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Showing 1–7 of 7 results
Advanced filters: Author: Daniel Muthas Clear advanced filters
  • A set of three papers in Nature reports a new proteomics resource from the UK Biobank and initial analysis of common and rare genetic variant associations with plasma protein levels.

    • Ryan S. Dhindsa
    • Oliver S. Burren
    • Slavé Petrovski
    ResearchOpen Access
    Nature
    Volume: 622, P: 339-347
  • Genome-wide association analysis of an improved telomere length score, calculated from quantitative PCR and whole-genome sequencing measurements in 462,666 individuals in the UK Biobank, identifies novel genes and variants underlying this trait.

    • Oliver S. Burren
    • Ryan S. Dhindsa
    • Slavé Petrovski
    ResearchOpen Access
    Nature Genetics
    Volume: 56, P: 1832-1840
  • In 2014, the Illuminating the Druggable Genome programme was launched to promote the exploration of currently understudied but potentially druggable proteins. This article discusses how the systematic collection and processing of a wide array of biological and chemical data as part of this programme has enabled the development of evidence-based criteria for tracking the target development level of human proteins, which indicates a substantial knowledge deficit for approximately one out of three proteins in the human proteome. It also highlights the nature of the unexplored therapeutic opportunities for major protein families.

    • Tudor I. Oprea
    • Cristian G. Bologa
    • Gergely Zahoránszky-Köhalmi
    Research
    Nature Reviews Drug Discovery
    Volume: 17, P: 317-332
  • Ryan Dhindsa et al. conducted an exome-wide association study to identify a rare variant in SPDL1 as a risk factor for idiopathic pulmonary fibrosis (IPF). Their findings implicate mitotic checkpoint signalling as a new mechanism underlying IPF.

    • Ryan S. Dhindsa
    • Johan Mattsson
    • Slavé Petrovski
    ResearchOpen Access
    Communications Biology
    Volume: 4, P: 1-8