Anne Seawright

2.6k total citations
22 papers, 1.9k citations indexed

About

Anne Seawright is a scholar working on Molecular Biology, Genetics and Organic Chemistry. According to data from OpenAlex, Anne Seawright has authored 22 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 9 papers in Genetics and 1 paper in Organic Chemistry. Recurrent topics in Anne Seawright's work include Renal and related cancers (11 papers), Developmental Biology and Gene Regulation (8 papers) and Animal Genetics and Reproduction (5 papers). Anne Seawright is often cited by papers focused on Renal and related cancers (11 papers), Developmental Biology and Gene Regulation (8 papers) and Animal Genetics and Reproduction (5 papers). Anne Seawright collaborates with scholars based in United Kingdom, United States and Hungary. Anne Seawright's co-authors include Veronica van Heyningen, Isabel M. Hanson, Nicholas D. Hastie, Shirley Hodgson, Penny Rashbass, Dieter Engelkamp, Dirk A. Kleinjan, Jane Prosser, Tim Jordan and Wendy A. Bickmore and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Anne Seawright

22 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anne Seawright United Kingdom 18 1.6k 580 161 145 139 22 1.9k
Carl C.T. Ton United States 13 1.8k 1.1× 661 1.1× 223 1.4× 218 1.5× 111 0.8× 16 2.2k
Kathleen A. Williamson United Kingdom 21 1.2k 0.7× 836 1.4× 228 1.4× 87 0.6× 72 0.5× 35 1.8k
Christine Vincent France 19 1.5k 0.9× 542 0.9× 108 0.7× 147 1.0× 139 1.0× 27 2.0k
Walter Pretsch Germany 19 1.1k 0.7× 322 0.6× 88 0.5× 84 0.6× 41 0.3× 60 1.4k
Jane Prosser United Kingdom 8 1.6k 1.0× 564 1.0× 253 1.6× 172 1.2× 109 0.8× 9 1.9k
Dirk A. Kleinjan United Kingdom 21 1.6k 1.0× 921 1.6× 164 1.0× 77 0.5× 67 0.5× 30 2.1k
Peter Gruss Germany 19 1.9k 1.2× 847 1.5× 93 0.6× 187 1.3× 133 1.0× 24 2.5k
Oleg V. Lagutin United States 16 2.0k 1.3× 500 0.9× 119 0.7× 342 2.4× 251 1.8× 27 2.6k
Claudia Walther Germany 8 2.5k 1.6× 733 1.3× 129 0.8× 381 2.6× 375 2.7× 8 2.9k
Xunlei Zhou Germany 20 1.6k 1.0× 478 0.8× 139 0.9× 226 1.6× 159 1.1× 29 2.0k

