Nicola Migone

6.9k total citations
81 papers, 3.8k citations indexed

About

Nicola Migone is a scholar working on Molecular Biology, Immunology and Genetics. According to data from OpenAlex, Nicola Migone has authored 81 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 22 papers in Immunology and 18 papers in Genetics. Recurrent topics in Nicola Migone's work include Monoclonal and Polyclonal Antibodies Research (13 papers), Tuberous Sclerosis Complex Research (10 papers) and T-cell and B-cell Immunology (10 papers). Nicola Migone is often cited by papers focused on Monoclonal and Polyclonal Antibodies Research (13 papers), Tuberous Sclerosis Complex Research (10 papers) and T-cell and B-cell Immunology (10 papers). Nicola Migone collaborates with scholars based in Italy, Switzerland and United States. Nicola Migone's co-authors include Giulia Casorati, Gennaro De Libero, Annalisa Petrelli, Alfredo Brusco, Antonio Lanzavecchia, Silvia Giordano, Paolo M. Comoglio, Giorgio F. Gilestro, Stefania Lanzardo and Caterina Carbonara and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Nicola Migone

80 papers receiving 3.7k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Nicola Migone Italy	33	1.7k	1.3k	726	565	435	81	3.8k
Christine Ambrose United States	29	2.4k 1.4×	4.1k 3.1×	564 0.8×	834 1.5×	531 1.2×	52	7.1k
Richard Pannell United Kingdom	30	2.1k 1.2×	2.5k 2.0×	393 0.5×	370 0.7×	219 0.5×	41	4.9k
E N Geissler United States	17	1.9k 1.1×	2.2k 1.7×	658 0.9×	443 0.8×	133 0.3×	19	4.5k
Ann Tsukamoto United States	26	2.3k 1.3×	542 0.4×	569 0.8×	1.0k 1.8×	357 0.8×	38	3.9k
Tobias Gedde‐Dahl Norway	39	1.8k 1.1×	1.2k 0.9×	1.0k 1.4×	770 1.4×	126 0.3×	225	5.3k
Arito Yamane Japan	22	3.4k 2.0×	1.2k 0.9×	318 0.4×	817 1.4×	118 0.3×	50	4.5k
Christophe Jamin France	34	764 0.5×	1.8k 1.4×	311 0.4×	324 0.6×	221 0.5×	136	3.7k
Kay M. Higgins United States	15	3.2k 1.9×	635 0.5×	943 1.3×	609 1.1×	154 0.4×	15	4.2k
Shulamit Katzav Israel	30	2.1k 1.3×	1.3k 1.0×	308 0.4×	940 1.7×	123 0.3×	73	3.8k
Alec M. Cheng United States	25	1.7k 1.0×	2.0k 1.5×	302 0.4×	545 1.0×	91 0.2×	28	3.9k

Countries citing papers authored by Nicola Migone

Since Specialization

Citations

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

Fields of papers citing papers by Nicola Migone

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nicola Migone

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

Brussino, Alessandro, Sandra D’Alfonso, Cinzia Cagnoli, et al.. (2009). Mutations in the lamin B1 gene are not present in multiple sclerosis. European Journal of Neurology. 16(4). 544–546. 3 indexed citations

Brussino, Alessandro, Giovanna Vaula, Cinzia Cagnoli, et al.. (2009). A novel family with Lamin B1 duplication associated with adult-onset leucoencephalopathy. Journal of Neurology Neurosurgery & Psychiatry. 80(2). 237–240. 32 indexed citations

Brussino, Alessandro, Flora Tassone, Carlo Arduino, et al.. (2005). An Enhanced Polymerase Chain Reaction Assay to Detect Pre- and Full Mutation Alleles of the Fragile X Mental Retardation 1 Gene. Journal of Molecular Diagnostics. 7(5). 605–612. 89 indexed citations

Brusco, Alfredo, Cinzia Gellera, Claudia Cagnoli, et al.. (2004). Molecular Genetics of Hereditary Spinocerebellar Ataxia. Archives of Neurology. 61(5). 727–727. 109 indexed citations

Saviozzi, Silvia, Maria Piane, Sabrina Prudente, et al.. (2003). Six novel ATM mutations in Italian patients with classical ataxia-telangiectasia. Human Mutation. 21(4). 450–450. 9 indexed citations

Petrelli, Annalisa, Giorgio F. Gilestro, Stefania Lanzardo, et al.. (2002). The endophilin–CIN85–Cbl complex mediates ligand-dependent downregulation of c-Met. Nature. 416(6877). 187–190. 373 indexed citations

