Stefano Bertolini

7.2k total citations
129 papers, 4.7k citations indexed

About

Stefano Bertolini is a scholar working on Surgery, Molecular Biology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Stefano Bertolini has authored 129 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 81 papers in Surgery, 44 papers in Molecular Biology and 40 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Stefano Bertolini's work include Lipoproteins and Cardiovascular Health (67 papers), Diabetes, Cardiovascular Risks, and Lipoproteins (29 papers) and Lipid metabolism and disorders (27 papers). Stefano Bertolini is often cited by papers focused on Lipoproteins and Cardiovascular Health (67 papers), Diabetes, Cardiovascular Risks, and Lipoproteins (29 papers) and Lipid metabolism and disorders (27 papers). Stefano Bertolini collaborates with scholars based in Italy, United States and United Kingdom. Stefano Bertolini's co-authors include S. Calandra, Livia Pisciotta, Patrizia Tarugi, Maurizio Averna, Claudio Franceschi, R. Fellin, Marcello Arca, Antonella Bellocchio, Giovanni Zuliani and Daniela Mari and has published in prestigious journals such as Science, The Lancet and Journal of Biological Chemistry.

In The Last Decade

Stefano Bertolini

125 papers receiving 4.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stefano Bertolini Italy	35	2.3k	1.4k	1.1k	963	821	129	4.7k
S. Calandra Italy	39	3.0k 1.3×	1.5k 1.1×	1.6k 1.4×	1.3k 1.4×	978 1.2×	187	5.2k
Judy G. Verstuyft United States	14	1.9k 0.9×	1.3k 1.0×	1.0k 0.9×	605 0.6×	732 0.9×	14	4.2k
J L Breslow United States	28	1.9k 0.8×	1.2k 0.9×	1.7k 1.5×	798 0.8×	791 1.0×	37	4.1k
Mary J. Malloy United States	45	2.6k 1.1×	1.6k 1.2×	1.9k 1.7×	1.7k 1.7×	878 1.1×	137	7.2k
Armin Steinmetz Germany	34	3.1k 1.4×	1.6k 1.1×	2.6k 2.3×	858 0.9×	1.1k 1.4×	112	5.2k
Atsushi Nohara Japan	37	2.5k 1.1×	877 0.6×	1.3k 1.1×	1.1k 1.2×	889 1.1×	178	4.3k
Gordon A. Francis Canada	39	2.4k 1.1×	2.3k 1.7×	843 0.7×	640 0.7×	895 1.1×	109	6.0k
Miguel Pocovı́ Spain	40	1.8k 0.8×	1.1k 0.8×	984 0.9×	684 0.7×	540 0.7×	167	4.4k
Harald Funke Germany	40	3.6k 1.6×	2.2k 1.6×	1.7k 1.5×	1.2k 1.2×	806 1.0×	141	6.4k
Hayes M. Dansky United States	32	1.8k 0.8×	843 0.6×	999 0.9×	831 0.9×	564 0.7×	51	3.9k

Countries citing papers authored by Stefano Bertolini

Since Specialization

Citations

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

Fields of papers citing papers by Stefano Bertolini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefano Bertolini

This figure shows the co-authorship network connecting the top 25 collaborators of Stefano Bertolini. A scholar is included among the top collaborators of Stefano Bertolini 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 Stefano Bertolini. Stefano Bertolini 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

Tarugi, Patrizia, Stefano Bertolini, S. Calandra, et al.. (2024). Consensus document on diagnosis and management of familial hypercholesterolemia from the Italian Society for the Study of Atherosclerosis (SISA). Nutrition Metabolism and Cardiovascular Diseases. 34(8). 1819–1836. 4 indexed citations

Larrea‐Sebal, Asier, Chiara Trenti, Shifa Jebari‐Benslaiman, et al.. (2023). Functional Characterization of p.(Arg160Gln) PCSK9 Variant Accidentally Found in a Hypercholesterolemic Subject. International Journal of Molecular Sciences. 24(4). 3330–3330. 1 indexed citations

Tarugi, Patrizia, Stefano Bertolini, & S. Calandra. (2018). Angiopoietin-like protein 3 (ANGPTL3) deficiency and familial combined hypolipidemia. Journal of Biomedical Research. 33(2). 73–73. 29 indexed citations

Rocco, Maja Di, Livia Pisciotta, Annalisa Madeo, Marta Bertamino, & Stefano Bertolini. (2018). Long term substrate reduction therapy with ezetimibe alone or associated with statins in three adult patients with lysosomal acid lipase deficiency. Orphanet Journal of Rare Diseases. 13(1). 24–24. 12 indexed citations

