Natascia Malerba

621 total citations
13 papers, 320 citations indexed

About

Natascia Malerba is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Natascia Malerba has authored 13 papers receiving a total of 320 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 1 paper in Surgery. Recurrent topics in Natascia Malerba's work include Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Epigenetics and DNA Methylation (2 papers). Natascia Malerba is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Epigenetics and DNA Methylation (2 papers). Natascia Malerba collaborates with scholars based in Italy, Switzerland and United States. Natascia Malerba's co-authors include Giuseppe Merla, Gabriella Maria Squeo, Maria Notarnicola, Maurizio Bifulco, Maria Grazia Refolo, Chiara Laezza, Valeria Tutino, Caterina Messa, Maria Gabriella Caruso and Rosalba D’Alessandro and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Human Molecular Genetics.

In The Last Decade

Natascia Malerba

13 papers receiving 316 citations

Peers

Natascia Malerba
Hwayong Park South Korea
Natascia Malerba
Citations per year, relative to Natascia Malerba Natascia Malerba (= 1×) peers Hwayong Park

Countries citing papers authored by Natascia Malerba

Since Specialization
Citations

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

Fields of papers citing papers by Natascia Malerba

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Natascia Malerba

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

All Works

13 of 13 papers shown
1.
Pacelli, Consiglia, Natascia Malerba, Gabriella Maria Squeo, et al.. (2020). Loss of Function of the Gene Encoding the Histone Methyltransferase KMT2D Leads to Deregulation of Mitochondrial Respiration. Cells. 9(7). 1685–1685. 15 indexed citations
2.
Zanella, Matteo, Alessandro Vitriolo, Thomas J. O’Rourke, et al.. (2020). Dosage analysis of the 7q11.23 Williams region identifies BAZ1B as a major human gene patterning the modern human face and underlying self-domestication. Yearbook of pediatric endocrinology. 1 indexed citations
3.
Malerba, Natascia, Pasquelena De Nittis, & Giuseppe Merla. (2019). The Emerging Role of Gβ Subunits in Human Genetic Diseases. Cells. 8(12). 1567–1567. 10 indexed citations
4.
Zanella, Matteo, Alessandro Vitriolo, Pedro Tiago Martins, et al.. (2019). Dosage analysis of the 7q11.23 Williams region identifies BAZ1B as a major human gene patterning the modern human face and underlying self-domestication. Science Advances. 5(12). eaaw7908–eaaw7908. 54 indexed citations
5.
Malerba, Natascia, Patrizia Benzoni, Gabriella Maria Squeo, et al.. (2019). Generation of the induced human pluripotent stem cell lines CSSi009-A from a patient with a GNB5 pathogenic variant, and CSSi010-A from a CRISPR/Cas9 engineered GNB5 knock-out human cell line. Stem Cell Research. 40. 101547–101547. 2 indexed citations
6.
Fusco, Carmela, Barbara Mandriani, Martina Di Rienzo, et al.. (2018). TRIM50 regulates Beclin 1 proautophagic activity. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1865(6). 908–919. 45 indexed citations
7.
Malerba, Natascia, et al.. (2018). A NGS-Targeted Autism/ID Panel Reveals Compound Heterozygous GNB5 Variants in a Novel Patient. Frontiers in Genetics. 9. 626–626. 9 indexed citations
8.
Cocciadiferro, Dario, Bartolomeo Augello, Pasquelena De Nittis, et al.. (2018). Dissecting KMT2D missense mutations in Kabuki syndrome patients. Human Molecular Genetics. 27(21). 3651–3668. 45 indexed citations
9.
Lepri, Francesca Romana, Dario Cocciadiferro, Bartolomeo Augello, et al.. (2017). Clinical and Neurobehavioral Features of Three Novel Kabuki Syndrome Patients with Mosaic KMT2D Mutations and a Review of Literature. International Journal of Molecular Sciences. 19(1). 82–82. 17 indexed citations
10.
Prontera, Paolo, Daniela Rogaia, Amedea Mencarelli, et al.. (2016). A novel MED12 mutation: Evidence for a fourth phenotype. American Journal of Medical Genetics Part A. 170(9). 2377–2382. 23 indexed citations
11.
Fusco, Carmela, Pasquelena De Nittis, Ali Abdullah Alfaiz, et al.. (2016). A New Split Hand/Foot Malformation with Long Bone Deficiency Familial Case. Journal of Pediatric Genetics. 6(2). 98–102. 4 indexed citations
12.
Refolo, Maria Grazia, Rosalba D’Alessandro, Natascia Malerba, et al.. (2015). Anti Proliferative and Pro Apoptotic Effects of Flavonoid Quercetin Are Mediated by CB1 Receptor in Human Colon Cancer Cell Lines. Journal of Cellular Physiology. 230(12). 2973–2980. 94 indexed citations
13.
Fusco, Carmela, Lucia Micale, Maria Teresa Pellico, et al.. (2015). Genomic and Genetic Disorders Biobank. SHILAP Revista de lepidopterología. 2. 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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