Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies
if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the
same subfield and year (this is the minimum needed to enter the top 1%, not the average
within it), or reaches the top citation threshold in at least one of its specific research
topics.
Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples
1999513 citationsAndrew F. Hill, R J Butterworth et al.The Lancetprofile →
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late)
cites ·
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This map shows the geographic impact of PL Lantos'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 PL Lantos with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites PL Lantos more than expected).
This network shows the impact of papers produced by PL Lantos. 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 PL Lantos. The network helps show where PL Lantos may publish in the future.
Co-authorship network of co-authors of PL Lantos
This figure shows the co-authorship network connecting the top 25 collaborators of PL Lantos.
A scholar is included among the top collaborators of PL Lantos 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 PL Lantos. PL Lantos is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
All Works
10 of 10 papers shown
1.
Hill, Andrew F., R J Butterworth, Sarah Joiner, et al.. (1999). Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples. The Lancet. 353(9148). 183–189.513 indexed citations breakdown →
Collinge, John, Andrew F. Hill, Ian Gowland, et al.. (1997). Unaltered susceptibility to BSE in transgenic mice expressing human prion protein (vol 378, pg 779, 1995). UCL Discovery (University College London).5 indexed citations
4.
Budka, Herbert, Adriano Aguzzi, Paul Brown, et al.. (1996). Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). UCL Discovery (University College London).1 indexed citations
5.
Davies, Jamie A., et al.. (1993). The contemporary AIDS database and brain bank--lessons from the past.. PubMed. 39. 77–85.5 indexed citations
6.
Lantos, PL. (1992). Neuropathology of unusual dementias: an overview.. PubMed. 1(3). 485–516.7 indexed citations
7.
Lantos, PL, et al.. (1991). Distribution and fine structural analysis of undifferentiated cells in the primate subependymal layer.. PubMed. 178. 45–63.21 indexed citations
Lantos, PL, et al.. (1976). Malignant meningioma with liver metastases and hypoglycaemia. A case report.. PubMed. 35(4). 357–61.18 indexed citations
10.
Lantos, PL, et al.. (1976). The fine structure of blood vessels in ethylnitrosourea-induced tumours of the rat nervous system: with special reference to the breakdown of the blood-brain barrier.. PubMed. 57(4). 419–30.42 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.