New method speeds diagnosis of rare genetic disease
Peer-Reviewed Publication
Updates every hour. Last Updated: 14-Sep-2025 08:11 ET (14-Sep-2025 12:11 GMT/UTC)
A Columbia study addresses a key challenge in the diagnosis of rare genetic disorders.
A novel study aimed at disentangling the neurological underpinnings of depression shows that multiple brain profiles may manifest as the same clinical symptoms, providing evidence to support the presence of both one-to-one and many-to-one heterogeneity in depression. The findings of the study in Biological Psychiatry, published by Elsevier, highlight the layered and complex interactions between clinical symptoms and neurobiological sources of variation.
Using adult human cells to produce novel multicellular organisms, researchers find that the cells express both ancient genes, which are shared with our predecessors as far back as single celled organisms, and embryonic genes. They also reverse age-related modifications to DNA. The studies may lead to insights into regenerative medicine