Researchers from Children's Hospital of Philadelphia (CHOP) have identified a causal genetic variant strongly associated with ...

The variant occurs on the fibronectin 1 (FN1) gene, which expresses fibronectin, an adhesive glycoprotein that lines the ...

In the past, research had focused on a single gene or variant. However, combining high-throughput DNA sequencing methods ...

A random-forest, machine-learning classifier, artificial intelligence-Model organism Aggregated Resources for Rare Variant ...

Researchers at Columbia University have identified a genetic variant that may lower the risk of Alzheimer's disease by as ...

A genetic change or variant in a gene called SCN2A is a known cause of infantile seizures, autism spectrum disorder, and ...

AIM is a machine-learning classifier that combines over 3.5 million variations from thousands of identified cases and ...

The BEQVEZ gene therapy inserts a working copy of the Factor IX (FIX) gene that codes for a high-activity FIX variant.

Results showed a reduction in annualized bleeding rate after a single infusion of fidanacogene elaparvovec compared with ...

The allele associated with obesity risk influenced how the FAIM2 gene was expressed and decreased the proportion of neurons produced when the stem cells differentiated, suggesting that the variant is ...

Pfizer Inc. (NYSE: PFE) announced today that the U.S. Food and Drug Administration (FDA) has approved BEQVEZ™ (fidanacogene ...