Mike Owen

10.6k total citations
76 papers, 3.4k citations indexed

About

Mike Owen is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Mike Owen has authored 76 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 23 papers in Molecular Biology and 13 papers in Psychiatry and Mental health. Recurrent topics in Mike Owen's work include Genetic Associations and Epidemiology (16 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Bipolar Disorder and Treatment (9 papers). Mike Owen is often cited by papers focused on Genetic Associations and Epidemiology (16 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Bipolar Disorder and Treatment (9 papers). Mike Owen collaborates with scholars based in United Kingdom, United States and Ireland. Mike Owen's co-authors include Peter McGuffin, Adrian Hayday, Nick Craddock, Michael O’Donovan, N. Craddock, Assen Jablensky, L Dianda, Nicholas A. Wright, AM Hanby and A. Sebesteny and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Mike Owen

76 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mike Owen United Kingdom 31 1.3k 1.1k 642 575 366 76 3.4k
Sang Hyuck Lee United States 31 568 0.4× 1.4k 1.3× 227 0.4× 499 0.9× 444 1.2× 97 4.4k
Anjali K. Henders Australia 35 3.3k 2.6× 1.8k 1.7× 359 0.6× 364 0.6× 258 0.7× 83 6.5k
Vivien J. Bubb United Kingdom 27 918 0.7× 1.6k 1.5× 256 0.4× 396 0.7× 510 1.4× 84 3.5k
Nicolás Ramoz France 31 765 0.6× 692 0.6× 538 0.8× 161 0.3× 461 1.3× 115 3.0k
Michio Takahashi Japan 34 532 0.4× 1.4k 1.2× 184 0.3× 707 1.2× 204 0.6× 222 4.6k
Josué Feingold France 34 791 0.6× 1.3k 1.2× 408 0.6× 227 0.4× 592 1.6× 89 3.8k
Joseph A. Majzoub United States 48 515 0.4× 1.1k 1.0× 101 0.2× 523 0.9× 475 1.3× 132 6.6k
Kyoko Watanabe Netherlands 16 1.9k 1.5× 1.3k 1.2× 333 0.5× 194 0.3× 159 0.4× 34 3.9k
Ignacio Camacho‐Arroyo Mexico 37 1.3k 1.0× 1.2k 1.1× 150 0.2× 710 1.2× 424 1.2× 205 4.6k
Saffron A.G. Willis‐Owen United Kingdom 27 509 0.4× 883 0.8× 127 0.2× 336 0.6× 316 0.9× 42 3.0k

Countries citing papers authored by Mike Owen

Since Specialization
Citations

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

Fields of papers citing papers by Mike Owen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mike Owen

This figure shows the co-authorship network connecting the top 25 collaborators of Mike Owen. A scholar is included among the top collaborators of Mike 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 Mike Owen. Mike 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
2.
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
3.
Samaan, Zainab, Anne Farmer, Nick Craddock, et al.. (2009). Migraine in recurrent depression: case–control study. The British Journal of Psychiatry. 194(4). 350–354. 39 indexed citations
4.
Jones, Ian, Marian L. Hamshere, Phillip R. Bennett, et al.. (2007). Bipolar Affective Puerperal Psychosis: Genome-Wide Significant Evidence for Linkage to Chromosome 16. American Journal of Psychiatry. 164(7). 1099–1104. 48 indexed citations
5.
Moskvina, Valentina, Anne Farmer, Cerisse Gunasinghe, et al.. (2006). Interrelationship of childhood trauma, neuroticism, and depressive phenotype. Depression and Anxiety. 24(3). 163–168. 40 indexed citations
6.
Harold, Denise, Silvia Paracchini, Thomas Scerri, et al.. (2006). Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Molecular Psychiatry. 11(12). 1085–1091. 127 indexed citations
7.
Dimitrova, A., et al.. (2004). Association study of myo-inositol monophosphatase 2 (IMPA2) polymorphisms with bipolar affective disorder and response to lithium treatment. The Pharmacogenomics Journal. 5(1). 35–41. 23 indexed citations
8.
Farmer, Anne, Gerome Breen, Shyama Brewster, et al.. (2004). The Depression Network (DeNT) Study: methodology and sociodemographic characteristics of the first 470 affected sibling pairs from a large multi-site linkage genetic study. BMC Psychiatry. 4(1). 42–42. 30 indexed citations
9.
Daly, Eileen, Dale N. Robertson, Jayne Henry, et al.. (2002). Brain anatomy in psychotic and non-psychotic adults with chromosome 22q11 deletion. Schizophrenia Research. 53(3). 76–76. 1 indexed citations
10.
Harold, Denise, T Peirce, Marian L. Hamshere, et al.. (2002). No association of polymorphisms in the chat locus with late-onset Alzheimer's disease. Neurobiology of Aging. 23(1). 1 indexed citations
11.
Austin, Jehannine, Paul R. Buckland, A.G. Cardno, et al.. (2000). The high affinity neurotensin receptor gene (NTSR1): comparative sequencing and association studies in schizophrenia. Molecular Psychiatry. 5(5). 552–557. 22 indexed citations
12.
Jones, Lisa, Alastair G. Cardno, Kieran C. Murphy, et al.. (2000). The Kings Schizotypy Questionnaire as a quantitative measure of schizophrenia liability. Schizophrenia Research. 45(3). 213–221. 16 indexed citations
13.
Rees, Mark I., T. Lewis, Geert Mortier, et al.. (2000). A transient hyperekplexia phenotype associated with compound heterozygote mutations in the human beta-subunit of the inhibitory glycine receptor (GLRB). ORCA Online Research @Cardiff (Cardiff University). 2 indexed citations
14.
Wright, Pádraig, Elisabeth Dawson, Peter T. Donaldson, et al.. (1998). A transmission/disequilibrium study of the DRB1*04 gene locus on chromosome 6p21.3 with schizophrenia. Schizophrenia Research. 32(2). 75–80. 21 indexed citations
15.
Peng, Stanford L., Jennifer M. McNiff, Michael P. Madaio, et al.. (1997). alpha beta T cell regulation and CD40 ligand dependence in murine systemic autoimmunity. The Journal of Immunology. 158(5). 2464–2470. 57 indexed citations
16.
Peng, Stanford L., Michael P. Madaio, David Hughes, et al.. (1996). Murine lupus in the absence of αβ T cells. The Journal of Immunology. 156(10). 4041–4049. 125 indexed citations
17.
Bayer, Antony, et al.. (1995). No evidence that common allelic variation in the Amyloid Precursor Protein (APP) gene confers susceptibility to Alzheimer's disease. Human Molecular Genetics. 4(5). 853–858. 18 indexed citations
18.
Craddock, Nick & Mike Owen. (1994). Chromosomal Aberrations and Bipolar Affective Disorder. The British Journal of Psychiatry. 164(4). 507–512. 37 indexed citations
19.
Craddock, Nick, Ian Brockington, R. Mant, et al.. (1994). Bipolar Affective Puerperal Psychosis Associated with Consanguinity. The British Journal of Psychiatry. 164(3). 359–364. 11 indexed citations
20.
Foerster, Alice, Shôn Lewis, Mike Owen, & Robin Murray. (1991). Low birth weight and a family history of schizophrenia predict poor premorbid functioning in psychosis. Schizophrenia Research. 5(1). 13–20. 81 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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