Filling the gap: connecting genes to diseases through proteins

Hundreds of connections between different human diseases have been uncovered through their shared origin in our genome by an international research team led by scientists at the Berlin Institute of Health at Charité (BIH) and the University of Cambridge, challenging the categorisation of diseases by organ, symptoms, or clinical speciality. A new study published in Science today generated data on thousands of proteins circulating in our blood and combined this with genetic data to produce a map showing how genetic differences that affect these proteins link together seemingly diverse as well as related diseases.

Quelle: IDW Informationsdienst Wissenschaft