Metabolic dysfunction-associated steatohepatitis (MASH) is a polygenic disorder influenced by multiple genes, but their specific roles in the progression of disease remain unknown. To address this gap ...

In a recent study published in the journal PLoS ONE, researchers investigated the effect of genetic variability based on accessory gene deletions on severe acute respiratory syndrome coronavirus 2 ...

LA JOLLA, CA—Genetic mutations kick start cancers. Some mutations shuffle the genetic code, others come from the deletion of key genes. At La Jolla Institute for Immunology (LJI), researchers have ...

Genetic mutations kick start cancers. Some mutations shuffle the genetic code, others come from the deletion of key genes. At La Jolla Institute for Immunology (LJI), researchers have made a major ...

Researchers have identified a promising strategy to improve memory and brain cell function in models of 22q11.2 Deletion Syndrome. The study, published in eLife, shows that reducing the levels of the ...

Patients with clinical features suggestive of either NS, NSML, CFC, NF1, Legius syndrome or Noonan-like syndrome; patients with a clinical diagnosis of any of these syndromes that previously tested ...

Researchers at Rutgers and Emory University have gained new insights into how schizophrenia (SCZ) develops, by studying 3q29 deletion syndrome, which represents the strongest-known genetic risk factor ...

Researcher discovers possible link of mitochondrial function to the development of schizophrenia. Researchers at Rutgers and Emory University are gaining insights into how schizophrenia develops by ...