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Intronic Polymorphisms in the CDKN2B-AS1 Gene Are Strongly Associated with the Risk of Myocardial Infarction and Coronary Artery Disease in the Saudi Population.
AbdulAzeez S, Al-Nafie AN, Al-Shehri A, Borgio JF, Baranova EV, Al-Madan MS, Al-Ali RA, Al-Muhanna F, Al-Ali A, Al-Mansori M, Ibrahim MF, Asselbergs FW, Keating B, Koeleman BP, Al-Ali AK. AbdulAzeez S, et al. Among authors: koeleman bp. Int J Mol Sci. 2016 Mar 17;17(3):395. doi: 10.3390/ijms17030395. Int J Mol Sci. 2016. PMID: 26999117 Free PMC article.
Exome-Wide Association Analysis of Coronary Artery Disease in the Kingdom of Saudi Arabia Population.
de Kovel CG, Mulder F, van Setten J, van 't Slot R, Al-Rubaish A, Alshehri AM, Al Faraidy K, Al-Ali A, Al-Madan M, Al Aqaili I, Larbi E, Al-Ali R, Alzahrani A, Asselbergs FW, Koeleman BP, Al-Ali A. de Kovel CG, et al. Among authors: koeleman bp. PLoS One. 2016 Feb 5;11(2):e0146502. doi: 10.1371/journal.pone.0146502. eCollection 2016. PLoS One. 2016. PMID: 26849363 Free PMC article.
Genetic variants associated with protein C levels.
Vossen CY, Koeleman BP, Hasstedt SJ, Nijman IJ, Renkens IJ, Callas PW, Rosendaal FR, Bovill EG. Vossen CY, et al. Among authors: koeleman bp. J Thromb Haemost. 2013 Apr;11(4):715-23. doi: 10.1111/jth.12157. J Thromb Haemost. 2013. PMID: 23387557 Free PMC article.
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index.
Hinney A, Kesselmeier M, Jall S, Volckmar AL, Föcker M, Antel J; GCAN; WTCCC3; Heid IM, Winkler TW; GIANT; Grant SF; EGG; Guo Y, Bergen AW, Kaye W, Berrettini W, Hakonarson H; Price Foundation Collaborative Group; Children’s Hospital of Philadelphia/Price Foundation; Herpertz-Dahlmann B, de Zwaan M, Herzog W, Ehrlich S, Zipfel S, Egberts KM, Adan R, Brandys M, van Elburg A, Boraska Perica V, Franklin CS, Tschöp MH, Zeggini E, Bulik CM, Collier D, Scherag A, Müller TD, Hebebrand J. Hinney A, et al. Mol Psychiatry. 2017 Feb;22(2):192-201. doi: 10.1038/mp.2016.71. Epub 2016 May 17. Mol Psychiatry. 2017. PMID: 27184124 Free PMC article.
Genetic polymorphisms in susceptibility to Type 1 Diabetes.
Alizadeh BZ, Koeleman BP. Alizadeh BZ, et al. Among authors: koeleman bp. Clin Chim Acta. 2008 Jan;387(1-2):9-17. doi: 10.1016/j.cca.2007.09.021. Epub 2007 Oct 2. Clin Chim Acta. 2008. PMID: 17963738 Review.
Functional variants of Fc gamma receptor (FCGR2A) and FCGR3A are not associated with susceptibility to systemic sclerosis in a large European Study (EUSTAR).
Alizadeh BZ, Broen J, Rueda B, Hesselstrand R, Wuttge D, Simeon C, Ortego-Centeno N, Gonzalez-Gay MA, Pros A, Herrick A, Worthington J, Denton C, Fonseca C, Riemekasten G, Vonk MC, van den Hoogen F, Guiducci S, Matucci-Cerinic M, Scorza R, Beretta L, Airó P, Coenen M, Martin J, Koeleman BP, Radstake TR; EUSTAR. Alizadeh BZ, et al. Among authors: koeleman bp. J Rheumatol. 2010 Aug 1;37(8):1673-9. doi: 10.3899/jrheum.091259. Epub 2010 Jun 15. J Rheumatol. 2010. PMID: 20551103
Endocrine autoimmune disease: genetics become complex.
Wiebolt J, Koeleman BP, van Haeften TW. Wiebolt J, et al. Among authors: koeleman bp. Eur J Clin Invest. 2010 Dec;40(12):1144-55. doi: 10.1111/j.1365-2362.2010.02366.x. Epub 2010 Aug 16. Eur J Clin Invest. 2010. PMID: 20718847 Review.
248 results