Chiara Fallerini

7.1k total citations
31 papers, 556 citations indexed

About

Chiara Fallerini is a scholar working on Molecular Biology, Immunology and Allergy and Genetics. According to data from OpenAlex, Chiara Fallerini has authored 31 papers receiving a total of 556 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 10 papers in Immunology and Allergy and 8 papers in Genetics. Recurrent topics in Chiara Fallerini's work include Cell Adhesion Molecules Research (10 papers), Renal and related cancers (7 papers) and Platelet Disorders and Treatments (5 papers). Chiara Fallerini is often cited by papers focused on Cell Adhesion Molecules Research (10 papers), Renal and related cancers (7 papers) and Platelet Disorders and Treatments (5 papers). Chiara Fallerini collaborates with scholars based in Italy, United States and France. Chiara Fallerini's co-authors include Alessandra Renieri, Francesca Mari, Francesca Ariani, Elisa Frullanti, Maria Antonietta Mencarelli, Margherita Baldassarri, Mirella Bruttini, Anna Maria Pinto, Simone Furini and Guido Garosi and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Brain.

In The Last Decade

Chiara Fallerini

31 papers receiving 548 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chiara Fallerini Italy 14 237 207 132 103 96 31 556
Atsuko Maeda Japan 12 307 1.3× 127 0.6× 36 0.3× 128 1.2× 62 0.6× 14 801
Simona Paris Italy 15 529 2.2× 192 0.9× 46 0.3× 88 0.9× 45 0.5× 21 957
Ortal Barel Israel 15 450 1.9× 16 0.1× 247 1.9× 47 0.5× 17 0.2× 63 868
Asaf Ta‐Shma Israel 16 450 1.9× 17 0.1× 224 1.7× 46 0.4× 29 0.3× 19 988
Adi Mory Israel 15 245 1.0× 86 0.4× 147 1.1× 46 0.4× 3 0.0× 40 592
Liisa Laitinen Finland 10 272 1.1× 106 0.5× 33 0.3× 25 0.2× 25 0.3× 14 492
Matthias Vockel Germany 9 388 1.6× 152 0.7× 7 0.1× 44 0.4× 17 0.2× 10 673
Florian Wessel Germany 5 226 1.0× 125 0.6× 10 0.1× 62 0.6× 9 0.1× 7 465
Alex‐Xianghua Zhou Sweden 11 333 1.4× 36 0.2× 51 0.4× 23 0.2× 10 0.1× 14 575
Akatsuki Kubota Japan 11 215 0.9× 40 0.2× 26 0.2× 26 0.3× 10 0.1× 35 442

Countries citing papers authored by Chiara Fallerini

Since Specialization
Citations

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

Fields of papers citing papers by Chiara Fallerini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chiara Fallerini

