Hypertriglyceridemia, a commonly encountered phenotype in cardiovascular and metabolic
clinics, is surprisingly complex. A range of genetic variants, from single-nucleotide variants …

Combined hyperlipidemia: familial but not (usually) monogeni... : Current Opinion in Lipidology
Combined hyperlipidemia: familial but not (usually) monogenic : Current Opinion in Lipidology …

Background—Epigenetic alterations may contribute to the development of atherosclerosis.
In particular, DNA methylation, a reversible and highly regulated DNA modification, could …

MicroRNAs (miRNAs) are strongly up‐regulated under pathological stress and in a wide
range of diseases. In recent years, miRNAs are under investigation for their potential use as …

Genome-wide association studies (GWAS) are a powerful tool for investigators to examine
the human genome to detect genetic risk factors, reveal the genetic architecture of diseases …

There is a growing literature on the impact of genetic variation on outcome in traumatic brain
injury (TBI). Whereas a substantial proportion of these publications have focused on the …

Biomarkers, quantitatively measurable indicators of biological or pathogenic processes,
once validated play a critical role in disease diagnostics, the prediction of disease …

This study aims to demonstrate that the application of miRNA expression in forensic
pathology, in cases of hanging, applying the method on skin samples. The proposed …

MicroRNAs (miRNAs) are a class of short non-coding regulatory RNA molecules which play
an important role in intracellular communication and cell signaling and which influence …

Omics is a form of high-throughput systems science. However, taxonomies for omics studies
are limited, inviting us to rethink new ways in which we classify, prioritize, and rank various …