Elliott Rees

11.8k total citations
54 papers, 2.5k citations indexed

About

Elliott Rees is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Elliott Rees has authored 54 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Genetics, 20 papers in Molecular Biology and 5 papers in Psychiatry and Mental health. Recurrent topics in Elliott Rees's work include Genomic variations and chromosomal abnormalities (38 papers), Genomics and Rare Diseases (30 papers) and Genetic Associations and Epidemiology (26 papers). Elliott Rees is often cited by papers focused on Genomic variations and chromosomal abnormalities (38 papers), Genomics and Rare Diseases (30 papers) and Genetic Associations and Epidemiology (26 papers). Elliott Rees collaborates with scholars based in United Kingdom, United States and Netherlands. Elliott Rees's co-authors include Michael J. Owen, George Kirov, Michael O’Donovan, James Walters, Sophie E. Legge, Valentina Escott‐Price, Steven A. McCarroll, Jennifer L. Moran, Kimberley Kendall and Kimberly D. Chambert and has published in prestigious journals such as Nature Communications, Neuron and SHILAP Revista de lepidopterología.

In The Last Decade

Elliott Rees

54 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elliott Rees United Kingdom 27 1.6k 1.1k 443 424 216 54 2.5k
Detelina Grozeva United Kingdom 21 1.2k 0.7× 857 0.8× 305 0.7× 575 1.4× 264 1.2× 40 2.2k
Johannes L. Roos South Africa 19 1.4k 0.9× 1.2k 1.1× 329 0.7× 235 0.6× 287 1.3× 76 2.4k
Ann E. Pulver United States 24 987 0.6× 663 0.6× 502 1.1× 818 1.9× 258 1.2× 36 2.6k
Guiqing Cai United States 22 747 0.5× 717 0.7× 504 1.1× 221 0.5× 214 1.0× 37 1.9k
Sophie E. Legge United Kingdom 20 902 0.5× 469 0.4× 243 0.5× 552 1.3× 88 0.4× 52 1.6k
Hugh Gurling United Kingdom 26 1.0k 0.6× 834 0.8× 389 0.9× 573 1.4× 417 1.9× 58 2.1k
Alexey Shadrin Norway 24 984 0.6× 538 0.5× 267 0.6× 405 1.0× 68 0.3× 102 1.9k
Thomas W. Mühleisen Germany 21 472 0.3× 874 0.8× 323 0.7× 299 0.7× 190 0.9× 47 1.7k
Amy Deep‐Soboslay United States 24 660 0.4× 1.2k 1.1× 326 0.7× 256 0.6× 458 2.1× 42 2.2k
M. Trixler Hungary 21 777 0.5× 543 0.5× 269 0.6× 451 1.1× 306 1.4× 49 1.8k

