Human Genome Epidemiology Literature Finder
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Records 1 - 23 (of 23 Records) |
| Query Trace: Hypertension and HFE[original query] |
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| A prospective study of coronary heart disease and the hemochromatosis gene (HFE) C282Y mutation: the Atherosclerosis Risk in Communities (ARIC) study. Atherosclerosis 2001 Feb 154 (3): 739-46. Rasmussen M L, Folsom A R, Catellier D J, Tsai M Y, Garg U, Eckfeldt J |
| Haemochromatosis mutations and ferritin in myocardial infarction: a case-control study. European journal of clinical investigation 2002 Mar 32 Suppl 1 (): 3-8. Claeys Dirk, Walting M, Julmy F, Wuillemin W A, Meyer B |
| Mutations in the hemochromatosis gene (HFE) and stroke. Stroke; a journal of cerebral circulation 2002 Oct 33 (10): 2363-6. Njajou Omer T, Hollander Monika, Koudstaal Peter J, Hofman Albert, Witteman Jacqueline C M, Breteler Monique M B, van Duijn Cornelia |
| Hemochromatosis-causing mutations C282Y and H63D are not risk factors for atherothrombotic cerebral infarction. Medical science monitor : international medical journal of experimental and clinical research 2005 Jul 11 (7): BR248-52. Hruskovicová Helena, Milanez Tomaz, Kobal Jan, Potisk Karmen Peterlin, Petrovic Danijel, Peterlin Bor |
| HFE H63D polymorphism as a modifier of the effect of cumulative lead exposure on pulse pressure: the Normative Aging Study. Environmental health perspectives 2010 Sep 118 (9): 1261-6. Zhang Aimin, Park Sung Kyun, Wright Robert O, Weisskopf Marc G, Mukherjee Bhramar, Nie Huiling, Sparrow David, Hu Howa |
| Genetic susceptibility to anthracycline-related congestive heart failure in survivors of haematopoietic cell transplantation. British journal of haematology 2013 Oct 163 (2): 205-13. Armenian Saro H, Ding Yan, Mills George, Sun Canlan, Venkataraman Kalyanasundaram, Wong Florence Lennie, Neuhausen Susan L, Senitzer David, Wang Shirong, Forman Stephen J, Bhatia Smi |
Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension.
Human molecular genetics 2015 Feb 24 (3): 865-74. Lu Xiangfeng, Wang Laiyuan, Lin Xu, Huang Jianfeng, Charles Gu C, He Meian, Shen Hongbing, He Jiang, Zhu Jingwen, Li Huaixing, Hixson James E, Wu Tangchun, Dai Juncheng, Lu Ling, Shen Chong, Chen Shufeng, He Lin, Mo Zengnan, Hao Yongchen, Mo Xingbo, Yang Xueli, Li Jianxin, Cao Jie, Chen Jichun, Fan Zhongjie, Li Ying, Zhao Liancheng, Li Hongfan, Lu Fanghong, Yao Cailiang, Yu Lin, Xu Lihua, Mu Jianjun, Wu Xianping, Deng Ying, Hu Dongsheng, Zhang Weidong, Ji Xu, Guo Dongshuang, Guo Zhirong, Zhou Zhengyuan, Yang Zili, Wang Renping, Yang Jun, Zhou Xiaoyang, Yan Weili, Sun Ningling, Gao Pingjin, Gu Dongfe |
| Effects of established blood pressure loci on blood pressure values and hypertension risk in an Algerian population sample. Journal of human hypertension 2015 May 29 (5): 296-302. Lardjam-Hetraf S A, Mediene-Benchekor S, Ouhaibi-Djellouli H, Meroufel D N, Boulenouar H, Hermant X, Hamani-Medjaoui I, Saidi-Mehtar N, Amouyel P, Houti L, Goumidi L, Meirhaeghe |
| [Molecular genetic analysis and clinical aspects of patients with hereditary hemochromatosis]. Der Orthopäde 2014 Aug 43 (8): 772-9. Lange U, Teichmann J, Dischereit |
| Association of the apolipoprotein E 2 allele with concurrent occurrence of endometrial hyperplasia and endometrial carcinoma. Oxidative medicine and cellular longevity 2015 2015 593658. Ivanova Tatiana I, Krikunova Ludmila I, Ryabchenko Nikolay I, Mkrtchyan Liana S, Khorokhorina Vera A, Salnikova Lyubov |
| Genetic variant coding for iron regulatory protein HFE contributes to hypertension, the TAMRISK study. Medicine 2015 Jan 94 (4): e464. Määttä Kirsi M, Nikkari Seppo T, Kunnas Tarja |
| Minor variant of rs 16827043 in the iron regulator hemojuvelin gene (HJV) contributes to hypertension: The TAMRISK study. Medicine 2017 Feb 96 (5): e6052. Nikkari Seppo T, Visto Anni-Laura, Määttä Kirsi M, Kunnas Tarja |
| HFE H63D Polymorphism and the Risk for Systemic Hypertension, Myocardial Remodeling, and Adverse Cardiovascular Events in the ARIC Study. Hypertension (Dallas, Tex. : 1979) 2019 Jan 73 (1): 68-74. Selvaraj Senthil, Seidelmann Sara, Silvestre Odilson M, Claggett Brian, Ndumele Chiadi E, Cheng Susan, Yu Bing, Fernandes-Silva Miguel M, Grove Megan L, Boerwinkle Eric, Shah Amil M, Solomon Scott |
| Prediction of features of the course of chronic hepatitis C using Bayesian networks. Terapevticheskii arkhiv 2019 Mar 91 (2): 32-39. Samokhodskaya L M, Starostina E E, Sulimov A V, Krasnova ? N, Rosina T P, Avdeev V G, Savkin I A, Sulimov V B, Mukhin N A, Tkachuk V A, Sadovnichii V |
| Varicose veins of lower extremities: Insights from the first large-scale genetic study.