This figure shows the co-authorship network connecting the top 25 collaborators of Chiara Fallerini. A scholar is included among the top collaborators of Chiara Fallerini 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 Chiara Fallerini. Chiara Fallerini 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.
Cittadini, Camilla, Elena Germinario, Lucrezia Gambardella, et al.. (2023). Effects of the Rho GTPase‐activating toxin CNF1 on fibroblasts derived from Rett syndrome patients: A pilot study. Journal of Cellular and Molecular Medicine. 27(10). 1315–1326. 2 indexed citations
2.
Palmieri, Maria, Chiara Fallerini, Francesca Ariani, et al.. (2023). Case report: PIK3CA somatic mutation leading to Klippel Trenaunay Syndrome and multiple tumors. Frontiers in Genetics. 14. 1213283–1213283. 2 indexed citations
3.
Valentino, Floriana, Gabriella Doddato, Chiara Fallerini, et al.. (2022). Heterozygosity for neuronal ceroid lipofuscinosis predisposes to bipolar disorder. Brazilian Journal of Psychiatry. 45(1). 11–19. 1 indexed citations
4.
Zguro, Kristina, Chiara Fallerini, Francesca Fava, Simone Furini, & Alessandra Renieri. (2022). Host genetic basis of COVID-19: from methodologies to genes. European Journal of Human Genetics. 30(8). 899–907. 12 indexed citations
5.
Monticelli, Maria, Bruno Hay Mele, Elisa Benetti, et al.. (2021). Protective Role of a TMPRSS2 Variant on Severe COVID-19 Outcome in Young Males and Elderly Women. Genes. 12(4). 596–596. 40 indexed citations
6.
Doddato, Gabriella, Alessandra Fabbiani, Chiara Fallerini, et al.. (2021). Spondyloocular Syndrome: A Novel XYLT2 Variant with Description of the Neonatal Phenotype. Frontiers in Genetics. 12. 761264–761264. 5 indexed citations
7.
Cupaioli, Francesca Anna, Chiara Fallerini, Maria Antonietta Mencarelli, et al.. (2021). Autism Spectrum Disorders: Analysis of Mobile Elements at 7q11.23 Williams–Beuren Region by Comparative Genomics. Genes. 12(10). 1605–1605. 1 indexed citations
8.
Onat, Onur Emre, Şeref Gül, Kaya Bilgüvar, et al.. (2020). Human CRY1 variants associate with attention deficit/hyperactivity disorder. Journal of Clinical Investigation. 130(7). 3885–3900. 33 indexed citations
9.
Cupaioli, Francesca Anna, Ettore Mosca, Chiara Magri, et al.. (2020). Assessment of haptoglobin alleles in autism spectrum disorders. Scientific Reports. 10(1). 7758–7758. 4 indexed citations
10.
Mastrangelo, Antonio, Marisa Giani, Pierangela Castorina, et al.. (2020). X-Linked Alport Syndrome in Women: Genotype and Clinical Course in 24 Cases. Frontiers in Medicine. 7. 580376–580376. 13 indexed citations
11.
Palmieri, Maria, Aurora Currò, Andrea Tommasi, et al.. (2020). Cell-free DNA next-generation sequencing liquid biopsy as a new revolutionary approach for arteriovenous malformation. SHILAP Revista de lepidopterología. 1. 176–180. 22 indexed citations
12.
Palmieri, Maria, Laura Di Sarno, Andrea Tommasi, et al.. (2020). MET somatic activating mutations are responsible for lymphovenous malformation and can be identified using cell-free DNA next generation sequencing liquid biopsy. Journal of Vascular Surgery Venous and Lymphatic Disorders. 9(3). 740–744. 6 indexed citations
13.
Fallerini, Chiara, Floriana Valentino, Annarita Giliberti, et al.. (2020). RB1 Germline Variant Predisposing to a Rare Ovarian Germ Cell Tumor: A Case Report. Frontiers in Oncology. 10. 1467–1467. 1 indexed citations
14.
Daga, Sergio, Francesco Donati, Katia Capitani, et al.. (2019). New frontiers to cure Alport syndrome: COL4A3 and COL4A5 gene editing in podocyte-lineage cells. European Journal of Human Genetics. 28(4). 480–490. 30 indexed citations
15.
Daga, Sergio, Chiara Fallerini, Simone Furini, et al.. (2019). Non-collagen genes role in digenic Alport syndrome. BMC Nephrology. 20(1). 70–70. 14 indexed citations
16.
Baldassarri, Margherita, Chiara Fallerini, Francesco Cetta, et al.. (2017). Omic Approach in Non-smoker Female with Lung Squamous Cell Carcinoma Pinpoints to Germline Susceptibility and Personalized Medicine. Cancer Research and Treatment. 50(2). 356–365. 17 indexed citations
17.
Mencarelli, Maria Antonietta, Chiara Fallerini, Laura Bianciardi, et al.. (2016). Potentially Treatable Disorder Diagnosed Post Mortem by Exome Analysis in a Boy with Respiratory Distress. International Journal of Molecular Sciences. 17(3). 306–306. 6 indexed citations
18.
Mencarelli, Maria Antonietta, Laurence Heidet, Helen Storey, et al.. (2015). Evidence of digenic inheritance in Alport syndrome. Journal of Medical Genetics. 52(3). 163–174. 107 indexed citations
19.
Amato, Teresa, Francesco Abate, Pier Paolo Piccaluga, et al.. (2015). Clonality Analysis of Immunoglobulin Gene Rearrangement by Next-Generation Sequencing in Endemic Burkitt Lymphoma Suggests Antigen Drive Activation of BCR as Opposed to Sporadic Burkitt Lymphoma. American Journal of Clinical Pathology. 145(1). 116–127. 23 indexed citations
20.
Rotondi, Mario, Chiara Fallerini, Barbara Pirali, et al.. (2012). A Unique Patient Presenting With Concomitant Klinefelter Syndrome, Alport Syndrome, and Craniopharyngioma. Journal of Andrology. 33(6). 1155–1159. 4 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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