Matthew Wyles

5.2k total citations
13 papers, 706 citations indexed

About

Matthew Wyles is a scholar working on Neurology, Molecular Biology and Genetics. According to data from OpenAlex, Matthew Wyles has authored 13 papers receiving a total of 706 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Neurology, 7 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Matthew Wyles's work include Amyotrophic Lateral Sclerosis Research (8 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Prion Diseases and Protein Misfolding (3 papers). Matthew Wyles is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (8 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Prion Diseases and Protein Misfolding (3 papers). Matthew Wyles collaborates with scholars based in United Kingdom, Germany and Saudi Arabia. Matthew Wyles's co-authors include Pamela J. Shaw, Ke Ning, Chiara F. Valori, Mimoun Azzouz, Andrew J. Grierson, Richard J. Mead, Paul R. Heath, Janine Kirby, Adrian Higginbottom and Johnathan Cooper‐Knock and has published in prestigious journals such as PLoS ONE, Human Molecular Genetics and Science Translational Medicine.

In The Last Decade

Matthew Wyles

13 papers receiving 693 citations

Peers

Matthew Wyles
Kathryn Koszka United States
Tristan H. Coady United States
Tara Martinez United States
Zhihua Feng United States
Andrew G. L. Douglas United Kingdom
Marianna Falcone Italy
Valentina Sardone United Kingdom
Mélissa Bowerman United Kingdom
Julianne Aebischer France
Marián Hruška-Plocháň United States
Kathryn Koszka United States
Matthew Wyles
Citations per year, relative to Matthew Wyles Matthew Wyles (= 1×) peers Kathryn Koszka

Countries citing papers authored by Matthew Wyles

Since Specialization
Citations

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

Fields of papers citing papers by Matthew Wyles

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthew Wyles

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

All Works

13 of 13 papers shown
1.
Waller, Rachel, Joanna J. Bury, Matthew Wyles, et al.. (2023). Establishing mRNA and microRNA interactions driving disease heterogeneity in amyotrophic lateral sclerosis patient survival. Brain Communications. 6(1). fcad331–fcad331. 2 indexed citations
2.
Waller, Rachel, Yoshiki Hase, Julie E. Simpson, et al.. (2022). Transcriptomic Profiling Reveals Discrete Poststroke Dementia Neuronal and Gliovascular Signatures. Translational Stroke Research. 14(3). 383–396. 3 indexed citations
3.
Weinreich, Michael, Stephanie Shepheard, Nick Verber, et al.. (2019). Neuropathological characterization of a novel TANK binding kinase (TBK1) gene loss of function mutation associated with amyotrophic lateral sclerosis. Neuropathology and Applied Neurobiology. 46(3). 279–291. 14 indexed citations
4.
Waller, Rachel, Matthew Wyles, Paul R. Heath, et al.. (2018). Small RNA Sequencing of Sporadic Amyotrophic Lateral Sclerosis Cerebrospinal Fluid Reveals Differentially Expressed miRNAs Related to Neural and Glial Activity. Frontiers in Neuroscience. 11. 731–731. 73 indexed citations
5.
Cooper‐Knock, Johnathan, Gabriel Altschuler, Wenbin Wei, et al.. (2017). A data-driven approach links microglia to pathology and prognosis in amyotrophic lateral sclerosis. Acta Neuropathologica Communications. 5(1). 23–23. 54 indexed citations
6.
Cooper‐Knock, Johnathan, H. Ian Robins, Matthew Wyles, et al.. (2017). Targeted Genetic Screen in Amyotrophic Lateral Sclerosis Reveals Novel Genetic Variants with Synergistic Effect on Clinical Phenotype. Frontiers in Molecular Neuroscience. 10. 370–370. 24 indexed citations
7.
Cooper‐Knock, Johnathan, Joanna J. Bury, Paul R. Heath, et al.. (2015). C9ORF72 GGGGCC Expanded Repeats Produce Splicing Dysregulation which Correlates with Disease Severity in Amyotrophic Lateral Sclerosis. PLoS ONE. 10(5). e0127376–e0127376. 77 indexed citations
8.
Bayatti, Nadhim, Johnathan Cooper‐Knock, Joanna J. Bury, et al.. (2014). Comparison of Blood RNA Extraction Methods Used for Gene Expression Profiling in Amyotrophic Lateral Sclerosis. PLoS ONE. 9(1). e87508–e87508. 22 indexed citations
9.
Little, Daniel, Chiara F. Valori, Chantal A. Mutsaers, et al.. (2014). PTEN Depletion Decreases Disease Severity and Modestly Prolongs Survival in a Mouse Model of Spinal Muscular Atrophy. Molecular Therapy. 23(2). 270–277. 43 indexed citations
10.
Higginbottom, Adrian, Chiara F. Valori, Matthew Wyles, et al.. (2013). Viral Delivery of Antioxidant Genes as a Therapeutic Strategy in Experimental Models of Amyotrophic Lateral Sclerosis. Molecular Therapy. 21(8). 1486–1496. 39 indexed citations
11.
Ning, Ke, Carsten Drepper, Chiara F. Valori, et al.. (2010). PTEN depletion rescues axonal growth defect and improves survival in SMN-deficient motor neurons. Human Molecular Genetics. 19(16). 3159–3168. 106 indexed citations
12.
Valori, Chiara F., Ke Ning, Matthew Wyles, et al.. (2010). Systemic Delivery of scAAV9 Expressing SMN Prolongs Survival in a Model of Spinal Muscular Atrophy. Science Translational Medicine. 2(35). 35ra42–35ra42. 224 indexed citations
13.
Valori, Chiara F., Ke Ning, Matthew Wyles, & Mimoun Azzouz. (2008). Development and Applications of Non-HIV-Based Lentiviral Vectors in Neurological Disorders. Current Gene Therapy. 8(6). 406–418. 25 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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