Theodore Morley

637 total citations
7 papers, 103 citations indexed

About

Theodore Morley is a scholar working on Genetics, Cancer Research and Molecular Biology. According to data from OpenAlex, Theodore Morley has authored 7 papers receiving a total of 103 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 2 papers in Cancer Research and 1 paper in Molecular Biology. Recurrent topics in Theodore Morley's work include Genomics and Rare Diseases (3 papers), Genetic Associations and Epidemiology (2 papers) and Cancer Genomics and Diagnostics (2 papers). Theodore Morley is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetic Associations and Epidemiology (2 papers) and Cancer Genomics and Diagnostics (2 papers). Theodore Morley collaborates with scholars based in United States and Canada. Theodore Morley's co-authors include Douglas M. Ruderfer, Donald Hucks, Annika Faucon, Nancy J. Cox, Péter Straub, Slavina B. Goleva, Jordan W. Smoller, Julia Sealock, Kritika Singh and Jessica Dennis and has published in prestigious journals such as Nature Medicine, Scientific Reports and Genetics in Medicine.

In The Last Decade

Theodore Morley

6 papers receiving 103 citations

Peers

Theodore Morley
Bradley Jermy United Kingdom
Elinor M Jones United Kingdom
Emilie M. Wigdor United States
Susan Love United States
Carly M. O’Donnell United States
Theodore Morley
Citations per year, relative to Theodore Morley Theodore Morley (= 1×) peers Anna Carreras

Countries citing papers authored by Theodore Morley

Since Specialization
Citations

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

Fields of papers citing papers by Theodore Morley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Theodore Morley

This figure shows the co-authorship network connecting the top 25 collaborators of Theodore Morley. A scholar is included among the top collaborators of Theodore Morley 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 Theodore Morley. Theodore Morley is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

7 of 7 papers shown
1.
Morley, Theodore, Hyunjoon Lee, Yu Zhou, et al.. (2024). Evaluating the impact of modeling choices on the performance of integrated genetic and clinical models. Genetics in Medicine. 27(4). 101353–101353.
2.
Lee, Hyunjoon, Karmel W. Choi, Siwei Zhang, et al.. (2024). Integrating Electronic Health Records and Polygenic Risk to Identify Genetically Unrelated Comorbidities of Schizophrenia That May Be Modifiable. Biological Psychiatry Global Open Science. 4(3). 100297–100297. 1 indexed citations
3.
Liao, Calwing, Mariana Moysés‐Oliveira, Xander Nuttle, et al.. (2023). Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies. Cell Genomics. 3(4). 100277–100277. 5 indexed citations
4.
Richter, Lucas, Theodore Morley, Gillian W. Hooker, et al.. (2022). Leveraging electronic health records to inform genetic counseling practice surrounding psychiatric disorders. Journal of Genetic Counseling. 31(4). 1008–1015. 2 indexed citations
5.
Bejan, Cosmin A., et al.. (2022). Improving ascertainment of suicidal ideation and suicide attempt with natural language processing. Scientific Reports. 12(1). 15146–15146. 17 indexed citations
6.
Morley, Theodore, Lide Han, Víctor M. Castro, et al.. (2021). Phenotypic signatures in clinical data enable systematic identification of patients for genetic testing. Nature Medicine. 27(6). 1097–1104. 19 indexed citations
7.
Dennis, Jessica, Julia Sealock, Péter Straub, et al.. (2021). Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Genome Medicine. 13(1). 6–6. 59 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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