Aaron R. Jeffries

7.6k total citations
48 papers, 1.3k citations indexed

About

Aaron R. Jeffries is a scholar working on Molecular Biology, Genetics and Infectious Diseases. According to data from OpenAlex, Aaron R. Jeffries has authored 48 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 18 papers in Genetics and 4 papers in Infectious Diseases. Recurrent topics in Aaron R. Jeffries's work include Epigenetics and DNA Methylation (9 papers), Genetics and Neurodevelopmental Disorders (7 papers) and RNA Research and Splicing (7 papers). Aaron R. Jeffries is often cited by papers focused on Epigenetics and DNA Methylation (9 papers), Genetics and Neurodevelopmental Disorders (7 papers) and RNA Research and Splicing (7 papers). Aaron R. Jeffries collaborates with scholars based in United Kingdom, United States and Australia. Aaron R. Jeffries's co-authors include Jonathan Mill, Leonard C. Schalkwyk, Emma L. Meaburn, Robert Plomin, Jack Price, Emma Dempster, Nicholas J. Bray, Matthew N Davies, Rebecca G. Smith and Thomas S. Price and has published in prestigious journals such as Nature Communications, Blood and PLoS ONE.

In The Last Decade

Aaron R. Jeffries

45 papers receiving 1.3k citations

Peers

Aaron R. Jeffries
Noriyoshi Usui Japan
Alicia Guemez‐Gamboa United States
Hui Guo China
Sandrine Passemard France
Michael S. Breen United States
Ayyappan Anitha Japan
Julia K. Pinsonneault United States
Eric Strengman Netherlands
Laëtitia Davidovic France
Edmund C. Jenkins United States
Noriyoshi Usui Japan
Aaron R. Jeffries
Citations per year, relative to Aaron R. Jeffries Aaron R. Jeffries (= 1×) peers Noriyoshi Usui

Countries citing papers authored by Aaron R. Jeffries

Since Specialization
Citations

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

Fields of papers citing papers by Aaron R. Jeffries

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aaron R. Jeffries. 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 Aaron R. Jeffries. The network helps show where Aaron R. Jeffries may publish in the future.

