The recent bankruptcy of genetic testing firm 23andMe has raised alarms for privacy advocates and consumers worried about ...

Cleft lip and cleft palate are among the most common birth defects, occurring in about one in 1,050 births in the United ...

Researchers from Children's Hospital of Philadelphia (CHOP) and the Perelman School of Medicine at the University of ...

SARPLLM leverages large language modeling and quantum algorithms to predict Salmonella AMR, offering robust analysis and user ...

A new set of genes that contribute to Parkinson’s disease risk has been identified.

Certain common genetic changes might make some people with focal epilepsy less responsive to seizure medications, finds a new global study.

Rady study uses PacBio long-read sequencing for RFX3 variant in adolescent patient with autism, showcasing clinical genomics ...

Health Secretary Robert F. Kennedy Jr. said the agency will soon announce autism studies aimed at identifying “environmental ...

A scientific statement regarding direct-to-consumer genetic testing for cardiovascular disease has been published by the AHA.

Nongenetic factors and rare genetic variants were sources of variation that could influence the association between age at menarche and CAD.

Researchers from the Epilepsy Neurogenetics Initiative (ENGIN) at Children's Hospital of Philadelphia (CHOP) have completed a comprehensive natural history study of SCN8A-related disorders, which ...