D. S. Brar

8.6k total citations · 1 hit paper
89 papers, 5.3k citations indexed

About

D. S. Brar is a scholar working on Plant Science, Genetics and Molecular Biology. According to data from OpenAlex, D. S. Brar has authored 89 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 77 papers in Plant Science, 45 papers in Genetics and 22 papers in Molecular Biology. Recurrent topics in D. S. Brar's work include Genetic Mapping and Diversity in Plants and Animals (45 papers), Plant Disease Resistance and Genetics (24 papers) and GABA and Rice Research (20 papers). D. S. Brar is often cited by papers focused on Genetic Mapping and Diversity in Plants and Animals (45 papers), Plant Disease Resistance and Genetics (24 papers) and GABA and Rice Research (20 papers). D. S. Brar collaborates with scholars based in Philippines, Japan and United States. D. S. Brar's co-authors include G. S. Khush, R. K. Aggarwal, Yu-Ting Huang, Takashige Ishii, Kshirod K. Jena, Olivier Panaud, Zhongyi Li, Dilbag S. Multani, Sunit Jain and Ji‐Ung Jeung and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Scientific Reports.

In The Last Decade

D. S. Brar

85 papers receiving 4.9k citations

Hit Papers

Functional Characteristics of an Endophyte Community Colo... 2011 2026 2016 2021 2011 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
D. S. Brar Philippines 33 4.9k 1.9k 1.6k 399 275 89 5.3k
Belén Picó Spain 38 3.6k 0.7× 1.7k 0.9× 1.1k 0.7× 392 1.0× 190 0.7× 152 4.3k
Jordi García-Más Spain 43 4.1k 0.9× 2.0k 1.1× 1.7k 1.1× 164 0.4× 264 1.0× 103 5.1k
Hiroyuki Kanamori Japan 36 4.3k 0.9× 1.4k 0.8× 1.8k 1.2× 155 0.4× 223 0.8× 98 5.1k
Bao‐Rong Lu China 41 4.9k 1.0× 2.1k 1.1× 2.1k 1.3× 199 0.5× 908 3.3× 165 5.7k
Joe Tohmé Colombia 47 6.3k 1.3× 1.5k 0.8× 1.1k 0.7× 141 0.4× 459 1.7× 141 7.2k
T. M. Fulton United States 15 3.6k 0.7× 1.5k 0.8× 1.3k 0.8× 122 0.3× 223 0.8× 15 3.9k
K. M. Soliman United States 13 4.1k 0.9× 1.5k 0.8× 1.4k 0.9× 106 0.3× 415 1.5× 35 4.9k
S. D. Tanksley United States 34 6.6k 1.4× 2.9k 1.6× 2.1k 1.4× 205 0.5× 425 1.5× 54 7.5k
Takashige Ishii Japan 27 3.6k 0.7× 2.3k 1.2× 879 0.6× 131 0.3× 234 0.9× 81 4.0k
Antonio J. Monforte Spain 45 4.6k 1.0× 2.5k 1.4× 1.7k 1.1× 169 0.4× 228 0.8× 121 5.6k

Countries citing papers authored by D. S. Brar

Since Specialization
Citations

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

Fields of papers citing papers by D. S. Brar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of D. S. Brar

