M.L. Mostacciuolo

641 total citations
18 papers, 466 citations indexed

About

M.L. Mostacciuolo is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, M.L. Mostacciuolo has authored 18 papers receiving a total of 466 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 6 papers in Genetics. Recurrent topics in M.L. Mostacciuolo's work include Hereditary Neurological Disorders (6 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Neurological diseases and metabolism (3 papers). M.L. Mostacciuolo is often cited by papers focused on Hereditary Neurological Disorders (6 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Neurological diseases and metabolism (3 papers). M.L. Mostacciuolo collaborates with scholars based in Italy, United States and United Kingdom. M.L. Mostacciuolo's co-authors include C. Angelini, G Danieli, Giovanni Vazza, Andrea Vettori, Manuela Miorelli, C Villanova, Paola Melacini, M.P. Freda, G Fasoli and Sergio Dalla Volta and has published in prestigious journals such as Circulation, Neurology and Genome Research.

In The Last Decade

M.L. Mostacciuolo

17 papers receiving 457 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.L. Mostacciuolo Italy 12 289 119 113 88 65 18 466
Robyn Labrum United Kingdom 14 488 1.7× 145 1.2× 400 3.5× 44 0.5× 93 1.4× 21 772
Carmen Serrano Spain 14 501 1.7× 98 0.8× 267 2.4× 68 0.8× 43 0.7× 31 844
Jordan T. Gladman United States 10 210 0.7× 50 0.4× 76 0.7× 48 0.5× 46 0.7× 13 406
Anne‐Catherine Passaquin Switzerland 12 460 1.6× 54 0.5× 110 1.0× 31 0.4× 20 0.3× 18 616
Tiziana Mongini Italy 14 399 1.4× 117 1.0× 141 1.2× 48 0.5× 8 0.1× 46 595
Loredana Boccone Italy 15 560 1.9× 35 0.3× 97 0.9× 46 0.5× 8 0.1× 21 779
Tara Newcomb United States 10 263 0.9× 22 0.2× 119 1.1× 101 1.1× 37 0.6× 12 454
Valentina Pegoraro Italy 14 399 1.4× 86 0.7× 91 0.8× 109 1.2× 19 0.3× 25 626
Alberto A. Zambon Italy 11 226 0.8× 60 0.5× 61 0.5× 44 0.5× 9 0.1× 26 324
Monica Traverso Italy 13 348 1.2× 61 0.5× 66 0.6× 30 0.3× 53 0.8× 32 488

Countries citing papers authored by M.L. Mostacciuolo

Since Specialization
Citations

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

Fields of papers citing papers by M.L. Mostacciuolo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M.L. Mostacciuolo

