M.L. Mostacciuolo

641 citations

18 papers · 466 indexed · h-index 12

Impact in

Genetics top 10%
- Neurogenetic and Muscular Disorders Research
Neurology
- Neurological diseases and metabolism

Papers in ⓘ

Molecular Biology 11
- RNA Research and Splicing 3
- RNA modifications and cancer 3
- Muscle Physiology and Disorders 2
Cellular and Molecular Neuroscience 7
- Hereditary Neurological Disorders 6
- Genetic Neurodegenerative Diseases 3

Co-authors: C. Angelini (6 shared papers)G Danieli (4 shared papers)Giovanni Vazza (5 shared papers)Andrea Vettori (5 shared papers)C Villanova (1 shared paper)Sergio Dalla Volta (1 shared paper)M.P. Freda (1 shared paper)G Fasoli (1 shared paper)
Journals: Neuroepidemiology (2 papers)Neurology (2 papers)Neuromuscular Disorders (2 papers)Gene (1 paper)Human Molecular Genetics (1 paper)
Partner nations: Italy United States United Kingdom

In The Last Decade

M.L. Mostacciuolo

17 papers receiving 457 citations

Peers

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-authors

The 25 scholars most cited alongside M.L. Mostacciuolo, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with M.L. Mostacciuolo Line = papers co-authored together M.L. Mostacciuolo links everyone, so they are left out of the graph.

