Ubaldo Caruso

1.4k total citations
21 papers, 662 citations indexed

About

Ubaldo Caruso is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ubaldo Caruso has authored 21 papers receiving a total of 662 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Clinical Biochemistry, 11 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ubaldo Caruso's work include Metabolism and Genetic Disorders (14 papers), Peroxisome Proliferator-Activated Receptors (5 papers) and Cystic Fibrosis Research Advances (4 papers). Ubaldo Caruso is often cited by papers focused on Metabolism and Genetic Disorders (14 papers), Peroxisome Proliferator-Activated Receptors (5 papers) and Cystic Fibrosis Research Advances (4 papers). Ubaldo Caruso collaborates with scholars based in Italy, Netherlands and United States. Ubaldo Caruso's co-authors include Cristiano Rizzo, Carlo Dionisi‐Vici, Damiano Abeni, Gaetano Sabetta, Alberto Burlina, Graziella Uziel, Ronald J. A. Wanders, Maria Cristina Schiaffino, Maja Di Rocco and R. Cerone and has published in prestigious journals such as Annals of Neurology, The Journal of Pediatrics and International Journal of Environmental Research and Public Health.

In The Last Decade

Ubaldo Caruso

21 papers receiving 645 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ubaldo Caruso Italy	15	349	338	150	136	108	21	662
Ksenija Fumić Croatia	15	498 1.4×	329 1.0×	286 1.9×	248 1.8×	78 0.7×	62	868
J. M. Saudubray France	18	717 2.1×	615 1.8×	93 0.6×	164 1.2×	100 0.9×	49	1.0k
W.O. Renier Netherlands	16	532 1.5×	324 1.0×	164 1.1×	143 1.1×	67 0.6×	32	849
Cristina Amat Di San Filippo United States	13	554 1.6×	594 1.8×	115 0.8×	178 1.3×	134 1.2×	13	858
Dimitar Gavrilov United States	15	403 1.2×	437 1.3×	152 1.0×	345 2.5×	200 1.9×	35	901
Fatih Süheyl Ezgü Türkiye	15	296 0.8×	136 0.4×	139 0.9×	262 1.9×	84 0.8×	100	724
Dorothea Möslinger Austria	14	274 0.8×	358 1.1×	133 0.9×	177 1.3×	98 0.9×	31	572
T. Ohura Japan	15	495 1.4×	543 1.6×	198 1.3×	114 0.8×	145 1.3×	33	959
Jean-Marie Saudubray France	14	383 1.1×	397 1.2×	43 0.3×	133 1.0×	115 1.1×	15	952
Jun Ye China	15	312 0.9×	305 0.9×	156 1.0×	127 0.9×	105 1.0×	50	590

Countries citing papers authored by Ubaldo Caruso

Since Specialization

Citations

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

Fields of papers citing papers by Ubaldo Caruso

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ubaldo Caruso

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

All Works

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20 of 20 papers shown

Salvatore, Marco, Annalisa Amato, Giovanna Floridia, et al.. (2020). The Italian External Quality Assessment Program for Cystic Fibrosis Sweat Chloride Test: Does Active Participation Improve the Quality?. International Journal of Environmental Research and Public Health. 17(9). 3196–3196. 2 indexed citations

Salvatore, Marco, Giovanna Floridia, Annalisa Amato, et al.. (2016). The Italian pilot external quality assessment program for cystic fibrosis sweat test. Clinical Biochemistry. 49(7-8). 601–605. 8 indexed citations

Cassanello, Michela, Valentina D’Onofrio, Paola Puccinelli, et al.. (2013). A neonatal case of 3-hydroxy-3-methylglutaric-coenzyme A lyase deficiency. The Italian Journal of Pediatrics/Italian journal of pediatrics. 39(1). 33–33. 23 indexed citations

Porta, Francesco, Anna Caciotti, Serena Catarzi, et al.. (2012). Sudden unexpected infant death (SUDI) in a newborn due to medium chain acyl CoA dehydrogenase (MCAD) deficiency with an unusual severe genotype. The Italian Journal of Pediatrics/Italian journal of pediatrics. 38(1). 59–59. 11 indexed citations

Giribaldi, Gaia, Roberta Biancheri, Mariasavina Severino, et al.. (2011). Intermittent‐relapsing pyruvate dehydrogenase complex deficiency: a case with clinical, biochemical, and neuroradiological reversibility. Developmental Medicine & Child Neurology. 54(5). 472–476. 17 indexed citations

