Studies

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

Identification of novel genetic causes of ocular maldevelopment

Speciality area
Genomics and Rare Diseases

Study type
Participant re-contact

Researcher type
Academic

Research lead
Mariya Moosajee

RNA phenotyping in blood cell autoimmunity

Speciality area
Genomics and Rare Diseases, Haematology

Study type
Participant re-contact

Researcher type
Academic

Research lead
Nichola Cooper

RNA phenotyping in primary biliary cholangitis

Speciality area
Genomics and Rare Diseases, Liver

Study type
Participant re-contact

Researcher type
Academic

Research lead
George Mells

Very early Intervention through RNA analysis on Leukocytes in Scleroderma

Speciality area
Genomics and Rare Diseases

Study type
Participant re-contact

Researcher type
Academic

Research lead
Francesco Del Galdo

The leukocyte RNA imprint of splicing-factor retinitis pigmentosa

Speciality area
Genomics and Rare Diseases

Study type
Participant re-contact

Researcher type
Academic

Research lead
Andrew Webster

Quality checks, curation and methodological enhancement of the UK LLC Partner Studies using linked data

Speciality area
COVID, Public Health and Prevention, Infection

Study type
Data only

Researcher type
Academic

Research lead
Julie von Ziegenweidt

The role of genetics in liver disease during pregnancy

Speciality area
Genomics and Rare Diseases, Liver, Reproductive Health

Study type
Data only

Researcher type
Academic

Research lead
Dr Peter Dixon

Effect of genetic variants associated with risk for inflammatory disease on immune cell phenotype and function

Speciality area
Gastroenterology, Genomics and Rare Diseases

Study type
Data only

Researcher type
Academic

Research lead
Dr Carl Anderson