M. Rolleri

574 total citations
13 papers, 335 citations indexed

About

M. Rolleri is a scholar working on Surgery, Molecular Biology and Cancer Research. According to data from OpenAlex, M. Rolleri has authored 13 papers receiving a total of 335 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Surgery, 7 papers in Molecular Biology and 3 papers in Cancer Research. Recurrent topics in M. Rolleri's work include Lipoproteins and Cardiovascular Health (9 papers), Protein Kinase Regulation and GTPase Signaling (3 papers) and Diabetes, Cardiovascular Risks, and Lipoproteins (2 papers). M. Rolleri is often cited by papers focused on Lipoproteins and Cardiovascular Health (9 papers), Protein Kinase Regulation and GTPase Signaling (3 papers) and Diabetes, Cardiovascular Risks, and Lipoproteins (2 papers). M. Rolleri collaborates with scholars based in Italy, United States and Armenia. M. Rolleri's co-authors include Stefano Bertolini, S. Calandra, M. Ghisellini, P Masturzo, Rita Garuti, Giovanni Mario Pes, Livia Pisciotta, C. Stefanutti, Alfredo Cantàfora and Maria Luisa Simone and has published in prestigious journals such as Neurology, Arteriosclerosis Thrombosis and Vascular Biology and Journal of Lipid Research.

In The Last Decade

M. Rolleri

13 papers receiving 325 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Rolleri Italy	10	232	98	72	72	49	13	335
Yilun Deng United States	11	135 0.6×	99 1.0×	85 1.2×	131 1.8×	37 0.8×	29	417
Maria Ginalska-Malinowska Poland	8	109 0.5×	196 2.0×	189 2.6×	79 1.1×	29 0.6×	16	438
Kaida Ji China	11	86 0.4×	59 0.6×	170 2.4×	87 1.2×	95 1.9×	15	429
Michitaka Tsuzuki Japan	10	72 0.3×	44 0.4×	180 2.5×	81 1.1×	96 2.0×	12	376
Kirsty R. Greenow United Kingdom	9	100 0.4×	55 0.6×	185 2.6×	74 1.0×	33 0.7×	13	383
Sachi Hoshi Japan	7	65 0.3×	47 0.5×	247 3.4×	60 0.8×	43 0.9×	8	547
Wojciech Garczorz Poland	12	95 0.4×	168 1.7×	173 2.4×	57 0.8×	42 0.9×	28	411
Hyung-Min Chin South Korea	15	209 0.9×	41 0.4×	71 1.0×	65 0.9×	22 0.4×	28	453
Yuichi Fujinaka Japan	11	235 1.0×	135 1.4×	201 2.8×	17 0.2×	37 0.8×	17	463
Jeong-Yoon Song South Korea	11	149 0.6×	60 0.6×	79 1.1×	113 1.6×	11 0.2×	21	441

Countries citing papers authored by M. Rolleri

Since Specialization

Citations

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

Fields of papers citing papers by M. Rolleri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Rolleri

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

All Works

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13 of 13 papers shown

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

Cefalù, Angelo B., Carlo M. Barbagallo, Rosalia Caldarella, et al.. (2001). Italian familial defective apolipoprotein B patients share a unique haplotype with other Caucasian patients. Clinical and Experimental Medicine. 1(3). 151–154. 2 indexed citations

Sessa, Adalberto, Graziana Battini, Mietta Meroni, et al.. (2001). Hypocomplementemic Type II Membranoproliferative Glomerulonephritis in a Male Patient with Familial Lecithin-Cholesterol Acyltransferase Deficiency due to Two Different Allelic Mutations. The Nephron journals/Nephron journals. 88(3). 268–272. 10 indexed citations

Bertolini, Stefano, Giovanni Mario Pes, M. Ghisellini, et al.. (2000). Pseudodominance of lipoprotein lipase (LPL) deficiency due to a nonsense mutation (Tyr₃₀₂>Term) in exon 6 of LPL gene in an Italian family from Sardinia (LPL_Olbia). Clinical Genetics. 57(2). 140–147. 15 indexed citations

Bertolini, Stefano, Alfredo Cantàfora, Maurizio Averna, et al.. (2000). Clinical Expression of Familial Hypercholesterolemia in Clusters of Mutations of the LDL Receptor Gene That Cause a Receptor-Defective or Receptor-Negative Phenotype. Arteriosclerosis Thrombosis and Vascular Biology. 20(9). E41–52. 123 indexed citations

Deiana, Luca, Rita Garuti, Giovanni Mario Pes, et al.. (2000). Influence of β⁰-Thalassemia on the Phenotypic Expression of Heterozygous Familial Hypercholesterolemia. Arteriosclerosis Thrombosis and Vascular Biology. 20(1). 236–243. 25 indexed citations

Bertolini, Stefano, Stefano Cassanelli, Rita Garuti, et al.. (1999). Analysis of LDL Receptor Gene Mutations in Italian Patients With Homozygous Familial Hypercholesterolemia. Arteriosclerosis Thrombosis and Vascular Biology. 19(2). 408–418. 54 indexed citations

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

Matteï, Simone, M. Rolleri, P Masturzo, et al.. (1997). 1.P.236 A founder-related LDL receptor gene mutation in the Liguria region of Italy. Atherosclerosis. 134(1-2). 66–66. 1 indexed citations

10.

Tabaton, Massimo, M. Rolleri, P Masturzo, et al.. (1995). Apolipoprotein E element 4 allele frequency is not increased in progressive supranuclear palsy. Neurology. 45(9). 1764–1765. 32 indexed citations

11.

Garuti, Rita, M. Ghisellini, Roberta Tiozzo, et al.. (1995). Occurrence of multiple aberrantly spliced mRNAs of the LDL-receptor gene upon a donor splice site mutation that causes familial hypercholesterolemia (FHBenevento).. Journal of Lipid Research. 36(6). 1315–1324. 19 indexed citations

12.

Bertolini, Stefano, Rita Garuti, M. Rolleri, et al.. (1995). Four Novel Partial Deletions of LDL-Receptor Gene in Italian Patients With Familial Hypercholesterolemia. Arteriosclerosis Thrombosis and Vascular Biology. 15(1). 81–88. 22 indexed citations

13.

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

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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