Introduction Inherited cardiac conditions, including dilated cardiomyopathy (DCM) and hypertrophic cardiomyopathy (HCM), may ...

As genetic sequencing technology becomes more accessible and efficient, researchers have made significant strides in understanding the genetic underpinnings of various diseases. This knowledge has led ...

Genetic variants that cause rare disorders may remain elusive even after expansive testing, such as exome sequencing. The diagnostic yield of genome sequencing, particularly after a negative ...

VIENNA — Advances in genetic testing and newly discovered biomarkers can help screen newborns and monitor inflammation and pulmonary exacerbations in patients diagnosed with cystic fibrosis. At the ...

Mystery infections—persistent and unexplained illnesses—are a rising global health challenge, often delaying critical treatment as patients and clinicians search for answers. Today, advanced genetic ...

A new consensus statement recommended genetic testing for all categories of kidney diseases whenever a genetic cause is suspected and offered guidance on who to test, which tests are the most useful, ...

When the Human Genome Project concluded 21 years ago, it opened the door for genetic testing and a promise for lifesaving screenings and personalized medicine. An innovation that serves as a key ...

Genetic testing analyzes a person's DNA to determine their risk for certain diseases. It was a game-changer for one Montgomery County woman. Genetic testing is a simple mouth swab that can uncover ...

The treatment of clinical depression presents unique challenges, with many patients voicing concerns that echo a disheartening struggle: "I have tried every medication for depression, and nothing ...

Researchers have discovered 195 genomic regions jointly associated with schizophrenia and osteoporosis-related traits, mapping to 1376 protein-coding genes involved in metabolism and anatomical ...