Research on plant abiotic stress responses in the post‐genome era: past, present and future

Europe-wide reduction in primary productivity caused by the heat and drought in 2003

Ciais, P., Reichstein, M., Viovy, N., Granier, A., Ogée, J., Allard, V., Aubinet, M., Buchmann, N., Bernhofer, C., Carrara, A., et al. (2005) · Nature · doi:10.1038/nature03972 · Cited by 4,153

Abiotic stress, the field environment and stress combination

Mittler, R. (2006) · Trends in Plant Science · doi:10.1016/j.tplants.2005.11.002 · Cited by 3,083

Abscisic Acid Inhibits Type 2C Protein Phosphatases via the PYR/PYL Family of START Proteins

Park, S., Fung, P., Nishimura, N., Jensen, D. R., Fujii, H., Zhao, Y., Lumba, S., Santiago, J., Rodrigues, A., Chow, T.-F. F., et al. (2009) · Science · doi:10.1126/science.1173041 · Cited by 2,986

TRANSCRIPTIONAL REGULATORY NETWORKS IN CELLULAR RESPONSES AND TOLERANCE TO DEHYDRATION AND COLD STRESSES

Yamaguchi‐Shinozaki, K., & Shinozaki, K. (2006) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.57.032905.105444 · Cited by 2,935

Salinity tolerance in halophytes*

Flowers, T. J., & Colmer, T. D. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02531.x · Cited by 2,789

The complex language of chromatin regulation during transcription

Berger, S. L. (2007) · Nature · doi:10.1038/nature05915 · Cited by 2,768

MicroRNAs AND THEIR REGULATORY ROLES IN PLANTS

Jones-Rhoades, M. W., Bartel, D. P., & Bartel, B. (2006) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.57.032905.105218 · Cited by 2,720

Gene networks involved in drought stress response and tolerance

Shinozaki, K., & Yamaguchi‐Shinozaki, K. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erl164 · Cited by 2,641

Drought and Salt Tolerance in Plants

Bartels, D., & Sunkar, R. (2005) · Critical Reviews in Plant Sciences · doi:10.1080/07352680590910410 · Cited by 2,611

Regulators of PP2C Phosphatase Activity Function as Abscisic Acid Sensors

Ma, Y., Szostkiewicz, I., Korte, A., Moes, D., Yang, Y., Christmann, A., & Grill, E. (2009) · Science · doi:10.1126/science.1172408 · Cited by 2,467

PsnERF75 Transcription Factor from Populus simonii × P. nigra Confers Salt Tolerance in Transgenic Arabidopsis

Wang, S., Zhou, B., Yao, W., & Jiang, T. (2018) · Journal of Plant Biology · doi:10.1007/s12374-017-0450-z · Cited by 14

Designing sustainable urban landscape and meeting the challenge of climate change: a study of plant species adaptation and fitness under different climate change scenarios in public landscape of UK

Alizadeh, B., & Hitchmough, J. D. (2019) · Landscape Research · doi:10.1080/01426397.2019.1606185 · Cited by 14

Overexpression of wheat α-mannosidase gene TaMP impairs salt tolerance in transgenic Brachypodium distachyon

Wang, W., Wu, Y., Shi, R., Sun, M., Li, Q., Zhang, G., Wu, J., Wang, W., & Wang, W. (2020) · Plant Cell Reports · doi:10.1007/s00299-020-02522-2 · Cited by 14

Role of abiotic stress responsive miRNAs in Arabidopsis root development

Singh, A., Gandhi, N., Mishra, V., Yadav, S., Rai, V., & Sarkar, A. K. (2020) · Journal of Plant Biochemistry and Biotechnology · doi:10.1007/s13562-020-00626-0 · Cited by 15

Genome-Wide Identification and Expression Analysis of Tomato ADK Gene Family during Development and Stress

Yang, L., Cao, H., Zhang, X., Gui, L., Chen, Q., Qian, G., Xiao, J., & Li, Z. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147708 · Cited by 14

Cloning and Characterization of TaSAP7-A, a Member of the Stress-Associated Protein Family in Common Wheat

Li, W., Wang, Y., Li, R., Chang, X., Yuan, X., & Jing, R. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.609351 · Cited by 14

Genome Editing: A Tool from the Vault of Science for Engineering Climate-Resilient Cereals

