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Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation.
Luijk R, Wu H, Ward-Caviness CK, Hannon E, Carnero-Montoro E, Min JL, Mandaviya P, Müller-Nurasyid M, Mei H, van der Maarel SM; BIOS Consortium; Relton C, Mill J, Waldenberger M, Bell JT, Jansen R, Zhernakova A, Franke L, 't Hoen PAC, Boomsma DI, van Duijn CM, van Greevenbroek MMJ, Veldink JH, Wijmenga C, van Meurs J, Daxinger L, Slagboom PE, van Zwet EW, Heijmans BT. Luijk R, et al. Among authors: van zwet ew, van duijn cm, van der maarel sm, van greevenbroek mmj, van meurs j. Nat Commun. 2018 Sep 14;9(1):3738. doi: 10.1038/s41467-018-05714-3. Nat Commun. 2018. PMID: 30218040 Free PMC article.
Genetic dissection of familial combined hyperlipidemia.
Eurlings PM, van der Kallen CJ, Geurts JM, van Greevenbroek MM, de Bruin TW. Eurlings PM, et al. Mol Genet Metab. 2001 Sep-Oct;74(1-2):98-104. doi: 10.1006/mgme.2001.3232. Mol Genet Metab. 2001. PMID: 11592807 Review.
Subclasses of low-density lipoprotein and very low-density lipoprotein in familial combined hyperlipidemia: relationship to multiple lipoprotein phenotype.
Georgieva AM, van Greevenbroek MM, Krauss RM, Brouwers MC, Vermeulen VM, Robertus-Teunissen MG, van der Kallen CJ, de Bruin TW. Georgieva AM, et al. Arterioscler Thromb Vasc Biol. 2004 Apr;24(4):744-9. doi: 10.1161/01.ATV.0000119681.47218.a4. Epub 2004 Jan 29. Arterioscler Thromb Vasc Biol. 2004. PMID: 14751815
242 results