Human Genome Epidemiology Literature Finder
|
Records 1 - 23 (of 23 Records) |
| Query Trace: Hypercholesterolemia and ABCG5[original query] |
|---|
| ATP binding cassette transporter G5 and G8 genotypes and plasma lipoprotein levels before and after treatment with atorvastatin. Journal of lipid research 2004 Apr 45 (4): 653-6. Kajinami Kouji, Brousseau Margaret E, Nartsupha Chorthip, Ordovas Jose M, Schaefer Ernst |
| Significant association of ABCG8:D19H gene polymorphism with hypercholesterolemia and insulin resistance. Journal of human genetics 2008 53 (8): 757-63. Chen Zhih-Cherng, Shin Shyi-Jang, Kuo Kung-Kai, Lin Kun-Der, Yu Ming-Lung, Hsiao Pi-Ju |
| Single nucleotide polymorphisms in ABCG5 and ABCG8 genes in Chilean subjects with polygenic hypercholesterolemia and controls. Clinical chemistry and laboratory medicine : CCLM / FESCC 2008 46 (11): 1581-5. Caamaño José M, Pacheco Alejandro, Lanas Fernando, Salazar Luis |
| Genetic variations at ABCG5/G8 genes modulate plasma lipids concentrations in patients with familial hypercholesterolemia. Atherosclerosis 2010 Jun 210 (2): 486-92. Garcia-Rios A, Perez-Martinez P, Fuentes F, Mata P, Lopez-Miranda J, Alonso R, Rodriguez F, Garcia-Olid A, Ruano J, Ordovas J M, Perez-Jimenez |
| Genetic variability within the cholesterol lowering pathway and the effectiveness of statins in reducing the risk of MI. Atherosclerosis 2011 Aug 217 (2): 458-64. Peters Bas J M, Pett Helmi, Klungel Olaf H, Stricker Bruno H Ch, Psaty Bruce M, Glazer Nicole L, Wiggins Kerri L, Bis Josh C, de Boer Anthonius, Maitland-van der Zee Anke-Hil |
| Refinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countries. Clinical chemistry 2015 Jan 61 (1): 231-8. Futema Marta, Shah Sonia, Cooper Jackie A, Li KaWah, Whittall Ros A, Sharifi Mahtab, Goldberg Olivia, Drogari Euridiki, Mollaki Vasiliki, Wiegman Albert, Defesche Joep, D'Agostino Maria N, D'Angelo Antonietta, Rubba Paolo, Fortunato Giuliana, Walu?-Miarka Ma?gorzata, Hegele Robert A, Aderayo Bamimore Mary, Durst Ronen, Leitersdorf Eran, Mulder Monique T, Roeters van Lennep Jeanine E, Sijbrands Eric J G, Whittaker John C, Talmud Philippa J, Humphries Steve |
| ABCG5/G8 gene is associated with hypercholesterolemias without mutation in candidate genes and noncholesterol sterols. Journal of clinical lipidology 2017 Oct . Lamiquiz-Moneo Itziar, Baila-Rueda Lucía, Bea Ana M, Mateo-Gallego Rocío, Pérez-Calahorra Sofía, Marco-Benedí Victoria, Martín-Navarro Antonio, Ros Emilio, Cofán Montserrat, Rodríguez-Rey José Carlos, Pocovi Miguel, Cenarro Ana, Civeira Fernan |
| Oligogenic familial hypercholesterolemia, LDL cholesterol, and coronary artery disease. Journal of clinical lipidology 2018 Aug . Tada Hayato, Kawashiri Masa-Aki, Nomura Akihiro, Teramoto Ryota, Hosomichi Kazuyoshi, Nohara Atsushi, Inazu Akihiro, Mabuchi Hiroshi, Tajima Atsushi, Yamagishi Masaka |
| Unusual genetic variants associated with hypercholesterolemia in Argentina. Atherosclerosis 2018 10 277 256-261. Corral Pablo, Geller Andrew S, Polisecki Eliana Y, Lopez Graciela I, Bañares Virginia G, Cacciagiu Leonardo, Berg Gabriela, Hegele Robert A, Schaefer Ernst J, Schreier Laura |
| Whole-Gene Duplication of PCSK9 as a Novel Genetic Mechanism for Severe Familial Hypercholesterolemia. The Canadian journal of cardiology 2018 10 34 (10): 1316-1324. Iacocca Michael A, Wang Jian, Sarkar Samantha, Dron Jacqueline S, Lagace Thomas, McIntyre Adam D, Lau Paulina, Robinson John F, Yang Ping, Knoll Joan H, Cao Henian, McPherson Ruth, Hegele Robert |
| Rare and Deleterious Mutations in ABCG5/ABCG8 Genes Contribute to Mimicking and Worsening of Familial Hypercholesterolemia Phenotype. Circulation journal : official journal of the Japanese Circulation Society 2019 7 83 (9): 1917-1924. Tada Hayato, Okada Hirofumi, Nomura Akihiro, Yashiro Satoshi, Nohara Atsushi, Ishigaki Yasushi, Takamura Masayuki, Kawashiri Masa-A |
