David S. Lynch

2.0k total citations
30 papers, 578 citations indexed

About

David S. Lynch is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, David S. Lynch has authored 30 papers receiving a total of 578 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 10 papers in Neurology and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in David S. Lynch's work include RNA regulation and disease (8 papers), Hereditary Neurological Disorders (6 papers) and Neurological diseases and metabolism (5 papers). David S. Lynch is often cited by papers focused on RNA regulation and disease (8 papers), Hereditary Neurological Disorders (6 papers) and Neurological diseases and metabolism (5 papers). David S. Lynch collaborates with scholars based in United Kingdom, Italy and Brazil. David S. Lynch's co-authors include Henry Houlden, Peter M. Bingham, Jeremy Chataway, Elaine H. Zackai, Donna M. McDonald‐McGinn, Indran Davagnanam, Elaine Murphy, Nick C. Fox, Nicholas Wood and Jonathan M. Schott and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Neurology.

In The Last Decade

David S. Lynch

28 papers receiving 570 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David S. Lynch United Kingdom 13 346 210 145 104 97 30 578
Óscar G. Vidaurre Spain 10 290 0.8× 105 0.5× 161 1.1× 52 0.5× 64 0.7× 12 506
Hanna Mierzewska Poland 15 444 1.3× 61 0.3× 105 0.7× 82 0.8× 98 1.0× 57 728
Daniela Sinske Germany 12 310 0.9× 75 0.4× 155 1.1× 53 0.5× 115 1.2× 17 550
Reza Maroofian United Kingdom 15 307 0.9× 165 0.8× 55 0.4× 61 0.6× 44 0.5× 57 667
Ramesh Menon Italy 10 371 1.1× 137 0.7× 170 1.2× 49 0.5× 64 0.7× 11 605
Ryan G. Lim United States 11 309 0.9× 173 0.8× 151 1.0× 49 0.5× 74 0.8× 18 565
Yujiro Higuchi Japan 13 206 0.6× 161 0.8× 381 2.6× 47 0.5× 135 1.4× 53 551
Masayoshi Tada Japan 11 299 0.9× 157 0.7× 174 1.2× 86 0.8× 209 2.2× 29 598
Akop Seksenyan United States 10 150 0.4× 120 0.6× 84 0.6× 90 0.9× 79 0.8× 15 454
Terri L. Petkau Canada 12 189 0.5× 171 0.8× 82 0.6× 259 2.5× 390 4.0× 18 618

Countries citing papers authored by David S. Lynch

Since Specialization
Citations

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

Fields of papers citing papers by David S. Lynch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David S. Lynch. 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 David S. Lynch. The network helps show where David S. Lynch may publish in the future.

