Ruth Armstrong

6.2k total citations
16 papers, 108 citations indexed

About

Ruth Armstrong is a scholar working on Surgery, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Ruth Armstrong has authored 16 papers receiving a total of 108 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Surgery, 4 papers in Molecular Biology and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Ruth Armstrong's work include Parathyroid Disorders and Treatments (2 papers), Chromatin Remodeling and Cancer (2 papers) and Cancer Genomics and Diagnostics (2 papers). Ruth Armstrong is often cited by papers focused on Parathyroid Disorders and Treatments (2 papers), Chromatin Remodeling and Cancer (2 papers) and Cancer Genomics and Diagnostics (2 papers). Ruth Armstrong collaborates with scholars based in United Kingdom, France and Australia. Ruth Armstrong's co-authors include Jane May, Wolfgang Lösche, Stan Heptinstall, Ruth Casey, Katrina Andrews, Edward H. Thompson, Soo‐Mi Park, Mamta Joshi, Mary Jane Platt and Ian Seetho and has published in prestigious journals such as SHILAP Revista de lepidopterología, British Journal of Cancer and Thrombosis and Haemostasis.

In The Last Decade

Ruth Armstrong

14 papers receiving 96 citations

Peers

Ruth Armstrong

GENET

EPIDE

NEPHR

PFM

Caragh P. Stapleton Ireland

Paloma García de la Peña Spain

Shinichi Namba Japan

Constantinos G. Zografos Greece

Farid F. Kadyrov United States

Maria Kareva Russia

Hiroaki Obayashi Japan

S. Busco Italy

Navaratnam Kotea Mauritius

Joanna Lazier Canada

Caragh P. Stapleton Ireland

Ruth Armstrong

25 ×0.9

GENET

30 ×1.2

15 ×0.7

EPIDE

47 ×2.2

NEPHR

9 ×0.5

PFM

Citations per year, relative to Ruth Armstrong Ruth Armstrong (= 1×) peers Caragh P. Stapleton

Countries citing papers authored by Ruth Armstrong

Since Specialization

Citations

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

Fields of papers citing papers by Ruth Armstrong

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ruth Armstrong

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

All Works

Sort: Min cites: Since: Top N: Style:

16 of 16 papers shown

Whitworth, James, Ruth Armstrong, & Eamonn R. Maher. (2024). Wilms tumour resulting from paternal transmission of a TRIM28 pathogenic variant—A first report. European Journal of Human Genetics. 32(3). 361–364. 1 indexed citations

Watkins, James, John A. Tadross, Jennifer Harrington, et al.. (2024). Introduction and impact of routine whole genome sequencing in the diagnosis and management of sarcoma. British Journal of Cancer. 131(5). 860–869. 4 indexed citations

Monahan, Kevin, Neil Ryan, Laura Monje‐Garcia, et al.. (2023). The English National Lynch Syndrome transformation project: an NHS Genomic Medicine Service Alliance (GMSA) programme. SHILAP Revista de lepidopterología. 2(1). e000124–e000124. 9 indexed citations

Harper, Inês, Luigi Aloj, Ruth Armstrong, et al.. (2022). The use of temozolomide in paediatric metastatic phaeochromocytoma/paraganglioma: A case report and literature review. Frontiers in Endocrinology. 13. 1066208–1066208. 3 indexed citations

Andrews, Katrina, Edward H. Thompson, Ben Challis, et al.. (2020). Genetic testing for hereditary hyperparathyroidism and familial hypocalciuric hypercalcaemia in a large UK cohort. Clinical Endocrinology. 93(4). 409–418. 25 indexed citations

Armstrong, Ruth. (2019). Why We Sleep: The new science of sleep and dreams. Clinical Psychology Forum. 1(318). 55–56. 5 indexed citations

Andrews, Katrina, et al.. (2019). Genetic testing for hereditary hyperparathyroidism in a large UK cohort. Endocrine Abstracts. 2 indexed citations

Blyth, Moira, Ingrid Scurr, Peter D. Turnpenny, et al.. (2018). Extending the clinical and genetic spectrum of ARID2 related intellectual disability. A case series of 7 patients. European Journal of Medical Genetics. 62(1). 27–34. 9 indexed citations

Jedraszak, Guillaume, Bénédicte Demeer, Michèle Mathieu‐Dramard, et al.. (2015). Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: Six new patients. American Journal of Medical Genetics Part A. 167(3). 504–511. 17 indexed citations

10.

Tavares, Ana Lisa Taylor, Lionel Willatt, Ruth Armstrong, Ingrid Simonic, & Soo‐Mi Park. (2013). Mosaic Deletion of the NF1 Gene in a Patient With Cognitive Disability and Dysmorphic Features But Without Diagnostic Features of NF1. American Journal of Medical Genetics Part A. 161(5). 1185–1188. 4 indexed citations

11.

Jones, Todd C., et al.. (2013). Verbal Description Benefits for Faces When Description Conditions are Unknown a Priori. Quarterly Journal of Experimental Psychology. 66(9). 1818–1839. 5 indexed citations

12.

Armstrong, Ruth & Ann Gregory. (2012). Layers of complexity. The Medical Journal of Australia. 197(6). 311–311. 1 indexed citations

13.

Armstrong, Ruth, Emma McCann, Alan Fryer, Leanne Bricker, & Mary Jane Platt. (2009). A review of prenatally detected femoral abnormalities. Clinical Dysmorphology. 18(3). 127–130. 3 indexed citations

14.

Armstrong, Ruth, Alan Fryer, Sailaja Pisipati, & Edwin C. Jesudason. (2007). Evaluating the association between congenital cystic adenomatoid malformation of the lung and abdominal wall laxity. Clinical Dysmorphology. 16(2). 77–80.

15.

Armstrong, Ruth, Jane May, Wolfgang Lösche, & Stan Heptinstall. (1995). Factors that Contribute to Spontaneous Platelet Aggregation and Streptokinase-Induced Aggregation in Whole Blood. Thrombosis and Haemostasis. 73(2). 297–303. 19 indexed citations

16.

Armstrong, Ruth. (1969). The Fulton Report The Tasks of the Civil Service. Public Administration. 47(1). 1–12. 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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