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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 361-369 of 421
Progressing from Genetics to Function and Clinical Translation in Crohn’s Disease & Ulcerative Colitis
Speciality areaGastroenterology, Genomics and Rare Diseases
Study typeData only
Researcher typeAcademic
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
Speciality areaGenomics and Rare Diseases
Research leadDr Paul Lyons
Contribution of polygenic scores to haematological traits and diseases
Research leadDr Dragana Vuckovic
NIHR BioResource access
Research leadDr Christopher Penkett