Leonor Morais–Cecílio

1.1k total citations
40 papers, 703 citations indexed

About

Leonor Morais–Cecílio is a scholar working on Plant Science, Molecular Biology and Genetics. According to data from OpenAlex, Leonor Morais–Cecílio has authored 40 papers receiving a total of 703 indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Plant Science, 28 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Leonor Morais–Cecílio's work include Chromosomal and Genetic Variations (18 papers), Plant Disease Resistance and Genetics (13 papers) and Plant Molecular Biology Research (11 papers). Leonor Morais–Cecílio is often cited by papers focused on Chromosomal and Genetic Variations (18 papers), Plant Disease Resistance and Genetics (13 papers) and Plant Molecular Biology Research (11 papers). Leonor Morais–Cecílio collaborates with scholars based in Portugal, United Kingdom and United States. Leonor Morais–Cecílio's co-authors include Wanda Viegas, Margarida Delgado, Teresa Ribeiro, Ana D. Caperta, Robert N. Jones, Margarida Rocheta, Nuno Neves, Maria Manuela Ribeiro Costa, Álvaro Antônio Alencar de Queiroz and T. Mello-Sampayo and has published in prestigious journals such as PLoS ONE, The Plant Cell and Journal of Cell Science.

In The Last Decade

Leonor Morais–Cecílio

40 papers receiving 682 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Leonor Morais–Cecílio Portugal 18 613 404 83 61 42 40 703
Andrew Spriggs Australia 11 824 1.3× 423 1.0× 98 1.2× 161 2.6× 9 0.2× 14 976
Satya Chintamanani United States 12 930 1.5× 396 1.0× 108 1.3× 54 0.9× 59 1.4× 13 1.0k
B. Worland United Kingdom 15 747 1.2× 750 1.9× 54 0.7× 49 0.8× 22 0.5× 18 955
Guihua Jin China 14 376 0.6× 278 0.7× 74 0.9× 129 2.1× 63 1.5× 24 645
Michael Schwall Germany 6 415 0.7× 167 0.4× 105 1.3× 55 0.9× 27 0.6× 7 505
Alexandra B. Rebocho United Kingdom 10 524 0.9× 519 1.3× 59 0.7× 123 2.0× 15 0.4× 10 698
Jugpreet Singh United States 16 617 1.0× 161 0.4× 156 1.9× 57 0.9× 96 2.3× 31 708
Timothy Kelliher United States 13 1.2k 2.0× 1.1k 2.8× 158 1.9× 131 2.1× 23 0.5× 16 1.4k
Luís M. Muñiz Spain 13 593 1.0× 449 1.1× 100 1.2× 27 0.4× 27 0.6× 20 732
Nathalie Ladouce France 13 402 0.7× 451 1.1× 33 0.4× 20 0.3× 50 1.2× 17 632

Countries citing papers authored by Leonor Morais–Cecílio

Since Specialization
Citations

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

Fields of papers citing papers by Leonor Morais–Cecílio

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Leonor Morais–Cecílio. 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 Leonor Morais–Cecílio. The network helps show where Leonor Morais–Cecílio may publish in the future.

