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 424-429 of 429
Hypertropic Cardiomyopathy (HCM)
Speciality areaCardiovascular Disease, Genomics and Rare Diseases
Study typeData only
Researcher typeAcademic
Research leadHugh Watkins
Steroid Resistant Nephrotic Syndrome (SRNS)
Speciality areaKidney Disorders, Genomics and Rare Diseases
Research leadAnia Koziell
The role of mitochondrial DNA variants in common disease
Speciality areaGenomics and Rare Diseases
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
