Veronica J. Buckle

9.1k total citations
91 papers, 6.5k citations indexed

About

Veronica J. Buckle is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Veronica J. Buckle has authored 91 papers receiving a total of 6.5k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Molecular Biology, 33 papers in Genetics and 17 papers in Plant Science. Recurrent topics in Veronica J. Buckle's work include Genomics and Chromatin Dynamics (23 papers), Chromosomal and Genetic Variations (16 papers) and Genomic variations and chromosomal abnormalities (14 papers). Veronica J. Buckle is often cited by papers focused on Genomics and Chromatin Dynamics (23 papers), Chromosomal and Genetic Variations (16 papers) and Genomic variations and chromosomal abnormalities (14 papers). Veronica J. Buckle collaborates with scholars based in United Kingdom, United States and India. Veronica J. Buckle's co-authors include Douglas R. Higgs, Jill M. Brown, Andrew O.M. Wilkie, William R. Brown, Ian Craig, Jonathan Flint, E.P. Evans, Jim R. Hughes, W. G. Wood and Nigel K. Spurr and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Veronica J. Buckle

90 papers receiving 6.3k citations

Peers

Veronica J. Buckle

GENET

PHYSI

HEMAT

Stephen T. Reeders United States

P. Pearson Netherlands

Arthur I. Skoultchi United States

Elizabeth Baker Australia

Mariano Rocchi Italy

T. Mohandas United States

Richard J. Gibbons United Kingdom

Monica J. Justice United States

John J. Wasmuth United States

Yasuhisa Matsui Japan

Stephen T. Reeders United States

Veronica J. Buckle

2.9k ×0.6

2.9k ×1.3

GENET

849 ×0.7

359 ×0.5

PHYSI

468 ×0.9

HEMAT

Citations per year, relative to Veronica J. Buckle Veronica J. Buckle (= 1×) peers Stephen T. Reeders

Countries citing papers authored by Veronica J. Buckle

Since Specialization

Citations

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

Fields of papers citing papers by Veronica J. Buckle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Veronica J. Buckle. 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 Veronica J. Buckle. The network helps show where Veronica J. Buckle may publish in the future.

Co-authorship network of co-authors of Veronica J. Buckle

This figure shows the co-authorship network connecting the top 25 collaborators of Veronica J. Buckle. A scholar is included among the top collaborators of Veronica J. Buckle 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 Veronica J. Buckle. Veronica J. Buckle 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

Jeziorska, Danuta M., Edward Tunnacliffe, Jill M. Brown, et al.. (2022). On-microscope staging of live cells reveals changes in the dynamics of transcriptional bursting during differentiation. Nature Communications. 13(1). 6641–6641. 7 indexed citations

Oldenkamp, Roel, Jill M. Brown, David Miguel Susano Pinto, et al.. (2020). Chromatin arranges in chains of mesoscale domains with nanoscale functional topography independent of cohesin. Science Advances. 6(39). 121 indexed citations

Oudelaar, A. Marieke, Robert A. Beagrie, Matthew Gosden, et al.. (2020). Dynamics of the 4D genome during in vivo lineage specification and differentiation. Nature Communications. 11(1). 2722–2722. 77 indexed citations

Cheong, Pak Leng, Aude-Anaïs Olijnik, Jill M. Brown, et al.. (2018). Robust CRISPR/Cas9 Genome Editing of the HUDEP-2 Erythroid Precursor Line Using Plasmids and Single-Stranded Oligonucleotide Donors. Methods and Protocols. 1(3). 28–28. 17 indexed citations

Oudelaar, A. Marieke, James Davies, Lars L. P. Hanssen, et al.. (2018). Single-allele chromatin interactions identify regulatory hubs in dynamic compartmentalized domains. Nature Genetics. 50(12). 1744–1751. 134 indexed citations

Kowalczyk, Monika S., Jim R. Hughes, David Garrick, et al.. (2012). Intragenic Enhancers Act as Alternative Promoters. Molecular Cell. 45(4). 447–458. 194 indexed citations

Renella, Raffaele, Nigel Roberts, Jill M. Brown, et al.. (2011). Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1α localization in erythroblasts. Blood. 117(25). 6928–6938. 34 indexed citations

Hong, Dengli, Rajeev Gupta, Philip Ancliff, et al.. (2008). Initiating and Cancer-Propagating Cells in TEL-AML1 -Associated Childhood Leukemia. Science. 319(5861). 336–339. 260 indexed citations

Buckle, Veronica J. & Robert E. Kearney. (2001). Cytogenetics in haematology. 2 indexed citations

10.

Harris, Peter C., Raymond L. Stallings, Martijn H. Breuning, et al.. (1994). A Large Duplicated Area in the Polycystic Kidney Disease 1 (PKD1) Region of Chromosome 16 Is Prone to Rearrangement. Genomics. 23(2). 321–330. 12 indexed citations

11.

Boultwood, Jacqueline, et al.. (1993). MOLECULAR MAPPING OF THE 7Q-DELETION IN MYELOID DISORDERS. Blood. 82. 3 indexed citations

12.

Flynn, Geraldine, Mark C. Hirst, Samantha J.L. Knight, et al.. (1993). Identification of the FRAXE fragile site in two families ascertained for X linked mental retardation.. Journal of Medical Genetics. 30(2). 97–100. 52 indexed citations

13.

Buckle, Veronica J., E.P. Evans, Andrew C.G. Porter, et al.. (1993). Telomere directed fragmentation of mammalian chromosomes. Nucleic Acids Research. 21(1). 27–36. 124 indexed citations

14.

Itzhaki, Jane E., et al.. (1992). Targeted breakage of a human chromosome mediated by cloned human telomeric DNA. Nature Genetics. 2(4). 283–287. 71 indexed citations

15.

Boultwood, Jacqueline, Gail Abrahamson, Veronica J. Buckle, et al.. (1990). Structure of the granulocyte macrophage colony‐stimulating factor gene in patients with the myelodysplastic syndromes. American Journal of Hematology. 34(2). 157–158. 2 indexed citations

16.

Ballabio, Andrea, Giancarlo Parenti, Rosalba Carrozzo, et al.. (1987). Isolation and characterization of a steroid sulfatase cDNA clone: genomic deletions in patients with X-chromosome-linked ichthyosis.. Proceedings of the National Academy of Sciences. 84(13). 4519–4523. 115 indexed citations

17.

Buckle, Veronica J., Yvonne Boyd, Niall J. Fraser, et al.. (1987). Localisation of Y chromosome sequences in normal and 'XX' males.. Journal of Medical Genetics. 24(4). 197–203. 27 indexed citations

18.

Buckle, Veronica J., Peter Scambler, & Brandon J. Wainwright. (1987). Localisation of a sequence, 7C22, showing close linkage to the cystic fibrosis locus. Cytogenetic and Genome Research. 44(1). 41–42. 7 indexed citations

19.

Searle, A.G., J. Peters, Mary F. Lyon, et al.. (1987). Chromosome maps of man and mouse, III. Genomics. 1(1). 3–18. 148 indexed citations

20.

Craig, S.P., Veronica J. Buckle, A. Lamouroux, Jacques Mallet, & Ian Craig. (1986). Localization of the human tyrosine hydroxylase gene to 11p15: gene duplication and evolution of metabolic pathways. Cytogenetic and Genome Research. 42(1-2). 29–32. 58 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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