Pages that link to "Q24598765"
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The following pages link to Common variants at 30 loci contribute to polygenic dyslipidemia (Q24598765):
Displaying 50 items.
- Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution (Q21092459) (← links)
- Differential binding and co-binding pattern of FOXA1 and FOXA3 and their relation to H3K4me3 in HepG2 cells revealed by ChIP-seq (Q21092861) (← links)
- Non-cholesterol sterol levels predict hyperglycemia and conversion to type 2 diabetes in Finnish men (Q21133002) (← links)
- Genome-wide association of lipid-lowering response to statins in combined study populations (Q21142620) (← links)
- Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis (Q21144992) (← links)
- A genome-wide association study of the metabolic syndrome in Indian Asian men (Q21562180) (← links)
- Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits (Q21563350) (← links)
- RNAi-based functional profiling of loci from blood lipid genome-wide association studies identifies genes with cholesterol-regulatory function (Q21563361) (← links)
- Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability (Q21563383) (← links)
- The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease (Q21819337) (← links)
- Genetic diagnosis by whole exome capture and massively parallel DNA sequencing (Q22066282) (← links)
- Finding the missing heritability of complex diseases (Q22122198) (← links)
- Complex Diseases, Complex Genes (Q24289171) (← links)
- TM6SF2 is a regulator of liver fat metabolism influencing triglyceride secretion and hepatic lipid droplet content (Q24299190) (← links)
- Single nucleotide polymorphisms in the FADS gene cluster are associated with delta-5 and delta-6 desaturase activities estimated by serum fatty acid ratios (Q24609420) (← links)
- Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (Q24609915) (← links)
- Association between a literature-based genetic risk score and cardiovascular events in women (Q24613965) (← links)
- Triglycerides as vascular risk factors: new epidemiologic insights (Q24618902) (← links)
- Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration (Q24622351) (← links)
- Biological, clinical and population relevance of 95 loci for blood lipids (Q24622541) (← links)
- Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC) (Q24622766) (← links)
- Genome-wide association analysis identifies multiple loci related to resting heart rate (Q24624928) (← links)
- Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk (Q24631195) (← links)
- Allelic expression imbalance at high-density lipoprotein cholesterol locus MMAB-MVK (Q24631350) (← links)
- From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus (Q24633183) (← links)
- Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples (Q24642868) (← links)
- Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants (Q24645076) (← links)
- Novel variants at KCTD10, MVK, and MMAB genes interact with dietary carbohydrates to modulate HDL-cholesterol concentrations in the Genetics of Lipid Lowering Drugs and Diet Network Study (Q24650019) (← links)
- OSBPL10, a novel candidate gene for high triglyceride trait in dyslipidemic Finnish subjects, regulates cellular lipid metabolism (Q24650988) (← links)
- Genome-wide association study of biochemical traits in Korcula Island, Croatia (Q24655944) (← links)
- Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region (Q24657139) (← links)
- Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip (Q24657931) (← links)
- A description of large-scale metabolomics studies: increasing value by combining metabolomics with genome-wide SNP genotyping and transcriptional profiling (Q26849757) (← links)
- Low-density lipoprotein cholesterol, apolipoprotein B, and risk of coronary heart disease: from familial hyperlipidemia to genomics (Q26853114) (← links)
- The gut microbial endocrine organ: bacterially derived signals driving cardiometabolic diseases (Q27021692) (← links)
- Arguments for the sake of endophenotypes: examining common misconceptions about the use of endophenotypes in psychiatric genetics (Q27027555) (← links)
- Sortilin, encoded by the cardiovascular risk gene SORT1, and its suggested functions in cardiovascular disease (Q28257511) (← links)
- Angiopoietin-like 4: a decade of research (Q28263089) (← links)
- Sortilin as a regulator of lipoprotein metabolism (Q28265389) (← links)
- New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Q28270700) (← links)
- Hepatocyte Nuclear Factor 1A Is a Cell-Intrinsic Transcription Factor Required for B Cell Differentiation and Development in Mice (Q28272446) (← links)
- Genetics of type 2 diabetes: pathophysiologic and clinical relevance (Q28302158) (← links)
- Genetic variants associated with fasting blood lipids in the U.S. population: Third National Health and Nutrition Examination Survey (Q28395880) (← links)
- Genetic determinants of age-related macular degeneration in diverse populations from the PAGE study (Q28396822) (← links)
- Meta-analysis of inter-species liver co-expression networks elucidates traits associated with common human diseases (Q28472207) (← links)
- Transcriptional profiling of human liver identifies sex-biased genes associated with polygenic dyslipidemia and coronary artery disease (Q28476544) (← links)
- Hypercholesterolemia is associated with the apolipoprotein C-III (APOC3) genotype in children receiving HAART: an eight-year retrospective study (Q28481552) (← links)
- A replication study of GWAS-derived lipid genes in Asian Indians: the chromosomal region 11q23.3 harbors loci contributing to triglycerides (Q28483829) (← links)
- Variants identified in a GWAS meta-analysis for blood lipids are associated with the lipid response to fenofibrate (Q28484684) (← links)
- Elevated high-density lipoprotein cholesterol and age-related macular degeneration: the Alienor study (Q28540642) (← links)