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Expression Quantitative Trait Locus Mapping in Pulmonary Arterial Hypertension.
Ulrich A, Otero-Núñez P, Wharton J, Swietlik EM, Gräf S, Morrell NW, Wang D, Lawrie A, Wilkins MR, Prokopenko I, Rhodes CJ, Consortium OBOTNBD, Consortium UPCS. Ulrich A, et al. Among authors: consortium upcs. Genes (Basel). 2020 Oct 22;11(11):1247. doi: 10.3390/genes11111247. Genes (Basel). 2020. PMID: 33105808 Free PMC article.
Bi-allelic mutations in MYL1 cause a severe congenital myopathy.
Ravenscroft G, Zaharieva IT, Bortolotti CA, Lambrughi M, Pignataro M, Borsari M, Sewry CA, Phadke R, Haliloglu G, Ong R, Goullée H, Whyte T, Consortium UK, Manzur A, Talim B, Kaya U, Osborn DPS, Forrest ARR, Laing NG, Muntoni F. Ravenscroft G, et al. Among authors: consortium uk. Hum Mol Genet. 2018 Dec 15;27(24):4263-4272. doi: 10.1093/hmg/ddy320. Hum Mol Genet. 2018. PMID: 30215711 Free PMC article.
Functional Analysis of the Coronary Heart Disease Risk Locus on Chromosome 21q22.
Beaney KE, Smith AJP, Folkersen L, Palmen J, Wannamethee SG, Jefferis BJ, Whincup P, Gaunt TR, Casas JP, Ben-Shlomo Y, Price JF, Kumari M, Wong A, Ong K, Hardy R, Kuh D, Wareham N, Kivimaki M, Eriksson P, Humphries SE, Consortium U. Beaney KE, et al. Among authors: consortium u. Dis Markers. 2017;2017:1096916. doi: 10.1155/2017/1096916. Epub 2017 Mar 28. Dis Markers. 2017. PMID: 28458444 Free PMC article.