Rosanna Gatti

1.3k total citations
35 papers, 808 citations indexed

About

Rosanna Gatti is a scholar working on Physiology, Molecular Biology and Organic Chemistry. According to data from OpenAlex, Rosanna Gatti has authored 35 papers receiving a total of 808 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Physiology, 19 papers in Molecular Biology and 10 papers in Organic Chemistry. Recurrent topics in Rosanna Gatti's work include Lysosomal Storage Disorders Research (21 papers), Carbohydrate Chemistry and Synthesis (10 papers) and Trypanosoma species research and implications (8 papers). Rosanna Gatti is often cited by papers focused on Lysosomal Storage Disorders Research (21 papers), Carbohydrate Chemistry and Synthesis (10 papers) and Trypanosoma species research and implications (8 papers). Rosanna Gatti collaborates with scholars based in Italy, United States and Australia. Rosanna Gatti's co-authors include Mirella Filocamo, Paolo Durand, Fabio Corsolini, Stefano Regis, C Borrone, John Darby, Jan E. Dumon, John S. O’Brien, Patrick J. Willems and Giancarlo Parenti and has published in prestigious journals such as FEBS Letters, The Journal of Pediatrics and Clinica Chimica Acta.

In The Last Decade

Rosanna Gatti

34 papers receiving 774 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rosanna Gatti Italy 17 422 298 195 167 151 35 808
N. U. Bosshard Switzerland 18 446 1.1× 338 1.1× 323 1.7× 164 1.0× 223 1.5× 27 972
Clare Beesley United Kingdom 17 607 1.4× 288 1.0× 241 1.2× 123 0.7× 240 1.6× 29 980
María Josep Coll Spain 19 703 1.7× 370 1.2× 180 0.9× 153 0.9× 218 1.4× 37 1.1k
R J Desnick United States 12 778 1.8× 245 0.8× 212 1.1× 205 1.2× 198 1.3× 20 941
Vũ Chí Dũng Vietnam 18 729 1.7× 298 1.0× 222 1.1× 191 1.1× 236 1.6× 38 1.1k
Helena Poupětová Czechia 17 932 2.2× 302 1.0× 207 1.1× 272 1.6× 196 1.3× 40 1.1k
J Jaeken Belgium 11 162 0.4× 421 1.4× 116 0.6× 58 0.3× 73 0.5× 19 760
Y T Chen United States 11 321 0.8× 187 0.6× 416 2.1× 41 0.2× 176 1.2× 11 769
E. Young United Kingdom 15 664 1.6× 175 0.6× 148 0.8× 179 1.1× 138 0.9× 23 768
Ali Dursun Türkiye 17 215 0.5× 434 1.5× 165 0.8× 109 0.7× 51 0.3× 97 995

Countries citing papers authored by Rosanna Gatti

Since Specialization
Citations

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

Fields of papers citing papers by Rosanna Gatti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rosanna Gatti

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

All Works

20 of 20 papers shown
1.
Melis, Daniela, Giancarlo Parenti, Paola Marcolongo, et al.. (2005). Genotype/phenotype correlation in glycogen storage disease type 1b: a multicentre study and review of the literature. European Journal of Pediatrics. 164(8). 501–508. 64 indexed citations
2.
Filocamo, Mirella, Marina Stroppiano, Marco Seri, et al.. (2002). Analysis of the glucocerebrosidase gene and mutation profile in 144 Italian gaucher patients. Human Mutation. 20(3). 234–235. 50 indexed citations
4.
Filocamo, Mirella, et al.. (2001). Molecular analysis of 40 Italian patients with mucopolysaccharidosis type II: New mutations in the iduronate-2-sulfatase (IDS) gene. Human Mutation. 18(2). 164–165. 32 indexed citations
5.
Filocamo, Mirella, Gloria Bonuccelli, Fabio Corsolini, et al.. (2000). Somatic Mosaicism in a Patient with Gaucher Disease Type 2: Implication for Genetic Counseling and Therapeutic Decision-Making. Blood Cells Molecules and Diseases. 26(6). 611–612. 11 indexed citations
6.
Filocamo, Mirella, et al.. (2000). Identification of a Novel Recombinant Allele in Three Unrelated Italian Gaucher Patients: Implications for Prognosis and Genetic Counseling. Blood Cells Molecules and Diseases. 26(4). 307–311. 11 indexed citations
7.
Galli, Lucia, Alfredo Orrico, Paola Marcolongo, et al.. (1999). Mutations in the glucose‐6‐phosphate transporter (G6PT) gene in patients with glycogen storage diseases type 1b and 1c. FEBS Letters. 459(2). 255–258. 43 indexed citations
9.
Pilia, Giuseppe, Manuela Uda, Fulvia Frau, et al.. (1999). Jagged-1 mutation analysis in Italian Alagille syndrome patients. Human Mutation. 14(5). 394–400. 36 indexed citations
10.
Parenti, Giancarlo, Mirella Filocamo, Luigi Titomanlio, et al.. (1998). A novel mutation of the β‐glucocererebrosidase gene associated with neurologic manifestations in three sibs. Clinical Genetics. 53(4). 281–285. 5 indexed citations
11.
Stroppiano, Marina, et al.. (1998). New mutation (S298P) in a patient with glycogen storage disease type IA. Human Mutation. 11(S1). S329–S329. 2 indexed citations
12.
Bonuccelli, Gloria, Stefano Regis, Mirella Filocamo, et al.. (1998). A deletion involving exons 2–4 in the iduronate‐2‐sulfatase gene of a patient with intermediate Hunter syndrome. Clinical Genetics. 53(6). 474–477. 12 indexed citations
13.
Regis, Stefano, Mirella Filocamo, Marina Stroppiano, Fabio Corsolini, & Rosanna Gatti. (1997). A T > C transition causing a Leu > Pro substitution in a conserved region of the arylsulfatase A gene in a late infantile metachromatic leukodystrophy patient. Clinical Genetics. 52(1). 65–67. 5 indexed citations
14.
Carrozzo, Romeo, Rossana Tonlorenzi, Fabio Corsolini, & Rosanna Gatti. (1996). Two New Nonsense mutations (Q80X; Q389X) in patients with severe hunter syndrome ( mucopolysaccharidosis type II). Human Mutation. 7(2). 184–185. 6 indexed citations
15.
16.
Rocco, Maja Di, Rosanna Gatti, Paolo Gandullia, et al.. (1993). Report on two patients with Costello syndrome and sialuria. American Journal of Medical Genetics. 47(7). 1135–1140. 38 indexed citations
17.
Palmieri, Giuseppe, Valeria Capra, Giovanna Romano, et al.. (1992). The iduronate sulfatase gene: Isolation of a 1.2-Mb YAC contig spanning the entire gene and identification of heterogeneous deletions in patients with Hunter syndrome. Genomics. 12(1). 52–57. 33 indexed citations
18.
Willems, Patrick J., Rosanna Gatti, John Darby, et al.. (1991). Fucosidosis revisited: A review of 77 patients. American Journal of Medical Genetics. 38(1). 111–131. 115 indexed citations
19.
Gatti, Rosanna, et al.. (1979). Características biológicas de las mucolipidosis II y III. Anales de Pediatría. 12(8). 563–574. 1 indexed citations
20.
Borrone, C, et al.. (1974). Fucosidosis: Clinical, biochemical, immunologic, and genetic studies in two new cases. The Journal of Pediatrics. 84(5). 727–730. 48 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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