Jonathan Stephens

26.1k total citations · 2 hit papers
60 papers, 3.2k citations indexed

About

Jonathan Stephens is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, Jonathan Stephens has authored 60 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 16 papers in Molecular Biology and 11 papers in Hematology. Recurrent topics in Jonathan Stephens's work include Genetic Associations and Epidemiology (12 papers), Platelet Disorders and Treatments (8 papers) and Helicobacter pylori-related gastroenterology studies (7 papers). Jonathan Stephens is often cited by papers focused on Genetic Associations and Epidemiology (12 papers), Platelet Disorders and Treatments (8 papers) and Helicobacter pylori-related gastroenterology studies (7 papers). Jonathan Stephens collaborates with scholars based in United Kingdom, United States and Netherlands. Jonathan Stephens's co-authors include Richard Judson, Gualberto Ruaño, Krishnan Nandabalan, Stephen B. Liggett, Catharine B. Stack, Dennis W. McGraw, Kevin Arnold, Andreas Windemuth, Benjamin A. Salisbury and Willem H. Ouwehand and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Jonathan Stephens

60 papers receiving 3.1k 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.

Complex promoter and coding region β ₂ -adrenergic receptor haplotypes alter receptor expression and predict in vivo responsiveness

2000 745 citations Jonathan Stephens, Richard Judson et al. profile →
Leukemia-Associated Somatic Mutations Drive Distinct Patterns of Age-Related Clonal Hemopoiesis

2015 357 citations Thomas McKerrell, Naomi Park et al. Cell Reports profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jonathan Stephens United Kingdom	25	1.3k	829	569	367	344	60	3.2k
Noor Kalsheker United Kingdom	34	2.0k 1.6×	662 0.8×	504 0.9×	234 0.6×	833 2.4×	114	5.1k
Michael Hubank United Kingdom	39	3.0k 2.3×	559 0.7×	344 0.6×	395 1.1×	296 0.9×	128	5.2k
Marcus Dittrich Germany	33	1.8k 1.4×	450 0.5×	299 0.5×	301 0.8×	239 0.7×	103	3.7k
Claire Summers United Kingdom	7	1.1k 0.9×	369 0.4×	282 0.5×	202 0.6×	96 0.3×	12	2.6k
Tadashi Matsumoto Japan	29	1.1k 0.9×	553 0.7×	183 0.3×	163 0.4×	226 0.7×	211	3.3k
Kirk A. Rockett United Kingdom	43	1.1k 0.8×	555 0.7×	311 0.5×	337 0.9×	980 2.8×	130	5.7k
Bernard H. Brownstein United States	27	2.2k 1.7×	668 0.8×	129 0.2×	126 0.3×	220 0.6×	62	5.0k
Lesley Heptinstall United Kingdom	13	1.1k 0.9×	395 0.5×	318 0.6×	52 0.1×	364 1.1×	19	2.5k
Quanhu Sheng United States	40	2.6k 2.0×	462 0.6×	106 0.2×	227 0.6×	230 0.7×	147	4.3k
Maeve O’Sullivan United States	31	2.0k 1.5×	968 1.2×	109 0.2×	62 0.2×	220 0.6×	108	4.3k

Countries citing papers authored by Jonathan Stephens

Since Specialization

Citations

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

Fields of papers citing papers by Jonathan Stephens

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jonathan Stephens

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

All Works

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20 of 20 papers shown

Gilbert, Edmund, Michaël Merrigan, Seamus O’Reilly, et al.. (2023). The Newfoundland and Labrador mosaic founder population descends from an Irish and British diaspora from 300 years ago. Communications Biology. 6(1). 469–469. 2 indexed citations

Lane, William J., Nicholas Gleadall, Sunitha Vege, et al.. (2020). Multiple GYPB gene deletions associated with the U− phenotype in those of African ancestry. Transfusion. 60(6). 1294–1307. 10 indexed citations

Westbury, Sarah K., Claire S. Whyte, Jonathan Stephens, et al.. (2020). A new pedigree with thrombomodulin‐associated coagulopathy in which delayed fibrinolysis is partially attenuated by co‐inherited TAFI deficiency. Journal of Thrombosis and Haemostasis. 18(9). 2209–2214. 21 indexed citations

