Jonathan Beck

2.6k total citations
25 papers, 1.6k citations indexed

About

Jonathan Beck is a scholar working on Molecular Biology, Neurology and Physiology. According to data from OpenAlex, Jonathan Beck has authored 25 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 9 papers in Neurology and 6 papers in Physiology. Recurrent topics in Jonathan Beck's work include Prion Diseases and Protein Misfolding (13 papers), Neurological diseases and metabolism (9 papers) and Alzheimer's disease research and treatments (6 papers). Jonathan Beck is often cited by papers focused on Prion Diseases and Protein Misfolding (13 papers), Neurological diseases and metabolism (9 papers) and Alzheimer's disease research and treatments (6 papers). Jonathan Beck collaborates with scholars based in United Kingdom, Australia and United States. Jonathan Beck's co-authors include John Collinge, Simon Mead, Elizabeth Fisher, Tracy Campbell, Jonathan D. F. Wadsworth, Mark Poulter, Martin N. Rossor, Andrew F. Hill, Jason D. Warren and Jonathan D. Rohrer and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Jonathan Beck

25 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jonathan Beck United Kingdom 20 1.0k 550 344 254 212 25 1.6k
R. D. Rudelli United States 18 1.2k 1.1× 310 0.6× 224 0.7× 220 0.9× 475 2.2× 40 2.2k
Mary T. Lucero United States 26 977 1.0× 82 0.1× 343 1.0× 111 0.4× 81 0.4× 51 2.1k
Anne E. Luebke United States 21 460 0.5× 397 0.7× 99 0.3× 51 0.2× 414 2.0× 47 1.6k
Azlina Ahmad‐Annuar Malaysia 16 540 0.5× 183 0.3× 29 0.1× 125 0.5× 79 0.4× 69 1.3k
Ryosei Minoda Japan 17 461 0.5× 310 0.6× 47 0.1× 211 0.8× 456 2.2× 71 1.8k
Shin‐ichi Kano United States 17 599 0.6× 223 0.4× 49 0.1× 117 0.5× 59 0.3× 33 1.9k
Patricia J. Fisher United States 10 629 0.6× 112 0.2× 44 0.1× 178 0.7× 113 0.5× 16 1.3k
Irene Corradini Italy 17 626 0.6× 221 0.4× 22 0.1× 200 0.8× 108 0.5× 24 1.3k
Harold G. Marks United States 24 840 0.8× 174 0.3× 14 0.0× 125 0.5× 127 0.6× 48 1.6k
Hirohiko Hohjoh Japan 29 1.8k 1.7× 87 0.2× 30 0.1× 151 0.6× 540 2.5× 70 3.0k

