Giuseppe Merla

17.4k total citations
97 papers, 2.9k citations indexed

About

Giuseppe Merla is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Giuseppe Merla has authored 97 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 33 papers in Genetics and 14 papers in Immunology. Recurrent topics in Giuseppe Merla's work include Genomics and Rare Diseases (19 papers), Williams Syndrome Research (13 papers) and Genomic variations and chromosomal abnormalities (12 papers). Giuseppe Merla is often cited by papers focused on Genomics and Rare Diseases (19 papers), Williams Syndrome Research (13 papers) and Genomic variations and chromosomal abnormalities (12 papers). Giuseppe Merla collaborates with scholars based in Italy, Switzerland and United States. Giuseppe Merla's co-authors include Alexandre Reymond, Lucia Micale, Carmela Fusco, Bartolomeo Augello, Santina Venuto, Stylianos E. Antonarakis, Charlotte N. Henrichsen, Cédric Howald, Nicola Brunetti‐Pierri and Catherine Ucla and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PLoS ONE.

In The Last Decade

Giuseppe Merla

97 papers receiving 2.8k citations

Peers

Giuseppe Merla

GENET

IMMUN

Jean Charron Canada

Dejan Lazarević Italy

Hoa Nguyen United States

Marianna Bugiani Netherlands

Abdel G. Elkahloun United States

Anne Schaefer United States

Alexander G. Bassuk United States

Philippe M. Campeau Canada

Jeremy M. Simon United States

Erik A. Sistermans Netherlands

Jean Charron Canada

Giuseppe Merla

2.1k ×1.3

481 ×0.6

GENET

343 ×0.7

IMMUN

133 ×0.4

341 ×1.2

Citations per year, relative to Giuseppe Merla Giuseppe Merla (= 1×) peers Jean Charron

Countries citing papers authored by Giuseppe Merla

Since Specialization

Citations

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

Fields of papers citing papers by Giuseppe Merla

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giuseppe Merla

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

All Works

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20 of 20 papers shown

Arduino, Ilaria, Antonella Santoro, Silvia De Santis, et al.. (2024). Microfluidic formulation of diazoxide-loaded solid lipid nanoparticles as a Novel approach for Friedreich's ataxia treatment. Journal of Drug Delivery Science and Technology. 97. 105837–105837. 2 indexed citations

Pignata, Laura, A. De Rosa, Paolo Salerno, et al.. (2024). Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors. Genes. 15(3). 321–321. 7 indexed citations

Coppedè, Fabio, et al.. (2023). DNA Methylation in the Fields of Prenatal Diagnosis and Early Detection of Cancers. International Journal of Molecular Sciences. 24(14). 11715–11715. 5 indexed citations

Romagnoli, Alessandra, Martina Di Rienzo, Elisa Petruccioli, et al.. (2023). The ubiquitin ligase TRIM32 promotes the autophagic response to Mycobacterium tuberculosis infection in macrophages. Cell Death and Disease. 14(8). 505–505. 17 indexed citations

Savino, Michelangelo, Bartolomeo Augello, Giuseppe Merla, et al.. (2022). Circadian Genes Expression Patterns in Disorders Due to Enzyme Deficiencies in the Heme Biosynthetic Pathway. Biomedicines. 10(12). 3198–3198. 3 indexed citations

Merla, Giuseppe, et al.. (2021). Ubiquitination, Biotech Startups, and the Future of TRIM Family Proteins: A TRIM-Endous Opportunity. Cells. 10(5). 1015–1015. 15 indexed citations

Rooney, Kathleen, Michael A. Levy, Sadegheh Haghshenas, et al.. (2021). Identification of a DNA Methylation Episignature in the 22q11.2 Deletion Syndrome. International Journal of Molecular Sciences. 22(16). 8611–8611. 13 indexed citations

Flex, Elisabetta, Giovanna Carpentieri, Alessandro Bruselles, et al.. (2021). A Rare Case of Brachyolmia with Amelogenesis Imperfecta Caused by a New Pathogenic Splicing Variant in LTBP3. Genes. 12(9). 1406–1406. 3 indexed citations

Bigoni, Stefania, et al.. (2020). Clinical Genetics Can Solve the Pitfalls of Genome-Wide Investigations: Lesson from Mismapping a Loss-of-Function Variant in KANSL1. Genes. 11(10). 1177–1177. 13 indexed citations

10.

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

11.

Merla, Giuseppe, et al.. (2020). Rise of TRIM8: A Molecule of Duality. Molecular Therapy — Nucleic Acids. 22. 434–444. 24 indexed citations

12.

Venuto, Santina & Giuseppe Merla. (2019). E3 Ubiquitin Ligase TRIM Proteins, Cell Cycle and Mitosis. Cells. 8(5). 510–510. 116 indexed citations

13.

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

14.

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

15.

Simone, Laura, Francesco Pisani, Maria Grazia Mola, et al.. (2019). AQP4 Aggregation State Is a Determinant for Glioma Cell Fate. Cancer Research. 79(9). 2182–2194. 41 indexed citations

16.

Prontera, Paolo, Daniela Rogaia, Amedea Mencarelli, et al.. (2019). Schilbach–Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene. European Journal of Human Genetics. 27(8). 1260–1266. 1 indexed citations

17.

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

18.

Prontera, Paolo, Daniela Rogaia, Amedea Mencarelli, et al.. (2017). Juvenile Moyamoya and Craniosynostosis in a Child with Deletion 1p32p31: Expanding the Clinical Spectrum of 1p32p31 Deletion Syndrome and a Review of the Literature. International Journal of Molecular Sciences. 18(9). 1998–1998. 8 indexed citations

19.

Merla, Giuseppe, et al.. (2013). Diagnóstico clínico en el síndrome de Kabuki: fenotipo y anomalías asociadas en dos casos nuevos. Archivos Argentinos de Pediatria. 112(1). e13–e17. 3 indexed citations

20.

Meroni, Germana, Alexandre Reymond, Stefano Cairo, et al.. (1999). Functional genomics of the B-box gene family reveals a possible role in subcellular compartmentalization. The American Journal of Human Genetics. 65(4). 80. 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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