Matilde Laurá

7.6k citations

75 papers · 3.4k indexed · h-index 30

Cellular and Molecular Neuroscience top 0.5%
- Hereditary Neurological Disorders 61
- Genetic Neurodegenerative Diseases 29
Neurology top 1%
- Botulinum Toxin and Related Neurological Disorders 31
- Peripheral Neuropathies and Disorders 14
- Neurological diseases and metabolism 8
Neurology top 1%
- Botulinum Toxin and Related Neurological Disorders 31
- Peripheral Neuropathies and Disorders 14
- Neurological diseases and metabolism 8
Cell Biology top 2%
- Cellular transport and secretion 6
Genetics top 5%
- Neurogenetic and Muscular Disorders Research 4
Molecular Biology
- RNA regulation and disease 4

Co-authors: Mary M. Reilly Alexander M. Rossor Henry Houlden Davide Pareyson Sinéad M. Murphy Menelaos Pipis James M. Polke Julian Blake
Cited by: Cellular and Molecular Neuroscience Neurology Cell Biology
Journals: Journal of the Peripheral Nervous System (12 papers)Neurology (11 papers)Journal of Neurology Neurosurgery & Psychiatry (9 papers)
Partner nations: United Kingdom Italy United States

In The Last Decade

Matilde Laurá

74 papers receiving 3.3k citations

Peers

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

The 25 scholars most cited alongside Matilde Laurá, 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 Matilde Laurá Line = papers co-authored together Matilde Laurá links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Intermediate conduction velocity in two cases of Charcot−Marie−Tooth disease type 1A European Journal of Neurology ·Pedro José Tomaselli,Julian Blake,James M. Polke,Osvaldo J. M. Nascimento,Mary M. Reilly,Wilson Marques,Matilde Laurá	2024	2
2	Whole genome sequencing increases the diagnostic rate in Charcot-Marie-Tooth disease Brain ·Christopher J. Record,Menelaos Pipis,Mariola Skorupinska,Julian Blake,Roy Poh,James M. Polke,A M El-Gatit,Tina Nanji,Stephan Züchner,Andrea Cortese,Henry Houlden,Alexander M. Rossor,Matilde Laurá,Mary M. Reilly	2024	13
3	Incidence and risk factors for patellofemoral dislocation in adults with Charcot‐Marie‐Tooth disease: An observational study Physiotherapy Research International ·順奥野,Sally Davenport,Claire Robertson,Matilde Laurá,Mariola Skorupinska,Mary M. Reilly,Gita Ramdharry	2023	2
4	Post-transcriptional microRNA repression of PMP22 dose in severe Charcot-Marie-Tooth disease type 1 Brain ·Menelaos Pipis,Kuldeep Singh,Roy Poh,Stéphanie Efthymiou,James M. Polke,Mariola Skorupinska,Julian Blake,Alexander M. Rossor,John J. Moran,Pinki Munot,Francesco Muntoni,Matilde Laurá,John Svaren,Mary M. Reilly	2023	3
5	Quantitative MRI outcome measures in CMT1A using automated lower limb muscle segmentation Journal of Neurology Neurosurgery & Psychiatry ·Luke O’Donnell,Menelaos Pipis,John S. Thornton,Baris Kanber,Stephen Wastling,Prospero Gulli,王长梅,Matilde Laurá,Mariola Skorupinska,Christopher J. Record,Volodymyr P. Komarnytskyi,David N. Herrmann,Henrik Zetterberg,Amanda Heslegrave,Alejandro Sanchez,Alexander M. Rossor,Jasper M. Morrow,Mary M. Reilly	2023	6
6	Charcot-Marie-Tooth disease type 2CC due toNEFHvariants causes a progressive, non-length-dependent, motor-predominant phenotype Journal of Neurology Neurosurgery & Psychiatry ·Menelaos Pipis,Andrea Cortese,James M. Polke,Roy Poh,Jana Vandrovcová,Matilde Laurá,Mariola Skorupinska,Arnaud Jacquier,Raúl Juntas‐Morales,Philippe Latour,Philippe Petiot,Guilhem Solé,Yves Fromes,Sachit Shah,Julian Blake,Byung‐Ok Choi,Ki Wha Chung,Tanya Stojkovic,Alexander M. Rossor,Mary M. Reilly	2021	11
7	Refining clinical trial inclusion criteria to optimize the standardized response mean of the CMTPedS Annals of Clinical and Translational Neurology ·Kayla Cornett,Manoj P. Menezes,Paula Bray,Rosemary Shy,Isabella Moroni,Emanuela Pagliano,Davide Pareyson,Tim Estilow,Sabrina W. Yum,Bijal C. Patel,Francesco Muntoni,Matilde Laurá,Mary M. Reilly,Richard S. Finkel,Katy Eichinger,David N. Herrmann,Michael E. Shy,Joshua Burns,(unknown)	2020	15
8	Next-generation sequencing in Charcot–Marie–Tooth disease: opportunities and challenges Nature Reviews Neurology ·Menelaos Pipis,Alexander M. Rossor,Matilde Laurá,Mary M. Reilly	2019	134