Countries citing papers authored by Elliott Rees

Since Specialization
Citations

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

Fields of papers citing papers by Elliott Rees

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elliott Rees

This figure shows the co-authorship network connecting the top 25 collaborators of Elliott Rees. A scholar is included among the top collaborators of Elliott Rees 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 Elliott Rees. Elliott Rees 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.
Dennison, Charlotte, Sarah J. Lewis, Amy Davies, et al.. (2025). Copy number variants and their implications for developmental and behavioural problems in cleft lip and/or palate. Human Molecular Genetics. 34(18). 1563–1574. 1 indexed citations
2.
Holmans, Peter, Darren Cameron, Detelina Grozeva, et al.. (2025). Whole-exome sequencing analysis identifies risk genes for schizophrenia. Nature Communications. 16(1). 7102–7102. 2 indexed citations
3.
Holmans, Peter, et al.. (2024). Genetic Implication of Specific Glutamatergic Neurons of the Prefrontal Cortex in the Pathophysiology of Schizophrenia. SHILAP Revista de lepidopterología. 4(5). 100345–100345. 1 indexed citations
4.
Kappel, Djenifer B., Elliott Rees, John A. Jansen, et al.. (2024). Rare variants in pharmacogenes influence clozapine metabolism in individuals with schizophrenia. European Neuropsychopharmacology. 80. 47–54. 1 indexed citations
5.
D’Andrea, Daniel, Mark O. Collins, Elliott Rees, et al.. (2022). Transcriptional programs regulating neuronal differentiation are disrupted in DLG2 knockout human embryonic stem cells and enriched for schizophrenia and related disorders risk variants. Nature Communications. 13(1). 27–27. 13 indexed citations
6.
Rees, Elliott, Hugo Creeth, Hai‐Gwo Hwu, et al.. (2021). Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations. Nature Communications. 12(1). 5353–5353. 50 indexed citations
7.
Clifton, Nicholas E., Elliott Rees, Peter Holmans, et al.. (2020). Genetic association of FMRP targets with psychiatric disorders. Molecular Psychiatry. 26(7). 2977–2990. 20 indexed citations
8.
Martin, Joanna, Sharifah Shameem Agha, K. Langley, et al.. (2020). A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder. Translational Psychiatry. 10(1). 135–135. 16 indexed citations
9.
Rees, Elliott & Michael J. Owen. (2020). Translating insights from neuropsychiatric genetics and genomics for precision psychiatry. Genome Medicine. 12(1). 43–43. 52 indexed citations
10.
Kendall, Kimberley, Ann John, Sze Chim Lee, et al.. (2020). Impact of schizophrenia genetic liability on the association between schizophrenia and physical illness: data-linkage study. BJPsych Open. 6(6). e139–e139. 5 indexed citations
11.
Hall, Lynsey S., Oliver Pain, Antonio F. Pardiñas, et al.. (2019). A transcriptome-wide association study implicates specific pre- and post-synaptic abnormalities in schizophrenia. Human Molecular Genetics. 29(1). 159–167. 43 indexed citations
12.
Legge, Sophie E., Charlotte Dennison, Antonio F. Pardiñas, et al.. (2019). Clinical indicators of treatment-resistant psychosis. The British Journal of Psychiatry. 216(5). 259–266. 57 indexed citations
13.
Kendall, Kimberley, et al.. (2019). Schizophrenia-associated genomic copy number variants and subcortical brain volumes in the UK Biobank. Molecular Psychiatry. 25(4). 854–862. 44 indexed citations
14.
Crawford, Karen, Matthew Bracher‐Smith, David Owen, et al.. (2018). Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank. Journal of Medical Genetics. 56(3). 131–138. 88 indexed citations
15.
Owen, David, Kimberley Kendall, Elliott Rees, et al.. (2018). Effects of pathogenic CNVs on physical traits in participants of the UK Biobank. BMC Genomics. 19(1). 867–867. 39 indexed citations
16.
Clifton, Nicholas E., Andrew Pocklington, Birger Scholz, et al.. (2016). Schizophrenia copy number variants and associative learning. Molecular Psychiatry. 22(2). 178–182. 16 indexed citations
17.
Richards, Alexander, Ganna Leonenko, James Walters, et al.. (2016). Exome arrays capture polygenic rare variant contributions to schizophrenia. Human Molecular Genetics. 25(5). 1001–1007. 35 indexed citations
18.
Pocklington, Andrew, Elliott Rees, James Walters, et al.. (2015). Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia. Neuron. 86(5). 1203–1214. 126 indexed citations
19.
Georgieva, Lyudmila, Elliott Rees, Jennifer L. Moran, et al.. (2014). De novo CNVs in bipolar affective disorder and schizophrenia. Human Molecular Genetics. 23(24). 6677–6683. 56 indexed citations
20.
Kirov, George, Elliott Rees, James Walters, et al.. (2013). The Penetrance of Copy Number Variations for Schizophrenia and Developmental Delay. Biological Psychiatry. 75(5). 378–385. 235 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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