Mario Tosi

6.0k total citations
87 papers, 4.3k citations indexed

About

Mario Tosi is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Mario Tosi has authored 87 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 30 papers in Genetics and 23 papers in Genetics. Recurrent topics in Mario Tosi's work include Coagulation, Bradykinin, Polyphosphates, and Angioedema (23 papers), Complement system in diseases (15 papers) and RNA and protein synthesis mechanisms (13 papers). Mario Tosi is often cited by papers focused on Coagulation, Bradykinin, Polyphosphates, and Angioedema (23 papers), Complement system in diseases (15 papers) and RNA and protein synthesis mechanisms (13 papers). Mario Tosi collaborates with scholars based in France, United States and Italy. Mario Tosi's co-authors include Christiane Duponchel, T Meo, Thierry Frébourg, Ueli Schibler, Tommaso Meo, Dominique Stoppa‐Lyonnet, Otto Hagenbüchle, Peter K. Wellauer, Richard A. Young and Alexandra Martins and has published in prestigious journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Mario Tosi

87 papers receiving 4.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mario Tosi France	38	2.1k	1.3k	922	703	580	87	4.3k
T.B. Shows United States	37	2.3k 1.1×	332 0.3×	798 0.9×	700 1.0×	370 0.6×	77	4.4k
Tom Kadesch United States	44	5.5k 2.6×	298 0.2×	878 1.0×	1.6k 2.2×	356 0.6×	56	7.5k
Michael L. Mucenski United States	33	3.0k 1.4×	275 0.2×	830 0.9×	1.3k 1.8×	767 1.3×	47	5.0k
Finbarr E. Cotter United Kingdom	38	2.6k 1.2×	872 0.7×	505 0.5×	792 1.1×	848 1.5×	111	5.0k
Lisa Garrett United States	25	3.1k 1.5×	235 0.2×	874 0.9×	540 0.8×	346 0.6×	50	5.0k
Annalisa Frattini Italy	26	2.0k 1.0×	229 0.2×	628 0.7×	1.0k 1.4×	181 0.3×	77	3.4k
Marieke von Lindern Netherlands	43	3.9k 1.8×	884 0.7×	507 0.5×	618 0.9×	1.4k 2.4×	134	5.7k
Daniel Afar United States	33	2.0k 0.9×	822 0.6×	209 0.2×	835 1.2×	1.5k 2.6×	68	4.0k
S Munemitsu United States	24	5.1k 2.4×	209 0.2×	893 1.0×	797 1.1×	321 0.6×	28	7.1k
Petra Moerer Netherlands	19	4.9k 2.3×	427 0.3×	1.2k 1.2×	594 0.8×	82 0.1×	23	6.1k

Countries citing papers authored by Mario Tosi

Since Specialization

Citations

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

Fields of papers citing papers by Mario Tosi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mario Tosi

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

Ponard, D., Christine Gaboriaud, Arije Ghannam, et al.. (2019). SERPING1 mutation update: Mutation spectrum and C1 Inhibitor phenotypes. Human Mutation. 41(1). 38–57. 66 indexed citations

Soukarieh, Omar, Pascaline Gaildrat, Mohamad Hamieh, et al.. (2016). Exonic Splicing Mutations Are More Prevalent than Currently Estimated and Can Be Predicted by Using In Silico Tools. PLoS Genetics. 12(1). e1005756–e1005756. 117 indexed citations

Huin, Vincent, Nathalie Drouot, Pascal Chambon, et al.. (2011). Development of a Nonfluorescent Multiplex Semiquantitative Polymerase Chain Reaction to Confirm Rearrangements Detected by Array-Comparative Genomic Hybridization. Genetic Testing and Molecular Biomarkers. 15(7-8). 469–474. 1 indexed citations

Gaildrat, Pascaline, Audrey Killian, Alexandra Martins, et al.. (2010). Use of Splicing Reporter Minigene Assay to Evaluate the Effect on Splicing of Unclassified Genetic Variants. Methods in molecular biology. 653. 249–257. 120 indexed citations

Bonnet, Céline, Sophie Krieger, Myriam Vézain, et al.. (2008). Screening BRCA1 and BRCA2 unclassified variants for splicing mutations using reverse transcription PCR on patient RNA and an ex vivo assay based on a splicing reporter minigene. Journal of Medical Genetics. 45(7). 438–446. 89 indexed citations