Dilawari, R., Kaur, N., Priyadarshi, N., Kumar, B., Abdelmotelb, K. F., Lal, S. K., Singh, B. P., Tripathi, A., Aggarwal, S. K., Jat, B. S., et al. (2021) · Springer eBooks · doi:10.1007/978-3-030-65912-7_3 · Cited by 14

Antioxidant Response and Calcium-Dependent Protein Kinases Involvement in Canola (Brassica napus L.) Tolerance to Drought

Ahmadi, H., Abbasi, A., Taleei, A., Mohammadi, V., & Pueyo, J. J. (2022) · Agronomy · doi:10.3390/agronomy12010125 · Cited by 14

Genome-Wide Analysis of U-box E3 Ubiquitin Ligase Family in Response to ABA Treatment in Salvia miltiorrhiza

Chen, C., Wang, C., Li, J., Gao, X., Huang, Q., Gong, Y., Hao, X., Maoz, I., Kai, G., & Zhou, W. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.829447 · Cited by 14

Critical roles of the activation of ethylene pathway genes mediated by DNA demethylation in Arabidopsis hyperhydricity

Gao, H., Xia, X., & An, L. (2022) · The Plant Genome · doi:10.1002/tpg2.20202 · Cited by 14

Global Integrated Genomic and Transcriptomic Analyses of MYB Transcription Factor Superfamily in C3 Model Plant Oryza sativa (L.) Unravel Potential Candidates Involved in Abiotic Stress Signaling

Muthuramalingam, P., Jeyasri, R., Selvaraj, A., Shin, H., Chen, J., Satish, L., Wu, Q., & Ramesh, M. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2022.946834 · Cited by 14

Targeted Genome Editing for Cotton Improvement

Khan, Z., Khan, S. H., Mubarik, M. S., & Ahmad, A. (2018) · InTech eBooks · doi:10.5772/intechopen.73600 · Cited by 14

Novel ASR isolated from drought stress responsive SSH library in pearl millet confers multiple abiotic stress tolerance in PgASR3 transgenic Arabidopsis

Meena, R. P., Vishwakarma, H., Ghosh, G. K., Gaikwad, K., Chellapilla, T. S., Singh, M. P., & Padaria, J. C. (2020) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2020.07.031 · Cited by 14

Revisión bibliográfica TOLERANCIA A ESTRÉS POR DÉFICIT HÍDRICO EN TOMATE (Solanum lycopersicum L.)

Bacallao, M. F., & Fundora, L. B. (2014) · DOAJ (DOAJ: Directory of Open Access Journals) · Cited by 14

A deep dive into plant metabolomics: Milestones, technologies, and translational impact

Rai, M., Dutta, M., Saito, K., & Rai, A. (2025) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiaf408 · Cited by 16

Differently expressed ‘Early’ flavonoid synthesis genes in wheat seedlings become to be co-regulated under salinity stress

Shoeva, O. Y., & Хлесткина, Е. К. (2015) · Cereal Research Communications · doi:10.1556/0806.43.2015.025 · Cited by 13

Overexpression of MpbHLH transcription factor, an encoding ICE1-like protein, enhances Foc TR4-resistance of Cavendish banana

Li, H., Hu, C., Xie, A., Wu, S., Bi, F., Dong, T., Li, C., Deng, G., He, W., Gao, H., et al. (2021) · Scientia Horticulturae · doi:10.1016/j.scienta.2021.110590 · Cited by 13

CRISPR/Cas-Mediated Abiotic Stress Tolerance in Crops

Ahmad, A., Ashraf, S., Munawar, N., Jamil, A., Ghaffar, A., & Shahbaz, M. (2021) · Springer eBooks · doi:10.1007/978-981-15-7142-8_6 · Cited by 13

Genome-wide analysis of BURP genes and identification of a BURP-V gene RcBURP4 in Rosa chinensis

Fu, L., Zhang, Z., Wang, H., Zhao, X., Su, L., Geng, L., Lu, Y., Tong, B., Liu, Q., & Jiang, X. (2021) · Plant Cell Reports · doi:10.1007/s00299-021-02815-0 · Cited by 13

Overexpression of OsHMGB707, a High Mobility Group Protein, Enhances Rice Drought Tolerance by Promoting Stress-Related Gene Expression

Xu, K., Chen, S., Li, T., Yu, S., Zhao, H., Liu, H., & Luo, L. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.711271 · Cited by 13

