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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:

Large-scale transcriptomics to dissect 2 years of the life of a fungal phytopathogen interacting with its host plant
Elise J. Gay, Jessica L. Soyer, Nicolas Lapalu, et al.
BMC Biology (2021) Vol. 19, Iss. 1
Open Access | Times Cited: 33

Showing 1-25 of 33 citing articles:

A new family of structurally conserved fungal effectors displays epistatic interactions with plant resistance proteins
Noureddine Lazar, Carl H. Mesarich, Yohann Petit, et al.
PLoS Pathogens (2022) Vol. 18, Iss. 7, pp. e1010664-e1010664
Open Access | Times Cited: 58
Two independent approaches converge to the cloning of a new Leptosphaeria maculans avirulence effector gene, AvrLmS‐Lep2
Ting Xiang Neik, Kaveh Ghanbarnia, Bénédicte Ollivier, et al.
Molecular Plant Pathology (2022) Vol. 23, Iss. 5, pp. 733-748
Open Access | Times Cited: 27
Regulation of effector gene expression as concerted waves in Leptosphaeria maculans: a two‐player game
Colin Clairet, Elise J. Gay, Antoine Porquier, et al.
New Phytologist (2024) Vol. 242, Iss. 1, pp. 247-261
Open Access | Times Cited: 5
A gene‐for‐gene interaction involving a ‘late’ effector contributes to quantitative resistance to the stem canker disease in Brassica napus
Audren Jiquel, Julie Gervais, Aude Geistodt‐Kiener, et al.
New Phytologist (2021) Vol. 231, Iss. 4, pp. 1510-1524
Open Access | Times Cited: 27
Slipping through the cracks: Challenges and prospects for investigating fungal plant disease complexes
Anne‐Lise Boixel, Thierry Rouxel, Didier Andrivon, et al.
Crop Protection (2024) Vol. 184, pp. 106826-106826
Closed Access | Times Cited: 4
From Lesions to Lessons: Two Decades of Filamentous Plant Pathogen Genomics
Wagner C. Fagundes, Yu-Seng Huang, Susanne Häußler, et al.
Molecular Plant-Microbe Interactions (2025)
Open Access
A Dual RNA-Seq Analysis Revealed Dynamic Arms Race during the Infestation of Wheat by the English Grain Aphid (Sitobion avenae)
Zhenyu Wang, Weixi Hao, Dong‐Hui Geng, et al.
Journal of Agricultural and Food Chemistry (2025)
Closed Access
The neighbouring genes AvrLm10A and AvrLm10B are part of a large multigene family of cooperating effector genes conserved in Dothideomycetes and Sordariomycetes
Nacèra Talbi, Like Fokkens, Corinne Audran, et al.
Molecular Plant Pathology (2023) Vol. 24, Iss. 8, pp. 914-931
Open Access | Times Cited: 10
Does fungal infection increase the palatability of oilseed rape to insects?
Barbora Jindřichová, Nikoleta Rubil, Jan Rezek, et al.
Pest Management Science (2024) Vol. 80, Iss. 5, pp. 2480-2494
Closed Access | Times Cited: 3
A new avirulence gene of Leptosphaeria maculans, AvrLm14, identifies a resistance source in American broccoli (Brassica oleracea) genotypes
Alexandre Degrave, Marine Wagner, Pierre George, et al.
Molecular Plant Pathology (2021) Vol. 22, Iss. 12, pp. 1599-1612
Open Access | Times Cited: 23
Molecular Interactions BetweenLeptosphaeria maculansandBrassicaSpecies
M. Hossein Borhan, Angela P. Van de Wouw, Nicholas J. Larkan
Annual Review of Phytopathology (2022) Vol. 60, Iss. 1, pp. 237-257
Open Access | Times Cited: 15
Improved gene annotation of the fungal wheat pathogenZymoseptoria triticibased on combined Iso-Seq and RNA-Seq evidence
Nicolas Lapalu, Lucie Lamothe, Yohann Petit, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2023)
Open Access | Times Cited: 9
The SET domain protein PsKMT3 regulates histone H3K36 trimethylation and modulates effector gene expression in the soybean pathogen Phytophthora sojae
Han Chen, Yujie Fang, Wenrui Song, et al.
Molecular Plant Pathology (2023) Vol. 24, Iss. 4, pp. 346-358
Open Access | Times Cited: 8
Polymorphism of Avirulence Genes and Adaptation to Brassica Resistance Genes Is Gene-Dependent in the Phytopathogenic Fungus Leptosphaeria maculans
Angélique Gautier, Valérie Laval, Sébastien Faure, et al.
Phytopathology (2023) Vol. 113, Iss. 7, pp. 1222-1232
Open Access | Times Cited: 8
Location and timing govern tripartite interactions of fungal phytopathogens and host in the stem canker species complex
Elise J. Gay, Noémie Jacques, Nicolas Lapalu, et al.
BMC Biology (2023) Vol. 21, Iss. 1
Open Access | Times Cited: 8
A new family of structurally conserved fungal effectors displays epistatic interactions with plant resistance proteins
Noureddine Lazar, Carl H. Mesarich, Yohann Petit, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 16
CusProSe: a customizable protein annotation software with an application to the prediction of fungal secondary metabolism genes
Leonor Oliveira, Nicolas Chevrollier, Jean‐Félix Dallery, et al.
Scientific Reports (2023) Vol. 13, Iss. 1
Open Access | Times Cited: 4
Breeding and management of major resistance genes to stem canker/blackleg in Brassica crops
Paula Vasquez‐Teuber, Thierry Rouxel, Annaliese S. Mason, et al.
Theoretical and Applied Genetics (2024) Vol. 137, Iss. 8
Open Access | Times Cited: 1
Dual RNA-seq reveals distinct families of co-regulated and structurally conserved effectors in Botrytis cinerea infection of Arabidopsis thaliana
Jinfeng Wei, Qian Zhou, Jing Zhang, et al.
BMC Biology (2024) Vol. 22, Iss. 1
Open Access | Times Cited: 1
“Late” effectors from Leptosphaeria maculans as tools for identifying novel sources of resistance in Brassica napus
Audren Jiquel, Elise J. Gay, Justine Mas, et al.
Plant Direct (2022) Vol. 6, Iss. 8
Open Access | Times Cited: 7
Plant Relationships
Jessica L. Soyer, Isabelle Fudal
˜The œmycota (2022)
Closed Access | Times Cited: 7
Regulation of effector gene expression as concerted waves inLeptosphaeria maculans: a two-players game
Colin Clairet, Elise J. Gay, Antoine Porquier, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 9
Constitutive expression of transcription factor SirZ blocks pathogenicity in Leptosphaeria maculans independently of sirodesmin production
Andrew S. Urquhart, Candace E. Elliott, Wei Zeng, et al.
PLoS ONE (2021) Vol. 16, Iss. 6, pp. e0252333-e0252333
Open Access | Times Cited: 6
Overexpression of rice acyl-CoA-binding protein OsACBP5 protects Brassica napus against seedling infection by fungal phytopathogens
Saritha Panthapulakkal Narayanan, Aruni Y. Alahakoon, Candace E. Elliott, et al.
Crop and Pasture Science (2023) Vol. 74, Iss. 5, pp. 459-469
Open Access | Times Cited: 2
Meiotic recombination in Leptosphaeria maculans favours the rise of transgressive isolates adapted to a nonhost species, Brassica carinata
Julie Noah, Mathilde Gorse, Carole‐Anne Romain, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
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