M. Muglia

4.2k total citations
72 papers, 1.8k citations indexed

About

M. Muglia is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, M. Muglia has authored 72 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Cellular and Molecular Neuroscience, 27 papers in Neurology and 26 papers in Molecular Biology. Recurrent topics in M. Muglia's work include Hereditary Neurological Disorders (25 papers), Neurological diseases and metabolism (13 papers) and Genetic Neurodegenerative Diseases (11 papers). M. Muglia is often cited by papers focused on Hereditary Neurological Disorders (25 papers), Neurological diseases and metabolism (13 papers) and Genetic Neurodegenerative Diseases (11 papers). M. Muglia collaborates with scholars based in Italy, United States and United Kingdom. M. Muglia's co-authors include Aldo Quattrone, A. Magariello, F. L. Conforti, Antonio Gambardella, Francesco Bono, Antonio Cerasa, A. Patitucci, R. Mazzei, Maria Cecilia Gioia and Alessandra Bolino and has published in prestigious journals such as Nature Genetics, NeuroImage and Neurology.

In The Last Decade

M. Muglia

70 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Muglia Italy 24 815 665 614 300 277 72 1.8k
Niccolò E. Mencacci United Kingdom 25 798 1.0× 675 1.0× 1.3k 2.1× 245 0.8× 315 1.1× 58 2.1k
Lis Hasholt Denmark 24 823 1.0× 835 1.3× 412 0.7× 152 0.5× 133 0.5× 86 1.6k
B. Ford United States 21 387 0.5× 494 0.7× 848 1.4× 206 0.7× 125 0.5× 36 1.8k
Perrine Charles France 26 1.4k 1.7× 1.3k 1.9× 608 1.0× 254 0.8× 237 0.9× 62 2.5k
Sharon Vinsant United States 20 965 1.2× 619 0.9× 480 0.8× 259 0.9× 118 0.4× 22 1.8k
Aislinn Williams United States 16 763 0.9× 1.2k 1.8× 420 0.7× 198 0.7× 256 0.9× 35 1.8k
Peter Raeymaekers Belgium 17 1.1k 1.3× 530 0.8× 366 0.6× 346 1.2× 182 0.7× 49 2.0k
Stefania Fasano Italy 22 867 1.1× 1.0k 1.6× 277 0.5× 251 0.8× 174 0.6× 31 2.0k
Paymaan Jafar‐Nejad United States 23 920 1.1× 1.6k 2.4× 610 1.0× 212 0.7× 165 0.6× 55 2.3k
Andrea Ciammola Italy 23 2.0k 2.4× 1.7k 2.5× 1.1k 1.8× 175 0.6× 154 0.6× 64 2.9k

Countries citing papers authored by M. Muglia

Since Specialization
Citations

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

Fields of papers citing papers by M. Muglia

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

All Works

20 of 20 papers shown
1.
Sprovieri, T., C Ungaro, Serena Sivo, et al.. (2019). Clinical features and genetic analysis of two siblings with startle disease in an Italian family: a case report. BMC Medical Genetics. 20(1). 40–40. 7 indexed citations
2.
3.
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.
4.
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
5.
Sprovieri, T., F. L. Conforti, Agata Fiumara, et al.. (2009). A novel mutation in the X‐linked cyclin‐dependent kinase‐like 5 (CDKL5) gene associated with a severe Rett phenotype. American Journal of Medical Genetics Part A. 149A(4). 722–725. 16 indexed citations
6.
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
7.
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
8.
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
9.
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
10.
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
11.
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
12.
Cannella, Milena, Cinzia Gellera, Vittorio Maglione, et al.. (2003). The gender effect in juvenile Huntington disease patients of Italian origin. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 125B(1). 92–98. 42 indexed citations
13.
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
14.
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
15.
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
16.
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
17.
Bolino, Alessandra, M. Muglia, F. L. Conforti, et al.. (2000). Genetic Refinement and Physical Mapping of the CMT4B Gene on Chromosome 11q22. Genomics. 63(2). 271–278. 14 indexed citations
18.
Bolino, Alessandra, M. Muglia, F. L. Conforti, et al.. (2000). Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2. Nature Genetics. 25(1). 17–19. 360 indexed citations
19.
Muglia, M., et al.. (1993). α-Thalassemia in a Southern Italian Population (Detection by a Non-Radioactive Procedure). Hemoglobin. 17(3). 285–287. 2 indexed citations
20.
Pepe, Guglielmina, M. Muglia, C. Brancati, & G. Modiano. (1990). Studies on Four Restriction Fragment Length Polymorphisms of the Type I Collagen Genes in Two Italian Populations. Human Heredity. 40(6). 368–380. 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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