Group of unique gene variants governing Estonians’ appetite | News
Researchers at the University of Tartu have uncovered new genetic links that help explain why some people gain…
Cancer hijacks embryonic gene editors to fuel growth
Cancer cells are known to reawaken embryonic genes to grow. A new study reveals the disease also hijacks…
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…
New insights can reshape psychiatric practice across continents
In a compelling Genomic Press Interview published today in Genomic Psychiatry, Dr. Bruce M. Cohen discusses results and…
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…
Human evolution and genes: culture rewrites science
For years, science was certain: genes determine who a person is. The latest report by American researchers overturns…
Fathers can pass on benefits of exercise to children, Chinese study suggests
Chinese scientists have found that the benefits of exercise can be inherited across generations, with a father’s level…
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…
Cleveland Clinic team uncovers genetic link to osteosarcoma
Researchers at Cleveland Clinic Children’s have helped identify a previously unknown gene that increases the risk of developing…
Newborn genomic screening may detect hundreds of additional childhood conditions
Adding genomic sequencing to newborn blood screening would detect hundreds of additional childhood conditions, providing much earlier diagnosis…