Works about HYPERTENSION genetics

Results: 295

Nutrigenetics and Nutritional Strategies in Systemic Arterial Hypertension: Evidence From a Scoping Review.

Published in:

Nutrition Reviews, 2025, v. 83, n. 3, p. 539, doi. 10.1093/nutrit/nuae112

By:

Holzbach, Luciana C;
Brandão-Lima, Paula N;
Duarte, Graziela B S;
Rogero, Marcelo M;
Cominetti, Cristiane

Publication type:

Article

Salt-sensitive hypertension: mechanisms and effects of dietary and other lifestyle factors.

Published in:

Nutrition Reviews, 2016, v. 74, n. 10, p. 645, doi. 10.1093/nutrit/nuw028

By:

Pilic, Leta;
Pedlar, Charles R.;
Mavrommatis, Yiannis

Publication type:

Article

Mutational analysis of CYP2C8 in hypertensive patients using denaturing high performance liquid chromatography L. K. Teh et al. Mutational analysis of CYP2C8 using DHPLC.

Published in:

Journal of Clinical Pharmacy & Therapeutics, 2010, v. 35, n. 6, p. 723, doi. 10.1111/j.1365-2710.2009.01146.x

By:

Teh, L. K.;
Zahri, M. K.;
Zakaria, Z. A.;
Ismail, R.;
Salleh, M. Z.

Publication type:

Article

Compound BMPR2 gene mutations in a malignant variant of idiopathic pulmonary arterial hypertension.

Published in:

Cardiogenetics, 2014, v. 4, n. 1, p. 27, doi. 10.4081/cardiogenetics.2014.4824

By:

Serra, Walter;
Marziliano, Nicola;
Corradi, Domenico;
Brigati, Francesca;
Intrieri, Mariano;
Sapere, Nadia;
Caporale, Vittoria;
Merlini, Piera Angelica;
Chetta, Alfredo;
Ardissino, Diego

Publication type:

Article

Mouse models of cerebral injury and cognitive impairment in hypertension.

Published in:

Frontiers in Aging Neuroscience, 2023, p. 1, doi. 10.3389/fnagi.2023.1199612

By:

Perrotta, Marialuisa;
Carnevale, Daniela;
Carnevale, Lorenzo

Publication type:

Article

DNA methylation and hypertension: emerging evidence and challenges.

Published in:

Briefings in Functional Genomics, 2016, v. 15, n. 6, p. 460, doi. 10.1093/bfgp/elw014

By:

Liyuan Han;
Yanfen Liu;
Shiwei Duan;
Perry, Benjamin;
Wen Li;
Yonghan He

Publication type:

Article

Microarray expression profiling and gene ontology analysis of long non-coding RNAs in spontaneously hypertensive rats and their potential roles in the pathogenesis of hypertension.

Published in:

Molecular Medicine Reports, 2016, v. 13, n. 1, p. 295, doi. 10.3892/mmr.2015.4554

By:

LIANGLEI HOU;
ZHENHAO LIN;
YUNJIE NI;
YIHAO WU;
DEZHUN CHEN;
LIJUAN SONG;
XIAOYAN HUANG;
HUANHUAN HU;
DEYE YANG

Publication type:

Article

2D-<sup>1</sup>H proton magnetic resonance spectroscopic imaging study on brain metabolite alterations in patients with diabetic hypertension.

Published in:

Molecular Medicine Reports, 2015, v. 11, n. 6, p. 4232, doi. 10.3892/mmr.2015.3305

By:

ZHEN CAO;
BI-DI YE;
ZHI-WEI SHEN;
XIAO-FANG CHENG;
ZHONG-XIAN YANG;
YAN-YAN LIU;
REN-HUA WU;
KUAN GENG;
YE-YU XIAO

Publication type:

Article

C242T polymorphism of the NADPH oxidase p22PHOX gene and its association with endothelial dysfunction in asymptomatic individuals with essential systemic hypertension.

Published in:

Molecular Medicine Reports, 2014, v. 9, n. 5, p. 1857, doi. 10.3892/mmr.2014.1992

By:

ADNAN RAFIQ;
KHURSHEED ASLAM;
ROUF MALIK;
DIL AFROZE

Publication type:

Article

The Genetics of Blood Pressure and Hypertension: The Role of Rare Variation.

Published in:

Cardiovascular Therapeutics, 2011, v. 29, n. 1, p. 37, doi. 10.1111/j.1755-5922.2010.00246.x

By:

Doris, Peter A.

Publication type:

Article

Mean platelet volume is increased in patients with hypertensive crises.

Published in:

Platelets, 2014, v. 25, n. 6, p. 423, doi. 10.3109/09537104.2013.830181

By:

Karabacak, Mustafa;
Dogan, Abdullah;
Turkdogan, Ahmet Kenan;
Kapci, Mucahit;
Duman, Ali;
Akpinar, Orhan

Publication type:

Article

A novel mutation in KLHL3 gene causes familial hyperkalemic hypertension.

Published in:

QJM: An International Journal of Medicine, 2016, v. 109, n. 7, p. 487, doi. 10.1093/qjmed/hcw043

By:

Kelly, D.;
Rodzlan, M. R.;
Jeunemaitre, X.;
Wall, C.

Publication type:

Article

Identification of genetic defects in pulmonary arterial hypertension by a new gene panel diagnostic tool.

Published in:

Clinical Science, 2016, v. 130, n. 22, p. 2043, doi. 10.1042/CS20160531

By:

Jie Song;
Eichstaedt, Christina A.;
Viales, Rebecca Rodríguez;
Benjamin, Nicola;
Harutyunova, Satenik;
Fischer, Christine;
Grünig, Ekkehard;
Hinderhofer, Katrin

Publication type:

Article

Localization of genes involved in the metabolic syndrome using multivariate linkage analysis.

Published in:

BMC Genetics, 2003, v. 4, p. S57, doi. 10.1186/1471-2156-4-S1-S57

By:

Olswold, Curtis;
De Andrade, Mariza

Publication type:

Article

Genome-wide linkage analysis of systolic blood pressure: a comparison of two approaches to phenotype definition.

Published in:

BMC Genetics, 2003, v. 4, p. S13, doi. 10.1186/1471-2156-4-S1-S13

By:

Slager, Susan L.;
Iturria, Stephen J.

Publication type:

Article

HYPEST study: profile of hypertensive patients in Estonia.

Published in:: BMC Cardiovascular Disorders, 2011, v. 11, n. 1, p. 55, doi. 10.1186/1471-2261-11-55
Publication type:: Article

eNOS and BDKRB2 genotypes affect the antihypertensive responses to enalapril.

Published in:

European Journal of Clinical Pharmacology, 2013, v. 69, n. 2, p. 167, doi. 10.1007/s00228-012-1326-2

By:

Silva, P.;
Fontana, V.;
Luizon, M.;
Lacchini, R.;
Silva, W.;
Biagi, C.;
Tanus-Santos, J.

Publication type:

Article

Genome-wide linkage analysis for uric acid in families enriched for hypertension.

Published in:

Nephrology Dialysis Transplantation, 2009, v. 24, n. 8, p. 2414, doi. 10.1093/ndt/gfp080

By:

Rule, Andrew D.;
Fridley, Brooke L.;
Hunt, Steven C.;
Asmann, Yan;
Boerwinkle, Eric;
Pankow, James S.;
Mosley, Thomas H.;
Turner, Stephen T.

Publication type:

Article

Strain-specific single-nucleotide polymorphisms in hypertensive ISIAH rats.

Published in:

Biochemistry (00062979), 2017, v. 82, n. 2, p. 224, doi. 10.1134/S0006297917020146

By:

Ershov, N.;
Markel, A.;
Redina, O.

Publication type:

Article

Comprehensive molecular characterization of hypertension-related genes in cancer.

Published in:

Cardio-Oncology, 2022, v. 8, n. 1, p. 1, doi. 10.1186/s40959-022-00136-z

By:

Jiang, Yanan;
Shi, Chunpeng;
Tian, Songyu;
Zhi, Fengnan;
Shen, Xiuyun;
Shang, Desi;
Tian, Jinwei

Publication type:

Article

Molecular mechanisms in vascular injury induced by hypertension: Expression and role of microRNA-34a.

