Researchers discover genetic cause of hearing loss and identify possible treatments
Researchers have understood for decades that some forms of deafness are inherited, yet until now, few of those…
Researchers develop new platform to expand genetic diversity in cannabis
Researchers at CRAG, in collaboration with the John Innes Centre (UK) and the company Front Range Biosciences…
TropiCODB: A Multi-Omics Database Unlocking the Genetic Potential of Tropical Crops
Newswise — By integrating genomic, transcriptomic, metabolomic, variomic, and phenotypic datasets for eight major crops—including cassava, sugarcane, and…
Epigenetic scars: Unveiling How Childhood Trauma Affects Our Genes
Child maltreatment, which includes abuse and neglect, is one of the most serious public health concerns worldwide. These…
High-proof alcohol preserved century-old fish DNA to enable ‘genomic time travel’
Key takeaways Fish specimens collected during a 1907–1910 U.S. expedition to the Philippines were stored in high-proof sugarcane…
How Genetics and Diet Helped the World’s Oldest Woman Live to 117
October 1, 2025 3 min read How the World’s Oldest Woman Lived to 117 Maria Branyas Morera was…
Family history, genetic testing important factors
Who: Brenda Broughton, of rural Cassville What: Infiltrating ductal carcinoma More: No chemo, no radiation Broughton: ‘Even my…
Precise gene editing technique changes one DNA base to correct heart disease
Researchers used a technique called base editing to correct a mutation in the lamin A gene. At 8…
“Google for DNA”: Scientists create the world’s first and fastest genetic search engine |
A team of researchers at ETH Zurich has developed MetaGraph, a groundbreaking tool that allows scientists to search…
MADS-Box Gene Family Discovered in Lavender Species
In an exciting development within the field of genomics, researchers have turned their attention to the MADS-box gene…
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…
NHS to screen newborns in England for rare genetic disorder
Hereditary tyrosinaemia type 1 (HT1) affects around seven babies a year in the UK. It prevents the normal…