Jill Clayton‐Smith
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- Pharmacological Effects and Toxicity Studies 31
- Prenatal Screening and Diagnostics 22
- Genetics top 0.1%
- Genetic Syndromes and Imprinting 41
- Genomic variations and chromosomal abnormalities 37
- Genetics and Neurodevelopmental Disorders 23
- Genomics and Rare Diseases 20
- Psychiatry and Mental health top 0.5%
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- Pregnancy and Medication Impact 28
- Molecular Biology top 2%
- Epigenetics and DNA Methylation 26
- Co-authors
- Gus A. BakerRebecca BromleyDian DonnaiKimford J. MeadorDavid W. LoringMorris J. CohenMichael PriviteraLaura A. Kalayjian
- Journals
- Journal of Medical Genetics (15 papers)European Journal of Medical Genetics (13 papers)European Journal of Human Genetics (9 papers)
- Partner nations
- United KingdomUnited StatesSouth Africa
In The Last Decade
Jill Clayton‐Smith
197 papers receiving 9.3k citations
Hit Papers
Peers
Comparison fields: 5 of 148
- Pediatrics, Perinatology and Child Health 4.1k
- Genetics 5.3k
- Psychiatry and Mental health 1.8k
- Public Health, Environmental and Occupational Health 2.0k
- Molecular Biology 3.7k
Countries citing papers authored by Jill Clayton‐Smith
This map shows the geographic impact of Jill Clayton‐Smith'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 Jill Clayton‐Smith with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jill Clayton‐Smith more than expected).
Fields of papers citing papers by Jill Clayton‐Smith
This network shows the impact of papers produced by Jill Clayton‐Smith. 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 Jill Clayton‐Smith. The network helps show where Jill Clayton‐Smith may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Jill Clayton‐Smith, 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 | 2025 | 1 | |
| 2 | 2023 | 12 | |
| 3 | 2023 | 7 | |
| 4 | 2021 | 27 | |
| 5 | 2019 | 6 | |
| 6 | 2017 | 3 | |
| 7 | 2017 | 24 | |
| 8 | 2017 | 18 | |
| 9 | 2015 | 11 | |
| 10 | 2014 | 166 | |
| 11 | 2009 | 0 | |
| 12 | BEHAVIORAL ABILITIES OF CHILDREN EXPOSED TO CARBAMAZEPINE OR SODIUM VALPROATE IN UTERO: PRELIMINARY PROSPECTIVE EVIDENCE FROM THE LIVERPOOL AND MANCHESTER NEURO-DEVELOPMENT GROUP | 2009 | 1 |
| 13 | 2007 | 2 | |
| 14 | 2006 | 420 | |
| 15 | Angelman syndrome phenotype associated with mutations in MECP2. | 2001 | 1 |
| 16 | A survey of TWIST for mutations in craniosynostosis reveals a variable length polyglycine tract in asymptomatic individuals. | 2001 | 2 |
| 17 | Somatic mutation in the MECP2 gene may be a cause of non-lethal neurodevelopmental diosrder in males. | 2000 | 6 |
| 18 | 1992 | 29 | |
| 19 | Angelman syndrome can result from uniparental paternal isodisomy | 1990 | 6 |
| 20 | 1990 | 46 |
About Jill Clayton‐Smith
Jill Clayton‐Smith is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Obstetrics and Gynecology, Genetics and Developmental Biology, having authored 201 papers that have together received 9.7k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (41 papers), Genomic variations and chromosomal abnormalities (37 papers), Pharmacological Effects and Toxicity Studies (31 papers), Pregnancy and Medication Impact (28 papers), Epigenetics and DNA Methylation (26 papers), Genetics and Neurodevelopmental Disorders (23 papers), Prenatal Screening and Diagnostics (22 papers) and Genomics and Rare Diseases (20 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (4.1k citations), Genetics (5.3k citations), Psychiatry and Mental health (1.8k citations), Public Health, Environmental and Occupational Health (2.0k citations) and Molecular Biology (3.7k citations). Jill Clayton‐Smith has collaborated with scholars based in United Kingdom, United States and South Africa. Frequent co-authors include Gus A. Baker, Rebecca Bromley, Dian Donnai, Kimford J. Meador, David W. Loring, Morris J. Cohen, Michael Privitera, Laura A. Kalayjian, Joyce Liporace and Page B. Pennell. Their work appears in journals such as Journal of Medical Genetics, European Journal of Medical Genetics, European Journal of Human Genetics, Clinical Genetics and The American Journal of Human 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.