Bruce E. Hayward

6.4k total citations
54 papers, 2.9k citations indexed

About

Bruce E. Hayward is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Bruce E. Hayward has authored 54 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 34 papers in Genetics and 9 papers in Surgery. Recurrent topics in Bruce E. Hayward's work include Genetics and Neurodevelopmental Disorders (19 papers), Genetic Syndromes and Imprinting (11 papers) and Epigenetics and DNA Methylation (8 papers). Bruce E. Hayward is often cited by papers focused on Genetics and Neurodevelopmental Disorders (19 papers), Genetic Syndromes and Imprinting (11 papers) and Epigenetics and DNA Methylation (8 papers). Bruce E. Hayward collaborates with scholars based in United Kingdom, United States and France. Bruce E. Hayward's co-authors include David T. Bonthron, Eamonn Sheridan, Lisa Strain, Veronica Moran, Karen Usdin, Ian Carr, Michel De Vos, Graham R. Taylor, Aruna Asipu and Márta Korbonits and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Bruce E. Hayward

53 papers receiving 2.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bruce E. Hayward United Kingdom 27 1.7k 1.3k 481 418 384 54 2.9k
Hidenobu Soejima Japan 35 2.6k 1.5× 1.2k 0.9× 655 1.4× 466 1.1× 91 0.2× 117 3.4k
Monique Losekoot Netherlands 34 1.4k 0.8× 1.3k 1.0× 310 0.6× 259 0.6× 762 2.0× 125 3.1k
Claudia Ruivenkamp Netherlands 31 1.8k 1.0× 1.8k 1.4× 393 0.8× 292 0.7× 296 0.8× 79 3.4k
Sarina G. Kant Netherlands 26 1.4k 0.8× 1.3k 1.0× 325 0.7× 131 0.3× 451 1.2× 70 2.7k
Michele Rubini Italy 25 1.7k 1.0× 841 0.6× 114 0.2× 535 1.3× 1.1k 2.9× 76 3.3k
Lawrence S. Mathews United States 28 3.0k 1.7× 1.1k 0.8× 242 0.5× 318 0.8× 1.9k 4.9× 35 4.7k
Laura K. Conlin United States 27 1.2k 0.7× 1.6k 1.2× 561 1.2× 161 0.4× 83 0.2× 73 2.5k
Elizabeth Robertson Germany 5 2.2k 1.2× 724 0.5× 378 0.8× 306 0.7× 1.4k 3.6× 12 3.6k
Digamber S. Borgaonkar United States 20 1.1k 0.7× 955 0.7× 226 0.5× 257 0.6× 192 0.5× 66 2.4k
Tsunehiro Mukai Japan 30 2.3k 1.3× 1.4k 1.1× 687 1.4× 304 0.7× 69 0.2× 78 2.8k

Countries citing papers authored by Bruce E. Hayward

Since Specialization
Citations

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

Fields of papers citing papers by Bruce E. Hayward

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bruce E. Hayward. 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 Bruce E. Hayward. The network helps show where Bruce E. Hayward may publish in the future.

