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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 370-378 of 422
NIHR BioResource access
Speciality areaGenomics and Rare Diseases
Study typeData only
Researcher typeAcademic
Research leadDr Christopher Penkett
Characterisation of the genetic landscapes of Myeloproliferative neoplasms (MPN) patients
Speciality areaCancer, Genomics and Rare Diseases
Research leadMarieke Oudelaar
Genetic Regulation of platelet GPVI Dimer Levels in Healthy Individuals
Speciality areaHaematology, Genomics and Rare Diseases
Research leadDr Kate Downes
BRIDGE genomic analysis of neuropathic pain disorders
Researcher typeNon-commercial
Research leadDr Georgios Baskozos
Nanopore sequencing project
Speciality areaGenomics and Rare Diseases, Haematology
Research leadProfessor Willem Ouwehand
Validation of spinal muscular atrophy copy-number caller using 13,000 whole-genome sequence data
Research leadMs Adeela Ahmad
Genetic Variation in Coagulation Factors and Risk of Haemorrhage
Research leadMs Erlinda Dedgjonaj
COvid-19 PsychIatry and Neurological Genetics (COPING) study
Speciality areaMental Health, Genomics and Rare Diseases, Neurological Disorders, COVID
Study typeParticipant re-contact
Research leadProfessor Gerome Breen
METRIC-EF: Magnetic Resonance Enterography and Small Bowel Ultrasound as predictors of disabling disease in newly-diagnosed Crohn’s disease
Speciality areaGastroenterology
Research leadProf. Stuart Taylor