| ANGPTL3 Mutations in Unrelated Chinese Han Patients with Familial Hypercholesterolemia. Current pharmaceutical design 2019 3 25 (2): 190-200. Yang Yunyun, Yang Song, Jiao Xiaolu, Li Juan, Zhu Miaomiao, Wang Luya, Qin Yanw |
| Targeted Genetic Analysis in a Chinese Cohort of 208 Patients Related to Familial Hypercholesterolemia. Journal of atherosclerosis and thrombosis 2020 Aug . Wang Hao, Yang Hang, Liu Zhaohui, Cui Kai, Zhang Yinhui, Zhang Yujing, Zhao Kun, Yin Kunlun, Li Wenke, Zhou Zh |
| Next-generation sequencing to confirm clinical familial hypercholesterolemia. European journal of preventive cardiology 2020 Jul 2047487320942996. Reeskamp Laurens F, Tromp Tycho R, Defesche Joep C, Grefhorst Aldo, Stroes Erik Sg, Hovingh G Kees, Zuurbier Lin |
| ABCG5 and ABCG8 genetic variants in familial hypercholesterolemia. Journal of clinical lipidology 2020 Jan . Reeskamp Laurens F, Volta Andrea, Zuurbier Linda, Defesche Joep C, Hovingh G Kees, Grefhorst Al |
| Cascade screening and genetic diagnosis of familial hypercholesterolemia in clusters of the Southeastern region from Brazil. Molecular biology reports 2020 11 47 (12): 9279-9288. de Paiva Silvino Júnea Paolucci, Jannes Cinthia Elim, Tada Mauricio Teruo, Lima Isabella Ramos, Silva Iêda de Fátima Oliveira, Pereira Alexandre Costa, Gomes Karina Bra |
| Next-generation sequencing to confirm clinical familial hypercholesterolemia. European journal of preventive cardiology 2021 7 28 (8): 875-883. Reeskamp Laurens F, Tromp Tycho R, Defesche Joep C, Grefhorst Aldo, Stroes Erik S G, Hovingh G Kees, Zuurbier Lin |
| Genetic Analysis of Japanese Children Clinically Diagnosed with Familial Hypercholesterolemia. Journal of atherosclerosis and thrombosis 2021 5 29 (5): 667-677. Nagahara Keiko, Nishibukuro Tsuyoshi, Ogiwara Yasuko, Ikegawa Kento, Tada Hayato, Yamagishi Masakazu, Kawashiri Masa-Aki, Ochi Ayako, Toyoda Junya, Nakano Yuya, Adachi Masanori, Mizuno Katsumi, Hasegawa Yukihiro, Dobashi Kazushi |
| Analysis of Rare Variants in Genes Related to Lipid Metabolism in Patients with Familial Hypercholesterolemia in Western Siberia (Russia). Journal of personalized medicine 2021 11 11 (11): . Shakhtshneider Elena, Ivanoshchuk Dinara, Timoshchenko Olga, Orlov Pavel, Semaev Sergey, Valeev Emil, Goonko Andrew, Ladygina Nataliya, Voevoda Mikha |
| [Identification of genetic variants associated with familial hypercholesterolemia in Chilean children and adolescents]. Revista medica de Chile 2022 3 149 (9): 1267-1274. Sánchez Andrea, Bustos Paulina, Honorato Paula, Sáez Katia, Elim-Jannes Cinthia, Barriga Natalia, Ibieta Guillermo, Pérez Luis, Alonso Rodrigo, Radojkovic Claudia, Asenjo Sylv |
| Improvement of Definite Diagnosis of Familial Hypercholesterolemia Using an Expanding Genetic Analysis. JACC. Asia 2022 11 1 (1): 82-89. Cao Ye-Xuan, Sun Di, Liu Hui-Hui, Jin Jing-Lu, Li Sha, Guo Yuan-Lin, Wu Na-Qiong, Zhu Cheng-Gang, Liu Geng, Dong Qian, Sun Jing, Chen Xie-Hui, Li Jian-J |
| Association of CELSR2, APOB100, ABCG5/8, LDLR, and APOE polymorphisms and their genetic risks with lipids among the Thai subjects. Saudi journal of biological sciences 2023 1 30 (2): 103554. Nuinoon Manit, Saiphak Wutthichai, Nawaka Nantiya, Rattanawan Chutima, Pussadhamma Burabha, Jeenduang Nutjar |
| Targeted sequencing of a gene panel in patients with Familial Hypercholesterolemia from Southern Poland. Polish archives of internal medicine 2023 1 . Toto?-?ura?ska Justyna, Wo?kow Pawe?, Kapusta Maria, Wójcik Ma?gorzata, Starzyk Jerzy, Kawalec Ewa, Idzior-Walu? Barbara, Walu?-Miarka Ma?gorza |
- Page last reviewed:Feb 1, 2023
- Page last updated:May 22, 2023
- Content source: