G. Sabetta

422 total citations
29 papers, 279 citations indexed

About

G. Sabetta is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, G. Sabetta has authored 29 papers receiving a total of 279 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Clinical Biochemistry, 7 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in G. Sabetta's work include Metabolism and Genetic Disorders (11 papers), Mitochondrial Function and Pathology (5 papers) and Neonatal Health and Biochemistry (4 papers). G. Sabetta is often cited by papers focused on Metabolism and Genetic Disorders (11 papers), Mitochondrial Function and Pathology (5 papers) and Neonatal Health and Biochemistry (4 papers). G. Sabetta collaborates with scholars based in Italy, Switzerland and United States. G. Sabetta's co-authors include Carlo Dionisi‐Vici, Enrico Bertini, Andrea Bartuli, M. Gambarara, Alberto Burlina, C. Bachmann, J. P. Colombo, Barbara Garavaglia, Mario Sabatelli and Cristiano Rizzo and has published in prestigious journals such as Annals of Neurology, Clinica Chimica Acta and Thrombosis and Haemostasis.

In The Last Decade

G. Sabetta

26 papers receiving 274 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
G. Sabetta Italy 11 145 103 66 44 43 29 279
Roshni Vara United Kingdom 13 221 1.5× 157 1.5× 85 1.3× 96 2.2× 115 2.7× 34 462
Rafael Muley Spain 9 94 0.6× 166 1.6× 44 0.7× 19 0.4× 11 0.3× 11 336
Angela Hosack Canada 9 121 0.8× 168 1.6× 217 3.3× 30 0.7× 36 0.8× 12 315
Yuqi Yang China 9 74 0.5× 138 1.3× 22 0.3× 13 0.3× 20 0.5× 32 367
Catherine Lynn T. Silao Philippines 9 124 0.9× 79 0.8× 61 0.9× 14 0.3× 43 1.0× 33 287
Soledad Kleppe United States 8 160 1.1× 153 1.5× 32 0.5× 54 1.2× 49 1.1× 12 333
Miguel Angel Alcántara‐Ortigoza Mexico 12 45 0.3× 163 1.6× 42 0.6× 25 0.6× 71 1.7× 57 386
Jaya Ganesh United States 14 239 1.6× 376 3.7× 33 0.5× 44 1.0× 55 1.3× 43 575
Naziha Kaabachi Tunisia 8 32 0.2× 84 0.8× 55 0.8× 56 1.3× 67 1.6× 19 329
U. van Haelst Netherlands 4 281 1.9× 324 3.1× 23 0.3× 63 1.4× 50 1.2× 7 467

Countries citing papers authored by G. Sabetta

Since Specialization
Citations

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

Fields of papers citing papers by G. Sabetta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of G. Sabetta