The Regulatory Networks of Plant Responses to Abscisic Acid

Umezawa, T., Hirayama, T., Kuromori, T., & Shinozaki, K. (2011) · Advances in botanical research · doi:10.1016/b978-0-12-387692-8.00006-0 · Cited by 13

Environmental Cues Contribute to Dynamic Plasma Membrane Organization of Nanodomains Containing Flotillin-1 and Hypersensitive Induced Reaction-1 Proteins in Arabidopsis thaliana

Xu, C., Abbas, S., Qian, H., Yu, M., Zhang, X., Li, X., Cui, Y., & Lin, J. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.897594 · Cited by 13

Effects of Exogenous Application of 5-Aminolevulinic Acid in Crop Plants

Korkmaz, A. (2011) · Springer eBooks · doi:10.1007/978-1-4614-0634-1_12 · Cited by 13

Suppression Substractive Hybridization and NGS Reveal Differential Transcriptome Expression Profiles in Wayfaring Tree (Viburnum lantana L.) Treated with Ozone

Gottardini, E., Cristofori, A., Pellegrini, E., Porta, N. L., Nali, C., Baldi, P., & Sablok, G. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00713 · Cited by 13

Physiological and biochemical changes in waterlog tolerant sesame genotypes

Saha, R., Ahmed, F., Mokarroma, N., Rohman, M., & Golder, P. C. (2017) · SAARC Journal of Agriculture · doi:10.3329/sja.v14i2.31243 · Cited by 13

Detection of changes in DNA methylation patterns in Pyropia haitanensis under high-temperature stress using a methylation-sensitive amplified polymorphism assay

Yu, C., Xu, K., Wang, W., Xu, Y., Ji, D., Chen, C., & Xie, C. (2017) · Journal of Applied Phycology · doi:10.1007/s10811-017-1363-4 · Cited by 13

Rhizospheric Microbial Diversity: An Important Component for Abiotic Stress Management in Crop Plants Toward Sustainable Agriculture

Goyal, D., Prakash, O., & Pandey, J. (2019) · Elsevier eBooks · doi:10.1016/b978-0-444-64191-5.00009-2 · Cited by 13

A natriuretic peptide from Arabidopsis thaliana (AtPNP-A) can modulate catalase 2 activity

Turek, I., Wheeler, J. I., Bartels, S., Szczurek, J., Wang, Y. H., Taylor, P., Gehring, C., & Irving, H. R. (2020) · Scientific Reports · doi:10.1038/s41598-020-76676-0 · Cited by 13

ArabidopsisPED2 positively modulates plant drought stress resistance

Shi, H., Ye, T., Yang, F., & Chan, Z. (2015) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12330 · Cited by 13

GpDSR7, a Novel E3 Ubiquitin Ligase Gene in Grimmia pilifera Is Involved in Tolerance to Drought Stress in Arabidopsis

Li, M., Li, Y., Zhao, J., Liu, H., Jia, S., Li, J., Zhao, H., Han, S., & Wang, Y. (2016) · PLoS ONE · doi:10.1371/journal.pone.0155455 · Cited by 13

Alternative splicing coupled to nonsense-mediated mRNA decay contributes to the high-altitude adaptation of maca (Lepidium meyenii)

Shi, Y., Su, Z., Yang, H. Y., Wang, W., Jin, G., He, G., Siddique, A. N., Zhang, L., Zhu, A., Xue, R., et al. (2019) · Gene · doi:10.1016/j.gene.2018.12.082 · Cited by 13

Systematic analysis and functional verification of sugarcane PYL gene family reveals that ScPYL61-ScPP2C49-ScSnRK2s module contributes to drought resistance

Dong, X., Lu, Y., Li, A., Jiang, S., Zhou, S., Peng, X., Bi, Z.-F., Mingjing, L. I. A. O., Hu, Q., Yao, W., et al. (2025) · Industrial Crops and Products · doi:10.1016/j.indcrop.2025.120743 · Cited by 12

The Roles of Epigenetics in the Interplay Between Beneficial Rhizobacteria and Plants

Zou, R., Lu, Z., Armin Djamei, A., Kragler, F., Lam, H., & Zhang, S. (2025) · Modern Agriculture · doi:10.1002/moda.70017 · Cited by 12

