Dario Strina

1.1k total citations
27 papers, 741 citations indexed

About

Dario Strina is a scholar working on Molecular Biology, Immunology and Genetics. According to data from OpenAlex, Dario Strina has authored 27 papers receiving a total of 741 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 11 papers in Immunology and 7 papers in Genetics. Recurrent topics in Dario Strina's work include Immunodeficiency and Autoimmune Disorders (5 papers), T-cell and B-cell Immunology (4 papers) and Virus-based gene therapy research (3 papers). Dario Strina is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (5 papers), T-cell and B-cell Immunology (4 papers) and Virus-based gene therapy research (3 papers). Dario Strina collaborates with scholars based in Italy, United States and Netherlands. Dario Strina's co-authors include Anna Villa, Paolo Vezzoni, Luigi D. Notarangelo, Paolo Macchi, Maria Grazia Sacco, Elide Mantuano, Alberto G. Ugazio, Duilio Brugnoni, M.C. Patrosso and Silvia Giliani and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and The Journal of Experimental Medicine.

In The Last Decade

Dario Strina

27 papers receiving 723 citations

Peers

Dario Strina

IMMUN

ONCOL

GENET

Marsha Grattan Canada

G W Krissansen New Zealand

Keisuke Aoyama Japan

Jun-ichi Yata Japan

Paola Porcedda Italy

Tomoaki Kuwaki Japan

Adam Asch United States

Kevin B. Leslie Canada

Jérôme Perrard United States

Paul A. Singer United States

Marsha Grattan Canada

Dario Strina

255 ×0.8

IMMUN

378 ×1.4

312 ×1.8

ONCOL

207 ×1.3

GENET

84 ×0.7

Citations per year, relative to Dario Strina Dario Strina (= 1×) peers Marsha Grattan

Countries citing papers authored by Dario Strina

Since Specialization

Citations

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

Fields of papers citing papers by Dario Strina

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dario Strina

This figure shows the co-authorship network connecting the top 25 collaborators of Dario Strina. A scholar is included among the top collaborators of Dario Strina 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 Dario Strina. Dario Strina 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

Strina, Dario, Roberto Leone, Sonia Valentino, et al.. (2024). Interleukin-1β Polymorphisms Are Genetic Markers of Susceptibility to Periprosthetic Joint Infection in Total Hip and Knee Arthroplasty. Genes. 15(5). 596–596. 3 indexed citations

Strina, Dario, et al.. (2023). Genetic Deficiency of the Long Pentraxin 3 Affects Osteogenesis and Osteoclastogenesis in Homeostatic and Inflammatory Conditions. International Journal of Molecular Sciences. 24(23). 16648–16648. 1 indexed citations

Palagano, Eleonora, Sharon Muggeo, Laura Crisafulli, et al.. (2020). Generation of an immunodeficient mouse model of tcirg1-deficient autosomal recessive osteopetrosis. Bone Reports. 12. 100242–100242. 6 indexed citations

Ritelli, Marco, Eleonora Palagano, Valeria Cinquina, et al.. (2020). Genome-first approach for the characterization of a complex phenotype with combined NBAS and CUL4B deficiency. Bone. 140. 115571–115571. 7 indexed citations

Paulis, Marianna, S. P. Lucia, Teruhiko Suzuki, et al.. (2020). Chromosome Transplantation: A Possible Approach to Treat Human X-linked Disorders. Molecular Therapy — Methods & Clinical Development. 17. 369–377. 11 indexed citations

Lucia, S. P., Ciro Menale, Sharon Muggeo, et al.. (2019). Chromosome Transplantation: Correction of the Chronic Granulomatous Disease Defect in Mouse Induced Pluripotent Stem Cells. Stem Cells. 37(7). 876–887. 5 indexed citations

Sobacchi, Cristina, Marco Erreni, Dario Strina, et al.. (2018). 3D Bone Biomimetic Scaffolds for Basic and Translational Studies with Mesenchymal Stem Cells. International Journal of Molecular Sciences. 19(10). 3150–3150. 26 indexed citations

Néri, Tui, Sharon Muggeo, Marianna Paulis, et al.. (2015). Targeted Gene Correction in Osteopetrotic-Induced Pluripotent Stem Cells for the Generation of Functional Osteoclasts. Stem Cell Reports. 5(4). 558–568. 18 indexed citations

Cassani, Barbara, Pietro Luigi Poliani, Veronica Marrella, et al.. (2010). Homeostatic expansion of autoreactive immunoglobulin-secreting cells in the Rag2 mouse model of Omenn syndrome. The Journal of Experimental Medicine. 207(7). 1525–1540. 44 indexed citations

10.

Sacco, Maria Grazia, Marco Ungari, Anna Villa, et al.. (2000). Lymphoid abnormalities in CD40 ligand transgenic mice suggest the need for tight regulation in gene therapy approaches to hyper immunoglobulin M (IgM) syndrome. Cancer Gene Therapy. 7(10). 1299–1306. 50 indexed citations

11.

Villa, Anna, Dario Strina, Annalisa Frattini, et al.. (1996). The ZNF75 Zinc Finger Gene Subfamily: Isolation and Mapping of the Four Members in Humans and Great Apes. Genomics. 35(2). 312–320. 9 indexed citations

12.

Bozzi, Fabio, et al.. (1996). The Exon–Intron Structure of HumanLHX1 Gene. Biochemical and Biophysical Research Communications. 229(2). 494–497. 11 indexed citations

13.

Villa, Anna, Luigi D. Notarangelo, Paolo Macchi, et al.. (1995). X–linked thrombocytopenia and Wiskott–Aldrich syndrome are allelic diseases with mutations in the WASP gene. Nature Genetics. 9(4). 414–417. 203 indexed citations

14.

Macchi, Paolo, Luigi D. Notarangelo, Silvia Giliani, et al.. (1995). The Genomic Organization of the Human Transcription Factor 3 (TFE3) Gene. Genomics. 28(3). 491–494. 9 indexed citations

15.

Villa, Anna, Dario Strina, Paolo Macchi, et al.. (1994). C to T mutation causing premature termination of CD40 ligand at amino acid 221 in a patient affected by Hyper IgM syndrome. Human Mutation. 3(1). 73–75. 11 indexed citations

16.

Villa, Anna, et al.. (1994). Rapid isolation of cDNA clones by aliquot testing via PCR amplification.. Genome Research. 4(2). 126–128. 2 indexed citations

17.

Frattini, Annalisa, Ileana Zucchi, Anna Villa, et al.. (1994). Genomic Organization of the Human VP16 Accessory Protein, a Housekeeping Gene (HCFC1) Mapping to Xq28. Genomics. 23(1). 30–35. 13 indexed citations

18.

Frattini, Annalisa, Ileana Zucchi, Anna Villa, et al.. (1993). Type 2 Vasopressin Receptor Gene, the Gene Responsible for Nephrogenic Diabetes Insipidus, Maps to XQ28 Close to the L1CAM Gene. Biochemical and Biophysical Research Communications. 193(3). 864–871. 6 indexed citations

19.

Villa, Anna, Ileana Zucchi, Giuseppe Pilia, et al.. (1993). ZNF75: Isolation of a cDNA Clone of the KRAB Zinc Finger Gene Subfamily Mapped in YACs 1 Mb Telomeric of HPRT. Genomics. 18(2). 223–229. 15 indexed citations

20.

Villa, Anna, Ida Biunno, Annalisa Frattini, et al.. (1992). Isolation of a zinc finger motif (ZNF75) mapping on chromosome Xq26. Genomics. 13(4). 1231–1236. 9 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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