Alessandro Marocchi

1.0k total citations
34 papers, 738 citations indexed

About

Alessandro Marocchi is a scholar working on Neurology, Genetics and Molecular Biology. According to data from OpenAlex, Alessandro Marocchi has authored 34 papers receiving a total of 738 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Neurology, 9 papers in Genetics and 5 papers in Molecular Biology. Recurrent topics in Alessandro Marocchi's work include Amyotrophic Lateral Sclerosis Research (10 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Intracranial Aneurysms: Treatment and Complications (5 papers). Alessandro Marocchi is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (10 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Intracranial Aneurysms: Treatment and Complications (5 papers). Alessandro Marocchi collaborates with scholars based in Italy, Germany and United Kingdom. Alessandro Marocchi's co-authors include Silvana Penco, Christian Lunetta, Paolo Mocarelli, Lorena Mosca, Maria Cristina Patrosso, Fabio Coppedè, Andrea Stoccoro, Lucia Migliore, Paolo Brambilla and Pier Mario Gerthoux and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of neurosurgery and Statistics in Medicine.

In The Last Decade

Alessandro Marocchi

34 papers receiving 715 citations

Peers

Alessandro Marocchi

NEURO

HTM

GENET

N Konishi Japan

Takaharu Nakamura Japan

Satoru Oshiro Japan

Ken Tachibana Japan

Kiyoshi Ozumi Japan

L.M. Garrick United States

Renate Thiel Germany

Netanya Y. Spencer United States

Andrea Mignarri Italy

N Konishi Japan

Alessandro Marocchi

540 ×2.3

63 ×0.3

NEURO

270 ×2.3

49 ×0.6

HTM

92 ×1.1

GENET

Citations per year, relative to Alessandro Marocchi Alessandro Marocchi (= 1×) peers N Konishi

Countries citing papers authored by Alessandro Marocchi

Since Specialization

Citations

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

Fields of papers citing papers by Alessandro Marocchi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alessandro Marocchi

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

Stoccoro, Andrea, Adam R. Smith, Lorena Mosca, et al.. (2020). Reduced mitochondrial D-loop methylation levels in sporadic amyotrophic lateral sclerosis. Clinical Epigenetics. 12(1). 137–137. 37 indexed citations

Marini, Valéria, Carmen Fucile, Francesca Mattioli, et al.. (2019). Combined evaluation of genotype and phenotype of thiopurine S-methyltransferase (TPMT) in the clinical management of patients in chronic therapy with azathioprine. Drug Metabolism and Personalized Therapy. 34(1). 2 indexed citations

Benedetti, Stefano De, Giorgio Lucchini, Cristian Del Bo’, et al.. (2017). Blood trace metals in a sporadic amyotrophic lateral sclerosis geographical cluster. BioMetals. 30(3). 355–365. 22 indexed citations

Mosca, Lorena, Francesca Rivieri, Raffaella Tanel, et al.. (2014). Mutational Screening of NOTCH3 Gene Reveals Two Novel Mutations: Complexity of CADASIL Diagnosis. Journal of Molecular Neuroscience. 54(4). 723–729. 2 indexed citations

Mosca, Lorena, Silvana Pileggi, Francesca Avemaria, et al.. (2012). De Novo MGC4607 Gene Heterozygous Missense Variants in a Child with Multiple Cerebral Cavernous Malformations. Journal of Molecular Neuroscience. 47(3). 475–480. 6 indexed citations

Avemaria, Francesca, Christian Lunetta, Claudia Tarlarini, et al.. (2011). Mutation in the senataxin gene found in a patient affected by familial ALS with juvenile onset and slow progression. Amyotrophic Lateral Sclerosis. 12(3). 228–230. 20 indexed citations

Mosca, Lorena, Silvana Penco, Maria Cristina Patrosso, et al.. (2011). Genetic variability of the fructosamine 3-kinase gene in diabetic patients. Clinical Chemistry and Laboratory Medicine (CCLM). 49(5). 803–808. 11 indexed citations

Pileggi, Silvana, Claudia Ricci, Maria Cristina Patrosso, et al.. (2010). Genetic Variations Within KRIT1/CCM1, MGC4607/CCM2 and PDCD10/CCM3 in a Large Italian Family Harbouring a Krit1/CCM1 Mutation. Journal of Molecular Neuroscience. 42(2). 235–242. 11 indexed citations

Penco, Silvana, Christian Lunetta, Lorena Mosca, et al.. (2010). Phenotypic Heterogeneity in a SOD1 G93D Italian ALS Family: An Example of Human Model to Study a Complex Disease. Journal of Molecular Neuroscience. 44(1). 25–30. 17 indexed citations

10.

Nannucci, Serena, Francesca Pescini, Anna Poggesi, et al.. (2009). Familial cerebral cavernous malformation: report of a further Italian family. Neurological Sciences. 30(2). 143–147. 7 indexed citations

11.

Cairoli, Roberto, Carla B. Ripamonti, Alessandro Beghini, et al.. (2009). Total serum tryptase: A predictive marker for KIT mutation in acute myeloid leukemia. Leukemia Research. 33(9). 1282–1284. 6 indexed citations

12.

Penco, Silvana, Massimo Buscema, Maria Cristina Patrosso, Alessandro Marocchi, & Enzo Grossi. (2008). New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background. BMC Bioinformatics. 9(1). 254–254. 19 indexed citations

13.

Battistini, Stefania, Raffaele Rocchi, Alfonso Cerase, et al.. (2007). Clinical, Magnetic Resonance Imaging, and Genetic Study of 5 Italian Families With Cerebral Cavernous Malformation. Archives of Neurology. 64(6). 843–843. 30 indexed citations

14.

Licastro, Federico, Alessandro Marocchi, Silvana Penco, et al.. (2006). Does Down's syndrome support the homocysteine theory of atherogenesis?. Archives of Gerontology and Geriatrics. 43(3). 381–387. 36 indexed citations

15.

Grossrubatscher, Erika, Paolo Dalino Ciaramella, Federico Vignati, et al.. (2006). The role of chromogranin A in the management of patients with phaeochromocytoma. Clinical Endocrinology. 65(3). 287–293. 49 indexed citations

16.

Guidugli, Federico, et al.. (2006). Unexpectedly Dangerous Escargot Stew: Oleandrin Poisoning through the Alimentary Chain*. Journal of Analytical Toxicology. 30(9). 683–686. 11 indexed citations

17.

Lando, Giuliana, Andrea Mosca, R Bonora, et al.. (2003). Frequency of butyrylcholinesterase gene mutations in individuals with abnormal inhibition numbers. Pharmacogenetics. 13(5). 265–270. 18 indexed citations

18.

Ceriotti, Ferruccio, et al.. (2002). A Two-Center Evaluation of the Blood Gas Immediate Response Mobile Analyzer (IRMA). Clinical Chemistry and Laboratory Medicine (CCLM). 40(2). 182–91. 6 indexed citations

19.

Sarto, Cecilia, Alessandro Marocchi, Jean‐Charles Sanchez, et al.. (1997). Renal cell carcinoma and normal kidney protein expression. Electrophoresis. 18(3-4). 599–604. 105 indexed citations

20.

Mocarelli, Paolo, Alessandro Marocchi, Donald G. Patterson, et al.. (1991). Serum concentrations of 2,3,7,8‐tetrachlorodibenzo‐p‐dioxin and test results from selected residents of Seveso, Italy. Journal of Toxicology and Environmental Health. 32(4). 357–366. 83 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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