Genetics
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Stanford Medicine scientists and colleagues discover bacterial genes can encode multiple versions of themselves, altering a core understanding of genetics.
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Ashley chair of Department of Medicine
Cardiology and genetics expert Euan Ashley will become the new chair of Stanford Medicine’s Department of Medicine.
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Lars Steinmetz new chair of genetics
Genomics and technology development expert Lars Steinmetz now leads Stanford Medicine’s genetics department.
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Howard Chang awarded Lurie Prize
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.
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Foretelling breast cancer
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.
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Bengal cat coats not so wild after all
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.
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Microbiomes are personal
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.
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Why women have higher autoimmunity risk
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.
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DNA shows Roman Empire migration
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.
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Tumor DNA levels in blood predict outcome
Circulating tumor DNA predicts recurrence and splits disease into two subgroups in Stanford Medicine-led study of Hodgkin lymphoma. New drug targets or changes in treatments may reduce toxicity.
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Role for ‘junk DNA’
Changes to short, repetitive sequences in the genome have been linked to diseases like autism and schizophrenia. New revelations about how such changes increase and decrease gene expression may provide insight into these and other disorders.
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