Anna Mateddu

1.5k total citations
28 papers, 1.1k citations indexed

About

Anna Mateddu is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cell Biology. According to data from OpenAlex, Anna Mateddu has authored 28 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 12 papers in Cardiology and Cardiovascular Medicine and 9 papers in Cell Biology. Recurrent topics in Anna Mateddu's work include Muscle Physiology and Disorders (16 papers), Cardiomyopathy and Myosin Studies (12 papers) and RNA Research and Splicing (10 papers). Anna Mateddu is often cited by papers focused on Muscle Physiology and Disorders (16 papers), Cardiomyopathy and Myosin Studies (12 papers) and RNA Research and Splicing (10 papers). Anna Mateddu collaborates with scholars based in Italy, United Kingdom and Israel. Anna Mateddu's co-authors include Maria Giovanna Marrosu, Maria Antonietta Melis, Francesco Muntoni, Francesco Muntoni, Gino Serra, Carlo Cianchetti, Antonio Cao, Milena Cau, Rita Congiu and G. Realdi and has published in prestigious journals such as New England Journal of Medicine, Human Molecular Genetics and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Anna Mateddu

28 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anna Mateddu Italy 15 897 576 160 119 95 28 1.1k
L. Feng United Kingdom 13 674 0.8× 254 0.4× 67 0.4× 107 0.9× 187 2.0× 19 795
Susana Quijano‐Roy France 18 1.0k 1.2× 379 0.7× 95 0.6× 233 2.0× 276 2.9× 32 1.2k
L M Kunkel United States 12 755 0.8× 193 0.3× 217 1.4× 142 1.2× 128 1.3× 19 914
Pietro Spitali Netherlands 20 1.0k 1.1× 191 0.3× 213 1.3× 132 1.1× 115 1.2× 55 1.1k
Hui Meng United States 17 593 0.7× 211 0.4× 105 0.7× 106 0.9× 145 1.5× 33 762
S. Britton United Kingdom 6 914 1.0× 240 0.4× 242 1.5× 227 1.9× 104 1.1× 9 1.0k
Jim Talbot Canada 2 553 0.6× 137 0.2× 141 0.9× 95 0.8× 66 0.7× 3 593
Rita C.M. Pavanello Brazil 18 899 1.0× 254 0.4× 93 0.6× 303 2.5× 210 2.2× 50 1.0k
I. Courdier-Fruh Switzerland 11 686 0.8× 105 0.2× 211 1.3× 115 1.0× 131 1.4× 13 829
Sean Germain United States 11 404 0.5× 109 0.2× 202 1.3× 83 0.7× 67 0.7× 13 593

Countries citing papers authored by Anna Mateddu

Since Specialization
Citations

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

Fields of papers citing papers by Anna Mateddu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Mateddu

