Items where Author is "O'Brien, K"
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Murthy, S, O'Brien, K, Agbor, A, Angedakin, S, Arandjelovic, M, Ayimisin, EA, Bailey, E, Bergl, RA, Brazzola, G, Dieguez, P, Eno-Nku, M, Eshuis, H, Fruth, B, Gillespie, TR, Ginath, Y, Gray, M, Herbinger, I, Jones, S, Kehoe, L, Kuhl, H , Kujirakwinja, D, Lee, K, Madinda, NF, Mitamba, G, Muhindo, E, Nishuli, R, Ormsby, LJ, Petrzelkova, KJ, Plumptre, AJ, Robbins, MM, Sommer, V, Ter Heegde, M, Todd, A, Tokunda, R, Wessling, E, Jarvis, MA, Leendertz, FH, Ehlers, B and Calvignac-Spencer, S (2019) Cytomegalovirus distribution and evolution in hominines. Virus Evolution, 5 (2). ISSN 2057-1577
Harris, M, Brathwaite, R, McGowan, CR, Ciccarone, D, Gilchrist, G, McCusker, M, O'Brien, K, Dunn, J, Scott, J and Hope, V (2018) 'Care and Prevent': rationale for investigating skin and soft tissue infections and AA amyloidosis among people who inject drugs in London. Harm Reduction Journal, 15 (1). ISSN 1477-7517
Fazey, I, Moug, P, Allen, S, Beckmann, K, Blackwood, D, Bonaventura, M, Burnett, K, Danson, M, Falconer, R, Gagnon, AS, Harkness, R, Hodgson, A, Holm, L, Irvine, KN, Low, R, Lyon, C, Moss, A, Moran, C, Naylor, L, O'Brien, K , Russell, S, Skerratt, S, Rao-Williams, J and Wolstenholme, R (2017) Transformation in a changing climate: a research agenda. Climate and Development, 10 (3). pp. 197-217. ISSN 1756-5529
Foley, AR, Menezes, MP, Pandraud, A, Gonzalez, MA, Al-Odaib, A, Abrams, AJ, Sugano, K, Yonezawa, A, Manzur, AY, Burns, J, Hughes, I, McCullagh, BG, Jungbluth, H, Lim, MJ, Lin, J-P, Megarbane, A, Urtizberea, JA, Shah, AH, Antony, J, Webster, R , Broomfield, A, Ng, J, Mathew, AA, O'Byrne, JJ, Forman, E, Scoto, M, Prasad, M, O'Brien, K, Olpin, S, Oppenheim, M, Hargreaves, IP, Land, JM, Wang, MX, Carpenter, K, Horvath, R, Straub, V, Lek, M, Gold, W, Farrell, MO, Brandner, S, Phadke, R, Matsubara, K, McGarvey, ML, Scherer, SS, Baxter, PS, King, MD, Clayton, P, Rahman, S, Reilly, MM, Ouvrier, RA, Christodoulou, J, Zuechner, S, Muntoni, F and Houlden, H (2013) Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2. Brain, 137 (1). pp. 44-56. ISSN 1460-2156