Karena Pryce

2.1k total citations · 1 hit paper
6 papers, 765 citations indexed

About

Karena Pryce is a scholar working on Genetics, Rheumatology and Immunology. According to data from OpenAlex, Karena Pryce has authored 6 papers receiving a total of 765 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Rheumatology and 2 papers in Immunology. Recurrent topics in Karena Pryce's work include Spondyloarthritis Studies and Treatments (3 papers), Liver Diseases and Immunity (2 papers) and Systemic Lupus Erythematosus Research (2 papers). Karena Pryce is often cited by papers focused on Spondyloarthritis Studies and Treatments (3 papers), Liver Diseases and Immunity (2 papers) and Systemic Lupus Erythematosus Research (2 papers). Karena Pryce collaborates with scholars based in Australia, United States and United Kingdom. Karena Pryce's co-authors include Matthew A. Brown, B P Wordsworth, J. D. Reveille, Philip C. Robinson, Manuel A. R. Ferreira, Patrick Danoy, Robert D. Inman, Johanna Hadler, Proton Rahman and Walter P. Maksymowych and has published in prestigious journals such as Nature Genetics, PLoS Genetics and Human Genetics.

In The Last Decade

Karena Pryce

6 papers receiving 756 citations

Hit Papers

align trajectories

What are hit papers?

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.

Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci

2013 627 citations Philip C. Robinson, Karena Pryce et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Karena Pryce Australia	5	506	391	208	169	147	6	765
Edward Flynn United Kingdom	17	363 0.7×	453 1.2×	231 1.1×	147 0.9×	143 1.0×	25	839
Rekha Parmar United Kingdom	12	416 0.8×	387 1.0×	105 0.5×	217 1.3×	45 0.3×	23	779
Animesh Singh United Kingdom	4	297 0.6×	800 2.0×	111 0.5×	89 0.5×	103 0.7×	7	1.1k
L Bradbury United Kingdom	9	432 0.9×	209 0.5×	113 0.5×	99 0.6×	128 0.9×	28	542
Ebun Omoyinmi United Kingdom	17	211 0.4×	498 1.3×	217 1.0×	530 3.1×	111 0.8×	45	961
Patrycja Hoffmann United States	11	239 0.5×	404 1.0×	110 0.5×	317 1.9×	65 0.4×	19	799
Chung‐E Tseng United States	13	505 1.0×	412 1.1×	52 0.3×	163 1.0×	131 0.9×	19	928
Nina Daha Netherlands	13	381 0.8×	249 0.6×	82 0.4×	141 0.8×	50 0.3×	22	699
Kazuro Yabuki Japan	16	385 0.8×	261 0.7×	181 0.9×	104 0.6×	39 0.3×	25	753
Xiangli Xiao United States	8	214 0.4×	171 0.4×	71 0.3×	164 1.0×	59 0.4×	11	503

Countries citing papers authored by Karena Pryce

Since Specialization

Citations

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

Fields of papers citing papers by Karena Pryce

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karena Pryce

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

All Works

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6 of 6 papers shown

1.

Danoy, Patrick, Karena Pryce, Johanna Hadler, et al.. (2015). Association of Variants at 1q32 and <em>STAT3</em> with Ankylosing Spondylitis Suggests Genetic Overlap with Crohn's Disease. Figshare. 82 indexed citations

2.

McInerney‐Leo, Aideen, Gareth Baynam, Craig F. Munns, et al.. (2014). The IFITM5 mutation c.-14C > T results in an elongated transcript expressed in human bone; and causes varying phenotypic severity of osteogenesis imperfecta type V. BMC Musculoskeletal Disorders. 15(1). 107–107. 20 indexed citations

3.

Robinson, Philip C., Karena Pryce, Manuel A. R. Ferreira, et al.. (2013). Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci. Nature Genetics. 45(7). 730–738. 627 indexed citations breakdown →

4.

Danoy, Patrick, Karena Pryce, Johanna Hadler, et al.. (2011). Correction: Association of Variants at 1q32 and STAT3 with Ankylosing Spondylitis Suggests Genetic Overlap with Crohn's Disease. PLoS Genetics. 7(2). 1 indexed citations

5.

Piret, Siân E., Patrick Danoy, Karin Dahan, et al.. (2010). Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21. Human Genetics. 129(1). 51–58. 21 indexed citations

6.

Danoy, Patrick, Karena Pryce, Johanna Hadler, et al.. (2010). Association of Variants at 1q32 and STAT3 with Ankylosing Spondylitis Suggests Genetic Overlap with Crohn's Disease. PLoS Genetics. 6(12). e1001195–e1001195. 14 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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