Some doctors told him he'd live with the disease forever, but Khaled Alsheebani never stopped believing treatments would advance one day.

BEAM-101, a genetically modified cell therapy for sickle cell, is designed to turn on HbF to counteract mutated adult ...

India faces a critical shortage of 41 million blood units annually. Doctors stress that the country needs lifelong donors for ...

In a world often divided by politics, borders and beliefs, this is one thing that unites us all. The same blood that flows ...

A team led by Rutgers University-New Brunswick engineers has developed a portable device capable of detecting rare genetic ...

A new portable device developed by Rutgers University researchers can detect genetic mutations linked to hereditary ...

Professor Vijay Chandru shares his storied career in academia and entrepreneurship, how to balance both sides of the AI coin, ...

Genes don’t cause epidemics. You need an environmental toxin,” Kennedy said in April when announcing his department’s new ...

Victoria Gray, the first person cured of sickle cell using CRISPR gene editing therapies, spoke in Fargo about her journey and the need to lower the $2M treatment cost.

Without the Sickle Cell Data Collection program, we will see greater burdens and higher costs for both families and health ...