Elisabetta Flex

4.0k total citations
39 papers, 1.3k citations indexed

About

Elisabetta Flex is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Elisabetta Flex has authored 39 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 8 papers in Genetics and 8 papers in Immunology. Recurrent topics in Elisabetta Flex's work include Protein Tyrosine Phosphatases (14 papers), RNA modifications and cancer (10 papers) and Galectins and Cancer Biology (8 papers). Elisabetta Flex is often cited by papers focused on Protein Tyrosine Phosphatases (14 papers), RNA modifications and cancer (10 papers) and Galectins and Cancer Biology (8 papers). Elisabetta Flex collaborates with scholars based in Italy, United States and Belgium. Elisabetta Flex's co-authors include Bruno Dallapiccola, Marco Tartaglia, Antonio Pizzuti, Simone Martinelli, Gianfranco Bocchinfuso, Antonio Palleschi, Lorenzo Stella, Giuseppe Zampino, Bruce D. Gelb and Tamara C. Petrucci and has published in prestigious journals such as Journal of Biological Chemistry, Blood and Diabetes.

In The Last Decade

Elisabetta Flex

39 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elisabetta Flex Italy	21	941	385	239	159	158	39	1.3k
Irene Franco Italy	16	682 0.7×	272 0.7×	169 0.7×	137 0.9×	230 1.5×	26	1.2k
Marion Jeanne United States	16	1.4k 1.5×	264 0.7×	242 1.0×	143 0.9×	335 2.1×	23	2.1k
Monika Goś Poland	19	769 0.8×	164 0.4×	331 1.4×	94 0.6×	134 0.8×	49	1.2k
Sherri L. Rankin United States	16	619 0.7×	644 1.7×	122 0.5×	99 0.6×	260 1.6×	25	1.4k
Christian Kosan Germany	21	616 0.7×	439 1.1×	297 1.2×	124 0.8×	260 1.6×	46	1.3k
Fred de Sauvage United States	5	821 0.9×	232 0.6×	80 0.3×	194 1.2×	245 1.6×	8	1.5k
Valeria Berno Italy	21	797 0.8×	155 0.4×	327 1.4×	94 0.6×	236 1.5×	33	1.4k
Alessandra Drusco United States	16	1.2k 1.3×	123 0.3×	139 0.6×	114 0.7×	139 0.9×	18	1.6k
Kumi Kawai Japan	22	1.0k 1.1×	175 0.5×	218 0.9×	179 1.1×	350 2.2×	36	1.8k
Caroline G. Humphries United States	13	1.2k 1.2×	318 0.8×	134 0.6×	155 1.0×	148 0.9×	17	1.7k

Countries citing papers authored by Elisabetta Flex

Since Specialization

Citations

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

Fields of papers citing papers by Elisabetta Flex

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisabetta Flex

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

All Works

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20 of 20 papers shown

Leoni, Chiara, Jacopo Gervasoni, Aniello Primiano, et al.. (2022). Metabolic profiling of Costello syndrome: Insights from a single-center cohort. European Journal of Medical Genetics. 65(3). 104439–104439. 5 indexed citations

Giuffrida, Maria Grazia, Marina Goldoni, Giovanna Carpentieri, et al.. (2022). 3′UTR Deletion of NONO Leads to Corpus Callosum Anomaly, Left Ventricular Non-Compaction and Ebstein’s Anomaly in a Male Fetus. Diagnostics. 12(10). 2354–2354. 3 indexed citations

Leoni, Chiara, Domenico M. Romeo, Roberta Onesimo, et al.. (2021). Musculo-skeletal phenotype of Costello syndrome and cardio-facio-cutaneous syndrome: insights on the functional assessment status. Orphanet Journal of Rare Diseases. 16(1). 43–43. 22 indexed citations

Leoni, Chiara, Roberta Onesimo, Valentina Giorgio, et al.. (2021). Bone tissue homeostasis and risk of fractures in Costello syndrome: A 4‐year follow‐up study. American Journal of Medical Genetics Part A. 188(2). 422–430. 6 indexed citations

Leoni, Chiara, Roberta Onesimo, Valentina Giorgio, et al.. (2021). Characterization of bone homeostasis in individuals affected by cardio‐facio‐cutaneous syndrome. American Journal of Medical Genetics Part A. 188(2). 414–421. 7 indexed citations

