Joseph W. Spatafora

30.3k total citations · 3 hit papers
163 papers, 12.0k citations indexed

About

Joseph W. Spatafora is a scholar working on Plant Science, Cell Biology and Molecular Biology. According to data from OpenAlex, Joseph W. Spatafora has authored 163 papers receiving a total of 12.0k indexed citations (citations by other indexed papers that have themselves been cited), including 122 papers in Plant Science, 98 papers in Cell Biology and 54 papers in Molecular Biology. Recurrent topics in Joseph W. Spatafora's work include Mycorrhizal Fungi and Plant Interactions (102 papers), Plant Pathogens and Fungal Diseases (98 papers) and Lichen and fungal ecology (31 papers). Joseph W. Spatafora is often cited by papers focused on Mycorrhizal Fungi and Plant Interactions (102 papers), Plant Pathogens and Fungal Diseases (98 papers) and Lichen and fungal ecology (31 papers). Joseph W. Spatafora collaborates with scholars based in United States, Netherlands and Canada. Joseph W. Spatafora's co-authors include Gi‐Ho Sung, Nigel L. Hywel‐Jones, Conrad L. Schoch, Meredith Blackwell, David S. Hibbett, Janet Jennifer Luangsa-ard, Bhushan Shrestha, P.W. Crous, Igor V. Grigoriev and Jason Stajich and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Joseph W. Spatafora

161 papers receiving 11.6k citations

Hit Papers

A phylum-level phylogenet... 2007 2026 2013 2019 2016 2007 2021 250 500 750

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Joseph W. Spatafora United States 59 8.4k 5.8k 3.5k 2.7k 2.6k 163 12.0k
David S. Hibbett United States 64 10.4k 1.2× 6.7k 1.1× 3.5k 1.0× 3.9k 1.4× 1.5k 0.6× 164 12.5k
Stephen A. Rehner United States 46 6.7k 0.8× 4.3k 0.7× 2.8k 0.8× 2.7k 1.0× 3.9k 1.5× 88 10.0k
A. Elizabeth Arnold United States 51 8.5k 1.0× 7.4k 1.3× 1.9k 0.5× 5.5k 2.0× 1.1k 0.4× 155 12.6k
Brenda D. Wingfield South Africa 60 10.8k 1.3× 10.7k 1.8× 4.7k 1.3× 1.4k 0.5× 2.2k 0.8× 523 14.8k
W. Gams Netherlands 51 8.5k 1.0× 7.2k 1.2× 3.1k 0.9× 2.1k 0.7× 1.4k 0.6× 248 12.2k
Karl‐Henrik Larsson Sweden 36 5.4k 0.6× 3.1k 0.5× 1.4k 0.4× 2.7k 1.0× 1.7k 0.7× 105 6.8k
Franz Oberwinkler Germany 50 7.2k 0.9× 4.2k 0.7× 3.6k 1.0× 2.3k 0.8× 958 0.4× 310 8.8k
François Lutzoni United States 57 7.7k 0.9× 5.3k 0.9× 2.2k 0.6× 6.3k 2.3× 615 0.2× 138 10.7k
David M. Geiser United States 52 10.7k 1.3× 9.8k 1.7× 3.0k 0.9× 1.3k 0.5× 608 0.2× 117 13.6k
Bernard Slippers South Africa 53 7.6k 0.9× 7.6k 1.3× 3.4k 1.0× 1.9k 0.7× 1.9k 0.7× 286 10.8k

Countries citing papers authored by Joseph W. Spatafora

Since Specialization
Citations

This map shows the geographic impact of Joseph W. Spatafora's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Joseph W. Spatafora with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Joseph W. Spatafora more than expected).

Fields of papers citing papers by Joseph W. Spatafora

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joseph W. Spatafora. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Joseph W. Spatafora. The network helps show where Joseph W. Spatafora may publish in the future.