Countries citing papers authored by Anne Seawright

Since Specialization
Citations

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

Fields of papers citing papers by Anne Seawright

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Seawright

This figure shows the co-authorship network connecting the top 25 collaborators of Anne Seawright. A scholar is included among the top collaborators of Anne Seawright 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 Anne Seawright. Anne Seawright 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.
Rainger, Joe, Kathleen A. Williamson, Dinesh C. Soares, et al.. (2017). A recurrent de novo mutation inACTG1causes isolated ocular coloboma. Human Mutation. 38(8). 942–946. 20 indexed citations
2.
Tate, Peri, Andrew J. Finch, Joseph Shaw, et al.. (2014). Kdm3a lysine demethylase is an Hsp90 client required for cytoskeletal rearrangements during spermatogenesis. Molecular Biology of the Cell. 25(8). 1216–1233. 30 indexed citations
3.
Kleinjan, Dirk A., Philippe Gautier, Ralf Dahm, et al.. (2008). Subfunctionalization of Duplicated Zebrafish pax6 Genes by cis-Regulatory Divergence. PLoS Genetics. 4(2). e29–e29. 128 indexed citations
4.
Kleinjan, Dirk A., Anne Seawright, Sébastien Mella, et al.. (2006). Long-range downstream enhancers are essential for Pax6 expression. Developmental Biology. 299(2). 563–581. 109 indexed citations
5.
Kleinjan, Dirk A., Anne Seawright, Andrew J. Childs, & Veronica van Heyningen. (2003). Conserved elements in Pax6 intron 7 involved in (auto)regulation and alternative transcription. Developmental Biology. 265(2). 462–477. 88 indexed citations
6.
Kleinjan, Dirk A., Anne Seawright, Greg Elgar, & Veronica van Heyningen. (2002). Characterization of a novel gene adjacent to PAX6, revealing synteny conservation with functional significance. Mammalian Genome. 13(2). 102–107. 38 indexed citations
7.
Axton, Richard A, et al.. (1997). Combined SSCP/heteroduplex analysis in the screening for PAX6 mutations. Molecular and Cellular Probes. 11(4). 287–292. 26 indexed citations
8.
Slorach, Euan M., Mihael H. Polymeropoulos, Kathryn L. Evans, et al.. (1995). Regional localisation of 19 brain expressed sequence tags to human chromosome 11 using PCR amplification of somatic cell hybrid DNAs. Cytogenetic and Genome Research. 70(1-2). 71–75. 3 indexed citations
9.
James, Michael R., Charles W. Richard, Rosella Mollicone, et al.. (1994). The gene encoding myeloid α-3-fucosyltransferase (FUT4) is located between D11S388 and D11S919 on 11q21. Cytogenetic and Genome Research. 66(2). 104–106. 24 indexed citations
10.
Hanson, Isabel M., et al.. (1993). PAX6 mutations in aniridia. Human Molecular Genetics. 2(7). 915–920. 147 indexed citations
11.
Sherrington, Paul D., A. Förster, Anne Seawright, Veronica van Heyningen, & Terence H. Rabbitts. (1992). Human RAG2, like RAGI, is on chromosome II band p13 and therefore not linked to ataxia telangiectasia complementation groups. Genes Chromosomes and Cancer. 5(4). 404–406. 6 indexed citations
12.
Hanson, Isabel M., Anne Seawright, & Veronica van Heyningen. (1992). The human BDNF gene maps between FSHB and HVBS1 at the boundary of 11p13–p14. Genomics. 13(4). 1331–1333. 67 indexed citations
13.
Jordan, Tim, Isabel M. Hanson, Shirley Hodgson, et al.. (1992). The human PAX6 gene is mutated in two patients with aniridia. Nature Genetics. 1(5). 328–332. 431 indexed citations
14.
Bickmore, Wendy A., et al.. (1992). Modulation of DNA Binding Specificity by Alternative Splicing of the Wilms Tumor wt1 Gene Transcript. Science. 257(5067). 235–237. 195 indexed citations
15.
Little, Melissa H., R. C. Dunn, Jennifer A. Byrne, et al.. (1992). Equivalent expression of paternally and maternally inherited WT1 alleles in normal fetal tissue and Wilms' tumours.. PubMed. 7(4). 635–41. 48 indexed citations
16.
Heyningen, Veronica van, Wendy A. Bickmore, Anne Seawright, et al.. (1990). Role for the Wilms tumor gene in genital development?. Proceedings of the National Academy of Sciences. 87(14). 5383–5386. 70 indexed citations
17.
Bickmore, Wendy A., David J. Porteous, Sheila Christie, et al.. (1989). CpG islands surround a DNA segment located between translocation breakpoints associated with genitourinary dysplasia and aniridia. Genomics. 5(4). 685–693. 17 indexed citations
18.
Seawright, Anne, Judy Fletcher, Judy Fantes, et al.. (1988). Analysis of WAGR deletions and related translocations with gene-specific DNA probes, using FACS-selected cell hybrids. Somatic Cell and Molecular Genetics. 14(1). 21–30. 18 indexed citations
19.
Porteous, David J., Wendy A. Bickmore, S. Christie, et al.. (1987). HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13.. Proceedings of the National Academy of Sciences. 84(15). 5355–5359. 64 indexed citations
20.
Boyd, Patricia A., Veronica van Heyningen, Anne Seawright, György Fekete, & Nicholas D. Hastie. (1986). Use of catalase polymorphisms in the study of sporadic aniridia. Human Genetics. 73(2). 171–174. 17 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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