Matilde Laurá

7.6k total citations
75 papers, 3.4k citations indexed

About

Matilde Laurá is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Matilde Laurá has authored 75 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Cellular and Molecular Neuroscience, 36 papers in Neurology and 20 papers in Molecular Biology. Recurrent topics in Matilde Laurá's work include Hereditary Neurological Disorders (61 papers), Botulinum Toxin and Related Neurological Disorders (31 papers) and Genetic Neurodegenerative Diseases (29 papers). Matilde Laurá is often cited by papers focused on Hereditary Neurological Disorders (61 papers), Botulinum Toxin and Related Neurological Disorders (31 papers) and Genetic Neurodegenerative Diseases (29 papers). Matilde Laurá collaborates with scholars based in United Kingdom, Italy and United States. Matilde Laurá's co-authors include Mary M. Reilly, Alexander M. Rossor, Henry Houlden, Davide Pareyson, Sinéad M. Murphy, Menelaos Pipis, James M. Polke, Julian Blake, Michael E. Shy and V. Scaioli and has published in prestigious journals such as Journal of Biological Chemistry, Brain and Neurology.

In The Last Decade

Matilde Laurá

74 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matilde Laurá United Kingdom 30 2.3k 1.2k 1.1k 701 533 75 3.4k
Paola Mandich Italy 28 1.3k 0.6× 1.1k 0.9× 1.0k 0.9× 561 0.8× 399 0.7× 124 2.8k
Marina Kennerson Australia 27 1.4k 0.6× 1.5k 1.2× 762 0.7× 658 0.9× 564 1.1× 95 3.0k
Pieter A. Bolhuis Netherlands 31 2.2k 1.0× 1.8k 1.5× 909 0.8× 844 1.2× 489 0.9× 63 4.0k
Albena Jordanova Belgium 32 1.7k 0.7× 1.9k 1.6× 518 0.5× 638 0.9× 570 1.1× 87 3.6k
Carsten Wessig Germany 31 1.1k 0.5× 1.0k 0.9× 939 0.8× 415 0.6× 331 0.6× 59 3.1k
Mario Sabatelli Italy 36 1.4k 0.6× 1.3k 1.1× 2.6k 2.3× 572 0.8× 345 0.6× 179 4.0k
Benoît Funalot France 26 813 0.4× 1.1k 0.9× 657 0.6× 314 0.4× 185 0.3× 87 2.3k
A E Harding United Kingdom 33 2.5k 1.1× 2.6k 2.2× 1.7k 1.5× 893 1.3× 359 0.7× 72 4.9k
Carla Taveggia Italy 27 1.6k 0.7× 1.0k 0.9× 259 0.2× 292 0.4× 378 0.7× 44 2.7k
Erik Storkebaum Germany 23 696 0.3× 1.4k 1.2× 704 0.6× 371 0.5× 174 0.3× 37 2.7k

