Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: Hypertension and LDLR[original query] |
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A common mutation of low-density lipoprotein receptor gene is associated with essential hypertension among Japanese. Journal of human hypertension 2001 Feb 15 (2): 125-30. Fu Y, Katsuya T, Higaki J, Asai T, Fukuda M, Takiuchi S, Hatanaka Y, Rakugi H, Ogihara |
Influence of LDL-receptor mutation type on age at first cardiovascular event in patients with familial hypercholesterolaemia. European heart journal 2007 Feb 28 (3): 299-304. Souverein Olga W, Defesche Joep C, Zwinderman Aeilko H, Kastelein John J P, Tanck Michael W |
Association of polymorphisms of ABCA1 and ROS1 with hypertension in Japanese individuals. International journal of molecular medicine 2008 Jan 21 (1): 83-9. Yamada Yoshiji, Kato Kimihiko, Yoshida Tetsuro, Yokoi Kiyoshi, Matsuo Hitoshi, Watanabe Sachiro, Ichihara Sahoko, Metoki Norifumi, Yoshida Hidemi, Satoh Kei, Aoyagi Yukitoshi, Yasunaga Akitomo, Park Hyuntae, Tanaka Masashi, Nozawa Yoshino |
Association of genetic variation in apolipoprotein E and low density lipoprotein receptor with ischemic stroke in Northern Han Chinese. Journal of the neurological sciences 2009 Jan 276 (1-2): 118-22. Wang Bin, Zhao Hongye, Zhou Li, Dai Xiaoxia, Wang Dayu, Cao Jun, Niu Wenqu |
Familial hypercholesterolemia in the danish general population: prevalence, coronary artery disease, and cholesterol-lowering medication. The Journal of clinical endocrinology and metabolism 2012 Nov 97 (11): 3956-64. Benn Marianne, Watts Gerald F, Tybjaerg-Hansen Anne, Nordestgaard Børge |
Spectrum of mutations and phenotypic expression in patients with autosomal dominant hypercholesterolemia identified in Italy. Atherosclerosis 2013 Jan . Bertolini S, Pisciotta L, Rabacchi C, Cefalù AB, Noto D, Fasano T, Signori A, Fresa R, Averna M, Calandra S |
Lipoprotein(a) in Familial Hypercholesterolemia With Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Gain-of-Function Mutations. Circulation journal : official journal of the Japanese Circulation Society 2015 Dec . Tada Hayato, Kawashiri Masa-Aki, Yoshida Taiji, Teramoto Ryota, Nohara Atsushi, Konno Tetsuo, Inazu Akihiro, Mabuchi Hiroshi, Yamagishi Masakazu, Hayashi Kens |
Genomic Study of Cardiovascular Continuum Comorbidity. Acta naturae 0 7 (3): 89-99. Makeeva O A, Sleptsov A A, Kulish E V, Barbarash O L, Mazur A M, Prokhorchuk E B, Chekanov N N, Stepanov V A, Puzyrev V |
Association of polymorphisms of genes involved in lipid metabolism with blood pressure and lipid values in mexican hypertensive individuals. Disease markers 2014 2014 150358. Ríos-González Blanca Estela, Ibarra-Cortés Bertha, Ramírez-López Guadalupe, Sánchez-Corona José, Magaña-Torres María Tere |
The Montreal-FH-SCORE: A new score to predict cardiovascular events in familial hypercholesterolemia. Journal of clinical lipidology 0 11 (1): 80-86. Paquette Martine, Dufour Robert, Baass Alex |
Reducing cardiovascular risk in patients with familial hypercholesterolemia: Risk prediction and lipid management. Progress in cardiovascular diseases 2019 11 62 (5): 414-422. Miname Marcio H, Santos Raul |
Heterozygosity in LDLR rs2228671 and rs72658855 Gene is Associated with Increased Risk of Developing Coronary Artery Disease in India -A Case-Control Study. Endocrine, metabolic & immune disorders drug targets 2019 Oct . Jha Chandan K, Mir Rashid, Banu Shaheena, Elfaki Imadeldin, Chahal Sukh M |
Molecular Characterization of Familial Hypercholesterolemia in a North American Cohort. Journal of the Endocrine Society 2020 1 4 (1): bvz015. Garg Abhimanyu, Fazio Sergio, Duell P Barton, Baass Alexis, Udata Chandrasekhar, Joh Tenshang, Riel Tom, Sirota Marina, Dettling Danielle, Liang Hong, Garzone Pamela D, Gumbiner Barry, Wan Ho |
LDLR gene polymorphism (rs688) affects susceptibility to cardiovascular disease in end-stage kidney disease patients. BMC nephrology 2021 Sep 22 (1): 316. Buraczynska Monika, Jacob Jerry, Gwiazda-Tyndel Karolina, Ksiazek Andrz |
Hypertension is associated with a variant in the RARRES2 gene in populations of Ouro Preto, Minas Gerais, Brazil: a cross-sectional study. International journal of molecular epidemiology and genetics 2021 12 (3): 40-51. Batista Aline Priscila, Barbosa Keila Furbino, de Azevedo Rafael Júnior, Vianna Valeska Natiely, de Queiroz Erica Maria, Marinho Carolina Coimbra, Machado-Coelho George Luiz Li |
Identification of genetic variants related to metabolic syndrome by next-generation sequencing. Diabetology & metabolic syndrome 2022 Aug 14 (1): 119. Lee Sanghoo, Kim Seol-A, Hong Jeonghoon, Kim Yejin, Hong Gayeon, Baik SaeYun, Choi Kyeonghwan, Lee Mi-Kyeong, Lee Kyoung-Ry |
The R93C Variant of PCSK9 Reduces the Risk of Premature MI in a Chinese Han Population. Frontiers in genetics 2022 4 13 875269. Yang Lincheng, Pu Tian, Zhang Yan, Yan Hua, Yu Haiyi, Gao W |
Gene Sequencing Identifies Perturbation in Nitric Oxide Signaling as a Nonlipid Molecular Subtype of Coronary Artery Disease. Circulation. Genomic and precision medicine 2022 Oct 101161CIRCGEN121003598. Khera Amit V, Wang Minxian, Chaffin Mark, Emdin Connor A, Samani Nilesh J, Schunkert Heribert, Watkins Hugh, McPherson Ruth, Erdmann Jeanette, Elosua Roberto, Boerwinkle Eric, Ardissino Diego, Butterworth Adam S, Di Angelantonio Emanuele, Naheed Aliya, Danesh John, Chowdhury Rajiv, Krumholz Harlan M, Sheu Wayne H-H, Rich Stephen S, Rotter Jerome I, Chen Yii-der Ida, Gabriel Stacey, Lander Eric S, Saleheen Danish, Kathiresan Sek |
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