Antagonistic coevolution accelerates molecular evolution S Paterson, T Vogwill, A Buckling, R Benmayor, AJ Spiers, NR Thomson, ... Nature 464 (7286), 275-278, 2010 | 628 | 2010 |
The genetic basis of the fitness costs of antimicrobial resistance: a meta‐analysis approach T Vogwill, RC MacLean Evolutionary applications 8 (3), 284-295, 2015 | 430 | 2015 |
Epistasis between antibiotic resistance mutations and genetic background shape the fitness effect of resistance across species of Pseudomonas T Vogwill, M Kojadinovic, RC Maclean Proceedings of the Royal Society B: Biological Sciences 283 (1830), 20160151, 2016 | 112 | 2016 |
Herbicide mixtures at high doses slow the evolution of resistance in experimentally evolving populations of Chlamydomonas reinhardtii M Lagator, T Vogwill, A Mead, N Colegrave, P Neve New Phytologist 198 (3), 938-945, 2013 | 100 | 2013 |
Persistence and resistance as complementary bacterial adaptations to antibiotics T Vogwill, AC Comfort, V Furió, RC MacLean Journal of evolutionary biology 29 (6), 1223-1233, 2016 | 84 | 2016 |
Limits to compensatory adaptation and the persistence of antibiotic resistance in pathogenic bacteria RC MacLean, T Vogwill Evolution, medicine, and public Health 2015 (1), 4-12, 2015 | 76 | 2015 |
Testing the role of genetic background in parallel evolution using the comparative experimental evolution of antibiotic resistance T Vogwill, M Kojadinovic, V Furió, RC MacLean Molecular biology and evolution 31 (12), 3314-3323, 2014 | 74 | 2014 |
Dispersal and natural enemies interact to drive spatial synchrony and decrease stability in patchy populations T Vogwill, A Fenton, MA Brockhurst Ecology Letters 12 (11), 1194-1200, 2009 | 53 | 2009 |
Identifying and exploiting genes that potentiate the evolution of antibiotic resistance DR Gifford, V Furió, A Papkou, T Vogwill, A Oliver, RC MacLean Nature ecology & evolution 2 (6), 1033-1039, 2018 | 49 | 2018 |
Divergent evolution peaks under intermediate population bottlenecks during bacterial experimental evolution T Vogwill, RL Phillips, DR Gifford, RC MacLean Proceedings of the Royal Society B: Biological Sciences 283 (1835), 20160749, 2016 | 48 | 2016 |
The impact of parasite dispersal on antagonistic host–parasite coevolution T Vogwill, A Fenton, MA Brockhurst Journal of Evolutionary Biology 21 (5), 1252-1258, 2008 | 43 | 2008 |
Herbicide cycling has diverse effects on evolution of resistance in Chlamydomonas reinhardtii M Lagator, T Vogwill, N Colegrave, P Neve Evolutionary applications 6 (2), 197-206, 2013 | 42 | 2013 |
Source populations act as coevolutionary pacemakers in experimental selection mosaics containing hotspots and coldspots T Vogwill, A Fenton, A Buckling, ME Hochberg, MA Brockhurst The American Naturalist 173 (5), E171-E176, 2009 | 38 | 2009 |
The experimental evolution of herbicide resistance in Chlamydomonas reinhardtii results in a positive correlation between fitness in the presence and absence of … T Vogwill, M Lagator, N Colegrave, P Neve Journal of Evolutionary Biology 25 (10), 1955-1964, 2012 | 32 | 2012 |
How does spatial dispersal network affect the evolution of parasite local adaptation? T Vogwill, A Fenton, MA Brockhurst Evolution 64 (6), 1795-1801, 2010 | 27 | 2010 |
Coevolving parasites enhance the diversity-decreasing effect of dispersal T Vogwill, A Fenton, MA Brockhurst Biology letters 7 (4), 578-580, 2011 | 16 | 2011 |
The genetic basis of the fitness costs of antimicrobial resistance: a meta-analysis approach. Evol Appl. 2015; 8 (3): 284–95 T Vogwill, RC MacLean Epub 2015/04/11. https://doi. org/10.1111/eva. 12202 PMID: 25861386, 0 | 7 | |
The genetic basis of the fitness costs of antimicrobial resistance: A meta‐analysis approach. Evolutionary Applications, 8 (3), 284–295 T Vogwill, RC MacLean | 6 | 2015 |
Using an “artificial fitness gradient” to unravel the effects of population-wide fitness variation on the cost of antibiotic resistance. JD Barber, T Vogwill | | |