Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: Syndrome and LDLR[original query] |
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Characterization and geographic distribution of the low density lipoprotein receptor (LDLR) gene mutations in northwestern Greece. Human mutation 2001 May 17 (5): 432-3. Miltiadous G, Elisaf M, Bairaktari H, Xenophontos S L, Manoli P, Cariolou M |
Evidence for substantial effect modification by gender in a large-scale genetic association study of the metabolic syndrome among coronary heart disease patients. Human genetics 2003 Dec 114 (1): 87-98. McCarthy Jeanette J, Meyer Joanne, Moliterno David J, Newby L Kristin, Rogers William J, Topol Eric J, |
Maternal apo E genotype is a modifier of the Smith-Lemli-Opitz syndrome. Journal of medical genetics 2004 Aug 41 (8): 577-84. Witsch-Baumgartner M, Gruber M, Kraft H G, Rossi M, Clayton P, Giros M, Haas D, Kelley R I, Krajewska-Walasek M, Utermann |
Genetic risk for metabolic syndrome: examination of candidate gene polymorphisms related to lipid metabolism in Japanese people. Journal of medical genetics 2008 Jan 45 (1): 22-8. Yamada Y, Ichihara S, Kato K, Yoshida T, Yokoi K, Matsuo H, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Yasunaga A, Park H, Tanaka M, Lee W, Nozawa |
Spectrum of LDLR gene mutations, including a novel mutation causing familial hypercholesterolaemia, in North-western Greece. European journal of internal medicine 2011 Oct 22 (5): e55-9. Diakou Maria, Miltiadous George, Xenophontos Stavroulla L, Manoli Panayiotis, Cariolou Marios A, Elisaf Mos |
Molecular basis of autosomal dominant hypercholesterolemia: assessment in a large cohort of hypercholesterolemic children. Circulation 2011 Mar 123 (11): 1167-73. van der Graaf Anouk, Avis Hans J, Kusters D Meeike, Vissers Maud N, Hutten Barbara A, Defesche Joep C, Huijgen Roeland, Fouchier Sigrid W, Wijburg Frits A, Kastelein John J P, Wiegman Albe |
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 |
Association between Pro12Ala, Pvull, Avall, Sstl and ADIPOQ single-nucleotide polymorphisms with lipid and glycemic profiles of patients with Berardinelli-Seip syndrome. Annals of nutrition & metabolism 2014 65 (4): 272-9. Baracho Maria F P, Nunes Adriana B, Hirata Mario H, Hirata Rosario D C, Fajardo Christina M, Santos Maria G N, Wajchenberg Bernardo L, De Marco Luiz A, Brandão-Neto Jo |
LDLR, ApoB and ApoE genes polymorphisms and classical risk factors in premature coronary artery disease. Gene 2016 May . Abd El-Aziz Tarek A, Mohamed Randa |
Genetically Confirmed Familial Hypercholesterolemia in Patients With Acute Coronary Syndrome. Journal of the American College of Cardiology 2017 Oct 70 (14): 1732-1740. Amor-Salamanca Almudena, Castillo Sergio, Gonzalez-Vioque Emiliano, Dominguez Fernando, Quintana Lucía, Lluís-Ganella Carla, Escudier Juan Manuel, Ortega Javier, Lara-Pezzi Enrique, Alonso-Pulpon Luis, Garcia-Pavia Pab |
Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib.
PloS one 2017 12 (7): e0182115. Yeo Astrid, Li Li, Warren Liling, Aponte Jennifer, Fraser Dana, King Karen, Johansson Kelley, Barnes Allison, MacPhee Colin, Davies Richard, Chissoe Stephanie, Tarka Elizabeth, O'Donoghue Michelle L, White Harvey D, Wallentin Lars, Waterworth Da |
The c.*52 A/G and c.*773 A/G Genetic Variants in the UTR'3 of the LDLR Gene Are Associated with the Risk of Acute Coronary Syndrome and Lower Plasma HDL-Cholesterol Concentration. Biomolecules 2020 10 10 (10): . Vargas-Alarcon Gilberto, Perez-Mendez Oscar, Ramirez-Bello Julian, Posadas-Sanchez Rosalinda, Gonzalez-Pacheco Hector, Escobedo Galileo, Nieto-Lima Betzabe, Carreon-Torres Elizabeth, Fragoso Jose Manu |
Familial Hypercholesterolemia in Patients with Acute Coronary Syndrome: Genetic Insights from EXPLORE-J. Journal of atherosclerosis and thrombosis 2021 9 29 (8): 1201-1212. Harada-Shiba Mariko, Ako Junya, Hirayama Atsushi, Nakamura Masato, Nohara Atsushi, Sato Kayoko, Murakami Yoshitaka, Koshida Ryusuke, Ozaki Asuka, Arai Hideno |
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 |
Genetic Determinants of Selenium Availability, Selenium-Response, and Risk of Polycystic Ovary Syndrome. Biological trace element research 2024 1 . Priya Sharma, Preeti Khetarp |
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- Page last updated:Apr 22, 2024
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