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.
Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor
20101.1k citationsWilliam McLaren, Bethan Pritchard et al.Bioinformaticsprofile →
Countries citing papers authored by Bethan Pritchard
Since
Specialization
Citations
This map shows the geographic impact of Bethan Pritchard'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 Bethan Pritchard with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bethan Pritchard more than expected).
Fields of papers citing papers by Bethan Pritchard
This network shows the impact of papers produced by Bethan Pritchard. 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 Bethan Pritchard. The network helps show where Bethan Pritchard may publish in the future.
Co-authorship network of co-authors of Bethan Pritchard
This figure shows the co-authorship network connecting the top 25 collaborators of Bethan Pritchard.
A scholar is included among the top collaborators of Bethan Pritchard 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 Bethan Pritchard. Bethan Pritchard is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
All Works
5 of 5 papers shown
#
Work
Indexed citations
1
Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor breakdown →
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.