Co-authorship network of co-authors of Joseph W. Spatafora

This figure shows the co-authorship network connecting the top 25 collaborators of Joseph W. Spatafora. A scholar is included among the top collaborators of Joseph W. Spatafora based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Joseph W. Spatafora. Joseph W. Spatafora is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
2.
Czajka, Jeffrey J., Yichao Han, Joonhoon Kim, et al.. (2024). Genome-scale model development and genomic sequencing of the oleaginous clade Lipomyces. Frontiers in Bioengineering and Biotechnology. 12. 1356551–1356551. 5 indexed citations
3.
Li, Yuanning, Jacob L. Steenwyk, Ying Chang, et al.. (2021). A genome-scale phylogeny of the kingdom Fungi. Current Biology. 31(8). 1653–1665.e5. 180 indexed citations breakdown →
4.
Gluck‐Thaler, Emile, Sajeet Haridas, Manfred Binder, et al.. (2020). The Architecture of Metabolism Maximizes Biosynthetic Diversity in the Largest Class of Fungi. Molecular Biology and Evolution. 37(10). 2838–2856. 37 indexed citations
5.
Tabima, Javier F., Ying Chang, Yan Wang, et al.. (2020). Phylogenomic Analyses of Non-Dikarya Fungi Supports Horizontal Gene Transfer Driving Diversification of Secondary Metabolism in the Amphibian Gastrointestinal Symbiont, Basidiobolus. G3 Genes Genomes Genetics. 10(9). 3417–3433. 25 indexed citations
7.
Knapp, Dániel G., Kerrie Barry, Matthieu Hainaut, et al.. (2018). Comparative genomics provides insights into the lifestyle and reveals functional heterogeneity of dark septate endophytic fungi. Scientific Reports. 8(1). 6321–6321. 129 indexed citations
8.
Walker, Allison K., Keith A. Seifert, J. David Miller, et al.. (2016). Full Genome of Phialocephala scopiformis DAOMC 229536, a Fungal Endophyte of Spruce Producing the Potent Anti-Insectan Compound Rugulosin. Genome Announcements. 4(1). 20 indexed citations
9.
Miettinen, Otto, Robert Riley, Kerrie Barry, et al.. (2016). Draft Genome Sequence of the White-Rot Fungus Obba rivulosa 3A-2. Genome Announcements. 4(5). 13 indexed citations
10.
Spatafora, Joseph W. & Kathryn E. Bushley. (2015). Phylogenomics and evolution of secondary metabolism in plant-associated fungi. Current Opinion in Plant Biology. 26. 37–44. 18 indexed citations
11.
Sanjuán, Tatiana, Javier F. Tabima, Silvia Restrepo, et al.. (2014). Entomopathogens of Amazonian stick insects and locusts are members of the Beauveria species complex ( Cordyceps sensu stricto). Mycologia. 106(2). 260–275. 36 indexed citations
12.
Kumar, T. K. Arun, Rosanne Healy, Joseph W. Spatafora, Meredith Blackwell, & David J. McLaughlin. (2012). Orbilia ultrastructure, character evolution and phylogeny of Pezizomycotina. Mycologia. 104(2). 462–476. 22 indexed citations
13.
Kepler, Ryan M., Gi‐Ho Sung, Sayaka Ban, et al.. (2012). New teleomorph combinations in the entomopathogenic genus Metacordyceps. Mycologia. 104(1). 182–197. 100 indexed citations
14.
Zhang, Qi, et al.. (2010). A species of Ophiocordyceps new to China.. Anhui Nongye Daxue xuebao. 37(4). 709–711. 2 indexed citations
15.
16.
Sullivan, Raymond F., et al.. (2001). Features and phylogenetic status of an enigmatic clavicipitalean fungus Neoclaviceps monostipa gen. et sp. nov.. Mycologia. 93(1). 90–99. 4 indexed citations
17.
Grubisha, Lisa C., James M. Trappe, Randy Molina, & Joseph W. Spatafora. (2001). Biology of the ectomycorrhizal genus Rhizopogon . V. Phylogenetic relationships in the Boletales inferred from LSU rDNA sequences. Mycologia. 93(1). 82–89. 34 indexed citations
18.
Kohlmeyer, Jan, Joseph W. Spatafora, & Brigitte Volkmann‐Kohlmeyer. (2000). Lulworthiales, a new order of marine Ascomycota. Mycologia. 92(3). 453–458. 22 indexed citations
19.
Suh, Sung‐Oui, et al.. (1998). Molecular phylogenetic study of a termite pathogen Cordycepioideus bisporus. Mycologia. 90(4). 611–617. 14 indexed citations
20.
Spatafora, Joseph W. & Meredith Blackwell. (1993). Molecular Systematics of Unitunicate Perithecial Ascomycetes: The Clavicipitales-Hypocreales Connection. Mycologia. 85(6). 912–922. 141 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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