Cestra, Gianluca, Luisa Castagnoli, Luciana Dente, et al.. (1999). The SH3 Domains of Endophilin and Amphiphysin Bind to the Proline-rich Region of Synaptojanin 1 at Distinct Sites That Display an Unconventional Binding Specificity. Journal of Biological Chemistry. 274(45). 32001–32007. 103 indexed citations

Migone, Nicola, Claudia Giachino, Giuseppe Matullo, et al.. (1995). Restriction of the T-cell receptor V delta gene repertoire is due to preferential rearrangement and is independent of antigen selection. Immunogenetics. 42(5). 323–332. 15 indexed citations

Perona, M, D. Dall’Amico, Enrico Grosso, et al.. (1994). Maternal serum markers. Estimation of the risk of Down's syndrome: a prospective study. International Journal of Clinical & Laboratory Research. 24(1). 49–53. 14 indexed citations

10.

Libero, Gennaro De, et al.. (1993). T cell receptor heterogeneity in γδ T cell clones from intestinal biopsies of patients with celiac disease. European Journal of Immunology. 23(2). 499–504. 33 indexed citations

11.

Pandolfi, Franco, Giulio Rossi, Renato Zambello, et al.. (1991). Clonally expanded CD3+, CD4−, CD8− cells bearing the or the T-cell receptor in patients with the lymphoproliferative disease of granular lymphocytes. Clinical Immunology and Immunopathology. 60(3). 371–383. 8 indexed citations

12.

Trentin, Livio, Nicola Migone, Renato Zambello, et al.. (1990). Mechanisms accounting for lymphocytic alveolitis in hypersensitivity pneumonitis.. The Journal of Immunology. 145(7). 2147–2154. 73 indexed citations

13.

Biondi, Andrea, Paola Francia di Celle, Vincenzo Rossi, et al.. (1990). High prevalence of T-cell receptor V delta 2-(D)-D delta 3 or D delta 1/2-D delta 3 rearrangements in B-precursor acute lymphoblastic leukemias. Blood. 75(9). 1834–1840. 55 indexed citations

14.

Casorati, Giulia, Gennaro De Libero, Antonio Lanzavecchia, & Nicola Migone. (1989). Molecular analysis of human gamma/delta+ clones from thymus and peripheral blood.. The Journal of Experimental Medicine. 170(5). 1521–1535. 164 indexed citations

15.

Moretta, Alessandro, Cristina Bottino, Ermanno Ciccone, et al.. (1988). Human peripheral blood lymphocytes bearing T cell receptor gamma/delta. Expression of CD8 differentiation antigen correlates with the expression of the 55-kD, C gamma 2-encoded gamma chain.. The Journal of Experimental Medicine. 168(6). 2349–2354. 31 indexed citations

16.

Ciccone, Ermanno, O Viale, Cristina Bottino, et al.. (1988). Antigen recognition by human T cell receptor gamma-positive lymphocytes. Specific lysis of allogeneic cells after activation in mixed lymphocyte culture.. The Journal of Experimental Medicine. 167(4). 1517–1522. 84 indexed citations

17.

Moretta, Lorenzo, Daniela Pende, Cristina Bottino, et al.. (1987). Human CD3⁺4⁻8⁻WT31⁻T lymphocyte expressing the putative T cell receptor γ‐gene product. A limiting dilution and clonal analysis. European Journal of Immunology. 17(9). 1229–1234. 32 indexed citations

18.

Foà, Robin, Giulia Casorati, M. C. Giubellino, et al.. (1987). Rearrangements of immunoglobulin and T cell receptor beta and gamma genes are associated with terminal deoxynucleotidyl transferase expression in acute myeloid leukemia.. The Journal of Experimental Medicine. 165(3). 879–890. 77 indexed citations

19.

Lauria, F., Robin Foà, Donatella Raspadori, et al.. (1987). Chronic T‐cell leukaemias. A variant of T‐prolymphocytic leukaemias: morphological, immunological and clinical characterization of 2 cases. European Journal Of Haematology. 39(1). 1–6. 1 indexed citations

20.

Foà, Robin, Pier Giuseppe Pelicci, Nicola Migone, et al.. (1986). Analysis of T-cell receptor beta chain (T beta) gene rearrangements demonstrates the monoclonal nature of T-cell chronic lymphoproliferative disorders.. Blood. 67(1). 247–50. 56 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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