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Genetics news

Genetics

Scientists find the genetic clues that let humans walk on two legs

Two small changes in human DNA may have played a big role in helping our ancestors walk upright, researchers say.

Genetics

Common gene variant linked to higher heart disease risk in people with African ancestry

Dilated cardiomyopathy (DCM), a leading cause of heart failure, is twice as common in Black individuals as in white individuals. This excess risk is not fully explained by known risk factors such as high blood pressure or ...

Oncology & Cancer

Mutation yields hot new clues for treating immune 'cold' tumors

Immune checkpoint inhibitors (ICIs) emerged in the US about 15 years ago as an exciting class of cancer treatments that have achieved complete and durable remissions for thousands of people with end-stage metastatic cancers. ...

Genetics

Common genetic causes across motor neuron diseases identified

Motor neuron diseases, such as amyotrophic lateral sclerosis (ALS) and hereditary spastic paraplegia (HSP), share physical similarities but have been largely viewed as genetically distinct. However, an analysis led by investigators ...

Genetics

MAGIC: AI-assisted 'laser tag' illuminates cancer origins

The human body relies on precise genetic instructions to function, and cancer begins when these instructions get scrambled. When cells accumulate genetic errors over time, they can break free of the normal controls on their ...

Genetics

3D genome mapping tool reveals hidden complexity in DNA

Standard laboratory tests can fail to detect many disease-causing DNA changes. Now, a novel 3D chromosome mapping method can reliably reveal these hidden structural variants and lead to new discoveries.

Genetics

Previously unknown genetic cause of microcephaly identified

Microcephaly is a congenital malformation that leads to a significantly reduced brain size and is often accompanied by developmental delay. An international research team led by Dr. Tran Tuoc from the Department of Human ...

Genetics

An X chromosome switch offers hope for girls with Rett syndrome

Researchers led by UC Davis Health scientist Sanchita Bhatnagar have developed a promising gene therapy that could treat Rett syndrome. The therapy works on reactivating healthy but silent genes responsible for this rare ...

Genetics

Research identifies genetic predictor of weight loss with GLP-1RAs

A new study published by Cleveland Clinic researchers in Diabetes, Obesity and Metabolism investigating the genetic underpinnings of weight loss response has identified a gene, neurobeachin (NBEA), as a predictor of how individuals ...