9	Community exercise is feasible for neuromuscular diseases and can improve aerobic capacity Neurology ·Amanda Wallace,NAGABHAIRAVA VENKATA SIDDARTHA,R Lee,Magdalena Dudziec,Katherine Jones,P. J. Hennis,Annette Sterr,Gianluca Baio,Pedro Machado,Matilde Laurá,Iwona Skorupinska,Mariola Skorupinska,하얀 남,Michael I. Trenell,Mary M. Reilly,Michael G. Hanna,Gita Ramdharry	2019	46
10	Autosomal-recessive cerebellar ataxia caused by a novel ADCK3 mutation that elongates the protein: clinical, genetic and biochemical characterisation Journal of Neurology Neurosurgery & Psychiatry ·Pengfei Bai,Joshua Hersheson,Vincent Plagnol,Katherine A. Fawcett,Kate Duberley,Elisavet Preza,Iain P. Hargreaves,Annapurna Chalasani,Matilde Laurá,Nicholas Wood,Mary M. Reilly,Henry Houlden	2013	43
11	Validation of the Charcot–Marie–Tooth disease pediatric scale as an outcome measure of disability Annals of Neurology ·Joshua Burns,Robert Ouvrier,Tim Estilow,Rosemary Shy,Matilde Laurá,Julie Pallant,Monkol Lek,Francesco Muntoni,Mary M. Reilly,Davide Pareyson,Gyula Acsádi,Michael E. Shy,Richard S. Finkel	2012	124
12	Charcot–Marie–Tooth disease: frequency of genetic subtypes and guidelines for genetic testing Journal of Neurology Neurosurgery & Psychiatry ·Sinéad M. Murphy,Matilde Laurá,Katherine A. Fawcett,Amelie Pandraud,Yo‐Tsen Liu,Gabrielle L. Davidson,Alexander M. Rossor,James M. Polke,Victoria Castleman,Hadi Manji,Michael P. Lunn,Jorg Matthys,Gita Ramdharry,Mary B. Davis,Julian Blake,Henry Houlden,Mary M. Reilly	2012	257
13	Hand weakness in Charcot-Marie-Tooth disease 1X Neuromuscular Disorders ·J. Guasch-Martínez,Sinéad M. Murphy,Matilde Laurá,Michael P. Lunn,Hadi Manji,J. Blake,Gita Ramdharry,E. A. Bartlett,Mary M. Reilly	2012	16
14	MFN2 mutations cause severe phenotypes in most patients with CMT2A Neurology ·Shawna Feely,Matilde Laurá,Carly E. Siskind,Yang-Qing Qiu,Mary B. Davis,Mahsa Kaviani Boroojeni,Mary M. Reilly,Michael E. Shy	2011	154
15	Conduction block and tonic pupils in Charcot-Marie-Tooth disease caused by a myelin protein zero p.Ile112Thr mutation Neuromuscular Disorders ·Sinéad M. Murphy,Matilde Laurá,Julian Blake,James M. Polke,Fion Bremner,Mary M. Reilly	2011	17
16	c-Jun expression in human neuropathies: a pilot study Journal of the Peripheral Nervous System ·Elspeth Hutton,Lucy Carty,Matilde Laurá,Henry Houlden,Michael P. Lunn,Sebastian Brandner,Rhona Mirsky,Kristján R. Jessen,Mary M. Reilly	2011	48
17	Variable phenotypes are associated with PMP22 missense mutations Neuromuscular Disorders ·Massimo Russo,Matilde Laurá,James M. Polke,Mary B. Davis,J. Blake,Sebastian Brandner,Richard AC Hughes,Henry Houlden,David Bennett,Michael P. Lunn,Mary M. Reilly	2010	42
18	Reliability of clinical outcome measures in Charcot-Marie-Tooth disease Neuromuscular Disorders ·Alessandra Solari,Matilde Laurá,Ettore Salsano,D. Radice,Davide Pareyson	2007	55
19	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 ·Matilde Laurá,M Milani,Michela Morbin,Laura Uberti Hughes,Michela Ripolone,S. Jann,V. Scaioli,Franco Taroni,Davide Pareyson	2007	26
20	Clinical and electrophysiological aspects of Charcot-Marie-Tooth disease NeuroMolecular Medicine ·Davide Pareyson,V. Scaioli,Matilde Laurá	2006	129

About Matilde Laurá

Matilde Laurá is a scholar working on Cellular and Molecular Neuroscience, Neurology, Neurology, Cell Biology and Genetics, having authored 75 papers that have together received 3.4k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (61 papers), Botulinum Toxin and Related Neurological Disorders (31 papers), Genetic Neurodegenerative Diseases (29 papers), Peripheral Neuropathies and Disorders (14 papers), Neurological diseases and metabolism (8 papers), Cellular transport and secretion (6 papers), RNA regulation and disease (4 papers) and Neurogenetic and Muscular Disorders Research (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (2.3k citations), Neurology (701 citations), Neurology (1.1k citations), Cell Biology (533 citations) and Genetics (312 citations). Matilde Laurá has collaborated with scholars based in United Kingdom, Italy and United States. Frequent 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. Their work appears in journals such as Journal of the Peripheral Nervous System, Neurology, Journal of Neurology Neurosurgery & Psychiatry, Neuromuscular Disorders and European Journal of Neurology.

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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