This map shows the geographic impact of Bryan Mowry'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 Bryan Mowry with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bryan Mowry more than expected).
This network shows the impact of papers produced by Bryan Mowry. 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 Bryan Mowry. The network helps show where Bryan Mowry may publish in the future.
Co-authorship network of co-authors of Bryan Mowry
This figure shows the co-authorship network connecting the top 25 collaborators of Bryan Mowry.
A scholar is included among the top collaborators of Bryan Mowry 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 Bryan Mowry. Bryan Mowry is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
McLean, Duncan, et al.. (2009). Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis. Queensland's institutional digital repository (The University of Queensland).1 indexed citations
Mowry, Bryan, David Chant, & Janet W. McGrath. (2002). Assessing the co-segregation of disorders within pedigrees: a comparison of two methods. 9(1). 29–33.1 indexed citations
12.
Martínez, María, et al.. (2002). Linkage disequillbrium analysis of 6ql3-q26 schizophrenia candidate genes.. The American Journal of Human Genetics. 71(4). 473–473.1 indexed citations
13.
Saha, Sukanta, et al.. (2002). The presence of quasi-psychotic phenomena is associated with minor physical anomalies and craniofacial measures in well controls. Schizophrenia Research. 53(3). 232–233.4 indexed citations
14.
Cao, Quanquan, Jennifer M. Taylor, Anibal Cravchik, et al.. (2000). Genetic diversity of the human serotonin receptor 1B (HTR1B).. American Journal of Medical Genetics Part A. 96(4). 564–564.2 indexed citations
Mowry, Bryan. (1998). Structured interview for DSM-IV personality: SIDP-IV. Australian & New Zealand Journal of Psychiatry. 32(6). 896–897.496 indexed citations
19.
Mowry, Bryan. (1998). Psychopathology: the evolving science of mental disorder. Australian & New Zealand Journal of Psychiatry. 32(2). 315–316.3 indexed citations
20.
Mowry, Bryan, et al.. (1995). The Potential of Isonymy in Psychiatric Genetics. eCite Digital Repository (University of Tasmania).1 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.