Background Amyloid transthyretin (ATTR) amyloidosis is a rare, life-threatening disease frequently manifesting with ...

Mount Sinai scientists developed V2P, a powerful new AI tool that predicts how specific DNA mutations translate into disease, unlocking faster diagnoses and new targets for therapy.

Down syndrome (DS) is one of the most frequent congenital birth defects, and the most common genetic cause of mental retardation; it presents with a complex clinical spectrum of variable features ...

Any organism is a by-product of both its genetic makeup and the environment. To understand this in detail, we must first appreciate some basic genetic vocabulary and concepts. Here, we provide ...

Obesity is not a single disease. New research shows distinct biological phenotypes that explain why weight gain and treatment ...

Researchers have uncovered novel insights into how brain function disruptions related to cerebrovascular disease (CeVD) ...

Northwestern University biophysicists have developed a new computational tool for identifying gene combinations underlying complex illnesses such as diabetes, cancer, and asthma. Unlike single-gene ...

The Food and Drug Administration (FDA) has approved Exdensur (depemokimab-ulaa), an interleukin-5 antagonist, for add-on maintenance treatment of severe asthma characterized by an eosinophilic ...

Genotype-phenotype models (GPM) of crops represent a significant advancement in understanding the intricate relationship between genetic information and physiological processes in plants. These models ...