Countries citing papers authored by Jonathan Beck

Since Specialization
Citations

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

Fields of papers citing papers by Jonathan Beck

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jonathan Beck

This figure shows the co-authorship network connecting the top 25 collaborators of Jonathan Beck. A scholar is included among the top collaborators of Jonathan 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 Jonathan Beck. Jonathan Beck 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.
Wadsworth, Jonathan D. F., Gary Adamson, Susan Joiner, et al.. (2017). Methods for Molecular Diagnosis of Human Prion Disease. Methods in molecular biology. 1658. 311–346. 11 indexed citations
2.
Scahill, Rachael I., Gerard R. Ridgway, Jonathan W. Bartlett, et al.. (2013). Genetic Influences on Atrophy Patterns in Familial Alzheimer's Disease: A Comparison of APP and PSEN1 Mutations. Journal of Alzheimer s Disease. 35(1). 199–212. 30 indexed citations
3.
Sergouniotis, Panagiotis I., Alice E. Davidson, Donna S. Mackay, et al.. (2011). Biallelic Mutations in PLA2G5, Encoding Group V Phospholipase A2, Cause Benign Fleck Retina. The American Journal of Human Genetics. 89(6). 782–791. 34 indexed citations
4.
Rohrer, Jonathan D., Jason D. Warren, James Uphill, et al.. (2011). A novel exon 2 I27V VCP variant is associated with dissimilar clinical syndromes. Journal of Neurology. 258(8). 1494–1496. 24 indexed citations
5.
Edgeworth, Julie Ann, Michael Farmer, Jonathan Beck, et al.. (2011). Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay. The Lancet. 377(9764). 487–493. 134 indexed citations
6.
Lukić, Ana, Jonathan Beck, Susan Joiner, et al.. (2010). Heterozygosity at Polymorphic Codon 219 in Variant Creutzfeldt-Jakob Disease. Archives of Neurology. 67(8). 1021–3. 17 indexed citations
7.
Rohrer, Jonathan D., Gerard R. Ridgway, Sebastian J. Crutch, et al.. (2009). Progressive logopenic/phonological aphasia: Erosion of the language network. NeuroImage. 49(1). 984–993. 192 indexed citations
8.
Rohrer, Jonathan D., Jason D. Warren, Rohani Omar, et al.. (2008). Parietal Lobe Deficits in Frontotemporal Lobar Degeneration Caused by a Mutation in the Progranulin Gene. Archives of Neurology. 65(4). 506–506. 42 indexed citations
9.
Rohrer, Jonathan D., Jason D. Warren, Josephine Barnes, et al.. (2008). Mapping the progression of progranulin-associated frontotemporal lobar degeneration. Nature Clinical Practice Neurology. 4(8). 455–460. 34 indexed citations
10.
Wadsworth, Jonathan D. F., Caroline Powell, Jonathan Beck, et al.. (2008). Molecular Diagnosis of Human Prion Disease. Methods in molecular biology. 459. 197–227. 38 indexed citations
11.
Mead, Simon, Jerome Whitfield, Mark Poulter, et al.. (2008). Genetic susceptibility, evolution and the kuru epidemic. Philosophical Transactions of the Royal Society B Biological Sciences. 363(1510). 3741–3746. 29 indexed citations
12.
Mead, Simon, Susan Joiner, Melanie Desbruslais, et al.. (2007). Creutzfeldt-Jakob Disease, Prion Protein Gene Codon 129VV, and a Novel PrPSc Type in a Young British Woman. Archives of Neurology. 64(12). 1780–1780. 18 indexed citations
13.
Hill, Andrew F., Susan Joiner, Jonathan Beck, et al.. (2006). Distinct glycoform ratios of protease resistant prion protein associated with PRNP point mutations. Brain. 129(3). 676–685. 78 indexed citations
14.
Lloyd, Sarah E., Simon R. Thompson, Jonathan Beck, et al.. (2004). Identification and characterization of a novel mouse prion gene allele. Mammalian Genome. 15(5). 383–389. 22 indexed citations
15.
Mead, Simon, Michael P. H. Stumpf, Jerome Whitfield, et al.. (2003). Balancing Selection at the Prion Protein Gene Consistent with Prehistoric Kurulike Epidemics. Science. 300(5619). 640–643. 276 indexed citations
16.
Wadsworth, Jonathan D. F., Andrew F. Hill, Jonathan Beck, & John Collinge. (2003). Molecular and clinical classification of human prion disease. British Medical Bulletin. 66(1). 241–254. 92 indexed citations
17.
Jackson, Graham S., Jonathan Beck, Cristina Navarrete, et al.. (2001). HLA-DQ7 antigen and resistance to variant CJD. Nature. 414(6861). 269–270. 38 indexed citations
18.
Mead, Simon, Jonathan Beck, Andrew Dickinson, Elizabeth Fisher, & John Collinge. (2000). Examination of the human prion protein-like gene Doppel for genetic susceptibility to sporadic and variant Creutzfeldt–Jakob disease. Neuroscience Letters. 290(2). 117–120. 49 indexed citations
19.
Palmer, Mark S., Jonathan Beck, Tracy Campbell, et al.. (1999). Pathogenic presenilin 1 mutations (P436S & I143F) in early-onset Alzheimer's disease in the UK. Human Mutation. 13(3). 256–256. 16 indexed citations
20.
Katsanis, Nicholas, Jonathan Beck, & Elizabeth Fisher. (1997). Mapping of a novel SH3 domain protein and two proteins of unknown function to human chromosome 21. Human Genetics. 100(3-4). 477–480. 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by R. D. Rudelli Breakdown of academic impact, for papers by Mary T. Lucero Breakdown of academic impact, for papers by Anne E. Luebke Breakdown of academic impact, for papers by Azlina Ahmad‐Annuar Breakdown of academic impact, for papers by Ryosei Minoda Breakdown of academic impact, for papers by Shin‐ichi Kano Breakdown of academic impact, for papers by Patricia J. Fisher Breakdown of academic impact, for papers by Irene Corradini Breakdown of academic impact, for papers by Harold G. Marks Breakdown of academic impact, for papers by Hirohiko Hohjoh
Rankless by CCL
2026