D. Jayarama Bhat

7.1k total citations · 1 hit paper
115 papers, 2.5k citations indexed

About

D. Jayarama Bhat is a scholar working on Cell Biology, Plant Science and Molecular Biology. According to data from OpenAlex, D. Jayarama Bhat has authored 115 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 106 papers in Cell Biology, 99 papers in Plant Science and 29 papers in Molecular Biology. Recurrent topics in D. Jayarama Bhat's work include Plant Pathogens and Fungal Diseases (106 papers), Mycorrhizal Fungi and Plant Interactions (87 papers) and Lichen and fungal ecology (21 papers). D. Jayarama Bhat is often cited by papers focused on Plant Pathogens and Fungal Diseases (106 papers), Mycorrhizal Fungi and Plant Interactions (87 papers) and Lichen and fungal ecology (21 papers). D. Jayarama Bhat collaborates with scholars based in Thailand, China and India. D. Jayarama Bhat's co-authors include Kevin D. Hyde, Eric H. C. McKenzie, Ekachai Chukeatirote, Ali H. Bahkali, Sajeewa S. N. Maharachchikumbura, Jian‐Kui Liu, Dhanushka N. Wanasinghe, Saranyaphat Boonmee, Nalin N. Wijayawardene and Dong-Qin Dai and has published in prestigious journals such as Frontiers in Microbiology, Mycologia and Frontiers in Cellular and Infection Microbiology.

In The Last Decade

D. Jayarama Bhat

107 papers receiving 2.4k citations

Hit Papers

Significance of precise documentation of hosts and geospa... 2024 2026 2025 2024 10 20 30 40

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
D. Jayarama Bhat Thailand 25 2.3k 2.2k 718 530 525 115 2.5k
Rungtiwa Phookamsak Thailand 23 2.4k 1.0× 2.3k 1.1× 762 1.1× 683 1.3× 534 1.0× 100 2.7k
Sinang Hongsanan Thailand 24 2.0k 0.9× 2.0k 0.9× 721 1.0× 709 1.3× 478 0.9× 99 2.4k
Hiran A. Ariyawansa Thailand 24 1.6k 0.7× 1.6k 0.7× 549 0.8× 469 0.9× 313 0.6× 83 1.9k
Saranyaphat Boonmee Thailand 24 2.0k 0.9× 2.0k 0.9× 597 0.8× 571 1.1× 466 0.9× 121 2.3k
Dhanushka N. Wanasinghe China 27 2.6k 1.1× 2.5k 1.1× 805 1.1× 704 1.3× 693 1.3× 154 3.0k
Erio Camporesi Thailand 24 2.0k 0.9× 1.9k 0.9× 690 1.0× 610 1.2× 397 0.8× 75 2.2k
Wen-Ying Zhuang China 23 1.6k 0.7× 1.8k 0.8× 545 0.8× 531 1.0× 350 0.7× 189 2.2k
Putarak Chomnunti Thailand 19 1.5k 0.7× 1.5k 0.7× 581 0.8× 430 0.8× 280 0.5× 62 1.8k
Mingkwan Doilom Thailand 18 1.2k 0.5× 1.1k 0.5× 359 0.5× 271 0.5× 351 0.7× 58 1.4k
Asha J. Dissanayake China 19 1.6k 0.7× 1.4k 0.6× 496 0.7× 279 0.5× 357 0.7× 38 1.7k

Countries citing papers authored by D. Jayarama Bhat

Since Specialization
Citations

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

Fields of papers citing papers by D. Jayarama Bhat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D. Jayarama Bhat. 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 D. Jayarama Bhat. The network helps show where D. Jayarama Bhat may publish in the future.

