Scientists at the Icahn School of Medicine at Mount Sinai have developed a novel artificial intelligence tool that not only ...

A mysterious genetic disease wiped out generations of one family before science uncovered its cause. This talk reveals how a ...

Scientists discovered that certain gene changes allow cells to function even when frataxin, the protein lost in Friedreich’s ...

Scientists at the Icahn School of Medicine at Mount Sinai have developed a novel artificial intelligence tool that not only identifies disease-causing genetic mutations but also predicts the type of ...

There is no cure for the rare disease Hereditary Spastic Paraplegia (HSP), but researchers from Drexel University’s College ...

With a rate of mutation 35 percent higher than random chance, this previously unknown weakness could be a major vector for ...

Their data suggests that tweaking the expression of FDX2 could make up for the loss of frataxin, the protein tied to FA's development.

A sperm donor with a rare genetic mutation linked to an increased risk of developing cancer fathered at least 197 children across Europe, some of whom have already died from the disease, according to ...

Childhood psychosis risk appears to increase significantly among carriers of this gene variant. In A Nutshell First ...

Mount Sinai scientists developed V2P, a powerful new AI tool that predicts how specific DNA mutations translate into disease, ...

When Meenu Hodiwalla gave birth to her son almost three decades ago, she imagined the early days unfolding like they do for most new parents - tiny fingers curling around hers, the baby's eyes ...

European fertility clinics used cancer-causing sperm for 17 years, prompting urgent calls for genetic screening reforms and ...