Emma L. Meaburn

3.5k total citations
46 papers, 2.0k citations indexed

About

Emma L. Meaburn is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Emma L. Meaburn has authored 46 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 21 papers in Molecular Biology and 11 papers in Cognitive Neuroscience. Recurrent topics in Emma L. Meaburn's work include Genetics and Neurodevelopmental Disorders (20 papers), Genetic Associations and Epidemiology (19 papers) and Autism Spectrum Disorder Research (11 papers). Emma L. Meaburn is often cited by papers focused on Genetics and Neurodevelopmental Disorders (20 papers), Genetic Associations and Epidemiology (19 papers) and Autism Spectrum Disorder Research (11 papers). Emma L. Meaburn collaborates with scholars based in United Kingdom, United States and Australia. Emma L. Meaburn's co-authors include Robert Plomin, Leonard C. Schalkwyk, Jonathan Mill, Oliver S. P. Davis, Ian Craig, Claire M. A. Haworth, Thomas S. Price, Aaron R. Jeffries, Lee M Butcher and Angelica Ronald and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and Scientific Reports.

In The Last Decade

Emma L. Meaburn

46 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emma L. Meaburn United Kingdom 24 1.1k 862 318 266 249 46 2.0k
Lee M Butcher United Kingdom 26 992 0.9× 1.6k 1.8× 417 1.3× 145 0.5× 174 0.7× 37 2.6k
Vickie Pasterski United Kingdom 20 626 0.6× 1.3k 1.5× 221 0.7× 202 0.8× 124 0.5× 30 2.0k
P R Raggatt United Kingdom 15 585 0.5× 868 1.0× 394 1.2× 325 1.2× 198 0.8× 29 2.1k
W. David Hill United Kingdom 24 1.4k 1.3× 649 0.8× 268 0.8× 546 2.1× 281 1.1× 44 2.8k
Zachary Kaminsky United States 30 989 0.9× 2.1k 2.5× 229 0.7× 147 0.6× 541 2.2× 56 3.8k
Kate Lawrence United Kingdom 23 601 0.6× 256 0.3× 615 1.9× 213 0.8× 241 1.0× 52 1.8k
Anna A. E. Vinkhuyzen Australia 20 947 0.9× 233 0.3× 651 2.0× 312 1.2× 435 1.7× 29 2.3k
Carole Samango‐Sprouse United States 24 1.2k 1.1× 846 1.0× 322 1.0× 66 0.2× 99 0.4× 71 2.0k
Pamela Flodman United States 34 1.4k 1.3× 1.1k 1.3× 928 2.9× 187 0.7× 383 1.5× 70 3.7k
Richard Anney United Kingdom 30 1.2k 1.1× 877 1.0× 996 3.1× 259 1.0× 635 2.6× 69 3.1k

Countries citing papers authored by Emma L. Meaburn

Since Specialization
Citations

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

Fields of papers citing papers by Emma L. Meaburn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Emma L. Meaburn. 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 Emma L. Meaburn. The network helps show where Emma L. Meaburn may publish in the future.

