Danielle E. Dye

2.3k total citations
46 papers, 1.6k citations indexed

About

Danielle E. Dye is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Danielle E. Dye has authored 46 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 11 papers in Cardiology and Cardiovascular Medicine and 10 papers in Genetics. Recurrent topics in Danielle E. Dye's work include Muscle Physiology and Disorders (14 papers), Cardiomyopathy and Myosin Studies (9 papers) and Neurogenetic and Muscular Disorders Research (4 papers). Danielle E. Dye is often cited by papers focused on Muscle Physiology and Disorders (14 papers), Cardiomyopathy and Myosin Studies (9 papers) and Neurogenetic and Muscular Disorders Research (4 papers). Danielle E. Dye collaborates with scholars based in Australia, United States and Germany. Danielle E. Dye's co-authors include Nigel G. Laing, Deirdre R. Coombe, Chee-Wai Wong, Steve D. Wilton, Emma J. Glasson, Miranda D. Grounds, A.H. Bittles, John C. Sparrow, Nicole Monnier and Beverley F. Kinnear and has published in prestigious journals such as PLoS ONE, Neurology and Annals of Neurology.

In The Last Decade

Danielle E. Dye

45 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Danielle E. Dye Australia 24 952 517 280 204 180 46 1.6k
William A. LaFramboise United States 27 963 1.0× 305 0.6× 194 0.7× 146 0.7× 201 1.1× 96 2.0k
Catherine Moreau France 24 863 0.9× 216 0.4× 177 0.6× 110 0.5× 264 1.5× 35 1.8k
Lawrence T. Bish United States 21 1.1k 1.2× 618 1.2× 298 1.1× 347 1.7× 74 0.4× 37 2.0k
Sabina Liechti‐Gallati Switzerland 23 1.8k 1.9× 490 0.9× 430 1.5× 481 2.4× 120 0.7× 59 2.8k
Francesca Andreetta Italy 28 1.6k 1.6× 141 0.3× 225 0.8× 158 0.8× 212 1.2× 78 2.7k
En Kimura Japan 24 1.1k 1.2× 209 0.4× 288 1.0× 270 1.3× 40 0.2× 86 1.7k
Alexis R. Demonbreun United States 25 1.2k 1.3× 217 0.4× 116 0.4× 89 0.4× 117 0.7× 59 1.7k
Gary R. Coulton United Kingdom 20 1.7k 1.8× 332 0.6× 374 1.3× 247 1.2× 62 0.3× 41 2.1k
Zhen‐Ao Zhao China 25 1.7k 1.8× 201 0.4× 154 0.6× 226 1.1× 409 2.3× 58 2.6k
Christina A. Pacak United States 21 1.6k 1.7× 405 0.8× 201 0.7× 651 3.2× 60 0.3× 68 2.4k

