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A common single-nucleotide variant in T is strongly associated with chordoma.
Pillay N, Plagnol V, Tarpey PS, Lobo SB, Presneau N, Szuhai K, Halai D, Berisha F, Cannon SR, Mead S, Kasperaviciute D, Palmen J, Talmud PJ, Kindblom LG, Amary MF, Tirabosco R, Flanagan AM. Pillay N, et al. Among authors: palmen j. Nat Genet. 2012 Nov;44(11):1185-7. doi: 10.1038/ng.2419. Epub 2012 Oct 14. Nat Genet. 2012. PMID: 23064415
Determination of the functionality of common APOA5 polymorphisms.
Talmud PJ, Palmen J, Putt W, Lins L, Humphries SE. Talmud PJ, et al. Among authors: palmen j. J Biol Chem. 2005 Aug 5;280(31):28215-20. doi: 10.1074/jbc.M502144200. Epub 2005 Jun 7. J Biol Chem. 2005. PMID: 15941721 Free article.
Common variants in the TCF7L2 gene and predisposition to type 2 diabetes in UK European Whites, Indian Asians and Afro-Caribbean men and women.
Humphries SE, Gable D, Cooper JA, Ireland H, Stephens JW, Hurel SJ, Li KW, Palmen J, Miller MA, Cappuccio FP, Elkeles R, Godsland I, Miller GJ, Talmud PJ. Humphries SE, et al. Among authors: palmen j. J Mol Med (Berl). 2006 Dec;84(12):1005-14. doi: 10.1007/s00109-006-0108-7. J Mol Med (Berl). 2006. PMID: 17665514
Genetic variants associated with Von Willebrand factor levels in healthy men and women identified using the HumanCVD BeadChip.
Zabaneh D, Gaunt TR, Kumari M, Drenos F, Shah S, Berry D, Power C, Hypponen E, Shah T, Palmen J, Pallas J, Talmud PJ, Casas JP, Sofat R, Lowe G, Rumley A, Morris RW, Whincup PH, Rodriguez S, Ebrahim S, Marmot MG, Smith GD, Lawlor DA, Kivimaki M, Whittaker J, Hingorani AD, Day IN, Humphries SE. Zabaneh D, et al. Among authors: palmen j. Ann Hum Genet. 2011 Jul;75(4):456-67. doi: 10.1111/j.1469-1809.2011.00654.x. Epub 2011 Apr 28. Ann Hum Genet. 2011. PMID: 21534939
78 results