Co-authorship network of co-authors of D. Jayarama Bhat

This figure shows the co-authorship network connecting the top 25 collaborators of D. Jayarama Bhat. A scholar is included among the top collaborators of D. Jayarama Bhat 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 D. Jayarama Bhat. D. Jayarama Bhat 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.
Shen, H. F., Dhanushka N. Wanasinghe, Sinang Hongsanan, et al.. (2025). Taxonomy and phylogeny of lignicolous freshwater fungi from plateau lakes in Yunnan Province, China. Fungal Diversity. 134(1). 635–899.
2.
Yang, Yanyan, Chitrabhanu S. Bhunjun, Vinodhini Thiyagaraja, et al.. (2025). Two novel species of Hermatomyces (Dothideomycetes) from Fagales in China. Mycological Progress. 24(1). 1 indexed citations
3.
Thiyagaraja, Vinodhini, et al.. (2024). New fungal taxa of Ascomycota from China. New Zealand Journal of Botany. 63(2-3). 228–250.
4.
Rathnayaka, Achala R., Danushka S. Tennakoon, E.B. Gareth Jones, et al.. (2024). Significance of precise documentation of hosts and geospatial data of fungal collections, with an emphasis on plant‐associated fungi. New Zealand Journal of Botany. 63(2-3). 462–489. 47 indexed citations breakdown →
5.
Phukhamsakda, Chayanard, Chitrabhanu S. Bhunjun, Achala R. Rathnayaka, et al.. (2024). Novel Hosts, Geographical Records, and A Global Checklist of molecularly confirmed Periconia species. Phytotaxa. 674(1). 18–54. 1 indexed citations
7.
Tennakoon, Danushka S., Chang-Hsin Kuo, Sajeewa S. N. Maharachchikumbura, et al.. (2021). Taxonomic and phylogenetic contributions to Celtis formosana, Ficus ampelas, F. septica, Macaranga tanarius and Morus australis leaf litter inhabiting microfungi. Fungal Diversity. 108(1). 1–215. 82 indexed citations
8.
Li, Wenjing, Eric H. C. McKenzie, Jian‐Kui Liu, et al.. (2020). Taxonomy and phylogeny of hyaline-spored coelomycetes. Fungal Diversity. 100(1). 279–801. 88 indexed citations
9.
Phukhamsakda, Chayanard, Eric H. C. McKenzie, Alan J. L. Phillips, et al.. (2020). Microfungi associated with Clematis (Ranunculaceae) with an integrated approach to delimiting species boundaries. Fungal Diversity. 102(1). 1–203. 143 indexed citations
10.
Mapook, Ausana, Kevin D. Hyde, Eric H. C. McKenzie, et al.. (2020). Taxonomic and phylogenetic contributions to fungi associated with the invasive weed Chromolaena odorata (Siam weed). Fungal Diversity. 101(1). 1–175. 126 indexed citations
11.
Liu, Ning-Guo, Yong‐Zhong Lu, D. Jayarama Bhat, et al.. (2019). Kevinhydea brevistipitata gen. et sp. nov. and Helicoma hydei sp. nov., (Tubeufiaceae) from decaying wood habitats. Mycological Progress. 18(5). 671–682. 9 indexed citations
12.
Tibpromma, Saowaluck, Kevin D. Hyde, Eric H. C. McKenzie, et al.. (2018). Fungal diversity notes 840–928: micro-fungi associated with Pandanaceae. Fungal Diversity. 93(1). 1–160. 186 indexed citations
13.
Zhang, Huang, Wei Dong, Kevin D. Hyde, et al.. (2017). Towards a natural classification of Annulatascaceae-like taxa: introducing Atractosporales ord. nov. and six new families. Fungal Diversity. 85(1). 75–110. 51 indexed citations
14.
Doilom, Mingkwan, Asha J. Dissanayake, Dhanushka N. Wanasinghe, et al.. (2016). Microfungi on Tectona grandis (teak) in Northern Thailand. Fungal Diversity. 82(1). 107–182. 148 indexed citations
15.
Dai, Dong, Rungtiwa Phookamsak, Nalin N. Wijayawardene, et al.. (2016). Bambusicolous fungi. Fungal Diversity. 82(1). 1–105. 175 indexed citations
16.
Thambugala, Kasun M., Hiran A. Ariyawansa, Yanmei Li, et al.. (2014). Dothideales. Fungal Diversity. 68(1). 105–158. 39 indexed citations
17.
Chomnunti, Putarak, D. Jayarama Bhat, E.B. Gareth Jones, et al.. (2012). Trichomeriaceae, a new sooty mould family of Chaetothyriales. Fungal Diversity. 56(1). 63–76. 60 indexed citations
18.
Maharachchikumbura, Sajeewa S. N., Liang‐Dong Guo, Lei Cai, et al.. (2012). A multi-locus backbone tree for Pestalotiopsis, with a polyphasic characterization of 14 new species. Fungal Diversity. 56(1). 95–129. 228 indexed citations
19.
Singh, Sanjay K., et al.. (2002). New conidial fungi from Andaman Islands, India. Mycotaxon. 82. 133–143. 1 indexed citations
20.
Prasad, Thottethodi Subrahmanya Keshava & D. Jayarama Bhat. (2002). Speiropsis rogergoosensis sp.nov. from India. Mycotaxon. 82. 127–131. 3 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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