Bartolomeo Augello

1.9k total citations
33 papers, 882 citations indexed

About

Bartolomeo Augello is a scholar working on Molecular Biology, Genetics and Epidemiology. According to data from OpenAlex, Bartolomeo Augello has authored 33 papers receiving a total of 882 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Genetics and 5 papers in Epidemiology. Recurrent topics in Bartolomeo Augello's work include Genomics and Rare Diseases (5 papers), Williams Syndrome Research (5 papers) and Epigenetics and DNA Methylation (4 papers). Bartolomeo Augello is often cited by papers focused on Genomics and Rare Diseases (5 papers), Williams Syndrome Research (5 papers) and Epigenetics and DNA Methylation (4 papers). Bartolomeo Augello collaborates with scholars based in Italy, Switzerland and United Kingdom. Bartolomeo Augello's co-authors include Giuseppe Merla, Lucia Micale, Carmela Fusco, Alexandre Reymond, Barbara Mandriani, Maria Teresa Pellico, Leopoldo Zelante, Angelo Andriulli, Massimo Carella and Dario Cocciadiferro and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Bartolomeo Augello

33 papers receiving 877 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bartolomeo Augello Italy 18 439 199 184 134 101 33 882
Haruna Takeda Japan 13 351 0.8× 93 0.5× 142 0.8× 84 0.6× 22 0.2× 28 968
Bruno Dipasquale United States 13 429 1.0× 39 0.2× 213 1.2× 132 1.0× 96 1.0× 17 1.1k
Isabelle Gloaguen Italy 13 281 0.6× 80 0.4× 246 1.3× 67 0.5× 45 0.4× 18 747
Frank Blaeser United States 10 435 1.0× 187 0.9× 714 3.9× 42 0.3× 56 0.6× 11 1.4k
Tomoya Ozaki Japan 16 320 0.7× 116 0.6× 98 0.5× 38 0.3× 16 0.2× 42 828
Susumu Hirabayashi Japan 19 640 1.5× 86 0.4× 135 0.7× 53 0.4× 15 0.1× 27 1.1k
Rehae Miller United States 10 325 0.7× 86 0.4× 76 0.4× 35 0.3× 60 0.6× 14 712
Heather A. Iocca United States 9 671 1.5× 42 0.2× 403 2.2× 56 0.4× 47 0.5× 20 973
Cédric Howald Switzerland 12 488 1.1× 168 0.8× 86 0.5× 24 0.2× 84 0.8× 13 776
Rita Lopes United Kingdom 9 622 1.4× 39 0.2× 97 0.5× 63 0.5× 46 0.5× 11 860

