John R. Stinchcombe

9.8k total citations
127 papers, 6.8k citations indexed

About

John R. Stinchcombe is a scholar working on Ecology, Evolution, Behavior and Systematics, Plant Science and Genetics. According to data from OpenAlex, John R. Stinchcombe has authored 127 papers receiving a total of 6.8k indexed citations (citations by other indexed papers that have themselves been cited), including 70 papers in Ecology, Evolution, Behavior and Systematics, 64 papers in Plant Science and 44 papers in Genetics. Recurrent topics in John R. Stinchcombe's work include Plant and animal studies (65 papers), Ecology and Vegetation Dynamics Studies (43 papers) and Genetic diversity and population structure (27 papers). John R. Stinchcombe is often cited by papers focused on Plant and animal studies (65 papers), Ecology and Vegetation Dynamics Studies (43 papers) and Genetic diversity and population structure (27 papers). John R. Stinchcombe collaborates with scholars based in Canada, United States and Germany. John R. Stinchcombe's co-authors include Hopi E. Hoekstra, Marc T. J. Johnson, Aneil F. Agrawal, Michael D. Purugganan, Johanna Schmitt, Mark D. Rausher, Cynthia Weinig, Katy D. Heath, Johanna Schmitt and Stephen Wright and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

John R. Stinchcombe

121 papers receiving 6.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
John R. Stinchcombe Canada 44 3.1k 2.9k 2.4k 1.6k 1.4k 127 6.8k
Christian Lexer Switzerland 49 3.6k 1.2× 3.1k 1.1× 4.4k 1.9× 1.6k 1.0× 2.3k 1.7× 126 8.3k
Martin Lascoux Sweden 44 2.4k 0.8× 2.8k 1.0× 4.3k 1.8× 1.4k 0.8× 2.6k 1.9× 160 7.7k
Kermit Ritland Canada 37 2.5k 0.8× 2.3k 0.8× 3.3k 1.4× 1.7k 1.0× 2.0k 1.4× 82 6.9k
John D. Nason United States 36 3.5k 1.1× 2.5k 0.9× 3.3k 1.4× 1.9k 1.2× 1.1k 0.8× 84 6.4k
Peter H. van Tienderen Netherlands 38 2.7k 0.9× 2.3k 0.8× 2.7k 1.1× 1.6k 1.0× 994 0.7× 78 6.8k
Isabelle Olivieri France 47 3.0k 1.0× 1.9k 0.7× 3.1k 1.3× 1.6k 1.0× 944 0.7× 113 6.4k
Carl D. Schlichting United States 40 4.3k 1.4× 2.5k 0.9× 2.6k 1.1× 2.4k 1.5× 1.4k 1.0× 80 8.8k
John H. Willis United States 42 3.0k 1.0× 3.1k 1.1× 4.2k 1.8× 1.1k 0.7× 2.3k 1.7× 62 7.5k
Outi Savolainen Finland 51 2.4k 0.8× 2.9k 1.0× 4.2k 1.8× 2.4k 1.5× 2.5k 1.8× 124 8.6k
Michael L. Arnold United States 39 2.5k 0.8× 1.9k 0.7× 2.5k 1.1× 1.1k 0.7× 1.3k 0.9× 76 5.0k

Countries citing papers authored by John R. Stinchcombe

Since Specialization
Citations

This map shows the geographic impact of John R. Stinchcombe'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 John R. Stinchcombe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites John R. Stinchcombe more than expected).

Fields of papers citing papers by John R. Stinchcombe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John R. Stinchcombe. 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 John R. Stinchcombe. The network helps show where John R. Stinchcombe may publish in the future.

