D. Warburton

41 papers receiving 1.4k citations

D. Warburton's Hit Papers

Location of Ribosomal DNA in the Human Chromosome Complement 1972 · 454 citations
4540+18+36Years since publication100200300400

Peers

D. Warburton
Comparison fields: 5 of 93
  • Genetics 539
  • Pediatrics, Perinatology and Child Health 283
  • Developmental Biology 30
  • Molecular Biology 824
  • Plant Science 405
Replace John R. Gosden with:
John R. Gosden United Kingdom
M W Kilpatrick United States
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D. Warburton relative to John R. Gosden United Kingdom John R. Gosden's profile →
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Countries citing papers authored by D. Warburton

Since Specialization
Citations

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

Fields of papers citing papers by D. Warburton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside D. Warburton, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with D. Warburton Line = papers co-authored together D. Warburton links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 42 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Location of Ribosomal DNA in the Human Chromosome Complement
Hit paper breakdown →
1972454
2
The 13q-deletion syndrome.
1969133
3 2000100
4 198265
5 197362
6
The relationship of maternal age and trisomy among trisomic spontaneous abortions.
198462
7 197256
8
Translocation heterozygosis: a cause of five cases of the cri du chat syndrome and two cases with a duplication of chromosome number five in three families.
196756
9
The relationship between maternal age and chromosome size in autosomal trisomy.
198656
10
Mosaic autosomal trisomy in cultures from spontaneous abortions.
197849
11
A stable human dicentric chromosome, t dic (12;14)(p13;p13) including an intercalary satellite region between centromeres.
197346
12 197541
13 197436
14
Preliminary communication: prenatal detection of the Fanconi Anemia gene by cytogenetic methods.
197929
15
Morphological characteristics of monosomy X in spontaneous abortions.
198828
16 197327
17 196327
18 197723
19 199022
20
Application of new staining techniques to the study of human chromosomes.
197322

About D. Warburton

D. Warburton is a scholar working on Molecular Biology, Genetics, Electrical and Electronic Engineering, Aerospace Engineering and Atomic and Molecular Physics, and Optics, having authored 42 papers that have together received 1.5k indexed citations. Recurring topics across this work include Particle Accelerators and Free-Electron Lasers (12 papers), Particle accelerators and beam dynamics (11 papers), Gyrotron and Vacuum Electronics Research (9 papers), Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (7 papers), Prenatal Screening and Diagnostics (7 papers), DNA and Nucleic Acid Chemistry (6 papers) and RNA Interference and Gene Delivery (3 papers). The work is most often cited by research in Genetics (539 citations), Pediatrics, Perinatology and Child Health (283 citations), Developmental Biology (30 citations), Molecular Biology (824 citations) and Plant Science (405 citations). D. Warburton has collaborated with scholars based in United States, Canada and Slovenia. Frequent co-authors include K.C. Atwood, A.S. Henderson, Jennie Kline, Zena Stein, O.J. Miller, Bernard F. Erlanger, Sam M. Beiser, O. J. Miller, Frederick E. Warburton and Terry Hassold. Their work appears in journals such as Human Genetics, Proceedings of the National Academy of Sciences, Chromosoma, The Lancet and Nuclear Instruments and Methods in Physics Research Section A Accelerators Spectrometers Detectors and Associated Equipment.

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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