Jon Beck

3.6k total citations
25 papers, 1.8k citations indexed

About

Jon Beck is a scholar working on Molecular Biology, Neurology and Neurology. According to data from OpenAlex, Jon Beck has authored 25 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Neurology and 9 papers in Neurology. Recurrent topics in Jon Beck's work include Neurological diseases and metabolism (12 papers), Prion Diseases and Protein Misfolding (10 papers) and Amyotrophic Lateral Sclerosis Research (8 papers). Jon Beck is often cited by papers focused on Neurological diseases and metabolism (12 papers), Prion Diseases and Protein Misfolding (10 papers) and Amyotrophic Lateral Sclerosis Research (8 papers). Jon Beck collaborates with scholars based in United Kingdom, United States and Australia. Jon Beck's co-authors include Simon Mead, Martin N. Rossor, Nick C. Fox, Jason D. Warren, Jonathan D. Rohrer, Tamás Révész, Tammaryn Lashley, John Hardy, Janice L. Holton and Mark Poulter and has published in prestigious journals such as New England Journal of Medicine, Nature Communications and Brain.

In The Last Decade

Jon Beck

25 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jon Beck United Kingdom	17	1.0k	743	699	561	316	25	1.8k
Penelope Hogarth United States	21	1.0k 1.0×	833 1.1×	154 0.2×	703 1.3×	801 2.5×	43	2.1k
Ione Woollacott United Kingdom	16	816 0.8×	462 0.6×	465 0.7×	278 0.5×	210 0.7×	26	1.4k
Una‐Marie Sheerin United Kingdom	13	1.3k 1.2×	495 0.7×	296 0.4×	370 0.7×	567 1.8×	19	1.7k
R. Marconi Italy	14	645 0.6×	652 0.9×	167 0.2×	458 0.8×	660 2.1×	16	1.5k
Raffaele Ferrari United Kingdom	14	660 0.6×	312 0.4×	427 0.6×	253 0.5×	103 0.3×	21	980
Tim Van Langenhove Belgium	11	718 0.7×	316 0.4×	339 0.5×	367 0.7×	133 0.4×	23	1.1k
Manu Sharma Germany	17	1.0k 1.0×	680 0.9×	311 0.4×	380 0.7×	552 1.7×	41	1.6k
Koji Ogomori Japan	18	195 0.2×	598 0.8×	694 1.0×	268 0.5×	143 0.5×	41	1.3k
Eliza Lewandowska Poland	18	418 0.4×	279 0.4×	256 0.4×	480 0.9×	251 0.8×	62	1.2k
J. J. Martin Belgium	15	366 0.4×	269 0.4×	177 0.3×	318 0.6×	729 2.3×	33	1.1k

Countries citing papers authored by Jon Beck

Since Specialization

Citations

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

Fields of papers citing papers by Jon Beck

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jon Beck

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

All Works

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20 of 20 papers shown

Katrak, Sarosh M., et al.. (2019). Familial Creutzfeldt-Jakob disease in an Indian kindred. Annals of Indian Academy of Neurology. 22(4). 458–458. 6 indexed citations

Keogh, Michael J., Wei Wei, Juvid Aryaman, et al.. (2018). High prevalence of focal and multi-focal somatic genetic variants in the human brain. Nature Communications. 9(1). 4257–4257. 44 indexed citations

Ryan, Natalie S., Jennifer M. Nicholas, Philip S.J. Weston, et al.. (2016). Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer’s disease: a case series. The Lancet Neurology. 15(13). 1326–1335. 144 indexed citations

Ryan, Natalie S., Geert Jan Biessels, Lois G. Kim, et al.. (2015). Genetic determinants of white matter hyperintensities and amyloid angiopathy in familial Alzheimer's disease. Neurobiology of Aging. 36(12). 3140–3151. 44 indexed citations

Beck, Jon, Tracy Campbell, Gary Adamson, et al.. (2014). Predictive testing for inherited prion disease: report of 22 years experience. European Journal of Human Genetics. 22(12). 1351–1356. 16 indexed citations

Moss, Davina J. Hensman, Mark Poulter, Jon Beck, et al.. (2013). C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies. Neurology. 82(4). 292–299. 137 indexed citations

Fratta, Pietro, Mark Poulter, Tammaryn Lashley, et al.. (2013). Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia. Acta Neuropathologica. 126(3). 401–409. 104 indexed citations

Mahoney, Colin, Laura Downey, Jon Beck, et al.. (2013). The Presenilin 1 P264L Mutation Presenting as non-Fluent/Agrammatic Primary Progressive Aphasia. Journal of Alzheimer s Disease. 36(2). 239–243. 8 indexed citations

Mahoney, Colin, Laura Downey, Gerard R. Ridgway, et al.. (2012). Longitudinal neuroimaging and neuropsychological profiles of frontotemporal dementia with C9ORF72 expansions. Alzheimer s Research & Therapy. 4(5). 41–41. 80 indexed citations

10.

Mahoney, Colin, Jon Beck, Jonathan D. Rohrer, et al.. (2012). Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features. Brain. 135(3). 736–750. 317 indexed citations

11.

Kaski, Diego, Catherine Pennington, Jon Beck, et al.. (2011). Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factors. Brain. 134(6). 1829–1838. 24 indexed citations

12.

Mead, Simon, Jerome Whitfield, Mark Poulter, et al.. (2009). A Novel Protective Prion Protein Variant that Colocalizes with Kuru Exposure. New England Journal of Medicine. 361(21). 2056–2065. 119 indexed citations

13.

Beck, Jon, Jonathan D. Rohrer, Adrian M. Isaacs, et al.. (2008). A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series. Brain. 131(3). 706–720. 173 indexed citations

14.

Beck, Jon, T. A. Campbell, G Adamson, et al.. (2008). Association of a null allele of SPRN with variant Creutzfeldt–Jakob disease. Journal of Medical Genetics. 45(12). 813–817. 63 indexed citations

15.

Wild, Edward J., Ese Mudanohwo, Mary G. Sweeney, et al.. (2008). Huntington's disease phenocopies are clinically and genetically heterogeneous. Movement Disorders. 23(5). 716–720. 79 indexed citations

16.

Mead, Simon, Tom Webb, Tracy Campbell, et al.. (2007). Inherited prion disease with 5-OPRI. Neurology. 69(8). 730–738. 48 indexed citations

17.

Kovács, Tibor, Jon Beck, M Papp, et al.. (2006). Familial prion disease in a Hungarian family with a novel 144-base pair insertion in the prion protein gene. Journal of Neurology Neurosurgery & Psychiatry. 78(3). 321–323. 6 indexed citations

18.

Godbolt, Alison K., et al.. (2006). A second family with familial AD and the V717L APP mutation has a later age at onset. Neurology. 66(4). 611–612. 9 indexed citations

19.

Beck, Jon, Simon Mead, Tracy Campbell, et al.. (2001). Two-octapeptide repeat deletion of prion protein associated with rapidly progressive dementia. Neurology. 57(2). 354–356. 49 indexed citations

20.

Beck, Jon. (1956). [Méniere's disease].. PubMed. 98(12). 398–400. 1 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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