Ten Years of Hereditary Alpha-Tryptasemia: The Common Gene Variant Reshaping Anaphylaxis Care
A decade after its discovery, hereditary alpha-tryptasemia is recognized as the leading cause of elevated basal serum tryptase and an ...
A decade after its discovery, hereditary alpha-tryptasemia is recognized as the leading cause of elevated basal serum tryptase and an ...
A Mendelian randomization study links diuretic use to lower bipolar disorder risk and identifies the ADO gene as a potential ...
A large genetically informed analysis of nearly a million people finds that genetic liability to childhood maltreatment is linked to ...
A new Pediatric Research reflection by Alex Smith traces nearly twenty years of living alongside his son Harrison's Duchenne muscular ...
A landmark analysis of over 51,000 brain scans reveals that problematic substance use is linked to distinct, age-specific brain structural ...
A hybrid long-read and short-read sequencing study has identified a common CCG repeat in the FAM193B promoter as a genome-wide ...
A large genome-wide meta-analysis shows that the genetic architecture of social behaviour in humans varies systematically with behavioural domain, reporter, ...
A UK Biobank study of 46,843 people shows that genetic risk and lifestyle jointly drive MRI-based brain aging, with a ...
Research into naturally parasite-resistant St. Croix sheep is revealing how an early Th2 immune response blocks the deadly blood-feeding worm ...
Researchers at Baylor College of Medicine identified MECP2 regulatory variants on the X chromosome that may help explain why autism ...
© 2025 Scienmag - Science Magazine
© 2025 Scienmag - Science Magazine