This study provides a valuable new resource to investigate the molecular basis of the particular features characterizing the pipefish embryo. The authors found both unique and shared gene expression ...

Established in October 2024 and the largest of its kind in South-east Asia, the Ocular Genetics Service (OGS) provides a centralised and specialised approach to diagnosing and managing inherited ...

Nearly 300 new genetic variants have been linked to depression, according to a new study that included a large sample of nearly 5 million people. The international team, led by researchers at the ...

Polygenic scores (PGS) are metrics used to estimate the genetic predisposition of people to developing specific mental health conditions, personality traits or diseases. In recent years ...

For 30 years, researchers have known that Huntington's is caused by an inherited mutation in the Huntingtin (HTT) gene, but they didn't know how the mutation causes brain cell death. A study ...

In addition to opening a new window into how human genetic mutations can operate, the researchers hope that their insights lead to new strategies that improve or ultimately save the lives of people ...

Whole genome sequencing, which is also being used widely to improve treatments of difficult-to-diagnose diseases as well as for genetic screening of newborns, has given hope to patients with ...

Get Instant Summarized Text (Gist) The study identifies 106 genetic variants linked to occupational status, highlighting the interplay between genetics, family environment, and childhood ...

Scientists have found 697 genetic variants – or small changes within a gene – linked to depression, of which almost 300 were previously unknown. A Queensland scientist described the project as ...

A package for binary and continuous, single and multi-material, truss and continuum, 2D and 3D topology optimization on unstructured meshes using automatic differentiation in Julia.