M J Owen

2.6k total citations
36 papers, 1.6k citations indexed

About

M J Owen is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, M J Owen has authored 36 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 14 papers in Molecular Biology and 7 papers in Psychiatry and Mental health. Recurrent topics in M J Owen's work include Genetics and Neurodevelopmental Disorders (9 papers), Genetic Associations and Epidemiology (8 papers) and Genetic and rare skin diseases. (4 papers). M J Owen is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Genetic Associations and Epidemiology (8 papers) and Genetic and rare skin diseases. (4 papers). M J Owen collaborates with scholars based in United Kingdom, Germany and United States. M J Owen's co-authors include Michael O’Donovan, Nick Craddock, Nigel Williams, Peter McGuffin, George Kirov, Philip Asherson, Nick Jacobsen, Julie Williams, Hywel Williams and David Collier and has published in prestigious journals such as The Lancet, Nucleic Acids Research and Human Molecular Genetics.

In The Last Decade

M J Owen

36 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M J Owen United Kingdom 21 837 641 378 303 244 36 1.6k
M. Trixler Hungary 21 777 0.9× 543 0.8× 451 1.2× 306 1.0× 269 1.1× 49 1.8k
Hugh Gurling United Kingdom 24 681 0.8× 531 0.8× 318 0.8× 251 0.8× 221 0.9× 64 1.6k
Hugh Gurling United Kingdom 26 1.0k 1.2× 834 1.3× 573 1.5× 417 1.4× 389 1.6× 58 2.1k
Virginia K. Lasseter United States 18 956 1.1× 827 1.3× 310 0.8× 305 1.0× 198 0.8× 23 1.7k
Kyra Kanyas Israel 23 672 0.8× 572 0.9× 442 1.2× 256 0.8× 150 0.6× 31 1.6k
Pablo V. Gejman United States 21 910 1.1× 684 1.1× 212 0.6× 353 1.2× 155 0.6× 30 1.6k
Ivan Nikolov United Kingdom 13 681 0.8× 520 0.8× 376 1.0× 214 0.7× 224 0.9× 21 1.3k
Ann E. Pulver United States 24 987 1.2× 663 1.0× 818 2.2× 258 0.9× 502 2.1× 36 2.6k
Detelina Grozeva United Kingdom 21 1.2k 1.4× 857 1.3× 575 1.5× 264 0.9× 305 1.3× 40 2.2k
Johannes L. Roos South Africa 19 1.4k 1.7× 1.2k 1.9× 235 0.6× 287 0.9× 329 1.3× 76 2.4k

Countries citing papers authored by M J Owen

Since Specialization
Citations

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

Fields of papers citing papers by M J Owen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M J Owen. 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 M J Owen. The network helps show where M J Owen may publish in the future.

