Replication of a genome-wide association study on essential hypertension in Mongolians

References

• Kearney PM, Whelton M, Reynolds K, et al. Global burden of hypertension: Analysis of worldwide data. Lancet 2005;365(9455):217–23.
   PubMed Web of Science ®Google Scholar
• Liu LS; Writing Group of 2010 Chinese guidelines for the management of hypertension. 2010 chinese guidelines for the management of hypertension [in Chinese]. Chin J Hypertens 2011;19(8):701–43.
   Google Scholar
• Binder A. A review of the genetics of essential hypertension. Curr Opin Cardiol 2007;22(3):176–84.
   PubMed Web of Science ®Google Scholar
• Cowley AW Jr. The genetic dissection of essential hypertension. Nat Rev Genet 2006;7(11):829–40.
   PubMed Web of Science ®Google Scholar
• Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3000 shared controls. Nature 2007;447(7145):661–78.
   PubMed Web of Science ®Google Scholar
• Slavin TP, Feng T, Schnell A, et al. Two-marker association tests yield new disease associations for coronary artery disease and hypertension. Hum Genet 2011;130(6):725–33.
   PubMed Web of Science ®Google Scholar
• Guo Y, Tomlinson B, Chu T, et al. A genome-wide linkage and association scan reveals novel loci for hypertension and blood pressure traits. Plos One 2012;7(2):e31489.
   PubMed Web of Science ®Google Scholar
• Org E, Eyheramendy S, Juhanson P, et al. Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations. Hum Mol Genet 2009;18(12):2288–96.
   PubMed Web of Science ®Google Scholar
• Wang Y, O’Connell JR, McArdle PF, et al. From the cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene. Proc Natl Aaca Sci USA 2009;106(1):226–31.
   PubMed Web of Science ®Google Scholar
• Wang X, Chua HX, Chen P, et al. Comparing methods for performing trans-ethnic meta-analysis of genome-wide association studies. Hum Mol Genet 2013;22(11): 2303–11.
   PubMed Web of Science ®Google Scholar
• Chanock SJ, Manolio T, Boehnke M, et al. Replicating genotype-phenotype associations. Nature 2007;447(7145): 655–60.
   PubMed Web of Science ®Google Scholar
• Guidelines Subcommittee. World health organization-international society of hypertension guidelines for the management of hypertension. J Hypertens 1999;17(2):151–83.
   PubMed Web of Science ®Google Scholar
• Li HM, Du ZR, Zhang L, et al. The relationship between angiotensinogen gene polymorphisms and essential hypertension in a Northern Han Chinese population. Angiology 2014;65(7):614–9.
   PubMed Web of Science ®Google Scholar
• Ehret GB, Morrison AC, O’Connor AA, et al. Replication of the Wellcome Trust genome-wide association study of essential hypertension: The Family Blood Pressure Program. Eur J Hum Genet 2008;16(12):1507–11.
   PubMed Web of Science ®Google Scholar
• Hong KW, Jin HS, Cho YS, et al. Replication of the Wellcome Trust genome-wide association study on essential hypertension in a Korean population. Hypertens Res 2009;32(7):570–4.
   PubMed Web of Science ®Google Scholar
• Newton-Cheh C, Johnson T, Gateva V, et al. Genome-wide association study identifies eight loci associated with blood pressure. Nat Genet 2009;41(6):666–76.
   PubMed Web of Science ®Google Scholar
• Levy D, Ehret GB, Rice K, et al. Genome-wide association study of blood pressure and hypertension. Nat Genet 2009;41(6):677–87.
   PubMed Web of Science ®Google Scholar
• Hong KW, Jin HS, Lim JE, et al. Recapitulation of two genomewide association studies on blood pressure and essentialhypertension in the Korean population. J Hum Genet 2010;55(6):336–41.
   PubMed Web of Science ®Google Scholar
• Niu W, Zhang Y, Ji K, et al. Confirmation of top polymorphisms in hypertension genome-wide association study among Han Chinese. Clin Chim Acta 2010;411(19–20):1491–5.
