Vicki Fabian

1.0k total citations
20 papers, 596 citations indexed

About

Vicki Fabian is a scholar working on Epidemiology, Genetics and Neurology. According to data from OpenAlex, Vicki Fabian has authored 20 papers receiving a total of 596 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Epidemiology, 5 papers in Genetics and 5 papers in Neurology. Recurrent topics in Vicki Fabian's work include Inflammatory Myopathies and Dermatomyositis (6 papers), Glioma Diagnosis and Treatment (3 papers) and Hereditary Neurological Disorders (3 papers). Vicki Fabian is often cited by papers focused on Inflammatory Myopathies and Dermatomyositis (6 papers), Glioma Diagnosis and Treatment (3 papers) and Hereditary Neurological Disorders (3 papers). Vicki Fabian collaborates with scholars based in Australia, United States and Thailand. Vicki Fabian's co-authors include Frank Mastaglia, Merrilee Needham, Frank Christiansen, Alastair Corbett, Timothy Day, Byron A. Kakulas, B P Wood, Phillipa J. Lamont, P. J. Zilko and Hayley J. Durling and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and Acta Neuropathologica.

In The Last Decade

Vicki Fabian

18 papers receiving 588 citations

Peers

Vicki Fabian

EPIDE

CCM

NEURO

GENET

C. Sewry United Kingdom

Amal Y. Kentab Saudi Arabia

T. E. Bertoríni United States

Robert‐Yves Carlier France

Nicoletta Checcarelli Italy

Tracey Willis United Kingdom

Ichiro Kuki Japan

Mark A. Levenstien United States

Sara Bonato Italy

Maria Rita Murru Italy

C. Sewry United Kingdom

Vicki Fabian

382 ×1.4

170 ×0.8

EPIDE

122 ×0.9

CCM

35 ×0.3

NEURO

32 ×0.4

GENET

Citations per year, relative to Vicki Fabian Vicki Fabian (= 1×) peers C. Sewry

Countries citing papers authored by Vicki Fabian

Since Specialization

Citations

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

Fields of papers citing papers by Vicki Fabian

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vicki Fabian

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

All Works

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20 of 20 papers shown

Khan, Mumtaz J., Gabriel Lee, Sharon Lee, et al.. (2023). Long-term outcomes of symptomatic optic pathway glioma: 32-year experience at a single Western Australian tertiary pediatric oncology center. Frontiers in Oncology. 13. 1157909–1157909. 3 indexed citations

Speers, David, et al.. (2021). A detailed neuropathological assessment of a Western Australian case of Balamuthia mandrillaris amoebic encephalitis. Pathology. 53. S29–S30.

Valentine, Jane, Roslyn Ward, Ashleigh Thornton, et al.. (2019). Normative data of muscle fiber diameter of vastus lateralis during childhood: a field test. Muscle & Nerve. 59(5). 590–593. 2 indexed citations

Valentine, Jane, Katherine Stannage, Vicki Fabian, et al.. (2015). Muscle histopathology in children with spastic cerebral palsy receiving botulinum toxin type A. Muscle & Nerve. 53(3). 407–414. 28 indexed citations

Fabian, Vicki, et al.. (2015). Compliance with reporting guidelines by Australian pathologists: an audit of the quality of histopathology reporting in high-grade glioma. Neuro-Oncology Practice. 3(2). 97–104.

Luo, Yue‐Bei, Chalermchai Mitrpant, R. Johnsen, et al.. (2013). Investigation of splicing changes and post-translational processing of LMNA in sporadic inclusion body myositis.. PubMed. 6(9). 1723–33. 5 indexed citations

Rojana-udomsart, Arada, Merrilee Needham, Yue‐Bei Luo, et al.. (2011). The association of sporadic inclusion body myositis and Sjögren's syndrome in carriers of HLA-DR3 and the 8.1 MHC ancestral haplotype. Clinical Neurology and Neurosurgery. 113(7). 559–563. 36 indexed citations

Rojana-udomsart, Arada, Vicki Fabian, Peter Hollingsworth, et al.. (2010). Paraspinal and Scapular Myopathy Associated With Scleroderma. Journal of Clinical Neuromuscular Disease. 11(4). 213–222. 16 indexed citations

Holthouse, David, Peter B. Dallas, Jette Ford, et al.. (2008). Classic and desmoplastic medulloblastoma: Complete case reports and characterizations of two new cell lines. Neuropathology. 29(4). 398–409. 8 indexed citations

10.

Needham, Merrilee, Alastair Corbett, Timothy Day, et al.. (2008). Prevalence of sporadic inclusion body myositis and factors contributing to delayed diagnosis. Journal of Clinical Neuroscience. 15(12). 1350–1353. 115 indexed citations

11.

Needham, Merrilee, Alastair Corbett, Timothy Day, Vicki Fabian, & Francis Mastaglia. (2007). G.P.13.07 Prevalence and diagnosis of sporadic inclusion body myositis (sIBM) in Western Australia. Neuromuscular Disorders. 17(9-10). 850–851. 1 indexed citations

12.

Mastaglia, Frank, Patricia Price, Susan Walters, et al.. (2006). Familial inclusion body myositis in a mother and son with different ancestral MHC haplotypes. Neuromuscular Disorders. 16(11). 754–758. 12 indexed citations

13.

Kankirawatana, Pongkiat, Helen Leonard, Carolyn Ellaway, et al.. (2006). Early progressive encephalopathy in boys and MECP2 mutations. Neurology. 67(1). 164–166. 71 indexed citations

14.

Lamont, Phillipa J., David R. Thorburn, Vicki Fabian, et al.. (2004). Nemaline Rods and Complex I Deficiency in Three Infants with Hypotonia, Motor Delay and Failure to Thrive. Neuropediatrics. 35(5). 302–306. 17 indexed citations

15.

Meredith, Christopher S., Ralf Herrmann, Danielle E. Dye, et al.. (2004). Mutations in the Slow Skeletal Muscle Fiber Myosin Heavy Chain Gene (MYH7) Cause Laing Early-Onset Distal Myopathy (MPD1). The American Journal of Human Genetics. 75(4). 703–708. 156 indexed citations

16.

Halliday, Glenda M., Tony Ng, Michael Rodriguez, et al.. (2002). Consensus neuropathological diagnosis of common dementia syndromes: testing and standardising the use of multiple diagnostic criteria. Acta Neuropathologica. 104(1). 72–78. 44 indexed citations

17.

Panegyres, Peter K., Cyril Mamotte, Samuel D Vasikaran, et al.. (1999). Butyrylcholinesterase K variant and Alzheimer's disease. Journal of Neurology. 246(5). 369–370. 24 indexed citations

18.

Laing, Nigel G., Francis Mastaglia, Vicki Fabian, et al.. (1998). Genetic studies in a family with autosomal dominant rod and core disease. Journal of Leukocyte Biology. 97(2). 237–45. 1 indexed citations

19.

Stell, Rick, et al.. (1997). Linkage to the myelin protein zero locus in a family with intermediate HMSN. Neuromuscular Disorders. 7(6-7). 470–470. 1 indexed citations

20.

Fabian, Vicki, et al.. (1997). Herpes zoster brachial plexus neuritis.. PubMed. 16(2). 61–4. 56 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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