Suet‐Feung Chin

47.5k total citations · 5 hit papers
98 papers, 11.0k citations indexed

About

Suet‐Feung Chin is a scholar working on Molecular Biology, Cancer Research and Oncology. According to data from OpenAlex, Suet‐Feung Chin has authored 98 papers receiving a total of 11.0k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Molecular Biology, 50 papers in Cancer Research and 35 papers in Oncology. Recurrent topics in Suet‐Feung Chin's work include Cancer Genomics and Diagnostics (37 papers), Gene expression and cancer classification (17 papers) and Genomic variations and chromosomal abnormalities (17 papers). Suet‐Feung Chin is often cited by papers focused on Cancer Genomics and Diagnostics (37 papers), Gene expression and cancer classification (17 papers) and Genomic variations and chromosomal abnormalities (17 papers). Suet‐Feung Chin collaborates with scholars based in United Kingdom, United States and Netherlands. Suet‐Feung Chin's co-authors include Carlos Caldas, Mark Dunning, Ian O. Ellis, Oscar M. Rueda, Andrew E. Teschendorff, Andrew R. Green, Muhammed Murtaza, Sarah‐Jane Dawson, Tim Forshew and Dana W.Y. Tsui and has published in prestigious journals such as Nature, New England Journal of Medicine and Cell.

In The Last Decade

Suet‐Feung Chin

94 papers receiving 10.9k citations

Hit Papers

Analysis of Circulating T... 2007 2026 2013 2019 2013 2012 2013 2007 2022 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Suet‐Feung Chin United Kingdom 44 6.8k 5.7k 3.2k 2.1k 1.5k 98 11.0k
John W.M. Martens Netherlands 61 6.8k 1.0× 4.8k 0.8× 4.4k 1.4× 2.1k 1.0× 1.5k 1.0× 328 11.9k
Simon Forbes United Kingdom 21 7.6k 1.1× 4.0k 0.7× 2.8k 0.9× 2.2k 1.0× 1.4k 0.9× 46 11.2k
Nitzan Rosenfeld United Kingdom 37 7.7k 1.1× 7.7k 1.3× 3.7k 1.2× 3.3k 1.6× 1.2k 0.8× 75 13.3k
Anieta M. Sieuwerts Netherlands 51 6.5k 1.0× 4.9k 0.9× 4.3k 1.3× 1.6k 0.7× 1.3k 0.8× 152 10.8k
Alan Mackay United Kingdom 56 5.5k 0.8× 3.5k 0.6× 3.9k 1.2× 1.3k 0.6× 1.4k 0.9× 134 10.1k
James D. Brenton United Kingdom 47 5.9k 0.9× 6.2k 1.1× 4.0k 1.2× 2.6k 1.2× 1.2k 0.8× 167 12.5k
Nallasivam Palanisamy United States 50 5.5k 0.8× 3.4k 0.6× 1.9k 0.6× 2.1k 1.0× 837 0.5× 144 9.1k
Barry S. Taylor United States 46 5.5k 0.8× 3.0k 0.5× 3.3k 1.0× 2.7k 1.3× 933 0.6× 118 9.9k
Sally Bamford United Kingdom 12 5.6k 0.8× 3.1k 0.5× 2.1k 0.6× 1.2k 0.6× 1.3k 0.8× 19 8.1k
Nicholas E. Navin United States 36 6.6k 1.0× 5.5k 1.0× 2.8k 0.9× 1.1k 0.5× 2.6k 1.7× 74 10.5k

Countries citing papers authored by Suet‐Feung Chin

Since Specialization
Citations

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

Fields of papers citing papers by Suet‐Feung Chin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Suet‐Feung Chin. 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 Suet‐Feung Chin. The network helps show where Suet‐Feung Chin may publish in the future.

