The impact of low-frequency and rare variants on lipid levels.
about
Susceptibility of Different Mouse Wild Type Strains to Develop Diet-Induced NAFLD/AFLD-Associated Liver DiseaseMeta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levelsAssociation analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels.Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study.FINEMAP: efficient variable selection using summary data from genome-wide association studies.The impact of rare and low-frequency genetic variants in common diseaseGenome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.Identification of eight genetic variants as novel determinants of dyslipidemia in Japanese by exome-wide association studies.Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.A Protein Domain and Family Based Approach to Rare Variant Association AnalysisThe Contribution of GWAS Loci in Familial Dyslipidemias.Genomic approaches for understanding the genetics of complex disease.SCOPA and META-SCOPA: software for the analysis and aggregation of genome-wide association studies of multiple correlated phenotypes.MARV: a tool for genome-wide multi-phenotype analysis of rare variants.Admixture mapping in two Mexican samples identifies significant associations of locus ancestry with triglyceride levels in the BUD13/ZNF259/APOA5 region and fine mapping points to rs964184 as the main driver of the association signal.A rare-variant test for high-dimensional data.Resequencing of the CETP gene in American whites and African blacks: Association of rare and common variants with HDL-cholesterol levelsRole of TM6SF2 rs58542926 in the pathogenesis of nonalcoholic pediatric fatty liver disease: A multiethnic studyGenome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA.What can we learn about lipoprotein metabolism and coronary heart disease from studying rare variants?Minireview: Genome Editing of Human Pluripotent Stem Cells for Modeling Metabolic Disease.metaCCA: summary statistics-based multivariate meta-analysis of genome-wide association studies using canonical correlation analysisNext-generation sequencing-based molecular diagnosis of neonatal hypotonia in Chinese PopulationDiscovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.Regional heritability mapping method helps explain missing heritability of blood lipid traits in isolated populations.Recent Progress in the Understanding of Obesity: Contributions of Genome-Wide Association Studies.Genetic association studies in cardiovascular diseases: Do we have enough power?Genetics of Gestational Diabetes Mellitus and Maternal Metabolism.Human genetic insights into lipoproteins and risk of cardiometabolic disease.A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoforms.Genome-Wide Studies of Type 2 Diabetes and Lipid Traits in Hispanics.Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation.Hepatic Tm6sf2 overexpression affects cellular ApoB-trafficking, plasma lipid levels, hepatic steatosis and atherosclerosis.Comprehensive genotyping in dyslipidemia: mendelian dyslipidemias caused by rare variants and Mendelian randomization studies using common variants.Coding-sequence variants are associated with blood lipid levels in 14,473 Chinese.Blood triglyceride levels are associated with DNA methylation at the serine metabolism gene PHGDH.Analysis with the exome array identifies multiple new independent variants in lipid lociClinical Perspectives of Genetic Analyses on Dyslipidemia and Coronary Artery Disease.Prospects of Fine-Mapping Trait-Associated Genomic Regions by Using Summary Statistics from Genome-wide Association Studies.Exome-wide association study of plasma lipids in >300,000 individuals.
P2860
Q28551941-D5F64022-5673-4216-9135-341B3E797D17Q28596453-5F4A2C24-343B-4C8E-B25B-14D4C8D39325Q30252887-A0FE49A3-8538-4C93-A65C-CEAF8E6E2F4AQ30490746-2BE70361-4C59-4B94-B3B2-91B5E6E7FC1CQ31037165-709DABD6-FF5F-4F10-941E-B96618E5FDE5Q33613854-D9A90C4A-08DD-416B-B5CA-F62D563079A6Q33675161-7C7D4200-91DE-4822-9BBB-9621BA9062B7Q33889023-899A9174-80FC-41D9-B33E-2E5AA518A963Q34682478-23BA954D-FC9F-4758-8720-257CB13A42DEQ36003130-34815BD0-174A-4497-AD45-652978C45715Q36030162-FD13F955-9C0E-4C9F-9AED-C76F86105F92Q36084287-2928A3CA-7528-47F9-A9FD-792AD9010962Q36246589-E9A8FE49-34CF-4D04-BEF1-41D59555C26AQ36283337-AD08771D-1AF0-4FBB-ABD3-2A728CCD3FD1Q36292894-7C544B67-2642-4358-88C1-014EDA462E88Q36379034-D6F9EFA6-00EF-4E06-B171-CCEA9D4E703EQ36386737-D214F12B-78CF-4C55-A305-2917C4735470Q36396108-314D4A6A-F13F-4A12-BA90-5C4FF0696926Q36747275-D2307FA5-5818-458C-B289-CD5A04BF941BQ36760799-115BEFF3-8D5D-4CB7-90C3-A876FC4F7A1CQ36945218-9C39AFEF-A884-453B-A176-3BEA054B6E27Q37036051-655F8706-6E0B-4A11-8DF3-D2AFCD712C8EQ37050173-02F4D30E-AB04-4AC3-A404-F49F171B0659Q37613798-0E3F54F1-C3D0-4E5B-9110-47AC06986F15Q38382817-C7034625-FD13-4142-B3CD-9559616C1EEFQ38587726-8D58CB40-E3EA-4F94-A95F-C3CB676A2479Q38689422-62D79295-0E3A-4585-83FE-81F12D2B4E46Q38709349-BFBF22C9-F6F7-40D2-A6C8-5CEE58215827Q38774074-11D8F21A-CA2D-4678-8390-B7ABCF093169Q38781922-42FD2FE4-E1E1-4F41-9B18-163FB6E28150Q38786129-DD12A140-1723-4855-99C2-F8EA47205A49Q38803986-A9FBF499-EA16-4B9B-84CC-249DFCFB67DDQ38816682-56242FEC-6AE8-4B61-B394-9FA2626962B2Q39068223-601BBD46-407D-47FC-85B6-2F13A8C443FDQ39497026-3CDEAE46-520F-40D3-A4E5-A02DD8876665Q40046496-367F768B-A942-4460-BDB4-3C1F4EE5FD71Q41731666-55A674B2-9C01-4F51-8A4E-6ECE2107542FQ42244280-02E1BB6B-4905-4818-BBAB-C7444B296D1DQ42692681-A5202D06-798F-4CC6-A847-C311DA90A3F3Q45071322-9CF1C46B-0DDE-4EBA-A5B3-4702AF6779B2
P2860
The impact of low-frequency and rare variants on lipid levels.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
The impact of low-frequency and rare variants on lipid levels.
@ast
The impact of low-frequency and rare variants on lipid levels.
@en
type
label
The impact of low-frequency and rare variants on lipid levels.
@ast
The impact of low-frequency and rare variants on lipid levels.
@en
prefLabel
The impact of low-frequency and rare variants on lipid levels.
@ast
The impact of low-frequency and rare variants on lipid levels.
@en
P2093
P2860
P50
P356
P1433
P1476
The impact of low-frequency and rare variants on lipid levels.
@en
P2093
Aaron Isaacs
Andrew P Morris
Anton J M de Craen
Antti-Pekka Sarin
Benjamin Miraglio
Brenda W J H Penninx
Christian Hengstenberg
Christina Willenborg
Christine Power
Claes Ladenvall
P2860
P2888
P304
P356
10.1038/NG.3300
P407
P50
P577
2015-05-11T00:00:00Z