Published in:

Experimental & Therapeutic Medicine, 2017, v. 14, n. 6, p. 5497, doi. 10.3892/etm.2017.5216

By:

XIN QU;
CHUNTING WANG;
SIGUAN LIU;
FANFAN YI;
WENWEI CHENG

Publication type:

Article

Association of a transcription factor 21 gene polymorphism with hypertension.

Published in:

Biomedical Reports, 2015, v. 3, n. 1, p. 118, doi. 10.3892/br.2014.371

By:

TETSUO FUJIMAKI;
MITSUTOSHI OGURI;
HIDEKI HORIBE;
KIMIHIKO KATO;
REIKO MATSUOKA;
SHINTARO ABE;
FUMITAKA TOKORO;
MASAZUMI ARAI;
TOSHIYUKI NODA;
SACHIRO WATANABE;
YOSHIJI YAMADA

Publication type:

Article

The VA Hypertension Primary Care Longitudinal Cohort: Electronic medical records in the post-genomic era.

Published in:

Health Informatics Journal, 2010, v. 16, n. 4, p. 274, doi. 10.1177/1460458210380527

By:

Salem, Rany M.;
Pandey, Braj;
Richard, Erin;
Fung, Maple M.;
Garcia, Erin P.;
Brophy, Victoria H.;
Schork, Nicholas J.;
O'Connor, Daniel T.;
Bhatnagar, Vibha

Publication type:

Article

Common variant of human NEDD4L activates a cryptic splice site to form a frameshifted transcript.

Published in:

Journal of Human Genetics, 2002, v. 47, n. 12, p. 665, doi. 10.1007/s100380200102

By:

Dunn, Diane M.;
Ishigami, Tomoaki;
Pankow, James;
von Niederhaussen, Andrew;
Alder, Jonathan;
Hunt, Steven C.;
Leppert, Mark F.;
Lalouel, Jean-Marc;
Weiss, Robert B.

Publication type:

Article

The ADD1 G460W polymorphism is not associated with variation in blood pressure in Canadian Oji-Cree.

Published in:

Journal of Human Genetics, 1999, v. 44, n. 4, p. 225, doi. 10.1007/s100380050148

By:

Busch, Christopher P.;
Harris, Stewart B.;
Hanley, Anthony J. G.;
Zinman, Bernard;
Hegele, Robert A.

Publication type:

Article

Searching for genes involved in hypertension development in special populations: children and pre-eclamptic women. Where are we standing now?

Published in:

Clinical Chemistry & Laboratory Medicine, 2013, v. 51, n. 12, p. 2253, doi. 10.1515/cclm-2013-0405

By:

Danese, Elisa;
Montagnana, Martina;
Fava, Cristiano

Publication type:

Article

Polymorphisms of the β1-adrenergic receptor gene are associated with essential hypertension in Chinese.

Published in:

Clinical Chemistry & Laboratory Medicine, 2009, v. 47, n. 10, p. 1227, doi. 10.1515/CCLM.2009.276

By:

Yingxin Peng;
Hao Xue;
Leiming Luo;
Wenjing Yao;
Rongbin Li

Publication type:

Article

Functional polymorphisms in ACE and CYP11B2 genes and atrial fibrillation in patients with hypertensive heart disease.

Published in:

Clinical Chemistry & Laboratory Medicine, 2009, v. 47, n. 1, p. 32, doi. 10.1515/CCLM.2009.023

By:

Huang, Mingfang;
Gai, Xiaobo;
Yang, Xiangyue;
Hou, Jianping;
Lan, Xiaopeng;
Zheng, Weixing;
Chen, Fengping;
He, Jiake

Publication type:

Article

Genetics in pulmonary arterial hypertension in a large homogeneous Japanese population.

Published in:

Clinical Genetics, 2018, v. 94, n. 1, p. 70, doi. 10.1111/cge.13154

By:

Gamou, S.;
Kataoka, M.;
Aimi, Y.;
Chiba, T.;
Momose, Y.;
Isobe, S.;
Hirayama, T.;
Yoshino, H.;
Fukuda, K.;
Satoh, T.

Publication type:

Article

Issue Information ‐ Editorial Board.