Co-authorship network of co-authors of Aaron R. Jeffries

This figure shows the co-authorship network connecting the top 25 collaborators of Aaron R. Jeffries. A scholar is included among the top collaborators of Aaron R. Jeffries 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 Aaron R. Jeffries. Aaron R. Jeffries 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.
Łapińska, Urszula, Bing Zhang, Wanida Phetsang, et al.. (2025). Heterogeneous efflux pump expression underpins phenotypic resistance to antimicrobial peptides. eLife. 13. 1 indexed citations
2.
Leung, Szi Kay, Rosemary A. Bamford, Aaron R. Jeffries, et al.. (2024). Long-read transcript sequencing identifies differential isoform expression in the entorhinal cortex in a transgenic model of tau pathology. Nature Communications. 15(1). 6458–6458. 5 indexed citations
3.
Franco, Elisa De, Christine S. Flaxman, Sarah J. Richardson, et al.. (2024). Developmentally dynamic changes in DNA methylation in the human pancreas. BMC Genomics. 25(1). 553–553. 3 indexed citations
4.
Maloney, Daniel, Nicholas Evens, Jonathan Porter, et al.. (2023). Comparison of metagenomic and targeted methods for sequencing human pathogenic viruses from wastewater. mBio. 14(6). e0146823–e0146823. 26 indexed citations
5.
Bamford, Rosemary A., Szi Kay Leung, Aaron R. Jeffries, et al.. (2023). 59. ULTRA-DEEP LONG READ TRANSCRIPTOME SEQUENCING REVEALS DRAMATIC ISOFORM DIVERSITY ACROSS HUMAN CORTEX DEVELOPMENT: RELEVANCE FOR GENETIC STUDIES OF PSYCHIATRIC DISORDERS. European Neuropsychopharmacology. 75. S88–S88.
6.
O’Neill, Paul, Karen Moore, William Rowe, et al.. (2023). Optimised protocol for monitoring SARS-CoV-2 in wastewater using reverse complement PCR-based whole-genome sequencing. PLoS ONE. 18(4). e0284211–e0284211. 9 indexed citations
7.
Flynn, Robert J., Aaron R. Jeffries, Gemma Shireby, et al.. (2022). Evaluation of nanopore sequencing for epigenetic epidemiology: a comparison with DNA methylation microarrays. Human Molecular Genetics. 31(18). 3181–3190. 8 indexed citations
8.
Smith, Ashley, Jehangir Cama, Brandon M. Invergo, et al.. (2021). Persister Escherichia coli Cells Have a Lower Intracellular pH than Susceptible Cells but Maintain Their pH in Response to Antibiotic Treatment. mBio. 12(4). e0090921–e0090921. 58 indexed citations
9.
Leung, Szi Kay, Aaron R. Jeffries, Isabel Castanho, et al.. (2021). Full-length transcript sequencing of human and mouse cerebral cortex identifies widespread isoform diversity and alternative splicing. Cell Reports. 37(7). 110022–110022. 84 indexed citations
10.
Pishva, Ehsan, Muhammad Ali, Talitha L. Kerrigan, et al.. (2021). Characterization of DNA Methylomic Signatures in Induced Pluripotent Stem Cells During Neuronal Differentiation. Frontiers in Cell and Developmental Biology. 9. 647981–647981. 7 indexed citations
11.
Borsini, Alessandra, Doris Stangl, Aaron R. Jeffries, Carmine M. Pariante, & Sandrine Thuret. (2020). The role of omega-3 fatty acids in preventing glucocorticoid-induced reduction in human hippocampal neurogenesis and increase in apoptosis. Translational Psychiatry. 10(1). 219–219. 38 indexed citations
12.
Castanho, Isabel, Tracey K. Murray, Eilís Hannon, et al.. (2020). Transcriptional Signatures of Tau and Amyloid Neuropathology. Cell Reports. 30(6). 2040–2054.e5. 41 indexed citations
13.
Mizuno, Keiko, Aaron R. Jeffries, Ted Abel, & Karl-Peter Giese. (2020). Long-lasting transcription in hippocampal area CA1 after contextual fear conditioning. Neurobiology of Learning and Memory. 172. 107250–107250. 5 indexed citations
14.
Wong, Chloe C. Y., Emma L. Meaburn, Angelica Ronald, et al.. (2013). Methylomic analysis of monozygotic twins discordant for autism spectrum disorder and related behavioural traits. Molecular Psychiatry. 19(4). 495–503. 208 indexed citations
15.
Cocks, Graham, Sarah Curran, Priya Gami‐Patel, et al.. (2013). The utility of patient specific induced pluripotent stem cells for the modelling of Autistic Spectrum Disorders. Psychopharmacology. 231(6). 1079–1088. 33 indexed citations
16.
El–Akabawy, Gehan, et al.. (2011). Purmorphamine Increases DARPP-32 Differentiation in Human Striatal Neural Stem Cells Through the Hedgehog Pathway. Stem Cells and Development. 20(11). 1873–1887. 53 indexed citations
17.
Hill, Matthew, Aaron R. Jeffries, Richard Dobson, Jack Price, & Nicholas J. Bray. (2011). Knockdown of the psychosis susceptibility gene ZNF804A alters expression of genes involved in cell adhesion. Human Molecular Genetics. 21(5). 1018–1024. 78 indexed citations
18.
Schalkwyk, Leonard C., Emma L. Meaburn, Rebecca G. Smith, et al.. (2010). Allelic Skewing of DNA Methylation Is Widespread across the Genome. The American Journal of Human Genetics. 86(2). 196–212. 185 indexed citations
19.
Morgan, Sarah C., Shireena A. Yasin, Dafe Uwanogho, Aaron R. Jeffries, & Jack Price. (2009). Positional Specification in a Neural Stem Cell Line Involves Modulation of Musashi1 Expression. Stem Cells and Development. 19(4). 579–592. 2 indexed citations
20.
Jeffries, Aaron R., Sarah Curran, Frances Elmslie, et al.. (2005). Molecular and phenotypic characterization of ring chromosome 22. American Journal of Medical Genetics Part A. 137A(2). 139–147. 85 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Noriyoshi Usui Breakdown of academic impact, for papers by Alicia Guemez‐Gamboa Breakdown of academic impact, for papers by Hui Guo Breakdown of academic impact, for papers by Sandrine Passemard Breakdown of academic impact, for papers by Michael S. Breen Breakdown of academic impact, for papers by Ayyappan Anitha Breakdown of academic impact, for papers by Julia K. Pinsonneault Breakdown of academic impact, for papers by Eric Strengman Breakdown of academic impact, for papers by Laëtitia Davidovic Breakdown of academic impact, for papers by Edmund C. Jenkins
Rankless by CCL
2026