Co-authorship network of co-authors of Leonor Morais–Cecílio

This figure shows the co-authorship network connecting the top 25 collaborators of Leonor Morais–Cecílio. A scholar is included among the top collaborators of Leonor Morais–Cecílio 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 Leonor Morais–Cecílio. Leonor Morais–Cecílio 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.
Ribeiro, Teresa, et al.. (2024). Genetic and epigenetic control of dormancy transitions throughout the year in the monoecious cork oak. Physiologia Plantarum. 176(6). e14620–e14620. 2 indexed citations
2.
Oliveira, Helena, João Loureiro, Sílvia Castro, et al.. (2023). Contribution to the knowledge of genome size variation in Calendula L. (Asteraceae) with special focus on the SW Mediterranean region. Plant Biosystems - An International Journal Dealing with all Aspects of Plant Biology. 157(2). 312–324. 2 indexed citations
3.
Talhinhas, Pedro, S. C. C. de H. Tavares, Teresa Ribeiro, et al.. (2023). Diploid Nuclei Occur throughout the Life Cycles of Pucciniales Fungi. Microbiology Spectrum. 11(4). e0153223–e0153223. 4 indexed citations
4.
5.
Graça, José, et al.. (2022). Epigenetics at the crossroads of secondary growth regulation. Frontiers in Plant Science. 13. 970342–970342. 4 indexed citations
6.
Graça, José, et al.. (2021). Cork cells in cork oak periderms undergo programmed cell death and proanthocyanidin deposition. Tree Physiology. 41(9). 1701–1713. 4 indexed citations
7.
Morais–Cecílio, Leonor, et al.. (2020). Genome-Wide Identification of Epigenetic Regulators in Quercus suber L.. International Journal of Molecular Sciences. 21(11). 3783–3783. 17 indexed citations
8.
Graça, José, et al.. (2018). Cork Oak Young and Traumatic Periderms Show PCD Typical Chromatin Patterns but Different Chromatin-Modifying Genes Expression. Frontiers in Plant Science. 9. 1194–1194. 20 indexed citations
9.
Barbosa, Pedro, Ana Usié, A. M. Ramos, et al.. (2018). ChIP-Seq reveals that QsMYB1 directly targets genes involved in lignin and suberin biosynthesis pathways in cork oak (Quercus suber). BMC Plant Biology. 18(1). 198–198. 38 indexed citations
10.
Barros, Pedro M., Augusta Costa, Elsa Gonçalves, et al.. (2017). Differential DNA Methylation Patterns Are Related to Phellogen Origin and Quality of Quercus suber Cork. PLoS ONE. 12(1). e0169018–e0169018. 20 indexed citations
11.
Carvalho, Ana, et al.. (2016). Oak ribosomal DNA: characterization by FISH and polymorphism assessed by IGS PCR–RFLP. Österreichische Botanische Zeitschrift. 302(5). 527–544. 6 indexed citations
12.
Rocheta, Margarida, Isabel Amorim, Teresa Ribeiro, et al.. (2014). Comparative transcriptomic analysis of male and female flowers of monoecious Quercus suber. Frontiers in Plant Science. 5. 599–599. 39 indexed citations
13.
Rocheta, Margarida, Luísa C. Carvalho, Wanda Viegas, & Leonor Morais–Cecílio. (2012). Corky, a gypsy-like retrotransposon is differentially transcribed in Quercus suber tissues. BMC Research Notes. 5(1). 432–432. 11 indexed citations
14.
Ribeiro, Teresa, et al.. (2012). Genomic organization and dynamics of repetitive DNA sequences in representatives of three Fagaceae genera. Genome. 55(5). 348–359. 5 indexed citations
15.
Ribeiro, Teresa, et al.. (2010). Presence ofenv-like sequences inQuercus suber retrotransposons. Journal of Applied Genetics. 51(4). 461–467. 6 indexed citations
16.
Delgado, Margarida, Teresa Ribeiro, Pedro Costa‐Nunes, et al.. (2007). Transcriptionally Active Heterochromatin in Rye B Chromosomes. The Plant Cell. 19(6). 1738–1749. 68 indexed citations
17.
Castilho, Alexandra, et al.. (2005). Genomic characterization and physical mapping of two fucosyltransferase genes inMedicago truncatula. Genome. 48(1). 168–176. 3 indexed citations
18.
Delgado, Margarida, Ana D. Caperta, Teresa Ribeiro, et al.. (2004). Different numbers of rye B chromosomes induce identical compaction changes in distinct A chromosome domains. Cytogenetic and Genome Research. 106(2-4). 320–324. 10 indexed citations
19.
Morais–Cecílio, Leonor, Margarida Delgado, Robert N. Jones, & Wanda Viegas. (2000). Modification of wheat rDNA loci by rye B chromosomes: a chromatin organization model. Chromosome Research. 8(4). 341–351. 24 indexed citations
20.
Morais–Cecílio, Leonor, Margarida Delgado, Robert N. Jones, & Wanda Viegas. (1997). Interphase arrangement of rye B chromosomes in rye and wheat. Chromosome Research. 5(3). 177–181. 9 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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