Genome-wide studies and expression profiling of GhWRKY41 family genes in different tissues and stress conditions in upland cotton (Gossypium hirsutum)

Adjibolosoo, D., Nartey, M. A., Aboagye, E. T., Danso, B., Fatima, I., Hua, J., & Guo, A. (2024) · Industrial Crops and Products · doi:10.1016/j.indcrop.2024.118486 · Cited by 12

Getting the ‘MOST’ out of crop improvement

Hu, S., & Lübberstedt, T. (2015) · Trends in Plant Science · doi:10.1016/j.tplants.2015.03.002 · Cited by 12

Functional Mechanisms Underlying the Antimicrobial Activity of the Oryza sativa Trx-like Protein

Park, S., Kim, I. R., Hwang, J. E., Kim, J., Jung, Y. J., Choi, W., Lee, Y., Jang, M.-K., & Lee, J. R. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20061413 · Cited by 12

The protein elicitor Hrip1 enhances resistance to insects and early bolting and flowering in Arabidopsis thaliana

Miao, X.-Y., Qu, H.-P., Han, Y.-L., He, C., Qiu, D., & Cheng, Z.-W. (2019) · PLoS ONE · doi:10.1371/journal.pone.0216082 · Cited by 12

Abiotic Stress Signaling in Wheat Crop

Tounsi, S., Feki, K., & Brini, F. (2019) · Springer eBooks · doi:10.1007/978-981-13-6883-7_12 · Cited by 12

Transcriptome Profiling of Gossypium anomalum Seedlings Reveals Key Regulators and Metabolic Pathways in Response to Drought Stress

Ji, W., Yu, H., Shangguan, Y., Cao, J., Chen, X., Zhao, L., Guo, Q., Xu, P., Shen, X., & Xu, Z. (2023) · Plants · doi:10.3390/plants12020312 · Cited by 12

Genome-wide identification of MATE, functional analysis and molecular dynamics of DcMATE21 involved in anthocyanin accumulation in Daucus carota

Saad, K. R., Kumar, G., Puthusseri, B., Srinivasa, S. M., Giridhar, P., & Shetty, N. P. (2023) · Phytochemistry · doi:10.1016/j.phytochem.2023.113676 · Cited by 12

Microarray Analysis of bacterial blight resistance 1 mutant rice infected with Xanthomonas oryzae pv. oryzae

Yi, S. Y., Lee, H. Y., Kim, H. A., Lim, C. J., Kim, W. B., Jang, H. A., Jeon, J., & Kwon, S. (2013) · Plant Breeding and Biotechnology · doi:10.9787/pbb.2013.1.4.354 · Cited by 12

Regulatory mechanism of abscisic acid signaling

Miyakawa, T., & Tanokura, M. (2011) · BIOPHYSICS · doi:10.2142/biophysics.7.123 · Cited by 12

Identification of Genes Involved in the Responses of Tangor(C. reticulata×C. sinensis)to Drought Stress

Xiao, J., Zhang, L., Zhang, H., & Miao, L. (2017) · BioMed Research International · doi:10.1155/2017/8068725 · Cited by 12

Genome-wide identification of abiotic stress-regulated and novel microRNAs in mulberry leaf

Wu, P., Han, S., Zhao, W., Chen, T., JiaChun, Z., & Li, L. (2015) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2015.07.007 · Cited by 12

Reactive Oxygen in Abiotic Stress Perception - From Genes to Proteins

Wrzaczek, M., Julia, P., Gauthier, A., Overmyer, K., & Kangasjärvi, J. (2011) · InTech eBooks · doi:10.5772/24891 · Cited by 12

Homeobox Genes as Potential Candidates for Crop Improvement Under Abiotic Stress

Bhattacharjee, A., & Jain, M. (2012) · Springer eBooks · doi:10.1007/978-1-4614-5001-6_7 · Cited by 12

Genomic Approaches and Abiotic Stress Tolerance in Plants

Rashıd, B., Husnaın, T., & Riazuddin, S. A. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-800876-8.00001-1 · Cited by 14

ROS and autophagy in plant stress responses: adaptive partners in survival

Cadena‐Ramos, A. I., Rodríguez-Piña, A. L., & De‐la‐Peña, C. (2025) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2025.110991 · Cited by 12

Identification and characterization of a novel multi-stress responsive gene in Arabidopsis