Published in:: Clinical Genetics, 2018, v. 94, n. 1, p. 1, doi. 10.1111/cge.13114
Publication type:: Article

A family-based association test to detect gene-gene interactions in the presence of linkage.

Published in:

European Journal of Human Genetics, 2012, v. 20, n. 9, p. 973, doi. 10.1038/ejhg.2012.45

By:

De Lobel, Lizzy;
Thijs, Lutgarde;
Kouznetsova, Tatiana;
Staessen, Jan A;
Van Steen, Kristel

Publication type:

Article

The tRNA<sup>Met</sup> 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree.

Published in:

European Journal of Human Genetics, 2011, v. 19, n. 11, p. 1181, doi. 10.1038/ejhg.2011.111

By:

Lu, Zhongqiu;
Chen, Hong;
Meng, Yanzi;
Wang, Yan;
Xue, Ling;
Zhi, Shaoce;
Qiu, Qiaomeng;
Yang, Li;
Mo, Jun Qin;
Guan, Min-Xin

Publication type:

Article

A clustering approach to identify rare variants associated with hypertension.

Published in:

BMC Proceedings, 2016, v. 10, p. 153, doi. 10.1186/s12919-016-0022-0

By:

Rui Sun;
Qiao Deng;
Inchi Hu;
Benny Chung-Ying Zee;
Maggie Haitian Wang

Publication type:

Article

Prediction of hypertension based on the genetic analysis of longitudinal phenotypes: a comparison of different modeling approaches for the binary trait of hypertension.

Published in:

BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S78

By:

Yun-Hee Choi;
Chowdhury, Rafiqul;
Swaminathan, Balakumar

Publication type:

Article

Practical investigation of the performance of robust logistic regression to predict the genetic risk of hypertension.

Published in:

BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S65

By:

Kesselmeier, Miriam;
Legrand, Carine;
Peil, Barbara;
Kabisch, Maria;
Fischer, Christine;
Hamann, Ute;
Bermejo, Justo Lorenzo

Publication type:

Article

Testing optimally weighted combination of variants for hypertension.

Published in:

BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S59

By:

Xingwang Zhao;
Qiuying Sha;
Shuanglin Zhang;
Xuexia Wang

Publication type:

Article

Haplotype approach for association analysis on hypertension.

Published in:

BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S57

By:

Xiaowei Shen;
Espin-Garcia, Osvaldo;
Xin Qiu;
Brhane, Yonathan;
Liu, Geoffrey;
Wei Xu

Publication type:

Article

Identifying rare variants associated with hypertension using the C-alpha test.

Published in:

BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S56

By:

Faino, Anna;
Powell, Amber;
Williams, André;
Silveira, Lori

Publication type:

Article

Detection of imprinting effects for hypertension based on general pedigrees utilizing all affected and unaffected individuals.

Published in:

BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S52

By:

Fangyuan Zhang;
Shili Lin

Publication type:

Article

Familial Dyslipidemic Hypertension: Evidence From 58 Utah Families for a Syndrome Present in Approximately 12% of Patients With Essential Hypertension.

Published in:

Diabetes Spectrum, 1990, v. 3, n. 5, p. 314

By:

Kaplan, N. M.

Publication type:

Article

Genetic and BMI Risks for Predicting Blood Pressure in Three Generations of West African Dogon Women.

Published in:

2013

By:

Taylor, Jacquelyn Y.;
Sampson, Deborah;
Taylor, Andre D.;
Caldwell, Dennis;
Sun, Yan V.

Publication type:

Journal Article

Gene-Environment Interaction for Hypertension Among African American Women Across Generations.

Published in:

2010

By:

Taylor, Jacquelyn Y.;
Sun, Yan V.;
Hunt, Steven C.;
Kardia, Sharon L.R.

Publication type:

Journal Article

Selected Abstracts from the National Congress of the Italian Society of Hypertension (SIIA 2011).

Published in:: 2011
Publication type:: Abstract

KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron.

