Amanda J. Walne

4.9k total citations
36 papers, 3.0k citations indexed

About

Amanda J. Walne is a scholar working on Physiology, Molecular Biology and Immunology. According to data from OpenAlex, Amanda J. Walne has authored 36 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Physiology, 21 papers in Molecular Biology and 9 papers in Immunology. Recurrent topics in Amanda J. Walne's work include Telomeres, Telomerase, and Senescence (28 papers), DNA Repair Mechanisms (7 papers) and Neutrophil, Myeloperoxidase and Oxidative Mechanisms (5 papers). Amanda J. Walne is often cited by papers focused on Telomeres, Telomerase, and Senescence (28 papers), DNA Repair Mechanisms (7 papers) and Neutrophil, Myeloperoxidase and Oxidative Mechanisms (5 papers). Amanda J. Walne collaborates with scholars based in United Kingdom, United States and Germany. Amanda J. Walne's co-authors include Inderjeet Dokal, Tom Vulliamy, Anna Marrone, Michael Kirwan, Richard Beswick, Philip J. Mason, Vincent Plagnol, Richard Szydlo, S. W. Knight and Hemanth Tummala and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Amanda J. Walne

36 papers receiving 3.0k citations

Peers

Amanda J. Walne

PHYSI

GENET

IMMUN

HEMAT

Anna Marrone United Kingdom

Goro Sashida Japan

Seishi Kyoizumi Japan

Johan Flygare Sweden

Yojiro Arinobu Japan

Yoshiaki Kubo Japan

Stella T. Chou United States

Bodil Strömbeck Sweden

Carmela P. Morales United States

Ming Tang China

Anna Marrone United Kingdom

Amanda J. Walne

2.1k ×1.1

PHYSI

1.6k ×1.0

278 ×0.6

GENET

278 ×0.7

IMMUN

237 ×0.7

HEMAT

Citations per year, relative to Amanda J. Walne Amanda J. Walne (= 1×) peers Anna Marrone

Countries citing papers authored by Amanda J. Walne

Since Specialization

Citations

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

Fields of papers citing papers by Amanda J. Walne

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amanda J. Walne

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

Tummala, Hemanth, Amanda J. Walne, Roberto Buccafusca, et al.. (2022). Germline thymidylate synthase deficiency impacts nucleotide metabolism and causes dyskeratosis congenita. The American Journal of Human Genetics. 109(8). 1472–1483. 13 indexed citations

Norris, Kevin, Amanda J. Walne, Mark Ponsford, et al.. (2021). High-throughput STELA provides a rapid test for the diagnosis of telomere biology disorders. Human Genetics. 140(6). 945–955. 16 indexed citations

Tummala, Hemanth, Amanda J. Walne, Findlay Bewicke‐Copley, et al.. (2020). A frameshift variant in specificity protein 1 triggers superactivation of Sp1-mediated transcription in familial bone marrow failure. Proceedings of the National Academy of Sciences. 117(29). 17151–17155. 4 indexed citations

Tummala, Hemanth, Amanda J. Walne, Mike Williams, et al.. (2016). DNAJC21 Mutations Link a Cancer-Prone Bone Marrow Failure Syndrome to Corruption in 60S Ribosome Subunit Maturation. The American Journal of Human Genetics. 99(1). 115–124. 73 indexed citations

Collopy, Laura C., Amanda J. Walne, Shirleny Cardoso, et al.. (2015). Triallelic and epigenetic-like inheritance in human disorders of telomerase. Blood. 126(2). 176–184. 33 indexed citations

Tummala, Hemanth, Amanda J. Walne, Laura C. Collopy, et al.. (2015). Poly(A)-specific ribonuclease deficiency impacts telomere biology and causes dyskeratosis congenita. Journal of Clinical Investigation. 125(5). 2151–2160. 134 indexed citations

Tummala, Hemanth, Michael Kirwan, Amanda J. Walne, et al.. (2014). ERCC6L2 Mutations Link a Distinct Bone-Marrow-Failure Syndrome to DNA Repair and Mitochondrial Function. The American Journal of Human Genetics. 94(2). 246–256. 43 indexed citations

Kirwan, Michael, Amanda J. Walne, Vincent Plagnol, et al.. (2012). Exome Sequencing Identifies Autosomal-Dominant SRP72 Mutations Associated with Familial Aplasia and Myelodysplasia. The American Journal of Human Genetics. 90(5). 888–892. 71 indexed citations

Blaydon, Diana C., Paolo Biancheri, Wei‐Li Di, et al.. (2011). Inflammatory Skin and Bowel Disease Linked toADAM17Deletion. New England Journal of Medicine. 365(16). 1502–1508. 235 indexed citations

10.

Kirwan, Michael, Richard Beswick, Amanda J. Walne, et al.. (2011). Dyskeratosis congenita and the DNA damage response. British Journal of Haematology. 153(5). 634–643. 26 indexed citations

11.

Vulliamy, Tom, Michael Kirwan, Richard Beswick, et al.. (2011). Differences in Disease Severity but Similar Telomere Lengths in Genetic Subgroups of Patients with Telomerase and Shelterin Mutations. PLoS ONE. 6(9). e24383–e24383. 70 indexed citations

12.

Walne, Amanda J., Tom Vulliamy, Richard Beswick, Michael Kirwan, & Inderjeet Dokal. (2010). Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund–Thomson syndrome. Human Molecular Genetics. 19(22). 4453–4461. 68 indexed citations

13.

Walne, Amanda J. & Inderjeet Dokal. (2009). Advances in the understanding of dyskeratosis congenita. British Journal of Haematology. 145(2). 164–172. 126 indexed citations

14.

Kirwan, Michael, Tom Vulliamy, Anna Marrone, et al.. (2009). Defining the pathogenic role of telomerase mutations in myelodysplastic syndrome and acute myeloid leukemia. Human Mutation. 30(11). 1567–1573. 88 indexed citations

15.

Vulliamy, Tom, Richard Beswick, Michael Kirwan, et al.. (2008). Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita. Proceedings of the National Academy of Sciences. 105(23). 8073–8078. 235 indexed citations

16.

Kirwan, Michael, Richard Beswick, Tom Vulliamy, et al.. (2008). Exogenous TERC alone can enhance proliferative potential, telomerase activity and telomere length in lymphocytes from dyskeratosis congenita patients. British Journal of Haematology. 144(5). 771–781. 29 indexed citations

17.

Walne, Amanda J. & Inderjeet Dokal. (2007). Dyskeratosis Congenita: A historical perspective. Mechanisms of Ageing and Development. 129(1-2). 48–59. 54 indexed citations

18.

Walne, Amanda J., Anna Marrone, & Inderjeet Dokal. (2005). Dyskeratosis Congenita: A Disorder of Defective Telomere Maintenance?. International Journal of Hematology. 82(3). 184–189. 34 indexed citations

19.

Vulliamy, Tom, Amanda J. Walne, Aroon Baskaradas, et al.. (2005). Mutations in the reverse transcriptase component of telomerase (TERT) in patients with bone marrow failure. Blood Cells Molecules and Diseases. 34(3). 257–263. 148 indexed citations

20.

Walne, Amanda J., Paul J. Jenkins, Ian James, & P.N. Plowman. (1997). Pyridinium crosslinks in the monitoring of patients with bone metastases from carcinoma of the breast. Clinical Oncology. 9(1). 30–34. 5 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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