Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies
if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the
same subfield and year (this is the minimum needed to enter the top 1%, not the average
within it), or reaches the top citation threshold in at least one of its specific research
topics.
Introduction of Gluten, HLA Status, and the Risk of Celiac Disease in Children
2014328 citationsElena Lionetti, Stefania Castellaneta et al.New England Journal of Medicineprofile →
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late)
cites ·
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This map shows the geographic impact of C Ughi'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 C Ughi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C Ughi more than expected).
This network shows the impact of papers produced by C Ughi. 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 C Ughi. The network helps show where C Ughi may publish in the future.
Co-authorship network of co-authors of C Ughi
This figure shows the co-authorship network connecting the top 25 collaborators of C Ughi.
A scholar is included among the top collaborators of C Ughi 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 C Ughi. C Ughi 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.
Lionetti, Elena, Stefania Castellaneta, Ruggiero Francavilla, et al.. (2014). Introduction of Gluten, HLA Status, and the Risk of Celiac Disease in Children. New England Journal of Medicine. 371(14). 1295–1303.328 indexed citations breakdown →
Fitzgerald, Joseph F., et al.. (1998). Clinical Quiz. Journal of Pediatric Gastroenterology and Nutrition. 26(4). 436–436.2 indexed citations
7.
Ughi, C, et al.. (1998). Clinical quiz. Trichobezoar, a rare and unique form of gastrointestinal foreign body.. PubMed. 26(4). 436, 453–436, 453.4 indexed citations
Ughi, C, et al.. (1995). DETERMINING ETIOLOGY OF PNEUMONIA. The Pediatric Infectious Disease Journal. 14(10). 920–920.6 indexed citations
11.
Chiaravalloti, G, et al.. (1995). [Williams-Beuren syndrome and celiac disease].. PubMed. 47(1-2). 43–6.4 indexed citations
12.
Olmi, Stefano, et al.. (1993). [Celiac disease associated with chronic autoimmune hepatitis. Description of a case].. PubMed. 45(12). 511–3.7 indexed citations
13.
Ceccarelli, Manuela, et al.. (1992). [Plasma L-carnitine levels in children with celiac disease].. PubMed. 44(9). 401–5.3 indexed citations
14.
Ceccarelli, Manuela, et al.. (1991). [Clinical aspects of celiac disease. Comparison of 2 periods: before and after the introduction of antigliadin antibody determination in clinical practice].. PubMed. 42(7-8). 263–6.3 indexed citations
Cortigiani, Lauro, et al.. (1991). [Anti-beta-lactoglobulin antibodies as an index of increased intestinal permeability in celiac disease].. PubMed. 12(5). 463–5.1 indexed citations
17.
Ceccarelli, Manuela, et al.. (1989). Recurrent meningitis: a case report. European Journal of Pediatrics. 148(7). 646–647.11 indexed citations
18.
Cortigiani, Lauro, et al.. (1989). [Selenium in celiac disease].. PubMed. 41(11). 539–42.6 indexed citations
19.
Ceccarelli, Manuela, et al.. (1988). [Initial experiences in the use of intravenous immunoglobulins in Guillain-Barré-Strohl syndrome].. PubMed. 9(6). 719–21.3 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.