Maggie Brett

1.8k total citations
32 papers, 738 citations indexed

About

Maggie Brett is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Maggie Brett has authored 32 papers receiving a total of 738 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 9 papers in Molecular Biology and 8 papers in Epidemiology. Recurrent topics in Maggie Brett's work include Genomic variations and chromosomal abnormalities (7 papers), Pneumonia and Respiratory Infections (5 papers) and Bacterial Infections and Vaccines (5 papers). Maggie Brett is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Pneumonia and Respiratory Infections (5 papers) and Bacterial Infections and Vaccines (5 papers). Maggie Brett collaborates with scholars based in Singapore, New Zealand and United States. Maggie Brett's co-authors include Bruce Bennetts, Lesley C. Adès, Katherine Holman, Andrew Biggin, J. Rocourt, John B. Luchansky, B. Ojeniyi, Roland Brosch, B. Catimel and Ene‐Choo Tan and has published in prestigious journals such as PLoS ONE, Gene and International Journal of Food Microbiology.

In The Last Decade

Maggie Brett

30 papers receiving 679 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maggie Brett Singapore 12 283 260 250 145 91 32 738
Hongyan Luo China 13 100 0.4× 47 0.2× 68 0.3× 192 1.3× 61 0.7× 40 534
Sílvia Yumi Bando Brazil 16 34 0.1× 125 0.5× 91 0.4× 183 1.3× 26 0.3× 43 694
Katharine G. Harris United States 10 98 0.3× 33 0.1× 61 0.2× 346 2.4× 20 0.2× 14 603
Jingfeng Zhang China 15 43 0.2× 64 0.2× 74 0.3× 499 3.4× 29 0.3× 47 828
Frans Tielen Netherlands 14 61 0.2× 172 0.7× 82 0.3× 234 1.6× 38 0.4× 18 553
Yulong He China 15 32 0.1× 36 0.1× 64 0.3× 315 2.2× 52 0.6× 44 645
Giulia Malferrari Italy 12 24 0.1× 85 0.3× 50 0.2× 233 1.6× 33 0.4× 22 569
Hakim Echchannaoui Germany 15 67 0.2× 38 0.1× 41 0.2× 156 1.1× 158 1.7× 23 797
M D Sjaastad United States 8 17 0.1× 134 0.5× 86 0.3× 261 1.8× 17 0.2× 8 580
Mark Lucas United Kingdom 10 23 0.1× 77 0.3× 83 0.3× 331 2.3× 16 0.2× 11 1.1k

