Marina Stroppiano

1.1k total citations
34 papers, 822 citations indexed

About

Marina Stroppiano is a scholar working on Physiology, Molecular Biology and Organic Chemistry. According to data from OpenAlex, Marina Stroppiano has authored 34 papers receiving a total of 822 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Physiology, 13 papers in Molecular Biology and 11 papers in Organic Chemistry. Recurrent topics in Marina Stroppiano's work include Lysosomal Storage Disorders Research (27 papers), Carbohydrate Chemistry and Synthesis (11 papers) and Cellular transport and secretion (9 papers). Marina Stroppiano is often cited by papers focused on Lysosomal Storage Disorders Research (27 papers), Carbohydrate Chemistry and Synthesis (11 papers) and Cellular transport and secretion (9 papers). Marina Stroppiano collaborates with scholars based in Italy, United Kingdom and Slovakia. Marina Stroppiano's co-authors include Mirella Filocamo, Fabio Corsolini, Stefano Regis, Bruno Bembi, Maja Di Rocco, Giancarlo Parenti, Susanna Lualdi, Andrea Dardis, María Gabriela Pittis and Giovanni Ciana and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Nanoscale.

In The Last Decade

Marina Stroppiano

33 papers receiving 797 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marina Stroppiano Italy 17 634 271 233 223 210 34 822
Tina Rozaklis Australia 17 659 1.0× 236 0.9× 145 0.6× 253 1.1× 231 1.1× 24 835
Vivienne Muller Australia 17 786 1.2× 291 1.1× 327 1.4× 243 1.1× 333 1.6× 26 1.0k
E. Young United Kingdom 15 664 1.0× 175 0.6× 138 0.6× 179 0.8× 281 1.3× 23 768
Ya. V. Voznyi Russia 12 592 0.9× 206 0.8× 140 0.6× 171 0.8× 248 1.2× 19 685
Cordula Steglich Germany 16 609 1.0× 226 0.8× 158 0.7× 132 0.6× 358 1.7× 24 805
Leanne K. Hein Australia 17 522 0.8× 232 0.9× 129 0.6× 193 0.9× 288 1.4× 34 734
Takahiro Tsukimura Japan 18 769 1.2× 243 0.9× 310 1.3× 222 1.0× 380 1.8× 47 868
Sean N. Prater United States 12 720 1.1× 167 0.6× 194 0.8× 53 0.2× 235 1.1× 19 875
Susanna Bunge Germany 18 1.0k 1.6× 299 1.1× 279 1.2× 224 1.0× 559 2.7× 26 1.2k
Daniëlle te Vruchte United Kingdom 12 505 0.8× 448 1.7× 142 0.6× 162 0.7× 194 0.9× 18 939

Countries citing papers authored by Marina Stroppiano

Since Specialization
Citations

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

Fields of papers citing papers by Marina Stroppiano

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marina Stroppiano

This figure shows the co-authorship network connecting the top 25 collaborators of Marina Stroppiano. A scholar is included among the top collaborators of Marina Stroppiano 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 Marina Stroppiano. Marina Stroppiano 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.
Siri, Laura, Andrea Rossi, Marina Stroppiano, et al.. (2014). A novel homozygous splicing mutation in PSAP gene causes metachromatic leukodystrophy in two Moroccan brothers. Neurogenetics. 15(2). 101–106. 9 indexed citations
2.
Costa, Roberto, Marika Salvalaio, Marina Stroppiano, et al.. (2014). Glucocerebrosidase deficiency in zebrafish affects primary bone ossification through increased oxidative stress and reduced Wnt/β-catenin signaling. Human Molecular Genetics. 24(5). 1280–1294. 44 indexed citations
3.
Tappino, Barbara, Roberta Biancheri, Matthew Mort, et al.. (2010). Identification and characterization of 15 novel GALC gene mutations causing Krabbe disease. Human Mutation. 31(12). E1894–E1914. 90 indexed citations
4.
5.
Zampieri, Stefania, Mirella Filocamo, Emanuele Buratti, et al.. (2008). Molecular and functional analysis of the HEXB gene in Italian patients affected with Sandhoff disease: identification of six novel alleles. Neurogenetics. 10(1). 49–58. 24 indexed citations
6.
Bembi, Bruno, Mirella Filocamo, Giancarlo Parenti, et al.. (2006). Mutation profile of theGAA gene in 40 Italian patients with late onset glycogen storage disease type II. Human Mutation. 27(10). 999–1006. 103 indexed citations
7.
Lualdi, Susanna, Maja Di Rocco, Fabio Corsolini, et al.. (2006). Identification of nine new IDS alleles in mucopolysaccharidosis II. Quantitative evaluation by real-time RT-PCR of mRNAs sensitive to nonsense-mediated and nonstop decay mechanisms. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1762(4). 478–484. 27 indexed citations
8.
Lualdi, Susanna, Stefano Regis, Maja Di Rocco, et al.. (2005). Characterization of iduronate-2-sulfatase gene-pseudogene recombinations in eight patients with Mucopolysaccharidosis type II revealed by a rapid PCR-based method. Human Mutation. 25(5). 491–497. 29 indexed citations
9.
Biasio, Pierangela De, et al.. (2005). First-trimester fetal nuchal translucency and inherited metabolic disorders. Prenatal Diagnosis. 26(1). 77–80. 7 indexed citations
10.
Stroppiano, Marina, Fabio Corsolini, Maja Di Rocco, et al.. (2004). Screening of 25 Italian patients with Niemann-Pick a reveals fourteen new mutations, one common and thirteen private, inSMPD1. Human Mutation. 24(1). 105–105. 25 indexed citations
11.
Pittis, María Gabriela, Veronica Ileana Guerci, Christophe Marçais, et al.. (2004). Acid sphingomyelinase: Identification of nine novel mutations among Italian Niemann Pick type B patients and characterization ofin vivofunctional in-frame start codon. Human Mutation. 24(2). 186–187. 43 indexed citations
12.
Filocamo, Mirella, Stefano Regis, Fabio Corsolini, et al.. (2003). Expression studies of two novel in CIS‐mutations identified in an intermediate case of Hunter syndrome. American Journal of Medical Genetics Part A. 120A(1). 84–87. 13 indexed citations
13.
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
14.
Regis, Stefano, Fabio Corsolini, Marina Stroppiano, Roberto Cusano, & Mirella Filocamo. (2002). Contribution of arylsulfatase A mutations located on the same allele to enzyme activity reduction and metachromatic leukodystrophy severity. Human Genetics. 110(4). 351–355. 25 indexed citations
15.
Miano, Maurizio, Edoardo Lanino, R. Gatti, et al.. (2001). Four year follow-up of a case of fucosidosis treated with unrelated donor bone marrow transplantation. Bone Marrow Transplantation. 27(7). 747–751. 38 indexed citations
16.
Regis, Stefano, Mirella Filocamo, Roberto Cusano, et al.. (2001). Prenatal diagnosis of Pelizaeus‐Merzbacher disease: detection of proteolipid protein gene duplication by quantitative fluorescent multiplex PCR. Prenatal Diagnosis. 21(8). 668–671. 13 indexed citations
17.
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
18.
Stroppiano, Marina, et al.. (2000). Evidence for a Founder Effect in Sicilian Patients with Glycogen Storage Disease Type II. Human Heredity. 50(6). 331–333. 14 indexed citations
19.
20.
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

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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