Whole-genome sequencing of 100 genomes identifies a distinctive genetic susceptibility profile of Qatari patients with hypertension

AM Alsamman, H Almabrazi, H Zayed - Journal of Personalized Medicine, 2022 - mdpi.com
Essential hypertension (EH) is a leading risk condition for cardiovascular and renal
complications. While multiple genes are associated with EH, little is known about its genetic …

Genome-wide and candidate gene association analyses identify a 14-SNP combination for hypertension in patients with type 2 diabetes

CF Cheng, AR Hsieh, WM Liang… - American Journal of …, 2021 - academic.oup.com
Background High blood pressure is common and comorbid with type 2 diabetes (T2D).
Almost 50% of patients with T2D have high blood pressure. Patients with both conditions of …

Effects of rare and common blood pressure gene variants on essential hypertension: results from the Family Blood Pressure Program, CLUE, and Atherosclerosis Risk …

KDH Nguyen, V Pihur, SK Ganesh, A Rakha… - Circulation …, 2013 - Am Heart Assoc
Rationale: Hypertension affects≈ 30% of adults in industrialized countries and is the major
risk factor for cardiovascular disease. Objective: We sought to study the genetic effect of …

Male-specific genetic effect on hypertension and metabolic disorders

SG Heo, JY Hwang, S Uhmn, MJ Go, B Oh, JY Lee… - Human genetics, 2014 - Springer
Genetic risk factors for hypertension may have age or gender specificity and pleiotropic
effects. This study aims to measure the risk of genetic and non-genetic factors in the …

[HTML][HTML] Identifying susceptibility genes for essential hypertension by transcriptome-wide association study

L Huang, Q Zhang, RK Valenzuela, J Xu, F Yan… - … and Biophysics Reports, 2022 - Elsevier
Hypertension is a leading risk factor of cardiovascular disease and mortality in the
population worldwide. Recently, hundreds of genomic loci were reported for hypertension by …

Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension

P Surendran, F Drenos, R Young, H Warren, JP Cook… - Nature …, 2016 - nature.com
High blood pressure is a major risk factor for cardiovascular disease and premature death.
However, there is limited knowledge on specific causal genes and pathways. To better …

Recapitulation of genome-wide association studies on pulse pressure and mean arterial pressure in the Korean population

KW Hong, H Min, BM Heo, S Eun Joo… - Journal of human …, 2012 - nature.com
Increased pulse pressure (PP) and decreased mean arterial pressure (MAP) are strong
prognostic predictors of adverse cardiovascular events. Recently, the International …

Common variants in the ATP2B1 gene are associated with susceptibility to hypertension: the Japanese Millennium Genome Project

Y Tabara, K Kohara, Y Kita, N Hirawa, T Katsuya… - …, 2010 - Am Heart Assoc
Hypertension is one of the most common complex genetic disorders. We have described
previously 38 single nucleotide polymorphisms (SNPs) with suggestive association with …

CYP17A1–ATP2B1 SNPs and Gene–Gene and Gene–Environment Interactions on Essential Hypertension

BL Wei, RX Yin, CX Liu, GX Deng, YZ Guan… - Frontiers in …, 2021 - frontiersin.org
Background: The association between the CYP17A1 and ATP2B1 SNPs and essential
hypertension (referred to as hypertension) is far from being consistent. In addition to the …

Silencing of Atp2b1 increases blood pressure through vasoconstriction

YB Shin, JE Lim, SM Ji, HJ Lee, SY Park… - Journal of …, 2013 - journals.lww.com
Background: Recent genome-wide association studies (GWASs) have identified 30 genetic
loci that regulate blood pressure, increasing our understanding of the cause of hypertension …