M. Rolleri

579 citations

13 papers · 341 · h-index 10

Impact in

Surgery
- Lipoproteins and Cardiovascular Health
- Cholesterol and Lipid Metabolism
Endocrinology, Diabetes and Metabolism
- Diabetes, Cardiovascular Risks, and Lipoproteins

Papers in

Surgery 8
- Lipoproteins and Cardiovascular Health 8
Molecular Biology 7
- Protein Kinase Regulation and GTPase Signaling 3
- Amyloidosis: Diagnosis, Treatment, Outcomes 2
- RNA and protein synthesis mechanisms 2
- Plant biochemistry and biosynthesis 2

Co-authors: Stefano Bertolini (12 shared papers)S. Calandra (9 shared papers)M. Ghisellini (6 shared papers)P Masturzo (6 shared papers)Rita Garuti (5 shared papers)Giovanni Mario Pes (3 shared papers)Livia Pisciotta (3 shared papers)Alfredo Cantàfora (2 shared papers)
Journals: Arteriosclerosis Thrombosis and Vascular Biology (4 papers)Clinical Genetics (2 papers)Journal of Lipid Research (1 paper)The Nephron journals/Nephron journals (1 paper)Neurology (1 paper)
Partner nations: Italy United States Armenia

In The Last Decade

M. Rolleri

13 papers receiving 330 citations

Peers

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-authors

The 25 scholars most cited alongside M. Rolleri, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with M. Rolleri Line = papers co-authored together M. Rolleri links everyone, so they are left out of the graph.