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Mateddu. A scholar is included among the top collaborators of Anna Mateddu 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 Anna Mateddu. Anna Mateddu 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.
Lachowicz, Joanna Izabela, Anna Mateddu, Pierpaolo Coni, et al.. (2022). Study of the DNA binding mechanism and in vitro activity against cancer cells of iron(iii) and aluminium(iii) kojic acid derivative complexes. Dalton Transactions. 51(16). 6254–6263. 2 indexed citations
2.
Cau, Milena, Loredana Boccone, Anna Mateddu, et al.. (2012). A new deletion in 5′-end of dystrophin gene removing M and P promoters and dystrophin muscle enhancers. Gene. 511(2). 437–440. 1 indexed citations
3.
Carboni, Nicola, Claudia Sardu, Eleonora Cocco, et al.. (2012). Cardiac involvement in patients with lamin A/C gene mutations: A cohort observation. Muscle & Nerve. 46(2). 187–192. 10 indexed citations
4.
Carboni, Nicola, Giovanni Marrosu, Maurizio Porcu, et al.. (2011). Dilated cardiomyopathy with conduction defects in a patient with partial merosin deficiency due to mutations in the laminin‐α2‐chain gene: A chance association or a novel phenotype?. Muscle & Nerve. 44(5). 826–828. 23 indexed citations
5.
Carboni, Nicola, Marco Mura, Eugenio Mercuri, et al.. (2011). Cardiac and muscle imaging findings in a family with X-linked Emery–Dreifuss muscular dystrophy. Neuromuscular Disorders. 22(2). 152–158. 14 indexed citations
6.
Carboni, Nicola, Matteo Floris, Anna Mateddu, et al.. (2011). Aberrant splicing in the LMNA gene caused by a novel mutation on the polypyrimidine tract of intron 5. Muscle & Nerve. 43(5). 688–693. 11 indexed citations
7.
Carboni, Nicola, Marco Mura, Giovanni Marrosu, et al.. (2009). Muscle imaging analogies in a cohort of patients with different clinical phenotypes caused by LMNA gene mutations. Muscle & Nerve. 41(4). 458–463. 28 indexed citations
8.
Carboni, Nicola, Marco Mura, Giovanni Marrosu, et al.. (2008). Muscle MRI findings in patients with an apparently exclusive cardiac phenotype due to a novel LMNA gene mutation. Neuromuscular Disorders. 18(4). 291–298. 22 indexed citations
9.
Maioli, Maria Antonietta, Giovanni Marrosu, Anna Mateddu, et al.. (2007). A novel mutation in the central rod domain of lamin A/C producing a phenotype resembling the Emery–Dreifuss muscular dystrophy phenotype. Muscle & Nerve. 36(6). 828–832. 5 indexed citations
10.
Ferlini, Alessandra, et al.. (1999). X-linked dilated cardiomyopathy and the dystrophin gene. Neuromuscular Disorders. 9(5). 339–346. 82 indexed citations
11.
Melis, MA, M. Cau, Francesco Muntoni, et al.. (1998). Elevation of serum creatine kinase as the only manifestation of an intragenic deletion of the dystrophin gene in three unrelated families. European Journal of Paediatric Neurology. 2(5). 255–261. 56 indexed citations
12.
Cau, Milena, Antonio Cao, Daniela Loi, et al.. (1998). Two novel mutations (10410 T→G; 10296 del C) at carboxy-terminus of the dystrophin gene associated with mental retardation. Human Mutation. 12(1). 70–70. 6 indexed citations
13.
Melis, Maria Antonietta, Francesco Muntoni, Milena Cau, et al.. (1998). Novel nonsense mutation (C→A nt 10512) in exon 72 of dystrophin gene leading to exon skipping in a patient with a mild dystrophinopathy. Human Mutation. 11(S1). S137–S138. 23 indexed citations
14.
Milas̆in, Jelena, Francesco Muntoni, Giovanni Maria Severini, et al.. (1996). A Point Mutation in the 5' Splice Site of the Dystrophin Gene First Intron Responsible for X-Linked Dilated Cardiomyopathy. Human Molecular Genetics. 5(1). 73–79. 125 indexed citations
15.
Muntoni, Francesco, Gualtiero Catani, Anna Mateddu, et al.. (1994). Familial cardiomyopathy, mental retardation and myopathy associated with desmin-type intermediate filaments. Neuromuscular Disorders. 4(3). 233–241. 44 indexed citations
16.
Muntoni, Francesco, et al.. (1993). Muscular weakness in the mdx mouse. Journal of the Neurological Sciences. 120(1). 71–77. 75 indexed citations
17.
Muntoni, Francesco, Milena Cau, Antonello Ganau, et al.. (1993). Deletion of the Dystrophin Muscle-Promoter Region Associated with X-Linked Dilated Cardiomyopathy. New England Journal of Medicine. 329(13). 921–925. 300 indexed citations
18.
Muntoni, Francesco, Anna Mateddu, M. Cau, et al.. (1993). Diagnosis of DMD Carrier Status in a Family with No Known Affected Males. Developmental Medicine & Child Neurology. 35(1). 70–73. 1 indexed citations
19.
Muntoni, Francesco, Anna Mateddu, Maria Giovanna Marrosu, et al.. (1992). Variable dystrophin expression in different muscles of a Duchenne muscular dystrophy carrier. Clinical Genetics. 42(1). 35–38. 11 indexed citations
20.
Muntoni, Francesco, Anna Mateddu, & Gino Serra. (1991). Passive avoidance behaviour deficit in the mdx mouse. Neuromuscular Disorders. 1(2). 121–123. 88 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by L. Feng Breakdown of academic impact, for papers by Susana Quijano‐Roy Breakdown of academic impact, for papers by L M Kunkel Breakdown of academic impact, for papers by Pietro Spitali Breakdown of academic impact, for papers by Hui Meng Breakdown of academic impact, for papers by S. Britton Breakdown of academic impact, for papers by Jim Talbot Breakdown of academic impact, for papers by Rita C.M. Pavanello Breakdown of academic impact, for papers by I. Courdier-Fruh Breakdown of academic impact, for papers by Sean Germain
Rankless by CCL
2026