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 109-117 of 136
BRIDGE Bleeding and Platelet Disorders study
Speciality areaHaematology, Genomics and Rare Diseases
Study typeData only
Researcher typeAcademic
Research leadErnest Turro
Blood platelet disorders (access to 'Chromoscope' data platform)
Speciality areaGenomics and Rare Diseases
Research leadDr Floor Heubel-Moenen
Progressing from Genetics to Function and Clinical Translation in Crohn’s Disease & Ulcerative Colitis
Speciality areaGastroenterology, Genomics and Rare Diseases
Research leadCarl Anderson
von Wiilebrand factor - access to Gene Docs
Speciality areaGenomics and Rare Diseases, Haematology
Research leadDr Reuben Bierings
Whole Genome Sequencing and Analysis to identify new isease genes for hypertrophic cardiomyopathy
Speciality areaCardiovascular Disease, Genomics and Rare Diseases
Research leadDr Ashley Pritchard
PMG (Primary Membranoproliferative glomerulonephritis and C3 Glomerulopathy)
Speciality areaKidney Disorders, Genomics and Rare Diseases
Research leadProf. John Armour
Genetics of Leber hereditary optic neuropathy (access to 'Chromoscope' data platform)
Speciality areaChildren and Young People, Neurological Disorders, Genomics and Rare Diseases
Research leadProf. Lucy Raymond
Idiopathic Nephrotic Syndrome
Research leadDr Amy Osborne
Primary Immunodeficieny
Research leadDr Paul Lyons