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Each summary is provided by the research team.
Please note: The views expressed may not reflect those of the NIHR BioResource.
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Studies 100-108 of 421
Genetic association analyses of computationally derived phenotypes implicate extracellular matrix in the pathogenesis of pulmonary arterial hypertension
Speciality areaCardiovascular Disease
Study typeSamples and data
Researcher typeAcademic
Research leadDr Emilia Swietlik
Clinical evaluation of potentially actionable ‘additional findings’ in inherited cardiac condition genes (SCARFE)
Study typeParticipant re-contact
Research leadProf. Hugh Watkins
Gene regulatory Sequence Variation Effects on automimmune diseases and platelet traits
Speciality areaDiabetes
Research leadProfessor John Todd
Speciality areaMental Health
Study typeData only
Research leadProfessor James Walters
ToWards Immunisations that Last: the Immunology andGerontology of Helper T cells (TWILIGHT)
Speciality areaAgeing
Research leadDr Michelle Linterman
The genetic analysis of multiple sclerosis
Speciality areaNeurological Disorders
Research leadProfessor Stephen Sawcer
IBD Gene Discovery - UK IBD Genetics Consortium
Speciality areaGastroenterology
Research leadProfessor Miles Parkes
Genetic variation in SAMHD1
Speciality areaInfection
Research leadDr Harriet Groom
Towards an understanding of Multiple Sclerosis (TUMS)