Matthew Bishop

2.9k total citations
49 papers, 1.8k citations indexed

About

Matthew Bishop is a scholar working on Molecular Biology, Neurology and Nutrition and Dietetics. According to data from OpenAlex, Matthew Bishop has authored 49 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 9 papers in Neurology and 6 papers in Nutrition and Dietetics. Recurrent topics in Matthew Bishop's work include Prion Diseases and Protein Misfolding (27 papers), Neurological diseases and metabolism (9 papers) and Trace Elements in Health (6 papers). Matthew Bishop is often cited by papers focused on Prion Diseases and Protein Misfolding (27 papers), Neurological diseases and metabolism (9 papers) and Trace Elements in Health (6 papers). Matthew Bishop collaborates with scholars based in United Kingdom, United States and China. Matthew Bishop's co-authors include Frank E. Karasz, Kenneth H. Langley, Robert Will, Jean Manson, Paul S. Russo, James W. Ironside, Xigao Jin, Thomas Sayers Ellis, Diane Ritchie and Linda McCardle and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Physical Review Letters.

In The Last Decade

Matthew Bishop

47 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matthew Bishop United Kingdom 20 959 452 341 253 232 49 1.8k
Chenyang Wei China 22 241 0.3× 79 0.2× 389 1.1× 814 3.2× 85 0.4× 52 1.8k
Mengmeng Feng China 21 269 0.3× 29 0.1× 269 0.8× 166 0.7× 93 0.4× 79 1.4k
Yutong Guo China 18 177 0.2× 35 0.1× 151 0.4× 694 2.7× 172 0.7× 62 1.3k
Yang Wei Taiwan 20 347 0.4× 14 0.0× 213 0.6× 222 0.9× 61 0.3× 56 1.2k
Hiroto Kudo Japan 26 288 0.3× 20 0.0× 512 1.5× 388 1.5× 565 2.4× 137 1.9k
Olivier Frey Switzerland 25 482 0.5× 27 0.1× 444 1.3× 1.7k 6.6× 51 0.2× 66 2.5k
Shuning Liu China 19 171 0.2× 26 0.1× 267 0.8× 360 1.4× 173 0.7× 59 1.3k
Suqin Chen China 16 127 0.1× 37 0.1× 300 0.9× 59 0.2× 89 0.4× 44 818
Taegyu Kang South Korea 17 522 0.5× 26 0.1× 590 1.7× 1.4k 5.6× 341 1.5× 39 2.6k
Shinichiro Mori Japan 20 253 0.3× 23 0.1× 510 1.5× 25 0.1× 87 0.4× 63 1.3k

Countries citing papers authored by Matthew Bishop

Since Specialization
Citations

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

Fields of papers citing papers by Matthew Bishop

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthew Bishop

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew Bishop. A scholar is included among the top collaborators of Matthew Bishop 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 Bishop. Matthew Bishop 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.
Bishop, Matthew, et al.. (2019). Mechanical Characterization of Thermally Annealed Tablets Containing Polyethylene Oxide for Abuse Deterrence. AAPS PharmSciTech. 21(1). 2–2. 4 indexed citations
2.
Tomatis, Marco, Honghui Xu, Chaohui Wei, et al.. (2018). A Comparative Study of Mn/Co Binary Metal Catalysts Supported on Two Commercial Diatomaceous Earths for Oxidation of Benzene. Catalysts. 8(3). 111–111. 6 indexed citations
4.
Bishop, Matthew, Abigail B. Diack, Diane Ritchie, et al.. (2013). Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt–Jakob disease. Brain. 136(4). 1139–1145. 43 indexed citations
5.
Bishop, Matthew, Pascual Sánchez‐Juan, & Richard Knight. (2013). Splice site SNPs of phospholipase PLCXD3 are significantly associated with variant and sporadic Creutzfeldt-Jakob disease. BMC Medical Genetics. 14(1). 91–91. 9 indexed citations
6.
Head, Mark, Helen Yull, Diane Ritchie, et al.. (2012). Comparison of two different protocols for the detection of PrPres type 1 and 2 co-occurrence in sporadic CJD. Prion. 6. 129–130. 1 indexed citations
7.
Jansen, Casper, Piero Parchi, Sabina Capellari, et al.. (2012). Human Prion Diseases in The Netherlands (1998–2009): Clinical, Genetic and Molecular Aspects. PLoS ONE. 7(4). e36333–e36333. 40 indexed citations
8.
Moda, Fabio, Silvia Suardi, Giuseppe Di Fede, et al.. (2012). MM2‐Thalamic Creutzfeldt–Jakob Disease: Neuropathological, Biochemical and Transmission Studies Identify a Distinctive Prion Strain. Brain Pathology. 22(5). 662–669. 54 indexed citations
9.
Head, Mark, Helen Yull, Diane Ritchie, et al.. (2012). Variably protease sensitive prionopathy in the United Kingdom. Clinical Neuropathology. 31(4). 272–273. 1 indexed citations
10.
Sánchez‐Juan, Pascual, Matthew Bishop, Esther A. Croes, et al.. (2011). A polymorphism in the regulatory region of PRNPis associated with increased risk of sporadic Creutzfeldt-Jakob disease. BMC Medical Genetics. 12(1). 73–73. 14 indexed citations
11.
Sánchez‐Juan, Pascual, Matthew Bishop, Yurii S. Aulchenko, et al.. (2011). Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk. Neurobiology of Aging. 33(7). 1487.e21–1487.e28. 38 indexed citations
12.
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
13.
Bishop, Matthew, et al.. (2010). Variant CJD strain remains stable after secondary transmission. Prion. 4(3). 2 indexed citations
14.
Pells, Steve, Enrico Cancellotti, Matthew Bishop, et al.. (2010). Human embryonic stem cells rapidly take up and then clear exogenous human and animal prions in vitro. The Journal of Pathology. 223(5). 635–645. 10 indexed citations
15.
Peden, Alexander, M. G. K. Jones, Helen Yull, et al.. (2008). Human platelets as a substrate source for the in vitro amplification of the abnormal prion protein (PrPSc) associated with variant Creutzfeldt-Jakob disease. Prion.
16.
Bishop, Matthew, Diane Ritchie, Robert Will, et al.. (2008). No Major Change in vCJD Agent Strain after Secondary Transmission via Blood Transfusion. PLoS ONE. 3(8). e2878–e2878. 12 indexed citations
17.
Bishop, Matthew, Gábor G. Kovács, Pascual Sánchez‐Juan, & Richard Knight. (2008). Cathepsin D SNP associated with increased risk of variant Creutzfeldt-Jakob disease. BMC Medical Genetics. 9(1). 31–31. 18 indexed citations
18.
Sánchez‐Juan, Pascual, Matthew Bishop, Alison Green, et al.. (2007). No evidence for association between taugene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease. BMC Medical Genetics. 8(1). 77–77. 10 indexed citations
19.
Cancellotti, Enrico, Rona Barron, Matthew Bishop, et al.. (2006). The role of host PrP in Transmissible Spongiform Encephalopathies. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1772(6). 673–680. 22 indexed citations
20.
Head, Mark, Diane Ritchie, William H. Nailon, et al.. (2004). Peripheral Tissue Involvement in Sporadic, Iatrogenic, and Variant Creutzfeldt-Jakob Disease. American Journal Of Pathology. 164(1). 143–153. 133 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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