Countries citing papers authored by Danielle E. Dye

Since Specialization
Citations

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

Fields of papers citing papers by Danielle E. Dye

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Danielle E. Dye

This figure shows the co-authorship network connecting the top 25 collaborators of Danielle E. Dye. A scholar is included among the top collaborators of Danielle E. Dye 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 Danielle E. Dye. Danielle E. Dye 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.
Wong, Chee-Wai, Beverley F. Kinnear, Simon Denil, et al.. (2025). Keratinocyte self-renewal and differentiation is dictated by extrinsic signals from dermal extracellular matrices. Open Biology. 15(10). 240417–240417.
2.
Dye, Danielle E., et al.. (2023). Immune evasion on the nanoscale: Small extracellular vesicles in pancreatic ductal adenocarcinoma immunity. Seminars in Cancer Biology. 96. 36–47. 8 indexed citations
3.
Kirk, T.B., et al.. (2021). Contribution of glycosaminoglycans to the structural and mechanical properties of tendons – A multiscale study. Journal of Biomechanics. 128. 110796–110796. 11 indexed citations
4.
Wong, Chee-Wai, Beverley F. Kinnear, Radoslaw M. Sobota, et al.. (2019). In Vitro Expansion of Keratinocytes on Human Dermal Fibroblast-Derived Matrix Retains Their Stem-Like Characteristics. Scientific Reports. 9(1). 18561–18561. 34 indexed citations
5.
Jackaman, Connie, Federica Tomay, Danielle E. Dye, et al.. (2019). CD8+cytotoxic T cell responses to dominant tumor-associated antigens are profoundly weakened by aging yet subdominant responses retain functionality and expand in response to chemotherapy. OncoImmunology. 8(4). e1564452–e1564452. 9 indexed citations
6.
Dye, Danielle E., et al.. (2019). Crab Ash Extract has Anti-Proliferative Effects on SK-MEL-28 Melanoma Cells and Induces a Cellular Stress Response and Metabolic Changes. Tropical Journal of Natural Product Research. 3(4). 113–123. 2 indexed citations
7.
Brameld, Kate, Danielle E. Dye, Susannah Maxwell, et al.. (2014). The Western Australian Family Connections Genealogical Project: Detection of Familial Occurrences of Single Gene and Chromosomal Disorders. Genetic Testing and Molecular Biomarkers. 18(2). 77–82. 3 indexed citations
8.
Jackaman, Connie, Danielle E. Dye, & Delia J. Nelson. (2014). IL-2/CD40-activated macrophages rescue age and tumor-induced T cell dysfunction in elderly mice. AGE. 36(3). 9655–9655. 25 indexed citations
9.
Fyfe, Sue, et al.. (2013). Use of Anatomage tables in a large first year core unit. ASCILITE Publications. 298–302. 19 indexed citations
10.
Wong, Chee-Wai, Danielle E. Dye, & Deirdre R. Coombe. (2012). The Role of Immunoglobulin Superfamily Cell Adhesion Molecules in Cancer Metastasis. International Journal of Cell Biology. 2012. 1–9. 148 indexed citations
11.
Dye, Danielle E., Kate Brameld, Susannah Maxwell, et al.. (2010). The Impact of Single Gene and Chromosomal Disorders on Hospital Admissions of Children and Adolescents: A Population-Based Study. Public Health Genomics. 14(3). 153–161. 26 indexed citations
12.
Dye, Danielle E., Leanne Youngs, Beverley McNamara, Jack Goldblatt, & Peter O’Leary. (2010). The Disclosure of Genetic Information: A Human Research Ethics Perspective. Journal of Bioethical Inquiry. 7(1). 103–109. 1 indexed citations
13.
Dye, Danielle E., et al.. (2009). hShroom1 links a membrane bound protein to the actin cytoskeleton. Cellular and Molecular Life Sciences. 66(4). 681–696. 14 indexed citations
14.
Laing, Nigel G., Danielle E. Dye, Carina Wallgren‐Pettersson, et al.. (2009). Mutations and polymorphisms of the skeletal muscle α-actin gene (ACTA1). Human Mutation. 30(9). 1267–1277. 173 indexed citations
15.
Clarke, Nigel F., Hanna Kolski, Danielle E. Dye, et al.. (2008). Mutations in TPM3 are a common cause of congenital fiber type disproportion. Annals of Neurology. 63(3). 329–337. 102 indexed citations
16.
Wallefeld, William, Sabine Krause, Kristen L. Nowak, et al.. (2006). Severe nemaline myopathy caused by mutations of the stop codon of the skeletal muscle alpha actin gene (ACTA1). Neuromuscular Disorders. 16(9-10). 541–547. 27 indexed citations
17.
Shingde, Meena, Penelope J. Spring, E. J. Wills, et al.. (2006). Myosin storage (hyaline body) myopathy: A case report. Neuromuscular Disorders. 16(12). 882–886. 23 indexed citations
18.
Dye, Danielle E., Biagio Azzarelli, Hans H. Goebel, & Nigel G. Laing. (2006). Novel slow-skeletal myosin (MYH7) mutation in the original myosin storage myopathy kindred. Neuromuscular Disorders. 16(6). 357–360. 32 indexed citations
19.
Leonard, Helen, Sue Fyfe, Danielle E. Dye, Athel Hockey, & John Christodoulou. (2000). Family data in Rett syndrome: Association with other genetic disorders. Journal of Paediatrics and Child Health. 36(4). 336–339. 3 indexed citations
20.
Kalaydjieva, Luba, Anna Pérez-Lezaun, Dora Angelicheva, et al.. (1999). A Founder Mutation in the GK1 Gene Is Responsible for Galactokinase Deficiency in Roma (Gypsies). The American Journal of Human Genetics. 65(5). 1299–1307. 55 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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