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Carina Brehony

Researcher at University of Oxford

Publications -  30
Citations -  1589

Carina Brehony is an academic researcher from University of Oxford. The author has contributed to research in topics: Meningococcal vaccine & Multilocus sequence typing. The author has an hindex of 15, co-authored 29 publications receiving 1354 citations. Previous affiliations of Carina Brehony include Health Service Executive & National University of Ireland, Galway.

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Ribosomal multilocus sequence typing: universal characterization of bacteria from domain to strain.

TL;DR: This work proposes ribosomal multilocus sequence typing (rMLST), an approach which indexes variation of the 53 genes encoding the bacterial ribosome protein subunits (rps genes), as a means of integrating microbial genealogy and typing, and employs curated reference sequences to identify gene variants efficiently and rapidly.
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Molecular typing of meningococci: recommendations for target choice and nomenclature

TL;DR: The diversity and dynamics of Neisseria meningitidis populations generate a requirement for high resolution, comprehensive, and portable typing schemes for meningococcal disease surveillance, and the following target genes are recommended.
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A surveillance network for meningococcal disease in Europe

TL;DR: A major decline in the incidence of invasive disease in those countries that have introduced routine vaccination against serogroup C infection is demonstrated and case fatality was found to vary with clonal complex, suggesting that genotype can be a marker for hypervirulence.
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Multilocus sequence typing for global surveillance of meningococcal disease

TL;DR: The 'Impact of meningococcal epidemiology and population biology on public health in Europe (EU-MenNet)' project has shown the distribution of a relatively small number of STs, clonal complexes and PorA types that account for a large proportion of the disease-associated isolates in Europe.
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Variation of the factor H-binding protein of Neisseria meningitidis.

TL;DR: A survey of the diversity of the fHbp gene and the encoded protein confirmed that variability in this protein is structured into two or three major groups, each with a substantial number of alleles that have some association with meningococcal clonal complexes and serogroups.