Genetics

Researchers used artificial intelligence to predict the activity of thousands of genes in tumors based on routinely collected images of tumor biopsies. It could guide treatment without costly genomic tests.

Tiny circles called ecDNA are critical in cancer development and drug resistance. An international Stanford Medicine-led team publishes landmark studies detailing new findings and potential therapies.

Stanford Medicine scientists and colleagues discover bacterial genes can encode multiple versions of themselves, altering a core understanding of genetics.

Cardiology and genetics expert Euan Ashley will become the new chair of Stanford Medicine’s Department of Medicine.

Genomics and technology development expert Lars Steinmetz now leads Stanford Medicine’s genetics department.

The professor of dermatology and genetics was honored with the 2024 Lurie Prize for his studies into the role of long noncoding RNA in health and disease.

In a finding that vastly expands the understanding of tumor evolution, researchers discover genetic biomarkers that can predict the breast cancer subtype a patient is likely to develop.

Researchers studied hundreds of Bengal cats to uncover the genetic origins of their leopard-like patterns and found that their appearance stems largely from domesticated cats.

Stanford Medicine researchers and their colleagues tracked the gut, mouth, nose and skin bacteria of 86 people for as long as six years to try to gauge what constitutes a healthy microbiome.

Research throws light on the mystery of why women are much more prone to autoimmune disorders: A molecule made by one X chromosome in every female cell can generate antibodies to a woman’s own tissues.

The team led by Stanford Medicine analyzed thousands of genomes, including those newly sequenced from 204 skeletons, to gain insight into how and where people moved during the Roman Empire.