D A Couzin

561 total citations
23 papers, 367 citations indexed

About

D A Couzin is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, D A Couzin has authored 23 papers receiving a total of 367 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 10 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in D A Couzin's work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (8 papers) and Chromosomal and Genetic Variations (4 papers). D A Couzin is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (8 papers) and Chromosomal and Genetic Variations (4 papers). D A Couzin collaborates with scholars based in United Kingdom, Sri Lanka and Germany. D A Couzin's co-authors include J L Watt, Gordon S. Stephen, D. P. Fox, D.G. Papworth, Alan Johnston, John Dean, Ken Ward, A W Johnston, Elizabeth Gray and E. Boyd and has published in prestigious journals such as Experimental Cell Research, Journal of Theoretical Biology and BJOG An International Journal of Obstetrics & Gynaecology.

In The Last Decade

D A Couzin

23 papers receiving 328 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
D A Couzin United Kingdom	12	226	135	124	117	39	23	367
G. R. Stalder Switzerland	12	256 1.1×	146 1.1×	98 0.8×	87 0.7×	22 0.6×	21	387
Ko–ichiro Yoshiura Japan	12	251 1.1×	304 2.3×	107 0.9×	69 0.6×	49 1.3×	22	505
Sandra Peacock United States	9	308 1.4×	183 1.4×	207 1.7×	71 0.6×	25 0.6×	11	489
Gordon S. Stephen United Kingdom	8	171 0.8×	100 0.7×	66 0.5×	62 0.5×	24 0.6×	15	239
Kirsten Bruun Petersen Denmark	8	157 0.7×	206 1.5×	45 0.4×	159 1.4×	12 0.3×	8	357
Morag N. Collinson United Kingdom	14	381 1.7×	210 1.6×	123 1.0×	97 0.8×	25 0.6×	21	473
Sue Ann Berend United States	15	432 1.9×	174 1.3×	336 2.7×	149 1.3×	39 1.0×	20	584
Elisabeth A. Keitges United States	11	439 1.9×	249 1.8×	85 0.7×	105 0.9×	16 0.4×	13	529
C Baccichetti Italy	14	539 2.4×	287 2.1×	204 1.6×	207 1.8×	54 1.4×	32	686
Petrea Jacobsen Denmark	10	347 1.5×	195 1.4×	90 0.7×	97 0.8×	21 0.5×	16	491

Countries citing papers authored by D A Couzin

Since Specialization

Citations

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

Fields of papers citing papers by D A Couzin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D A Couzin. 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 D A Couzin. The network helps show where D A Couzin may publish in the future.

Co-authorship network of co-authors of D A Couzin

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

All Works

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20 of 20 papers shown

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

Carothers, A D, E. Boyd, Gordon Lowther, et al.. (1999). Trends in prenatal diagnosis of Down syndrome and other autosomal trisomies in Scotland 1990 to 1994, with associated cytogenetic and epidemiological findings. Genetic Epidemiology. 16(2). 179–190. 25 indexed citations

Drummond, Jennifer, et al.. (1998). Mosaicism for a tandem duplication dup(1)(q12q22) in an 18 year old female.. Journal of Medical Genetics. 35(7). 600–603. 6 indexed citations

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

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

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

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

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

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

10.

Couzin, D A, N E Haites, J L Watt, & A W Johnston. (1986). Partial trisomy 7 (q32----qter) syndrome in two children.. Journal of Medical Genetics. 23(5). 461–465. 11 indexed citations

11.

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

12.

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

13.

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

14.

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

15.

Watt, J L & D A Couzin. (1983). De novo translocation heterozygote with three reciprocal translocations.. Journal of Medical Genetics. 20(5). 385–388. 18 indexed citations

16.

Watt, J L, D A Couzin, A W Johnston, V. Jandial, & Elizabeth Gray. (1981). Prenatal detection of Turner's syndrome in conjunction with trisomy 20 mosaicism (45,X/46, X, +0).. Journal of Medical Genetics. 18(3). 225–227. 10 indexed citations

17.

Couzin, D A. (1979). Frequency changes with time in vivo of radiation-induced chromosomal aberrations in skin fibroblasts. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 60(3). 367–380. 5 indexed citations

18.

Couzin, D A. (1978). Plating efficiency measurements and the experimental control of ageing of adult human skin fibroblasts in vitro. Experimental Cell Research. 116(1). 115–126. 8 indexed citations

19.

Couzin, D A & D. P. Fox. (1974). Variation in chiasma frequency during tulip anther development. Chromosoma. 46(2). 173–179. 24 indexed citations

20.

Couzin, D A & D. P. Fox. (1973). U-type exchange in tulip meiosis. Chromosoma. 41(4). 421–436. 5 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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