Laura Arthur

452 total citations
21 papers, 271 citations indexed

About

Laura Arthur is a scholar working on Oncology, Cancer Research and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Laura Arthur has authored 21 papers receiving a total of 271 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Oncology, 11 papers in Cancer Research and 6 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Laura Arthur's work include Breast Cancer Treatment Studies (9 papers), HER2/EGFR in Cancer Research (6 papers) and Advanced Breast Cancer Therapies (5 papers). Laura Arthur is often cited by papers focused on Breast Cancer Treatment Studies (9 papers), HER2/EGFR in Cancer Research (6 papers) and Advanced Breast Cancer Therapies (5 papers). Laura Arthur collaborates with scholars based in United Kingdom, United States and France. Laura Arthur's co-authors include Arran Turnbull, Andrew H. Sims, Jeremy Thomas, Lorna Renshaw, J. Michael Dixon, J. Michael Dixon, Alexey A. Larionov, Charlene Kay, Mitch Dowsett and Anita K. Dunbier and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Oncology and Blood.

In The Last Decade

Laura Arthur

19 papers receiving 268 citations

Peers

Laura Arthur
Elisabeth Breit Germany
Orsolya Rusz Hungary
Christoph Suppan Austria
Ning Liao China
Nieves Perdigones United States
Max Salm United Kingdom
Wenbo Zheng China
Anna Barbro Sætersdal Norway
Judit Matito Spain
Elisabeth Breit Germany
Laura Arthur
Citations per year, relative to Laura Arthur Laura Arthur (= 1×) peers Elisabeth Breit

Countries citing papers authored by Laura Arthur

Since Specialization
Citations

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

Fields of papers citing papers by Laura Arthur

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Arthur

This figure shows the co-authorship network connecting the top 25 collaborators of Laura Arthur. A scholar is included among the top collaborators of Laura Arthur 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 Laura Arthur. Laura Arthur 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.
Vadakekolathu, Jayakumar, Laura Arthur, Melissa Tran, et al.. (2024). W-NK1 Choreographs Innate and Adaptive Immune Responses to Provide a Robust and Durable Anti-AML Response. Blood. 144(Supplement 1). 916–916. 3 indexed citations
2.
Rutella, Sergio, Amanda F. Cashen, John Muth, et al.. (2023). S129: ADOPTIVELY INFUSED MEMORY-LIKE (ML) NATURAL KILLER (NK) CELLS ELICIT ADAPTIVE IMMUNE RESPONSES IN PATIENTS WITH ACUTE MYELOID LEUKEMIA (AML). HemaSphere. 7(S3). e4299744–e4299744. 1 indexed citations
3.
Rutella, Sergio, John Muth, Jayakumar Vadakekolathu, et al.. (2023). WU-NK-101 (W-NK), a Memory-like (ML) NK Cell, Intrinsically Overcomes Factors Restricting Adoptive Cell Therapy (ACT) in Acute Myeloid Leukemia (AML). Blood. 142(Supplement 1). 466–466. 1 indexed citations
4.
Bhatnagar, Nupur, Vincent Petit, Jayakumar Vadakekolathu, et al.. (2023). WU-NK-101 (W-NK), a Memory-like (ML) NK Cell, Naturally Overcomes Tumor Microenvironment (TME) Metabolic Challenges, Retaining Anti-Tumor Potency. Blood. 142(Supplement 1). 4834–4834. 2 indexed citations
5.
6.
Turnbull, Arran, Laura Arthur, Carlos Martínez-Pérez, et al.. (2020). Abstract P1-18-07: Can some ER+/HER2+ patients be safely spared from treatment with chemotherapy plus herceptin?. Cancer Research. 80(4_Supplement). P1–18. 3 indexed citations
7.
Martínez-Pérez, Carlos, Charlene Kay, Laura Arthur, et al.. (2020). Abstract P6-16-04: IL6ST, a biomarker of endocrine therapy response, has potential in identifying a subgroup of women with ER+ DCIS who are more likely to benefit from adjuvant endocrine therapy. Cancer Research. 80(4_Supplement). P6–16. 1 indexed citations
8.
Dixon, J. Michael, David Cameron, Laura Arthur, et al.. (2019). Accurate Estrogen Receptor Quantification in Patients with Negative and Low-Positive Estrogen-Receptor-Expressing Breast Tumors: Sub-Analyses of Data from Two Clinical Studies. Advances in Therapy. 36(4). 828–841. 12 indexed citations
9.
Arthur, Laura, Carlos Martínez-Pérez, Lorna Renshaw, et al.. (2019). Abstract P3-10-26: Predicting benefit from HER2-targeted therapies in patients with ER+/HER2+ breast cancer. Cancer Research. 79(4_Supplement). P3–10. 1 indexed citations
10.
Arthur, Laura, Arran Turnbull, Lucy R. Khan, & J. Michael Dixon. (2017). Pre-operative Endocrine Therapy. Current Breast Cancer Reports. 9(4). 202–209. 17 indexed citations
11.
Turnbull, Arran, et al.. (2017). Margin width and local recurrence after breast conserving surgery for ductal carcinoma in situ. European Journal of Surgical Oncology. 43(11). 2029–2035. 10 indexed citations
12.
Martínez-Pérez, Carlos, Arran Turnbull, Laura Arthur, et al.. (2017). Current treatment trends and the need for better predictive tools in the management of ductal carcinoma in situ of the breast. Cancer Treatment Reviews. 55. 163–172. 29 indexed citations
13.
Arthur, Laura, Arran Turnbull, Lorna Renshaw, et al.. (2016). Tumour sampling method can significantly influence gene expression profiles derived from neoadjuvant window studies. Scientific Reports. 6(1). 29434–29434. 12 indexed citations
14.
Dixon, J. Michael, Arran Turnbull, Lorna Renshaw, et al.. (2015). Abstract P3-06-35: Association of estrogen receptor (ER) levels and prediction of antiproliferative effect of hormone therapy (HT) in lower ER-expressing tumors. Cancer Research. 75(9_Supplement). P3–6. 1 indexed citations
15.
Turnbull, Arran, Laura Arthur, Lorna Renshaw, et al.. (2015). Accurate Prediction and Validation of Response to Endocrine Therapy in Breast Cancer. Journal of Clinical Oncology. 33(20). 2270–2278. 72 indexed citations
16.
Arthur, Laura, Arran Turnbull, Alexey A. Larionov, et al.. (2014). Molecular Changes in Lobular Breast Cancers in Response to Endocrine Therapy. Cancer Research. 74(19). 5371–5376. 25 indexed citations
17.
18.
Arthur, Laura, Arran Turnbull, Lorna Renshaw, et al.. (2014). Changes in PIK3CA mutation status are not associated with recurrence, metastatic disease or progression in endocrine-treated breast cancer. Breast Cancer Research and Treatment. 147(1). 211–219. 31 indexed citations
19.
Moront, Matthew, et al.. (2014). Vacuum-Assisted Closure: A Novel Method of Managing Surgical Necrotizing Enterocolitis. European Journal of Pediatric Surgery. 25(1). 41–45. 7 indexed citations
20.
Arthur, Laura. (2004). Structural and functional analysis of Mre11-3. Nucleic Acids Research. 32(6). 1886–1893. 42 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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