- The map of this key organ of the digestive system analyses more than four million cells and cell nuclei from pancreatic tissue samples donated by 57 people, covering different stages of life, from fetal development to healthy adulthood, as well as type 2 diabetes (T2D).   - The single-cell...

- A new study, published in Human Mutation and led by Dr Pedro Rodríguez from CNAG, reports the first genetically confirmed cases of the rare disorder CAMRQ1 on the African continent. - Genetic analysis revealed a novel variant in the VLDLR gene, contributing to a better understanding of this...

- Helping researchers discover relevant clinical data across institutions using different data models can open new opportunities for collaboration in precision medicine. A CNAG-led study offers practical ways for IMPaCT-Data partners using OMOP to make their data discoverable to other partners too....

- An international study identifies a genetic variant at the SUSD1 locus associated with the risk of renal impairment in people with decompensated cirrhosis.   - More than 70 researchers, including scientists from CNAG, analysed genetic and clinical data from over 5,000 people of diverse...

A new role for Dr Holger Heyn, Single Cell Genomics Group Leader at CNAG and ICREA Research Professor, strengthens CNAG’s contribution to the Human Cell Atlas (HCA), an international initiative seeking to build a comprehensive picture of the cells that...

- Researchers have discovered a window of opportunity to eliminate metastasis at an early stage, before it causes symptoms. - The finding, published in Cancer Cell, opens a potential route to stopping the disease before it becomes clinically apparent, effectively paving the way towards prevention....