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 82-90 of 136
Investigation into potential role for terminal degrons in PID (access to 'Chromoscope' data platform)
Speciality areaGenomics and Rare Diseases, Infection
Study typeData only
Researcher typeAcademic
Research leadDr Richard Timms
Genome wide identification of CTCF site disruption resulting in aberrant enhancer: promoter interactions as a recurrent mechanism of human disease
Speciality areaGenomics and Rare Diseases, Neurological Disorders
Research leadDr Christopher Cummings
Molecular Pathology of Human Genetic Disease
Speciality areaKidney Disorders, Genomics and Rare Diseases
Research leadAvgi Andreou
Primary Immune Deficiency (access to 'Chromoscope' data platform)
Research leadProf. Christoph Hess
Determining ethnic differences in IBD phenotype and response to treatment; determining differences in disease course and management of IBD in the elderly
Speciality areaGastroenterology
Research leadDr Sharmili Balarajah
DAA - EpiCov database
Speciality areaInfection
Research leadProfessor Willem Ouwehand
Use of long-read nanopore sequencing and short-read whole genome sequencing to resolve individuals with antithrombin deficiency, a rare disease which increase the risk of thrombosis, with unknown molecular base.
Speciality areaGenomics and Rare Diseases, Haematology
Research leadDr Belén de la Morena-Barrio
Diagnostic sequence analysis in patients with renal diseases
Speciality areaLiver, Genomics and Rare Diseases
Research leadAli Gharavi
Investigation of Omics in Chronic Widespread Pain
Speciality areaGenomics and Rare Diseases, Anaesthesia, Perioperative Medicine and Pain Management
Research leadFrances Williams
