Mark Busby

1.1k total citations
6 papers, 224 citations indexed

About

Mark Busby is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Mark Busby has authored 6 papers receiving a total of 224 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Neurology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Mark Busby's work include Peripheral Neuropathies and Disorders (2 papers), Muscle Physiology and Disorders (2 papers) and Hereditary Neurological Disorders (2 papers). Mark Busby is often cited by papers focused on Peripheral Neuropathies and Disorders (2 papers), Muscle Physiology and Disorders (2 papers) and Hereditary Neurological Disorders (2 papers). Mark Busby collaborates with scholars based in United Kingdom. Mark Busby's co-authors include Michael Donaghy, Michelle Eagle, Francesco Muntoni, John Bourke, K. Bushby, Maja Poppe, Andy J. Wills, Daniel Birchall, Martin Brockington and M. Buddles and has published in prestigious journals such as Neurology, Journal of Neurology and Orphanet Journal of Rare Diseases.

In The Last Decade

Mark Busby

6 papers receiving 214 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mark Busby United Kingdom	4	139	106	65	45	24	6	224
Dongxue Ding China	11	108 0.8×	69 0.7×	46 0.7×	15 0.3×	24 1.0×	26	235
Reinhard Rohkamm Germany	10	172 1.2×	97 0.9×	39 0.6×	88 2.0×	15 0.6×	16	288
Miriam Rodrigues New Zealand	9	165 1.2×	187 1.8×	71 1.1×	14 0.3×	16 0.7×	24	295
Mary S. Carvalho Brazil	11	215 1.5×	42 0.4×	20 0.3×	65 1.4×	7 0.3×	27	267
Irene Sanz‐Gallego Spain	11	187 1.3×	221 2.1×	165 2.5×	7 0.2×	13 0.5×	14	357
Satu Sandell Finland	10	232 1.7×	89 0.8×	46 0.7×	114 2.5×	3 0.1×	21	313
C. Cini United Kingdom	5	103 0.7×	38 0.4×	12 0.2×	40 0.9×	11 0.5×	5	148
Jenni Jonasson Sweden	10	242 1.7×	93 0.9×	28 0.4×	73 1.6×	5 0.2×	14	307
E. Bonifazi Italy	12	366 2.6×	348 3.3×	149 2.3×	52 1.2×	11 0.5×	18	472
María A. Ramos-Arroyo Spain	8	144 1.0×	172 1.6×	136 2.1×	12 0.3×	5 0.2×	9	336

Countries citing papers authored by Mark Busby

Since Specialization

Citations

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

Fields of papers citing papers by Mark Busby

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark Busby

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

All Works

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6 of 6 papers shown

1.

Cosgrove, Jeremy, et al.. (2014). Adult onset Brown–Vialetto–Van Laere syndrome with opsoclonus and a novel heterozygous mutation: A case report. Clinical Neurology and Neurosurgery. 128. 1–3. 18 indexed citations

2.

Wood, Libby, Teresinha Evangelista, Fiona Norwood, et al.. (2014). UK Facioscapulohumeral Muscular Dystrophy (FSHD) Patient Registry. Orphanet Journal of Rare Diseases. 9(S1). 2 indexed citations

3.

Cosgrove, Jeremy & Mark Busby. (2013). Hemiatrophy and seizures: a case of adult-onset Rasmussen encephalitis. Practical Neurology. 13(1). 54–55. 4 indexed citations

4.

Poppe, Maja, Lynsey Cree, John Bourke, et al.. (2003). The phenotype of limb-girdle muscular dystrophy type 2I. Neurology. 60(8). 1246–1251. 136 indexed citations

5.

Busby, Mark & Michael Donaghy. (2003). Chronic dysimmune neuropathy. Journal of Neurology. 250(6). 714–724. 61 indexed citations

6.

Busby, Mark & Michael Donaghy. (2000). Predominant arm weakness in acute idiopathic polyneuritis: a distinct regional variant. Journal of Neurology. 247(5). 343–345. 3 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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