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

All Works

18 of 18 papers shown
1.
Manno, Nicola, Francesca Boaretto, Salvatore Musumeci, et al.. (2014). High prevalence of chitotriosidase deficiency in Peruvian Amerindians exposed to chitin-bearing food and enteroparasites. Carbohydrate Polymers. 113. 607–614. 10 indexed citations
2.
Vazza, Giovanni, Francesca Boaretto, Andrea Vettori, et al.. (2013). A novel SACS mutation results in non‐ataxic spastic paraplegia and peripheral neuropathy. European Journal of Neurology. 20(11). 1486–1491. 22 indexed citations
3.
Boaretto, Francesca, Andrea Vettori, Alberto Casarin, et al.. (2010). SEVERE CMT TYPE 2 WITH FATAL ENCEPHALOPATHY ASSOCIATED WITH A NOVEL MFN2 SPLICING MUTATION. Neurology. 74(23). 1919–1921. 23 indexed citations
4.
Simonati, Alessandro, et al.. (2006). A novel missense mutation in the L1CAM gene in a boy with L1 disease. Neurological Sciences. 27(2). 114–117. 6 indexed citations
5.
Soragna, D., Andrea Vettori, Gianni Carraro, et al.. (2003). A Locus for Migraine without Aura Maps on Chromosome 14q21.2-q22.3. The American Journal of Human Genetics. 72(1). 161–167. 70 indexed citations
6.
Opocher, Giuseppe, Francesca Schiavi, Andrea Vettori, et al.. (2003). Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma. Clinical Endocrinology. 59(6). 707–715. 15 indexed citations
7.
Vazza, Giovanni, et al.. (2003). Identification and characterization of C3orf6, a new conserved human gene mapping to chromosome 3q28. Gene. 314. 113–120. 13 indexed citations
8.
Rossetto, Marta, Elena Sartori, M.L. Mostacciuolo, et al.. (2003). Infancy onset hereditary spastic paraplegia associated with a novel atlastin mutation. Neurology. 61(4). 580–581. 26 indexed citations
9.
Capon, Francesca, Luciano Merlini, C. Angelini, et al.. (1996). Discordant clinical outcome in type III spinal muscular atrophy sibships showing the same deletion pattern. Neuromuscular Disorders. 6(4). 261–264. 14 indexed citations
10.
Melacini, Paola, G Danieli, C Villanova, et al.. (1996). Myocardial Involvement Is Very Frequent Among Patients Affected With Subclinical Becker's Muscular Dystrophy. Circulation. 94(12). 3168–3175. 139 indexed citations
11.
Mostacciuolo, M.L., et al.. (1995). Frequency of Duplication at 17p11.2 in Families of Northeast Italy with Charcot-Marie-Tooth Disease Type 1. Neuroepidemiology. 14(2). 49–53. 16 indexed citations
12.
Bell, C., Susan M. Cochrane, Jamel Chelly, et al.. (1994). Mutations in the connexin 32 gene in X-linked dominant Charcot—Marie—Tooth disease (CMTX1). Human Molecular Genetics. 3(6). 1033–1034. 9 indexed citations
13.
Saad, Fawzy A., Libero Vitiello, Salvatore Oliviero, M.L. Mostacciuolo, & G. A. Danieli. (1993). Detection of unknown gene mutations by multiplex single-strand conformation polymorphism (MSSCP).. Genome Research. 3(1). 60–62. 4 indexed citations
14.
Martinuzzi, Andrea, Luigi Bartolomei, Rosalba Carrozzo, et al.. (1992). Correlation between clinical and molecular features in two MELAS families. Journal of the Neurological Sciences. 113(2). 222–229. 35 indexed citations
15.
Mostacciuolo, M.L., et al.. (1992). Epidemiology of Spinal Muscular Atrophies in a Sample of the Italian Population. Neuroepidemiology. 11(1). 34–38. 35 indexed citations
16.
Kausch, Katrin, Frank Kullmann, M.L. Mostacciuolo, et al.. (1992). Multipoint linkage mapping of the Emery-Dreifuss muscular dystrophy gene. Neuromuscular Disorders. 2(2). 111–115. 7 indexed citations
17.
Vitiello, Libero, et al.. (1992). Screening for mutations in the muscle promoter region and for exonic deletions in a series of 115 DMD and BMD patients.. Journal of Medical Genetics. 29(2). 127–130. 22 indexed citations
18.
Mostacciuolo, M.L., et al.. (1991). A linkage study in a large family by using 12 probes of the pericentromeric region.

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Robyn Labrum Breakdown of academic impact, for papers by Carmen Serrano Breakdown of academic impact, for papers by Jordan T. Gladman Breakdown of academic impact, for papers by Anne‐Catherine Passaquin Breakdown of academic impact, for papers by Tiziana Mongini Breakdown of academic impact, for papers by Loredana Boccone Breakdown of academic impact, for papers by Tara Newcomb Breakdown of academic impact, for papers by Valentina Pegoraro Breakdown of academic impact, for papers by Alberto A. Zambon Breakdown of academic impact, for papers by Monica Traverso
Rankless by CCL
2026