Flex, Elisabetta, Giovanna Carpentieri, Alessandro Bruselles, et al.. (2021). A Rare Case of Brachyolmia with Amelogenesis Imperfecta Caused by a New Pathogenic Splicing Variant in LTBP3. Genes. 12(9). 1406–1406. 3 indexed citations

Camero, Simona, Paola Pontecorvi, Simona Ceccarelli, et al.. (2021). DNMT3A and DNMT3B Targeting as an Effective Radiosensitizing Strategy in Embryonal Rhabdomyosarcoma. Cells. 10(11). 2956–2956. 21 indexed citations

Lorca, Rebeca, Luca Pannone, Elías Cuesta‐Llavona, et al.. (2020). Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2 ‐related disorders. Clinical Genetics. 99(3). 457–461. 3 indexed citations

Martinelli, Simone, Luca Pannone, Christina Lißewski, et al.. (2020). Pathogenic PTPN11 variants involving the poly‐glutamine Gln ²⁵⁵ ‐Gln ²⁵⁶ ‐Gln ²⁵⁷ stretch highlight the relevance of helix B in SHP2's functional regulation. Human Mutation. 41(6). 1171–1182. 1 indexed citations

10.

Ciolfi, Andrea, Erfan Aref‐Eshghi, Simone Pizzi, et al.. (2020). Frameshift mutations at the C-terminus of HIST1H1E result in a specific DNA hypomethylation signature. Clinical Epigenetics. 12(1). 7–7. 28 indexed citations

11.

Hornakova, Tekla, Sandrine Degryse, Olga Gielen, et al.. (2015). Distinct Acute Lymphoblastic Leukemia (ALL)-associated Janus Kinase 3 (JAK3) Mutants Exhibit Different Cytokine-Receptor Requirements and JAK Inhibitor Specificities. Journal of Biological Chemistry. 290(48). 29022–29034. 37 indexed citations

12.

Silengo, Margherita, Claudio Defilippi, Elga Fabia Belligni, et al.. (2013). Progressive extreme heterotopic calcification. American Journal of Medical Genetics Part A. 161(7). 1706–1713. 3 indexed citations

13.

Ferrero, Giovanni Battista, Gabriele Picco, Giuseppina Baldassarre, et al.. (2012). Transcriptional hallmarks of noonan syndrome and noonan‐like syndrome with loose anagen hair. Human Mutation. 33(4). 703–709. 10 indexed citations

14.

Martinelli, Simone, Aurelio Pio Nardozza, Paola Torreri, et al.. (2012). Counteracting Effects Operating on Src Homology 2 Domain-containing Protein-tyrosine Phosphatase 2 (SHP2) Function Drive Selection of the Recurrent Y62D and Y63C Substitutions in Noonan Syndrome*. Journal of Biological Chemistry. 287(32). 27066–27077. 26 indexed citations

15.

Hornakova, Tekla, Judith Staerk, Yohan Royer, et al.. (2009). Acute Lymphoblastic Leukemia-associated JAK1 Mutants Activate the Janus Kinase/STAT Pathway via Interleukin-9 Receptor α Homodimers. Journal of Biological Chemistry. 284(11). 6773–6781. 54 indexed citations

16.

Torrente, Isabella, Salvatore De Cosmo, Valentina Guida, et al.. (2007). Interaction of DIO2 T92A and PPARγ2 P12A Polymorphisms in the Modulation of Metabolic Syndrome. Obesity. 15(12). 2889–2895. 22 indexed citations

17.

Flex, Elisabetta, Antonio Pizzuti, Carlo Di Bonaventura, et al.. (2005). LGI1 gene mutation screening in sporadic partial epilepsy with auditory features. Journal of Neurology. 252(1). 62–66. 11 indexed citations

18.

Flex, Elisabetta, et al.. (2003). Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12. Journal of Medical Genetics. 40(4). 278–281. 8 indexed citations

19.

Mangino, Massimo, Elisabetta Flex, M. Cristina Digilio, Aldo Giannotti, & Bruno Dallapiccola. (2002). Identification of a novel NOG gene mutation (P35S) in an Italian family with symphalangism. Human Mutation. 19(3). 308–308. 30 indexed citations

20.

Mangino, Massimo, Elisabetta Flex, Francesca Capon, et al.. (2001). Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26. European Journal of Human Genetics. 9(9). 667–671. 10 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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