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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Adaptive potential of ash (Fraxinus excelsior) populations against the novel emerging pathogenHymenoscyphus pseudoalbidus
Erik Dahl Kjær, Lea Vig McKinney, Lene Rostgaard Nielsen, et al.
Evolutionary Applications (2011) Vol. 5, Iss. 3, pp. 219-228
Open Access | Times Cited: 121

Showing 1-25 of 121 citing articles:

Suitability of close-to-nature silviculture for adapting temperate European forests to climate change
Peter Brang, Peter Spathelf, J. B. Larsen, et al.
Forestry An International Journal of Forest Research (2014) Vol. 87, Iss. 4, pp. 492-503
Open Access | Times Cited: 401
European ash (Fraxinus excelsior) dieback – A conservation biology challenge
Marco Pautasso, Gregor Aas, Valentin Queloz, et al.
Biological Conservation (2012) Vol. 158, pp. 37-49
Closed Access | Times Cited: 359
Impacts of climate change on plant diseases—opinions and trends
Marco Pautasso, Thomas Döring, Matteo Garbelotto, et al.
European Journal of Plant Pathology (2012) Vol. 133, Iss. 1, pp. 295-313
Closed Access | Times Cited: 320
Hymenoscyphus pseudoalbidus, the causal agent ofEuropean ash dieback
Andrin Gross, Ottmar Holdenrieder, Marco Pautasso, et al.
Molecular Plant Pathology (2013) Vol. 15, Iss. 1, pp. 5-21
Open Access | Times Cited: 315
The ash dieback crisis: genetic variation in resistance can prove a long‐term solution
Lea Vig McKinney, Lene Rostgaard Nielsen, David B. Collinge, et al.
Plant Pathology (2014) Vol. 63, Iss. 3, pp. 485-499
Open Access | Times Cited: 218
Ash dieback in the UK: A review of the ecological and conservation implications and potential management options
Ruth J. Mitchell, Joan K. Beaton, Paul E. Bellamy, et al.
Biological Conservation (2014) Vol. 175, pp. 95-109
Closed Access | Times Cited: 151
Drivers of emerging fungal diseases of forest trees
Luisa Ghelardini, Alessia Lucia Pepori, Nicola Luchi, et al.
Forest Ecology and Management (2016) Vol. 381, pp. 235-246
Closed Access | Times Cited: 125
Plant Microbe Interactions in Post Genomic Era: Perspectives and Applications
Jahangir Imam, Puneet Kumar Singh, Pratyoosh Shukla
Frontiers in Microbiology (2016) Vol. 7
Open Access | Times Cited: 98
Biological Flora of the British Isles:Fraxinus excelsior
Peter A. Thomas
Journal of Ecology (2016) Vol. 104, Iss. 4, pp. 1158-1209
Open Access | Times Cited: 88
Ash dieback: From Asia to Europe
Dáire Carroll, E. Boa
Plant Pathology (2024) Vol. 73, Iss. 4, pp. 741-759
Open Access | Times Cited: 15
Reproductive mode and life cycle of the ash dieback pathogen Hymenoscyphus pseudoalbidus
Andrin Gross, Pascal L. Zaffarano, Angelo Duò, et al.
Fungal Genetics and Biology (2012) Vol. 49, Iss. 12, pp. 977-986
Closed Access | Times Cited: 106
Clonal differences in susceptibility to the dieback ofFraxinus excelsiorin southern Sweden
Lars-Göran Stener
Scandinavian Journal of Forest Research (2012) Vol. 28, Iss. 3, pp. 205-216
Closed Access | Times Cited: 90
Molecular markers for tolerance of European ash (Fraxinus excelsior) to dieback disease identified using Associative Transcriptomics
Andrea L. Harper, Lea Vig McKinney, Lene Rostgaard Nielsen, et al.
Scientific Reports (2016) Vol. 6, Iss. 1
Open Access | Times Cited: 78
Silvicultural strategies for Fraxinus excelsior in response to dieback caused by Hymenoscyphus fraxineus
Jens Peter Skovsgaard, Georg Wilhelm, I. M. Thomsen, et al.
Forestry An International Journal of Forest Research (2017) Vol. 90, Iss. 4, pp. 455-472
Open Access | Times Cited: 75
Forest community response to invasive pathogens: the case of ash dieback in a British woodland
Jessica Needham, Cory Merow, Nathalie Butt, et al.
Journal of Ecology (2016) Vol. 104, Iss. 2, pp. 315-330
Open Access | Times Cited: 66
Demography beyond the population
Alden B. Griffith, Roberto Salguero‐Gómez, Cory Merow, et al.
Journal of Ecology (2016) Vol. 104, Iss. 2, pp. 271-280
Open Access | Times Cited: 63
The Natural Evolutionary Potential of Tree Populations to Cope with Newly Introduced Pests and Pathogens—Lessons Learned From Forest Health Catastrophes in Recent Decades
Katharina B. Budde, Lene Rostgaard Nielsen, Hans Peter Ravn, et al.
Current Forestry Reports (2016) Vol. 2, Iss. 1, pp. 18-29
Open Access | Times Cited: 61
The viability of a breeding programme for ash in the British Isles in the face of ash dieback
William J. Plumb, Timothy Coker, Jonathan Stocks, et al.
Plants People Planet (2019) Vol. 2, Iss. 1, pp. 29-40
Open Access | Times Cited: 56
Temporal development of ash dieback symptoms and spatial distribution of collar rots in a provenance trial of Fraxinus excelsior
Rasmus Enderle, F. E. Peters, Aikaterini Nakou, et al.
European Journal of Forest Research (2013) Vol. 132, Iss. 5-6, pp. 865-876
Closed Access | Times Cited: 66
Can we protect forests by harnessing variation in resistance to pests and pathogens?
Annika Telford, Stephen Cavers, Richard A. Ennos, et al.
Forestry An International Journal of Forest Research (2014) Vol. 88, Iss. 1, pp. 3-12
Open Access | Times Cited: 65
Hymenoscyphus albidoides sp. nov. and H. pseudoalbidus from China
Huan-Di Zheng, Wen-Ying Zhuang
Mycological Progress (2013) Vol. 13, Iss. 3, pp. 625-638
Closed Access | Times Cited: 60
Fungal communities associated with species of Fraxinus tolerant to ash dieback, and their potential for biological control
Chatchai Kosawang, Daniel Buchvaldt Amby, Boonsom Bussaban, et al.
Fungal Biology (2017) Vol. 122, Iss. 2-3, pp. 110-120
Closed Access | Times Cited: 55
Tree disease and pest epidemics in the Anthropocene: A review of the drivers, impacts and policy responses in the UK
Clive Potter, Julie Urquhart
Forest Policy and Economics (2016) Vol. 79, pp. 61-68
Open Access | Times Cited: 53
Genetic variation in dieback resistance in Fraxinus excelsior confirmed by progeny inoculation assay
Albin Lobo, Lea Vig McKinney, Jon Kehlet Hansen, et al.
Forest Pathology (2015) Vol. 45, Iss. 5, pp. 379-387
Closed Access | Times Cited: 50
Collapsing foundations: The ecology of the British oak, implications of its decline and mitigation options
Ruth J. Mitchell, Paul E. Bellamy, Christopher J. Ellis, et al.
Biological Conservation (2019) Vol. 233, pp. 316-327
Closed Access | Times Cited: 49
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