Drew Duckett

535 total citations
23 papers, 353 citations indexed

About

Drew Duckett is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Surgery. According to data from OpenAlex, Drew Duckett has authored 23 papers receiving a total of 353 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 9 papers in Pediatrics, Perinatology and Child Health and 6 papers in Surgery. Recurrent topics in Drew Duckett's work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (9 papers) and Congenital Anomalies and Fetal Surgery (4 papers). Drew Duckett is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (9 papers) and Congenital Anomalies and Fetal Surgery (4 papers). Drew Duckett collaborates with scholars based in United Kingdom, United States and South Africa. Drew Duckett's co-authors include Susan Roberts, I D Young, M E Oude Luttikhuis, Jane Wolstenholme, Jonathan Flint, I D Young, David J. Taylor, Lakshmi Mehta, J. C. Konje and David Williams and has published in prestigious journals such as Journal of Clinical Oncology, Journal of Medical Genetics and Modern Pathology.

In The Last Decade

Drew Duckett

22 papers receiving 334 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Drew Duckett United Kingdom 9 249 142 128 63 36 23 353
Cantú Jm Mexico 12 259 1.0× 165 1.2× 104 0.8× 83 1.3× 41 1.1× 67 405
Catherine Metaxotou Greece 12 188 0.8× 130 0.9× 140 1.1× 66 1.0× 27 0.8× 35 334
Jean‐Marie Rival France 12 186 0.7× 191 1.3× 72 0.6× 40 0.6× 69 1.9× 24 370
Morag N. Collinson United Kingdom 14 381 1.5× 210 1.5× 123 1.0× 97 1.5× 25 0.7× 21 473
Barbara Delle Chiaie Belgium 7 251 1.0× 195 1.4× 136 1.1× 38 0.6× 30 0.8× 10 423
M. Crocker United Kingdom 9 183 0.7× 88 0.6× 68 0.5× 52 0.8× 15 0.4× 16 245
Constance J. Sandlin United States 8 316 1.3× 132 0.9× 239 1.9× 138 2.2× 63 1.8× 10 397
M. Barr United States 6 144 0.6× 199 1.4× 93 0.7× 24 0.4× 62 1.7× 6 346
H. F. de France Netherlands 13 324 1.3× 144 1.0× 180 1.4× 129 2.0× 33 0.9× 24 459
Ioannis Papoulidis Greece 13 251 1.0× 116 0.8× 195 1.5× 51 0.8× 40 1.1× 52 388

Countries citing papers authored by Drew Duckett

Since Specialization
Citations

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

Fields of papers citing papers by Drew Duckett

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Drew Duckett

This figure shows the co-authorship network connecting the top 25 collaborators of Drew Duckett. A scholar is included among the top collaborators of Drew Duckett 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 Drew Duckett. Drew Duckett 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.
Jennings, Lawrence J., Drew Duckett, Borislav A. Alexiev, et al.. (2025). 91 Novel Low-Grade Fibroblastic Neoplasm with Co-Expression of MUC4 and Beta-catenin: Clinicopathologic and Molecular Characterization of Eight Cases. Laboratory Investigation. 105(3). 102314–102314. 1 indexed citations
2.
Duckett, Drew, Pouya Jamshidi, Madina Sukhanova, et al.. (2025). Accurate identification of primary site in tumors of unknown origin (TUO) using DNA methylation. npj Precision Oncology. 9(1). 8–8. 1 indexed citations
3.
Duckett, Drew, Jared T. Ahrendsen, Lawrence J. Jennings, et al.. (2025). Meningiomas With Chromosomal Polysomies Reveal Nonrandom Gain of Chromosomes, Distinct Methylation Signature, and Lower Risk of Recurrence. Modern Pathology. 38(7). 100775–100775.
4.
Alexiev, Borislav A., Lucas Santana‐Santos, Drew Duckett, et al.. (2023). Methylation classifier array and classification of solitary fibrous tumors.. Journal of Clinical Oncology. 41(16_suppl). e23522–e23522. 1 indexed citations
5.
Thomas, Shery, et al.. (2004). Ocular manifestations of mosaic trisomy 22: A case report and review of the literature. Ophthalmic Genetics. 25(1). 53–56. 13 indexed citations
6.
Howarth, E. S., J. C. Konje, Karen Healey, et al.. (2002). Invasive testing for the karyotyping of mid‐trimester intrauterine fetal death (IUFD): a pilot study. Prenatal Diagnosis. 22(6). 453–455. 19 indexed citations
7.
Konje, J. C., et al.. (1999). Genetic amniocentesis: gestation-specific pregnancy outcome and comparison of outcome following early and traditional amniocentesis. Prenatal Diagnosis. 19(9). 803–807. 28 indexed citations
8.
Konje, J. C., et al.. (1999). Genetic amniocentesis: gestation‐specific pregnancy outcome and comparison of outcome following early and traditional amniocentesis. Prenatal Diagnosis. 19(9). 803–807. 3 indexed citations
9.
Duckett, Drew, et al.. (1998). Triplication of 15q11-q13 with inv dup(15) in a female with developmental delay.. Journal of Medical Genetics. 35(5). 425–428. 34 indexed citations
10.
Luttikhuis, M E Oude, et al.. (1995). Brachydactyly and mental retardation: an Albright hereditary osteodystrophy-like syndrome localized to 2q37.. PubMed. 56(2). 400–7. 105 indexed citations
11.
Duckett, Drew, et al.. (1990). Origin of the X chromosomes in a patient with the 49,XXXXY syndrome.. Journal of Medical Genetics. 27(3). 203–204. 6 indexed citations
12.
Collacott, R. A., et al.. (1990). Down's syndrome and fragile‐X syndrome in a single patient. Journal of Intellectual Disability Research. 34(1). 81–86. 7 indexed citations
13.
Duckett, Drew, et al.. (1990). Prenatal diagnosis of trisomy for the distal two‐thirds of the long arm of chromosome 14 (q21→qter). Prenatal Diagnosis. 10(4). 261–264. 2 indexed citations
14.
Roberts, E., Drew Duckett, & G Lang. (1988). Maternal cell contamination in chorionic villus samples assessed by direct preparations and three different culture methods. Prenatal Diagnosis. 8(9). 635–640. 14 indexed citations
15.
Duckett, Drew & I D Young. (1988). A recombinant X chromosome in a short statured girl resulting from a maternal pericentric inversion. Human Genetics. 79(3). 251–254. 8 indexed citations
16.
Dalgleish, Raymond, Drew Duckett, Margaret Woodhouse, R S Shannon, & I D Young. (1988). Apparent monosomy 21 owing to a ring 21 chromosome: parental origin revealed by DNA analysis.. Journal of Medical Genetics. 25(12). 851–854. 6 indexed citations
17.
Mehta, Laxmi S., R S Shannon, Drew Duckett, & I D Young. (1986). Trisomy 18 in a 13 year old girl.. Journal of Medical Genetics. 23(3). 256–257. 16 indexed citations
18.
Duckett, Drew. (1982). Proximal 15q monosomy.. Journal of Medical Genetics. 19(5). 393.2–394. 3 indexed citations
19.
Roberts, Susan, et al.. (1982). Recurrent spontaneous abortions due to a homologous Robertsonian translocation (14q14q). Journal of Medical Genetics. 19(6). 465–467. 6 indexed citations
20.
Roberts, Susan & Drew Duckett. (1978). Trisomy 16p in a liveborn infant and a review of partial and full trisomy 16.. Journal of Medical Genetics. 15(5). 375–381. 44 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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