Giuseppe Borsani

6.4k total citations
90 papers, 4.7k citations indexed

About

Giuseppe Borsani is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Giuseppe Borsani has authored 90 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Molecular Biology, 21 papers in Genetics and 18 papers in Cell Biology. Recurrent topics in Giuseppe Borsani's work include Glycosylation and Glycoproteins Research (15 papers), Cellular transport and secretion (13 papers) and Amino Acid Enzymes and Metabolism (8 papers). Giuseppe Borsani is often cited by papers focused on Glycosylation and Glycoproteins Research (15 papers), Cellular transport and secretion (13 papers) and Amino Acid Enzymes and Metabolism (8 papers). Giuseppe Borsani collaborates with scholars based in Italy, United States and Germany. Giuseppe Borsani's co-authors include Andrea Ballabio, Eugenio Monti, Maria Teresa Bassi, Marta Manzoni, Augusto Preti, Bruno Venerando, Roberto Bresciani, Mirko Riboni, Elena I. Rugarli and Sandro Banfi and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Giuseppe Borsani

89 papers receiving 4.6k citations

Peers

Giuseppe Borsani
Lynne Chantranupong United States
Christopher A. Wassif United States
Kuang Shen United States
Marc Hild United States
Sandra Lacas‐Gervais France
Kevin Docherty United Kingdom
A Kahn France
Daniel W. Carr United States
Guangwei Du United States
John W.M. Creemers Belgium
Lynne Chantranupong United States
Giuseppe Borsani
Citations per year, relative to Giuseppe Borsani Giuseppe Borsani (= 1×) peers Lynne Chantranupong

Countries citing papers authored by Giuseppe Borsani

Since Specialization
Citations

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

Fields of papers citing papers by Giuseppe Borsani

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giuseppe Borsani

This figure shows the co-authorship network connecting the top 25 collaborators of Giuseppe Borsani. A scholar is included among the top collaborators of Giuseppe Borsani 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 Borsani. Giuseppe Borsani 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.
Via, Luca La, Giulia Carini, Alice Filippini, et al.. (2025). Functional impact of CYFIP2 RNA editing on actin regulation, axon growth, and spinogenesis. Neurochemistry International. 191. 106084–106084.
2.
Facchinello, Nicola, Natascia Tiso, Cosetta Ravelli, et al.. (2023). Deficiency of AP1 Complex Ap1g1 in Zebrafish Model Led to Perturbation of Neurodevelopment, Female and Male Fertility; New Insight to Understand Adaptinopathies. International Journal of Molecular Sciences. 24(8). 7108–7108. 3 indexed citations
3.
Zizioli, Daniela, Simona Bernardi, Mirko Farina, et al.. (2021). Development of BCR-ABL1 Transgenic Zebrafish Model Reproducing Chronic Myeloid Leukemia (CML) Like-Disease and Providing a New Insight into CML Mechanisms. Cells. 10(2). 445–445. 6 indexed citations
4.
Marchina, Eleonora, et al.. (2021). Molecular characterization of a complex small supernumerary marker chromosome derived from chromosome 18p: an addition to the literature. Molecular Cytogenetics. 14(1). 6–6. 3 indexed citations
5.
Mazzola, Laure, Karen Oliver, Audrey Labalme, et al.. (2020). Progressive Myoclonus Epilepsy Caused by a Homozygous Splicing Variant of SLC7A6OS. Annals of Neurology. 89(2). 402–407. 2 indexed citations
6.
7.
Tobia, Chiara, Paola Chiodelli, Simone Buraschi, et al.. (2019). Atypical Chemokine Receptor 3 Generates Guidance Cues for CXCL12-Mediated Endothelial Cell Migration. Frontiers in Immunology. 10. 1092–1092. 8 indexed citations
8.
Giacopuzzi, Edoardo, Mattia Laffranchi, Ilaria Ferrarotti, et al.. (2018). Real-world clinical applicability of pathogenicity predictors assessed onSERPINA1mutations in alpha-1-antitrypsin deficiency. Human Mutation. 39(9). 1203–1213. 32 indexed citations
9.
Borsani, Giuseppe, et al.. (2016). Amplicon-based semiconductor sequencing of human exomes: performance evaluation and optimization strategies. Human Genetics. 135(5). 499–511. 22 indexed citations
10.
Zizioli, Daniela, Natascia Tiso, Nicola Facchinello, et al.. (2016). Down-regulation of coasy, the gene associated with NBIA-VI, reduces Bmp signaling, perturbs dorso-ventral patterning and alters neuronal development in zebrafish. Scientific Reports. 6(1). 37660–37660. 36 indexed citations
11.
Zizioli, Daniela, Chiara Tobia, Giuseppe Borsani, et al.. (2014). Molecular cloning and knockdown of galactocerebrosidase in zebrafish: New insights into the pathogenesis of Krabbe's disease. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1842(4). 665–675. 29 indexed citations
12.
Micale, Lucia, Maria Nicla Loviglio, Marta Manzoni, et al.. (2012). A Fish-Specific Transposable Element Shapes the Repertoire of p53 Target Genes in Zebrafish. PLoS ONE. 7(10). e46642–e46642. 16 indexed citations
13.
Chiarelli, Nicola, Marco Ritelli, Nicoletta Zoppi, et al.. (2011). Characterization and expression pattern analysis of the facilitative glucose transporter 10 gene (slc2a10) in Danio rerio. The International Journal of Developmental Biology. 55(2). 229–236. 8 indexed citations
14.
Barlati, Sergio, et al.. (2008). Gene expression profiling of mucolipidosis type IV fibroblasts reveals deregulation of genes with relevant functions in lysosome physiology. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1782(4). 250–258. 11 indexed citations
15.
Piovani, Giovanna, Giuseppe Borsani, Vera M. Kalscheuer, et al.. (2005). Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype. European Journal of Medical Genetics. 49(3). 215–223. 9 indexed citations
16.
Bassi, Maria Teresa, Marta Manzoni, Marta Pineda, et al.. (2001). Identification and characterisation of human xCT that co-expresses, with 4F2 heavy chain, the amino acid transport activity system x c -. Pflügers Archiv - European Journal of Physiology. 442(2). 286–296. 134 indexed citations
17.
Grandi, Alessandro De, Vladimiro Calvari, Veronica Bertini, et al.. (2000). The expression pattern of a mouse doublesex-related gene is consistent with a role in gonadal differentiation. Mechanisms of Development. 90(2). 323–326. 104 indexed citations
18.
Piccini, Monica, Francesca Vitelli, Mirella Bruttini, et al.. (1998). FACL4, a New Gene Encoding Long-Chain Acyl-CoA Synthetase 4, Is Deleted in a Family with Alport Syndrome, Elliptocytosis, and Mental Retardation. Genomics. 47(3). 350–358. 92 indexed citations
19.
Mills, K., Katherine D. Mathews, Titia Scherpbier-Heddema, et al.. (1996). Genetic and Physical Mapping of a Voltage-Dependent Chloride Channel Gene to Human 4q32 and to Mouse 8. Genomics. 36(2). 374–376. 6 indexed citations
20.
Agulnik, Alexander I., Michael Mitchell, Marie‐Geneviève Mattéi, et al.. (1994). A novel X gene with a widely transcribed Y-linked homologue escapes X-inactivation in mouse and human. Human Molecular Genetics. 3(6). 879–884. 142 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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