Ancient lead exposure may have shaped human evolution and language
A groundbreaking international study changes the view that exposure to the toxic metal lead is largely a post-industrial…
Child maltreatment leaves measurable biological scars on children’s DNA
Child maltreatment, which includes abuse and neglect, is one of the most serious public health concerns worldwide. These…
Pioneering personalized medicine by deciphering depression’s complex biological web
In a compelling Genomic Press Interview published today in Genomic Psychiatry, Dr. Najaf Amin unveils transformative insights that…
Purespring Therapeutics to Present at Chardan’s 9th Annual Genetic Medicines Conference
Purespring Therapeutics to Present at Chardan’s 9th Annual Genetic Medicines Conference London – 14 October 2025 – Purespring…
500 babies now recruited to world-leading genetic study
500 babies now recruited to world-leading genetic study
Over 500 babies…
How genomic screening in newborns found 16 hidden disorders standard tests overlooked
By uncovering life-altering genetic conditions before symptoms appear, genomic screening could redefine newborn care if health systems can…
New method can create reliable growth charts for children with rare genetic disorders
Growth charts for children with rare genetic disorders – giving healthcare professionals and families clearer guidance on how…
Microbial genetic variation shapes neurocognitive behavior in sheep
The researchers used Merino sheep as an animal model, systematically collecting samples of their hindgut and ruminal microbiota,…
Living near Superfund sites increases risk of aggressive breast cancer
Women living close to federally designated Superfund sites are more likely to develop aggressive breast cancers – including…
Lifestyle choices and hormonal imbalances can impact men’s reproductive health
A new research paper was published in Volume 12 of Oncoscience on September 30, 2025, titled “Lifestyle and hormonal factors affecting…
Genetic study reveals unique mutations in Chinese patients with hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy (HCM), a common genetic heart disorder, is often caused by mutations in sarcomere-related genes. While extensively…
Evolutionary mutation in cGAS enhances naked mole-rat DNA repair
The secret to the naked mole-rats’ extraordinarily long life may lie in subtle changes to just four amino…