Studies

Genome wide identification of CTCF site disruption resulting in aberrant enhancer: promoter interactions as a recurrent mechanism of human disease

Speciality area
Genomics and Rare Diseases, Neurological Disorders

Study type
Data only

Researcher type
Academic

Research lead
Dr Christopher Cummings

The role of leptin in mediating the response to COVID vaccination in severely obese people

Speciality area
Infection, COVID

Study type
Participant re-contact

Researcher type
Academic

Research lead
Sadaf Farooqi

Pfizer vaccine allergy clinic

Speciality area
Infection, COVID

Study type
Participant re-contact

Researcher type
Academic

Research lead
Shuaib Nasser

VIP Study: SARS-CoV2 Vaccine Immunogenicity in immunosuppressed IBD Patients

Speciality area
Infection, COVID

Study type
Participant re-contact

Researcher type
Academic

Research lead
Dr Nick Powell

Molecular Pathology of Human Genetic Disease

Speciality area
Kidney Disorders, Genomics and Rare Diseases

Study type
Data only

Researcher type
Academic

Research lead
Avgi Andreou

Analysis of plasma BMP9/BMP10/sEng and markers of endothelial dysfunction in patients with COVID-19

Speciality area
Infection, COVID

Study type
Samples and data

Researcher type
Academic

Research lead
Professor Nicholas Morrell

Primary Immune Deficiency (access to 'Chromoscope' data platform)

Speciality area
Genomics and Rare Diseases, Infection

Study type
Data only

Researcher type
Academic

Research lead
Prof. Christoph Hess

QwikZyme SARS-CoV-2 Clinical Evaluation

Speciality area
Infection, COVID

Study type
Samples and data

Researcher type
Commercial

Research lead
Professor Molly Stevens

Effects of APOE genotype on episodic memory in mid life

Speciality area
Dementias and Neurodegeneration

Study type
Online

Researcher type
Academic

Research lead
Dr Claire Lancaster