Bruce Bennetts

5.7k total citations
101 papers, 3.2k citations indexed

About

Bruce Bennetts is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Bruce Bennetts has authored 101 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Genetics, 36 papers in Molecular Biology and 19 papers in Immunology. Recurrent topics in Bruce Bennetts's work include Genomic variations and chromosomal abnormalities (12 papers), T-cell and B-cell Immunology (12 papers) and Genetics and Neurodevelopmental Disorders (12 papers). Bruce Bennetts is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), T-cell and B-cell Immunology (12 papers) and Genetics and Neurodevelopmental Disorders (12 papers). Bruce Bennetts collaborates with scholars based in Australia, United States and United Kingdom. Bruce Bennetts's co-authors include John Christodoulou, Brian J. Morris, Lynette J. Schedlich, Graeme J. Stewart, Robert Heard, Suzy Teutsch, Katherine Holman, Bridget Wilcken, Sarah Williamson and Helen Leonard and has published in prestigious journals such as The Lancet, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Bruce Bennetts

99 papers receiving 3.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bruce Bennetts Australia 31 1.4k 1.3k 471 328 325 101 3.2k
Marwan Shinawi United States 32 1.5k 1.1× 2.4k 1.8× 415 0.9× 223 0.7× 226 0.7× 137 4.3k
Marco Seri Italy 38 1.4k 1.0× 2.3k 1.8× 488 1.0× 121 0.4× 345 1.1× 193 5.3k
Slavé Petrovski Australia 33 1.6k 1.2× 1.7k 1.3× 177 0.4× 104 0.3× 194 0.6× 71 3.8k
Robert J. Hopkin United States 40 1.1k 0.8× 1.5k 1.2× 160 0.3× 153 0.5× 449 1.4× 189 5.8k
Erik A. Sistermans Netherlands 37 2.7k 2.0× 2.9k 2.2× 395 0.8× 128 0.4× 280 0.9× 123 5.6k
Ituro Inoue Japan 35 637 0.5× 1.5k 1.2× 475 1.0× 197 0.6× 235 0.7× 101 3.6k
Jan Wahlström Sweden 38 1.1k 0.8× 1.3k 1.0× 865 1.8× 93 0.3× 955 2.9× 136 4.3k
Kenjiro Kosaki Japan 35 1.8k 1.3× 2.7k 2.1× 335 0.7× 103 0.3× 565 1.7× 363 5.2k
Michele D’Urso Italy 35 1.4k 1.0× 2.8k 2.1× 186 0.4× 182 0.6× 227 0.7× 100 4.2k
Pekka Ellonen Finland 29 802 0.6× 1.3k 1.0× 521 1.1× 107 0.3× 265 0.8× 70 3.1k