Co-authorship network of co-authors of John R. Stinchcombe

This figure shows the co-authorship network connecting the top 25 collaborators of John R. Stinchcombe. A scholar is included among the top collaborators of John R. Stinchcombe 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 John R. Stinchcombe. John R. Stinchcombe 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
1.
Carey, Sarah B., Baharul I. Choudhury, Jane Grimwood, et al.. (2025). Testing for the Genomic Footprint of Conflict Between Life Stages in an Angiosperm and Moss Species. Genome Biology and Evolution. 17(8).
2.
Stinchcombe, John R., et al.. (2024). Elevated Rates of Molecular Evolution Genome-wide in Mutualist Legumes and Rhizobia. Molecular Biology and Evolution. 41(12).
3.
Frederickson, Megan E., et al.. (2024). Genetic architecture of heritable leaf microbes. Microbiology Spectrum. 12(7). e0061024–e0061024. 1 indexed citations
4.
Frederickson, Megan E., et al.. (2023). Is there a latitudinal diversity gradient for symbiotic microbes? A case study with sensitive partridge peas. Molecular Ecology. 33(1). e17191–e17191. 2 indexed citations
5.
Afkhami, Michelle E., Maren Friesen, & John R. Stinchcombe. (2021). Multiple Mutualism Effects generate synergistic selection and strengthen fitness alignment in the interaction between legumes, rhizobia and mycorrhizal fungi. Ecology Letters. 24(9). 1824–1834. 24 indexed citations
6.
Stinchcombe, John R., et al.. (2021). Introduced populations of ragweed show as much evolutionary potential as native populations. Evolutionary Applications. 14(5). 1436–1449. 12 indexed citations
7.
Kreiner, Julia M., et al.. (2021). Selective ancestral sorting and de novo evolution in the agricultural invasion of Amaranthus tuberculatus. Evolution. 76(1). 70–85. 9 indexed citations
8.
Josephs, Emily B., Young Wha Lee, Corlett W. Wood, et al.. (2020). The Evolutionary Forces Shaping Cis- and Trans-Regulation of Gene Expression within a Population of Outcrossing Plants. Molecular Biology and Evolution. 37(8). 2386–2393. 12 indexed citations
9.
Batstone, Rebecca T., et al.. (2020). Environmental variation impacts trait expression and selection in the legume–rhizobium symbiosis. American Journal of Botany. 107(2). 195–208. 21 indexed citations
10.
Kreiner, Julia M., Darci A. Giacomini, Felix Bemm, et al.. (2019). Multiple modes of convergent adaptation in the spread of glyphosate-resistant Amaranthus tuberculatus. Proceedings of the National Academy of Sciences. 116(42). 21076–21084. 84 indexed citations
11.
Uzunović, Jasmina, Emily B. Josephs, John R. Stinchcombe, & Stephen Wright. (2019). Transposable Elements Are Important Contributors to Standing Variation in Gene Expression in Capsella Grandiflora. Molecular Biology and Evolution. 36(8). 1734–1745. 31 indexed citations
12.
Rosenthal, David M., et al.. (2019). The remarkable morphological diversity of leaf shape in sweet potato (Ipomoea batatas): the influence of genetics, environment, and G×E. New Phytologist. 225(5). 2183–2195. 33 indexed citations
13.
Austen, Emily J., Locke Rowe, John R. Stinchcombe, & Jessica R. K. Forrest. (2017). Explaining the apparent paradox of persistent selection for early flowering. New Phytologist. 215(3). 929–934. 81 indexed citations
14.
Wood, Corlett W., et al.. (2017). Geographically structured genetic variation in the Medicago lupulinaEnsifer mutualism. Evolution. 71(7). 1787–1801. 21 indexed citations
15.
Wood, Corlett W., et al.. (2017). No evidence for adaptation to local rhizobial mutualists in the legume Medicago lupulina. Ecology and Evolution. 7(12). 4367–4376. 20 indexed citations
16.
Sicard, Adrien, Christian Kappel, Young Wha Lee, et al.. (2016). Standing genetic variation in a tissue-specific enhancer underlies selfing-syndrome evolution in Capsella. Proceedings of the National Academy of Sciences. 113(48). 13911–13916. 46 indexed citations
17.
Weiß, Clemens L., Verena J. Schuenemann, Gautam Shirsekar, et al.. (2016). Temporal patterns of damage and decay kinetics of DNA retrieved from plant herbarium specimens. Royal Society Open Science. 3(6). 160239–160239. 85 indexed citations
18.
Josephs, Emily B., Young Wha Lee, John R. Stinchcombe, & Stephen Wright. (2015). Association mapping reveals the role of purifying selection in the maintenance of genomic variation in gene expression. Proceedings of the National Academy of Sciences. 112(50). 15390–15395. 73 indexed citations
19.
Stinchcombe, John R., Cynthia Weinig, Mark C. Ungerer, et al.. (2004). A latitudinal cline in flowering time in Arabidopsis thaliana modulated by the flowering time gene FRIGIDA. Proceedings of the National Academy of Sciences. 101(13). 4712–4717. 387 indexed citations
20.
Schmitt, Johanna, John R. Stinchcombe, & Heidrun Huber. (2002). Adaptive evolution of shade avoidance responses in natural plant populations. Radboud Repository (Radboud University). 1 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026