Alexander Richards

25.0k total citations
36 papers, 1.3k citations indexed

About

Alexander Richards is a scholar working on Genetics, Psychiatry and Mental health and Molecular Biology. According to data from OpenAlex, Alexander Richards has authored 36 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 10 papers in Psychiatry and Mental health and 8 papers in Molecular Biology. Recurrent topics in Alexander Richards's work include Genetic Associations and Epidemiology (21 papers), Schizophrenia research and treatment (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Alexander Richards is often cited by papers focused on Genetic Associations and Epidemiology (21 papers), Schizophrenia research and treatment (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Alexander Richards collaborates with scholars based in United Kingdom, United States and Netherlands. Alexander Richards's co-authors include Michael O’Donovan, Michael J. Owen, James Walters, George Kirov, Elliott Rees, Steven A. McCarroll, Jennifer L. Moran, Sophie E. Legge, Kimberly D. Chambert and Lyudmila Georgieva and has published in prestigious journals such as Nature Communications, Biological Psychiatry and Human Molecular Genetics.

In The Last Decade

Alexander Richards

33 papers receiving 1.3k citations

Peers

Alexander Richards
Sophie E. Legge United Kingdom
Nicholas Craddock United Kingdom
Michael Escamilla United States
J. Loftus United Kingdom
Sridevi Kalidindi United Kingdom
Hugh Gurling United Kingdom
Kayla A. Chase United States
Sophie E. Legge United Kingdom
Alexander Richards
Citations per year, relative to Alexander Richards Alexander Richards (= 1×) peers Sophie E. Legge

Countries citing papers authored by Alexander Richards

Since Specialization
Citations

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

Fields of papers citing papers by Alexander Richards

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alexander Richards

This figure shows the co-authorship network connecting the top 25 collaborators of Alexander Richards. A scholar is included among the top collaborators of Alexander Richards 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 Alexander Richards. Alexander Richards 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.
Richards, Alexander, Nicholas E. Clifton, Darren Cameron, et al.. (2025). Effects of Shared and Nonshared Schizophrenia and Bipolar Disorder Alleles on Cognition and Educational Attainment in the UK Biobank. Biological Psychiatry Global Open Science. 5(6). 100601–100601.
2.
Richards, Alexander, Alastair G. Cardno, Gordon T. Harold, et al.. (2022). Genetic Liabilities Differentiating Bipolar Disorder, Schizophrenia, and Major Depressive Disorder, and Phenotypic Heterogeneity in Bipolar Disorder. JAMA Psychiatry. 79(10). 1032–1032. 20 indexed citations
3.
Paquin, Vincent, Lotta-Katrin Pries, Margreet ten Have, et al.. (2022). Age- and sex-specific associations between risk scores for schizophrenia and self-reported health in the general population. Social Psychiatry and Psychiatric Epidemiology. 58(1). 43–52. 2 indexed citations
4.
Montagnese, Marcella, Franziska Knolle, Joost Haarsma, et al.. (2020). Reinforcement learning as an intermediate phenotype in psychosis? Deficits sensitive to illness stage but not associated with polygenic risk of schizophrenia in the general population. Schizophrenia Research. 222. 389–396. 19 indexed citations
5.
Richards, Alexander, L. John Horwood, Joseph M. Boden, et al.. (2018). Associations between schizophrenia genetic risk, anxiety disorders and manic/hypomanic episode in a longitudinal population cohort study. The British Journal of Psychiatry. 214(2). 96–102. 11 indexed citations
6.
Quattrone, Diego, Pak C. Sham, Evangelos Vassos, et al.. (2018). 5.4 BIOLOGICAL AND EPIDEMIOLOGICAL EXAMINATION OF TRANSDIAGNOSTIC AND SPECIFIC SYMPTOM DIMENSIONS AT PSYCHOSIS ONSET: FINDINGS FROM THE EUGEI STUDY. Schizophrenia Bulletin. 44(suppl_1). S7–S7.
7.
Donohoe, Gary, Jimmie C. Holland, David Mothersill, et al.. (2018). Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation. Psychological Medicine. 48(10). 1608–1615. 28 indexed citations
8.
Mothersill, Omar, Kimberley Kendall, Bettina Konte, et al.. (2017). Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working Memory. Neuropsychopharmacology. 42(13). 2612–2622. 29 indexed citations
9.
Leonenko, Ganna, Alexander Richards, James Walters, et al.. (2017). Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 174(7). 724–731. 16 indexed citations
10.
Riglin, Lucy, Stephan Collishaw, Alexander Richards, et al.. (2017). The impact of schizophrenia and mood disorder risk alleles on emotional problems: investigating change from childhood to middle age. Psychological Medicine. 48(13). 2153–2158. 18 indexed citations
11.
Riglin, Lucy, Stephan Collishaw, Alexander Richards, et al.. (2016). Schizophrenia risk alleles and neurodevelopmental outcomes in childhood: a population-based cohort study. The Lancet Psychiatry. 4(1). 57–62. 96 indexed citations
12.
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
13.
Loohuis, Loes M. Olde, Jacob Vorstman, Anil P. S. Ori, et al.. (2015). Genome-wide burden of deleterious coding variants increased in schizophrenia. Nature Communications. 6(1). 7501–7501. 18 indexed citations
14.
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
15.
Rees, Elliott, James Walters, Lyudmila Georgieva, et al.. (2013). Analysis of copy number variations at 15 schizophrenia-associated loci. The British Journal of Psychiatry. 204(2). 108–114. 266 indexed citations
16.
Zammit, Stanley, Marian L. Hamshere, Sarah Dwyer, et al.. (2013). A Population-Based Study of Genetic Variation and Psychotic Experiences in Adolescents. Schizophrenia Bulletin. 40(6). 1254–1262. 61 indexed citations
17.
Knight, Deborah A., Hywel Williams, Sarah Dwyer, et al.. (2011). Analysis of neurogranin (NRGN) in schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(5). 532–535. 13 indexed citations
18.
Richards, Alexander, Lisa Jones, Valentina Moskvina, et al.. (2011). Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain. Molecular Psychiatry. 17(2). 193–201. 82 indexed citations
19.
Bray, Nicholas J., Peter Holmans, Marianne van den Bree, et al.. (2008). Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1. Human Molecular Genetics. 17(8). 1169–1174. 15 indexed citations
20.
Campbell, J. A., et al.. (1989). The Course of Tardive Dyskinesia in Patients on Long-Term Neuroleptics. The British Journal of Psychiatry. 154(4). 523–528. 49 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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