Francesco Calı̀

4.4k total citations
86 papers, 1.2k citations indexed

About

Francesco Calı̀ is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Francesco Calı̀ has authored 86 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 44 papers in Genetics and 10 papers in Clinical Biochemistry. Recurrent topics in Francesco Calı̀'s work include Genetics and Neurodevelopmental Disorders (19 papers), Forensic and Genetic Research (13 papers) and Genomic variations and chromosomal abnormalities (10 papers). Francesco Calı̀ is often cited by papers focused on Genetics and Neurodevelopmental Disorders (19 papers), Forensic and Genetic Research (13 papers) and Genomic variations and chromosomal abnormalities (10 papers). Francesco Calı̀ collaborates with scholars based in Italy, United Kingdom and United States. Francesco Calı̀'s co-authors include Valentino Romano, Mirella Vinci, Giacomo De Leo, Stefano Puglisi‐Allegra, Rossella Ventura, Andrea Novelletto, Simona Cabib, Tiziana Pascucci, Mario G. Mirisola and Maurizio Elia and has published in prestigious journals such as PLoS ONE, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Francesco Calı̀

83 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Francesco Calı̀ Italy 19 683 467 186 159 94 86 1.2k
Olga Derbeneva United States 15 461 0.7× 1.0k 2.2× 412 2.2× 149 0.9× 163 1.7× 21 1.5k
Bharti Morar Australia 17 759 1.1× 503 1.1× 27 0.1× 141 0.9× 62 0.7× 30 1.4k
Cristina Santos Spain 22 467 0.7× 649 1.4× 134 0.7× 138 0.9× 67 0.7× 79 1.2k
Chiara Rengo Italy 18 1.1k 1.6× 884 1.9× 266 1.4× 452 2.8× 53 0.6× 22 1.9k
Chiara Magri Italy 17 780 1.1× 435 0.9× 69 0.4× 229 1.4× 43 0.5× 40 1.2k
Anna Pluzhnikov United States 14 797 1.2× 594 1.3× 76 0.4× 7 0.0× 193 2.1× 17 1.7k
Irene Pichler Italy 21 273 0.4× 401 0.9× 16 0.1× 16 0.1× 114 1.2× 45 1.2k
V. Ferák Slovakia 11 442 0.6× 305 0.7× 102 0.5× 100 0.6× 39 0.4× 21 937
Missy Dixon United States 6 430 0.6× 361 0.8× 20 0.1× 66 0.4× 46 0.5× 8 839
Hassan Rouba Morocco 22 739 1.1× 762 1.6× 21 0.1× 19 0.1× 36 0.4× 83 1.4k

