Frances Busfield

1.7k total citations
19 papers, 577 citations indexed

About

Frances Busfield is a scholar working on Molecular Biology, Rheumatology and Genetics. According to data from OpenAlex, Frances Busfield has authored 19 papers receiving a total of 577 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Rheumatology and 4 papers in Genetics. Recurrent topics in Frances Busfield's work include Porphyrin Metabolism and Disorders (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Folate and B Vitamins Research (3 papers). Frances Busfield is often cited by papers focused on Porphyrin Metabolism and Disorders (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Folate and B Vitamins Research (3 papers). Frances Busfield collaborates with scholars based in Australia, United States and United Kingdom. Frances Busfield's co-authors include Janine Kesting, Joanne T.E. Shaw, David L. Duffy, David A. Good, Paul K. Lovelock, John Roger Andersen, Alison Goate, Corinne Lendon, Joanne Norton and Dorothy H. Crawford and has published in prestigious journals such as Hepatology, Neurology and The American Journal of Human Genetics.

In The Last Decade

Frances Busfield

19 papers receiving 556 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Frances Busfield Australia 10 214 158 142 97 85 19 577
Taissa M. Kasahara Brazil 19 140 0.7× 63 0.4× 91 0.6× 29 0.3× 104 1.2× 33 846
Annette Sauter Switzerland 12 124 0.6× 26 0.2× 111 0.8× 103 1.1× 150 1.8× 23 594
Tobias Moser Austria 11 94 0.4× 33 0.2× 118 0.8× 32 0.3× 141 1.7× 33 544
Ruthann Kibler United States 6 177 0.8× 39 0.2× 114 0.8× 63 0.6× 31 0.4× 11 658
Takehiro Higashi Japan 12 113 0.5× 73 0.5× 72 0.5× 19 0.2× 23 0.3× 25 540
Tiziana Del Beato Italy 16 139 0.6× 49 0.3× 263 1.9× 59 0.6× 11 0.1× 68 830
F. T. A. Fitzpatrick United Kingdom 10 65 0.3× 81 0.5× 62 0.4× 153 1.6× 14 0.2× 10 698
Cornelia M. Spies Germany 13 155 0.7× 62 0.4× 82 0.6× 123 1.3× 15 0.2× 17 597
C J Mumford United Kingdom 11 303 1.4× 25 0.2× 32 0.2× 57 0.6× 154 1.8× 25 798
Shuan-Pei Lin Taiwan 19 239 1.1× 371 2.3× 21 0.1× 158 1.6× 14 0.2× 39 793

