Tammaryn Lashley

21.9k total citations · 4 hit papers
158 papers, 9.1k citations indexed

About

Tammaryn Lashley is a scholar working on Physiology, Neurology and Molecular Biology. According to data from OpenAlex, Tammaryn Lashley has authored 158 papers receiving a total of 9.1k indexed citations (citations by other indexed papers that have themselves been cited), including 93 papers in Physiology, 87 papers in Neurology and 65 papers in Molecular Biology. Recurrent topics in Tammaryn Lashley's work include Alzheimer's disease research and treatments (93 papers), Parkinson's Disease Mechanisms and Treatments (49 papers) and Amyotrophic Lateral Sclerosis Research (37 papers). Tammaryn Lashley is often cited by papers focused on Alzheimer's disease research and treatments (93 papers), Parkinson's Disease Mechanisms and Treatments (49 papers) and Amyotrophic Lateral Sclerosis Research (37 papers). Tammaryn Lashley collaborates with scholars based in United Kingdom, United States and Sweden. Tammaryn Lashley's co-authors include Tamás Révész, Janice L. Holton, Andrew J. Lees, Jorge Ghiso, Agueda Rostagno, Jonathan D. Rohrer, Gordon T. Plant, Blas Frangione, Nick C. Fox and Simon Mead and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Tammaryn Lashley

154 papers receiving 9.0k citations

Hit Papers

Lewy bodies in grafted ne... 2008 2026 2014 2020 2008 2011 2022 2023 400 800 1.2k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tammaryn Lashley United Kingdom 48 4.7k 4.4k 3.3k 2.1k 1.9k 158 9.1k
Thomas Arzberger Germany 46 4.3k 0.9× 3.3k 0.7× 3.6k 1.1× 1.7k 0.8× 2.2k 1.2× 116 9.7k
Edward B. Lee United States 53 4.9k 1.0× 4.2k 0.9× 3.7k 1.1× 1.9k 0.9× 1.5k 0.8× 208 10.6k
Ekaterina Rogaeva Canada 53 3.4k 0.7× 3.4k 0.8× 3.6k 1.1× 1.4k 0.6× 1.6k 0.9× 188 8.3k
Vivianna M. Van Deerlin United States 53 6.0k 1.3× 4.1k 0.9× 2.4k 0.7× 2.1k 1.0× 1.3k 0.7× 148 9.6k
Mark S. Forman United States 47 4.7k 1.0× 4.0k 0.9× 2.9k 0.9× 1.7k 0.8× 1.5k 0.8× 82 9.1k
Michael Hutton United States 48 2.6k 0.6× 5.3k 1.2× 2.9k 0.9× 1.9k 0.9× 1.8k 0.9× 107 8.2k
Stuart Pickering‐Brown United Kingdom 43 4.5k 1.0× 3.2k 0.7× 2.1k 0.6× 1.5k 0.7× 929 0.5× 111 6.6k
Kuniaki Tsuchiya Japan 35 4.9k 1.0× 2.5k 0.6× 2.4k 0.7× 1.7k 0.8× 1.4k 0.7× 157 7.4k
Yuko Saito Japan 44 2.9k 0.6× 2.8k 0.6× 2.0k 0.6× 1.6k 0.8× 1.5k 0.8× 191 6.6k
Takahiko Tokuda Japan 42 3.3k 0.7× 2.5k 0.6× 2.3k 0.7× 970 0.5× 1.5k 0.8× 171 6.9k

Countries citing papers authored by Tammaryn Lashley

Since Specialization
Citations

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

Fields of papers citing papers by Tammaryn Lashley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tammaryn Lashley

