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Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach.
Versmissen J, Oosterveer DM, Yazdanpanah M, Dehghan A, Hólm H, Erdman J, Aulchenko YS, Thorleifsson G, Schunkert H, Huijgen R, Vongpromek R, Uitterlinden AG, Defesche JC, van Duijn CM, Mulder M, Dadd T, Karlsson HD, Ordovas J, Kindt I, Jarman A, Hofman A, van Vark-van der Zee L, Blommesteijn-Touw AC, Kwekkeboom J, Liem AH, van der Ouderaa FJ, Calandra S, Bertolini S, Averna M, Langslet G, Ose L, Ros E, Almagro F, de Leeuw PW, Civeira F, Masana L, Pintó X, Simoons ML, Schinkel AF, Green MR, Zwinderman AH, Johnson KJ, Schaefer A, Neil A, Witteman JC, Humphries SE, Kastelein JJ, Sijbrands EJ. Versmissen J, et al. Among authors: blommesteijn touw ac. Eur J Hum Genet. 2015 Mar;23(3):381-7. doi: 10.1038/ejhg.2014.101. Epub 2014 Jun 11. Eur J Hum Genet. 2015. PMID: 24916650 Free PMC article.
Apolipoprotein isoform E4 does not increase coronary heart disease risk in carriers of low-density lipoprotein receptor mutations.
Versmissen J, Oosterveer DM, Hoekstra M, Out R, Berbée JF, Blommesteijn-Touw AC, van Vark-van der Zee L, Vongpromek R, Vanmierlo T, Defesche JC, Mulder M, Kastelein JJ, Sijbrands EJ. Versmissen J, et al. Among authors: blommesteijn touw ac. Circ Cardiovasc Genet. 2011 Dec;4(6):655-60. doi: 10.1161/CIRCGENETICS.111.959858. Epub 2011 Oct 18. Circ Cardiovasc Genet. 2011. PMID: 22010136