Countries citing papers authored by Matilde Laurá

Since Specialization
Citations

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

Fields of papers citing papers by Matilde Laurá

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matilde Laurá

This figure shows the co-authorship network connecting the top 25 collaborators of Matilde Laurá. A scholar is included among the top collaborators of Matilde Laurá 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 Matilde Laurá. Matilde Laurá 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.
Tomaselli, Pedro José, Julian Blake, James M. Polke, et al.. (2024). Intermediate conduction velocity in two cases of Charcot−Marie−Tooth disease type 1A. European Journal of Neurology. 31(5). e16199–e16199. 2 indexed citations
2.
Record, Christopher J., Menelaos Pipis, Mariola Skorupinska, et al.. (2024). Whole genome sequencing increases the diagnostic rate in Charcot-Marie-Tooth disease. Brain. 147(9). 3144–3156. 13 indexed citations
3.
Davenport, Sally, Claire Robertson, Matilde Laurá, et al.. (2023). Incidence and risk factors for patellofemoral dislocation in adults with Charcot‐Marie‐Tooth disease: An observational study. Physiotherapy Research International. 28(3). e1996–e1996. 2 indexed citations
4.
Pipis, Menelaos, Roy Poh, Stéphanie Efthymiou, et al.. (2023). Post-transcriptional microRNA repression of PMP22 dose in severe Charcot-Marie-Tooth disease type 1. Brain. 146(10). 4025–4032. 3 indexed citations
5.
O’Donnell, Luke, Menelaos Pipis, John S. Thornton, et al.. (2023). Quantitative MRI outcome measures in CMT1A using automated lower limb muscle segmentation. Journal of Neurology Neurosurgery & Psychiatry. 95(6). 500–503. 6 indexed citations
6.
Pipis, Menelaos, Andrea Cortese, James M. Polke, et al.. (2021). Charcot-Marie-Tooth disease type 2CC due toNEFHvariants causes a progressive, non-length-dependent, motor-predominant phenotype. Journal of Neurology Neurosurgery & Psychiatry. 93(1). 48–56. 11 indexed citations
7.
Cornett, Kayla, Manoj P. Menezes, Paula Bray, et al.. (2020). Refining clinical trial inclusion criteria to optimize the standardized response mean of the CMTPedS. Annals of Clinical and Translational Neurology. 7(9). 1713–1715. 15 indexed citations
8.
Pipis, Menelaos, Alexander M. Rossor, Matilde Laurá, & Mary M. Reilly. (2019). Next-generation sequencing in Charcot–Marie–Tooth disease: opportunities and challenges. Nature Reviews Neurology. 15(11). 644–656. 134 indexed citations
9.
Wallace, Amanda, Magdalena Dudziec, Katherine Jones, et al.. (2019). Community exercise is feasible for neuromuscular diseases and can improve aerobic capacity. Neurology. 92(15). e1773–e1785. 46 indexed citations
10.
Hersheson, Joshua, Vincent Plagnol, Katherine A. Fawcett, et al.. (2013). Autosomal-recessive cerebellar ataxia caused by a novel ADCK3 mutation that elongates the protein: clinical, genetic and biochemical characterisation. Journal of Neurology Neurosurgery & Psychiatry. 85(5). 493–498. 43 indexed citations
11.
Burns, Joshua, Robert Ouvrier, Tim Estilow, et al.. (2012). Validation of the Charcot–Marie–Tooth disease pediatric scale as an outcome measure of disability. Annals of Neurology. 71(5). 642–652. 124 indexed citations
12.
Murphy, Sinéad M., Matilde Laurá, Katherine A. Fawcett, et al.. (2012). Charcot–Marie–Tooth disease: frequency of genetic subtypes and guidelines for genetic testing. Journal of Neurology Neurosurgery & Psychiatry. 83(7). 706–710. 257 indexed citations
13.
Murphy, Sinéad M., Matilde Laurá, Michael P. Lunn, et al.. (2012). Hand weakness in Charcot-Marie-Tooth disease 1X. Neuromuscular Disorders. 22(7). 622–626. 16 indexed citations
14.
Feely, Shawna, Matilde Laurá, Carly E. Siskind, et al.. (2011). MFN2 mutations cause severe phenotypes in most patients with CMT2A. Neurology. 76(20). 1690–1696. 154 indexed citations
15.
Murphy, Sinéad M., Matilde Laurá, Julian Blake, et al.. (2011). Conduction block and tonic pupils in Charcot-Marie-Tooth disease caused by a myelin protein zero p.Ile112Thr mutation. Neuromuscular Disorders. 21(3). 223–226. 17 indexed citations
16.
Hutton, Elspeth, Lucy Carty, Matilde Laurá, et al.. (2011). c-Jun expression in human neuropathies: a pilot study. Journal of the Peripheral Nervous System. 16(4). 295–303. 48 indexed citations
17.
Russo, Massimo, Matilde Laurá, James M. Polke, et al.. (2010). Variable phenotypes are associated with PMP22 missense mutations. Neuromuscular Disorders. 21(2). 106–114. 42 indexed citations
18.
Solari, Alessandra, Matilde Laurá, Ettore Salsano, D. Radice, & Davide Pareyson. (2007). Reliability of clinical outcome measures in Charcot-Marie-Tooth disease. Neuromuscular Disorders. 18(1). 19–26. 55 indexed citations
19.
Laurá, Matilde, M Milani, Michela Morbin, et al.. (2007). Rapid progression of late onset axonal Charcot Marie Tooth disease associated with a novel MPZ mutation in the extracellular domain. Journal of Neurology Neurosurgery & Psychiatry. 78(11). 1263–1266. 26 indexed citations
20.
Pareyson, Davide, V. Scaioli, & Matilde Laurá. (2006). Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease. NeuroMolecular Medicine. 8(1-2). 3–22. 129 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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