Studies

Primary Biliary Cirrhosis (PBC): identification of genes associated with liver disease.

Speciality area
Liver

Study type
Participant re-contact

Researcher type
Academic

Research lead
Professor Richard Sandford

Generation of Patient-Specific Stem Cells for Research into Stroke

Speciality area
Stroke

Study type
Participant re-contact

Researcher type
Academic

Research lead
Professor Hugh Markus

Genotype and Phenotype in Inherited Neurodegenerative Diseases

Speciality area
Neurological Disorders, Infection

Study type
Participant re-contact

Researcher type
Academic

Research lead
Professor Patrick Chinnery

Modulating Emerging Memory Responses to Immunisation (MEMRI)

Speciality area
Infection, Primary Care, Ageing

Study type
Participant re-contact

Researcher type
Academic

Research lead
Dr Eoin McKinney

Elucidating genetic modulation of T cell – monocyte interactions and activation (Mono activation)

Speciality area
Infection

Study type
Participant re-contact

Researcher type
Academic

Research lead
Dr Michael Morgan

RNA phenotyping in Ataxia telangiectasia

Speciality area
Neurological Disorders, Genomics and Rare Diseases

Study type
Participant re-contact

Researcher type
Academic

Research lead
Rita Horvath and Anke Hensiek

Molecular mechanisms of Neuroferritinopathy

Speciality area
Neurological Disorders, Genomics and Rare Diseases

Study type
Participant re-contact

Researcher type
Academic

Research lead
Patrick Chinnery

Applying transcriptomic data to identify novel genes and disease clusters in congenital neutropenia

Speciality area
Genomics and Rare Diseases, Haematology

Study type
Participant re-contact

Researcher type
Academic

Research lead
Sarah Westbury

RNA phenotyping in C3 glomerulopathy

Speciality area
Kidney Disorders, Genomics and Rare Diseases

Study type
Participant re-contact

Researcher type
Academic

Research lead
Daniel Gale