Co-authorship network of co-authors of Emma L. Meaburn

This figure shows the co-authorship network connecting the top 25 collaborators of Emma L. Meaburn. A scholar is included among the top collaborators of Emma L. Meaburn 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 Emma L. Meaburn. Emma L. Meaburn 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.
Nyström, Pär, Teodora Gliga, Jannath Begum Ali, et al.. (2021). Development of the pupillary light reflex from 9 to 24 months: association with common autism spectrum disorder (ASD) genetic liability and 3‐year ASD diagnosis. Journal of Child Psychology and Psychiatry. 62(11). 1308–1319. 12 indexed citations
2.
Dumontheil, Iroise, et al.. (2021). Evidence for specificity of polygenic contributions to attainment in English, maths and science during adolescence. Scientific Reports. 11(1). 3851–3851. 7 indexed citations
3.
Jones, Emily J. H., Chloe C. Y. Wong, Emma L. Meaburn, et al.. (2020). Leveraging epigenetics to examine differences in developmental trajectories of social attention: A proof-of-principle study of DNA methylation in infants with older siblings with autism. Infant Behavior and Development. 60. 101409–101409. 11 indexed citations
4.
Saffari, Ayden, Angelica Ronald, Chloe C. Y. Wong, et al.. (2019). RNA sequencing of identical twins discordant for autism reveals blood-based signatures implicating immune and transcriptional dysregulation. Molecular Autism. 10(1). 38–38. 18 indexed citations
5.
Meaburn, Emma L., et al.. (2018). The specificity of associations between cognition and attainment in English, maths and science during adolescence. Learning and Individual Differences. 69. 84–93. 16 indexed citations
6.
Thomas, Michael S. C., Yulia Kovas, Emma L. Meaburn, & Andrew Tolmie. (2015). What Can the Study of Genetics Offer to Educators?. Mind Brain and Education. 9(2). 72–80. 13 indexed citations
7.
Kovas, Yulia, et al.. (2015). What can the study of genetics offer to educators? Mind, Brain, and Education. Research Online (Goldsmiths University of London). 2 indexed citations
8.
Harlaar, Nicole, Emma L. Meaburn, Marianna E. Hayiou‐Thomas, et al.. (2014). Genome-Wide Association Study of Receptive Language Ability of 12-Year-Olds. Journal of Speech Language and Hearing Research. 57(1). 96–105. 18 indexed citations
9.
Trzaskowski, Maciej, Thalia C. Eley, Oliver S. P. Davis, et al.. (2013). First Genome-Wide Association Study on Anxiety-Related Behaviours in Childhood. PLoS ONE. 8(4). e58676–e58676. 45 indexed citations
10.
Plomin, Robert, Claire M. A. Haworth, Emma L. Meaburn, Thomas S. Price, & Oliver S. P. Davis. (2013). Common DNA Markers Can Account for More Than Half of the Genetic Influence on Cognitive Abilities. Psychological Science. 24(4). 562–568. 86 indexed citations
11.
Trzaskowski, Maciej, Thalia C. Eley, Oliver S. P. Davis, et al.. (2013). Correction: First Genome-Wide Association Study on Anxiety-Related Behaviours in Childhood. PLoS ONE. 8(6). 6 indexed citations
12.
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
13.
Davies, Matthew N, Emma L. Meaburn, & Leonard C. Schalkwyk. (2010). Gene set enrichment; a problem of pathways. Briefings in Functional Genomics. 9(5-6). 385–390. 5 indexed citations
14.
Docherty, Sophia, Oliver S. P. Davis, Yulia Kovas, et al.. (2009). A genome‐wide association study identifies multiple loci associated with mathematics ability and disability. Genes Brain & Behavior. 9(2). 234–247. 71 indexed citations
15.
Haworth, Claire M. A., Susan Carnell, Emma L. Meaburn, et al.. (2008). Increasing Heritability of BMI and Stronger Associations With the FTO Gene Over Childhood. Obesity. 16(12). 2663–2668. 132 indexed citations
16.
Haworth, Claire M. A., Emma L. Meaburn, Nicole Harlaar, & Robert Plomin. (2007). Reading and Generalist Genes. Mind Brain and Education. 1(4). 173–180. 21 indexed citations
17.
Meaburn, Emma L., Nicole Harlaar, Ian Craig, Leonard C. Schalkwyk, & Robert Plomin. (2007). Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children. Molecular Psychiatry. 13(7). 729–740. 79 indexed citations
18.
Butcher, Lee M, Emma L. Meaburn, Lin Liu, et al.. (2004). Genotyping Pooled DNA on Microarrays: A Systematic Genome Screen of Thousands of SNPs in Large Samples to Detect QTLs for Complex Traits. Behavior Genetics. 34(5). 549–555. 78 indexed citations
19.
Butcher, Lee M, Emma L. Meaburn, Linzy Hill, Robert Plomin, & Leonard C. Schalkwyk. (2002). How many non-synonymous SNPS are available on public databases?. American Journal of Medical Genetics Part A. 114(7). 1 indexed citations
20.
Meaburn, Emma L., Philip S. Dale, Ian Craig, & Robert Plomin. (2002). Language-impaired children: No sign of the FOXP2 mutation. Neuroreport. 13(8). 1075–1077. 47 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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