University of Geneva

Researchers identified somatic KRAS mutations in affected tissue from more than 60 percent of people with sporadic arteriovenous malformations of the brain.

HUG's genetic medicine arm will use Saphetor's software and variant knowledgebase in clinical projects focused on developmental and neurological disorders.

An international team has uncovered roles for MYCN, PTPN14, and LATS1 mutations in the development and progression of skin basal cell carcinoma.

NEW YORK (GenomeWeb News) – Widespread genetic variation affects the regulation of most human genes, according to a study of functional variation appearing in the online early edition of Nat

The University of Geneva, Geneva University Hospitals, and the SIB Swiss Institute of Bioinformatics are partnering with Roche in a deal initially be directed at basic research, bioinformatics, and biomarker development.

AB Sciex plans to introduce later this year a new mass spec platform that combines qualitative and quantitative analysis.

Using SNP and expression microarrays, a team of researchers from Switzerland, the UK, and the US has uncovered cell type-specific differences in regulatory variant function within three different human cell types.

CNN reports that researchers have tied a new variant to opioid addiction risk.

Organoids derived from patients' tumors may help determine what chemotherapy treatment patients would benefit from, according to New Scientist.

An initiative from GenomeAsia 100K hopes to increase the number of South Asians in genetic research, according to NBC News.

In Science this week: genomic analysis of ancient and modern horses indicates population turnover, and more.