M. Mezzina

1.5k total citations
24 papers, 1.2k citations indexed

About

M. Mezzina is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, M. Mezzina has authored 24 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Oncology. Recurrent topics in M. Mezzina's work include DNA Repair Mechanisms (9 papers), Carcinogens and Genotoxicity Assessment (3 papers) and Polyomavirus and related diseases (3 papers). M. Mezzina is often cited by papers focused on DNA Repair Mechanisms (9 papers), Carcinogens and Genotoxicity Assessment (3 papers) and Polyomavirus and related diseases (3 papers). M. Mezzina collaborates with scholars based in France, Italy and Netherlands. M. Mezzina's co-authors include Alain Sarasin, Jan H.J. Hoeijmakers, Geert Weeda, Laurent Schaeffer, Adrien Staub, Jean‐Marc Egly, Vincent Moncollin, Richard Roy, Wim Vermeulen and Pascale Bouillé and has published in prestigious journals such as Nucleic Acids Research, The EMBO Journal and Journal of Virology.

In The Last Decade

M. Mezzina

24 papers receiving 1.2k citations

Peers

M. Mezzina

GENET

ONCOL

Christian Maercker Germany

Petra Jakobs United States

Peter K. Seperack United States

Erica M. Selva United States

Liyun Sang United States

Orr Barak United States

Steven C. Miller United States

Ciro Bonetti Italy

Nicole Bäumer Germany

Alexander R. Ball United States

Christian Maercker Germany

M. Mezzina

755 ×0.7

204 ×0.9

138 ×0.6

GENET

175 ×0.9

174 ×1.1

ONCOL

Citations per year, relative to M. Mezzina M. Mezzina (= 1×) peers Christian Maercker

Countries citing papers authored by M. Mezzina

Since Specialization

Citations

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

Fields of papers citing papers by M. Mezzina

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Mezzina

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

Gonin, Patrick, Christian J. Buchholz, Marc Pallardy, & M. Mezzina. (2005). Gene therapy bio-safety: scientific and regulatory issues. Gene Therapy. 12(S1). S146–S152. 24 indexed citations

Duan, Maoli, et al.. (2004). Treatment of peripheral sensorineural hearing loss: gene therapy. Gene Therapy. 11(S1). S51–S56. 25 indexed citations

Mezzina, M.. (2002). First Meeting of the Gene Vector Production Network, 4–5 October 2001, Evry, France. The Journal of Gene Medicine. 4(1). 105–108. 2 indexed citations

Mulleman, Denis, et al.. (2000). Adeno-associated virus-mediated delivery of IL-4 prevents collagen-induced arthritis. Gene Therapy. 7(22). 1930–1939. 70 indexed citations

Jabre, P., M. Mezzina, & André Mégarbané. (1999). [Cockayne syndrome in Lebanon. Description of 3 cases and review of the literature].. PubMed. 47(2). 144–7. 1 indexed citations

Mégarbané, André, et al.. (1999). Microcephaly, microphthalmia, congenital cataract, optic atrophy, short stature, hypotonia, severe psychomotor retardation, and cerebral malformations: a second family with micro syndrome or a new syndrome?. Journal of Medical Genetics. 36(8). 637–640. 17 indexed citations

Zeng, Lin, A Sarasin, & M. Mezzina. (1998). Retrovirus-mediated DNA repair gene transfer into xeroderma pigmentosum cells: Perspectives for a gene therapy. Cell Biology and Toxicology. 14(2). 105–110. 11 indexed citations

Zeng, Lin, et al.. (1997). Retrovirus-mediated gene transfer corrects DNA repair defect of xeroderma pigmentosum cells of complementation groups A, B and C. Gene Therapy. 4(10). 1077–1084. 50 indexed citations

Eveno, Éric, Wim Vermeulen, Odile Chevallier-Lagente, et al.. (1997). A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy.. PubMed. 60(2). 320–9. 121 indexed citations

10.

Eveno, Éric, Xavier Quilliet, Odile Chevallier-Lagente, et al.. (1995). Stable SV40-transformation and characterisation of some DNA repair properties of fibroblasts from a trichothiodystrophy patient. Biochimie. 77(11). 906–912. 8 indexed citations

11.

Vermeulen, Wim, Anneke J. van Vuuren, Laurent Schaeffer, et al.. (1994). Three Unusual Repair Deficiencies Associated with Transcription Factor BTF2(TFIIH): Evidence for the Existence of a Transcription Syndrome. Cold Spring Harbor Symposia on Quantitative Biology. 59(0). 317–329. 120 indexed citations

12.

Mezzina, M., Éric Eveno, Odile Chevallier-Lagente, et al.. (1994). Correction by the ERCC2 gene of UV sensitivity and repair deficiency phenotype in a subset of trichothiodystrophy cells. Carcinogenesis. 15(8). 1493–1498. 16 indexed citations

13.

Schaeffer, Laurent, Vincent Moncollin, Richard Roy, et al.. (1994). The ERCC2/DNA repair protein is associated with the class II BTF2/TFIIH transcription factor.. The EMBO Journal. 13(10). 2388–2392. 316 indexed citations

14.

Chang, Cheng, et al.. (1993). Characterization of the DNA double strand break repair defect in scid mice.. PubMed. 53(6). 1244–8. 75 indexed citations

15.

Stefanini, Miria, Wim Vermeulen, Geert Weeda, et al.. (1993). A new nucleotide-excision-repair gene associated with the disorder trichothiodystrophy.. PubMed. 53(4). 817–21. 94 indexed citations

16.

Mezzina, M., et al.. (1988). N-Acetoxy-N-2-acetylaminofluorene-induced damage on SV40 DNA: inhibition of DNA replication and visualization of DNA lesions. Carcinogenesis. 9(5). 789–795. 7 indexed citations

17.

Mezzina, M., et al.. (1988). Replication of simian virus 40 DNA after UV irradiation: evidence of growing fork blockage and single-stranded gaps in daughter strands. Journal of Virology. 62(11). 4249–4258. 26 indexed citations

18.

Elder, Rhoderick H., Alessandro Dell’Aquila, M. Mezzina, Alain Sarasin, & Daphne J. Osborne. (1987). DNA ligase in repair and replication in the embryos of rye, Secale cereale. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 181(1). 61–71. 47 indexed citations

19.

Mezzina, M., H. G. Suarez, R. Cassingéna, & Alain Sarasin. (1982). Increased activity of polynucleotide ligase in 5-iodo-2′-deoxyuridine and mitomycin C-pretreated simian virus 40 (SV40)-infected monkey kidney cells. Nucleic Acids Research. 10(16). 5073–5084. 13 indexed citations

20.

Mezzina, M., A. Gentil, & Alain Sarasin. (1981). Simian virus 40 as a probe for studying inducible repair functions in mammalian cells. PubMed. 17(2). 121–131. 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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