Celia Donaghue

938 total citations
16 papers, 629 citations indexed

About

Celia Donaghue is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Celia Donaghue has authored 16 papers receiving a total of 629 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 12 papers in Pediatrics, Perinatology and Child Health and 5 papers in Molecular Biology. Recurrent topics in Celia Donaghue's work include Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (10 papers) and Fetal and Pediatric Neurological Disorders (4 papers). Celia Donaghue is often cited by papers focused on Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (10 papers) and Fetal and Pediatric Neurological Disorders (4 papers). Celia Donaghue collaborates with scholars based in United Kingdom, Australia and Germany. Celia Donaghue's co-authors include Kathy Mann, Caroline Mackie Ogilvie, Zoe Docherty, Alison Hills, B R Westley, F. E. B. May, Angharad M. Roberts, Jonathan J. Waters, Joo Wook Ahn and Caroline Sullivan and has published in prestigious journals such as Molecular Endocrinology, Journal of Histochemistry & Cytochemistry and Human Genetics.

In The Last Decade

Celia Donaghue

16 papers receiving 586 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Celia Donaghue United Kingdom	14	479	437	155	68	65	16	629
Sandra Peacock United States	9	308 0.6×	207 0.5×	183 1.2×	71 1.0×	58 0.9×	11	489
E. J. Maher United Kingdom	8	440 0.9×	342 0.8×	173 1.1×	129 1.9×	28 0.4×	11	613
Anna Ruggeri Italy	10	197 0.4×	255 0.6×	122 0.8×	31 0.5×	76 1.2×	13	402
Francesca Dulcetti Italy	10	203 0.4×	301 0.7×	83 0.5×	29 0.4×	84 1.3×	12	387
Andrea Nuccitelli Italy	10	256 0.5×	446 1.0×	104 0.7×	23 0.3×	69 1.1×	16	593
Eftychia Dimitriadou Belgium	15	315 0.7×	488 1.1×	251 1.6×	92 1.4×	47 0.7×	26	715
G. Lefort France	16	377 0.8×	290 0.7×	189 1.2×	217 3.2×	33 0.5×	34	632
Maria Carla Pittalis Italy	13	254 0.5×	419 1.0×	132 0.9×	34 0.5×	69 1.1×	26	564
Ioannis Papoulidis Greece	13	251 0.5×	195 0.4×	116 0.7×	51 0.8×	24 0.4×	52	388
G. L. Terzoli Italy	10	397 0.8×	517 1.2×	237 1.5×	143 2.1×	44 0.7×	14	843

Countries citing papers authored by Celia Donaghue

Since Specialization

Citations

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

Fields of papers citing papers by Celia Donaghue

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Celia Donaghue. 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 Celia Donaghue. The network helps show where Celia Donaghue may publish in the future.

Co-authorship network of co-authors of Celia Donaghue

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

All Works

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16 of 16 papers shown

Donaghue, Celia, et al.. (2017). Efficient and cost-effective genetic analysis of products of conception and fetal tissues using a QF-PCR/array CGH strategy; five years of data. Molecular Cytogenetics. 10(1). 12–12. 17 indexed citations

Mann, Kathy, et al.. (2012). Quantitative fluorescence PCR analysis of >40 000 prenatal samples for the rapid diagnosis of trisomies 13, 18 and 21 and monosomy X. Prenatal Diagnosis. 32(12). 1197–1204. 23 indexed citations

Hills, Alison, Celia Donaghue, Jonathan J. Waters, et al.. (2010). QF‐PCR as a stand‐alone test for prenatal samples: the first 2 years' experience in the London region. Prenatal Diagnosis. 30(6). 509–517. 57 indexed citations

Irving, Melita, Karin Buiting, Deniz Kanber, et al.. (2010). Segmental paternal uniparental disomy (patUPD) of 14q32 with abnormal methylation elicits the characteristic features of complete patUPD14. American Journal of Medical Genetics Part A. 152A(8). 1942–1950. 27 indexed citations

Hills, Alison, et al.. (2010). MLPA for confirmation of array CGH results and determination of inheritance. Molecular Cytogenetics. 3(1). 19–19. 22 indexed citations

Donaghue, Celia, et al.. (2009). Combined QF‐PCR and MLPA molecular analysis of miscarriage products: an efficient and robust alternative to karyotype analysis. Prenatal Diagnosis. 30(2). 133–137. 32 indexed citations

Vandersteen, Anthony M., et al.. (2009). Genetic diagnosis in clinical psychiatry: A case report of a woman with a 47, XXX karyotype and Fragile X syndrome. The European Journal of Psychiatry. 23(1). 3 indexed citations

Waters, Jonathan J., Kathy Mann, Caroline Mackie Ogilvie, et al.. (2007). Complete discrepancy between QF‐PCR analysis of uncultured villi and karyotyping of cultured cells in the prenatal diagnosis of trisomy 21 in three CVS. Prenatal Diagnosis. 27(4). 332–339. 27 indexed citations

Ahn, Joo Wook, et al.. (2007). Detection of subtelomere imbalance using MLPA: validation, development of an analysis protocol, and application in a diagnostic centre. BMC Medical Genetics. 8(1). 9–9. 39 indexed citations

10.

Donaghue, Celia, Kathy Mann, Zoe Docherty, & Caroline Mackie Ogilvie. (2005). Detection of mosaicism for primary trisomies in prenatal samples by QF-PCR and karyotype analysis. Prenatal Diagnosis. 25(1). 65–72. 76 indexed citations

11.

Ogilvie, Caroline Mackie, et al.. (2005). Rapid Prenatal Diagnosis of Aneuploidy Using Quantitative Fluorescence-PCR (QF-PCR). Journal of Histochemistry & Cytochemistry. 53(3). 285–288. 52 indexed citations

12.

Mann, Kathy, et al.. (2004). Strategies for the rapid prenatal diagnosis of chromosome aneuploidy. European Journal of Human Genetics. 12(11). 907–915. 112 indexed citations

13.

Donaghue, Celia, Angharad M. Roberts, Kathy Mann, & Caroline Mackie Ogilvie. (2003). Development and targeted application of a rapid QF‐PCR test for sex chromosome imbalance. Prenatal Diagnosis. 23(3). 201–210. 53 indexed citations

14.

Mann, Kathy, Celia Donaghue, & Caroline Mackie Ogilvie. (2003). In vivo somatic microsatellite mutations identified in non-malignant human tissue. Human Genetics. 114(1). 110–114. 14 indexed citations

15.

Donaghue, Celia, Helen J. Bates, & Sue Cotterill. (2001). Identification and characterisation of the Drosophila homologue of the yeast Uba2 gene. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1518(1-2). 210–214. 10 indexed citations

16.

Donaghue, Celia, B R Westley, & F. E. B. May. (1999). Selective Promoter Usage of the Human Estrogen Receptor-α Gene and Its Regulation by Estrogen. Molecular Endocrinology. 13(11). 1934–1950. 65 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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