Maria Luisa Simone

679 total citations
17 papers, 518 citations indexed

About

Maria Luisa Simone is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Maria Luisa Simone has authored 17 papers receiving a total of 518 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Surgery and 5 papers in Genetics. Recurrent topics in Maria Luisa Simone's work include Lipoproteins and Cardiovascular Health (6 papers), Genetic factors in colorectal cancer (3 papers) and Protein Kinase Regulation and GTPase Signaling (3 papers). Maria Luisa Simone is often cited by papers focused on Lipoproteins and Cardiovascular Health (6 papers), Genetic factors in colorectal cancer (3 papers) and Protein Kinase Regulation and GTPase Signaling (3 papers). Maria Luisa Simone collaborates with scholars based in Italy, United States and Spain. Maria Luisa Simone's co-authors include Antonella Grottola, Sara Tagliazucchi, Monica Pecorari, Giuseppe Longo, Fabio Rumpianesi, Rossella Lelli, Giovanni Savini, William Gennari, Federica Monaco and S. Calandra and has published in prestigious journals such as Scientific Reports, Biochemical and Biophysical Research Communications and Arteriosclerosis Thrombosis and Vascular Biology.

In The Last Decade

Maria Luisa Simone

17 papers receiving 504 citations

Peers

Maria Luisa Simone
Satoshi UNE Japan
Maria Rosaria Bassi Denmark
J. Smith Leser United States
Shannon Townsend United States
José Ramos‐Castañeda Mexico
Jérémy Boussier France
Pritesh Lalwani Brazil
Alexandra Davies United Kingdom
Fela Mendlovic Mexico
K Yagami Japan
Satoshi UNE Japan
Maria Luisa Simone
Citations per year, relative to Maria Luisa Simone Maria Luisa Simone (= 1×) peers Satoshi UNE

Countries citing papers authored by Maria Luisa Simone

Since Specialization
Citations

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

Fields of papers citing papers by Maria Luisa Simone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maria Luisa Simone. 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 Maria Luisa Simone. The network helps show where Maria Luisa Simone may publish in the future.

Co-authorship network of co-authors of Maria Luisa Simone

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

All Works

17 of 17 papers shown
1.
2.
Costa, Sónia, et al.. (2024). Fibroblasts’ secretome from calcified and non-calcified dermis in Pseudoxanthoma elasticum differently contributes to elastin calcification. Communications Biology. 7(1). 577–577. 3 indexed citations
3.
Cefalù, Angelo B., Rossella Spina, Davide Noto, et al.. (2022). Comparison of two polygenic risk scores to identify non-monogenic primary hypocholesterolemias in a large cohort of Italian hypocholesterolemic subjects. Journal of clinical lipidology. 16(4). 530–537. 2 indexed citations
4.
Pascale, Maria Rosaria, Antonella Grottola, Maria Luisa Simone, et al.. (2020). Evaluation of MALDI–TOF Mass Spectrometry in Diagnostic and Environmental Surveillance of Legionella Species: A Comparison With Culture and Mip-Gene Sequencing Technique. Frontiers in Microbiology. 11. 589369–589369. 24 indexed citations
5.
Rabacchi, Claudio, Maria Luisa Simone, Livia Pisciotta, et al.. (2019). In vitro functional characterization of splicing variants of the APOB gene found in familial hypobetalipoproteinemia. Journal of clinical lipidology. 13(6). 960–969. 3 indexed citations
6.
Simone, Maria Luisa, Claudio Rabacchi, Zarife Kuloğlu, et al.. (2019). Novel mutations of SAR1B gene in four children with chylomicron retention disease. Journal of clinical lipidology. 13(4). 554–562. 6 indexed citations
7.
Bernardis, Isabella, Elena Tenedini, Lucia Artuso, et al.. (2016). Unravelling the Complexity of Inherited Retinal Dystrophies Molecular Testing: Added Value of Targeted Next-Generation Sequencing. BioMed Research International. 2016. 1–14. 39 indexed citations
8.
Pedroni, Monica, Carmela Di Gregorio, Laura Cortesi, et al.. (2013). Double heterozygosity for BRCA1 and hMLH1 gene mutations in a 46-year-old woman with five primary tumors. Techniques in Coloproctology. 18(3). 285–289. 12 indexed citations
9.
Alboni, Silvia, Cristina Benatti, Johanna Maria Catharina Blom, et al.. (2010). Constitutive and LPS-regulated expression of interleukin-18 receptor beta variants in the mouse brain. Brain Behavior and Immunity. 25(3). 483–493. 31 indexed citations
10.
Marino, Marco, Claudio Rabacchi, Maria Luisa Simone, et al.. (2009). A novel deletion of BRCA1 gene that eliminates the ATG initiation codon without affecting the promoter region. Clinica Chimica Acta. 403(1-2). 249–253. 9 indexed citations
11.
Pecorari, Monica, Giuseppe Longo, William Gennari, et al.. (2009). First human case of Usutu virus neuroinvasive infection, Italy, August-September 2009. Eurosurveillance. 14(50). 211 indexed citations
12.
13.
Bellincampi, Lorenza, Maria Luisa Simone, Corradino Motti, et al.. (2001). Identification of an Alternative Transcript of ABCA1 Gene in Different Human Cell Types. Biochemical and Biophysical Research Communications. 283(3). 590–597. 13 indexed citations
14.
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
15.
Garuti, Rita, Roberta Tiozzo, M. Ghisellini, et al.. (1996). Two novel partial deletions of LDL-receptor gene in Italian patients with familial hypercholesterolemia (FHSiracusa and FHReggio Emilia). Atherosclerosis. 121(1). 105–117. 8 indexed citations
16.
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
17.
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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