D E Rooney

794 total citations
14 papers, 631 citations indexed

About

D E Rooney is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Surgery. According to data from OpenAlex, D E Rooney has authored 14 papers receiving a total of 631 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Pediatrics, Perinatology and Child Health and 3 papers in Surgery. Recurrent topics in D E Rooney's work include Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic Syndromes and Imprinting (3 papers). D E Rooney is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic Syndromes and Imprinting (3 papers). D E Rooney collaborates with scholars based in United Kingdom, Canada and Saudi Arabia. D E Rooney's co-authors include Barbara Czepulkowski, Jackie Wolstenholme, E. V. Davison, F. E. Loeffler, R. W. Beard, George Rebello, D. V. Coleman, JA Smith, Charlie Gray and Gerald Hackett and has published in prestigious journals such as Journal of Medical Genetics, American Journal of Medical Genetics and Prenatal Diagnosis.

In The Last Decade

D E Rooney

13 papers receiving 608 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
D E Rooney United Kingdom	10	291	245	243	86	84	14	631
Rolf‐Dieter Wegner Germany	16	226 0.8×	270 1.1×	227 0.9×	60 0.7×	51 0.6×	38	626
Nataline B. Kardon United States	13	329 1.1×	232 0.9×	281 1.2×	108 1.3×	66 0.8×	26	640
Jan Rydnert Sweden	8	173 0.6×	424 1.7×	116 0.5×	80 0.9×	53 0.6×	12	735
Joy D.A. Delhanty United Kingdom	17	290 1.0×	267 1.1×	423 1.7×	60 0.7×	128 1.5×	30	796
Elena Kolomietz Canada	11	269 0.9×	305 1.2×	225 0.9×	104 1.2×	45 0.5×	23	734
V. Cacheux France	8	129 0.4×	165 0.7×	156 0.6×	43 0.5×	135 1.6×	10	453
Kavita S. Reddy United States	19	380 1.3×	254 1.0×	163 0.7×	144 1.7×	57 0.7×	55	846
Sara Kaffe United States	16	546 1.9×	235 1.0×	399 1.6×	111 1.3×	89 1.1×	30	768
Silvana Guerneri Italy	17	406 1.4×	357 1.5×	344 1.4×	121 1.4×	110 1.3×	50	902
Voula Velissariou Greece	17	444 1.5×	354 1.4×	390 1.6×	78 0.9×	55 0.7×	40	784

Countries citing papers authored by D E Rooney

Since Specialization

Citations

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

Fields of papers citing papers by D E Rooney

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of D E Rooney

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

All Works

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14 of 14 papers shown

1.

Wolstenholme, Jane & D E Rooney. (2010). Cytogenetics in the 1970s and 1980s. Prenatal Diagnosis. 30(7). 605–607. 5 indexed citations

2.

Rooney, D E. (2001). Constitutional analysis : a practical approach. Oxford University Press eBooks. 1 indexed citations

3.

Rooney, D E. (2001). Malignancy and acquired abnormalities : a practical approach. Oxford University Press eBooks.

4.

Rooney, D E. (2001). Human Cytogenetics: malignancy and acquired Abnormalities. 54 indexed citations

5.

Rooney, D E, et al.. (1999). Case of partial trisomy 2q3 with clinical manifestations of Marshall-Smith syndrome. American Journal of Medical Genetics. 85(2). 185–188. 20 indexed citations

6.

Czepulkowski, Barbara & D E Rooney. (1997). Human Chromosome Preparation: Essential Techniques. Medical Entomology and Zoology. 16 indexed citations

7.

Rooney, D E & Barbara Czepulkowski. (1994). Human cytogenetics : essential data. John Wiley eBooks. 9 indexed citations

8.

Wolstenholme, Jackie, D E Rooney, & E. V. Davison. (1994). Confined placental mosaicism, IUGR, and adverse pregnancy outcome: A controlled retrospective U.K. collaborative survey. Prenatal Diagnosis. 14(5). 345–361. 97 indexed citations

9.

Rooney, D E & Barbara Czepulkowski. (1992). Malignancy and acquired abnormalities. 17 indexed citations

10.

Rebello, George, Charlie Gray, D E Rooney, et al.. (1991). Cytogenetic studies of amniotic fluid taken before the 15th week of pregnancy for earlier prenatal diagnosis: A report of 114 consecutive cases. Prenatal Diagnosis. 11(1). 35–40. 21 indexed citations

11.

Hackett, Gerald, JA Smith, George Rebello, et al.. (1991). Early amniocentesis at 11–14 weeks' gestation for the diagnosis of fetal chromosomal abnormality—a clinical evaluation. Prenatal Diagnosis. 11(5). 311–315. 32 indexed citations

12.

Rooney, D E, Neil MacLachlan, John A. Smith, et al.. (1989). Early amniocentesis: a cytogenetic evaluation.. BMJ. 299(6690). 25.1–25. 32 indexed citations

13.

Rooney, D E, et al.. (1989). A case of interstitial deletion of 10q25.2----q26.1.. Journal of Medical Genetics. 26(1). 58–60. 16 indexed citations

14.

Rooney, D E & Barbara Czepulkowski. (1986). Human cytogenetics : a practical approach. 311 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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