E. Martoni

770 total citations
15 papers, 462 citations indexed

About

E. Martoni is a scholar working on Molecular Biology, Immunology and Allergy and Cell Biology. According to data from OpenAlex, E. Martoni has authored 15 papers receiving a total of 462 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Immunology and Allergy and 5 papers in Cell Biology. Recurrent topics in E. Martoni's work include Muscle Physiology and Disorders (9 papers), Cell Adhesion Molecules Research (8 papers) and Cellular Mechanics and Interactions (5 papers). E. Martoni is often cited by papers focused on Muscle Physiology and Disorders (9 papers), Cell Adhesion Molecules Research (8 papers) and Cellular Mechanics and Interactions (5 papers). E. Martoni collaborates with scholars based in Italy, Germany and United Kingdom. E. Martoni's co-authors include Francesca Gualandi, Patrizia Sabatelli, Luciano Merlini, Paolo Bonaldo, Alessandra Ferlini, Anna Urciuolo, Stefano Squarzoni, Paolo Grumati, Matteo Bovolenta and Eugenio Mercuri and has published in prestigious journals such as Neurology, Human Molecular Genetics and Journal of Investigative Dermatology.

In The Last Decade

E. Martoni

14 papers receiving 456 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
E. Martoni Italy	10	310	131	101	96	58	15	462
AK Lampe United Kingdom	6	310 1.0×	97 0.7×	113 1.1×	83 0.9×	55 0.9×	8	453
G. Joost Jöbsis Netherlands	8	338 1.1×	122 0.9×	101 1.0×	95 1.0×	63 1.1×	10	459
Matteo Bovolenta Italy	16	448 1.4×	52 0.4×	111 1.1×	67 0.7×	75 1.3×	36	569
Sabine Nedbal Germany	6	192 0.6×	139 1.1×	87 0.9×	98 1.0×	37 0.6×	6	485
Jachinta E. Rooney United States	7	452 1.5×	147 1.1×	44 0.4×	104 1.1×	74 1.3×	9	530
Claudia Di Blasi Italy	16	582 1.9×	77 0.6×	61 0.6×	107 1.1×	119 2.1×	26	657
Diane E. Frank United States	9	529 1.7×	115 0.9×	106 1.0×	155 1.6×	96 1.7×	15	716
Franziska Schatzmann Switzerland	6	316 1.0×	213 1.6×	66 0.7×	165 1.7×	82 1.4×	6	588
Patrizia Barzaghi Switzerland	8	555 1.8×	130 1.0×	76 0.8×	132 1.4×	79 1.4×	9	653
Kinga I. Gawlik Sweden	16	716 2.3×	294 2.2×	82 0.8×	154 1.6×	74 1.3×	22	832

Countries citing papers authored by E. Martoni

Since Specialization

Citations

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

Fields of papers citing papers by E. Martoni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. Martoni

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

All Works

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15 of 15 papers shown

Hicks, Debbie, S.H. Laval, James J. Collins, et al.. (2013). Mutations in the collagen XII gene define a new form of extracellular matrix-related myopathy. Human Molecular Genetics. 23(9). 2353–2363. 81 indexed citations

Martoni, E., Stefania Petrini, Cecilia Trabanelli, et al.. (2013). Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-Terminal domain: a case report. BMC Medical Genetics. 14(1). 59–59. 12 indexed citations

Sabatelli, Patrizia, Francesca Gualandi, Sudheer Kumar Gara, et al.. (2011). Expression of collagen VI α5 and α6 chains in human muscle and in Duchenne muscular dystrophy-related muscle fibrosis. Matrix Biology. 31(3). 187–196. 61 indexed citations

Gualandi, Francesca, Rosa Curci, Patrizia Sabatelli, et al.. (2011). Macrophages: A minimally invasive tool for monitoring collagen VI myopathies. Muscle & Nerve. 44(1). 80–84. 9 indexed citations

Sabatelli, Patrizia, Sudheer Kumar Gara, Paolo Grumati, et al.. (2010). Expression of the Collagen VI α5 and α6 Chains in Normal Human Skin and in Skin of Patients with Collagen VI-Related Myopathies. Journal of Investigative Dermatology. 131(1). 99–107. 66 indexed citations

Bovolenta, Matteo, Marcella Neri, E. Martoni, et al.. (2010). Identification of a deep intronic mutation in the COL6A2 gene by a novel custom oligonucleotide CGH array designed to explore allelic and genetic heterogeneity in collagen VI-related myopathies. BMC Medical Genetics. 11(1). 44–44. 26 indexed citations

Martoni, E., Anna Urciuolo, Patrizia Sabatelli, et al.. (2009). Identification and characterization of novel collagen VI non-canonical splicing mutations causing ullrich congenital muscular dystrophy. Human Mutation. 30(5). E662–E672. 34 indexed citations

Gualandi, Francesca, Anna Urciuolo, E. Martoni, et al.. (2009). Autosomal recessive Bethlem myopathy. Neurology. 73(22). 1883–1891. 57 indexed citations

Gualandi, Francesca, Anna Urciuolo, E. Martoni, et al.. (2009). EM.P.4.07 Autosomal recessive Bethlem myopathy. Neuromuscular Disorders. 19(8-9). 608–609. 1 indexed citations

10.

Gualandi, Francesca, Marcella Neri, Matteo Bovolenta, et al.. (2008). Transcriptional behavior of DMD gene duplications in DMD/BMD males. Human Mutation. 30(2). E310–E319. 14 indexed citations

11.

Merlini, Luciano, E. Martoni, Paolo Grumati, et al.. (2008). Autosomal recessive myosclerosis myopathy is a collagen VI disorder. Neurology. 71(16). 1245–1253. 98 indexed citations

12.

Bovolenta, Matteo, Marcella Neri, M. Fabris, et al.. (2008). G.P.7.04 High Density-comparative genomic hybridization (HD-CGH) array as a tool to detect deep intronic mutations in the dystrophin gene. Neuromuscular Disorders. 18(9-10). 777–777. 1 indexed citations

13.

Merlini, Luciano, Patrizia Sabatelli, Pascale Guicheney, et al.. (2007). C.P.2.07 Autosomal recessive myosclerosis myopathy is a collagen type VI disorder. Neuromuscular Disorders. 17(9-10). 845–845.

14.

Spitali, Pietro, M. Fabris, Matteo Bovolenta, et al.. (2007). G.P.3.07 Intronic conserved non-coding sequences (CNSs) as a tool to detect non-coding RNAs (ncRNAs) and putative regulatory motifs within the dystrophin gene. Neuromuscular Disorders. 17(9-10). 784–784. 1 indexed citations

15.

Cocco, Lucio, Silvano Capitani, E. Martoni, Patrizia Santi, & Adriano Torres Antonucci. (1976). [Chromosomal proteins during ontogenesis of Gallus gallus. I. Non-histone proteins in the liver].. PubMed. 52(13). 945–5. 1 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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