Elisa Giorgio

5.8k total citations
46 papers, 622 citations indexed

About

Elisa Giorgio is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Elisa Giorgio has authored 46 papers receiving a total of 622 indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 19 papers in Genetics and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Elisa Giorgio's work include RNA Research and Splicing (8 papers), RNA regulation and disease (7 papers) and Genomics and Rare Diseases (6 papers). Elisa Giorgio is often cited by papers focused on RNA Research and Splicing (8 papers), RNA regulation and disease (7 papers) and Genomics and Rare Diseases (6 papers). Elisa Giorgio collaborates with scholars based in Italy, United States and Russia. Elisa Giorgio's co-authors include Alfredo Brusco, Eleonora Di Gregorio, Alessandro Brussino, Cecilia Mancini, Fabio Sirchia, Laura Gasparini, Simona Cavalieri, Giovanna Vaula, Malte Spielmann and Giovanni Battista Ferrero and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Scientific Reports.

In The Last Decade

Elisa Giorgio

44 papers receiving 622 citations

Peers

Elisa Giorgio
Nisha Patel Saudi Arabia
Tadashi Kaname Japan
Marcello Niceta Italy
Aleksandra Jezela‐Stanek Poland
Matthew A. Lines Canada
Hamad Alzaidan Saudi Arabia
Xianfeng Li China
Soo‐Mi Park United Kingdom
Katharina Steindl Switzerland
Jeroen Vreijling Netherlands
Nisha Patel Saudi Arabia
Elisa Giorgio
Citations per year, relative to Elisa Giorgio Elisa Giorgio (= 1×) peers Nisha Patel

