S. Marinoni

401 total citations
7 papers, 326 citations indexed

About

S. Marinoni is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, S. Marinoni has authored 7 papers receiving a total of 326 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 1 paper in Cellular and Molecular Neuroscience and 1 paper in Neurology. Recurrent topics in S. Marinoni's work include DNA Repair Mechanisms (5 papers), Prion Diseases and Protein Misfolding (3 papers) and RNA regulation and disease (3 papers). S. Marinoni is often cited by papers focused on DNA Repair Mechanisms (5 papers), Prion Diseases and Protein Misfolding (3 papers) and RNA regulation and disease (3 papers). S. Marinoni collaborates with scholars based in Italy, United Kingdom and Greece. S. Marinoni's co-authors include Miria Stefanini, Tiziana Nardò, Giusto Trevisan, Fiorella Nuzzo, Bernard C. Broughton, Alan R. Lehmann, Elena Botta, P. Lagomarsini, C.F. Arlett and G Cordone and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Human Genetics.

In The Last Decade

S. Marinoni

7 papers receiving 316 citations

Peers

Countries citing papers authored by S. Marinoni

Since Specialization

Citations

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

Fields of papers citing papers by S. Marinoni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. Marinoni

This figure shows the co-authorship network connecting the top 25 collaborators of S. Marinoni. A scholar is included among the top collaborators of S. Marinoni 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 S. Marinoni. S. Marinoni is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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7 of 7 papers shown

#	Work	Indexed citations
1	Analysis of Mutations in the XPD Gene in Italian Patients with Trichothiodystrophy: Site of Mutation Correlates with Repair Deficiency, but Gene Dosage Appears to Determine Clinical Severity 1998 ·The American Journal of Human Genetics ·Elena Botta, Tiziana Nardò, Bernard C. Broughton, S. Marinoni, Alan R. Lehmann, Miria Stefanini	91
2	Trichothiodystrophic Hair Reveals an Abnormal Pattern of Viscoelastic Parameters 1994 ·Skin Pharmacology and Physiology ·D. Tsambaos, Georgios Nikiforidis, (unknown), S. Marinoni	2
3	DNA repair investigations in nine Italian patients affected by trichothiodystrophy 1992 ·Mutation Research/DNA Repair ·Miria Stefanini, Silvia Giliani, Tiziana Nardò, S. Marinoni, V. Nazzaro, Renata Rizzo, Giusto Trevisan	67
4	Immune defects in families and patients with xeroderma pigmentosum and trichothiodystrophy 1992 ·Clinical & Experimental Immunology ·Erminia Mariani, A. Facchini, M.C. Honorati, Enzo Lalli, Enzo Berardesca, (unknown), S. Marinoni, Fiorella Nuzzo, G. Ricotti, Miria Stefanini	43
5	Search for consanguinity within and among families of patients with trichothiodystrophy associated with xeroderma pigmentosum. 1990 ·Journal of Medical Genetics ·Fiorella Nuzzo, G. Zei, Miria Stefanini, (unknown), (unknown), P. Lagomarsini, S. Marinoni, L. Salvaneschi	10
6	Chromosome and blood marker studies in families of patients affected by xeroderma pigmentosum and trichothiodystrophy 1988 ·Mutation Research Letters ·Fiorella Nuzzo, Miria Stefanini, Mariano Rocchi, (unknown), (unknown), P. Lagomarsini, S. Marinoni, Rosaria Scozzari	6
7	Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity 1986 ·Human Genetics ·Miria Stefanini, P. Lagomarsini, C.F. Arlett, S. Marinoni, C Borrone, Franco Crovato, Giusto Trevisan, G Cordone, Fiorella Nuzzo	107

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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