Aliana Egeo

1.1k total citations
15 papers, 842 citations indexed

About

Aliana Egeo is a scholar working on Molecular Biology, Oncology and Genetics. According to data from OpenAlex, Aliana Egeo has authored 15 papers receiving a total of 842 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 5 papers in Oncology and 4 papers in Genetics. Recurrent topics in Aliana Egeo's work include Congenital heart defects research (6 papers), Peptidase Inhibition and Analysis (5 papers) and Glycosylation and Glycoproteins Research (3 papers). Aliana Egeo is often cited by papers focused on Congenital heart defects research (6 papers), Peptidase Inhibition and Analysis (5 papers) and Glycosylation and Glycoproteins Research (3 papers). Aliana Egeo collaborates with scholars based in Italy, Spain and United Kingdom. Aliana Egeo's co-authors include Paolo Scartezzini, Michela Mazzocco, Federica Sotgia, Michael P. Lisanti, Paolo Broda, F. Dagna Bricarelli, M. Bado, Federico Zara, Carlo Minetti and G Cordone and has published in prestigious journals such as Nature Genetics, Biochemical and Biophysical Research Communications and Gene.

In The Last Decade

Aliana Egeo

15 papers receiving 827 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Aliana Egeo Italy 12 691 319 139 101 84 15 842
Norio Takizawa United States 13 599 0.9× 297 0.9× 142 1.0× 44 0.4× 48 0.6× 20 813
Jaclyn P. Kerr United States 15 615 0.9× 211 0.7× 132 0.9× 70 0.7× 103 1.2× 19 783
Sophie Currier United States 7 682 1.0× 122 0.4× 79 0.6× 156 1.5× 141 1.7× 7 811
Barbara Lucke Germany 9 649 0.9× 163 0.5× 48 0.3× 95 0.9× 102 1.2× 10 875
Suzanne Lillis United Kingdom 13 609 0.9× 143 0.4× 388 2.8× 105 1.0× 138 1.6× 21 829
Alice Steinbrecher Germany 5 638 0.9× 118 0.4× 83 0.6× 93 0.9× 125 1.5× 7 725
Kiyomasa Nishii Japan 13 618 0.9× 83 0.3× 225 1.6× 90 0.9× 56 0.7× 18 791
Eric Fabbrizio France 17 1.1k 1.6× 105 0.3× 65 0.5× 97 1.0× 78 0.9× 33 1.2k

Countries citing papers authored by Aliana Egeo

Since Specialization
Citations

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

Fields of papers citing papers by Aliana Egeo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aliana Egeo

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

All Works

15 of 15 papers shown
1.
Platonova, Natalia, Gloria Bertoli, Vasco Meneghini, et al.. (2007). TBX3, the gene mutated in ulnar-mammary syndrome, promotes growth of mammary epithelial cells via repression of p19ARF, independently of p53. Cell and Tissue Research. 328(2). 301–316. 26 indexed citations
2.
Meneghini, Vasco, Sylvie Odent, Natalia Platonova, Aliana Egeo, & Giorgio R. Merlo. (2005). Novel TBX3 mutation data in families with Ulnar–Mammary syndrome indicate a genotype–phenotype relationship: mutations that do not disrupt the T-domain are associated with less severe limb defects. European Journal of Medical Genetics. 49(2). 151–158. 52 indexed citations
3.
Levi, Giovanni, Adam C. Puché, Stefano Mantero, et al.. (2003). The Dlx5 homeodomain gene is essential for olfactory development and connectivity in the mouse. Molecular and Cellular Neuroscience. 22(4). 530–543. 61 indexed citations
4.
Vidal, José, Salvador Bergoñón, Aliana Egeo, et al.. (2002). Characterisation and expression analysis of the WDR9 gene, located in the Down critical region-2 of the human chromosome 21. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1577(3). 377–383. 11 indexed citations
5.
6.
Mazzocco, Michela, Patrizio Arrigo, Aliana Egeo, et al.. (2001). A Novel Human Homologue of the SH3BGR Gene Encodes a Small Protein Similar to Glutaredoxin 1 of Escherichia coli. Biochemical and Biophysical Research Communications. 285(2). 540–545. 17 indexed citations
7.
Egeo, Aliana, Raffaella Di Lisi, Claudia Sandri, et al.. (2000). Developmental expression of the SH3BGR gene, mapping to the Down syndrome heart critical region. Mechanisms of Development. 90(2). 313–316. 24 indexed citations
8.
Vidal, José, et al.. (1998). Identification and Characterization of a New Gene from Human Chromosome 21 between Markers D21S343 and D21S268 Encoding a Leucine-Rich Protein. Biochemical and Biophysical Research Communications. 250(3). 547–554. 12 indexed citations
9.
Egeo, Aliana, Michela Mazzocco, Patrizio Arrigo, et al.. (1998). Identification and Characterization of a New Human Gene Encoding a Small Protein with High Homology to the Proline-Rich Region of the SH3BGR Gene. Biochemical and Biophysical Research Communications. 247(2). 302–306. 26 indexed citations
10.
Egeo, Aliana, Michela Mazzocco, Federica Sotgia, et al.. (1998). Identification and characterization of a new human cDNA from chromosome 21q22.3 encoding a basic nuclear protein. Human Genetics. 102(3). 289–293. 26 indexed citations
11.
Vidal, José, Salvador Bergoñón, Jürgen Groet, et al.. (1998). High Resolution Physical Mapping and Identification of Transcribed Sequences in the Down Syndrome Region-2. Biochemical and Biophysical Research Communications. 243(2). 572–578. 8 indexed citations
12.
Egeo, Aliana, Paolo Scartezzini, Giancarlo Rappazzo, et al.. (1998). Human NRD Convertase: A Highly Conserved Metalloendopeptidase Expressed at Specific Sites during Development and in Adult Tissues. Genomics. 47(2). 238–245. 29 indexed citations
13.
Minetti, Carlo, Federica Sotgia, Claudio Bruno, et al.. (1998). Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy. Nature Genetics. 18(4). 365–368. 456 indexed citations
14.
Scartezzini, Paolo, Aliana Egeo, Stefano Colella, et al.. (1997). Cloning a new human gene from chromosome 21q22.3 encoding a glutamic acid-rich protein expressed in heart and skeletal muscle. Human Genetics. 99(3). 387–392. 32 indexed citations
15.
Vidal, José, Salvador Bergoñón, Paolo Scartezzini, et al.. (1997). High-Resolution Physical Map and Identification of Potentially Regulatory Sequences of the Human SH3BGR Located in the Down Syndrome Chromosomal Region. Biochemical and Biophysical Research Communications. 241(2). 321–326. 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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