This figure shows the co-authorship network connecting the top 25 collaborators of G. Sabetta. A scholar is included among the top collaborators of G. Sabetta 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 G. Sabetta. G. Sabetta 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.
Cioffi, Raffaella, Paolo Ivo Cavoretto, G. Sabetta, et al.. (2025). Additional value of uterine artery Doppler pulsatility index for ultrasound diagnosis of placental site trophoblastic tumor: prospective cohort study. Ultrasound in Obstetrics and Gynecology. 66(1). 73–80.
2.
Cioffi, Raffaella, Robert Fruscio, G. Sabetta, et al.. (2025). Consolidation courses in low-risk gestational trophoblastic neoplasia and relapse rate: A MITO-9 retrospective study. Gynecologic Oncology. 196. 54–58.
3.
Sabetta, G., et al.. (2025). Pathophysiology and Management of Placenta Accreta Spectrum. Journal of Developmental Biology. 13(4). 45–45.
4.
Bergamini, Alice, Giorgia Mangili, Alessandro Ambrosi, et al.. (2023). Endometriosis-Related Ovarian Cancers: Evidence for a Dichotomy in the Histogenesis of the Two Associated Histotypes. Diagnostics. 13(8). 1425–1425. 9 indexed citations
5.
Bergamini, Alice, Miriam Dellino, Vera Loizzi, et al.. (2022). Fertility sparing surgery in sex-cord stromal tumors: oncological and reproductive outcomes. International Journal of Gynecological Cancer. 32(8). 1063–1070. 15 indexed citations
6.
Simonini, Marco, G. Sabetta, Alice Bergamini, et al.. (2022). [Anti-angiogenic drugs and hypertension: from multidisciplinary collaboration to greater care].. PubMed. 39(6). 1 indexed citations
7.
Mangili, Giorgia, G. Sabetta, Raffaella Cioffi, et al.. (2022). Current Evidence on Immunotherapy for Gestational Trophoblastic Neoplasia (GTN). Cancers. 14(11). 2782–2782. 20 indexed citations
8.
Dionisi‐Vici, Carlo, Lidia De Felice, May El Hachem, et al.. (1998). Intravenous immune globulin in lysinuric protein intolerance. Journal of Inherited Metabolic Disease. 21(2). 95–102. 11 indexed citations
9.
Dionisi‐Vici, Carlo, W. Ruitenbeek, G. Fariello, et al.. (1997). New familial mitochondrial encephalopathy with macrocephaly, cardiomyopathy, and complex I deficiency. Annals of Neurology. 42(4). 661–665. 10 indexed citations
10.
Bertini, Enrico, Carlo Dionisi‐Vici, Barbara Garavaglia, et al.. (1992). Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiency. European Journal of Pediatrics. 151(2). 121–126. 48 indexed citations
11.
Sebastio, Gianfranco, R. de Franchis, Pietro Strisciuglio, et al.. (1991). Aldolase B mutations in Italian families affected by hereditary fructose intolerance.. Journal of Medical Genetics. 28(4). 241–243. 15 indexed citations
12.
Bartuli, Andrea, et al.. (1990). Early Introduction of Uncooked Cornstarch for the Treatment of Glycogen Storage Disease Type I. Acta Paediatrica. 79(10). 978–979. 2 indexed citations
13.
Bachmann, C., et al.. (1990). Prenatal exclusion of ornithine transcarbamylase (OTC) by using RFLP analysis. Journal of Inherited Metabolic Disease. 13(6). 888–890. 2 indexed citations
14.
Burlina, Alberto, Barbara Garavaglia, Daniel E. Hale, et al.. (1990). 170 NEUROMUSCOLAR INVOLVMENT IN TWO UNRELATED CHELDHEN WTIH LONG-CHAIN 3-HYDROXYACYL-CoA DHEYDHOGENASE (LCHAD) DEFICIENCY. Pediatric Research. 28(3). 305–305. 4 indexed citations
15.
Gambarara, M., et al.. (1990). Therapeutical approaches of ald: Problems with diet in Italy. 181–193. 1 indexed citations
17.
Sabetta, G., C. Bachmann, O Giardini, et al.. (1987). β‐Ketothiolase deficiency with favourable evolution. Journal of Inherited Metabolic Disease. 10(4). 405–406. 6 indexed citations
18.
Baumgartner, R., O Giardini, A Cantani, G. Sabetta, & María Cecilia Castro. (1981). Methylmalonic acidaemia due to mutase apoenzyme defect: Responsive to vitamin B12 in intact fibroblasts but notin vivo. Journal of Inherited Metabolic Disease. 5(3). 137–141. 6 indexed citations
19.
Iannetti, Paola, et al.. (1975). [Electroencephalographic findings in children with acute lymphatic leukemia during treatment with vincristine].. PubMed. 27(12). 727–8. 1 indexed citations
20.
Principe, Domenico Del, et al.. (1973). Phosphatidylserine metabolism in normal and hemophylic human plasma. Clinica Chimica Acta. 49(2). 211–213. 1 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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