Countries citing papers authored by Elisa Giorgio

Since Specialization
Citations

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

Fields of papers citing papers by Elisa Giorgio

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisa Giorgio

This figure shows the co-authorship network connecting the top 25 collaborators of Elisa Giorgio. A scholar is included among the top collaborators of Elisa Giorgio 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 Elisa Giorgio. Elisa Giorgio 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.
Castagnoli, Riccardo, Thomas Foiadelli, Elisa Giorgio, et al.. (2025). Mitochondrial Complex I Deficiency: Unraveling the Relevance of NDUFAF1 in Pediatric Hypertrophic Cardiomyopathy. American Journal of Medical Genetics Part A. 197(5). e63994–e63994. 1 indexed citations
2.
Jokela, Manu, Meriel McEntagart, Tessa Homfray, et al.. (2023). The crucial role of titin in fetal development: recurrent miscarriages and bone, heart and muscle anomalies characterise the severe end of titinopathies spectrum. Journal of Medical Genetics. 60(9). 866–873. 8 indexed citations
3.
Ramazzotti, Giulia, Isabella Rusciano, Sara Mongiorgi, et al.. (2023). Lamin B1 as a key modulator of the developing and aging brain. Frontiers in Cellular Neuroscience. 17. 1263310–1263310. 9 indexed citations
4.
Pasca, Ludovica, Samantha Bruno, Elisa Giorgio, et al.. (2023). Expanding the phenotype of Brunner syndrome from childhood to adulthood: Description of the second pediatric patient and his mother. American Journal of Medical Genetics Part A. 194(1). 82–87.
5.
Ramazzotti, Giulia, Sara Mongiorgi, Isabella Rusciano, et al.. (2023). Understanding the Ultra-Rare Disease Autosomal Dominant Leukodystrophy: an Updated Review on Morpho-Functional Alterations Found in Experimental Models. Molecular Neurobiology. 60(11). 6362–6372. 5 indexed citations
6.
Rubino, Elisa, Silvia Boschi, Elisa Giorgio, et al.. (2022). Analysis of the DNA methylation pattern of the promoter region of calcitonin gene-related peptide 1 gene in patients with episodic migraine: An exploratory case-control study. SHILAP Revista de lepidopterología. 11. 100089–100089. 14 indexed citations
7.
Sirchia, Fabio, Elisa Giorgio, Laura Cucinella, Enza Maria Valente, & Rossella E. Nappi. (2022). Biallelic mutations in PSMC3IP are associated with secondary amenorrhea: expanding the spectrum of premature ovarian insufficiency. Journal of Assisted Reproduction and Genetics. 39(5). 1177–1181. 9 indexed citations
8.
Birolo, Giovanni, Serena Aneli, Cornelia Di Gaetano, et al.. (2020). Functional and clinical implications of genetic structure in 1686 Italian exomes. Human Mutation. 42(3). 272–289. 6 indexed citations
9.
Nardello, Rosaria, Giuseppe Donato Mangano, Vincenzo Antona, et al.. (2020). Electroclinical features and outcome of ANKRD11-related KBG syndrome: A novel report and literature review. Seizure. 85. 151–154. 5 indexed citations
10.
Pozzi, Elisa, Elisa Giorgio, Cecilia Mancini, et al.. (2020). In vitro dexamethasone treatment does not induce alternative ATM transcripts in cells from Ataxia–Telangiectasia patients. Scientific Reports. 10(1). 20182–20182. 2 indexed citations
11.
Navarra, Chiara Ottavia, Marco Bobbo, Pio D’Adamo, et al.. (2020). Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: a case report. BMC Pediatrics. 20(1). 201–201. 5 indexed citations
12.
Piro, Ettore, Gregorio Serra, Vincenzo Antona, et al.. (2020). Novel LRPPRC compound heterozygous mutation in a child with early-onset Leigh syndrome French-Canadian type: case report of an Italian patient. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 46(1). 140–140. 22 indexed citations
13.
Giorgio, Elisa, Emanuela Garelli, Adriana Carando, et al.. (2019). Design of a multiplex ligation-dependent probe amplification assay for SLC20A2: identification of two novel deletions in primary familial brain calcification. Journal of Human Genetics. 64(11). 1083–1090. 4 indexed citations
14.
Giorgio, Elisa, Fabio Sirchia, Martino Bosco, et al.. (2018). A novel case of Greenberg dysplasia and genotype–phenotype correlation analysis for LBR pathogenic variants: An instructive example of one gene‐multiple phenotypes. American Journal of Medical Genetics Part A. 179(2). 306–311. 9 indexed citations
15.
Cagnoli, Claudia, Alessandro Brussino, Cecilia Mancini, et al.. (2018). Spinocerebellar Ataxia Tethering PCR. Journal of Molecular Diagnostics. 20(3). 289–297. 15 indexed citations
16.
Giorgio, Elisa, Alessandro Brussino, Elisa Biamino, et al.. (2016). Exome sequencing in children of women with skewed X-inactivation identifies atypical cases and complex phenotypes. European Journal of Paediatric Neurology. 21(3). 475–484. 11 indexed citations
17.
Bartoletti‐Stella, Anna, Laura Gasparini, Caterina Giacomini, et al.. (2015). Messenger RNA processing is altered in autosomal dominant leukodystrophy. Human Molecular Genetics. 24(10). 2746–2756. 25 indexed citations
18.
Biamino, Elisa, Eleonora Di Gregorio, Elga Fabia Belligni, et al.. (2015). A novel 3q29 deletion associated with autism, intellectual disability, psychiatric disorders, and obesity. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 171(2). 290–299. 25 indexed citations
19.
Mancini, Cecilia, Yiran Guo, Yulan Chen, et al.. (2014). Adult-onset autosomal recessive ataxia associated with neuronal ceroid lipofuscinosis type 5 gene (CLN5) mutations. Journal of Neurology. 262(1). 173–178. 30 indexed citations
20.
Giorgio, Elisa, C. Caroti, Francesca Mattioli, et al.. (2011). Severe fluoropyrimidine-related toxicity: clinical implications of DPYD analysis and UH2/U ratio evaluation. Cancer Chemotherapy and Pharmacology. 68(5). 1355–1361. 12 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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