Co-authorship network of co-authors of Suet‐Feung Chin

This figure shows the co-authorship network connecting the top 25 collaborators of Suet‐Feung Chin. A scholar is included among the top collaborators of Suet‐Feung Chin 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 Suet‐Feung Chin. Suet‐Feung Chin 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.
Nguyen, Long, Suet‐Feung Chin, Stephen‐John Sammut, et al.. (2025). Fitness and transcriptional plasticity of human breast cancer single-cell-derived clones. Cell Reports. 44(5). 115699–115699.
2.
Hasan, Siti Norhidayu, Tania Islam, Li‐Ying Teoh, et al.. (2024). Clustering of HR + /HER2− breast cancer in an Asian cohort is driven by immune phenotypes. Breast Cancer Research. 26(1). 67–67.
3.
Young, Cameron C., Katherine Eason, Sach Mukherjee, et al.. (2024). Development and validation of a reliable DNA copy-number-based machine learning algorithm (CopyClust) for breast cancer integrative cluster classification. Scientific Reports. 14(1). 11861–11861. 2 indexed citations
4.
Sammut, Stephen‐John, Jacob D. Galson, Ralph Minter, et al.. (2024). Predictability of B cell clonal persistence and immunosurveillance in breast cancer. Nature Immunology. 25(5). 916–924. 10 indexed citations
5.
Hasan, Siti Norhidayu, Tania Islam, Li‐Ying Teoh, et al.. (2024). Gene expression signature for predicting homologous recombination deficiency in triple-negative breast cancer. npj Breast Cancer. 10(1). 60–60. 2 indexed citations
6.
Mattos‐Arruda, Leticia De, Javier Cortés, Daniel Guimarães Tiezzi, et al.. (2021). The temporal mutational and immune tumour microenvironment remodelling of HER2-negative primary breast cancers. npj Breast Cancer. 7(1). 73–73. 7 indexed citations
7.
Howarth, Karen, Susanna L. Cooke, Suet‐Feung Chin, et al.. (2021). NRG1 fusions in breast cancer. Breast Cancer Research. 23(1). 3–3. 17 indexed citations
8.
Ng, Pei Sze, Pathmanathan Rajadurai, Cheng Har Yip, et al.. (2021). Characterisation of PALB2 tumours through whole-exome and whole-transcriptomic analyses. npj Breast Cancer. 7(1). 46–46. 6 indexed citations
9.
Fuks, Garold, Suet‐Feung Chin, Oscar M. Rueda, et al.. (2020). Transcriptional profiling reveals a subset of human breast tumors that retain wt TP53 but display mutant p53‐associated features. Molecular Oncology. 14(8). 1640–1652. 7 indexed citations
10.
Hasan, Siti Norhidayu, Stephen‐John Sammut, Cheng Har Yip, et al.. (2020). The molecular landscape of Asian breast cancers reveals clinically relevant population-specific differences. Nature Communications. 11(1). 6433–6433. 52 indexed citations
11.
Cox, Órla T., Shelley J. Edmunds, Katja Simon‐Keller, et al.. (2019). PDLIM2 Is a Marker of Adhesion and β-Catenin Activity in Triple-Negative Breast Cancer. Cancer Research. 79(10). 2619–2633. 17 indexed citations
12.
McDonald, Bradon R., Tania Contente‐Cuomo, Stephen‐John Sammut, et al.. (2019). Personalized circulating tumor DNA analysis to detect residual disease after neoadjuvant therapy in breast cancer. Science Translational Medicine. 11(504). 201 indexed citations
13.
Silwal‐Pandit, Laxmi, Hans Kristian Moen Vollan, Suet‐Feung Chin, et al.. (2014). TP53 Mutation Spectrum in Breast Cancer Is Subtype Specific and Has Distinct Prognostic Relevance. Clinical Cancer Research. 20(13). 3569–3580. 215 indexed citations
14.
Quigley, David A., Laxmi Silwal‐Pandit, Ruth Dannenfelser, et al.. (2014). Lymphocyte Invasion in IC10/Basal-Like Breast Tumors Is Associated with Wild-Type TP53. Molecular Cancer Research. 13(3). 493–501. 47 indexed citations
15.
Ross-Innes, Caryn S., Rory Stark, Andrew E. Teschendorff, et al.. (2012). Differential oestrogen receptor binding is associated with clinical outcome in breast cancer. Nature. 481(7381). 389–393. 1304 indexed citations breakdown →
17.
Obrador‐Hevia, Antònia, Suet‐Feung Chin, Sara González, et al.. (2010). Oncogenic KRAS is not necessary for Wnt signalling activation in APC‐associated FAP adenomas. The Journal of Pathology. 221(1). 57–67. 17 indexed citations
18.
Veerakumarasivam, Abhi, Helen E. Scott, Suet‐Feung Chin, et al.. (2008). High-Resolution Array-Based Comparative Genomic Hybridization of Bladder Cancers Identifies Mouse Double Minute 4 ( MDM4 ) as an Amplification Target Exclusive of MDM2 and TP53. Clinical Cancer Research. 14(9). 2527–2534. 27 indexed citations
19.
Chin, Suet‐Feung, Andrew E. Teschendorff, John C. Marioni, et al.. (2007). High-resolution aCGH and expression profiling identifies a novel genomic subtype of ER negative breast cancer. Genome biology. 8(10). R215–R215. 239 indexed citations
20.
Chin, Suet‐Feung, Christophe Ginestier, Valérie‐Jeanne Bardou, et al.. (2004). A Recurrent Chromosome Breakpoint in Breast Cancer at the NRG1 / Neuregulin 1 / Heregulin Gene. Cancer Research. 64(19). 6840–6844. 73 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026