Countries citing papers authored by Maggie Brett

Since Specialization
Citations

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

Fields of papers citing papers by Maggie Brett

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maggie Brett

This figure shows the co-authorship network connecting the top 25 collaborators of Maggie Brett. A scholar is included among the top collaborators of Maggie Brett 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 Maggie Brett. Maggie Brett 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.
Haag, Natja, Ene‐Choo Tan, Matthias Begemann, et al.. (2021). Biallelic loss-of-function variants in WDR11 are associated with microcephaly and intellectual disability. European Journal of Human Genetics. 29(11). 1663–1668. 6 indexed citations
2.
Wei, Heming, Angeline Lai, Ee Shien Tan, et al.. (2020). Genetic landscape of congenital disorders in patients from Southeast Asia: results from sequencing using a gene panel for Mendelian phenotypes. Archives of Disease in Childhood. 106(1). 38–43. 5 indexed citations
3.
Koh, Mark Jean Aan, et al.. (2018). Piebaldism with multiple café-au-lait–like hyperpigmented macules and inguinal freckling caused by a novel KIT mutation. JAAD Case Reports. 4(4). 318–321. 2 indexed citations
4.
Brett, Maggie, et al.. (2017). Intragenic multi-exon deletion in the FBN1 gene in a child with mildly dilated aortic sinus: a retrotransposal event. Journal of Human Genetics. 62(7). 711–715. 7 indexed citations
5.
Jamuar, Saumya Shekhar, Jyn Ling Kuan, Maggie Brett, et al.. (2016). Incidentalome from Genomic Sequencing: A Barrier to Personalized Medicine?. EBioMedicine. 5. 211–216. 17 indexed citations
6.
Lim, Eileen C.P., Maggie Brett, Angeline Lai, et al.. (2015). Next-generation sequencing using a pre-designed gene panel for the molecular diagnosis of congenital disorders in pediatric patients. Human Genomics. 9(1). 33–33. 27 indexed citations
7.
Lim, Eileen C.P., et al.. (2014). Chromosome 15q11-q13 copy number gain detected by array-CGH in two cases with a maternal methylation pattern. Molecular Cytogenetics. 7(1). 32–32. 7 indexed citations
8.
Brett, Maggie, John R. McPherson, Zhi Jiang Zang, et al.. (2014). Massively Parallel Sequencing of Patients with Intellectual Disability, Congenital Anomalies and/or Autism Spectrum Disorders with a Targeted Gene Panel. PLoS ONE. 9(4). e93409–e93409. 28 indexed citations
9.
10.
Watson, Michael, et al.. (2007). Pneumococci responsible for invasive disease and discharging ears in children in Sydney, Australia. Journal of Medical Microbiology. 56(6). 819–823. 8 indexed citations
11.
Adès, Lesley C., Kathleen E. Sullivan, Andrew Biggin, et al.. (2006). FBN1, TGFBR1, and the Marfan‐craniosynostosis/mental retardation disorders revisited. American Journal of Medical Genetics Part A. 140A(10). 1047–1058. 69 indexed citations
12.
Biggin, Andrew, Katherine Holman, Maggie Brett, Bruce Bennetts, & Lesley C. Adès. (2003). Detection of thirty novelFBN1mutations in patients with Marfan syndrome or a related fibrillinopathy. Human Mutation. 23(1). 99–99. 49 indexed citations
13.
Hood, Derek W., et al.. (2002). Series of incidents of Listeria monocytogenes non-invasive febrile gastroenteritis involving ready-to-eat meats. Letters in Applied Microbiology. 35(5). 409–413. 76 indexed citations
14.
Brett, Maggie. (2001). Emergence of a high-level cefotaxime-resistant Streptococcus pneumoniae strain in New Zealand. Journal of Medical Microbiology. 50(2). 173–176. 5 indexed citations
15.
Pagotto, Franco, et al.. (2000). Sequence Analysis of the Family of Penicillinase-Producing Plasmids of Neisseria gonorrhoeae. Plasmid. 43(1). 24–34. 52 indexed citations
16.
Brett, Maggie, Philip Short, & Scott A. Beatson. (1998). The comparative in-vitro activity of roxithromycin and other antibiotics against Bordetella pertussis. Journal of Antimicrobial Chemotherapy. 41(suppl 2). 23–27. 9 indexed citations
17.
Brett, Maggie, et al.. (1998). Laboratory investigation and comparison of Salmonella Brandenburg cases in New Zealand. Epidemiology and Infection. 121(1). 49–55. 5 indexed citations
18.
Brett, Maggie. (1998). A small outbreak of listeriosis associated with smoked mussels. International Journal of Food Microbiology. 43(3). 223–229. 139 indexed citations
19.
Brosch, Roland, Maggie Brett, B. Catimel, et al.. (1996). Genomic fingerprinting of 80 strains from the WHO multicenter international typing study of Listeria monocytogenes via pulsed-field gel electrophoresis (PFGE). International Journal of Food Microbiology. 32(3). 343–355. 90 indexed citations
20.
Brett, Maggie. (1989). Conjugal transfer of gonococcal βlactamase and conjugative plasmids to Neisseria meningitidis. Journal of Antimicrobial Chemotherapy. 24(6). 875–879. 6 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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