Archie Campbell

27.9k total citations · 2 hit papers
94 papers, 2.9k citations indexed

About

Archie Campbell is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Archie Campbell has authored 94 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 32 papers in Genetics and 20 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Archie Campbell's work include Epigenetics and DNA Methylation (31 papers), Genetic Associations and Epidemiology (28 papers) and Birth, Development, and Health (19 papers). Archie Campbell is often cited by papers focused on Epigenetics and DNA Methylation (31 papers), Genetic Associations and Epidemiology (28 papers) and Birth, Development, and Health (19 papers). Archie Campbell collaborates with scholars based in United Kingdom, United States and Australia. Archie Campbell's co-authors include David J. Porteous, Caroline Hayward, Andrew M. McIntosh, Ian J. Deary, Riccardo E. Marioni, Blair H. Smith, Sandosh Padmanabhan, Kathryn L. Evans, Mark J. Adams and Rosie M. Walker and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Circulation and Nature Communications.

In The Last Decade

Archie Campbell

93 papers receiving 2.9k 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.

Cardiac Troponin T and Troponin I in the General Population

2019 211 citations Paul Welsh, Caroline Hayward et al. profile →
Refining epigenetic prediction of chronological and biological age

2023 65 citations Elena Bernabeu, Daniel L. McCartney et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Archie Campbell United Kingdom	31	974	709	462	361	356	94	2.9k
Ravindranath Duggirala United States	36	1.2k 1.3×	1.4k 2.0×	388 0.8×	239 0.7×	529 1.5×	116	4.4k
Alexander Teumer Germany	31	625 0.6×	613 0.9×	236 0.5×	186 0.5×	313 0.9×	107	2.6k
Andrew Wong United Kingdom	33	1.2k 1.2×	862 1.2×	213 0.5×	683 1.9×	661 1.9×	114	3.9k
Lise Bathum Denmark	30	520 0.5×	577 0.8×	272 0.6×	347 1.0×	515 1.4×	72	2.6k
Felix R. Day United Kingdom	27	1.1k 1.1×	2.3k 3.2×	255 0.6×	484 1.3×	562 1.6×	58	4.6k
Ilja Demuth Germany	34	1.7k 1.7×	348 0.5×	190 0.4×	172 0.5×	859 2.4×	170	4.1k
Aladdin H. Shadyab United States	29	427 0.4×	324 0.5×	436 0.9×	278 0.8×	787 2.2×	283	3.2k
Bernet Kato United Kingdom	27	935 1.0×	401 0.6×	221 0.5×	184 0.5×	756 2.1×	49	2.9k
John R. B. Perry United Kingdom	30	1.4k 1.4×	2.6k 3.6×	266 0.6×	491 1.4×	542 1.5×	75	5.2k
Sara Hägg Sweden	33	1.3k 1.3×	507 0.7×	215 0.5×	458 1.3×	1.5k 4.3×	135	4.2k

Countries citing papers authored by Archie Campbell

Since Specialization

Citations

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

Fields of papers citing papers by Archie Campbell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Archie Campbell

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Belsky, Daniel W., Kejun Ying, Mahdi Moqri, et al.. (2025). An unbiased comparison of 14 epigenetic clocks in relation to 174 incident disease outcomes. Nature Communications. 16(1). 11164–11164.

Valo, Erkka, Anne Richmond, Stefan Mutter, et al.. (2025). Genome-wide characterization of 54 urinary metabolites reveals molecular impact of kidney function. Nature Communications. 16(1). 325–325. 1 indexed citations

Bernabeu, Elena, Paul Yousefi, Matthew Suderman, et al.. (2025). A blood- and brain-based EWAS of smoking. Nature Communications. 16(1). 3210–3210. 1 indexed citations

Mischak, Harald, Antonia Vlahou, Justyna Siwy, et al.. (2024). Multiple urinary peptides are associated with hypertension: a link to molecular pathophysiology. Journal of Hypertension. 42(8). 1331–1339. 2 indexed citations