All Works

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13 of 13 papers shown

#	Work
1	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 ·Stefano Bertolini, Alfredo Cantàfora, Maurizio Averna, Claudio Cortese, Corradino Motti, S. Martini, Giovanni Mario Pes, A. Postiglione, C. Stefanutti, I. Blotta, Livia Pisciotta, M. Rolleri, Silvia Langheim, M. Ghisellini, Ivana Rabbone, S. Calandra	2000	125
2	Analysis of LDL Receptor Gene Mutations in Italian Patients With Homozygous Familial Hypercholesterolemia Arteriosclerosis Thrombosis and Vascular Biology ·Stefano Bertolini, Stefano Cassanelli, Rita Garuti, M. Ghisellini, Maria Luisa Simone, M. Rolleri, P Masturzo, S. Calandra	1999	54
3	Apolipoprotein E element 4 allele frequency is not increased in progressive supranuclear palsy Neurology ·Massimo Tabaton, M. Rolleri, P Masturzo, S. Cammarata, Giovanna Angelini, Lawrence A. Hansen, T Saitoh, Robert B. Petersen, George Perry, Peggy L. Richey, P. Gambetti, Stefano Bertolini	1995	33
4	Influence of β⁰-Thalassemia on the Phenotypic Expression of Heterozygous Familial Hypercholesterolemia Arteriosclerosis Thrombosis and Vascular Biology ·Luca Deiana, Rita Garuti, Giovanni Mario Pes, Ciriaco Carru, Alessandra Errigo, M. Rolleri, Livia Pisciotta, P Masturzo, Alfredo Cantàfora, S. Calandra, Stefano Bertolini	2000	26
5	Four Novel Partial Deletions of LDL-Receptor Gene in Italian Patients With Familial Hypercholesterolemia Arteriosclerosis Thrombosis and Vascular Biology ·Stefano Bertolini, Rita Garuti, W. Lelli, M. Rolleri, Roberta Tiozzo, M. Ghisellini, Maria Luisa Simone, P Masturzo, N Elicio, C. Stefanutti, Domenico Coviello, C. Carabbio, G Orecchini, S. Calandra	1995	23
6	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 ·Nicoletta Lelli, Rita Garuti, M. Ghisellini, Roberta Tiozzo, M. Rolleri, V Aimale, E Ginocchio, Aldo Naselli, Stefano Bertolini, S. Calandra	1995	19
7	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 ·Stefano Bertolini, Ml Simone, Giovanni Mario Pes, M. Ghisellini, M. Rolleri, Antonella Bellocchio, N Elicio, P Masturzo, S. Calandra	2000	15
8	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 ·M. Rolleri, Nicoletta Vivona, Giovanni Emmanuele, Angelo B. Cefalù, Livia Pisciotta, V. Guido, Davide Noto, B. Fiore, Carlo M. Barbagallo, A Notarbartoló, Salvatore Travali, Stefano Bertolini, Maurizio Averna	2003	15
9	A ‘de novo’ point mutation of the low‐density lipoprotein receptor gene in an Italian subject with primary hypercholesterolemia Clinical Genetics ·Stefano Cassanelli, Stefano Bertolini, M. Rolleri, (unknown), Lucia Casarino, N Elicio, Aldo Naselli, S. Calandra	1998	13
10	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 ·Adalberto Sessa, Graziana Battini, Mietta Meroni, Giuseppe Daidone, Ida Carnera, Pier Luigi Brambilla, Giovanni Viganò, Ferdinando Giordano, Francesco Pallotti, Laura Torri Tarelli, Laura Calabresi, M. Rolleri, S Bertolini	2001	10
11	A new missense mutation (Cys297?Phe) of the low density lipoprotein receptor in Italian patients with familial hypercholesterolemia (FHTrieste) Human Genetics ·Nicoletta Lelli, Rita Garuti, Paola Pedrazzi, M. Ghisellini, Maria Luisa Simone, Roberta Tiozzo, Luigi Cattin, M. Valenti, M. Rolleri, Stefano Bertolini, C. Stefanutti, S. Calandra	1994	4
12	Italian familial defective apolipoprotein B patients share a unique haplotype with other Caucasian patients Clinical and Experimental Medicine ·Angelo B. Cefalù, Carlo M. Barbagallo, E. Sesti, Rosalia Caldarella, F Polizzi, G. Marino, Davide Noto, M. Rolleri, Salvatore Travali, Giuseppe Scalisi, A Notarbartoló, Alberto Corsini, Stefano Bertolini, Maurizio Averna	2001	3
13	1.P.236 A founder-related LDL receptor gene mutation in the Liguria region of Italy Atherosclerosis ·Simone Matteï, M. Rolleri, P Masturzo, V Fascetti, N Elicio, Corradino Motti, Cherise Cortese, S. Calandra, Stefano Bertolini	1997	1

About M. Rolleri

M. Rolleri is a scholar working on Surgery, Molecular Biology, Endocrinology, Diabetes and Metabolism, Immunology and Allergy and Cancer Research, having authored 13 papers that have together received 341 indexed citations. Recurring topics across this work include Lipoproteins and Cardiovascular Health (8 papers), Protein Kinase Regulation and GTPase Signaling (3 papers), Amyloidosis: Diagnosis, Treatment, Outcomes (2 papers), RNA and protein synthesis mechanisms (2 papers), Plant biochemistry and biosynthesis (2 papers), Cancer, Lipids, and Metabolism (2 papers), Cell Adhesion Molecules Research (2 papers) and Diabetes, Cardiovascular Risks, and Lipoproteins (2 papers). The work is most often cited by research in Surgery (225 citations), Endocrinology, Diabetes and Metabolism (71 citations), Cancer Research (47 citations), Genetics (24 citations) and Cardiology and Cardiovascular Medicine (43 citations). M. Rolleri has collaborated with scholars based in Italy, United States and Armenia. Frequent co-authors include Stefano Bertolini, S. Calandra, M. Ghisellini, P Masturzo, Rita Garuti, Giovanni Mario Pes, Livia Pisciotta, Alfredo Cantàfora, Maurizio Averna and Maria Luisa Simone. Their work appears in journals such as Arteriosclerosis Thrombosis and Vascular Biology, Clinical Genetics, Journal of Lipid Research, The Nephron journals/Nephron journals and Neurology.

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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