J A Hurst
Impact in
- Genetics top 10%
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
- Genetics and Neurodevelopmental Disorders
- Connective tissue disorders research
- Genomic variations and chromosomal abnormalities
- Genetic and rare skin diseases.
Papers in
- Genetics 5
- Craniofacial Disorders and Treatments 2
- Genetics and Neurodevelopmental Disorders 2
- Connective tissue disorders research 1
- Cleft Lip and Palate Research 1
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- RNA modifications and cancer 1
- Co-authors
- C. Michael Hall (1 shared paper)Andrew O.M. Wilkie (1 shared paper)Michael Oldridge (1 shared paper)Sarah F. Slaney (1 shared paper)L. J. Butler (1 shared paper)M Baraitser (1 shared paper)Sandra Hing (1 shared paper)I. Karen Temple (1 shared paper)
- Journals
- Neurology (1 paper)The American Journal of Human Genetics (1 paper)Journal of Medical Genetics (1 paper)PubMed (2 papers)UCL Discovery (University College London) (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
- Developmental Biology 8
- Psychiatry and Mental health 39
- Molecular Biology 149
- Cell Biology 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-authors
The 25 scholars most cited alongside J A Hurst, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome. | 1996 | 174 |
| 2 | 2007 | 105 | |
| 3 | 1990 | 54 | |
| 4 | A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom. | 1996 | 37 |
| 5 | A novel transcription factor is mutated in a severe speech and language disorder | 2001 | 1 |
| 6 | Mutations of the homeobox gene MSX2 cause symmetric parietal foramina: contrasting effects of loss and gain of function mutations for skull development. | 1999 | 1 |
About J A Hurst
J A Hurst is a scholar working on Genetics, Molecular Biology, Dermatology, General Health Professions and Rheumatology, 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), Williams Syndrome Research (1 paper), Hermeneutics and Narrative Identity (1 paper), Connective tissue disorders research (1 paper), Cleft Lip and Palate Research (1 paper), Health, Medicine and Society (1 paper) and RNA modifications and cancer (1 paper). The work is most often cited by research in Genetics (319 citations), Developmental Biology (8 citations), Psychiatry and Mental health (39 citations), Molecular Biology (149 citations) and Cell Biology (28 citations). J A Hurst has collaborated with scholars based in United Kingdom and Italy. Frequent co-authors include C. Michael Hall, Andrew O.M. Wilkie, Michael Oldridge, Sarah F. Slaney, L. J. Butler, M Baraitser, Sandra Hing, I. Karen Temple, Renzo Guerrini and Mitsuhiro Kato. Their work appears in journals such as Neurology, The American Journal of Human Genetics, Journal of Medical Genetics, PubMed and UCL Discovery (University College London).
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.