Co-authorship network of co-authors of Bruce E. Hayward

This figure shows the co-authorship network connecting the top 25 collaborators of Bruce E. Hayward. A scholar is included among the top collaborators of Bruce E. Hayward 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 Bruce E. Hayward. Bruce E. Hayward 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.
Hayward, Bruce E., et al.. (2025). Repeat expansion in a fragile X model is independent of double strand break repair mediated by Pol θ, RAD52, RAD54 or RAD54B. Scientific Reports. 15(1). 5033–5033. 1 indexed citations
2.
Aishworiya, Ramkumar, Bruce E. Hayward, Karen Usdin, et al.. (2023). Clinical implications of somatic allele expansion in female FMR1 premutation carriers. Scientific Reports. 13(1). 7050–7050. 5 indexed citations
3.
Zhao, Xiao-Nan, Daman Kumari, Carson J. Miller, et al.. (2021). Modifiers of Somatic Repeat Instability in Mouse Models of Friedreich Ataxia and the Fragile X-Related Disorders: Implications for the Mechanism of Somatic Expansion in Huntington’s Disease. Journal of Huntington s Disease. 10(1). 149–163. 18 indexed citations
4.
Hayward, Bruce E., Peter Steinbach, & Karen Usdin. (2020). A point mutation in the nuclease domain of MLH3 eliminates repeat expansions in a mouse stem cell model of the Fragile X-related disorders. Nucleic Acids Research. 48(14). 7856–7863. 24 indexed citations
5.
Gazy, Inbal, et al.. (2018). Double-strand break repair plays a role in repeat instability in a fragile X mouse model. DNA repair. 74. 63–69. 21 indexed citations
6.
Diggle, Christine P., Isabel Martínez‐Garay, Zoltán Molnár, et al.. (2017). A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain development. PLoS ONE. 12(4). e0174264–e0174264. 23 indexed citations
7.
Hayward, Bruce E., Daman Kumari, & Karen Usdin. (2017). Recent advances in assays for the fragile X-related disorders. Human Genetics. 136(10). 1313–1327. 8 indexed citations
8.
Yudkin, Dmitry V., Bruce E. Hayward, Mirit I. Aladjem, Daman Kumari, & Karen Usdin. (2014). Chromosome fragility and the abnormal replication of the FMR1 locus in fragile X syndrome. Human Molecular Genetics. 23(11). 2940–2952. 39 indexed citations
9.
Rehwinkel, Jan, Jonathan Maelfait, Anne Bridgeman, et al.. (2013). SAMHD1‐dependent retroviral control and escape in mice. The EMBO Journal. 32(18). 2454–2462. 123 indexed citations
10.
Parry, David, Clare V. Logan, Bruce E. Hayward, et al.. (2011). Mutations Causing Familial Biparental Hydatidiform Mole Implicate C6orf221 as a Possible Regulator of Genomic Imprinting in the Human Oocyte. The American Journal of Human Genetics. 89(3). 451–458. 174 indexed citations
11.
Wood, Henry M., Ornella Belvedere, Caroline Conway, et al.. (2010). Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens. Nucleic Acids Research. 38(14). e151–e151. 83 indexed citations
12.
Abdollahi, Mohammad Reza, Ewan E. Morrison, Tamara Sirey, et al.. (2009). Mutation of the Variant α-Tubulin TUBA8 Results in Polymicrogyria with Optic Nerve Hypoplasia. The American Journal of Human Genetics. 85(5). 737–744. 122 indexed citations
13.
Hayward, Bruce E., Michel De Vos, Elizabeth M. A. Valleley, et al.. (2007). Extensive gene conversion at thePMS2DNA mismatch repair locus. Human Mutation. 28(5). 424–430. 43 indexed citations
14.
Vos, Michel De, Bruce E. Hayward, Ruth Charlton, et al.. (2006). PMS2 Mutations in Childhood Cancer. JNCI Journal of the National Cancer Institute. 98(5). 358–361. 63 indexed citations
15.
16.
Hayward, Bruce E., et al.. (2002). A global disorder of imprinting in the human female germ line. Nature. 416(6880). 539–542. 170 indexed citations
17.
Kozak, Maciej, Bruce E. Hayward, Dominika Borek, David T. Bonthron, & Mariusz Jaskólski. (2001). Expression, purification and preliminary crystallographic studies of human ketohexokinase. Acta Crystallographica Section D Biological Crystallography. 57(4). 586–588. 4 indexed citations
18.
Hayward, Bruce E., Anne Barlier, Márta Korbonits, et al.. (2001). Imprinting of the Gsα gene GNAS1 in the pathogenesis of acromegaly. Journal of Clinical Investigation. 107(6). R31–R36. 231 indexed citations
19.
Hayward, Bruce E., et al.. (1997). Recombination Creates Novel L1 (LINE-1) Elements in Rattus norvegicus. Genetics. 146(2). 641–654. 44 indexed citations
20.
Hayward, Bruce E., Judy Fantes, Jon Warner, et al.. (1996). Co-localization of the ketohexokinase and glucokinase regulator genes to a 500-kb region of Chromosome 2p23. Mammalian Genome. 7(6). 454–458. 21 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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