence from the Rotterdam Study.

Eijgelsheim M, Newton-Cheh C, Aarnoudse AL, van Noord C, Witteman JC, Hofman A, Uitterlinden AG, Stricker BH. Eijgelsheim M, et al. Among authors: witteman jc. Hum Mol Genet. 2009 Nov 1;18(21):4213-8. doi: 10.1093/hmg/ddp356. Epub 2009 Jul 30. Hum Mol Genet. 2009. PMID: 19643915 Free PMC article.

10

Genetic variance in CYP2C8 and increased risk of myocardial infarction.

Rodenburg EM, Visser LE, Danser AH, Hofman A, van Noord C, Witteman JC, Uitterlinden AG, Stricker BH. Rodenburg EM, et al. Among authors: witteman jc. Pharmacogenet Genomics. 2010 Jul;20(7):426-34. doi: 10.1097/FPC.0b013e32833a96d8. Pharmacogenet Genomics. 2010. PMID: 20436375

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