National Institute for Health Research Blood and Transplant Unit
19 papers found
Identification of rare sequence variation underlying heritable pulmonary arterial hypertension
Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps
Genome-wide Association Studies Identify Genetic Loci Associated with Albuminuria in Diabetes
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
Height-reducing variants and selection for short stature in Sardinia
Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index
Whole-genome sequence-based analysis of thyroid function
An atlas of genetic influences on human blood metabolites.
Loci influencing blood pressure identified using a cardiovascular gene-centric array
Collaborative Meta-analysis: Associations of 150 Candidate Genes With Osteoporosis and Osteoporotic Fracture
Association of genetic loci: replication or not, that is the question.
Genetic association studies: web-based resources for effective screening and assessment of candidate genes and pathways
Patterns of variation at a mitochondrial sequence-tagged-site locus provides new insights into the postglacial history of European Pinus sylvestris populations
A low mutation rate for chloroplast microsatellites.
Amplified Fragment Length Polymorphism (AFLP) analysis of genetic variation in Moringa oleifera Lam
Characterization of microsatellite loci in Pinus sylvestris L
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