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 10-17 of 17
RNA phenotyping in mitochondrial diseases
Speciality areaGenomics and Rare Diseases, Neurological Disorders
Study typeParticipant re-contact
Researcher typeAcademic
Research leadPatrick Chinnery
Investigating the risk of progressive kidney disease
Speciality areaKidney Disorders, Genomics and Rare Diseases
Research leadJonathan Barratt
RNA phenotyping in heritable platelet disorders
Speciality areaHaematology, Genomics and Rare Diseases
Research leadAndrew Mumford, Sarah Westbury
RNA phenotyping in unexplained inherited thrombosis
Research leadSuthesh Sivapalaratnam
RNA phenotyping in early progressive lung disease
Speciality areaRespiratory Disorders, Genomics and Rare Diseases
Research leadAlice Turner
RNA phenotyping in inherited optic neuropathies
Speciality areaGenomics and Rare Diseases
Research leadPatrick Yu Wai Man
RNA phenotyping in SAPHO/CNO/CRMO inflammatory conditions
Speciality areaMusculoskeletal Disorders, Genomics and Rare Diseases
Research leadJudith Bubbear
RNA phenotyping in newly diagnosed and flare giant cell arteritis
Research leadAnn Morgan
