Hayley Spearman

973 total citations
17 papers, 726 citations indexed

About

Hayley Spearman is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Hayley Spearman has authored 17 papers receiving a total of 726 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Neurology and 5 papers in Genetics. Recurrent topics in Hayley Spearman's work include Virus-based gene therapy research (5 papers), Myasthenia Gravis and Thymoma (4 papers) and Ion channel regulation and function (4 papers). Hayley Spearman is often cited by papers focused on Virus-based gene therapy research (5 papers), Myasthenia Gravis and Thymoma (4 papers) and Ion channel regulation and function (4 papers). Hayley Spearman collaborates with scholars based in United Kingdom, Malaysia and Denmark. Hayley Spearman's co-authors include David Beeson, Susan M. Kingsman, Judy Cossins, Osamu Higuchi, Yuji Yamanashi, Susan Maxwell, K. Binley, Sharifah Iqball, Clarke R. Slater and John Newsom–Davis and has published in prestigious journals such as Science, Journal of Biological Chemistry and Blood.

In The Last Decade

Hayley Spearman

17 papers receiving 716 citations

Peers

Hayley Spearman

NEURO

GENET

Vincent Abramowski France

Nikola Holtkamp Germany

Adrienne L. Watson United States

Monica Z. Wang United States

Jan Gronych Germany

P. Cornaglia‐Ferraris Italy

Jussara Hagen United States

Raimund Fahsold Germany

Yusuke Suenaga Japan

Yasuo Tohma Japan

Vincent Abramowski France

Hayley Spearman

555 ×1.5

309 ×1.5

NEURO

93 ×0.6

GENET

81 ×0.6

203 ×1.8

Citations per year, relative to Hayley Spearman Hayley Spearman (= 1×) peers Vincent Abramowski

Countries citing papers authored by Hayley Spearman

Since Specialization

Citations

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

Fields of papers citing papers by Hayley Spearman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hayley Spearman

This figure shows the co-authorship network connecting the top 25 collaborators of Hayley Spearman. A scholar is included among the top collaborators of Hayley Spearman 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 Hayley Spearman. Hayley Spearman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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17 of 17 papers shown

Johnson, Carrie E., Katharina Köhler, Hayley Spearman, et al.. (2025). Interactions between daily sleep-wake rhythms, γ-secretase, and amyloid-β peptide pathology point to complex underlying relationships. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1871(6). 167840–167840. 2 indexed citations

Brown, Philip J., Linden Lyne, Hayley Spearman, et al.. (2016). N-terminally truncated FOXP1 protein expression and alternate internal FOXP1 promoter usage in normal and malignant B cells. Haematologica. 101(7). 861–871. 7 indexed citations

Wong, Kah Keng, Duncan M. Gascoyne, Elizabeth J. Soilleux, et al.. (2016). FOXP2-positive diffuse large B-cell lymphomas exhibit a poor response to R-CHOP therapy and distinct biological signatures. Oncotarget. 7(33). 52940–52956. 17 indexed citations

Gascoyne, Duncan M., Linden Lyne, Hayley Spearman, et al.. (2016). Vitamin D Receptor Expression in Plasmablastic Lymphoma and Myeloma Cells Confers Susceptibility to Vitamin D. Endocrinology. 158(3). 503–515. 17 indexed citations

Gascoyne, Duncan M., Hayley Spearman, Linden Lyne, et al.. (2015). The Forkhead Transcription Factor FOXP2 Is Required for Regulation of p21WAF1/CIP1 in 143B Osteosarcoma Cell Growth Arrest. PLoS ONE. 10(6). e0128513–e0128513. 25 indexed citations

Brown, P., Kah Keng Wong, Suet Ling Felce, et al.. (2015). FOXP1 suppresses immune response signatures and MHC class II expression in activated B-cell-like diffuse large B-cell lymphomas. Leukemia. 30(3). 605–616. 46 indexed citations

Webster, Richard, Susan Maxwell, Hayley Spearman, et al.. (2012). A novel congenital myasthenic syndrome due to decreased acetylcholine receptor ion-channel conductance. Brain. 135(4). 1070–1080. 14 indexed citations

Lashley, Daniel, et al.. (2010). P51 Ephedrine treatment in DOK7 CMS and investigation of potential mechanisms. Neuromuscular Disorders. 20. S18–S18. 1 indexed citations

Beeson, David, Richard Webster, Judith Cossins, et al.. (2008). Congenital Myasthenic Syndromes and the Formation of the Neuromuscular Junction. Annals of the New York Academy of Sciences. 1132(1). 99–103. 20 indexed citations

10.

Vogt, Julie, Benjamin J. Harrison, Hayley Spearman, et al.. (2008). Mutation Analysis of CHRNA1, CHRNB1, CHRND, and RAPSN Genes in Multiple Pterygium Syndrome/Fetal Akinesia Patients. The American Journal of Human Genetics. 82(1). 222–227. 75 indexed citations

11.

Higuchi, Osamu, Kumiko Okada, Shun‐ichiro Iemura, et al.. (2007). Mutations Causing DOK7 Congenital Myasthenia Ablate Functional Motifs in Dok-7. Journal of Biological Chemistry. 283(9). 5518–5524. 55 indexed citations

12.

Beeson, David, Osamu Higuchi, Jackie Palace, et al.. (2006). Dok-7 Mutations Underlie a Neuromuscular Junction Synaptopathy. Science. 313(5795). 1975–1978. 201 indexed citations

13.

Binley, K., et al.. (2003). Hypoxia-mediated tumour targeting. Gene Therapy. 10(7). 540–549. 75 indexed citations

14.

Binley, Katie, Sharifah Iqball, Hayley Spearman, et al.. (2002). Long-term reversal of chronic anemia using a hypoxia-regulated erythropoietin gene therapy. Blood. 100(7). 2406–2413. 74 indexed citations

15.

Kan, O., Leigh G. Griffiths, Dilair Baban, et al.. (2001). Direct retroviral delivery of human cytochrome P450 2B6 for gene-directed enzyme prodrug therapy of cancer. Cancer Gene Therapy. 8(7). 473–482. 40 indexed citations

16.

Binley, K., Sharifah Iqball, Toby Price, et al.. (1999). Characterization of Physiologically Regulated Vectors for the Treatment of Ischemic Disease. Human Gene Therapy. 10(13). 2197–2208. 56 indexed citations

17.

Kan, O., Leigh G. Griffiths, Sharifah Iqball, et al.. (1999). Preclinical Evaluation of Human Cytochrome P450 2b6 (Cyp2b6) as a Therapeutic Gene Delivered by a Retroviral Vehicle for Gene-Directed Enzyme Prodrug Therapy (GDEPT) of Cancer. Nature Biotechnology. 17(S4). 37–37. 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.

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