Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Hypercholesterolemia and CELSR2[original query] |
---|
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 |
Bidirectional causal relationship between hypercholesterolemia and ischemic heart disease: a Mendelian randomization study. Frontiers in cardiovascular medicine 2023 12 10 1302282. Ying Jiang, Wenpeng Yu, Jianliang Zhou, Xiao Do |
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, 2024
- Content source: