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:

The Botrytis cinerea phytotoxin botcinic acid requires two polyketide synthases for production and has a redundant role in virulence with botrydial
Bérengère Dalmais, Julia Schumacher, Javier Moraga, et al.
Molecular Plant Pathology (2011) Vol. 12, Iss. 6, pp. 564-579
Open Access | Times Cited: 168

Showing 1-25 of 168 citing articles:

Genomic Analysis of the Necrotrophic Fungal Pathogens Sclerotinia sclerotiorum and Botrytis cinerea
Joëlle Amselem, Christina A. Cuomo, J.A.L. van Kan, et al.
PLoS Genetics (2011) Vol. 7, Iss. 8, pp. e1002230-e1002230
Open Access | Times Cited: 970

Regulation and Role of Fungal Secondary Metabolites
Juliane Macheleidt, Derek J. Mattern, Juliane Fischer, et al.
Annual Review of Genetics (2016) Vol. 50, Iss. 1, pp. 371-392
Open Access | Times Cited: 358

A gapless genome sequence of the fungus Botrytis cinerea
J.A.L. van Kan, Joost H. M. Stassen, Andreas Mosbach, et al.
Molecular Plant Pathology (2016) Vol. 18, Iss. 1, pp. 75-89
Open Access | Times Cited: 264

Three Pectin Methylesterase Inhibitors Protect Cell Wall Integrity for Arabidopsis Immunity to Botrytis
Vincenzo Lionetti, Eleonora Fabri, Monica De Caroli, et al.
PLANT PHYSIOLOGY (2017) Vol. 173, Iss. 3, pp. 1844-1863
Open Access | Times Cited: 172

Killing softly: a roadmap of Botrytis cinerea pathogenicity
Kai Bi, Yong Liang, Tesfaye Mengiste, et al.
Trends in Plant Science (2022) Vol. 28, Iss. 2, pp. 211-222
Open Access | Times Cited: 162

Multiple knockout mutants reveal a high redundancy of phytotoxic compounds contributing to necrotrophic pathogenesis of Botrytis cinerea
Thomas Leisen, J.A. Werner, Patrick Pattar, et al.
PLoS Pathogens (2022) Vol. 18, Iss. 3, pp. e1010367-e1010367
Open Access | Times Cited: 75

The Transcription Factor BcLTF1 Regulates Virulence and Light Responses in the Necrotrophic Plant Pathogen Botrytis cinerea
Julia Schumacher, Adeline Simon, Kim C. Cohrs, et al.
PLoS Genetics (2014) Vol. 10, Iss. 1, pp. e1004040-e1004040
Open Access | Times Cited: 143

Tomato transcriptome and mutant analyses suggest a role for plant stress hormones in the interaction between fruit and Botrytis cinerea
Bárbara Blanco-Ulate, Estefania Vincenti, Ann L. T. Powell, et al.
Frontiers in Plant Science (2013) Vol. 4
Open Access | Times Cited: 134

Changes in the Sclerotinia sclerotiorum transcriptome during infection of Brassica napus
Shirin Seifbarghi, M. Hossein Borhan, Yangdou Wei, et al.
BMC Genomics (2017) Vol. 18, Iss. 1
Open Access | Times Cited: 123

Oxaloacetate acetylhydrolase gene mutants of Sclerotinia sclerotiorum do not accumulate oxalic acid, but do produce limited lesions on host plants
Xiaofei Liang, Daniele Liberti, Moyi Li, et al.
Molecular Plant Pathology (2014) Vol. 16, Iss. 6, pp. 559-571
Open Access | Times Cited: 121

Infection Strategies Deployed by Botrytis cinerea, Fusarium acuminatum, and Rhizopus stolonifer as a Function of Tomato Fruit Ripening Stage
Stefan Petrasch, Christian J. Silva, Saskia D. Mesquida‐Pesci, et al.
Frontiers in Plant Science (2019) Vol. 10
Open Access | Times Cited: 97

CRISPR/Cas with ribonucleoprotein complexes and transiently selected telomere vectors allows highly efficient marker-free and multiple genome editing in Botrytis cinerea
Thomas Leisen, Fabian Bietz, J.A. Werner, et al.
PLoS Pathogens (2020) Vol. 16, Iss. 8, pp. e1008326-e1008326
Open Access | Times Cited: 89