Soni, Sanooj, et al.. (2020). Surgical cancellation rates due to peri‐operative hypertension: implementation of multidisciplinary guidelines across primary and secondary care. Anaesthesia. 75(10). 1314–1320. 7 indexed citations

McKerrell, Thomas, Naomi Park, Thaidy Moreno-Rodriguez, et al.. (2015). Leukemia-Associated Somatic Mutations Drive Distinct Patterns of Age-Related Clonal Hemopoiesis. Cell Reports. 10(8). 1239–1245. 357 indexed citations breakdown →

Good, Richard, Rory Sheehan, H. Miller, et al.. (2014). Variation in thromboxane B2 concentrations in serum and plasma in patients taking regular aspirin before and after clopidogrel therapy. Platelets. 26(1). 17–24. 11 indexed citations

Paul, Dirk S., Cornelis A. Albers, Augusto Rendon, et al.. (2013). Maps of open chromatin highlight cell type–restricted patterns of regulatory sequence variation at hematological trait loci. Genome Research. 23(7). 1130–1141. 25 indexed citations

Iperen, Erik P.A. van, Suthesh Sivapalaratnam, S. Matthijs Boekholdt, et al.. (2013). Common genetic variants do not associate with CAD in familial hypercholesterolemia. European Journal of Human Genetics. 22(6). 809–813. 4 indexed citations

Albers, Cornelis A., Ana Cvejic, Rémi Favier, et al.. (2011). Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome. Nature Genetics. 43(8). 735–737. 160 indexed citations

10.

Walker, Adam, Nicholas Pugh, Stephen F. Garner, et al.. (2009). Single domain antibodies against the collagen signalling receptor glycoprotein VI are inhibitors of collagen induced thrombus formation. Platelets. 20(4). 268–276. 13 indexed citations

11.

Guthery, Stephen L., Benjamin A. Salisbury, Manish Pungliya, Jonathan Stephens, & Michael J. Bamshad. (2007). The Structure of Common Genetic Variation in United States Populations. The American Journal of Human Genetics. 81(6). 1221–1231. 38 indexed citations

12.

Jones, Chris I., Stephen F. Garner, Will Angenent, et al.. (2007). Mapping the platelet profile for functional genomic studies and demonstration of the effect size of the GP6 locus. Journal of Thrombosis and Haemostasis. 5(8). 1756–1765. 54 indexed citations

13.

Smethurst, Peter A., Christopher G. Knight, Marie O’Connor, et al.. (2006). Production of calmodulin-tagged proteins in Drosophila Schneider S2 cells: A novel system for antigen production and phage antibody isolation. Journal of Immunological Methods. 316(1-2). 75–83. 10 indexed citations

14.

Schneider, Julie A., Manish Pungliya, Julie Choi, et al.. (2003). DNA variability of human genes. Mechanisms of Ageing and Development. 124(1). 17–25. 39 indexed citations

15.

Salisbury, Benjamin A., et al.. (2003). SNP and haplotype variation in the human genome. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 526(1-2). 53–61. 125 indexed citations

16.

Judson, Richard, Benjamin A. Salisbury, Julie A. Schneider, Andreas Windemuth, & Jonathan Stephens. (2002). How Many SNPs Does a Genome-Wide Haplotype Map Require?. Pharmacogenomics. 3(3). 379–391. 71 indexed citations

17.

Judson, Richard, Jonathan Stephens, & Andreas Windemuth. (2000). Genotyping:The predictive power of haplotypes in clinical response. Pharmacogenomics. 1(1). 15–26. 112 indexed citations

18.

Stephens, Jonathan, et al.. (1998). Helicobacter pylori cagA status, vacA genotypes and ulcer disease. European Journal of Gastroenterology & Hepatology. 10(5). 381–384. 27 indexed citations

19.

Stephens, Jonathan, Audrey Larkins, Roger F.L. James, & B J Rathbone. (1996). Production of a monoclonal antibody against the 128 kDa (CagA) protein of Helicobacter pylori. Journal of Immunological Methods. 190(2). 163–169. 8 indexed citations

20.

Martin, John H. & Jonathan Stephens. (1955). The culture and use of sorghums for forage.. University of North Texas Digital Library (University of North Texas). 5 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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