Michela Faleschini

653 total citations
20 papers, 293 citations indexed

About

Michela Faleschini is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Michela Faleschini has authored 20 papers receiving a total of 293 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Hematology, 7 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Michela Faleschini's work include Platelet Disorders and Treatments (9 papers), DNA Repair Mechanisms (5 papers) and Blood disorders and treatments (5 papers). Michela Faleschini is often cited by papers focused on Platelet Disorders and Treatments (9 papers), DNA Repair Mechanisms (5 papers) and Blood disorders and treatments (5 papers). Michela Faleschini collaborates with scholars based in Italy, United States and Australia. Michela Faleschini's co-authors include Anna Savoia, Roberta Bottega, Valeria Capaci, Libero Santarpia, Giannino Del Sal, Vera Cappelletti, Silvano Piazza, Reuven Agami, Federico Zampa and Maria Grazia Daidone and has published in prestigious journals such as Blood, Scientific Reports and Journal of Cellular Physiology.

In The Last Decade

Michela Faleschini

19 papers receiving 292 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michela Faleschini Italy 7 149 107 85 48 39 20 293
Isabel Moreno–Miralles United States 9 200 1.3× 92 0.9× 35 0.4× 24 0.5× 45 1.2× 9 291
Milica Vukovic United Kingdom 8 249 1.7× 174 1.6× 130 1.5× 19 0.4× 61 1.6× 10 433
Benjamin T. Goetz United States 9 184 1.2× 61 0.6× 33 0.4× 20 0.4× 60 1.5× 12 300
Muhammad Zaki Hidayatullah Fadlullah United Kingdom 11 232 1.6× 82 0.8× 51 0.6× 19 0.4× 80 2.1× 26 388
Jean‐Loup Huret France 6 165 1.1× 99 0.9× 83 1.0× 46 1.0× 40 1.0× 13 348
Valentina Fragliasso Italy 9 176 1.2× 45 0.4× 46 0.5× 19 0.4× 41 1.1× 25 295
Chaitanya R. Badwe United States 5 177 1.2× 85 0.8× 36 0.4× 17 0.4× 70 1.8× 9 276
Matthew Curran United States 5 192 1.3× 98 0.9× 42 0.5× 20 0.4× 68 1.7× 6 309
Simon Renders Germany 9 121 0.8× 126 1.2× 38 0.4× 18 0.4× 113 2.9× 17 295
Kelly R. Ostler United States 8 304 2.0× 115 1.1× 59 0.7× 55 1.1× 41 1.1× 9 369

Countries citing papers authored by Michela Faleschini

Since Specialization
Citations

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

Fields of papers citing papers by Michela Faleschini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michela Faleschini

This figure shows the co-authorship network connecting the top 25 collaborators of Michela Faleschini. A scholar is included among the top collaborators of Michela Faleschini 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 Michela Faleschini. Michela Faleschini 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.
2.
Marzollo, Antonio, Stefania Zampieri, Serena Barozzi, et al.. (2024). Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene. British Journal of Haematology. 205(1). 306–315. 6 indexed citations
3.
Barozzi, Serena, Caterina Marconi, Roberta Bottega, et al.. (2024). ACTN1‐related thrombocytopenia: Homozygosity for an ACTN1 variant results in a more severe phenotype. British Journal of Haematology. 204(6). 2453–2457. 2 indexed citations
4.
Marzollo, Antonio, Roberta Bottega, Valeria Capaci, et al.. (2023). A novel mutation in MECOM affects MPL regulation in vitro and results in thrombocytopenia and bone marrow failure. British Journal of Haematology. 203(5). 852–859. 2 indexed citations
5.
Faleschini, Michela, et al.. (2023). Phenotype reversion as “natural gene therapy” in Fanconi anemia by a gene conversion event. Frontiers in Genetics. 14. 1240758–1240758.
6.
Faleschini, Michela, Enrico Cappelli, Fabio Corsolini, et al.. (2023). A self-repair history: compensatory effect of a de novo variant on the FANCA c.2778+83C>G splicing mutation. Frontiers in Genetics. 14. 1209138–1209138. 2 indexed citations
7.
Faleschini, Michela, Caterina Alfano, Roberta Bottega, et al.. (2022). ETV6-related thrombocytopenia: dominant negative effect of mutations as common pathogenic mechanism. Haematologica. 107(9). 2249–2254. 6 indexed citations
8.
Marconi, Caterina, Alessandro Pecci, Flavia Palombo, et al.. (2022). Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workup. Haematologica. 108(7). 1909–1919. 1 indexed citations
9.
10.
Faleschini, Michela, Fabio Sirchia, Flavio Faletra, et al.. (2022). Things come in threes: A new complex allele and a novel deletion within the CFTR gene complicate an accurate diagnosis of cystic fibrosis. Molecular Genetics & Genomic Medicine. 10(6). e1926–e1926. 2 indexed citations
11.
Faleschini, Michela, Marie‐Christine Morel‐Kopp, Caterina Marconi, et al.. (2021). Dysregulation of oncogenic factors by GFI1B p32: investigation of a novel <I>GFI1B</I> germline mutation. Haematologica. 107(1). 260–267. 1 indexed citations
12.
Bottega, Roberta, Silvia Ravera, Luisa M. R. Napolitano, et al.. (2021). Genomic integrity and mitochondrial metabolism defects in Warsaw syndrome cells: a comparison with Fanconi anemia. Journal of Cellular Physiology. 236(8). 5664–5675. 3 indexed citations
13.
Marconi, Caterina, Christian A. Di Buduo, Serena Barozzi, et al.. (2018). Loss-of-function mutations in PTPRJ cause a new form of inherited thrombocytopenia. Blood. 133(12). 1346–1357. 37 indexed citations
14.
Faleschini, Michela, Federica Melazzini, Caterina Marconi, et al.. (2018). ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia. British Journal of Haematology. 183(2). 276–288. 16 indexed citations
15.
Bottega, Roberta, Elena Nicchia, Enrico Cappelli, et al.. (2017). Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia. Haematologica. 103(3). 417–426. 27 indexed citations
16.
Ravera, Silvia, Carlo Dufour, Simone Cesaro, et al.. (2016). Evaluation of energy metabolism and calcium homeostasis in cells affected by Shwachman-Diamond syndrome. Scientific Reports. 6(1). 25441–25441. 38 indexed citations
17.
Dufour, Carlo, Silvia Ravera, Simone Cesaro, et al.. (2015). Shwachman-Diamond Syndrome: Energetic Stress, Calcium Homeostasis and mTOR Pathway. Blood. 126(23). 2410–2410. 1 indexed citations
18.
Nicchia, Elena, Francesco Benedicenti, Daniela De Rocco, et al.. (2015). Clinical aspects of Fanconi anemia individuals with the same mutation of FANCF identified by next generation sequencing. Birth Defects Research Part A Clinical and Molecular Teratology. 103(12). 1003–1010. 5 indexed citations
19.
Bottega, Roberta, Caterina Marconi, Michela Faleschini, et al.. (2014). ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization. Blood. 125(5). 869–872. 40 indexed citations
20.
Bisso, Andrea, Michela Faleschini, Federico Zampa, et al.. (2013). Oncogenic miR-181a/b affect the DNA damage response in aggressive breast cancer. Cell Cycle. 12(11). 1679–1687. 96 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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