Marı́lia Gaspar

1.3k total citations
35 papers, 903 citations indexed

About

Marı́lia Gaspar is a scholar working on Plant Science, Ecology, Evolution, Behavior and Systematics and Molecular Biology. According to data from OpenAlex, Marı́lia Gaspar has authored 35 papers receiving a total of 903 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Plant Science, 12 papers in Ecology, Evolution, Behavior and Systematics and 8 papers in Molecular Biology. Recurrent topics in Marı́lia Gaspar's work include Plant Stress Responses and Tolerance (13 papers), Plant nutrient uptake and metabolism (11 papers) and Fern and Epiphyte Biology (8 papers). Marı́lia Gaspar is often cited by papers focused on Plant Stress Responses and Tolerance (13 papers), Plant nutrient uptake and metabolism (11 papers) and Fern and Epiphyte Biology (8 papers). Marı́lia Gaspar collaborates with scholars based in Brazil, France and Germany. Marı́lia Gaspar's co-authors include Marcos Silveira Buckeridge, Marcos Pereira Marinho Aidar, Lourdes Isabel Velho do Amaral, Emerson Alves da Silva, Milton Yutaka Nishiyama, Alessandro Jaquiel Waclawovsky, Gláucia Mendes Souza, E. C. Ulian, Amanda P. De Souza and Renato Vicentini and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and New Phytologist.

In The Last Decade

Marı́lia Gaspar

33 papers receiving 878 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marı́lia Gaspar Brazil	14	748	237	114	104	82	35	903
Haruto Sasaki Japan	16	756 1.0×	233 1.0×	110 1.0×	52 0.5×	47 0.6×	31	962
Zaigham Shahzad France	17	1.4k 1.9×	404 1.7×	85 0.7×	47 0.5×	44 0.5×	26	1.6k
Zhouping Sun China	12	576 0.8×	171 0.7×	191 1.7×	51 0.5×	19 0.2×	46	710
Jinyoung Y. Barnaby United States	17	774 1.0×	226 1.0×	65 0.6×	60 0.6×	33 0.4×	36	959
A. San Bautista Spain	18	1.1k 1.5×	184 0.8×	74 0.6×	41 0.4×	59 0.7×	84	1.3k
Chunxia Zhang China	18	856 1.1×	286 1.2×	52 0.5×	34 0.3×	41 0.5×	51	1.0k
Anja van Dijken Netherlands	12	1.3k 1.7×	767 3.2×	72 0.6×	81 0.8×	36 0.4×	15	1.5k
Alexandre Grondin France	16	1.2k 1.6×	494 2.1×	128 1.1×	53 0.5×	103 1.3×	27	1.5k
Celso Jamil Marur Brazil	14	1.2k 1.6×	394 1.7×	77 0.7×	64 0.6×	51 0.6×	34	1.4k
Rabiye Terzi Türkiye	19	1.1k 1.4×	239 1.0×	103 0.9×	64 0.6×	25 0.3×	35	1.2k

Countries citing papers authored by Marı́lia Gaspar

Since Specialization

Citations

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

Fields of papers citing papers by Marı́lia Gaspar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marı́lia Gaspar. 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 Marı́lia Gaspar. The network helps show where Marı́lia Gaspar may publish in the future.

Co-authorship network of co-authors of Marı́lia Gaspar

This figure shows the co-authorship network connecting the top 25 collaborators of Marı́lia Gaspar. A scholar is included among the top collaborators of Marı́lia Gaspar 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 Marı́lia Gaspar. Marı́lia Gaspar is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Gaspar, Marı́lia, et al.. (2025). Surviving water scarcity: seasonal contrasts in drought and desiccation tolerance of co-occurring Barbacenia gentianoides and Vellozia caruncularis. Frontiers in Plant Science. 16. 1642013–1642013.

Oliveira, Halley Caixeta, et al.. (2024). Interplay between nitric oxide and inorganic nitrogen sources in root development and abiotic stress responses. Journal of Plant Physiology. 297. 154241–154241. 11 indexed citations

Hayashi, Adriana Hissae, et al.. (2024). Unveiling morphophysiological and metabolic adaptive strategies of the CAM epiphytic bromeliad Acanthostachys pitcairnioides to drought. Plant Physiology and Biochemistry. 216. 109076–109076. 1 indexed citations

Gomes, Diego Genuário, Artur Berbel Lírio Rondina, Rodrigo Mendes Pereira, et al.. (2024). Influence of light intensity on the responses of seedlings of neotropical tree species to nitrogen source. Environmental and Experimental Botany. 228. 106007–106007.