Countries citing papers authored by Bartolomeo Augello

Since Specialization
Citations

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

Fields of papers citing papers by Bartolomeo Augello

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bartolomeo Augello

This figure shows the co-authorship network connecting the top 25 collaborators of Bartolomeo Augello. A scholar is included among the top collaborators of Bartolomeo Augello 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 Bartolomeo Augello. Bartolomeo Augello 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.
Savino, Michelangelo, Bartolomeo Augello, Giuseppe Merla, et al.. (2022). Circadian Genes Expression Patterns in Disorders Due to Enzyme Deficiencies in the Heme Biosynthetic Pathway. Biomedicines. 10(12). 3198–3198. 3 indexed citations
2.
Fusco, Carmela, Bartolomeo Augello, Francesca Boccafoschi, et al.. (2020). Pro-Fibrotic Phenotype in a Patient with Segmental Stiff Skin Syndrome via TGF-β Signaling Overactivation. International Journal of Molecular Sciences. 21(14). 5141–5141. 12 indexed citations
3.
Micale, Lucia, Vito Guarnieri, Bartolomeo Augello, et al.. (2019). Novel TNXB Variants in Two Italian Patients with Classical-Like Ehlers-Danlos Syndrome. Genes. 10(12). 967–967. 9 indexed citations
4.
Lepri, Francesca Romana, Dario Cocciadiferro, Bartolomeo Augello, et al.. (2017). Clinical and Neurobehavioral Features of Three Novel Kabuki Syndrome Patients with Mosaic KMT2D Mutations and a Review of Literature. International Journal of Molecular Sciences. 19(1). 82–82. 17 indexed citations
5.
Scrima, Rosella, Olga Cela, Giuseppe Merla, et al.. (2016). Clock-genes and mitochondrial respiratory activity: Evidence of a reciprocal interplay. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1857(8). 1344–1351. 43 indexed citations
6.
Micale, Lucia, Carmela Fusco, Andrea Fontana, et al.. (2015). TRIM8 downregulation in glioma affects cell proliferation and it is associated with patients survival. BMC Cancer. 15(1). 470–470. 42 indexed citations
7.
Fusco, Carmela, Lucia Micale, Maria Teresa Pellico, et al.. (2015). Genomic and Genetic Disorders Biobank. SHILAP Revista de lepidopterología. 2. 1 indexed citations
8.
Prontera, Paolo, Valerio Napolioni, Daniela Rogaia, et al.. (2014). DPP6 gene disruption in a family with Gilles de la Tourette syndrome. Neurogenetics. 15(4). 237–242. 22 indexed citations
9.
Augello, Bartolomeo, et al.. (2013). A 1.3-Mb 7q11.23 Atypical Deletion Identified in a Cohort of Patients with Williams-Beuren Syndrome. Molecular Syndromology. 4(3). 143–147. 9 indexed citations
10.
Latiano, Anna, Orazio Palmieri, Luca Pastorelli, et al.. (2013). Associations between Genetic Polymorphisms in IL-33, IL1R1 and Risk for Inflammatory Bowel Disease. PLoS ONE. 8(4). e62144–e62144. 76 indexed citations
11.
Fusco, Carmela, Lucia Micale, Bartolomeo Augello, et al.. (2013). HDAC6 mediates the acetylation of TRIM50. Cellular Signalling. 26(2). 363–369. 14 indexed citations
12.
Ratbi, Ilham, Lucia Micale, Bartolomeo Augello, et al.. (2013). Report of the First Clinical Case of a Moroccan Kabuki Patient with a Novel <b><i>MLL2</i></b> Mutation. Molecular Syndromology. 4(3). 152–156. 2 indexed citations
13.
Fusco, Carmela, Lucia Micale, Bartolomeo Augello, et al.. (2013). Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traits. European Journal of Human Genetics. 22(1). 64–70. 47 indexed citations
14.
Micale, Lucia, Maria Nicla Loviglio, Marta Manzoni, et al.. (2012). A Fish-Specific Transposable Element Shapes the Repertoire of p53 Target Genes in Zebrafish. PLoS ONE. 7(10). e46642–e46642. 16 indexed citations
15.
Priolo, Manuela, Lucia Micale, Bartolomeo Augello, et al.. (2012). Absence of deletion and duplication of MLL2 and KDM6A genes in a large cohort of patients with Kabuki syndrome. Molecular Genetics and Metabolism. 107(3). 627–629. 18 indexed citations
16.
Caratozzolo, Mariano Francesco, Lucia Micale, Carmela Fusco, et al.. (2012). TRIM8 modulates p53 activity to dictate cell cycle arrest. Cell Cycle. 11(3). 511–523. 55 indexed citations
17.
Micale, Lucia, Bartolomeo Augello, Carmela Fusco, et al.. (2009). GPR143 Mutational Analysis in Two Italian Families with X-Linked Ocular Albinism. Genetic Testing and Molecular Biomarkers. 13(4). 527–531. 1 indexed citations
18.
Bisceglia, Luigi, Lucia Fischetti, Patrizia De Bonis, et al.. (2009). Large rearrangements detected by MLPA, point mutations, and survey of the frequency of mutations within the SLC3A1 and SLC7A9 genes in a cohort of 172 cystinuric Italian patients. Molecular Genetics and Metabolism. 99(1). 42–52. 28 indexed citations
19.
Ferrero, Giovanni Battista, Cédric Howald, Lucia Micale, et al.. (2009). An atypical 7q11.23 deletion in a normal IQ Williams–Beuren syndrome patient. European Journal of Human Genetics. 18(1). 33–38. 48 indexed citations
20.
Micale, Lucia, Carmela Fusco, Bartolomeo Augello, et al.. (2008). Williams–Beuren syndrome TRIM50 encodes an E3 ubiquitin ligase. European Journal of Human Genetics. 16(9). 1038–1049. 43 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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