Carrozzo, Rosalba, Carlo Bellini, S. Lucioli, et al.. (2008). Peroxisomal acyl‐CoA‐oxidase deficiency: Two new cases. American Journal of Medical Genetics Part A. 146A(13). 1676–1681. 27 indexed citations

Nogueira, Célia, Chiara Aiello, R. Cerone, et al.. (2008). Spectrum of MMACHC mutations in Italian and Portuguese patients with combined methylmalonic aciduria and homocystinuria, cblC type. Molecular Genetics and Metabolism. 93(4). 475–480. 72 indexed citations

Mancardi, Maria Margherita, Ubaldo Caruso, Maria Cristina Schiaffino, et al.. (2007). Severe Epilepsy in X‐Linked Creatine Transporter Defect (CRTR‐D). Epilepsia. 48(6). 1211–1213. 35 indexed citations

Verrina, Enrico, Ubaldo Caruso, Maria Grazia Calevo, et al.. (2007). Effect of carnitine supplementation on lipid profile and anemia in children on chronic dialysis. Pediatric Nephrology. 22(5). 727–733. 14 indexed citations

10.

Rocco, Maja Di, Ubaldo Caruso, Egill Briem, et al.. (2006). A case of ethylmalonic encephalopathy with atypical clinical and biochemical presentation. Molecular Genetics and Metabolism. 89(4). 395–397. 20 indexed citations

11.

Levreri, Isabella, et al.. (2005). The secretion of ibuprofen metabolites interferes with the capillary chromatography of urinary homovanillic acid and 4-hydroxy-3-methoxymandelic acid in neuroblastoma diagnosis. Clinical Chemistry and Laboratory Medicine (CCLM). 43(2). 173–7. 3 indexed citations

12.

Schiaffino, Maria Cristina, Carlo Bellini, Ubaldo Caruso, et al.. (2005). X-linked creatine transporter deficiency. Neurogenetics. 6(3). 165–168. 21 indexed citations

13.

Svahn, Johanna, Maria Cristina Schiaffino, Ubaldo Caruso, et al.. (2003). Severe Lactic Acidosis Due to Thiamine Deficiency in a Patient With B-Cell Leukemia/Lymphoma on Total Parenteral Nutrition During High-Dose Methotrexate Therapy. Journal of Pediatric Hematology/Oncology. 25(12). 965–968. 31 indexed citations

14.

Rizzo, Cristiano, Sara Boenzi, Ronald J. A. Wanders, et al.. (2003). Characteristic Acylcarnitine Profiles in Inherited Defects of Peroxisome Biogenesis: A Novel Tool for Screening Diagnosis Using Tandem Mass Spectrometry. Pediatric Research. 53(6). 1013–1018. 43 indexed citations

15.

Biancheri, Roberta, R. Cerone, Andrea Rossi, et al.. (2002). Early‐onset Cobalamin C/D Deficiency: Epilepsy and Electroencephalographic Features. Epilepsia. 43(6). 616–622. 24 indexed citations

16.

Dionisi‐Vici, Carlo, Cristiano Rizzo, Alberto Burlina, et al.. (2002). Inborn errors of metabolism in the Italian pediatric population: A national retrospective survey. The Journal of Pediatrics. 140(3). 321–329. 167 indexed citations

17.

Houten, Sander M., Janet Koster, Joost Frenkel, et al.. (2001). Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome. European Journal of Human Genetics. 9(4). 253–259. 64 indexed citations

18.

Rocco, Maja Di, et al.. (2001). Monozygotic twins with X‐linked adrenoleukodystrophy and different phenotypes. Annals of Neurology. 50(3). 424–424. 29 indexed citations

19.

Galietta, Luis J. V., Luciana Musante, Leila Romio, et al.. (1998). An electrogenic amino acid transporter in the apical membrane of cultured human bronchial epithelial cells. American Journal of Physiology-Lung Cellular and Molecular Physiology. 275(5). L917–L923. 40 indexed citations

20.

Parini, Rossella, Ubaldo Caruso, C. Dorche, et al.. (1997). Spherophakia associated with molybdenum cofactor deficiency. American Journal of Medical Genetics. 73(3). 272–275. 9 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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