Telomere length and polygenic risk scores (PRS) are linked to idiopathic pulmonary fibrosis (IPF) risk, especially in noncarriers of rare genetic variants. The study identified rare damaging variants ...

Dr. Rebecca Ahrens-Nicklas and Dr. Kiran Musunru crafted a bespoke treatment that has successfully corrected the genetic defect.

New York Magazine published a profile in which multiple former Mace staffers alleged late-night alcohol requests and personal ...

While the leading cause of kidney disease is diabetes, many other factors can lead to kidney disease and failure - including a collection of rare and genetic conditions. According to the National ...

A large global genetics study shows that many key drivers of Type 2 diabetes operate outside the bloodstream. Scientists are ...

The DGIST Center for Synapse Diversity and Specificity has identified MDGA2 as a novel causative gene for developmental and epileptic encephalopathy (DEE), a rare and intractable neurological disorder ...

Explore the Q4 2025 Alger Weatherbie Specialized Growth Fund performance. Read about the top contributors and detractors in ...

The agreement grants MeiraGTx exclusive rights to ZipBio’s first-in-class therapies targeting the complement pathway for Geographic Atrophy, a progressive eye disease with significant unmet medical ...

Huntington’s disease is a rare inherited neurological disorder that progressively affects movement, cognition and mental health due to a genetic mutation ...

"I got a double dose of the Celtic Curse," said Campbell. She has suffered fatigue and muscle pain since childhood but specialists were unable to identify the cause. "I got used to living with pain, ...

People from the Outer Hebrides and north-west Ireland have the highest risk of developing a genetic disease that causes a dangerous build-up of iron in the body, a study suggests.

While the kidneys are mostly affected, advanced or severe hyperoxaluria can affect multiple organ systems due to the ...