Countries citing papers authored by Francesco Calı̀

Since Specialization
Citations

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

Fields of papers citing papers by Francesco Calı̀

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesco Calı̀

This figure shows the co-authorship network connecting the top 25 collaborators of Francesco Calı̀. A scholar is included among the top collaborators of Francesco Calı̀ 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 Francesco Calı̀. Francesco Calı̀ 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.
Greco, Donatella, Simone Treccarichi, Maria Bottitta, et al.. (2025). Clinical Application of a Customized Gene Panel for Identifying Autism Spectrum Disorder-Associated Variants. Medicina. 61(7). 1273–1273.
2.
Musumeci, Antonino, Mirella Vinci, Simone Treccarichi, et al.. (2025). Potential Role of ABCF2 Gene in Pudendal Nerve Neuropathy and Interstitial Cystitis. Genes. 16(3). 281–281. 1 indexed citations
3.
Treccarichi, Simone, Mirella Vinci, Antonino Musumeci, et al.. (2025). Investigating the Role of the Zinc Finger Protein ZC2HC1C on Autism Spectrum Disorder Susceptibility. Medicina. 61(4). 574–574. 3 indexed citations
4.
Vinci, Mirella, et al.. (2025). Dissecting the Genetic Contribution of Tooth Agenesis. International Journal of Molecular Sciences. 26(21). 10485–10485.
5.
Vinci, Mirella, Antonino Musumeci, Salvatore Saccone, et al.. (2025). Strengthening the Role of PSMC5 as a Potential Gene Associated with Neurodevelopmental Disorders. International Journal of Molecular Sciences. 26(13). 6386–6386. 1 indexed citations
6.
Calı̀, Francesco, Simone Treccarichi, Antonino Musumeci, et al.. (2025). ZNF496 as Candidate Gene for Neurodevelopmental Disorders: Identification of a Pathogenic De Novo Frameshift Variant. International Journal of Molecular Sciences. 26(15). 7586–7586. 1 indexed citations
7.
Vinci, Mirella, Donatella Greco, Simone Treccarichi, et al.. (2025). Investigating the role of a novel hemizygous FAAH2 variant in neurological and metabolic disorders. Gene. 966. 149703–149703. 2 indexed citations
8.
Vetri, Luigi, Francesco Calı̀, Salvatore Saccone, et al.. (2024). Whole Exome Sequencing as a First-Line Molecular Genetic Test in Developmental and Epileptic Encephalopathies. International Journal of Molecular Sciences. 25(2). 1146–1146. 6 indexed citations
9.
Musumeci, Antonino, Mirella Vinci, Simone Treccarichi, et al.. (2024). PPP2R5E: New gene potentially involved in specific learning disorders and myopathy. Gene. 933. 148945–148945. 3 indexed citations
10.
Treccarichi, Simone, Pinella Failla, Mirella Vinci, et al.. (2024). UNC5C: Novel Gene Associated with Psychiatric Disorders Impacts Dysregulation of Axon Guidance Pathways. Genes. 15(3). 306–306. 6 indexed citations
11.
Vinci, Mirella, Donatella Greco, Simone Treccarichi, et al.. (2024). Exploring the Role of FICD, a New Potential Gene Involved in Borderline Intellectual Functioning, Psychological and Metabolic Disorders. Genes. 15(12). 1655–1655. 2 indexed citations
12.
Calı̀, Francesco, Mirella Vinci, Simone Treccarichi, et al.. (2024). PLEKHG1: New Potential Candidate Gene for Periventricular White Matter Abnormalities. Genes. 15(8). 1096–1096. 5 indexed citations
13.
Treccarichi, Simone, Francesco Calı̀, Mirella Vinci, et al.. (2024). Implications of a De Novo Variant in the SOX12 Gene in a Patient with Generalized Epilepsy, Intellectual Disability, and Childhood Emotional Behavioral Disorders. Current Issues in Molecular Biology. 46(7). 6407–6422. 2 indexed citations
14.
Vinci, Mirella, Simone Treccarichi, Salvatore Saccone, et al.. (2023). STXBP6 Gene Mutation: A New Form of SNAREopathy Leads to Developmental Epileptic Encephalopathy. International Journal of Molecular Sciences. 24(22). 16436–16436. 14 indexed citations
15.
Calı̀, Francesco, Emanuela Avola, Mirella Vinci, et al.. (2023). Specific Learning Disorders: Variation Analysis of 15 Candidate Genes in 9 Multiplex Families. Medicina. 59(8). 1503–1503. 4 indexed citations
16.
Musumeci, Antonino, Mirella Vinci, Francesca L’Episcopo, et al.. (2021). Implementation of Sample Pooling Procedure Using a Rapid SARS-CoV-2 Diagnostic Real-Time PCR Test Performed Prior to Hospital Admission of People with Intellectual Disabilities. International Journal of Environmental Research and Public Health. 18(17). 9317–9317. 2 indexed citations
17.
Lanza, Giuseppe, et al.. (2020). Late-onset oro-facial dyskinesia in Spinocerebellar Ataxia type 2: a case report. BMC Neurology. 20(1). 156–156. 7 indexed citations
18.
Lanza, Giuseppe, Francesco Calı̀, Mirella Vinci, et al.. (2020). A Customized Next-Generation Sequencing-Based Panel to Identify Novel Genetic Variants in Dementing Disorders: A Pilot Study. Neural Plasticity. 2020. 1–10. 6 indexed citations
19.
Romano, Valentino, Mirella Vinci, Salvatore Miccichè, et al.. (2010). Exon deletions of the PAH gene in Italian hyperphenylalaninemics. Experimental & Molecular Medicine. 42. 1 indexed citations
20.
Bosco, Paolo, Raffaele Ferri, Francesco Calı̀, et al.. (1995). Analysis of the FMR-1 gene and correlation with phenotype in Sicilian families with the fragile X syndrome. 20. 149–151. 1 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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