M.C. Patrosso

424 total citations
9 papers, 318 citations indexed

About

M.C. Patrosso is a scholar working on Cell Biology, Molecular Biology and Ophthalmology. According to data from OpenAlex, M.C. Patrosso has authored 9 papers receiving a total of 318 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Cell Biology, 3 papers in Molecular Biology and 2 papers in Ophthalmology. Recurrent topics in M.C. Patrosso's work include Protein Kinase Regulation and GTPase Signaling (2 papers), Cell Adhesion Molecules Research (2 papers) and Cellular transport and secretion (2 papers). M.C. Patrosso is often cited by papers focused on Protein Kinase Regulation and GTPase Signaling (2 papers), Cell Adhesion Molecules Research (2 papers) and Cellular transport and secretion (2 papers). M.C. Patrosso collaborates with scholars based in Italy, United States and Germany. M.C. Patrosso's co-authors include Paolo Vezzoni, Anna Villa, Dario Strina, Paolo Macchi, Luigi D. Notarangelo, Alberto G. Ugazio, Ugo Ramenghi, Elide Mantuano, Giovanni Cavagni and Duilio Brugnoni and has published in prestigious journals such as Nature Genetics, Neuroscience and Investigative Ophthalmology & Visual Science.

In The Last Decade

M.C. Patrosso

9 papers receiving 315 citations

Peers

M.C. Patrosso

CB

IA

MB

IMMUN

GENET

Michelle Ryan Ireland

Linda M. Ritter United States

Tuula Helander Finland

Virva Huotari Finland

Ines Nasdala Germany

Dietmar Seiffert United States

Nicole L. Prokopishyn Canada

RA Hirst United Kingdom

Jonathan T. Pribila United States

Laura I. Salazar‐Fontana United States

Michelle Ryan Ireland

M.C. Patrosso

61 ×0.5

CB

40 ×0.4

IA

131 ×1.3

MB

85 ×1.1

IMMUN

36 ×0.5

GENET

Citations per year, relative to M.C. Patrosso M.C. Patrosso (= 1×) peers Michelle Ryan

Countries citing papers authored by M.C. Patrosso

Since Specialization

Citations

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

Fields of papers citing papers by M.C. Patrosso

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M.C. Patrosso

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

All Works

Sort: Min cites: Since: Top N: Style:

9 of 9 papers shown

1.

Mauri, Lucia, Steffen Uebe, Heinrich Sticht, et al.. (2016). Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucoma. Orphanet Journal of Rare Diseases. 11(1). 108–108. 28 indexed citations

2.

Gianfrancesco, Fernando, Teresa Esposito, Silvana Penco, et al.. (2008). ZPLD1 gene is disrupted in a patient with balanced translocation that exhibits cerebral cavernous malformations. Neuroscience. 155(2). 345–349. 23 indexed citations

3.

Lando, Giuliana, Adriano Magli, Paolo Frezzotti, et al.. (2007). Molecular Analysis of Italian Patients Affected by Congenital Glaucoma. Investigative Ophthalmology & Visual Science. 48(13). 2811–2811. 1 indexed citations

4.

Patrosso, M.C., Fabrizio Salvi, D. De Grandis, et al.. (1998). Novel transthyretin missense mutation (Thr34) in an Italian family with hereditary amyloidosis. American Journal of Medical Genetics. 77(2). 135–138. 10 indexed citations

5.

Patrosso, M.C., Paolo Vezzoni, Paola Gobbi, et al.. (1996). Two new mutations in the transthyretin gene, leading to polyneuropathy and cardiomyopathy in two unrelated ITalian families. Neuromuscular Disorders. 6. S23–S23. 2 indexed citations

6.

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

7.

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

8.

Patrosso, M.C., Monica Repetto, Anna Villa, et al.. (1994). The Exon-Intron Organization of the Human X-Linked Gene (FLN1) Encoding Actin-Binding Protein 280. Genomics. 21(1). 71–76. 27 indexed citations

9.

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

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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