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 28-36 of 108
UNRAVEL: Understanding the genetics of Ring Chromosome 20 Syndrome
Speciality areaGenomics and Rare Diseases
Study typeSamples and data
Researcher typeAcademic
Research leadProfessor Sameer Zuberi
The Genetics of Osteoarthritis (GO) Consortium - GWAS meta-analysis
Speciality areaMusculoskeletal Disorders, Genomics and Rare Diseases
Study typeData only
Research leadEleftheria Zeggini
Systematic temporal analysis of transcriptomic datasets using TrendCatcher identifies early and persistent neutrophil activation as a hallmark of severe COVID-19
Speciality areaInfection, Genomics and Rare Diseases, COVID
Research leadJalees Rehman
Looking at Immune receptors during viral infections at a single-cell level
Speciality areaInfection, Genomics and Rare Diseases
Research leadDr. Anunya Opasawatchai
Analysis of the role of HLA-type on T-cell state in Covid-19 infection
Research leadSoumya Raychaudhuri
Analysis of Structural Variants in 15,370 Individuals from the NIHR BioResource and Integration with Large-Scale Rare Disease Cohorts
Research leadDr Alba Sanchis-Juan
Bleeding and Platelet Disorders (access to 'Chromoscope' data platform)
Speciality areaGenomics and Rare Diseases, Haematology
Research leadMr Koenraad De Wispelaere
Partcipants' data from UCL to be held locally, to help enable local research.
Speciality areaCross-cutting, Genomics and Rare Diseases
Research leadNicholas Wood
Predicting disease trajectory and response to treatment in primary open-angle glaucoma
Speciality areaOphthalmology, Genomics and Rare Diseases
Research leadAnthony Khawaja
