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Erzurumluoglu, A. M. et al. (2020) Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci. Molecular Psychiatry, 25(10), pp. 2392-2409. (doi: 10.1038/s41380-018-0313-0) (PMID:30617275) (PMCID:PMC7515840)

Noordam, R. et al. (2019) Effects of calcium, magnesium, and potassium concentrations on ventricular repolarization in unselected individuals. Journal of the American College of Cardiology, 73(24), pp. 3118-3131. (doi: 10.1016/j.jacc.2019.03.519) (PMID:31221261)

Van Setten, J. et al. (2018) PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity. Nature Communications, 9, 2904. (doi: 10.1038/s41467-018-04766-9) (PMID:30046033) (PMCID:PMC6060178)

Prins, B. P. et al. (2018) Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6. Genome Biology, 19, 87. (doi: 10.1186/s13059-018-1457-6) (PMID:30012220) (PMCID:PMC6048820)

Surendran, P. et al. (2016) Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. Nature Genetics, 48(10), pp. 1151-1161. (doi: 10.1038/ng.3654) (PMID:27618447) (PMCID:PMC5056636)

Ehret, G. B. et al. (2016) The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Nature Genetics, 48(10), pp. 1171-1184. (doi: 10.1038/ng.3667) (PMID:27618452) (PMCID:PMC5042863)

Menni, C. et al. (2015) Metabolomic study of carotid–femoral pulse-wave velocity in women. Journal of Hypertension, 33(4), pp. 791-796. (doi: 10.1097/HJH.0000000000000467) (PMID:25490711) (PMCID:PMC4354457)

Yoneyama, S. et al. (2014) Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations. Human Molecular Genetics, 23(9), pp. 2498-2510. (doi: 10.1093/hmg/ddt626)

Tragante, V. et al. (2014) Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci. American Journal of Human Genetics, 94(3), pp. 349-360. (doi: 10.1016/j.ajhg.2013.12.016) (PMID:24560520) (PMCID:PMC3951943)

Graham, L. A. et al. (2014) Validation of uromodulin as a candidate gene for human essential hypertension. Hypertension, 63(3), pp. 551-558. (doi: 10.1161/HYPERTENSIONAHA.113.01423)

McDonough, C.W., Gong, Y., Padmanabhan, S. , Burkley, B., Langaee, T.Y., Melander, O., Pepine, C.J., Dominiczak, A.F. , Cooper-DeHoff, R.M. and Johnson, J.A. (2013) Pharmacogenomic association of nonsynonymous SNPs in SIGLEC12, A1BG, and the selectin region and cardiovascular outcomes. Hypertension, 62(1), pp. 48-54. (doi: 10.1161/HYPERTENSIONAHA.111.00823)

Sanna-Cherchi, S. et al. (2012) Copy-number disorders are a common cause of congenital kidney malformations. American Journal of Human Genetics, 91(6), pp. 987-997. (doi: 10.1016/j.ajhg.2012.10.007)

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