Attilio Pane

1.7k total citations
26 papers, 1.2k citations indexed

About

Attilio Pane is a scholar working on Molecular Biology, Insect Science and Plant Science. According to data from OpenAlex, Attilio Pane has authored 26 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 9 papers in Insect Science and 9 papers in Plant Science. Recurrent topics in Attilio Pane's work include Chromosomal and Genetic Variations (7 papers), Insect symbiosis and bacterial influences (6 papers) and Trypanosoma species research and implications (6 papers). Attilio Pane is often cited by papers focused on Chromosomal and Genetic Variations (7 papers), Insect symbiosis and bacterial influences (6 papers) and Trypanosoma species research and implications (6 papers). Attilio Pane collaborates with scholars based in Brazil, United States and Italy. Attilio Pane's co-authors include Trudi Schüpbach, Giuseppe Saccone, Kristina Wehr, Nicola Iovino, Catello Polito, Ulrike Gaul, Marco Salvemini, Yu Chen, Lino C. Polito and Pasquale Delli Bovi and has published in prestigious journals such as SHILAP Revista de lepidopterología, The EMBO Journal and Development.

In The Last Decade

Attilio Pane

25 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Attilio Pane Brazil 13 848 443 378 287 117 26 1.2k
Keisuke Shoji Japan 15 665 0.8× 416 0.9× 348 0.9× 321 1.1× 93 0.8× 31 1.1k
Shinpei Kawaoka Japan 18 1.1k 1.3× 577 1.3× 377 1.0× 396 1.4× 97 0.8× 35 1.6k
Nicolas Nègre France 25 2.1k 2.5× 534 1.2× 285 0.8× 339 1.2× 89 0.8× 51 2.4k
Gilberto dos Santos United States 9 1.3k 1.5× 217 0.5× 154 0.4× 226 0.8× 87 0.7× 11 1.6k
Rolando Rivera‐Pomar Argentina 18 1.4k 1.6× 165 0.4× 257 0.7× 349 1.2× 80 0.7× 34 1.8k
Nicholas J. Brideau United States 7 1.2k 1.4× 244 0.6× 88 0.2× 410 1.4× 99 0.8× 7 1.5k
Renjie Jiao China 18 1.1k 1.2× 171 0.4× 153 0.4× 187 0.7× 76 0.6× 39 1.3k
Jun Duan China 16 854 1.0× 192 0.4× 519 1.4× 287 1.0× 92 0.8× 48 1.4k
Brian Oliver United States 12 811 1.0× 147 0.3× 101 0.3× 452 1.6× 130 1.1× 14 1.2k
Jeongsil Kim‐Ha South Korea 17 1.3k 1.6× 174 0.4× 150 0.4× 227 0.8× 83 0.7× 34 1.8k