Rabacchi, Claudio, Sergio D’Addato, Silvia Palmisano, et al.. (2016). Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene. Journal of clinical lipidology. 10(4). 915–921.e4. 22 indexed citations

Rabacchi, Claudio, Federico Bigazzi, Francesco Sbrana, et al.. (2016). Phenotypic variability in 4 homozygous familial hypercholesterolemia siblings compound heterozygous for LDLR mutations. Journal of clinical lipidology. 10(4). 944–952.e1. 9 indexed citations

Calandra, S., Patrizia Tarugi, Helen E. Speedy, et al.. (2011). Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease risk. Journal of Lipid Research. 52(11). 1885–1926. 63 indexed citations

Tarugi, Patrizia, Maurizio Averna, Enza Di Leo, et al.. (2007). Molecular diagnosis of hypobetalipoproteinemia: An ENID review. Atherosclerosis. 195(2). e19–e27. 122 indexed citations

Mannucci, L., Ornella Guardamagna, Pierfrancesco Bertucci, et al.. (2007). Beta‐sitosterolaemia: a new nonsense mutation in the ABCG5 gene. European Journal of Clinical Investigation. 37(12). 997–1000. 28 indexed citations

10.

Belleudi, Francesca, Filomena Campagna, Tina Garofalo, et al.. (2005). Adaptor Protein ARH Is Recruited to the Plasma Membrane by Low Density Lipoprotein (LDL) Binding and Modulates Endocytosis of the LDL/LDL Receptor Complex in Hepatocytes. Journal of Biological Chemistry. 280(46). 38416–38423. 28 indexed citations

11.

Bertolini, Stefano, Livia Pisciotta, Lilla Di Scala, et al.. (2004). Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia. Atherosclerosis. 174(1). 57–65. 68 indexed citations

12.

Leo, Enza Di, et al.. (2003). Hypobetalipoproteinemia with an apparently recessive inheritance due to a “de novo” mutation of apolipoprotein B. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1688(1). 61–67. 9 indexed citations

13.

Rolleri, M., Giovanni Emmanuele, Angelo B. Cefalù, et al.. (2003). Two Italian kindreds carrying the Arg136→Ser mutation of the Apo E gene: development of premature and severe atherosclerosis in the presence of epsilon 2 as second allele. Nutrition Metabolism and Cardiovascular Diseases. 13(2). 93–99. 15 indexed citations

14.

Cantàfora, Alfredo, I. Blotta, N. Bruzzese, S. Calandra, & Stefano Bertolini. (2001). Rapid sizing of microsatellite alleles by gel electrophoresis on microfabricated channels: Application to the D19S394 tetranucleotide repeat for cosegregation study of familial hypercholesterolemia. Electrophoresis. 22(18). 4012–4015. 15 indexed citations

15.

Rose, Giuseppina, Giuseppe Passarino, Giuseppina Carrieri, et al.. (2001). Paradoxes in longevity: sequence analysis of mtDNA haplogroup J in centenarians. European Journal of Human Genetics. 9(9). 701–707. 94 indexed citations

16.

Licastro, Federico, Steve Pedrini, Marzia Govoni, et al.. (1999). Apolipoprotein E and α-1-antichymotrypsin allele polymorphism in sporadic and familial Alzheimer's disease. Neuroscience Letters. 270(3). 129–132. 38 indexed citations

17.

Cassanelli, Stefano, Stefano Bertolini, M. Rolleri, et al.. (1998). A ‘de novo’ point mutation of the low‐density lipoprotein receptor gene in an Italian subject with primary hypercholesterolemia. Clinical Genetics. 53(5). 391–395. 13 indexed citations

18.

Stefanutti, C., A Notarbartoló, V. Colloridi, et al.. (1997). LDL Apheresis in a Homozygous Familial Hypercholesterolemic Child Aged 4.5. Artificial Organs. 21(10). 1126–1127. 15 indexed citations

19.

Garuti, Rita, Paola Pedrazzi, M. Ghisellini, et al.. (1994). A new missense mutation (Cys297?Phe) of the low density lipoprotein receptor in Italian patients with familial hypercholesterolemia (FHTrieste). Human Genetics. 93(5). 538–40. 4 indexed citations

20.

Bertolini, Stefano, et al.. (1987). Effects of Three Low‐Dose Oral Contraceptive Formulations on Lipid Metabolism. Acta Obstetricia Et Gynecologica Scandinavica. 66(4). 327–332. 20 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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