PLoS genetics 2019 Apr 15 (4): e1008110. Shadrina Alexandra S, Sharapov Sodbo Z, Shashkova Tatiana I, Tsepilov Yakov |
| Histologic Lesions of Porto-Sinusoidal Vascular Disease Following Phlebotomy in Hemochromatosis. Gastroenterology research 2020 2 13 (1): 32-39. El Jabbour Tony, McHugh Kelsey E, Patil Deepa T, Zuo Chunlai, Koo Brandon H, Kim Sungeun, Lee Hwajeo |
| Hepcidin is potential regulator for renin activity. PloS one 2022 4 17 (4): e0267343. Piesanen Jaakko, Valjakka Jarkko, Niemelä Sanna, Borgenström Marjut, Nikkari Seppo, Hytönen Vesa, Määttä Juha, Kunnas Tar |
| An exploratory pilot study on the involvement of APOE, HFE, C9ORF72 variants and comorbidities in neurocognitive and physical performance in a group of HIV-infected people. Metabolic brain disease 2022 3 37 (5): 1569-1583. Zanella Isabella, Zacchi Eliana, Fornari Chiara, Fumarola Benedetta, Antoni Melania Degli, Zizioli Daniela, Quiros-Roldan Eugenia, |
| A haemochromatosis-causing HFE mutation is associated with SARS-CoV-2 susceptibility in the Czech population. Clinica chimica acta; international journal of clinical chemistry 2022 12 538 211-215. Hubacek J A, Philipp T, Adamkova V, Majek O, Dusek |
| Polymorphisms of hypertension susceptibility genes as a risk factors of preeclampsia in the Caucasian population of central Russia. Placenta 2022 Sep 129 51-61. Churnosov Mikhail, Abramova Maria, Reshetnikov Evgeny, Lyashenko Igor V, Efremova Olesya, Churnosova Maria, Ponomarenko Iri |
| Hereditary hemochromatosis beyond hyperferritinemia: Clinical and laboratory investigation of the patient's profile submitted to phlebotomy in two reference centers in southern Brazil. Genetics and molecular biology 2023 5 46 (2): e20220230. Nathalia Kersting, Juliana Cristine Fontana, Fabiane Pohlmann de Athayde, Fernanda Marcante Carlotto, Bruna Accorsi Machado, Cristiane da Silva Rodrigues de Araújo, Leo Sekine, Tor Gunnar Hugo Onsten, Sandra Leistner-Seg |
| Risk Effects of rs1799945 Polymorphism of the HFE Gene and Intergenic Interactions of GWAS-Significant Loci for Arterial Hypertension in the Caucasian Population of Central Russia. International journal of molecular sciences 2023 5 24 (9): . Tatiana Ivanova, Maria Churnosova, Maria Abramova, Irina Ponomarenko, Evgeny Reshetnikov, Inna Aristova, Inna Sorokina, Mikhail Churnos |
| Sex-Specific Features of the Correlation between GWAS-Noticeable Polymorphisms and Hypertension in Europeans of Russia. International journal of molecular sciences 2023 5 24 (9): . Tatiana Ivanova, Maria Churnosova, Maria Abramova, Denis Plotnikov, Irina Ponomarenko, Evgeny Reshetnikov, Inna Aristova, Inna Sorokina, Mikhail Churnos |
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