This figure shows the co-authorship network connecting the top 25 collaborators of Tammaryn Lashley. A scholar is included among the top collaborators of Tammaryn Lashley 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 Tammaryn Lashley. Tammaryn Lashley 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.
Schott, Jonathan M., et al.. (2025). Pathological Characterisation of Posterior Cortical Atrophy in Comparison With Amnestic Alzheimer's Disease. Neuropathology and Applied Neurobiology. 51(2). e70007–e70007. 1 indexed citations
2.
Sproviero, Daisy, César Payán‐Gómez, Chiara Milanese, et al.. (2025). A blood-based DNA damage signature in patients with Parkinson’s disease is associated with disease progression. Nature Aging. 5(9). 1844–1861. 2 indexed citations
3.
Vincent, Alec, Dongwei Xu, David Osumi-Sutherland, et al.. (2025). Differential neuronal vulnerability to C9orf72 repeat expansion driven by Xbp1-induced endoplasmic reticulum-associated degradation. Cell Reports. 44(4). 115459–115459. 1 indexed citations
4.
Ge, Junyue, Maciej Dulewicz, Kaj Blennow, et al.. (2025). Chemical imaging delineates Aβ plaque polymorphism across the Alzheimer’s disease spectrum. Nature Communications. 16(1). 3889–3889. 3 indexed citations
5.
Andrews, Rebecca, Christina E. Toomey, Tammaryn Lashley, et al.. (2024). RASP: Optimal Single Puncta Detection in Complex Cellular Backgrounds. The Journal of Physical Chemistry B. 128(15). 3585–3597. 1 indexed citations
6.
Banerjee, Gargi, John Collinge, Nick C. Fox, et al.. (2023). Clinical considerations in early-onset cerebral amyloid angiopathy. Brain. 146(10). 3991–4014. 30 indexed citations
7.
Tetter, Stephan, Diana Arseni, Alexey G. Murzin, et al.. (2023). TAF15 amyloid filaments in frontotemporal lobar degeneration. Nature. 625(7994). 345–351. 23 indexed citations
8.
Gatt, Ariana, et al.. (2022). HnRNP K mislocalisation in neurons of the dentate nucleus is a novel neuropathological feature of neurodegenerative disease and ageing. Neuropathology and Applied Neurobiology. 48(4). e12793–e12793. 14 indexed citations
9.
Shireby, Gemma, Yasuo Miki, Emmanuelle Viré, et al.. (2022). Epigenetic age acceleration is associated with oligodendrocyte proportions in MSA and control brain tissue. Neuropathology and Applied Neurobiology. 49(1). e12872–e12872. 9 indexed citations
10.
Michno, Wojciech, Rafael Camacho, Christina E. Toomey, et al.. (2022). Chemical traits of cerebral amyloid angiopathy in familial British‐, Danish‐, and non‐Alzheimerʼs dementias. Journal of Neurochemistry. 163(3). 233–246. 6 indexed citations
11.
Rossi, Pierre De, Amanda J. Lewis, Carlo Scialò, et al.. (2021). FTLD‐TDP assemblies seed neoaggregates with subtype‐specific features via a prion‐like cascade. EMBO Reports. 22(12). e53877–e53877. 18 indexed citations
12.
O’Connor, Antoinette, Emily K. Abel, Natalie S. Ryan, et al.. (2021). A novel presenilin 1 duplication mutation (Ile168dup) causing Alzheimer's disease associated with myoclonus, seizures and pyramidal features. Neurobiology of Aging. 103. 137.e1–137.e5. 3 indexed citations
13.
Goodman, James R., Chintan A. Trivedi, Sandrine C. Foti, et al.. (2019). Structural and functional conservation of non-lumenized lymphatic endothelial cells in the mammalian leptomeninges. Acta Neuropathologica. 139(2). 383–401. 33 indexed citations
14.
Lamb, Ruth, Jonathan D. Rohrer, Raquel Real, et al.. (2019). A novel TBK1 mutation in a family with diverse frontotemporal dementia spectrum disorders. Molecular Case Studies. 5(3). a003913–a003913. 22 indexed citations
15.
Michno, Wojciech, Sofie Nyström, Tammaryn Lashley, et al.. (2019). Pyroglutamation of amyloid-βx-42 (Aβx-42) followed by Aβ1–40 deposition underlies plaque polymorphism in progressing Alzheimer’s disease pathology. Journal of Biological Chemistry. 294(17). 6719–6732. 53 indexed citations
16.
Kvartsberg, Hlin, Tammaryn Lashley, Christina E. Murray, et al.. (2018). The intact postsynaptic protein neurogranin is reduced in brain tissue from patients with familial and sporadic Alzheimer’s disease. Acta Neuropathologica. 137(1). 89–102. 67 indexed citations
17.
Révész, Tamás, et al.. (2009). Genetics and molecular pathogenesis of sporadic and hereditary cerebral amyloid angiopathies (vol 118, pg 115, 2009). UCL Discovery (University College London).
18.
Li, Jiayi, Elisabet Englund, Janice L. Holton, et al.. (2008). Lewy bodies in grafted neurons in subjects with Parkinson's disease suggest host-to-graft disease propagation. Nature Medicine. 14(5). 501–503. 1325 indexed citations breakdown →
19.
Hope, Andrew, Tammaryn Lashley, Andrew J. Lees, & Rohan de Silva. (2004). Failure in heat-shock protein expression in response to UBB+1 protein in progressive supranuclear palsy in humans. Neuroscience Letters. 359(1-2). 94–98. 5 indexed citations
20.
Morris, Huw R., Graham Gibb, Regina Katzenschlager, et al.. (2002). Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy. Brain. 125(5). 969–975. 54 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

Rankless by CCL
2026