Carvalho, Victória, et al.. (2024). Succulence and aquaporin expression during drought and recovery in the CAM epiphytic bromeliad Acanthostachys strobilacea (Schult. & Schult.f.) Klotzsch. Environmental and Experimental Botany. 228. 105985–105985. 2 indexed citations

Gaspar, Marı́lia, et al.. (2024). Desiccation tolerance in the resurrection plant Barbacenia graminifolia involves changes in redox metabolism and carotenoid oxidation. Frontiers in Plant Science. 15. 1344820–1344820. 7 indexed citations

Rossi, Mônica Lanzoni, et al.. (2022). Water retention and metabolic changes improve desiccation tolerance in Barbacenia graminifolia (Velloziaceae). Physiologia Plantarum. 174(5). e13783–e13783. 11 indexed citations

Moreira, Keila Aparecida, Marcos Antônio de Morais, Rita de Cássia L. Figueiredo-Ribeiro, et al.. (2022). A comparative study between Fusarium solani and Neocosmospora vasinfecta revealed differential profile of fructooligosaccharide production. Folia Microbiologica. 67(6). 873–889. 3 indexed citations

Carvalho, Victória, et al.. (2020). Juvenile plants of an epiphytic bromeliad exhibit rapid changes in carbohydrate content and antioxidant capacity to cope with water withholding. Theoretical and Experimental Plant Physiology. 32(2). 89–98. 6 indexed citations

10.

Carvalho, Victória, Marı́lia Gaspar, & Catarina Carvalho Nievola. (2020). Short-term drought triggers defence mechanisms faster than ABA accumulation in the epiphytic bromeliad Acanthostachys strobilacea. Plant Physiology and Biochemistry. 160. 62–72. 8 indexed citations

11.

Cambuí, Camila Aguetoni, Nicolas Richet, Paulo Tamaso Mioto, et al.. (2019). Involvement of aquaporins on nitrogen-acquisition strategies of juvenile and adult plants of an epiphytic tank-forming bromeliad. Planta. 250(1). 319–332. 13 indexed citations

12.

Faria, Ana Maria Caetano, et al.. (2018). The increase of current atmospheric CO2 and temperature can benefit leaf gas exchanges, carbohydrate content and growth in C4 grass invaders of the Cerrado biome. Plant Physiology and Biochemistry. 127. 608–616. 16 indexed citations

13.

Santiago, Thaís Ribeiro, Wagner Rodrigo de Souza, Andrei Stecca Steindorff, et al.. (2018). Genome-wide identification, characterization and expression profile analysis of expansins gene family in sugarcane (Saccharum spp.). PLoS ONE. 13(1). e0191081–e0191081. 39 indexed citations

14.

Carvalho, Maria Ângela Machado de, et al.. (2015). Effects of different carbohydrate sources on fructan metabolism in plants of Chrysolaena obovata grown in vitro. Frontiers in Plant Science. 6. 681–681. 7 indexed citations

15.

Gaspar, Marı́lia, et al.. (2015). Endogenous hormone concentrations correlate with fructan metabolism throughout the phenological cycle inChrysolaena obovata. Annals of Botany. 115(7). 1163–1175. 19 indexed citations

16.

Grombone‐Guaratini, Maria Tereza, et al.. (2013). Atmospheric CO ₂ enrichment markedly increases photosynthesis and growth in a woody tropical bamboo from the Brazilian Atlantic Forest. New Zealand Journal of Botany. 51(4). 275–285. 18 indexed citations

17.

Cambuí, Camila Aguetoni, Marı́lia Gaspar, & Helenice Mercier. (2009). Detection of urease in the cell wall and membranes from leaf tissues of bromeliad species. Physiologia Plantarum. 136(1). 86–93. 24 indexed citations

18.

Lopez, Félicie, et al.. (2003). Diurnal Regulation of Water Transport and Aquaporin Gene Expression in Maize Roots: Contribution of PIP2 Proteins. Plant and Cell Physiology. 44(12). 1384–1395. 109 indexed citations

19.

Gaspar, Marı́lia, et al.. (2001). Transient variations of water transfer induced by HgCl 2 in excised roots of young maize plants: new data on the inhibition process. Australian Journal of Plant Physiology. 28(12). 1175–1186. 5 indexed citations

20.

Ottoboni, Laura M. M., et al.. (1997). Somaclonal-variation-induced aluminum-sensitive mutant from an aluminum-inbred maize tolerant line. Plant Cell Reports. 16(10). 686–691. 22 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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