Tawab, F., Munir, I., Nasim, Z., Khan, M. S., Tawab, S., Nasim, A., Iqbal, A., Ahmad, M. A., Ali, W., Munir, R., et al. (2020) · PLoS ONE · doi:10.1371/journal.pone.0244030 · Cited by 11

Difference in the ligand affinity among redundant plant hormone receptors of rice OsCOI1a/1b/2-OsJAZs

Okumura, T., Kitajima, T., Kaji, T., Urano, H., Matsumoto, K., Inagaki, H., Miyamoto, K., Okada, K., & Ueda, M. (2023) · Bioscience Biotechnology and Biochemistry · doi:10.1093/bbb/zbad092 · Cited by 11

CsABF8 mediates drought-induced ABA signaling in the regulation of raffinose biosynthesis in Camellia sinensis leaves

Zheng, D., Fu, M., Sun, C., Yang, Q., Zhang, X., Lü, J., Chang, M., Liu, L., Wan, X., & Chen, Q. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.143521 · Cited by 11

Plant Performance and Defensive Role of β-Amino Butyric Acid Under Environmental Stress

Choudhary, A., Kumar, A., Kaur, H., Balamurugan, A., Padhy, A. K., & Mehta, S. (2021) · Springer eBooks · doi:10.1007/978-3-030-78521-5_10 · Cited by 11

Plant Defense Mechanisms

Kimatu, J. N. (2021) · IntechOpen eBooks · doi:10.5772/intechopen.95214 · Cited by 11

CaCP15 Gene Negatively Regulates Salt and Osmotic Stress Responses in Capsicum annuum L

Zhou, L., Yang, S., Chen, C., Li, M., Du, Q., Wang, J., Yin, Y., & Xiao, H. (2023) · Genes · doi:10.3390/genes14071409 · Cited by 11

Microbe‐induced plant resistance against insect pests depends on timing of inoculation but is consistent across climatic conditions

Sanchez‐Mahecha, O., Klink, S., Rothballer, M., Sturm, S., Weisser, W. W., Zytynska, S. E., & Heinen, R. (2024) · Functional Ecology · doi:10.1111/1365-2435.14529 · Cited by 11

Multiple hormone treatment revealed novel cooperative relationships between abscisic acid and biotic stress hormones in cultured cells

Okamoto, M., Tsuboi, Y., Goda, H., Yoshizumi, T., Shimada, Y., & Hirayama, T. (2012) · Plant Biotechnology · doi:10.5511/plantbiotechnology.11.1130a · Cited by 11

Potential for recovery of Campomanesia xanthocarpa Mart. ex O. berg seedlings from water deficit

Larissa, F. B., Silvana, D. P. Q. A. O. S., Dresch, D. M., & Pereira, Z. V. (2016) · African Journal of Agricultural Research · doi:10.5897/ajar2016.11231 · Cited by 13

Biochemical and Molecular Mechanisms of Abiotic Stress Tolerance

Khan, M., Jannat, A., Munir, F., Fatima, N., & Amir, R. (2020) · Springer eBooks · doi:10.1007/978-981-15-2172-0_9 · Cited by 11

Identification of drought-induced transcription factors in Sorghum bicolor using GO term semantic similarity

Sekhwal, M. K., Swami, A. K., Sharma, V., & Sarin, R. (2014) · Cellular & Molecular Biology Letters · doi:10.2478/s11658-014-0223-3 · Cited by 11

Drought Stress Tolerance in Plants: Insights from Transcriptomic Studies

Kido, É. A., Ferreira‐Neto, J. R. C., Pandolfi, V., Souza, A. C. D. M., & Benko‐Iseppon, A. M. (2016) · Springer eBooks · doi:10.1007/978-3-319-32423-4_6 · Cited by 12

Genomic Designing for Biotic Stress Resistance in Mulberry

Vijayan, K., Arunakumar, G. S., Gnanesh, B. N., Sangannavar, P. A., Ramesha, A., & Zhao, W. (2022) · Springer eBooks · doi:10.1007/978-3-031-09293-0_8 · Cited by 10

Physiological and biochemical characteristics of cucumber seedlings under different levels drought stress (PEG 6000 concentrations)

Wang, X., Sun, H., Lian, X., Feng, J., Zhao, J., Wang, Y., & Liu, Y. (2024) · Horticultural Science · doi:10.17221/53/2023-hortsci · Cited by 10