This figure shows the co-authorship network connecting the top 25 collaborators of D. S. Brar. A scholar is included among the top collaborators of D. S. Brar 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. S. Brar. D. S. Brar 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.
Thakur, Vivek, Robert A. Coe, Jacqueline Dionora, et al.. (2020). Natural Diversity in Stomatal Features of Cultivated and Wild Oryza Species. Rice. 13(1). 58–58. 23 indexed citations
2.
Sanada‐Morimura, Sachiyo, Masaya Matsumura, P. S. Virk, et al.. (2019). The Development and Characterization of Near-Isogenic and Pyramided Lines Carrying Resistance Genes to Brown Planthopper with the Genetic Background of Japonica Rice (Oryza sativa L.). Plants. 8(11). 498–498. 22 indexed citations
3.
Pabuayon, Isaiah Catalino M., Hajime Ohyanagi, Masahiro Fujita, et al.. (2018). Potential of Oryza officinalis to augment the cold tolerance genetic mechanisms of Oryza sativa by network complementation. Scientific Reports. 8(1). 16346–16346. 17 indexed citations
4.
Piégu, Benoît, Romain Guyot, Nathalie Picault, et al.. (2011). Doubling genome size without polyploidization: dynamics of retrotransposition-driven genomic expansions in Oryza australiensis, a wild relative of rice (Genome Research (2006) 16, (1262-1269)). Genome Research. 21(7). 19 indexed citations
5.
Rahman, Md Lutfor, Wenzhu Jiang, Sang‐Ho Chu, et al.. (2009). High-resolution mapping of two rice brown planthopper resistance genes, Bph20(t) and Bph21(t), originating from Oryza minuta. Theoretical and Applied Genetics. 119(7). 1237–1246. 128 indexed citations
6.
Khush, G. S., E. R. Angeles, & D. S. Brar. (2007). Genetic analysis of resistance to green leafhopper, Nephotettix virescens (Distant), in IR rice varieties.. SABRAO Journal of Breeding and Genetics. 39(2). 79–88. 1 indexed citations
7.
Zhang, Shibo, Yong Gu, Jaswinder Singh, et al.. (2007). New insights into Oryza genome evolution: high gene colinearity and differential retrotransposon amplification. Plant Molecular Biology. 64(5). 589–600. 14 indexed citations
8.
Kim, Ki Jae, et al.. (2006). Characterization of Grain Quality under Lodging Time and Grade at Ripening. The Korean Journal of Crop Science. 51(5). 440–444. 6 indexed citations
9.
Piégu, Benoît, Romain Guyot, Nathalie Picault, et al.. (2006). Doubling genome size without polyploidization: Dynamics of retrotransposition-driven genomic expansions in Oryza australiensis , a wild relative of rice. Genome Research. 16(10). 1262–1269. 434 indexed citations
10.
Lang, Nguyen Thi, Prasanta K. Subudhi, S. S. Virmani, et al.. (2004). Development of PCR-based Markers for Thermosensitive Genetic Male Sterility Gene tms3(t) in Rice (Oryza Sativa L.). Hereditas. 131(2). 121–127. 20 indexed citations
11.
Murai, Hiroshi, Kazumasa Murata, Shigeo Takumi, et al.. (2003). Constructing linkage maps of brown planthopper resistance genes Bph1, bph2, and Bph9 on rice chromosome 12.. 263–265. 2 indexed citations
12.
Mendoza, R. D., et al.. (2003). Genetic variability of tolerance for iron toxicity in different species of Oryza and their derivatives.. 154–157. 4 indexed citations
13.
Nguyen, Bay, et al.. (2003). Identification and mapping of the QTL for aluminum tolerance introgressed from the new source, ORYZA RUFIPOGON Griff., into indica rice (Oryza sativa L.). Theoretical and Applied Genetics. 106(4). 583–593. 134 indexed citations
14.
Panaud, Olivier, et al.. (2002). Characterization of transposable elements in the genome of rice (Oryza sativa L.) using Representational Difference Analysis (RDA). Molecular Genetics and Genomics. 268(1). 113–121. 40 indexed citations
15.
16.
Cho, Young‐Chan, et al.. (1999). DNA Fingerprinting of Rice Cultivars using AFLP and RAPD Markers. The Korean Journal of Crop Science. 44(1). 26–31. 5 indexed citations
17.
Jelodar, Nadali Babaeian, N. W. Blackhall, T. P. V. Hartman, et al.. (1999). Intergeneric somatic hybrids of rice [Oryza sativa L. (+) Porteresia coarctata (Roxb.) Tateoka]. Theoretical and Applied Genetics. 99(3-4). 570–577. 22 indexed citations
18.
Brar, D. S. & A. S. Sidhu. (1995). Effect of soil water on pattern of nitrogen release during decomposition of added greenmanure residue. Journal of the Indian Society of Soil Science. 43(1). 14–17. 3 indexed citations
19.
Cocking, E. C., N. W. Blackhall, D. S. Brar, et al.. (1994). Biotechnological approaches to rice genetic improvement. Rothamsted Repository (Rothamsted Repository). 1 indexed citations
20.
Multani, Dilbag S., Kshirod K. Jena, D. S. Brar, et al.. (1994). Development of monosomic alien addition lines and introgression of genes from Oryza australiensis Domin. to cultivated rice O. sativa L.. Theoretical and Applied Genetics. 88(1). 102–109. 81 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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