A. J. Jeffreys

1.5k total citations
25 papers, 1.2k citations indexed

About

A. J. Jeffreys is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, A. J. Jeffreys has authored 25 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 14 papers in Genetics and 3 papers in Hematology. Recurrent topics in A. J. Jeffreys's work include CRISPR and Genetic Engineering (5 papers), DNA Repair Mechanisms (4 papers) and Genetic Mapping and Diversity in Plants and Animals (4 papers). A. J. Jeffreys is often cited by papers focused on CRISPR and Genetic Engineering (5 papers), DNA Repair Mechanisms (4 papers) and Genetic Mapping and Diversity in Plants and Animals (4 papers). A. J. Jeffreys collaborates with scholars based in United Kingdom, Switzerland and Netherlands. A. J. Jeffreys's co-authors include Andrew Collick, Robert G. Kelly, Mark Gibbs, Grahame Bulfield, Zeng Hao Wong, Christopher G. Mathew, Karen L. Thorpe, Bruce A.J. Ponder, Barbara A. Smith and Nicola J. Royle and has published in prestigious journals such as Nature, Nucleic Acids Research and Cancer.

In The Last Decade

A. J. Jeffreys

25 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. J. Jeffreys United Kingdom 17 697 470 223 160 110 25 1.2k
Gregory B. Peters Australia 21 773 1.1× 420 0.9× 116 0.5× 120 0.8× 92 0.8× 33 1.3k
Heinz-Ulrich Weier United States 13 1.1k 1.6× 658 1.4× 363 1.6× 155 1.0× 189 1.7× 16 1.8k
Zeng Hao Wong United Kingdom 8 389 0.6× 292 0.6× 76 0.3× 85 0.5× 48 0.4× 12 783
Judith Stamberg United States 18 606 0.9× 208 0.4× 242 1.1× 55 0.3× 242 2.2× 53 1.2k
Pierre Fouchet France 21 878 1.3× 336 0.7× 114 0.5× 177 1.1× 233 2.1× 46 1.5k
Tommy Gerdes Denmark 20 620 0.9× 859 1.8× 358 1.6× 201 1.3× 27 0.2× 31 1.4k
Richard J. Shaw United States 3 566 0.8× 437 0.9× 155 0.7× 271 1.7× 26 0.2× 6 1.0k
H. D. Hager Germany 7 745 1.1× 442 0.9× 397 1.8× 197 1.2× 44 0.4× 10 1.1k
S. A. Schonberg United States 12 1.1k 1.5× 627 1.3× 227 1.0× 361 2.3× 210 1.9× 14 1.8k
Ignasi Roig Spain 24 1.7k 2.4× 483 1.0× 311 1.4× 238 1.5× 385 3.5× 45 2.2k