Deciphering the ABA and GA biosynthesis approach of Bacillus pumilus, mechanistic approach, explaining the role of metabolic region as an aid in improving the stress tolerance

Shaffique, S., Shah, A. A., Odongkara, P., Elansary, H. O., Khan, A. L., Adhikari, A., Kang, ⋅.-M., & Lee, I.-J. (2024) · Scientific Reports · doi:10.1038/s41598-024-78227-3 · Cited by 10

The CsUGT87A1 gene enhances drought stress tolerance in tea plants by modulating IAA homeostasis

Ndombi, S. N., Chen, Y., Duan, Y., Jiang, J., Shen, Q., Yin, J., Ma, Y., Fang, W., & Zhu, X. (2025) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2025.110158 · Cited by 10

A Proteome Translocation Response to Complex Desert Stress Environments in Perennial Phragmites Sympatric Ecotypes with Contrasting Water Availability

Li, L., Chen, X., Shi, L., Wang, C., Fu, B., Qiu, T., & Cui, S. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.00511 · Cited by 10

Yield Comparisons between Cotton Variety Xin Nong Mian 1 and Its Transgenic ScALDH21 Lines under Different Water Deficiencies in a Desert-Oasis Ecotone

Yang, H., Bozorov, T. A., Chen, X., Zhang, D., Wang, J., Li, X., Dongwei, G. U. I., Qi, Z., & Zhang, D. (2021) · Agronomy · doi:10.3390/agronomy11051019 · Cited by 10

Overexpression of Rice OsS1Fa1 Gene Confers Drought Tolerance in Arabidopsis

Kim, S., Lee, K. H., Kwak, J. S., Kwon, D. H., Song, J. T., & Seo, H. S. (2021) · Plants · doi:10.3390/plants10102181 · Cited by 10

Allantoin mediated regulation of miRNAs for short term salinity stress tolerance in Oryza sativa L. cv. IR-29

Nishad, J., Panda, A. K., Chowrasia, S., Chongtham, N., & Mondal, T. K. (2022) · Journal of Plant Biochemistry and Biotechnology · doi:10.1007/s13562-022-00774-5 · Cited by 10

Analysis of Potato Physiological and Molecular Adaptation in Response to Different Water and Nitrogen Combined Regimes

Yan, W., Qin, J., Jian, Y., Liu, J., Bian, C., Jin, L., & Li, G. (2023) · Plants · doi:10.3390/plants12081671 · Cited by 10

Impact of water stress to plant epigenetic mechanisms in stress and adaptation

Aanniz, T., Baaboua, A. E., Aboulaghras, S., Bouyahya, A., Benali, T., Balahbib, A., Omari, N. E., Butnariu, M., Muzammil, K., Yadav, K. K., et al. (2025) · Physiologia Plantarum · doi:10.1111/ppl.70058 · Cited by 10

Two organobromines trigger lifespan, growth, reproductive and transcriptional changes in Caenorhabditis elegans

Saul, N., Baberschke, N., Chakrabarti, S., Stürzenbaum, S. R., Lieke, T., Menzel, R., Jonáš, A., & Steinberg, C. E. W. (2014) · Environmental Science and Pollution Research · doi:10.1007/s11356-014-2932-6 · Cited by 10

Identification of a putative stearoyl acyl-carrier-protein desaturase gene from Saussurea involucrata

Liu, H., Shen, H., Chen, C., Zhou, X., Liu, H., & Zhu, J. (2015) · Biologia Plantarum · doi:10.1007/s10535-015-0487-0 · Cited by 10

Abiotic Stress-Induced Redox Changes and Programmed Cell Death in Plants—A Path to Survival or Death?

Kumar, S. R., Mohanapriya, G., & Sathishkumar, R. (2016) · Springer eBooks · doi:10.1007/978-3-319-44081-1_11 · Cited by 11

Targeting of Metabolic Pathways for Genetic Engineering to Combat Abiotic Stress Tolerance in Crop Plants

Chamoli, S., & Verma, A. (2013) · Springer eBooks · doi:10.1007/978-81-322-1620-9_2 · Cited by 10

Epigenetic Chromatin Regulators as Mediators of Abiotic Stress Responses in Cereals

Kapazoglou, A., & Tsaftaris, A. S. (2011) · InTech eBooks · doi:10.5772/36025 · Cited by 10