Tournier, Isabelle, Myriam Vézain, Alexandra Martins, et al.. (2008). A large fraction of unclassified variants of the mismatch repair genesMLH1andMSH2is associated with splicing defects. Human Mutation. 29(12). 1412–1424. 126 indexed citations

Ruminy, Philippe, Jean Pierre Kerckaert, F Parmentier, et al.. (2008). Detection of somatic quantitative genetic alterations by multiplex polymerase chain reaction for the prediction of outcome in diffuse large B-cell lymphomas. Haematologica. 93(4). 543–550. 23 indexed citations

Bastard, Christian, Grégory Raux, Christophe Fruchart, et al.. (2007). Comparison of a quantitative PCR method with FISH for the assessment of the four aneuploidies commonly evaluated in CLL patients. Leukemia. 21(7). 1460–1463. 20 indexed citations

Vézain, Myriam, Pascale Saugier-Véber, Judith Melki, et al.. (2007). A sensitive assay for measuring SMN mRNA levels in peripheral blood and in muscle samples of patients affected with spinal muscular atrophy. European Journal of Human Genetics. 15(10). 1054–1062. 32 indexed citations

10.

Saugier-Véber, Pascale, Alice Goldenberg, Valérie Drouin‐Garraud, et al.. (2006). Simple detection of genomic microdeletions and microduplications using QMPSF in patients with idiopathic mental retardation. European Journal of Human Genetics. 14(9). 1009–1017. 27 indexed citations

11.

Roche, O., Alvaro Blanch, Christiane Duponchel, et al.. (2005). Hereditary angioedema: The mutation spectrum ofSERPING1/C1NHin a large Spanish cohort. Human Mutation. 26(2). 135–144. 62 indexed citations

12.

Pagès, Sabine, et al.. (2001). Screening of male breast cancer and of breast-ovarian cancer families for BRCA2 mutations using large bifluorescent amplicons. British Journal of Cancer. 84(4). 482–488. 10 indexed citations

13.

Pappalardo, Emanuela, Marco Cicardi, Christiane Duponchel, et al.. (2000). Frequent de novo mutations and exon deletions in the C1inhibitor gene of patients with angioedema. Journal of Allergy and Clinical Immunology. 106(6). 1147–1154. 174 indexed citations

14.

Verpy, Elisabeth, Evelyne Couture‐Tosi, Eric Eldering, et al.. (1995). Crucial residues in the carboxy-terminal end of C1 inhibitor revealed by pathogenic mutants impaired in secretion or function.. Journal of Clinical Investigation. 95(1). 350–359. 58 indexed citations

15.

Thielens, Nicole M., Jean Gagnon, Péter Gál, et al.. (1992). Recombinant human complement subcomponent C1s lacking .beta.-hydroxyasparagine, sialic acid, and one of its two carbohydrate chains still reassembles with C1q and C1r to form a functional C1 complex. Biochemistry. 31(17). 4254–4262. 33 indexed citations

16.

Carter, Philip E., Christiane Duponchel, Mario Tosi, & John E. Fothergill. (1991). Complete nucleotide sequence of the gene for human C1 inhibitor with an unusually high density of Alu elements. European Journal of Biochemistry. 197(2). 301–308. 99 indexed citations

17.

Gaspar, Marı́a-Luisa, P Bourgarel, T Meo, & Mario Tosi. (1991). [Structure of messenger RNA of androgen receptor in mice and molecular characterization in Tfm mutant].. PubMed. 185(6). 510–9. 2 indexed citations

18.

Tosi, Mario, Agnès Journet, Christiane Duponchel, Evelyne Couture‐Tosi, & T Meo. (1989). Human complement C1r and C1s proteins and genes: studies with molecular probes.. PubMed. 65–71. 7 indexed citations

19.

Tosi, Mario, Christiane Duponchel, P Bourgarel, Maurice G. Colomb, & Tommaso Meo. (1986). Molecular cloning of human C1 inhibitor: sequence homologies with α1-antitrypsin and other members of the serpins superfamily. Gene. 42(3). 265–272. 53 indexed citations

20.

Schibler, Ueli, Mario Tosi, Anne-Cécile Pittet, Lucia Fabiani, & Peter K. Wellauer. (1980). Tissue-specific expression of mouse α-amylase genes. Journal of Molecular Biology. 142(1). 93–116. 182 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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