Countries citing papers authored by A. J. Jeffreys

Since Specialization
Citations

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

Fields of papers citing papers by A. J. Jeffreys

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. J. Jeffreys

This figure shows the co-authorship network connecting the top 25 collaborators of A. J. Jeffreys. A scholar is included among the top collaborators of A. J. Jeffreys 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 A. J. Jeffreys. A. J. Jeffreys 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.
Buard, Jérôme, Andrew Collick, Jane Brown, & A. J. Jeffreys. (2000). Somatic versus Germline Mutation Processes at Minisatellite CEB1 (D2S90) in Humans and Transgenic Mice. Genomics. 65(2). 95–103. 34 indexed citations
2.
Jeffreys, A. J.. (2000). High resolution analysis of haplotype diversity and meiotic crossover in the human TAP2 recombination hotspot. Human Molecular Genetics. 9(5). 725–733. 169 indexed citations
3.
Signer, Esther, A. J. Jeffreys, & Yuri E. Dubrova. (2000). Are DNA profiles breed‐specific? A pilot study in pigs. Animal Genetics. 31(4). 273–276. 4 indexed citations
4.
Tamaki, Keiji, Celia A. May, Yuri E. Dubrova, & A. J. Jeffreys. (1999). Extremely Complex Repeat Shuffling during Germline Mutation at Human Minisatellite B6.7. Human Molecular Genetics. 8(5). 879–888. 47 indexed citations
5.
Bois, Philippe R.J., John D. H. Stead, Jill Williamson, et al.. (1998). Isolation and Characterization of Mouse Minisatellites. Genomics. 50(3). 317–330. 25 indexed citations
6.
Jeffreys, A. J.. (1997). Somatic mutation processes at a human minisatellite. Human Molecular Genetics. 6(1). 129–132. 86 indexed citations
7.
Allen, Maxine, et al.. (1994). Tandemly repeated transgenes of the human minisatellite MS32 (D1S8), with novel mouse gamma satellite integration. Nucleic Acids Research. 22(15). 2976–2981. 21 indexed citations
8.
Allen, Maxine, Andrew Collick, & A. J. Jeffreys. (1994). Use of vectorette and subvectorette PCR to isolate transgene flanking DNA.. Genome Research. 4(2). 71–75. 21 indexed citations
9.
Signer, Esther, et al.. (1994). DNA variability and parentage testing in captive Waldrapp ibises. Molecular Ecology. 3(4). 291–300. 23 indexed citations
10.
Royle, Nicola J., John A.L. Armour, Moira Crosier, & A. J. Jeffreys. (1993). Abnormal segregation of alleles in CEPH pedigree DNAs arising from allele loss in lymphoblastoid DNA. Trends in Genetics. 9(7). 232–232. 1 indexed citations
11.
Armour, John A.L. & A. J. Jeffreys. (1992). Biology and applications of human minisatellite loci. Current Opinion in Genetics & Development. 2(6). 850–856. 42 indexed citations
12.
Fisher, Rosemary A., A. J. Jeffreys, Geoffrey M. Boxer, et al.. (1992). Gestational and nongestational trophoblastic tumors distinguished by DNA analysis. Cancer. 69(3). 839–845. 86 indexed citations
13.
Jeffreys, A. J., Victoria Wilson, & S L Thein. (1992). Hypervariable 'minisatellite' regions in human DNA. 1985.. PubMed. 24. 467–72. 21 indexed citations
14.
Kelly, Robert G., Mark Gibbs, Andrew Collick, & A. J. Jeffreys. (1991). Spontaneous mutation at the hypervariable mouse minisatellite locusMs6-hm: flanking DNA sequence and analysis of germline and early somatic mutation events. Proceedings of the Royal Society B Biological Sciences. 245(1314). 235–245. 53 indexed citations
15.
Bellamy, Richard, et al.. (1991). Increased band sharing in DNA fingerprints of an inbred human population. Human Genetics. 87(3). 341–7. 11 indexed citations
16.
Hillel, J., T. Schaap, A. Haberfeld, et al.. (1990). DNA fingerprints applied to gene introgression in breeding programs.. Genetics. 124(3). 783–789. 110 indexed citations
17.
Kelly, Robert G., Grahame Bulfield, Andrew Collick, Mark Gibbs, & A. J. Jeffreys. (1989). Characterization of a highly unstable mouse minisatellite locus: Evidence for somatic mutation during early development. Genomics. 5(4). 844–856. 169 indexed citations
18.
Hutchinson, R. M., et al.. (1989). Rapid identification of donor and recipient cells after allogeneic bone marrow transplantation using specific genetic markers. British Journal of Haematology. 72(2). 133–140. 16 indexed citations
19.
Thein, SL, D G Oscier, A. J. Jeffreys, et al.. (1988). Detection of chromosomal 7 loss in myelodysplasia using an extremely polymorphic DNA probe. British Journal of Cancer. 57(2). 131–134. 13 indexed citations
20.
Clarke, B. C., Amy K. Robertson, & A. J. Jeffreys. (1987). The evolution of DNA sequences. OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information). 1 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026