Single-cell profiling of nearly 2,000 people brings scientists closer to understanding the link between genetic variation, ...

Alpha-1 antitrypsin deficiency (AATM) is a congenital metabolic disorder. It is caused by a genetic defect, which results in ...

Gallstone disease is common, but its genetic basis remains incompletely understood. Here, the authors conduct a ...

My parent has dementia, so will I eventually get it too?”I sometimes hear such concerns.Certainly, genetic factors are ...

Genetic analysis of nearly 50,000 people identified carriers of sickle cell and beta-thalassemia traits, many of whom lacked ...

Setara brings together an experienced team and a proven genetics-driven approach to design and development of small molecule ...

Opus Genetics is a clinical-stage biopharmaceutical company developing gene therapies to restore vision and prevent blindness in patients with inherited retinal diseases (IRDs). The Company is ...

Have you ever seen the item "PLT" on a health checkup or hospital blood test?PLT stands for Platelet, a component of blood involved in stopping bleeding.If your test results indicate that your ...

In three studies published in Nature today, Australian researchers have made advances in our understanding of how genetic ...

A new biotech born from Jazz Pharmaceuticals' acquisition deal is betting that rare disease genetics can unlock treatments ...

AIIMS Delhi and five national medical centres have launched a four-year, ICMR-funded study to investigate why autoimmune ...

Whole-genome embryo screening is expanding what prospective parents can learn during IVF. Instead of checking only chromosome ...