Kaite Honeyman

1.6k total citations
13 papers, 1.1k citations indexed

About

Kaite Honeyman is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Kaite Honeyman has authored 13 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Kaite Honeyman's work include Muscle Physiology and Disorders (11 papers), RNA Interference and Gene Delivery (7 papers) and Virus-based gene therapy research (4 papers). Kaite Honeyman is often cited by papers focused on Muscle Physiology and Disorders (11 papers), RNA Interference and Gene Delivery (7 papers) and Virus-based gene therapy research (4 papers). Kaite Honeyman collaborates with scholars based in Australia, United States and United Kingdom. Kaite Honeyman's co-authors include Steve D. Wilton, Sue Fletcher, Frances Lloyd, Christopher J. Mann, Abbie Fall, Penny L Harding, R. Johnsen, Andy Cheng, Jennifer E. Morgan and Terry Partridge and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Molecular Therapy and Human Mutation.

In The Last Decade

Kaite Honeyman

13 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kaite Honeyman Australia	10	1.1k	337	214	179	97	13	1.1k
Suzan M. Hammond United Kingdom	17	1.2k 1.2×	207 0.6×	385 1.8×	107 0.6×	45 0.5×	32	1.4k
Stephanie F. Phelps United States	7	1.2k 1.2×	506 1.5×	88 0.4×	269 1.5×	101 1.0×	8	1.3k
Yusuke Echigoya Japan	20	960 0.9×	196 0.6×	236 1.1×	185 1.0×	22 0.2×	33	1.0k
Hans Heemskerk Netherlands	10	691 0.6×	150 0.4×	136 0.6×	73 0.4×	47 0.5×	12	744
Penny L Harding Australia	6	513 0.5×	168 0.5×	104 0.5×	64 0.4×	55 0.6×	7	589
Michael J. Blankinship United States	13	1.5k 1.4×	963 2.9×	120 0.6×	475 2.7×	51 0.5×	14	1.7k
Courtney S. Young United States	12	862 0.8×	216 0.6×	126 0.6×	71 0.4×	28 0.3×	20	991
Carmen Bertoni United States	17	662 0.6×	246 0.7×	74 0.3×	51 0.3×	32 0.3×	27	763
Takako I. Jones United States	19	909 0.9×	120 0.4×	242 1.1×	225 1.3×	18 0.2×	32	948
Kristin N. Heller United States	14	569 0.5×	180 0.5×	91 0.4×	137 0.8×	17 0.2×	20	644

Countries citing papers authored by Kaite Honeyman

Since Specialization

Citations

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

Fields of papers citing papers by Kaite Honeyman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kaite Honeyman

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

All Works

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13 of 13 papers shown

1.

Fletcher, Sue, Kaite Honeyman, Abbie Fall, et al.. (2007). Morpholino Oligomer–Mediated Exon Skipping Averts the Onset of Dystrophic Pathology in the mdx Mouse. Molecular Therapy. 15(9). 1587–1592. 124 indexed citations

2.

Harding, Penny L, Abbie Fall, Kaite Honeyman, Sue Fletcher, & Steve D. Wilton. (2006). The Influence of Antisense Oligonucleotide Length on Dystrophin Exon Skipping. Molecular Therapy. 15(1). 157–166. 74 indexed citations

3.

Fall, Abbie, R. Johnsen, Kaite Honeyman, et al.. (2006). Induction of revertant fibres in the mdx mouse using antisense oligonucleotides. PubMed. 4(1). 3–3. 31 indexed citations

4.

Fletcher, Sue, Kaite Honeyman, Abbie Fall, et al.. (2005). Dystrophin expression in the mdx mouse after localised and systemic administration of a morpholino antisense oligonucleotide. The Journal of Gene Medicine. 8(2). 207–216. 142 indexed citations

5.

Mann, Christopher J., Kaite Honeyman, Graham McClorey, Sue Fletcher, & Steve D. Wilton. (2002). Improved antisense oligonucleotide induced exon skipping in the mdx mouse model of muscular dystrophy. The Journal of Gene Medicine. 4(6). 644–654. 119 indexed citations

6.

Mann, Christopher J., Kaite Honeyman, Andy Cheng, et al.. (2000). Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouse. Proceedings of the National Academy of Sciences. 98(1). 42–47. 311 indexed citations

7.

Honeyman, Kaite, et al.. (1999). Development of a snapback method of single-strand conformation polymorphism analysis for genotyping Golden Retrievers for the X-linked muscular dystrophy allele. American Journal of Veterinary Research. 60(6). 734–737. 25 indexed citations

8.

Wilton, Steve D., Frances Lloyd, Kylie Carville, et al.. (1999). Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotides. Neuromuscular Disorders. 9(5). 330–338. 175 indexed citations

9.

Wilton, Steve D., Kaite Honeyman, Sue Fletcher, & Nigel G. Laing. (1998). Snapback SSCP analysis: Engineered conformation changes for the rapid typing of known mutations. Human Mutation. 11(3). 252–258. 3 indexed citations

10.

Wilton, Steve D., Kaite Honeyman, Sue Fletcher, & Nigel G. Laing. (1998). Snapback SSCP analysis: Engineered conformation changes for the rapid typing of known mutations. Human Mutation. 11(3). 252–258. 12 indexed citations

11.

Laing, Nigel G., B.A. Laing, Christopher S. Meredith, et al.. (1995). Autosomal dominant distal myopathy: linkage to chromosome 14.. PubMed. 56(2). 422–7. 96 indexed citations

12.

Meredith, Christopher S., Steve D. Wilton, Kaite Honeyman, et al.. (1994). Autosomal dominant distal myopathy linkage on Chromosome 14. UWA Profiles and Research Repository (University of Western Australia). 1 indexed citations

13.

Laing, Nigel G., B.A. Laing, Christopher S. Meredith, et al.. (1993). Autosomal dominant distal myopathy: linkage to chromosome 14. UWA Profiles and Research Repository (UWA). 1 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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