By health condition
By demographic
Each summary is provided by the external research team. The views expressed may not reflect those of the NIHR BioResource.
We’ve also created a few study collections:
Studies 91-99 of 136
Genome medicine for platelet disorders (access to 'Chromoscope' data platform)
Speciality areaGenomics and Rare Diseases, Haematology
Study typeData only
Researcher typeAcademic
Research leadDr Hugo Ferreira Ponte
Gene discovery for cardiomyopathies
Speciality areaGenomics and Rare Diseases, Cardiovascular Disease
Research leadDr Dhandapany Perundurai
Monogenic immune deficiency diseases
Speciality areaGenomics and Rare Diseases
Research leadManish Butte
Testing biotx.ai's AI for wide data in Rare Diseases
Researcher typeCommercial
Research leadMarco Schmidt
Can Covid-19 outcome be revealed by single cell analysis?
Speciality areaInfection, COVID
Research leadPaul Lyons
IBD drug therapies and COVID-19
Speciality areaGastroenterology, Infection, COVID
Research leadNick Kennedy
Investigation of the underlying genetic variation of idiopathic and heritable pulmonary arterial hypertension (PAH)
Research leadDr Stefan Gräf
Investigating polygenic risk for immune-mediated disease in a sporadic primary immunodeficiency cohort.
Research leadHannah Huang
BRIDGE- EDS (Ehlers-Danlos Syndrome)
Research leadHeather Cordell