Countries citing papers authored by Bruce Bennetts

Since Specialization
Citations

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

Fields of papers citing papers by Bruce Bennetts

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bruce Bennetts

This figure shows the co-authorship network connecting the top 25 collaborators of Bruce Bennetts. A scholar is included among the top collaborators of Bruce Bennetts 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 Bruce Bennetts. Bruce Bennetts 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.
Leffler, Melanie, Louise Christie, Anna Hackett, et al.. (2023). Further delineation of dosage‐sensitive K/L mediated Xq28 duplication syndrome includes incomplete penetrance. Clinical Genetics. 103(6). 681–687. 1 indexed citations
2.
Bennetts, Bruce, Artur Darmanian, Luke Jones, et al.. (2023). SNP chromosome microarray genotyping for detection of uniparental disomy in the clinical diagnostic laboratory. Pathology. 55(6). 818–826. 1 indexed citations
3.
Kelada, Lauren, Claire E. Wakefield, David Armstrong, et al.. (2022). Genomic testing for children with interstitial and diffuse lung disease (chILD): parent satisfaction, understanding and health-related quality of life. BMJ Open Respiratory Research. 9(1). e001139–e001139. 2 indexed citations
4.
Nash, Benjamin M., Alan Ma, Gladys Ho, et al.. (2022). Whole Genome Sequencing, Focused Assays and Functional Studies Increasing Understanding in Cryptic Inherited Retinal Dystrophies. International Journal of Molecular Sciences. 23(7). 3905–3905. 7 indexed citations
5.
Archibald, Alison D., David Francis, Ling Ling, et al.. (2021). Paternal retraction of a fragile X allele to normal size, showing normal function over two generations. American Journal of Medical Genetics Part A. 188(1). 304–309. 1 indexed citations
6.
Nash, Benjamin M., Milan Fernando, James P. Robinson, et al.. (2021). Evaluation for Retinal Therapy for RPE65 Variation Assessed in hiPSC Retinal Pigment Epithelial Cells. Stem Cells International. 2021. 1–12. 4 indexed citations
7.
Holman, Katherine, Gladys Ho, Elizabeth Farnsworth, et al.. (2021). Australia and New Zealand renal gene panel testing in routine clinical practice of 542 families. npj Genomic Medicine. 6(1). 20–20. 15 indexed citations
8.
Ho, Gladys, Bruce Bennetts, Adviye Ayper Tolun, et al.. (2021). Challenges in Diagnosing Intermediate Maple Syrup Urine Disease by Newborn Screening and Functional Validation of Genomic Results Imperative for Reproductive Family Planning. International Journal of Neonatal Screening. 7(2). 25–25. 8 indexed citations
9.
Briody, Julie, Bruce Bennetts, Karen Wong, et al.. (2020). High Bone Mineral Density Osteogenesis Imperfecta in a Family with a Novel Pathogenic Variant in <b><i>COL1A2</i></b>. Hormone Research in Paediatrics. 93(4). 263–271. 2 indexed citations
10.
Wiley, Veronica, Bruce Bennetts, Louise Christie, et al.. (2018). Are We Ready for Fragile X Newborn Screening Testing?—Lessons Learnt from a Feasibility Study. International Journal of Neonatal Screening. 4(1). 9–9. 4 indexed citations
11.
Nash, Benjamin M., Richard J. Symes, Himanshu Goel, et al.. (2017). NMNAT1 variants cause cone and cone-rod dystrophy. European Journal of Human Genetics. 26(3). 428–433. 16 indexed citations
12.
Mallett, Andrew J., Dylan Mordaunt, A M Walker, et al.. (2015). Rmnd1 Mutations Are Associated with Autosomal Recessive Syndromic Nephropathy. Nephrology. 20. 42–42. 1 indexed citations
13.
Stark, Zornitza, et al.. (2011). Isolated hypogonadotropic hypogonadism with SOX2 mutation and anophthalmia/microphthalmia in offspring. European Journal of Human Genetics. 19(7). 753–756. 27 indexed citations
14.
Hamvas, Aaron, Lawrence M. Nogee, Daniel Wegner, et al.. (2009). Inherited Surfactant Deficiency Caused by Uniparental Disomy of Rare Mutations in the Surfactant Protein-B and ATP Binding Cassette, Subfamily A, Member 3 Genes. The Journal of Pediatrics. 155(6). 854–859.e1. 40 indexed citations
15.
Rudduck, Christina, et al.. (2009). Contiguous gene deletion syndrome in a female with ornithine transcarbamylase deficiency. Molecular Genetics and Metabolism. 99(1). 34–41. 28 indexed citations
16.
Waddell, Leigh B., Veronica Wiley, Kevin Carpenter, et al.. (2005). Medium-chain acyl-CoA dehydrogenase deficiency: Genotype–biochemical phenotype correlations. Molecular Genetics and Metabolism. 87(1). 32–39. 74 indexed citations
17.
Bennetts, Bruce, et al.. (1999). HLA-DMB gene and HLA-DRA promoter region polymorphisms in Australian multiple sclerosis patients. Human Immunology. 60(9). 886–893. 18 indexed citations
18.
Teutsch, Suzy, et al.. (1996). HLA‐DQA1 AND ‐DQB1 GENOTYPING BY PCR‐RFLP, HETERODUPLEX AND HOMODUPLEX ANALYSIS. International Journal of Immunogenetics. 23(2). 107–120. 10 indexed citations
19.
Huang, William Y. C., et al.. (1994). Fluorescence resonance energy transfer within the regulatory light chain of myosin. European Journal of Biochemistry. 219(1-2). 603–610. 10 indexed citations
20.
Schedlich, Lynette J., Bruce Bennetts, & Brian J. Morris. (1987). Primary Structure of a Human Glandular Kallikrein Gene. DNA. 6(5). 429–437. 256 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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