Manuela Mosconi

730 total citations
19 papers, 493 citations indexed

About

Manuela Mosconi is a scholar working on Surgery, Genetics and Immunology. According to data from OpenAlex, Manuela Mosconi has authored 19 papers receiving a total of 493 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Surgery, 3 papers in Genetics and 2 papers in Immunology. Recurrent topics in Manuela Mosconi's work include Congenital gastrointestinal and neural anomalies (13 papers), Intestinal Malrotation and Obstruction Disorders (6 papers) and Esophageal and GI Pathology (5 papers). Manuela Mosconi is often cited by papers focused on Congenital gastrointestinal and neural anomalies (13 papers), Intestinal Malrotation and Obstruction Disorders (6 papers) and Esophageal and GI Pathology (5 papers). Manuela Mosconi collaborates with scholars based in Italy, United States and Switzerland. Manuela Mosconi's co-authors include Claudio Gambini, Andrea Gregorio, Lorenzo Moretta, Marco Gattorno, Francesca Schena, Daniele Reverberi, Alberto Martini, Elisabetta Traggiai, Antonio Uccelli and Simona Casazza and has published in prestigious journals such as International Journal of Molecular Sciences, Heart and Cell Research.

In The Last Decade

Manuela Mosconi

17 papers receiving 483 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manuela Mosconi Italy 10 163 153 138 98 93 19 493
Isabelle Quintin‐Roué France 13 127 0.8× 145 0.9× 123 0.9× 138 1.4× 45 0.5× 45 494
Nagwa S. El‐Badri United States 12 110 0.7× 231 1.5× 146 1.1× 54 0.6× 129 1.4× 24 520
Jessica Cuerquis Canada 12 128 0.8× 198 1.3× 171 1.2× 92 0.9× 200 2.2× 17 529
Madhurima Kaushal United States 7 79 0.5× 63 0.4× 172 1.2× 70 0.7× 53 0.6× 11 368
Lingyang Hua China 15 114 0.7× 119 0.8× 176 1.3× 69 0.7× 39 0.4× 49 586
Miki Tomoeda Japan 11 118 0.7× 44 0.3× 234 1.7× 118 1.2× 45 0.5× 19 575
Rafaël Contreras Chile 9 155 1.0× 413 2.7× 234 1.7× 94 1.0× 183 2.0× 15 721
Yali Xuan Canada 6 130 0.8× 220 1.4× 245 1.8× 81 0.8× 38 0.4× 9 544
Safa Karandish United States 11 97 0.6× 395 2.6× 193 1.4× 136 1.4× 125 1.3× 13 733
Johannes Leibacher Germany 5 130 0.8× 232 1.5× 181 1.3× 56 0.6× 42 0.5× 6 464

Countries citing papers authored by Manuela Mosconi

Since Specialization
Citations

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

Fields of papers citing papers by Manuela Mosconi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manuela Mosconi

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

All Works

19 of 19 papers shown
1.
Avanzini, Stefano, et al.. (2023). Enterostomy-related complications in Hirschsprung's disease in a single cohort. Minerva Pediatrics. 75(5). 1 indexed citations
3.
Biassoni, Roberto, Eddi Di Marco, Margherita Squillario, et al.. (2021). Pathways and microbiome modifications related to surgery and enterocolitis in Hirschsprung disease. Pediatric Surgery International. 38(1). 83–98. 3 indexed citations
4.
Bachetti, Tiziana, Martina Bartolucci, Giuseppe Santamaria, et al.. (2021). The OSMR Gene Is Involved in Hirschsprung Associated Enterocolitis Susceptibility through an Altered Downstream Signaling. International Journal of Molecular Sciences. 22(8). 3831–3831. 7 indexed citations
5.
Avanzini, Stefano, et al.. (2019). Enterostomy-related complications in Hirschsprung's disease in a single cohort. Minerva Pediatrics. 75(5). 711–718. 2 indexed citations
6.
Prato, Alessio Pini, Casey Bartow‐McKenney, Kelly Hudspeth, et al.. (2019). A Metagenomics Study on Hirschsprung's Disease Associated Enterocolitis: Biodiversity and Gut Microbial Homeostasis Depend on Resection Length and Patient's Clinical History. Frontiers in Pediatrics. 7. 326–326. 20 indexed citations
7.
Prato, Alessio Pini, Enrico Felici, Fabrizio Racca, et al.. (2019). Hirschsprung disease and Down syndrome: From the reappraisal of risk factors to the impact of surgery. Journal of Pediatric Surgery. 54(9). 1838–1842. 10 indexed citations
8.
Lantieri, Francesca, Stefania Gimelli, Michela Malacarne, et al.. (2019). Copy number variations in candidate genomic regions confirm genetic heterogeneity and parental bias in Hirschsprung disease. Orphanet Journal of Rare Diseases. 14(1). 270–270. 4 indexed citations
10.
Prato, Alessio Pini, Clelia Zanaboni, Manuela Mosconi, et al.. (2016). Preliminary results of video-assisted anal fistula treatment (VAAFT) in children. Techniques in Coloproctology. 20(5). 279–285. 17 indexed citations
11.
Matera, Ivana, Marta Rusmini, Yiran Guo, et al.. (2016). Variants of the ACTG2 gene correlate with degree of severity and presence of megacystis in chronic intestinal pseudo-obstruction. European Journal of Human Genetics. 24(8). 1211–1215. 34 indexed citations
12.
Rossi, Valentina, Manuela Mosconi, Paolo Nozza, et al.. (2016). Chronic intestinal pseudo‐obstruction in a child harboring a founder Hirschsprung RET mutation. American Journal of Medical Genetics Part A. 170(9). 2400–2403. 4 indexed citations
13.
Tuo, Giulia, et al.. (2014). Hirschsprung’s Disease and Associated Congenital Heart Defects: A Prospective Observational Study from a Single Institution. Frontiers in Pediatrics. 2. 99–99. 9 indexed citations
14.
Prato, Alessio Pini, Valentina Rossi, Manuela Mosconi, et al.. (2014). Inguinal hernia in neonates and ex-preterm: complications, timing and need for routine contralateral exploration. Pediatric Surgery International. 31(2). 131–136. 13 indexed citations
15.
Prato, Alessio Pini, Valentina Rossi, Manuela Mosconi, et al.. (2013). A prospective observational study of associated anomalies in Hirschsprung’s disease. Orphanet Journal of Rare Diseases. 8(1). 184–184. 23 indexed citations
16.
Pezzolo, Annalisa, Federica Parodi, Danilo Marimpietri, et al.. (2011). Oct-4+/Tenascin C+ neuroblastoma cells serve as progenitors of tumor-derived endothelial cells. Cell Research. 21(10). 1470–1486. 54 indexed citations
17.
Disabella, Eliana, Maurizia Grasso, Fabiana Isabella Gambarin, et al.. (2011). Risk of dissection in thoracic aneurysms associated with mutations of smooth muscle alpha-actin 2 (ACTA2). Heart. 97(4). 321–326. 56 indexed citations
18.
Schena, Francesca, Claudio Gambini, Andrea Gregorio, et al.. (2010). Interferon‐γ–dependent inhibition of B cell activation by bone marrow–derived mesenchymal stem cells in a murine model of systemic lupus erythematosus. Arthritis & Rheumatism. 62(9). 2776–2786. 154 indexed citations
19.
Gregorio, Andrea, Maria Valeria Corrias, Roberta Castriconi, et al.. (2008). Small round blue cell tumours: diagnostic and prognostic usefulness of the expression of B7‐H3 surface molecule. Histopathology. 53(1). 73–80. 82 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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