SM Huson

882 total citations
14 papers, 600 citations indexed

About

SM Huson is a scholar working on Neurology, Epidemiology and Cellular and Molecular Neuroscience. According to data from OpenAlex, SM Huson has authored 14 papers receiving a total of 600 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Neurology, 4 papers in Epidemiology and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in SM Huson's work include Neurofibromatosis and Schwannoma Cases (13 papers), Meningioma and schwannoma management (4 papers) and Soft tissue tumor case studies (3 papers). SM Huson is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (13 papers), Meningioma and schwannoma management (4 papers) and Soft tissue tumor case studies (3 papers). SM Huson collaborates with scholars based in United Kingdom, United States and South Africa. SM Huson's co-authors include Margaret A. Ponder, Douglas F. Easton, B. A. J. Ponder, Lyn Beck, David Jones, D. Gareth Evans, A Shenton, Meena Upadhyaya, Rosalie E. Ferner and James M. Farnham and has published in prestigious journals such as Human Molecular Genetics, Archives of Disease in Childhood and British Journal of Ophthalmology.

In The Last Decade

SM Huson

13 papers receiving 588 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
SM Huson United Kingdom 7 487 177 168 132 125 14 600
Silke Frahm Germany 8 431 0.9× 82 0.5× 98 0.6× 197 1.5× 128 1.0× 8 534
Antonia Gaona Spain 13 474 1.0× 112 0.6× 203 1.2× 354 2.7× 165 1.3× 16 808
Clare Giblin United States 2 503 1.0× 271 1.5× 115 0.7× 98 0.7× 133 1.1× 4 648
Raimund Fahsold Germany 14 397 0.8× 90 0.5× 128 0.8× 130 1.0× 344 2.8× 27 777
Corinne Bouvier‐Labit France 11 193 0.4× 115 0.6× 63 0.4× 105 0.8× 102 0.8× 16 576
Mary Jo Wenning United States 8 390 0.8× 82 0.5× 79 0.5× 131 1.0× 182 1.5× 9 581
V.-F. Mautner Germany 12 512 1.1× 296 1.7× 145 0.9× 81 0.6× 51 0.4× 16 587
Masahito Fujimoto Japan 15 351 0.7× 164 0.9× 61 0.4× 88 0.7× 140 1.1× 30 641
Annegret Buske Germany 13 566 1.2× 143 0.8× 236 1.4× 215 1.6× 327 2.6× 18 908
Zhongxue Wu China 15 434 0.9× 85 0.5× 75 0.4× 118 0.9× 112 0.9× 57 622

Countries citing papers authored by SM Huson

Since Specialization
Citations

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

Fields of papers citing papers by SM Huson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of SM Huson

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

All Works

14 of 14 papers shown
1.
George, K. Joshi, et al.. (2018). Spinal Lesions in Neurofibromatosis Type 1: Analysis of 149 Cases. International Journal of Surgery. 55. S1–S1. 1 indexed citations
2.
3.
Hockett, Christine W., SM Huson, S. A. Roberts, et al.. (2013). Vitamin D status and muscle function in children with neurofibromatosis type 1 (NF1).. PubMed. 13(1). 111–9. 18 indexed citations
4.
Freeman, Simon, Simon Lloyd, Samantha J. Mills, et al.. (2012). Early Results of Bevacizumab Treatment in Spinal and Peripheral Nerve Schwannomas in Neurofibromatosis Type 2 and Schwannomatosis. Journal of Neurological Surgery Part B Skull Base. 73(S 02). 1 indexed citations
5.
Shenton, A, et al.. (2009). Further genotype – phenotype correlations in neurofibromatosis 2. Clinical Genetics. 77(2). 163–170. 62 indexed citations
6.
Shenton, A, et al.. (2009). Further genotypeâphenotype correlations in neurofibromatosis 2. Clinical Genetics. no–no. 1 indexed citations
7.
Messiaen, Ludwine, Tom Callens, Dusica Babovic‐Vuksanovic, et al.. (2007). Genotype-phenotype correlations in spinal NF. 4 indexed citations
8.
Trivedi, Ritu, James P. Byrne, SM Huson, & Michael Donaghy. (2001). Focal Amyotrophy In Neurofibromatosis 2. Journal of the Peripheral Nervous System. 6(1). 62–62. 1 indexed citations
9.
Upadhyaya, Meena, et al.. (1999). Unusual clustering of brain tumours in a family with NF1 and variable expression of cutaneous features. Journal of Medical Genetics. 36(12). 893–896. 5 indexed citations
10.
Huson, SM. (1999). Neurofibromatosis Type 1 in Childhood.. Archives of Disease in Childhood. 80(3). 301–301.
11.
Easton, Douglas F., Margaret A. Ponder, SM Huson, & B. A. J. Ponder. (1993). An analysis of variation in expression of neurofibromatosis (NF) type 1 (NF1): evidence for modifying genes.. PubMed. 53(2). 305–13. 298 indexed citations
12.
Upadhyaya, Meena, Ming Shen, James M. Farnham, et al.. (1992). Analysis of mutations at the neurofibromatosis 1 (NF1) locus.. Human Molecular Genetics. 1(9). 735–740. 58 indexed citations
13.
Huson, SM, David Jones, & Lyn Beck. (1987). Ophthalmic manifestations of neurofibromatosis.. British Journal of Ophthalmology. 71(3). 235–238. 74 indexed citations
14.
Shaw, Duncan J., Andrea L. Meredith, M. Sarfarazi, et al.. (1986). Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19. Human Genetics. 74(3). 262–6. 27 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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