Michael John Owen

1.8k total citations
27 papers, 485 citations indexed

About

Michael John Owen is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Michael John Owen has authored 27 papers receiving a total of 485 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Psychiatry and Mental health. Recurrent topics in Michael John Owen's work include Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers) and Attention Deficit Hyperactivity Disorder (3 papers). Michael John Owen is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (3 papers) and Attention Deficit Hyperactivity Disorder (3 papers). Michael John Owen collaborates with scholars based in United Kingdom, New Zealand and United States. Michael John Owen's co-authors include Peter McGuffin, Patrick G. Kehoe, Anita Thapar, Irving I. Gottesman, Peter S. Harper, Michael Krawczak, A. L. Jones, James Walters, Stanley Zammit and Michael O’Donovan and has published in prestigious journals such as Journal of Biological Chemistry, American Journal of Psychiatry and Biological Psychiatry.

In The Last Decade

Michael John Owen

26 papers receiving 475 citations

Peers

Michael John Owen
Elizabeth A. Lovejoy United Kingdom
T. Sander Germany
A.G. Cardno United Kingdom
N. Craddock United Kingdom
Liam Carroll United Kingdom
Roger Marchbanks United Kingdom
Elizabeth A. Lovejoy United Kingdom
Michael John Owen
Citations per year, relative to Michael John Owen Michael John Owen (= 1×) peers Elizabeth A. Lovejoy

Countries citing papers authored by Michael John Owen

Since Specialization
Citations

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

Fields of papers citing papers by Michael John Owen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael John Owen

This figure shows the co-authorship network connecting the top 25 collaborators of Michael John Owen. A scholar is included among the top collaborators of Michael John 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 Michael John Owen. Michael John 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.
Dennison, Charlotte, Joanna Martin, Lucy Riglin, et al.. (2025). Early Manifestations of Neurodevelopmental Copy Number Variants in Children: A Population-Based Investigation. Biological Psychiatry. 98(12). 924–933. 1 indexed citations
2.
Kendall, Kimberley, Elliott Rees, Matthew Bracher‐Smith, et al.. (2019). Association of Rare Copy Number Variants With Risk of Depression. JAMA Psychiatry. 76(8). 818–818. 69 indexed citations
3.
Kendall, Kimberley & Michael John Owen. (2015). Intellectual Disability and Psychiatric Comorbidity: Challenges and Clinical Issues. ORCA Online Research @Cardiff (Cardiff University). 3 indexed citations
4.
Niarchou, Maria, Stanley Zammit, James Walters, et al.. (2013). Defective Processing Speed and Nonclinical Psychotic Experiences in Children: Longitudinal Analyses in a Large Birth Cohort. American Journal of Psychiatry. 170(5). 550–557. 39 indexed citations
5.
Rees, Mark I., Kirsten Harvey, Hamish E. Ward, et al.. (2003). Isoform Heterogeneity of the Human Gephyrin Gene (GPHN), Binding Domains to the Glycine Receptor, and Mutation Analysis in Hyperekplexia. Journal of Biological Chemistry. 278(27). 24688–24696. 94 indexed citations
6.
Thapar, Anita, K. Langley, Lindsay Marshall, et al.. (2003). ADHD children with and without the dopamine D4 receptor 7-repeat allele: Evidence of differences in performance on neuropsychological tests. ORCA Online Research @Cardiff. 2 indexed citations
7.
Rees, Mark I., Kristin Baer, Hamish E. Ward, et al.. (2001). A missense mutation of human Gephyrin (GPHN) is associated with Hyperekplexia and transcript isoform analysis re-defines the genomic structure of GPHN. ORCA Online Research @Cardiff (Cardiff University). 1 indexed citations
8.
Thapar, Anita, Jane Holmes, Antony Payton, et al.. (2001). Evidence of association between DRD4 and ADHD with conduct disturbance. Behavior Genetics. 31(4). 470–471. 2 indexed citations
9.
McCarthy, Geraldine, Alastair G. Cardno, Lisa Jones, et al.. (2000). Investigating familiality of subtypes in schizophrenia. American Journal of Medical Genetics Part A. 96(4). 473–474. 1 indexed citations
10.
Payton, Antony, Joni Holmes, Jennifer H. Barrett, et al.. (2000). A family based candidate gene association study of Attention Deficit Hyperactivity Disorder. ORCA Online Research @Cardiff. 1 indexed citations
11.
Hill, LaBarron K., Michael J. Chorney, Karen Chorney, et al.. (1999). IGF2R and cognitive ability. Molecular Psychiatry. 4. 2 indexed citations
12.
Jones, Ian, Michael John Owen, & Nicholas Craddock. (1999). Further evidence of familial cosegregation of major affective disorder and Darier's disease. ORCA Online Research @Cardiff (Cardiff University). 4 indexed citations
13.
Thapar, Anita, Joni Holmes, R. Harrington, et al.. (1999). A quantitative trait loci study of attention deficit hyperactivity disorder. ORCA Online Research @Cardiff. 1 indexed citations
14.
Daly, Eileen, Hugo Critchley, Dene Robertson, et al.. (1999). An MRI and fMRI study on the effect of deletions on chromosome 22 on brain. ORCA Online Research @Cardiff (Cardiff University). 1 indexed citations
15.
Daniels, Judith K., Gillian Spurlock, Alastair G. Cardno, et al.. (1997). Linkage Study of Chromosome 6p in Sib-Pairs With Schizophrenia. American Journal of Medical Genetics. 74(3). 319–323. 14 indexed citations
16.
Thomas, N S, Katherine A. Davies, Tom R. Webb, et al.. (1997). Molecular genetic studies in familial Rett syndrome. ORCA Online Research @Cardiff (Cardiff University). 1 indexed citations
17.
Kehoe, Patrick G., Julie Williams, Simon Lovestone, Gordon Wilcock, & Michael John Owen. (1996). Presenilin-1 polymorphism and Alzheimer's disease. The UK Alzheimer's Disease Collaborative Group. Journal of Psychopharmacology. 347(9009). 1 indexed citations
18.
Craddock, Nicholas & Michael John Owen. (1996). Candidate gene association studies in psychiatric genetics: a SERTain future?. PubMed. 1(6). 434–6. 11 indexed citations
19.
McGuffin, Peter, et al.. (1994). Seminars in Psychiatric Genetics. ORCA Online Research @Cardiff. 89 indexed citations
20.
Owen, Michael John, E. Parfitt, Philip Asherson, et al.. (1991). Linkage studies of schizophrenia with markers of chromosome-11q. ORCA Online Research @Cardiff (Cardiff University). 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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