Alteration ofArabidopsis SLAC1promoter and its association with natural variation in drought tolerance

Imai, H., Noda, Y., & Tamaoki, M. (2015) · Plant Signaling & Behavior · doi:10.4161/15592324.2014.989761 · Cited by 10

Identification of differentially expressed genes potentially involved in the tolerance of Lotus tenuis to long-term alkaline stress

Paz, R. C., Rocco, R., Jiménez-Bremont, J. F., Rodríguez‐Kessler, M., Becerra-Flora, A., Menéndez, A. B., & RUIZ, O. A. (2014) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2014.06.009 · Cited by 10

Genetically Engineered Food Crops to Abiotic Stress Tolerance

dos Reis, S. P., Marques, D. N., Barros, N. L. F., Costa, C. D. N. M., & de Souza, C. R. B. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-811519-0.00010-8 · Cited by 10

Research Advances on Tall Fescue Salt Tolerance: From Root Signaling to Molecular and Metabolic Adjustment

Amombo, E., Li, H., & Fu, J. (2017) · Journal of the American Society for Horticultural Science · doi:10.21273/jashs04120-17 · Cited by 10

Plant Tolerance to Environmental Stress: Translating Research from Lab to Land

Suprasanna, P., & Ghag, S. B. (2019) · Wiley eBooks · doi:10.1002/9781119463665.ch1 · Cited by 10

HOS15 impacts DIL9 protein stability during drought stress in Arabidopsis

Zareen, S., Ali, A. A., Park, J., Kang, S., Lee, I., Pardo, J. M., Yun, D., & Xu, Z. (2025) · New Phytologist · doi:10.1111/nph.20398 · Cited by 9

Small but Mighty: Role of miRNA in Abiotic Stress Responses and Crop Improvement

Chatterjee, D., patra, S., & Mandal, A. (2025) · Journal of Plant Growth Regulation · doi:10.1007/s00344-025-11627-5 · Cited by 9

Overexpression of the receptor-like kinase gene OsNRRB enhances drought-stress tolerance in rice

Zhang, Y., & Chen, L. (2017) · Euphytica · doi:10.1007/s10681-017-1854-z · Cited by 9

Comparative proteomics analysis reveals important drought responsive proteins in the leaves of a potato variety tolerant to drought stress

Zhang, L., Liu, Z., Qi, X., pan, F., Wei, Q., & Shi, Y. (2020) · Pakistan Journal of Botany · doi:10.30848/pjb2020-5(26 · Cited by 9

The Omics Strategies for Abiotic Stress Responses and Microbe-Mediated Mitigation in Plants

Maitra, S., Bhadra, P., Yadav, A. N., Palai, J. B., Jena, J., & Shankar, T. (2021) · Sustainable development and biodiversity · doi:10.1007/978-3-030-73507-4_12 · Cited by 9

Phenological and physio-biochemical variations in Salicornia brachiata Roxb. under different soil and water treatments (salinity)

Rathore, A. P., Kumari, A., Chaudhary, D. R., & Rathore, M. S. (2021) · Aquatic Botany · doi:10.1016/j.aquabot.2021.103429 · Cited by 9

Transcriptome sequencing and gene expression profiling of Pinus sibirica under different cold stresses

Wang, F., Chen, S., Cai, K., Lu, Z., Yang, Y., Tigabu, M., & Zhao, X. (2021) · Ikushugaku zasshi · doi:10.1270/jsbbs.21009 · Cited by 9

ASPTF: A computational tool to predict abiotic stress-responsive transcription factors in plants by employing machine learning algorithms

Pradhan, U. K., Mahapatra, A., Naha, S., Gupta, A., Parsad, R., Gahlaut, V., Rath, S. N., & Meher, P. K. (2024) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2024.130597 · Cited by 9

RhMED15a-like, a subunit of the Mediator complex, is involved in the drought stress response in Rosa hybrida

Xie, N., Shi, H., Shang, X., Zhao, Z., Fang, Y. M., Wu, H., Luo, P., Cui, Y., & Chen, W. (2024) · BMC Plant Biology · doi:10.1186/s12870-024-05059-8 · Cited by 9

Phenotypic and Genomic Analysis of Enterobacter ludwigii Strains: Insights into Mechanisms Enhancing Plant Growth Both Under Normal Conditions and in Response to Supplementation with Mineral Fertilizers and Exposure to Stress Factors