   PubMed Web of Science ®Google Scholar
• Kato N, Takeuchi F, Tabara Y, et al. Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. Nat Genet 2011;43(6):531–8.
   PubMed Web of Science ®Google Scholar
• Qi Y, Zhao H, Wang Y, et al. Replication of the top 10 most significant polymorphisms from a large blood pressure genome-wide association study of northeast Han Chinese East Asian. Hypertens Res 2014;37(2):134–8.
   PubMed Web of Science ®Google Scholar
• Niu WQ, Zhang Y, Ji KD, et al. Contribution of five top whole-genome association signals to hypertension in Han Chinese. J Hum Hypertens 2011;25(4):278–80.
   PubMed Web of Science ®Google Scholar
• Hattangady NG, Olala LO, Bollag WB, Rainey WE. Acute and chronic regulation of aldosterone production. Mol Cell Endocrinol 2012;350(2):151–62.
   PubMed Web of Science ®Google Scholar
• Condon JC, Pezzi V, Drummond BM, et al. Calmodulin-dependent kinase I regulates adrenal cell expression of aldosterone synthase. Endocrinology 2002;143(9):3651–7.
   PubMed Web of Science ®Google Scholar
• Spät A, Hunyady L. Control of aldosterone secretion: A model for convergence in cellular signaling pathways. Physiol Rev 2004;84(2):489–39.
   PubMed Web of Science ®Google Scholar
• Sakagami H, Kamata A, Nishimura H, et al. Prominent expression and activity-dependent nuclear translocation of Ca2+/calmodulin-dependent protein kinase Idelta in hippocampal neurons. Eur J Neurosci 2005;22(11):2697–707.
   PubMed Web of Science ®Google Scholar
• Mulatero P, Monticone S, Rainey WE, et al. Role of KCNJ5 in familial and sporadic primary aldosteronism. Nat Rev Endocrinol 2013;9(2):104–12.
   PubMed Web of Science ®Google Scholar
• Beuschlein F, Boulkroun S, Osswald A, et al. Somatic mutations in ATP1A1 and ATP2B3 lead to aldosteroneproducing adenomas and secondary hypertension. Nat Genet 2013;45(4):440–4.
   PubMed Web of Science ®Google Scholar
• Vasan RS, Evans JC, Larson MG, et al. Serum aldosterone and the incidence of hypertension in nonhypertensive persons. N Engl J Med 2004;351(1):33–41.
   PubMed Web of Science ®Google Scholar
• Frau F, Zaninello R, Salvi E, et al. Genome-wide association study identifies CAMK1D variants involved in blood pressure response to losartan: The SOPHIA study. Pharmacogenomics 2014;15(13):1643–52.
   PubMed Web of Science ®Google Scholar
• Chou SH, Shulman JM, Keenan BT, et al. Genetic susceptibility for ischemic infarction and arteriolosclerosis based on neuropathologic evaluations. Cerebrovasc Dis 2013;36(3):181–8.
   PubMed Web of Science ®Google Scholar
• Yang Y, Wei M, Xiong Y, et al. Endophilin A1 regulates dendritic spine morphogenesis and stability through interaction with p140Cap. Cell Res 2015;25(4):496–516.
   PubMed Web of Science ®Google Scholar
• Shifman S, Darvasi A. The value of isolated populations. Nat Genet 2001;28(4):309–10.
   PubMed Web of Science ®Google Scholar
• Hei L, Tie Z. Shine Nairuulsan Mongol Undusten-ne dobch tuuh (Mongolian History): Inner Mongolian People Publishing Agency 2011
   Google Scholar
• Nima B. Mingan on ne dunji huun (Great Man of the Millennium): Inner Mongolian people publishing agency 2011
   Google Scholar
• Zhang M. Khoshuu nutug in temteglel (Mongolian Nomadic History). Beijing: Nationality Press 1988
   Google Scholar
• Xing J, Wuren T, Simonson TS, et al. Genomic analysis of natural selection and phenotypic variation in high-altitude Mongolians. PLos Genet 2013;9(7):e1003634.
   PubMed Web of Science ®Google Scholar