Welsh, Paul, Dorien M. Kimenai, Anoop Shah, et al.. (2023). Multiple Cardiac Biomarkers to Improve Prediction of Cardiovascular Events: Findings from the Generation Scotland Scottish Family Health Study. Clinical Chemistry. 70(2). 403–413. 6 indexed citations

Sherwood, Kitty, Lynn Martin, Archie Campbell, et al.. (2023). Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair. Nature Communications. 14(1). 3636–3636. 7 indexed citations

Shen, Xueyi, Claire Green, Robert F. Hillary, et al.. (2023). Structural brain correlates of childhood trauma with replication across two large, independent community-based samples. European Psychiatry. 66(1). e19–e19. 9 indexed citations

Hillary, Robert F., Daniel L. McCartney, Allan F. McRae, et al.. (2022). Identification of influential probe types in epigenetic predictions of human traits: implications for microarray design. Clinical Epigenetics. 14(1). 100–100. 4 indexed citations

Shenkin, Susan D., Andrew M. McIntosh, Mark E. Bastin, et al.. (2021). Early life predictors of late life cerebral small vessel disease in four prospective cohort studies. Brain. 144(12). 3769–3778. 26 indexed citations

10.

Stevenson, Anna J., Danni A. Gadd, Robert F. Hillary, et al.. (2021). Creating and Validating a DNA Methylation-Based Proxy for Interleukin-6. The Journals of Gerontology Series A. 76(12). 2284–2292. 20 indexed citations

11.

Shen, Xueyi, Aleks Stolicyn, Laura de Nooij, et al.. (2021). Spectral clustering based on structural magnetic resonance imaging and its relationship with major depressive disorder and cognitive ability. European Journal of Neuroscience. 54(6). 6281–6303. 5 indexed citations

12.

Barbu, Miruna C., Mathew A. Harris, Xueyi Shen, et al.. (2021). Epigenome-wide association study of global cortical volumes in generation Scotland: Scottish family health study. Epigenetics. 17(10). 1143–1158. 3 indexed citations

13.

Amador, Carmen, Yanni Zeng, M. Barber, et al.. (2021). Genome-wide methylation data improves dissection of the effect of smoking on body mass index. PLoS Genetics. 17(9). e1009750–e1009750. 5 indexed citations

14.

Barbu, Miruna C., Archie Campbell, Carmen Amador, et al.. (2021). Methylome-wide association study of antidepressant use in Generation Scotland and the Netherlands Twin Register implicates the innate immune system. Molecular Psychiatry. 27(3). 1647–1657. 10 indexed citations

15.

Meng, Weihua, Cameron Harris, Maxim B. Freidin, et al.. (2020). A genome-wide association study finds genetic variants associated with neck or shoulder pain in UK Biobank. Human Molecular Genetics. 29(8). 1396–1404. 27 indexed citations

16.

Docherty, Anna R., Andrey A. Shabalin, Daniel E. Adkins, et al.. (2020). Molecular Genetic Risk for Psychosis Is Associated With Psychosis Risk Symptoms in a Population-Based UK Cohort: Findings From Generation Scotland. Schizophrenia Bulletin. 46(5). 1045–1052. 13 indexed citations

17.

McCartney, Daniel L., Rosie M. Walker, Robert F. Hillary, et al.. (2020). Birth weight associations with DNA methylation differences in an adult population. Epigenetics. 16(7). 783–796. 16 indexed citations

18.

Howard, David M., Lasse Folkersen, Jonathan R. I. Coleman, et al.. (2020). Genetic stratification of depression in UK Biobank. Translational Psychiatry. 10(1). 163–163. 17 indexed citations

19.

Thormann, Anja, Mihail Halachev, William McLaren, et al.. (2019). Flexible and scalable diagnostic filtering of genomic variants using G2P with Ensembl VEP. Nature Communications. 10(1). 2373–2373. 53 indexed citations

20.

Amador, Carmen, Charley Xia, Réka Nagy, et al.. (2017). Regional variation in health is predominantly driven by lifestyle rather than genetics. Nature Communications. 8(1). 801–801. 12 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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