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Loci influencing blood pressure identified using a cardiovascular gene-centric array.
Ganesh SK, Tragante V, Guo W, Guo Y, Lanktree MB, Smith EN, Johnson T, Castillo BA, Barnard J, Baumert J, Chang YP, Elbers CC, Farrall M, Fischer ME, Franceschini N, Gaunt TR, Gho JM, Gieger C, Gong Y, Isaacs A, Kleber ME, Mateo Leach I, McDonough CW, Meijs MF, Mellander O, Molony CM, Nolte IM, Padmanabhan S, Price TS, Rajagopalan R, Shaffer J, Shah S, Shen H, Soranzo N, van der Most PJ, Van Iperen EP, Van Setten J, Vonk JM, Zhang L, Beitelshees AL, Berenson GS, Bhatt DL, Boer JM, Boerwinkle E, Burkley B, Burt A, Chakravarti A, Chen W, Cooper-Dehoff RM, Curtis SP, Dreisbach A, Duggan D, Ehret GB, Fabsitz RR, Fornage M, Fox E, Furlong CE, Gansevoort RT, Hofker MH, Hovingh GK, Kirkland SA, Kottke-Marchant K, Kutlar A, Lacroix AZ, Langaee TY, Li YR, Lin H, Liu K, Maiwald S, Malik R; CARDIOGRAM, METASTROKE; Murugesan G, Newton-Cheh C, O'Connell JR, Onland-Moret NC, Ouwehand WH, Palmas W, Penninx BW, Pepine CJ, Pettinger M, Polak JF, Ramachandran VS, Ranchalis J, Redline S, Ridker PM, Rose LM, Scharnag H, Schork NJ, Shimbo D, Shuldiner AR, Srinivasan SR, Stolk RP, Taylor HA, Thorand B, Trip MD, van Duijn CM, Verschuren WM, Wijmenga C, Winkelmann BR, Wyatt S,… See abstract for full author list ➔ Ganesh SK, et al. Among authors: van duijn cm, van setten j, van der harst p, van der most pj, van iperen ep, van der schouw yt. Hum Mol Genet. 2013 Apr 15;22(8):1663-78. doi: 10.1093/hmg/dds555. Epub 2013 Jan 8. Hum Mol Genet. 2013. PMID: 23303523 Free PMC article.
Association of 5' estrogen receptor alpha gene polymorphisms with bone mineral density, vertebral bone area and fracture risk.
van Meurs JB, Schuit SC, Weel AE, van der Klift M, Bergink AP, Arp PP, Colin EM, Fang Y, Hofman A, van Duijn CM, van Leeuwen JP, Pols HA, Uitterlinden AG. van Meurs JB, et al. Among authors: van duijn cm, van leeuwen jp, van der klift m. Hum Mol Genet. 2003 Jul 15;12(14):1745-54. doi: 10.1093/hmg/ddg176. Hum Mol Genet. 2003. PMID: 12837697 Free article.
ACE polymorphisms.
Sayed-Tabatabaei FA, Oostra BA, Isaacs A, van Duijn CM, Witteman JC. Sayed-Tabatabaei FA, et al. Among authors: van duijn cm. Circ Res. 2006 May 12;98(9):1123-33. doi: 10.1161/01.RES.0000223145.74217.e7. Circ Res. 2006. PMID: 16690893 Review.
TGF-beta1 polymorphisms and arterial stiffness; the Rotterdam Study.
Sie MP, Mattace-Raso FU, Uitterlinden AG, Arp PP, Hofman A, Hoeks AP, Reneman RS, Asmar R, van Duijn CM, Witteman JC. Sie MP, et al. Among authors: van duijn cm. J Hum Hypertens. 2007 Jun;21(6):431-7. doi: 10.1038/sj.jhh.1002175. Epub 2007 Mar 15. J Hum Hypertens. 2007. PMID: 17361195
GenABEL: an R library for genome-wide association analysis.
Aulchenko YS, Ripke S, Isaacs A, van Duijn CM. Aulchenko YS, et al. Among authors: van duijn cm. Bioinformatics. 2007 May 15;23(10):1294-6. doi: 10.1093/bioinformatics/btm108. Epub 2007 Mar 23. Bioinformatics. 2007. PMID: 17384015
Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene.
Kayser M, Liu F, Janssens AC, Rivadeneira F, Lao O, van Duijn K, Vermeulen M, Arp P, Jhamai MM, van Ijcken WF, den Dunnen JT, Heath S, Zelenika D, Despriet DD, Klaver CC, Vingerling JR, de Jong PT, Hofman A, Aulchenko YS, Uitterlinden AG, Oostra BA, van Duijn CM. Kayser M, et al. Among authors: van duijn k, van duijn cm, van ijcken wf. Am J Hum Genet. 2008 Feb;82(2):411-23. doi: 10.1016/j.ajhg.2007.10.003. Epub 2008 Jan 25. Am J Hum Genet. 2008. PMID: 18252221 Free PMC article.
Identification of DIO2 as a new susceptibility locus for symptomatic osteoarthritis.
Meulenbelt I, Min JL, Bos S, Riyazi N, Houwing-Duistermaat JJ, van der Wijk HJ, Kroon HM, Nakajima M, Ikegawa S, Uitterlinden AG, van Meurs JB, van der Deure WM, Visser TJ, Seymour AB, Lakenberg N, van der Breggen R, Kremer D, van Duijn CM, Kloppenburg M, Loughlin J, Slagboom PE. Meulenbelt I, et al. Among authors: van duijn cm, van der wijk hj, van meurs jb, van der breggen r, van der deure wm. Hum Mol Genet. 2008 Jun 15;17(12):1867-75. doi: 10.1093/hmg/ddn082. Epub 2008 Mar 11. Hum Mol Genet. 2008. PMID: 18334578
Eight-fold increased risk for congenital heart defects in children carrying the nicotinamide N-methyltransferase polymorphism and exposed to medicines and low nicotinamide.
van Driel LM, Smedts HP, Helbing WA, Isaacs A, Lindemans J, Uitterlinden AG, van Duijn CM, de Vries JH, Steegers EA, Steegers-Theunissen RP. van Driel LM, et al. Among authors: van duijn cm. Eur Heart J. 2008 Jun;29(11):1424-31. doi: 10.1093/eurheartj/ehn170. Epub 2008 Apr 25. Eur Heart J. 2008. PMID: 18441319
1,200 results