Robin N. Beaumont

12.3k total citations · 1 hit paper
57 papers, 2.0k citations indexed

About

Robin N. Beaumont is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Robin N. Beaumont has authored 57 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Genetics, 14 papers in Pediatrics, Perinatology and Child Health and 14 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Robin N. Beaumont's work include Genetic Associations and Epidemiology (22 papers), Birth, Development, and Health (13 papers) and Obesity, Physical Activity, Diet (12 papers). Robin N. Beaumont is often cited by papers focused on Genetic Associations and Epidemiology (22 papers), Birth, Development, and Health (13 papers) and Obesity, Physical Activity, Diet (12 papers). Robin N. Beaumont collaborates with scholars based in United Kingdom, United States and Australia. Robin N. Beaumont's co-authors include Andrew R. Wood, Jessica Tyrrell, Michael N. Weedon, Timothy M. Frayling, Samuel E. Jones, Rachel M. Freathy, Marcus A. Tuke, Hanieh Yaghootkar, Anna Murray and Katherine S. Ruth and has published in prestigious journals such as Nature Medicine, Nature Communications and Nature Genetics.

In The Last Decade

Robin N. Beaumont

55 papers receiving 2.0k citations

Hit Papers

Development and Standardization of an Improved Type 1 Dia... 2019 2026 2021 2023 2019 50 100 150 200

Peers

Robin N. Beaumont
Hanieh Yaghootkar United Kingdom
Rachel M. Freathy United Kingdom
Ilene Fennoy United States
Adam E. Locke United States
Rami Nassir United States
Sei Won Yang South Korea
Hyun Wook Chae South Korea
Hanieh Yaghootkar United Kingdom
Robin N. Beaumont
Citations per year, relative to Robin N. Beaumont Robin N. Beaumont (= 1×) peers Hanieh Yaghootkar

Countries citing papers authored by Robin N. Beaumont

Since Specialization
Citations

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

Fields of papers citing papers by Robin N. Beaumont

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robin N. Beaumont. 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 Robin N. Beaumont. The network helps show where Robin N. Beaumont may publish in the future.

Co-authorship network of co-authors of Robin N. Beaumont

This figure shows the co-authorship network connecting the top 25 collaborators of Robin N. Beaumont. A scholar is included among the top collaborators of Robin N. Beaumont 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 Robin N. Beaumont. Robin N. Beaumont 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.
Green, Harry, Ji Chen, Jonathan P Evans, et al.. (2024). Hyperglycaemia is a causal risk factor for upper limb pathologies. International Journal of Epidemiology. 53(1). 2 indexed citations
2.
Beaumont, Robin N., et al.. (2024). Genetic modifiers of rare variants in monogenic developmental disorder loci. Nature Genetics. 56(5). 861–868. 11 indexed citations
4.
Vedantam, Sailaja, Eirini Marouli, Robin N. Beaumont, et al.. (2023). Identification and analysis of individuals who deviate from their genetically-predicted phenotype. PLoS Genetics. 19(9). e1010934–e1010934. 4 indexed citations
5.
Bowden, Jack, Beverly M. Shields, Debbie A. Lawlor, et al.. (2022). Investigating a possible causal relationship between maternal serum urate concentrations and offspring birthweight: a Mendelian randomization study. International Journal of Epidemiology. 52(1). 178–189. 5 indexed citations
6.
Weedon, Michael N., Samuel E. Jones, Jacqueline M. Lane, et al.. (2022). The impact of Mendelian sleep and circadian genetic variants in a population setting. PLoS Genetics. 18(9). e1010356–e1010356. 4 indexed citations
7.
Beaumont, Robin N., et al.. (2021). Common genetic variants with fetal effects on birth weight are enriched for proximity to genes implicated in rare developmental disorders. Human Molecular Genetics. 30(11). 1057–1066. 1 indexed citations
8.
Thompson, William, Robin N. Beaumont, Alan Kuang, et al.. (2021). Fetal alleles predisposing to metabolically favorable adiposity are associated with higher birth weight. Human Molecular Genetics. 31(11). 1762–1775. 3 indexed citations
9.
Casanova, Francesco, Samuel E. Jones, Saskia P. Hagenaars, et al.. (2021). Using Mendelian Randomisation methods to understand whether diurnal preference is causally related to mental health. Molecular Psychiatry. 26(11). 6305–6316. 26 indexed citations
10.
Thompson, William, Robin N. Beaumont, Alan Kuang, et al.. (2021). Higher maternal adiposity reduces offspring birthweight if associated with a metabolically favourable profile. Diabetologia. 64(12). 2790–2802. 7 indexed citations
11.
Moen, Gunn-Helen, Robin N. Beaumont, Niels Grarup, et al.. (2020). Investigating the causal effect of maternal vitamin B12 and folate levels on offspring birthweight. International Journal of Epidemiology. 50(1). 179–189. 6 indexed citations
12.
Sharp, Seth A., Samuel E. Jones, Michael N. Weedon, et al.. (2020). A single nucleotide polymorphism genetic risk score to aid diagnosis of coeliac disease: a pilot study in clinical care. Alimentary Pharmacology & Therapeutics. 52(7). 1165–1173. 14 indexed citations
13.
Beaumont, Robin N., Sarah J. Kotecha, Andrew R. Wood, et al.. (2020). Common maternal and fetal genetic variants show expected polygenic effects on risk of small- or large-for-gestational-age (SGA or LGA), except in the smallest 3% of babies. PLoS Genetics. 16(12). e1009191–e1009191. 13 indexed citations
14.
Schnurr, Theresia M., Camilla S. Morgen, Dmitrii Borisevich, et al.. (2020). The influence of transmitted and non-transmitted parental BMI-associated alleles on the risk of overweight in childhood. Scientific Reports. 10(1). 4806–4806. 15 indexed citations
15.
Howe, Laura D, Sean Harrison, Robin N. Beaumont, et al.. (2019). Effects of body mass index on relationship status, social contact and socio-economic position: Mendelian randomization and within-sibling study in UK Biobank. International Journal of Epidemiology. 49(4). 1173–1184. 37 indexed citations
16.
Thompson, William, Jessica Tyrrell, Maria Carolina Borges, et al.. (2019). Association of maternal circulating 25(OH)D and calcium with birth weight: A mendelian randomisation analysis. PLoS Medicine. 16(6). e1002828–e1002828. 32 indexed citations
17.
Green, Harry, Robin N. Beaumont, Amanda Thomas, et al.. (2019). Genome-Wide Association Study of Microscopic Colitis in the UK Biobank Confirms Immune-Related Pathogenesis. Journal of Crohn s and Colitis. 13(12). 1578–1582. 31 indexed citations
18.
Kwasniok, Frank, Robin N. Beaumont, & John Thuburn. (2019). Vortex dynamics of stratospheric sudden warmings: A reanalysis data study using PV contour integral diagnostics. Quarterly Journal of the Royal Meteorological Society. 145(720). 1013–1033. 2 indexed citations
19.
Hughes, Alice E., Michael Nodzenski, Robin N. Beaumont, et al.. (2018). Fetal Genotype and Maternal Glucose Have Independent and Additive Effects on Birth Weight. Diabetes. 67(5). 1024–1029. 33 indexed citations
20.
Pilling, Luke C., Janice L. Atkins, Michael O. Duff, et al.. (2017). Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers. PLoS ONE. 12(9). e0185083–e0185083. 55 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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