Gordon S. Stephen

411 total citations
15 papers, 239 citations indexed

About

Gordon S. Stephen is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Gordon S. Stephen has authored 15 papers receiving a total of 239 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Gordon S. Stephen's work include Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (5 papers) and Congenital heart defects research (3 papers). Gordon S. Stephen is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (5 papers) and Congenital heart defects research (3 papers). Gordon S. Stephen collaborates with scholars based in United Kingdom. Gordon S. Stephen's co-authors include D A Couzin, J L Watt, Alan Johnston, John Dean, Ken Ward, E.L. McKay, Elizabeth Gray, R Rankin, Dongeun Yong and Sharon Simpson and has published in prestigious journals such as BJOG An International Journal of Obstetrics & Gynaecology, Journal of Medical Genetics and Clinical Genetics.

In The Last Decade

Gordon S. Stephen

14 papers receiving 211 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gordon S. Stephen United Kingdom 8 171 100 66 62 24 15 239
D A Couzin United Kingdom 12 226 1.3× 135 1.4× 124 1.9× 117 1.9× 39 1.6× 23 367
Patrick L. Wilmot United States 10 148 0.9× 95 0.9× 49 0.7× 29 0.5× 21 0.9× 26 238
Claudine Fear United Kingdom 10 229 1.3× 147 1.5× 74 1.1× 36 0.6× 30 1.3× 16 312
G. R. Stalder Switzerland 12 256 1.5× 146 1.5× 98 1.5× 87 1.4× 22 0.9× 21 387
Chiara Castronovo Italy 9 183 1.1× 122 1.2× 51 0.8× 49 0.8× 13 0.5× 16 275
Jacquelyn Roberson United States 10 223 1.3× 151 1.5× 50 0.8× 81 1.3× 28 1.2× 18 341
Rowena S. James United Kingdom 6 109 0.6× 91 0.9× 62 0.9× 32 0.5× 12 0.5× 6 242
Maria Paola Recalcati Italy 11 240 1.4× 191 1.9× 89 1.3× 46 0.7× 25 1.0× 21 378
M. Barr United States 6 144 0.8× 199 2.0× 93 1.4× 24 0.4× 62 2.6× 6 346
Hélène Moirot France 9 119 0.7× 76 0.8× 59 0.9× 45 0.7× 20 0.8× 13 198

Countries citing papers authored by Gordon S. Stephen

Since Specialization
Citations

This map shows the geographic impact of Gordon S. Stephen'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 Gordon S. Stephen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gordon S. Stephen more than expected).

Fields of papers citing papers by Gordon S. Stephen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gordon S. Stephen. 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 Gordon S. Stephen. The network helps show where Gordon S. Stephen may publish in the future.

Co-authorship network of co-authors of Gordon S. Stephen

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

All Works

15 of 15 papers shown
1.
Holman, Russell L. & Gordon S. Stephen. (2005). Thrombocytopenic purpura with depot medroxyprogesterone acetate and subsequent use of contraceptive implant: making decisions in the absence of evidence. Journal of Family Planning and Reproductive Health Care. 31(4). 333–334.
2.
Yong, Dongeun, et al.. (1999). Chromosome 22q11 microdeletion and congenital heart disease - a survey in a paediatric population. European Journal of Pediatrics. 158(7). 566–570. 15 indexed citations
3.
Turnpenny, Peter D., Alan Johnston, John Dean, et al.. (1992). Ectrodactyly-mandibulo-facial dysostosis. Clinical Dysmorphology. 1(2). 103???110–103???110. 1 indexed citations
4.
Dean, John, et al.. (1991). Apparent Fryns' syndrome and aneuploidy: evidence for a disturbance of the midline developmental field. Clinical Genetics. 40(5). 349–352. 17 indexed citations
5.
Dean, John, Sharon Simpson, D A Couzin, & Gordon S. Stephen. (1991). Interstitial deletion of chromosome 13: prognosis and adult phenotype.. Journal of Medical Genetics. 28(8). 533–535. 3 indexed citations
6.
Johnston, Alan, et al.. (1989). A fertile woman with non‐mosaic Turner's syndrome. Case report and review of the literature. BJOG An International Journal of Obstetrics & Gynaecology. 96(7). 876–880. 42 indexed citations
7.
Stephen, Gordon S., D A Couzin, J L Watt, & R Rankin. (1989). Prenatal diagnosis of a case of 46,XY, 18p — /46,XY, 18p + mosaicism. Prenatal Diagnosis. 9(1). 57–60. 7 indexed citations
8.
Couzin, D A, J L Watt, & Gordon S. Stephen. (1987). Structural rearrangements in the parents of children with primary trisomy 21.. Journal of Medical Genetics. 24(5). 280–282. 29 indexed citations
9.
Couzin, D A, et al.. (1986). The prenatal detection of a familial pericentric inversion of chromosome 19. Prenatal Diagnosis. 6(1). 79–82. 3 indexed citations
10.
Couzin, D A, Audrey A. Dawson, & Gordon S. Stephen. (1986). A possible case of chronic leukoerythroblastosis associated with t(12;14)(p13;q22) in bone marrow cells. Cancer Genetics and Cytogenetics. 22(3). 253–256. 1 indexed citations
11.
Watt, J L, et al.. (1986). A paracentric inversion of 7q illustrating a possible interchromosomal effect.. Journal of Medical Genetics. 23(4). 341–344. 24 indexed citations
12.
Watt, J L, et al.. (1985). A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome.. Journal of Medical Genetics. 22(4). 283–287. 65 indexed citations
13.
Watt, J L, et al.. (1984). A familial insertion involving an active nucleolar organiser within chromosome 12.. Journal of Medical Genetics. 21(5). 379–384. 14 indexed citations
14.
Allan, Sris, et al.. (1982). An unusual karyotype in preleukemia. Cancer Genetics and Cytogenetics. 7(1). 67–72. 6 indexed citations
15.
Stephen, Gordon S.. (1977). Mammalian chromosomes G-banded in four minutes. Genetica. 47(2). 115–116. 12 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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