Stuart Purvis‐Smith
Impact in
- Developmental Biology top 5%
- Congenital limb and hand anomalies
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Dermatoglyphics and Human Traits
- Genetic Syndromes and Imprinting
Papers in
- Genetics 27
- Dermatoglyphics and Human Traits 11
- Genomic variations and chromosomal abnormalities 7
- Genetic Syndromes and Imprinting 5
- Genetics and Neurodevelopmental Disorders 4
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- Prenatal Screening and Diagnostics 8
- Co-authors
- MargaretA. Menser (4 shared papers)Susan T. Laing (2 shared papers)Hazel M. Robinson (2 shared papers)Gillian Turner (2 shared papers)Gordon Turner (1 shared paper)P.R.L.C. Lam-Po-Tang (5 shared papers)Margaret A. Menser (3 shared papers)B. L. Duffy (1 shared paper)
- Journals
- The Lancet (5 papers)Prenatal Diagnosis (3 papers)Journal of Medical Genetics (2 papers)JAMA (1 paper)Australian and New Zealand Journal of Obstetrics and Gynaecology (1 paper)
- Partner nations
- AustraliaUnited KingdomSingapore
In The Last Decade
Stuart Purvis‐Smith
26 papers receiving 708 citations
Peers
Comparison fields: 5 of 65
- Developmental Biology 64
- Genetics 605
- Anatomy 27
- Pediatrics, Perinatology and Child Health 263
- Cognitive Neuroscience 124
Countries citing papers authored by Stuart Purvis‐Smith
This map shows the geographic impact of Stuart Purvis‐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 Stuart Purvis‐Smith with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stuart Purvis‐Smith more than expected).
Fields of papers citing papers by Stuart Purvis‐Smith
This network shows the impact of papers produced by Stuart Purvis‐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 Stuart Purvis‐Smith. The network helps show where Stuart Purvis‐Smith may publish in the future.
Co-authors
The 25 scholars most cited alongside Stuart Purvis‐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
Showing the 20 most-cited of 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1986 | 117 | |
| 2 | Uniparental disomy 15 resulting from "correction" of an initial trisomy 15. | 1992 | 103 |
| 3 | 1986 | 88 | |
| 4 | 1988 | 60 | |
| 5 | 1968 | 59 | |
| 6 | 1985 | 49 | |
| 7 | 1969 | 36 | |
| 8 | 1993 | 34 | |
| 9 | 1982 | 32 | |
| 10 | 1973 | 24 | |
| 11 | 1969 | 20 | |
| 12 | 1987 | 19 | |
| 13 | 1972 | 17 | |
| 14 | 1969 | 14 | |
| 15 | 1988 | 13 | |
| 16 | 1987 | 12 | |
| 17 | 1972 | 10 | |
| 18 | 1973 | 10 | |
| 19 | 1989 | 8 | |
| 20 | 1985 | 8 |
About Stuart Purvis‐Smith
Stuart Purvis‐Smith is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Plant Science and Developmental Biology, having authored 28 papers that have together received 765 indexed citations. Recurring topics across this work include Dermatoglyphics and Human Traits (11 papers), Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (7 papers), Genetic Syndromes and Imprinting (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Chromosomal and Genetic Variations (3 papers), Gestational Trophoblastic Disease Studies (2 papers) and Congenital limb and hand anomalies (2 papers). The work is most often cited by research in Developmental Biology (64 citations), Genetics (605 citations), Anatomy (27 citations), Pediatrics, Perinatology and Child Health (263 citations) and Cognitive Neuroscience (124 citations). Stuart Purvis‐Smith has collaborated with scholars based in Australia, United Kingdom and Singapore. Frequent co-authors include MargaretA. Menser, Susan T. Laing, Hazel M. Robinson, Gillian Turner, Gordon Turner, P.R.L.C. Lam-Po-Tang, Margaret A. Menser, B. L. Duffy, Don Leigh and Chris Tyler‐Smith. Their work appears in journals such as The Lancet, Prenatal Diagnosis, Journal of Medical Genetics, JAMA and Australian and New Zealand Journal of Obstetrics and Gynaecology.
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.