Stuart Purvis‐Smith

1.0k total citations
28 papers, 765 citations indexed

About

Stuart Purvis‐Smith is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Stuart Purvis‐Smith has authored 28 papers receiving a total of 765 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 8 papers in Pediatrics, Perinatology and Child Health and 5 papers in Molecular Biology. Recurrent topics in Stuart Purvis‐Smith's work include Dermatoglyphics and Human Traits (11 papers), Prenatal Screening and Diagnostics (8 papers) and Genomic variations and chromosomal abnormalities (7 papers). Stuart Purvis‐Smith is often cited by papers focused on Dermatoglyphics and Human Traits (11 papers), Prenatal Screening and Diagnostics (8 papers) and Genomic variations and chromosomal abnormalities (7 papers). Stuart Purvis‐Smith collaborates with scholars based in Australia, United Kingdom and Singapore. Stuart Purvis‐Smith's 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, Don Leigh, B. L. Duffy and Tsutomu Ogata and has published in prestigious journals such as New England Journal of Medicine, The Lancet and JAMA.

In The Last Decade

Stuart Purvis‐Smith

26 papers receiving 708 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Stuart Purvis‐Smith Australia 14 605 263 238 124 64 28 765
Ademar Freire‐Maia Brazil 13 233 0.4× 63 0.2× 127 0.5× 37 0.3× 164 2.6× 48 669
J Lafourcade France 16 476 0.8× 188 0.7× 216 0.9× 17 0.1× 54 0.8× 57 698
N R Dennis United Kingdom 13 520 0.9× 158 0.6× 242 1.0× 103 0.8× 10 0.2× 23 654
J Lejeune France 14 328 0.5× 163 0.6× 202 0.8× 11 0.1× 29 0.5× 50 576
J. Britt Ravnan United States 12 811 1.3× 494 1.9× 408 1.7× 83 0.7× 10 0.2× 19 1.1k
Stanley Walzer United States 8 270 0.4× 88 0.3× 145 0.6× 42 0.3× 16 0.3× 13 387
P. N. Howard‐Peebles United States 10 566 0.9× 513 2.0× 293 1.2× 32 0.3× 10 0.2× 16 778
M. A. C. Ridler United States 17 328 0.5× 153 0.6× 183 0.8× 14 0.1× 54 0.8× 36 572
Franz Binkert Switzerland 24 1.3k 2.2× 932 3.5× 585 2.5× 46 0.4× 31 0.5× 50 1.7k
Vikram Jaswaney United States 7 424 0.7× 154 0.6× 245 1.0× 43 0.3× 5 0.1× 12 489

Countries citing papers authored by Stuart Purvis‐Smith

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Stuart Purvis‐Smith

This figure shows the co-authorship network connecting the top 25 collaborators of Stuart Purvis‐Smith. A scholar is included among the top collaborators of Stuart Purvis‐Smith 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 Stuart Purvis‐Smith. Stuart Purvis‐Smith is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Perry, Jo K., Sara Nouri, Art Daniel, et al.. (2005). Molecular distinction between true centric fission and pericentric duplication-fission. Human Genetics. 116(4). 300–310. 7 indexed citations
2.
Soemantri, Ag, et al.. (1995). Fragile X mental retardation in an Indonesian family. Medical Journal of Indonesia. 17–17. 4 indexed citations
3.
Ogata, Tsutomu, Chris Tyler‐Smith, Stuart Purvis‐Smith, & Gillian Turner. (1993). Chromosomal localisation of a gene(s) for Turner stigmata on Yp.. Journal of Medical Genetics. 30(11). 918–922. 34 indexed citations
4.
Purvis‐Smith, Stuart, et al.. (1992). Uniparental disomy 15 resulting from "correction" of an initial trisomy 15.. PubMed. 50(6). 1348–50. 103 indexed citations
5.
Wilson, Meredith, et al.. (1989). Duplication of 5ql1.2→q13.1 from a familial (5;20) balanced insertion. American Journal of Medical Genetics. 33(2). 220–223. 8 indexed citations
6.
Purvis‐Smith, Stuart, et al.. (1988). Prenatal diagnosis of the fragile X – The Australasian experience. American Journal of Medical Genetics. 30(1-2). 337–345. 13 indexed citations
7.
Callen, David F., et al.. (1988). Extra embryonic/fetal karyotypic discordance during diagnostic chorionic villus sampling. Prenatal Diagnosis. 8(6). 453–460. 60 indexed citations
8.
Selikowitz, Mark, et al.. (1987). Deletion 15q21.1----q22.1 resulting from a paternal insertion into chromosome 5.. Journal of Medical Genetics. 24(11). 709–712. 19 indexed citations
9.
Turner, Gordon, Hazel M. Robinson, Susan T. Laing, & Stuart Purvis‐Smith. (1986). Preventive screening for fragile X syndrome.. PubMed. 2(10). 1191–2. 117 indexed citations
10.
Old, Julie M., Stuart Purvis‐Smith, Bridget Wilcken, et al.. (1985). PRENATAL EXCLUSION OF ORNITHINE TRANSCARBAMYLASE DEFICIENCY BY DIRECT GENE ANALYSIS. The Lancet. 325(8420). 73–75. 49 indexed citations
11.
Bell, Judith A., John Pearn, J. H. Ford, et al.. (1985). Utilization of prenatal cytogenetic diagnosis in women of advanced maternal age in Australia, 1979–1982. Prenatal Diagnosis. 5(1). 53–58. 8 indexed citations
12.
Purvis‐Smith, Stuart, et al.. (1983). Prenatal diagnosis of trisomy 9 mosaicism. Pathology. 15(1). 109–109. 7 indexed citations
13.
Purvis‐Smith, Stuart, Kathleen Hayes, & MargaretA. Menser. (1972). DERMATOGLYPHICS IN CHILDREN WITH PRENATAL CYTOMEGALOVIRUS INFECTION. The Lancet. 300(7784). 976–977. 17 indexed citations
14.
Menser, MargaretA. & Stuart Purvis‐Smith. (1972). DERMATOGLYPHICS IN LEUKÆMIA. The Lancet. 299(7757). 956–957. 6 indexed citations
15.
Purvis‐Smith, Stuart, et al.. (1970). DERMATOGLYPHIC DEFECTS AND RUBELLA TERATOGENESIS. Obstetrical & Gynecological Survey. 25(2). 141–143. 2 indexed citations
16.
Purvis‐Smith, Stuart. (1969). FINGER AND PALM PRINTING TECHNIQUES FOR THE CLINICIAN. The Medical Journal of Australia. 2(4). 189–191. 14 indexed citations
17.
Menser, MargaretA. & Stuart Purvis‐Smith. (1969). DERMATOGLYPHIC DEFECTS IN CHILDREN WITH LEUKÆMIA. The Lancet. 293(7605). 1076–1078. 36 indexed citations
18.
Purvis‐Smith, Stuart. (1969). Dermatoglyphic Defects and Rubella Teratogenesis. JAMA. 209(12). 1865–1865. 20 indexed citations
19.
Allan, G. S., et al.. (1968). CHROMOSOMAL SEX AND HERMAPHRODITISM. Australian Veterinary Journal. 44(10). 483–484.
20.
Purvis‐Smith, Stuart & MargaretA. Menser. (1968). DERMATOGLYPHICS IN ADULTS WITH CONGENITAL RUBELLA. The Lancet. 292(7560). 141–143. 59 indexed citations

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.

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