J A Hurst
- Co-authors
- Michael OldridgeAndrew O.M. WilkieSarah F. SlaneyC. Michael HallSandra HingL. J. ButlerM BaraitserI. Karen Temple
- Topics
- Craniofacial Disorders and Treatments (2 papers)Genetics and Neurodevelopmental Disorders (2 papers)RNA modifications and cancer (1 paper)
- Partner nations
- United KingdomItaly
In The Last Decade
J A Hurst
6 papers receiving 364 citations
Peers
Comparison fields: 5 of 43
- Genetics 319
- Molecular Biology 149
- Psychiatry and Mental health 39
- Cell Biology 28
- Surgery 28
Countries citing papers authored by J A Hurst
This map shows the geographic impact of J A Hurst'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 J A Hurst with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J A Hurst more than expected).
Fields of papers citing papers by J A Hurst
This network shows the impact of papers produced by J A Hurst. 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 J A Hurst. The network helps show where J A Hurst may publish in the future.
Co-authorship network of co-authors of J A Hurst
This figure shows the co-authorship network connecting the top 25 collaborators of J A Hurst. A scholar is included among the top collaborators of J A Hurst 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 J A Hurst. J A Hurst is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 105 | |
| 2 | A novel transcription factor is mutated in a severe speech and language disorder | 1 |
| 3 | Mutations of the homeobox gene MSX2 cause symmetric parietal foramina: contrasting effects of loss and gain of function mutations for skull development. | 1 |
| 4 | A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom. | 37 |
| 5 | Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome. | 174 |
| 6 | 54 |
About J A Hurst
J A Hurst is a scholar working on Developmental Neuroscience, Genetics and Dermatology, having authored 6 papers that have together received 372 indexed citations. Recurring topics across this work include Craniofacial Disorders and Treatments (2 papers), Genetics and Neurodevelopmental Disorders (2 papers) and RNA modifications and cancer (1 paper). The work is most often cited by research in Genetics (319 citations), Developmental Biology (8 citations) and Psychiatry and Mental health (39 citations). J A Hurst has collaborated with scholars based in United Kingdom and Italy. Frequent co-authors include Michael Oldridge, Andrew O.M. Wilkie, Sarah F. Slaney, C. Michael Hall, Sandra Hing, L. J. Butler, M Baraitser, I. Karen Temple, Francesca Moro and Kiyoshi Hayasaka. Their work appears in journals such as Neurology, The American Journal of Human Genetics 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.