Published in:

Nature Genetics, 2012, v. 44, n. 5, p. 609, doi. 10.1038/ng0512-609

By:

Louis-Dit-Picard, Hélène;
Barc, Julien;
Trujillano, Daniel;
Miserey-Lenkei, Stéphanie;
Bouatia-Naji, Nabila;
Pylypenko, Olena;
Beaurain, Geneviève;
Bonnefond, Amélie;
Sand, Olivier;
Simian, Christophe;
Vidal-Petiot, Emmanuelle;
Soukaseum, Christelle;
Mandet, Chantal;
Broux, Françoise;
Chabre, Olivier;
Delahousse, Michel;
Esnault, Vincent;
Fiquet, Béatrice;
Houillier, Pascal;
Bagnis, Corinne Isnard

Publication type:

Article

KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron.

Published in:

Nature Genetics, 2012, v. 44, n. 4, p. 456, doi. 10.1038/ng.2218

By:

Louis-Dit-Picard, Hélène;
Barc, Julien;
Trujillano, Daniel;
Miserey-Lenkei, Stéphanie;
Bouatia-Naji, Nabila;
Pylypenko, Olena;
Beaurain, Geneviève;
Bonnefond, Amélie;
Sand, Olivier;
Simian, Christophe;
Vidal-Petiot, Emmanuelle;
Soukaseum, Christelle;
Mandet, Chantal;
Broux, Françoise;
Chabre, Olivier;
Delahousse, Michel;
Esnault, Vincent;
Fiquet, Béatrice;
Houillier, Pascal;
Bagnis, Corinne Isnard

Publication type:

Article

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.

Published in:

Nature Genetics, 2011, v. 43, n. 10, p. 1005, doi. 10.1038/ng.922

By:

Wain, Louise V;
Verwoert, Germaine C;
O'Reilly, Paul F;
Shi, Gang;
Johnson, Toby;
Johnson, Andrew D;
Bochud, Murielle;
Rice, Kenneth M;
Henneman, Peter;
Smith, Albert V;
Ehret, Georg B;
Amin, Najaf;
Larson, Martin G;
Mooser, Vincent;
Hadley, David;
Dörr, Marcus;
Bis, Joshua C;
Aspelund, Thor;
Esko, Tõnu;
Janssens, A Cecile J W

Publication type:

Article

Identification of renal Cd36 as a determinant of blood pressure and risk for hypertension.

Published in:

Nature Genetics, 2008, v. 40, n. 8, p. 952, doi. 10.1038/ng.164

By:

Pravenec, Michal;
Churchill, Paul C.;
Churchill, Monique C.;
Viklicky, Ondrej;
Kazdova, Ludmila;
Aitman, Timothy J.;
Petretto, Enrico;
Hubner, Norbert;
AWallace, Caroline;
Zimdahl, Heike;
Zidek, Vaclav;
Landa, Vladimir;
Dunbar, Joseph;
Bidani, Anil;
Griffin, Karen;
Qi, Nathan;
Maxova, Martina;
Kren, Vladimir;
Mlejnek, Petr;
Jiaming Wang

Publication type:

Article

Use of biochip microarrays to discover genes for dyslipidaemia, insulin resistance and hypertension in rats and humans.

Published in:

1999

By:

Scott, James;
Naoumova, Rossi;
Shoulders, Carol C.;
Aitman, Timothy J.

Publication type:

Abstract

Characterization of VNTRs Within the Entire Region of SLC6A3 and Its Association with Hypertension.

Published in:

DNA & Cell Biology, 2017, v. 36, n. 3, p. 227, doi. 10.1089/dna.2016.3448

By:

Won-Tae Kim;
Se-Ra Lee;
Yun-Gil Roh;
Seung Il Kim;
Yung Hyun Choi;
Mi-Hye Mun;
Mi-So Jeong;
Sang Seok Koh;
Sun-Hee Leem

Publication type:

Article

Obesity-associated hypertension is ameliorated in patients with TLR4 single nucleotide polymorphism (SNP) rs4986790.

Published in:

Journal of Inflammation, 2015, v. 12, n. 1, p. 1, doi. 10.1186/s12950-015-0100-5

By:

Schneider, Simon;
Hoppmann, Petra;
Koch, Werner;
Kemmner, Stephan;
Schmaderer, Christoph;
Renders, Lutz;
Kastrati, Adnan;
Laugwitz, Karl-Ludwig;
Heemann, Uwe;
Baumann, Marcus

Publication type:

Article