Co-authorship network of co-authors of M J Owen

This figure shows the co-authorship network connecting the top 25 collaborators of M J Owen. A scholar is included among the top collaborators of M J Owen 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 M J Owen. M J Owen 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.
Cohen‐Woods, Sarah, Helen L. Fisher, Konstantinos Douroudis, et al.. (2017). Interaction between childhood maltreatment on immunogenetic risk in depression: Discovery and replication in clinical case-control samples. Brain Behavior and Immunity. 67. 203–210. 26 indexed citations
2.
Craddock, N., Detelina Grozeva, Ian Jones, et al.. (2009). Bipolar disorder risk allele at CACNA1C also confers risk to recurrent major depression and to schizophrenia. Bipolar Disorders. 11. 10–10. 6 indexed citations
3.
Williams, Hywel, M J Owen, & Michael O’Donovan. (2009). Schizophrenia genetics: new insights from new approaches. British Medical Bulletin. 91(1). 61–74. 56 indexed citations
4.
Kent, Lindsey, Ziarih Hawi, Aiveen Kirley, et al.. (2005). Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD. Molecular Psychiatry. 10(10). 939–943. 107 indexed citations
5.
O’Donovan, Michael, Nigel Williams, & M J Owen. (2003). Recent advances in the genetics of schizophrenia. Human Molecular Genetics. 12(suppl 2). R125–R133. 123 indexed citations
6.
Edwards, Deborah, P Burnard, M J Owen, et al.. (2003). A systematic review of the effectiveness of stress‐management interventions for mental health professionals. Journal of Psychiatric and Mental Health Nursing. 10(3). 370–371. 27 indexed citations
7.
West, Andrew, K. Langley, Marian L. Hamshere, et al.. (2002). Evidence to suggest biased phenotypes in children with Attention Deficit Hyperactivity Disorder from completely ascertained trios. Molecular Psychiatry. 7(9). 962–966. 19 indexed citations
8.
Saurin, Adrian T., Daniel J. Pennington, H. Raat, M J Owen, & Michael Marber. (2000). Ischemic preconditioning in isolated mouse hearts - An essential role for PKC-epsilon. Research Portal (King's College London). 102(18). 155–155. 1 indexed citations
9.
Bray, Nicholas J., Nigel Williams, Timothy Bowen, et al.. (2000). No evidence for association between a non-synonymous polymorphism in the gene encoding human metabotropic glutamate receptor 7 and schizophrenia. Psychiatric Genetics. 10(2). 83–86. 18 indexed citations
10.
Jacobsen, Nick, Gareth Elvidge, Ian Jones, et al.. (2000). Exclusion of the Darier's disease gene, ATP2A2, as a common susceptibility gene for bipolar disorder. Molecular Psychiatry. 6(1). 92–97. 37 indexed citations
11.
Owen, M J. (2000). Molecular genetic studies of schizophrenia. Brain Research Reviews. 31(2-3). 179–186. 20 indexed citations
12.
Williams, Nigel, Mark I. Rees, Peter Holmans, et al.. (1999). A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs. Human Molecular Genetics. 8(9). 1729–1739. 105 indexed citations
13.
Jacobsen, Nick, et al.. (1999). Mutational analysis of phospholipase A2A: a positional candidate susceptibility gene for bipolar disorder. Molecular Psychiatry. 4(3). 274–279. 22 indexed citations
14.
Murphy, Kevin, et al.. (1998). Chromosome 22qll deletions. The British Journal of Psychiatry. 172(2). 180–183. 50 indexed citations
15.
Bowen, Timothy, Nadine Norton, Nick Jacobsen, et al.. (1998). Linked polymorphisms upstream of exons 1 and 2 of the human cholecystokinin gene are not associated with schizophrenia or bipolar disorder. Molecular Psychiatry. 3(1). 67–71. 29 indexed citations
16.
Kunugi, Hiroshi, Homero Vallada, David Curtis, et al.. (1996). A transmission disequilibrium study on Catechol-O-Methyltransferase polymorphism in schizophrenia families. Schizophrenia Research. 18(2-3). 165–165. 1 indexed citations
17.
Daniels, Judith K., Julie Williams, Philip Asherson, Peter McGuffin, & M J Owen. (1995). No association between schizophrenia and polymorphisms within the genes for debrisoquine 4‐hydroxylase (CYP2D6) and the dopamine transporter (DAT). American Journal of Medical Genetics. 60(1). 85–87. 34 indexed citations
18.
Mant, R., Julie Williams, Philip Asherson, et al.. (1994). Relationship between homozygosity at the dopamine D3 receptor gene and schizophrenia. American Journal of Medical Genetics. 54(1). 21–26. 146 indexed citations
19.
Craddock, Nick & M J Owen. (1994). Is there an inverse relationship between Down's syndrome and bipolar affective disorder? Literature review and genetic implications. Journal of Intellectual Disability Research. 38(6). 613–620. 18 indexed citations
20.
Asherson, Philip, R. Mant, Christopher G. Taylor, et al.. (1993). Failure to find linkage between schizophrenia and genetic markers on chromosome 21. American Journal of Medical Genetics. 48(3). 161–165. 3 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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