Countries citing papers authored by Attilio Pane

Since Specialization
Citations

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

Fields of papers citing papers by Attilio Pane

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Attilio Pane

This figure shows the co-authorship network connecting the top 25 collaborators of Attilio Pane. A scholar is included among the top collaborators of Attilio Pane 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 Attilio Pane. Attilio Pane 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.
Ciabrelli, Filippo, et al.. (2024). Epigenetic inheritance and gene expression regulation in early Drosophila embryos. EMBO Reports. 25(10). 4131–4152. 5 indexed citations
2.
Cardoso, Maira Arruda, et al.. (2024). Embryonic piRNAs target horizontally transferred vertebrate transposons in assassin bugs. Frontiers in Cell and Developmental Biology. 12. 1481881–1481881. 2 indexed citations
3.
Miranda, Kildare, et al.. (2024). Knockdown of Sec16 causes early lethality and defective deposition of the protein Rp30 in the eggshell of the vector Rhodnius prolixus. Frontiers in Cell and Developmental Biology. 12. 1332894–1332894. 1 indexed citations
4.
Berni, Mateus, et al.. (2022). Atypical strategies for cuticle pigmentation in the blood-feeding hemipteran Rhodnius prolixus. Genetics. 221(2). 10 indexed citations
5.
Macharia, Lucy Wanjiku, Wanjiru Muriithi, Veronica Aran, et al.. (2021). The genotypic and phenotypic impact of hypoxia microenvironment on glioblastoma cell lines. BMC Cancer. 21(1). 1248–1248. 15 indexed citations
6.
Cardoso, Maira Arruda, et al.. (2021). Transovarial transmission of a core virome in the Chagas disease vector Rhodnius prolixus. PLoS Pathogens. 17(8). e1009780–e1009780. 10 indexed citations
7.
Cardoso, Maira Arruda, et al.. (2021). Analysis of ovarian transcriptomes reveals thousands of novel genes in the insect vector Rhodnius prolixus. Scientific Reports. 11(1). 1918–1918. 17 indexed citations
8.
Paes, Márcia Cristina, Felipe A. Dias, Ana Rossini, et al.. (2020). Gene expression profiling of Trypanosoma cruzi in the presence of heme points to glycosomal metabolic adaptation of epimastigotes inside the vector. PLoS neglected tropical diseases. 14(1). e0007945–e0007945. 7 indexed citations
9.
Berni, Mateus, et al.. (2018). Transcriptomic and functional analyses of the piRNA pathway in the Chagas disease vector Rhodnius prolixus. PLoS neglected tropical diseases. 12(10). e0006760–e0006760. 20 indexed citations
10.
Oti, Martin, Attilio Pane, & Michael Sammeth. (2017). Comparative Genomics in Drosophila. Methods in molecular biology. 1704. 433–450. 2 indexed citations
11.
12.
He, Bing, Amy A. Caudy, Lance Parsons, et al.. (2012). Mapping the pericentric heterochromatin by comparative genomic hybridization analysis and chromosome deletions in Drosophila melanogaster. Genome Research. 22(12). 2507–2519. 21 indexed citations
13.
Pane, Attilio, Peng Jiang, Dorothy Yanling Zhao, Mona Singh, & Trudi Schüpbach. (2011). The Cutoff protein regulates piRNA cluster expression and piRNA production in the Drosophila germline. The EMBO Journal. 30(22). 4601–4615. 94 indexed citations
14.
Iovino, Nicola, Attilio Pane, & Ulrike Gaul. (2009). miR-184 Has Multiple Roles in Drosophila Female Germline Development. Developmental Cell. 17(1). 123–133. 158 indexed citations
15.
Saccone, Giuseppe, Marco Salvemini, Attilio Pane, & Lino C. Polito. (2008). Masculinization of XX Drosophila transgenic flies expressing the Ceratitis capitata DoublesexM isoform. The International Journal of Developmental Biology. 52(8). 1051–1057. 41 indexed citations
16.
Pane, Attilio, Kristina Wehr, & Trudi Schüpbach. (2007). zucchini and squash Encode Two Putative Nucleases Required for rasiRNA Production in the Drosophila Germline. Developmental Cell. 12(6). 851–862. 249 indexed citations
17.
Chen, Yu, Attilio Pane, & Trudi Schüpbach. (2007). cutoff and aubergine Mutations Result in Retrotransposon Upregulation and Checkpoint Activation in Drosophila. Current Biology. 17(7). 637–642. 145 indexed citations
18.
Saccone, Giuseppe, Attilio Pane, & Lino C. Polito. (2002). Sex Determination in Flies, Fruitflies and Butterflies. Genetica. 116(1). 15–23. 96 indexed citations
19.
Pane, Attilio, Marco Salvemini, Pasquale Delli Bovi, Catello Polito, & Giuseppe Saccone. (2002). Thetransformergene inCeratitis capitataprovides a genetic basis for selecting and remembering the sexual fate. Development. 129(15). 3715–3725. 195 indexed citations
20.
Saccone, Giuseppe, Attilio Pane, Michele Santoro, et al.. (2000). Sex determination in Medfly: a molecular approach.. 491–496. 6 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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