Fleur Hammet

2.6k total citations
32 papers, 750 citations indexed

About

Fleur Hammet is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Fleur Hammet has authored 32 papers receiving a total of 750 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 18 papers in Genetics and 13 papers in Cancer Research. Recurrent topics in Fleur Hammet's work include BRCA gene mutations in cancer (13 papers), Cancer Genomics and Diagnostics (12 papers) and Molecular Biology Techniques and Applications (6 papers). Fleur Hammet is often cited by papers focused on BRCA gene mutations in cancer (13 papers), Cancer Genomics and Diagnostics (12 papers) and Molecular Biology Techniques and Applications (6 papers). Fleur Hammet collaborates with scholars based in Australia, United States and France. Fleur Hammet's co-authors include Melissa C. Southey, Deon J. Venter, Jane E. Armes, Anne‐Marie Hutchins, Tú Nguyen‐Dumont, Graham G. Giles, Daniel J. Park, John L. Hopper, Bernard J. Pope and David White and has published in prestigious journals such as Analytical Biochemistry, Oncogene and International Journal of Molecular Sciences.

In The Last Decade

Fleur Hammet

32 papers receiving 735 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fleur Hammet Australia 14 391 313 202 166 95 32 750
Jürgen Kunz Germany 15 511 1.3× 286 0.9× 68 0.3× 189 1.1× 65 0.7× 25 871
Maria Sofia Fernandes Portugal 13 343 0.9× 266 0.8× 94 0.5× 130 0.8× 95 1.0× 18 835
Y. Hey United Kingdom 16 587 1.5× 103 0.3× 155 0.8× 91 0.5× 66 0.7× 27 774
Sean F. Landrette United States 12 441 1.1× 83 0.3× 61 0.3× 108 0.7× 55 0.6× 18 663
Yu-Wei Leu Taiwan 13 800 2.0× 221 0.7× 165 0.8× 124 0.7× 39 0.4× 19 967
Malka Popliker Israel 12 485 1.2× 235 0.8× 139 0.7× 348 2.1× 36 0.4× 18 1.2k
Massimo Zani Italy 17 731 1.9× 345 1.1× 182 0.9× 180 1.1× 153 1.6× 31 1.1k
Roland Jurecic United States 17 794 2.0× 124 0.4× 89 0.4× 138 0.8× 25 0.3× 35 1.1k
Anna Díez-Villanueva Spain 13 598 1.5× 217 0.7× 179 0.9× 110 0.7× 49 0.5× 25 849
F. Apiou France 15 517 1.3× 245 0.8× 158 0.8× 144 0.9× 48 0.5× 31 835