Countries citing papers authored by Frances Busfield

Since Specialization
Citations

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

Fields of papers citing papers by Frances Busfield

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frances Busfield

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

All Works

19 of 19 papers shown
1.
Good, David A., et al.. (2019). Noncoding Variations in the Gene Encoding Ceramide Synthase 6 are Associated with Type 2 Diabetes in a Large Indigenous Australian Pedigree. Twin Research and Human Genetics. 22(2). 79–87. 1 indexed citations
2.
Morgan, Jess A. T., Frances Busfield, Mukesh Srivastava, et al.. (2012). Observation of a novel Babesia spp. in Eastern Grey Kangaroos (Macropus giganteus) in Australia. International Journal for Parasitology Parasites and Wildlife. 2. 54–61. 19 indexed citations
3.
Busfield, Frances, Brian Haluska, Adrian Barnett, et al.. (2005). Carotid artery intimal medial thickness, brachial artery flow-mediated vasodilation and cardiovascular risk factors in diabetic and non-diabetic indigenous Australians. Atherosclerosis. 180(2). 319–326. 11 indexed citations
4.
Good, David A., Frances Busfield, Paul K. Lovelock, et al.. (2004). Identification of SQSTM1 mutations in familial Paget's disease in Australian pedigrees. Bone. 35(1). 277–282. 48 indexed citations
5.
Chan, Lung, Frances Busfield, Brian Haluska, et al.. (2004). Carotid artery intimal medial thickness, brachial artery flow mediated vasodilation and cardiovascular disease risk factors in diabetic and non-diabetic indigenous Australians. Queensland's institutional digital repository (The University of Queensland). 242–242. 1 indexed citations
6.
Busfield, Frances, David L. Duffy, Janine Kesting, et al.. (2002). A Genomewide Search for Type 2 Diabetes–Susceptibility Genes in Indigenous Australians. The American Journal of Human Genetics. 70(2). 349–357. 68 indexed citations
7.
Good, David A., Frances Busfield, David L. Duffy, et al.. (2002). Linkage of Paget Disease of Bone to a Novel Region on Human Chromosome 18q23. The American Journal of Human Genetics. 70(2). 517–525. 65 indexed citations
8.
Good, David A., Frances Busfield, David L. Duffy, et al.. (2001). Familial Paget's Disease of Bone: Nonlinkage to the PDB1 and PDB2 Loci on Chromosomes 6p and 18q in a Large Pedigree. Journal of Bone and Mineral Research. 16(1). 33–38. 30 indexed citations
9.
Goldwurm, Stefano, Joanne Banyer, Lara M. Cullen, et al.. (1998). Generation of a transcription map distal to HLA-F. European Journal of Human Genetics. 6(5). 475–486. 1 indexed citations
10.
Stuart, Katherine, Frances Busfield, Elizabeth C. Jazwinska, et al.. (1998). The C282Y mutation in the haemochromatosis gene (HFE) and hepatitis C virus infection are independent cofactors for porphyria cutanea tarda in Australian patients. Journal of Hepatology. 28(3). 404–409. 92 indexed citations
11.
Lendon, Corinne, Timothy Lynch, Joanne Norton, et al.. (1998). Hereditary dysphasic disinhibition dementia A frontotemporal dementia linked to 17 q21‐‐22. Neurology. 50(6). 1546–1555. 111 indexed citations
12.
Olynyk, John K., Digby J Cullen, S. Aquilia, et al.. (1998). Clinical Expression of the Hemochromatosis Genotype CYS282TYR in the Busselton Population. UWA Profiles and Research Repository (UWA). 2 indexed citations
13.
Busfield, Frances, et al.. (1997). Association of the HFE C282Y mutation with porphyria cutanea tarda in Australian patients The 47th Annual Meeting of the American Society of Human Genetics was held in Baltimore, Maryland, October 28 to November 1, l997. The American Journal of Human Genetics. 61. 1 indexed citations
14.
Stuart, Katherine, et al.. (1997). The C282Y mutation in HFE is common in Australian patients and can act independently of HCV to precipitate porphyria cutanea tarda. Hepatology. 26. 1911–1911. 2 indexed citations
15.
Lendon, Corinne, Alonso Martínez, María Isabel Behrens, et al.. (1997). E280A PS-1 mutation causes Alzheimer's disease but age of onset is not modified by ApoE alleles. Human Mutation. 10(3). 186–195. 69 indexed citations
16.
Lendon, Corinne, Alonso Martínez, María Isabel Behrens, et al.. (1997). E280A PS‐1 mutation causes Alzheimer's disease but age of onset is not modified by ApoE alleles. Human Mutation. 10(3). 186–195. 9 indexed citations
17.
Clark, Robert, M. Hutton, Chris J. Talbot, et al.. (1996). . Cold Spring Harbor Symposia on Quantitative Biology. 61(1). 551–558. 6 indexed citations
18.
Lendon, Corinne, Stephen B. Shears, Frances Busfield, et al.. (1994). Molecular genetics of hereditary dysphasic dementia. Neurobiology of Aging. 15. S128–S128. 5 indexed citations
19.

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 Taissa M. Kasahara Breakdown of academic impact, for papers by Annette Sauter Breakdown of academic impact, for papers by Tobias Moser Breakdown of academic impact, for papers by Ruthann Kibler Breakdown of academic impact, for papers by Takehiro Higashi Breakdown of academic impact, for papers by Tiziana Del Beato Breakdown of academic impact, for papers by F. T. A. Fitzpatrick Breakdown of academic impact, for papers by Cornelia M. Spies Breakdown of academic impact, for papers by C J Mumford Breakdown of academic impact, for papers by Shuan-Pei Lin
Rankless by CCL
2026