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Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertension.
Copeland I, Wonkam-Tingang E, Gupta-Malhotra M, Hashmi SS, Han Y, Jajoo A, Hall NJ, Hernandez PP, Lie N, Liu D, Xu J, Rosenfeld J, Haldipur A, Desire Z, Coban-Akdemir ZH, Scott DA, Li Q, Chao HT, Zaske AM, Lupski JR, Milewicz DM, Shete S, Posey JE, Hanchard NA. Copeland I, et al. Among authors: gupta malhotra m. JCI Insight. 2024 May 8;9(9):e172152. doi: 10.1172/jci.insight.172152. JCI Insight. 2024. PMID: 38716726 Free PMC article.
Epidemiology of Childhood Onset Essential Hypertension.
Gupta-Malhotra M, Shete S, Barratt MS, Milewicz D, Hashmi SS. Gupta-Malhotra M, et al. J Hum Hypertens. 2018 Dec;32(12):808-813. doi: 10.1038/s41371-018-0110-x. Epub 2018 Sep 17. J Hum Hypertens. 2018. PMID: 30224771 Free PMC article.
Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel β-subunit in a case of early-onset phenotype of Liddle syndrome.
Polfus LM, Boerwinkle E, Gibbs RA, Metcalf G, Muzny D, Veeraraghavan N, Grove M, Shete S, Wallace S, Milewicz D, Hanchard N, Lupski JR, Hashmi SS, Gupta-Malhotra M. Polfus LM, et al. Among authors: gupta malhotra m. Cold Spring Harb Mol Case Stud. 2016 Nov;2(6):a001255. doi: 10.1101/mcs.a001255. Cold Spring Harb Mol Case Stud. 2016. PMID: 27900368 Free PMC article.
Childhood-Onset Essential Hypertension and the Family Structure.
Gupta-Malhotra M, Hashmi SS, Barratt MS, Milewicz DM, Shete S. Gupta-Malhotra M, et al. J Clin Hypertens (Greenwich). 2016 May;18(5):431-8. doi: 10.1111/jch.12701. Epub 2015 Oct 5. J Clin Hypertens (Greenwich). 2016. PMID: 26435293 Free PMC article.
35 results