Splicing

Les Turner Symposium on ALS brings researchers and clinicians to discuss new research findings

August 24, 2026

On the surface, amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD) and limbic-predominant age-related TDP-43 encephalopathy (LATE) might seem…

HHealth

'Resistin like molecule gamma' punches holes into heart cells after myocardial infarction

April 4, 2026

Myotonic dystrophy type 1 (DM1) is the most common cause of adult-onset muscular dystrophy, a genetic disorder that…

HHealth

Biallelic variants in RNU2-2 cause the most prevalent known recessive neurodevelopmental disorder

April 3, 2026

A major genetic study has uncovered a surprisingly common recessive cause of neurodevelopmental disorder, revealing how hidden changes…

HHealth

Enhanced Genomics extends Series A funding to USD $19 million to drive development of therapeutics pipeline

April 1, 2026

Hiroshima University researchers have developed a practical framework to identify candidate pathogenic variants hidden among the large number…

GGenetics

NYU Langone strengthens world-leading GI cancer program with renowned leaders

October 17, 2025

Cancer cells are known to reawaken embryonic genes to grow. A new study reveals the disease also hijacks…

SScience

Study: A genetic common factor underlying self-reported math ability and highest math class taken. Image Credit: Aree_S / Shutterstock

September 23, 2025

An exciting new study reveals the hidden genetic architecture of quantitative ability, showing how brain wiring and signaling…

Shared protein pathology redefines treatment for multiple neurodegenerative diseases

Toxic RNA drives progressive heart damage in myotonic dystrophy

Study identifies a common hidden genetic cause of neurodevelopmental disorder in children

Genomic study advances prioritization of variants in cancer diagnostics

Cancer hijacks embryonic gene editors to fuel growth

Scientists uncover 53 genetic clues that shape math ability beyond IQ