Co-authorship network of co-authors of David S. Lynch

This figure shows the co-authorship network connecting the top 25 collaborators of David S. Lynch. A scholar is included among the top collaborators of David S. Lynch 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 David S. Lynch. David S. Lynch 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.
Souza, Paulo Victor Sgobbi de, Pedro Braga‐Neto, Fernando Kok, et al.. (2024). Clinicogenetic characterization of cerebrotendinous xanthomatosis in Brazil. Clinical Genetics. 106(6). 721–732. 3 indexed citations
2.
Chataway, Jeremy, et al.. (2024). CSF1R -Related Disorder. Neurology Genetics. 10(4). e200179–e200179. 5 indexed citations
3.
O’Connor, Antoinette, Natalie S. Ryan, David S. Lynch, et al.. (2024). Genetic testing in dementia. Practical Neurology. 25(2). 127–136. 2 indexed citations
4.
Gagliardi, Delia, et al.. (2024). Analysis of GFAP variants in UK Biobank suggests underdiagnosis or incomplete penetrance of adult-onset Alexander disease. Journal of Neurology Neurosurgery & Psychiatry. 96(8). 728–735.
5.
Wade, Charles E. & David S. Lynch. (2024). Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia. Handbook of clinical neurology. 204. 263–271. 3 indexed citations
6.
Houlden, Henry, et al.. (2024). TTR associated leptomeningeal amyloidosis in a Sri Lankan patient. Journal of the Neurological Sciences. 466. 123273–123273.
7.
Papapetropoulos, Spyros, Angela Pontius, Elizabeth Finger, et al.. (2022). Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia: Review of Clinical Manifestations as Foundations for Therapeutic Development. Frontiers in Neurology. 12. 788168–788168. 36 indexed citations
8.
Nóbrega, Paulo Ribeiro, Anderson Rodrigues Brandão de Paiva, Lúcia Inês Macedo‐Souza, et al.. (2022). Arginase 1 deficiency presenting as complicated hereditary spastic paraplegia.. Molecular Case Studies. mcs.a006232–mcs.a006232. 4 indexed citations
9.
Shafat, Manar, Harpreet Hyare, Lorna Neill, et al.. (2021). Pembrolizumab for the treatment of progressive multifocal leukoencephalopathy following anti‐CD19 CAR‐T therapy: a case report. SHILAP Revista de lepidopterología. 2(4). 848–853. 7 indexed citations
10.
Williams, Thomas, Henry Houlden, Elaine Murphy, et al.. (2020). How to diagnose difficult white matter disorders. Practical Neurology. 20(4). 280–286. 5 indexed citations
11.
Bugiardini, Enrico, Rahul Phadke, David S. Lynch, et al.. (2019). Genetic and phenotypic characterisation of inherited myopathies in a tertiary neuromuscular centre. Neuromuscular Disorders. 29(10). 747–757. 10 indexed citations
12.
Lynch, David S., Anderson Rodrigues Brandão de Paiva, Nevin John, et al.. (2018). Practical approach to the diagnosis of adult-onset leukodystrophies: an updated guide in the genomic era. Journal of Neurology Neurosurgery & Psychiatry. 90(5). 543–555. 74 indexed citations
13.
Bugiardini, Enrico, Jasper M. Morrow, Sachit Shah, et al.. (2018). The Diagnostic Value of MRI Pattern Recognition in Distal Myopathies. Frontiers in Neurology. 9. 456–456. 33 indexed citations
14.
Chelban, Viorica, Nisha Patel, Jana Vandrovcová, et al.. (2017). Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination. The American Journal of Human Genetics. 100(6). 969–977. 36 indexed citations
15.
Lakshmanan, Rahul, Indran Davagnanam, Andrew G.B. Thompson, et al.. (2017). Brainstem phenotype of cathepsin A–related arteriopathy with strokes and leukoencephalopathy. Neurology Genetics. 3(4). e165–e165. 11 indexed citations
16.
Chelban, Viorica, Arianna Tucci, David S. Lynch, et al.. (2017). Truncating mutations inSPASTpatients are associated with a high rate of psychiatric comorbidities in hereditary spastic paraplegia. Journal of Neurology Neurosurgery & Psychiatry. 88(8). 681–687. 19 indexed citations
17.
Thomas, C., et al.. (2015). Novel Kidins220/ARMS Splice Isoforms: Potential Specific Regulators of Neuronal and Cardiovascular Development. PLoS ONE. 10(6). e0129944–e0129944. 12 indexed citations
18.
Koutsis, Georgios, David S. Lynch, Georgia Karadima, et al.. (2015). Charcot-Marie-Tooth disease type 2C and scapuloperoneal muscular atrophy overlap syndrome in a patient with the R232C TRPV4 mutation. Journal of Neurology. 262(8). 1972–1975. 5 indexed citations
19.
Lynch, David S., Zane Jaunmuktane, Una‐Marie Sheerin, et al.. (2015). Hereditary leukoencephalopathy with axonal spheroids: a spectrum of phenotypes from CNS vasculitis to parkinsonism in an adult onset leukodystrophy series. Journal of Neurology Neurosurgery & Psychiatry. 87(5). 512–519. 56 indexed citations
20.
McLaughlin, Russell L., Julie Phukan, David S. Lynch, et al.. (2010). Angiogenin Levels and ANG Genotypes: Dysregulation in Amyotrophic Lateral Sclerosis. PLoS ONE. 5(11). e15402–e15402. 14 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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