Josh Willoughby
- Co-authors
- Kate ChandlerMeena BalasubramanianJonathan BergWayne LamDaniela T. PilzCharu DeshpandeKay MetcalfeSusan Tomkins
- Topics
- Genomics and Rare Diseases (6 papers)Genetics and Neurodevelopmental Disorders (4 papers)Genomic variations and chromosomal abnormalities (4 papers)
- Cited by
- GeneticsNeurologyMolecular Biology
- Partner nations
- United KingdomAustraliaUnited States
In The Last Decade
Josh Willoughby
9 papers receiving 124 citations
Peers
Comparison fields: 5 of 32
- Genetics 84
- Molecular Biology 79
- Neurology 11
- Cognitive Neuroscience 8
- Genetics 6
Countries citing papers authored by Josh Willoughby
This map shows the geographic impact of Josh Willoughby'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 Josh Willoughby with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Josh Willoughby more than expected).
Fields of papers citing papers by Josh Willoughby
This network shows the impact of papers produced by Josh Willoughby. 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 Josh Willoughby. The network helps show where Josh Willoughby may publish in the future.
Co-authorship network of co-authors of Josh Willoughby
This figure shows the co-authorship network connecting the top 25 collaborators of Josh Willoughby. A scholar is included among the top collaborators of Josh Willoughby 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 Josh Willoughby. Josh Willoughby is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 2 | |
| 2 | 3 | |
| 3 | 21 | |
| 4 | 8 | |
| 5 | 4 | |
| 6 | 8 | |
| 7 | 5 | |
| 8 | 30 | |
| 9 | 44 |
About Josh Willoughby
Josh Willoughby is a scholar working on Genetics, Clinical Biochemistry and Neurology, having authored 9 papers that have together received 125 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Genetics (84 citations), Neurology (11 citations) and Molecular Biology (79 citations). Josh Willoughby has collaborated with scholars based in United Kingdom, Australia and United States. Frequent co-authors include Kate Chandler, Meena Balasubramanian, Jonathan Berg, Wayne Lam, Daniela T. Pilz, Charu Deshpande, Kay Metcalfe, Susan Tomkins, Andrew E. Fry and Astrid Weber. Their work appears in journals such as Gene, Archives of Disease in Childhood and Journal of Medical Genetics.
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.