A. Magariello

1.2k total citations
41 papers, 773 citations indexed

About

A. Magariello is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, A. Magariello has authored 41 papers receiving a total of 773 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Cellular and Molecular Neuroscience, 17 papers in Neurology and 10 papers in Molecular Biology. Recurrent topics in A. Magariello's work include Hereditary Neurological Disorders (11 papers), Neurological diseases and metabolism (10 papers) and Neurogenetic and Muscular Disorders Research (9 papers). A. Magariello is often cited by papers focused on Hereditary Neurological Disorders (11 papers), Neurological diseases and metabolism (10 papers) and Neurogenetic and Muscular Disorders Research (9 papers). A. Magariello collaborates with scholars based in Italy, United States and Czechia. A. Magariello's co-authors include M. Muglia, Aldo Quattrone, Antonio Cerasa, F. L. Conforti, R. Mazzei, Maria Cecilia Gioia, A. Patitucci, Luca Passamonti, Francesco Saverio Fera and A. L. Gabriele and has published in prestigious journals such as NeuroImage, Neurology and Biological Psychiatry.

In The Last Decade

A. Magariello

39 papers receiving 755 citations

Peers

A. Magariello

NEURO

CMN

NEURO

GENET

M. Muglia Italy

Hubertus M. Mehdorn Germany

Nancy Pavón Cuba

Anne Noreau Canada

Satoshi Kaneko Japan

Kathrin Müller Germany

Gilles‐Louis Defer France

Renée J. McCarter United Kingdom

Meghan G. Thomas Australia

Dan Geschwind United States

M. Muglia Italy

A. Magariello

614 ×1.8

NEURO

815 ×2.8

CMN

665 ×3.4

300 ×1.9

NEURO

200 ×1.3

GENET

Citations per year, relative to A. Magariello A. Magariello (= 1×) peers M. Muglia

Countries citing papers authored by A. Magariello

Since Specialization

Citations

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

Fields of papers citing papers by A. Magariello

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Magariello

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

Mazzei, R., et al.. (2025). From Hippocrates to Italian traditional medicine: Ethnopharmacological evidence for a potential pharmacological perspective in the management of polycystic ovary syndrome. Journal of Ethnopharmacology. 355(Pt B). 120730–120730. 1 indexed citations

Mazzei, R., et al.. (2024). Plants in Menstrual Diseases: A Systematic Study from Italian Folk Medicine on Current Approaches. Plants. 13(5). 589–589. 2 indexed citations

Muglia, M., Luigi Citrigno, Eustachio D’Errico, et al.. (2014). A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness. Journal of the Neurological Sciences. 343(1-2). 218–220. 8 indexed citations

Patitucci, A., A. Magariello, C Ungaro, et al.. (2012). SMN1 gene copy number analyses for SMA healthy carriers in Italian population.. Europe PMC (PubMed Central). 1(2). 99–102.

Cerasa, Antonio, Andrea Cherubini, Aldo Quattrone, et al.. (2010). Morphological correlates of MAO A VNTR polymorphism: New evidence from cortical thickness measurement. Behavioural Brain Research. 211(1). 118–124. 25 indexed citations

Magariello, A., M. Muglia, A. Patitucci, et al.. (2009). Mutation analysis of the SPG4 gene in Italian patients with pure and complicated forms of spastic paraplegia. Journal of the Neurological Sciences. 288(1-2). 96–100. 20 indexed citations

Conforti, F. L., T. Sprovieri, R. Mazzei, et al.. (2008). Further evidence that D90A-SOD1 mutation is recessively inherited in ALS patients in Italy. Amyotrophic Lateral Sclerosis. 10(1). 58–60. 11 indexed citations

Cerasa, Antonio, Maria Cecilia Gioia, Angelo Labate, et al.. (2008). MAO A VNTR polymorphism and variation in human morphology: a VBM study. Neuroreport. 19(11). 1107–1110. 23 indexed citations

Ungaro, C, R. Mazzei, F. L. Conforti, et al.. (2008). CADASIL: Extended polymorphisms and mutational analysis of the NOTCH3 gene. Journal of Neuroscience Research. 87(5). 1162–1167. 23 indexed citations

10.

Conforti, F. L., T. Sprovieri, R. Mazzei, et al.. (2007). A novel Angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy. Neuromuscular Disorders. 18(1). 68–70. 45 indexed citations

11.

Mazzei, R., Donata Guidetti, C Ungaro, et al.. (2007). First evidence of a pathogenic insertion in the NOTCH3 gene causing CADASIL. Journal of Neurology Neurosurgery & Psychiatry. 79(1). 108–110. 10 indexed citations

12.

Magariello, A., M. Muglia, A. Patitucci, et al.. (2006). Novel spastin (SPG4) mutations in Italian patients with hereditary spastic paraplegia. Neuromuscular Disorders. 16(6). 387–390. 14 indexed citations

13.

Conforti, F. L., T. Sprovieri, R. Mazzei, et al.. (2006). Sporadic ALS is not associated with VAPB gene mutations in Southern Italy. Journal of Negative Results in BioMedicine. 5(1). 7–7. 19 indexed citations

14.

Patitucci, A., M. Muglia, A. Magariello, et al.. (2005). Comparison of different techniques for detecting 17p12 duplication in CMT1A. Neuromuscular Disorders. 15(7). 488–492. 9 indexed citations

15.

Passamonti, Luca, Francesco Saverio Fera, A. Magariello, et al.. (2005). Monoamine Oxidase-A Genetic Variations Influence Brain Activity Associated with Inhibitory Control: New Insight into the Neural Correlates of Impulsivity. Biological Psychiatry. 59(4). 334–340. 125 indexed citations

16.

Conforti, F. L., M. Muglia, R. Mazzei, et al.. (2004). A new SBF2 mutation in a family with recessive demyelinating Charcot-Marie-Tooth (CMT4B2). Neurology. 63(7). 1327–1328. 11 indexed citations

17.

Mazzei, R., Antonio Gambardella, F. L. Conforti, et al.. (2003). Gene conversion events in adult-onset spinal muscular atrophy. Acta Neurologica Scandinavica. 109(2). 151–154. 11 indexed citations

18.

Muglia, M., Chiara Criscuolo, A. Magariello, et al.. (2003). Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus. Neurogenetics. 5(1). 49–54. 10 indexed citations

19.

Mazzei, R., F. L. Conforti, A. Magariello, et al.. (2002). A novel mutation in the CLN1 gene in a patient with juvenile neuronal ceroid lipofuscinosis. Journal of Neurology. 249(10). 1398–1400. 14 indexed citations

20.

Muglia, M., A. Magariello, Giuseppe Nicoletti, et al.. (2002). A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3. Journal of Neurology. 249(10). 1413–1416. 3 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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