Countries citing papers authored by Fleur Hammet

Since Specialization
Citations

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

Fields of papers citing papers by Fleur Hammet

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fleur Hammet

This figure shows the co-authorship network connecting the top 25 collaborators of Fleur Hammet. A scholar is included among the top collaborators of Fleur Hammet 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 Fleur Hammet. Fleur Hammet 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.
Hill, Rachel, Andrew S. Gibbons, Wittaya Suwakulsiri, et al.. (2022). Maternal SARS-CoV-2 exposure alters infant DNA methylation. Brain Behavior & Immunity - Health. 27. 100572–100572. 12 indexed citations
2.
Nguyen‐Dumont, Tú, James G. Dowty, Robert J. MacInnis, et al.. (2021). Rare Germline Pathogenic Variants Identified by Multigene Panel Testing and the Risk of Aggressive Prostate Cancer. Cancers. 13(7). 1495–1495. 15 indexed citations
3.
Dugué, Pierre‐Antoine, Chenglong Yu, Ee Ming Wong, et al.. (2021). VTRNA2-1: Genetic Variation, Heritable Methylation and Disease Association. International Journal of Molecular Sciences. 22(5). 2535–2535. 16 indexed citations
4.
Yu, Chenglong, Pierre‐Antoine Dugué, James G. Dowty, et al.. (2021). Repeatability of methylation measures using a QIAseq targeted methyl panel and comparison with the Illumina HumanMethylation450 assay. BMC Research Notes. 14(1). 394–394. 3 indexed citations
5.
Nguyen‐Dumont, Tú, Jason A. Steen, Ingrid Winship, et al.. (2020). Mismatch repair gene pathogenic germline variants in a population-based cohort of breast cancer. Familial Cancer. 19(3). 197–202. 5 indexed citations
6.
Nguyen‐Dumont, Tú, Paweł Karpiński, Maria Sąsiadek, et al.. (2020). Genetic testing in Poland and Ukraine: should comprehensive germline testing of BRCA1 and BRCA2 be recommended for women with breast and ovarian cancer?. Genetics Research. 102. e6–e6. 8 indexed citations
7.
Nguyen‐Dumont, Tú, Aleksander Myszka, Paweł Karpiński, et al.. (2018). FANCM and RECQL genetic variants and breast cancer susceptibility: relevance to South Poland and West Ukraine. BMC Medical Genetics. 19(1). 12–12. 20 indexed citations
8.
Nguyen‐Dumont, Tú, Zhi L. Teo, Fleur Hammet, et al.. (2018). Is RNASEL:p.Glu265* a modifier of early-onset breast cancer risk for carriers of high-risk mutations?. BMC Cancer. 18(1). 165–165. 7 indexed citations
9.
Pope, Bernard J., Fleur Hammet, Tú Nguyen‐Dumont, & Daniel J. Park. (2017). Hi-Plex for Simple, Accurate, and Cost-Effective Amplicon-based Targeted DNA Sequencing. Methods in molecular biology. 1712. 53–70. 3 indexed citations
10.
Myszka, Aleksander, Tú Nguyen‐Dumont, Paweł Karpiński, et al.. (2017). Targeted massively parallel sequencing characterises the mutation spectrum of PALB2 in breast and ovarian cancer cases from Poland and Ukraine. Familial Cancer. 17(3). 345–349. 8 indexed citations
11.
Nguyen‐Dumont, Tú, Fleur Hammet, Maryam Mahmoodi, et al.. (2015). Mutation screening of PALB2 in clinically ascertained families from the Breast Cancer Family Registry. Breast Cancer Research and Treatment. 149(2). 547–554. 18 indexed citations
12.
Pope, Bernard J., Tú Nguyen‐Dumont, Fleur Hammet, & Daniel J. Park. (2014). ROVER variant caller: read-pair overlap considerate variant-calling software applied to PCR-based massively parallel sequencing datasets. PubMed. 9(1). 3–3. 11 indexed citations
13.
Nguyen‐Dumont, Tú, Fleur Hammet, Trung Tran, et al.. (2014). Hi-Plex targeted sequencing is effective using DNA derived from archival dried blood spots. Analytical Biochemistry. 470. 48–51. 6 indexed citations
14.
Nguyen‐Dumont, Tú, Zhi L. Teo, Bernard J. Pope, et al.. (2013). Hi-Plex for high-throughput mutation screening: application to the breast cancer susceptibility gene PALB2. BMC Medical Genomics. 6(1). 48–48. 12 indexed citations
15.
Pope, Bernard J., Tú Nguyen‐Dumont, Fabrice Odefrey, et al.. (2013). FAVR (Filtering and Annotation of Variants that are Rare): methods to facilitate the analysis of rare germline genetic variants from massively parallel sequencing datasets. BMC Bioinformatics. 14(1). 65–65. 6 indexed citations
16.
Dite, Gillian S., Maryam Mahmoodi, Adrian Bickerstaffe, et al.. (2013). Using SNP genotypes to improve the discrimination of a simple breast cancer risk prediction model. Breast Cancer Research and Treatment. 139(3). 887–896. 33 indexed citations
17.
Park, Daniel J., Fabrice Odefrey, Fleur Hammet, et al.. (2011). FAN1 variants identified in multiple-case early-onset breast cancer families via exome sequencing: no evidence for association with risk for breast cancer. Breast Cancer Research and Treatment. 130(3). 1043–1049. 12 indexed citations
18.
Armes, Jane E., Fleur Hammet, Melanie de Silva, et al.. (2004). Candidate tumor-suppressor genes on chromosome arm 8p in early-onset and high-grade breast cancers. Oncogene. 23(33). 5697–5702. 86 indexed citations
19.
Willis, Simon N., Anne‐Marie Hutchins, Fleur Hammet, et al.. (2003). Detailed gene copy number and RNA expression analysis of the 17q12–23 region in primary breast cancers. Genes Chromosomes and Cancer. 36(4). 382–392. 22 indexed citations
20.
Allen, David G., Fleur Hammet, David White, et al.. (2002). Genetic aberrations detected by comparative genomic hybridisation in vulvar cancers. British Journal of Cancer. 86(6). 924–928. 40 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

Breakdown of academic impact, for papers by Jürgen Kunz Breakdown of academic impact, for papers by Maria Sofia Fernandes Breakdown of academic impact, for papers by Y. Hey Breakdown of academic impact, for papers by Sean F. Landrette Breakdown of academic impact, for papers by Yu-Wei Leu Breakdown of academic impact, for papers by Malka Popliker Breakdown of academic impact, for papers by Massimo Zani Breakdown of academic impact, for papers by Roland Jurecic Breakdown of academic impact, for papers by Anna Díez-Villanueva Breakdown of academic impact, for papers by F. Apiou
Rankless by CCL
2026