Pages that link to "Q36852391"

The following pages link to Copy number variation in the human genome and its implications for cardiovascular disease (Q36852391):

Displaying 32 items.

• Cellular hyperproliferation and cancer as evolutionary variables (Q27008923) (← links)
• Genetics of type 2 diabetes: pathophysiologic and clinical relevance (Q28302158) (← links)
• Genomic structural variations for cardiovascular and metabolic comorbidity (Q29248536) (← links)
• The variation game: Cracking complex genetic disorders with NGS and omics data (Q30945159) (← links)
• Computing power and sample size for case-control association studies with copy number polymorphism: application of mixture-based likelihood ratio test (Q33378466) (← links)
• Genetics and cardiovascular disease: Design and development of a DNA biobank. (Q33595709) (← links)
• Early identification of cardiovascular risk using genomics and proteomics (Q34129889) (← links)
• Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1. (Q34649789) (← links)
• Genetic Polymorphisms and Peritoneal Membrane Function (Q35419909) (← links)
• Variation in inflammation-related genes and risk of incident nonfatal myocardial infarction or ischemic stroke (Q36839359) (← links)
• The pressure of finding human hypertension genes: new tools, old dilemmas (Q37218698) (← links)
• Genome-wide association studies for atherosclerotic vascular disease and its risk factors (Q37339440) (← links)
• A common copy number variation on chromosome 6 association with the gene expression level of endothelin 1 in transformed B lymphocytes from three racial groups (Q37467116) (← links)
• The relationship between apolipoprotein E epsilon2/epsilon3/epsilon4 polymorphisms and hypertension: a meta-analysis of six studies comprising 1812 cases and 1762 controls (Q37611590) (← links)
• Predictive genetic testing for coronary artery disease (Q37643740) (← links)
• Cardiovascular genetic medicine: evolving concepts, rationale, and implementation. (Q37766139) (← links)
• The genome-wide association study--a new era for common polygenic disorders (Q37766201) (← links)
• Translating genomic analyses into improved management of coronary artery disease (Q37770573) (← links)
• Implications of gene copy-number variation in health and diseases. (Q37940158) (← links)
• Optimal Sparse Segment Identification with Application in Copy Number Variation Analysis (Q39384168) (← links)
• The utility of copy number variation (CNV) in studies of hypertension-related left ventricular hypertrophy (LVH): rationale, potential and challenges (Q41048467) (← links)
• Whole genome survey of copy number variation in the spontaneously hypertensive rat: relationship to quantitative trait loci, gene expression, and blood pressure (Q42227754) (← links)
• How Sensitive Is Genetic Data? (Q42688725) (← links)
• Use of next-generation sequencing to detect LDLR gene copy number variation in familial hypercholesterolemia (Q42993804) (← links)
• A genome-wide characterization of copy number variations in native populations of Peninsular Malaysia. (Q52687665) (← links)
• Identification of Copy Number Variations in Isolated Tetralogy of Fallot. (Q53480838) (← links)
• Analyses of copy number variation reveal putative susceptibility loci in MTX-induced mouse neural tube defects. (Q54223393) (← links)
• Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease (Q57828177) (← links)
• Perspective: DNA Copy Number Variations in Cardiovascular Diseases (Q60045435) (← links)
• Genetic Variations and Precision Medicine (Q64096804) (← links)
• GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death (Q97522251) (← links)
• Genetics of Hypertriglyceridemia (Q98465402) (← links)