Judith Symmons

1.9k total citations
9 papers, 416 citations indexed

About

Judith Symmons is a scholar working on Cancer Research, Molecular Biology and Oncology. According to data from OpenAlex, Judith Symmons has authored 9 papers receiving a total of 416 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Cancer Research, 5 papers in Molecular Biology and 3 papers in Oncology. Recurrent topics in Judith Symmons's work include Cancer Genomics and Diagnostics (4 papers), Cutaneous Melanoma Detection and Management (3 papers) and DNA Repair Mechanisms (2 papers). Judith Symmons is often cited by papers focused on Cancer Genomics and Diagnostics (4 papers), Cutaneous Melanoma Detection and Management (3 papers) and DNA Repair Mechanisms (2 papers). Judith Symmons collaborates with scholars based in Australia, Denmark and France. Judith Symmons's co-authors include Nicholas K. Hayward, Jane M. Palmer, Peter A. Johansson, Christopher Schmidt, Lauren G. Aoude, Anne‐Marie Gerdes, Karin Wadt, Nicholas G. Martin, Kevin J. Whitehead and Jens Folke Kiilgaard and has published in prestigious journals such as PLoS ONE, Journal of Investigative Dermatology and Oncotarget.

In The Last Decade

Judith Symmons

9 papers receiving 411 citations

Peers

Judith Symmons

MB

OPHTH

ONCOL

CR

IMMUN

Richard Yu United States

Berglind O. Einarsdottir Sweden

A T'Ang United States

Sophie Gardrat France

Johanne Lade‐Keller Denmark

Hanneke W. Mensink Netherlands

Gunnar B. Hansen Sweden

Wieke Zuidervaart Netherlands

Sophie Thornton United Kingdom

Linda Potter United Kingdom

Richard Yu United States

Judith Symmons

237 ×1.0

MB

123 ×0.7

OPHTH

177 ×1.0

ONCOL

95 ×0.8

CR

86 ×0.8

IMMUN

Citations per year, relative to Judith Symmons Judith Symmons (= 1×) peers Richard Yu

Countries citing papers authored by Judith Symmons

Since Specialization

Citations

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

Fields of papers citing papers by Judith Symmons

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Judith Symmons

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

All Works

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9 of 9 papers shown

1.

Pritchard, Antonia L., Peter A. Johansson, Vaishnavi Nathan, et al.. (2018). Germline mutations in candidate predisposition genes in individuals with cutaneous melanoma and at least two independent additional primary cancers. PLoS ONE. 13(4). e0194098–e0194098. 13 indexed citations

2.

Read, J, Judith Symmons, Jane M. Palmer, et al.. (2016). Increased incidence of bladder cancer, lymphoid leukaemia, and myeloma in a cohort of Queensland melanoma families. Familial Cancer. 15(4). 651–663. 4 indexed citations

3.

Stark, Mitchell, Vanessa Bonazzi, Glen M. Boyle, et al.. (2015). miR-514a regulates the tumour suppressor NF1 and modulates BRAFi sensitivity in melanoma. QUT ePrints (Queensland University of Technology). 1 indexed citations

4.

Aoude, Lauren G., Ellen Heitzer, Peter A. Johansson, et al.. (2015). POLE mutations in families predisposed to cutaneous melanoma. Familial Cancer. 14(4). 621–628. 33 indexed citations

5.

Aoude, Lauren G., Michael G. Gartside, Peter A. Johansson, et al.. (2015). Prevalence of GermlineBAP1, CDKN2A, andCDK4Mutations in an Australian Population-Based Sample of Cutaneous Melanoma Cases. Twin Research and Human Genetics. 18(2). 126–133. 19 indexed citations

6.

Stark, Mitchell, Vanessa Bonazzi, Glen M. Boyle, et al.. (2015). miR-514a regulates the tumour suppressor NF1 and modulates BRAFi sensitivity in melanoma. Oncotarget. 6(19). 17753–17763. 77 indexed citations

7.

Johansson, Peter A., Lauren G. Aoude, Karin Wadt, et al.. (2015). Deep sequencing of uveal melanoma identifies a recurrent mutation in PLCB4. Oncotarget. 7(4). 4624–4631. 215 indexed citations

8.

Aoude, Lauren G., Mai Xu, Zhen Zhao, et al.. (2014). Assessment of PALB2 as a Candidate Melanoma Susceptibility Gene. PLoS ONE. 9(6). e100683–e100683. 9 indexed citations

9.

Siskind, Victor, Maria Celia B. Hughes, Jane M. Palmer, et al.. (2010). Nevi, Family History, and Fair Skin Increase the Risk of Second Primary Melanoma. Journal of Investigative Dermatology. 131(2). 461–467. 45 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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