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Each summary is provided by the research team.
Please note: The views expressed may not reflect those of the NIHR BioResource.
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Studies 415-418 of 418
The role of mitochondrial DNA variants in common disease
Speciality areaGenomics and Rare Diseases
Study typeData only
Researcher typeAcademic
Research leadPatrick Chinnery
Identifying the molecular basis of congenital anaemias presenting in isolation or as bone marrow failure due to multilineage involvement (stem cell disorders)
Speciality areaGenomics and Rare Diseases, Haematology
Research leadChristian Babbs
Cerebral Small Vessel Disease
Speciality areaGenomics and Rare Diseases, Stroke
Research leadDr Stefan Graf
Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes.
Speciality areaCancer, Genomics and Rare Diseases
Research leadJames Whitworth