Sokolova, E. А., Mishukova, O. V., Khlistun, I. V., Tromenschleger, I. N., Chumanova, E. V., & Voronina, E. N. (2024) · Plants · doi:10.3390/plants13243551 · Cited by 9

Heterologous Expression of the DREB Transcription Factor AhDREB in Populus tomentosa Carrière Confers Tolerance to Salt without Growth Reduction under Greenhouse Conditions

Guo, Q., Lu, N., Sun, Y., Lv, W., Luo, Z., Zhang, H., Ji, Q., Yang, Q., Chen, S., Zhang, W., et al. (2019) · Forests · doi:10.3390/f10030214 · Cited by 9

Bioinformatics Resources for the Stress Biology of Plants

Kumar, S., & Shanker, A. (2018) · Springer eBooks · doi:10.1007/978-981-10-9029-5_14 · Cited by 9

Salt Stress and Plant Molecular Responses

Chaudhry, U. K., Gökçe, Z. N. Ö., & Gökçe, A. F. (2022) · IntechOpen eBooks · doi:10.5772/intechopen.101513 · Cited by 9

Role of microRNAs in Plant Adaptation to Environmental Stresses

Saini, A., Li, Y.-F., Jagadeeswaran, G., & Sunkar, R. (2012) · Signaling and communication in plants · doi:10.1007/978-3-642-27384-1_11 · Cited by 9

PHYSIOLOGICAL AND MOLECULAR MARKERS FOR SALT TOLERANCE IN FOUR BARLEY CULTIVARS

Abdel-Hamid, A. M. E. (2014) · European Scientific Journal ESJ · Cited by 9

Coping with Drought and Salinity Stresses: Role of Transcription Factors in Crop Improvement

Ribichich, K. F., Arce, A. L., & Chan, R. L. (2013) · Wiley eBooks · doi:10.1002/9783527675265.ch24 · Cited by 9

Barley: Omics Approaches for Abiotic Stress Tolerance

Pecchioni, N., Milc, J. A., Pasquariello, M., & Francia, E. (2012) · Wiley eBooks · doi:10.1002/9783527632930.ch34 · Cited by 9

Genome-wide identification and investigation of monosaccharide transporter gene family based on their evolution and expression analysis under abiotic stress and hormone treatments in maize (Zea mays L.)

Zhu, J., Li, T., Ma, J., Li, W., Zhang, H., Nadezhda, T., Zhu, Y., Dong, X., Li, C., & Fan, J. (2024) · BMC Plant Biology · doi:10.1186/s12870-024-05186-2 · Cited by 8

Integrating Multi-Omics Data for Plant Stress Response: Current Advances and Future Directions

Kajrolkar, A. (2025) · Premier Journal of Plant Biology · doi:10.70389/pjpb.100012 · Cited by 9

Comprehensive structural, evolutionary and functional analysis of superoxide dismutase gene family revealed critical role in salinity and drought stress responses in chickpea (Cicer arietinum L.)

Nehra, A., Kalwan, G., Taneja, D., Jangra, R., Joshi, K., Kumar, A., Jain, P. K., Nehra, K., Ansari, M. W., Singh, K., et al. (2025) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2025.110042 · Cited by 8

Arabidopsis thaliana: Model Plant for the Study of Abiotic Stress Responses

Raza, A., Charagh, S., Sadaqat, N., & Jin, W. (2020) · Springer eBooks · doi:10.1007/978-981-15-6345-4_3 · Cited by 25

Unraveling abiotic stress tolerance mechanisms – getting genomics going

Bohnert, H. J., Gong, Q., Li, P., & Ma, S. (2006) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2006.01.003 · Cited by 434

Emerging trends in the functional genomics of the abiotic stress response in crop plants

Vij, S., & Tyagi, A. K. (2007) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2007.00239.x · Cited by 265

Abiotic Stress Responses: Complexities in Gene Expression

Panjabi-Sabharwal, V., Karan, R., Khan, T., & Pareek, A. (2009) · Springer eBooks · doi:10.1007/978-90-481-3112-9_9 · Cited by 11

Genomic Approaches and Abiotic Stress Tolerance in Plants

Rashıd, B., Husnaın, T., & Riazuddin, S. A. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-800876-8.00001-1 · Cited by 14