All Works

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18 of 18 papers shown

#	Work
1	Myocardial Involvement Is Very Frequent Among Patients Affected With Subclinical Becker's Muscular Dystrophy Circulation ·Paola Melacini, (unknown), G Danieli, C Villanova, Flávia Martinello, Marta Miorin, M.P. Freda, Manuela Miorelli, M.L. Mostacciuolo, G Fasoli, C. Angelini, Sergio Dalla Volta	1996	139
2	A Locus for Migraine without Aura Maps on Chromosome 14q21.2-q22.3 The American Journal of Human Genetics ·D. Soragna, Andrea Vettori, Gianni Carraro, Enrico Marchioni, Giovanni Vazza, Silvia Bellini, Rossella Tupler, F Savoldi, M.L. Mostacciuolo	2003	70
3	Correlation between clinical and molecular features in two MELAS families Journal of the Neurological Sciences ·Andrea Martinuzzi, Luigi Bartolomei, Rosalba Carrozzo, M.L. Mostacciuolo, Costantino Carbonin, Vito Toso, Emma Ciafaloni, Sara Shanske, S. DiMauro, C. Angelini	1992	35
4	Epidemiology of Spinal Muscular Atrophies in a Sample of the Italian Population Neuroepidemiology ·M.L. Mostacciuolo, G Danieli, Caterina Trevisan, Erildo Vicente Müller, C. Angelini	1992	35
5	Infancy onset hereditary spastic paraplegia associated with a novel atlastin mutation Neurology ·F. Dalpozzo, Marta Rossetto, F. Boaretto, Elena Sartori, M.L. Mostacciuolo, Andrea Daga, Maria Teresa Bassi, Andrea Martinuzzi	2003	26
6	SEVERE CMT TYPE 2 WITH FATAL ENCEPHALOPATHY ASSOCIATED WITH A NOVEL MFN2 SPLICING MUTATION Neurology ·Francesca Boaretto, Andrea Vettori, Alberto Casarin, Giovanni Vazza, M. Muglia, Marta Rossetto, Tiziana Cavallaro, N. Rizzuto, Valério Carelli, Leonardo Salviati, M.L. Mostacciuolo, Andrea Martinuzzi	2010	23
7	A novel SACS mutation results in non‐ataxic spastic paraplegia and peripheral neuropathy European Journal of Neurology ·Elisa Gregianin, Giovanni Vazza, E. Scaramel, Francesca Boaretto, Andrea Vettori, Emanuela Leonardi, Silvio C. E. Tosatto, Renzo Manara, Elena Pegoraro, M.L. Mostacciuolo	2013	22
8	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 ·Libero Vitiello, M.L. Mostacciuolo, Salvatore Oliviero, F. Schiavon, L Nicoletti, C. Angelini, G. A. Danieli	1992	22
9	Frequency of Duplication at 17p11.2 in Families of Northeast Italy with Charcot-Marie-Tooth Disease Type 1 Neuroepidemiology ·M.L. Mostacciuolo, F. Schiavon, C. Angelini, Beatrice Miccoli, F. Piccolo, G Danieli	1995	16
10	Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma Clinical Endocrinology ·Giuseppe Opocher, Francesca Schiavi, Andrea Vettori, F. Pampinella, Libero Vitiello, Andrea Calderan, B. Vianello, Alessandra Murgia, Maddalena Martella, Augusto Taccaliti, Franco Mantero, M.L. Mostacciuolo	2003	15
11	Discordant clinical outcome in type III spinal muscular atrophy sibships showing the same deletion pattern Neuromuscular Disorders ·Francesca Capon, Chiarina Levato, Luciano Merlini, C. Angelini, M.L. Mostacciuolo, Luisa Politano, Giuseppe Novelli, Bruno Dallapiccola	1996	14
12	Identification and characterization of C3orf6, a new conserved human gene mapping to chromosome 3q28 Gene ·Giovanni Vazza, Simone Picelli, Andrea Bozzato, M.L. Mostacciuolo	2003	13
13	High prevalence of chitotriosidase deficiency in Peruvian Amerindians exposed to chitin-bearing food and enteroparasites Carbohydrate Polymers ·Nicola Manno, Sam Sherratt, Francesca Boaretto, Freddy Mejía Coico, C. Espinoza Camus, Cristina Campos, Salvatore Musumeci, Andrea Battisti, Rupert J. Quinnell, José Mostacero León, Giovanni Vazza, M.L. Mostacciuolo, Maurizio G. Paoletti, Franco H. Falcone	2014	10
14	Mutations in the connexin 32 gene in X-linked dominant Charcot—Marie—Tooth disease (CMTX1) Human Molecular Genetics ·N. Fairweather, C. Bell, Susan M. Cochrane, Jamel Chelly, S. Wang, M.L. Mostacciuolo, Anthony P. Monaco, N E Haites	1994	9
15	Multipoint linkage mapping of the Emery-Dreifuss muscular dystrophy gene Neuromuscular Disorders ·(unknown), Elvira Müller, Katrin Kausch, Frank Kullmann, M.L. Mostacciuolo, Marcella Rietschel, H. W. Rotthauwe, B. Schmalenberger, Gabriele Siciliano, Thomas Voit, U. Langenbeck, B. Mülluer, G Danieli, Klaus Zerres, Christina Müller, T. Grimm	1992	7
16	A novel missense mutation in the L1CAM gene in a boy with L1 disease Neurological Sciences ·Alessandro Simonati, Francesca Boaretto, Andrea Vettori, P. Dabrilli, L. Criscuolo, N. Rizzuto, M.L. Mostacciuolo	2006	6
17	Detection of unknown gene mutations by multiplex single-strand conformation polymorphism (MSSCP). Genome Research ·Fawzy A. Saad, Libero Vitiello, Salvatore Oliviero, M.L. Mostacciuolo, G. A. Danieli	1993	4
18	A linkage study in a large family by using 12 probes of the pericentromeric region M.L. Mostacciuolo, E. Miiller, P Fardin, Barbara Bardoni, Silvana Guioli, Giovanna Camerino, G. A. Danieli	1991	0

About M.L. Mostacciuolo

M.L. Mostacciuolo is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Neurology and Surgery, having authored 18 papers that have together received 466 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (6 papers), Neurogenetic and Muscular Disorders Research (5 papers), RNA Research and Splicing (3 papers), Genetic Neurodegenerative Diseases (3 papers), Neurological diseases and metabolism (3 papers), RNA modifications and cancer (3 papers), Cardiomyopathy and Myosin Studies (2 papers) and Muscle Physiology and Disorders (2 papers). The work is most often cited by research in Genetics (88 citations), Neurology (61 citations), Cellular and Molecular Neuroscience (113 citations), Cardiology and Cardiovascular Medicine (119 citations) and Clinical Biochemistry (33 citations). M.L. Mostacciuolo has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include C. Angelini, G Danieli, Giovanni Vazza, Andrea Vettori, C Villanova, Sergio Dalla Volta, M.P. Freda, G Fasoli, Paola Melacini and Marta Miorin. Their work appears in journals such as Neuroepidemiology, Neurology, Neuromuscular Disorders, Gene and Human Molecular Genetics.

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