The infection cushion of Botrytis cinerea: a fungal ‘weapon’ of plant‐biomass destruction
Mathias Choquer, Christine Rascle, Isabelle Gonçalves, et al.
Environmental Microbiology (2021) Vol. 23, Iss. 4, pp. 2293-2314
Open Access | Times Cited: 76

The Multiple Facets of Plant–Fungal Interactions Revealed Through Plant and Fungal Secretomics
Delphine Vincent, Maryam Rafiqi, Dominique Job
Frontiers in Plant Science (2020) Vol. 10
Open Access | Times Cited: 73

The Role of Yeasts as Biocontrol Agents for Pathogenic Fungi on Postharvest Grapes: A Review
Alessandra Di Canito, María Alejandra Mateo-Vargas, Monica Mazzieri, et al.
Foods (2021) Vol. 10, Iss. 7, pp. 1650-1650
Open Access | Times Cited: 56

Fungal biotechnology: From yesterday to tomorrow
Mitchell G. Roth, Nathaniel Westrick, Thomas Baldwin
Frontiers in Fungal Biology (2023) Vol. 4
Open Access | Times Cited: 36

The Sesquiterpene Botrydial Produced by Botrytis cinerea Induces the Hypersensitive Response on Plant Tissues and Its Action Is Modulated by Salicylic Acid and Jasmonic Acid Signaling
Franco R. Rossi, Andrés Gárriz, María Marina, et al.
Molecular Plant-Microbe Interactions (2011) Vol. 24, Iss. 8, pp. 888-896
Open Access | Times Cited: 102

BcAtf1, a global regulator, controls various differentiation processes and phytotoxin production inBotrytis cinerea
Nora Temme, Birgitt Oeser, Michelli Massaroli, et al.
Molecular Plant Pathology (2012) Vol. 13, Iss. 7, pp. 704-718
Open Access | Times Cited: 92

Transcriptome Profiling of Botrytis cinerea Conidial Germination Reveals Upregulation of Infection-Related Genes during the Prepenetration Stage
Michaela Leroch, Astrid Kleber, Evelyn Silva, et al.
Eukaryotic Cell (2013) Vol. 12, Iss. 4, pp. 614-626
Open Access | Times Cited: 89

The VELVET Complex in the Gray Mold FungusBotrytis cinerea: Impact of BcLAE1 on Differentiation, Secondary Metabolism, and Virulence
Julia Schumacher, Adeline Simon, Kim C. Cohrs, et al.
Molecular Plant-Microbe Interactions (2015) Vol. 28, Iss. 6, pp. 659-674
Open Access | Times Cited: 89

Patulin is a cultivar‐dependent aggressiveness factor favouring the colonization of apples by Penicillium expansum
Selma P. Snini, Joanna Tannous, Pauline Heuillard, et al.
Molecular Plant Pathology (2015) Vol. 17, Iss. 6, pp. 920-930
Open Access | Times Cited: 86

Natural Variation in the VELVET Gene bcvel1 Affects Virulence and Light-Dependent Differentiation in Botrytis cinerea
Julia Schumacher, Jean‐Marc Pradier, Adeline Simon, et al.
PLoS ONE (2012) Vol. 7, Iss. 10, pp. e47840-e47840
Open Access | Times Cited: 85

Plastic Transcriptomes Stabilize Immunity to Pathogen Diversity: The Jasmonic Acid and Salicylic Acid Networks within the Arabidopsis/Botrytis Pathosystem
Wei Zhang, Jason Corwin, Daniel Copeland, et al.
The Plant Cell (2017) Vol. 29, Iss. 11, pp. 2727-2752
Open Access | Times Cited: 84

Resistance to Botrytis cinerea in Solanum lycopersicoides involves widespread transcriptional reprogramming
Jonathon E. Smith, Bemnet Mengesha, Hua Tang, et al.
BMC Genomics (2014) Vol. 15, Iss. 1
Open Access | Times Cited: 82

Reactive oxygen species in development and infection processes
Robert Marschall, Paul Tudzynski
Seminars in Cell and Developmental Biology (2016) Vol. 57, pp. 138-146
Closed Access | Times Cited: 81

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