Sian Spacey

1.1k total citations
25 papers, 598 citations indexed

About

Sian Spacey is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Sian Spacey has authored 25 papers receiving a total of 598 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Cellular and Molecular Neuroscience, 10 papers in Molecular Biology and 8 papers in Neurology. Recurrent topics in Sian Spacey's work include Genetic Neurodegenerative Diseases (11 papers), Neurological disorders and treatments (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Sian Spacey is often cited by papers focused on Genetic Neurodegenerative Diseases (11 papers), Neurological disorders and treatments (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Sian Spacey collaborates with scholars based in Canada, United Kingdom and United States. Sian Spacey's co-authors include Terrance P. Snutch, Thomas D. Bird, Gordon Andrews, Ciarán Keogh, D A Graeb, Paul J. Adams, Nicholas Wood, Michael E. Hildebrand, Laurence S. David and Esperanza Garcı́a and has published in prestigious journals such as Neurology, Annals of Neurology and American Journal of Roentgenology.

In The Last Decade

Sian Spacey

25 papers receiving 580 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sian Spacey Canada 16 273 256 208 180 68 25 598
Tracey D. Graves United Kingdom 13 480 1.8× 461 1.8× 247 1.2× 105 0.6× 72 1.1× 25 766
Tiina Keränen Finland 11 206 0.8× 134 0.5× 211 1.0× 279 1.6× 55 0.8× 12 681
I. Rautakorpi Finland 8 174 0.6× 352 1.4× 206 1.0× 184 1.0× 71 1.0× 15 790
G. Gobbi Italy 14 195 0.7× 141 0.6× 115 0.6× 403 2.2× 27 0.4× 41 722
K. Meng Tan Australia 10 115 0.4× 129 0.5× 365 1.8× 169 0.9× 49 0.7× 25 637
Naomi Kanazawa Japan 17 138 0.5× 244 1.0× 342 1.6× 110 0.6× 32 0.5× 55 781
Waleed Altwaijri Saudi Arabia 11 52 0.2× 122 0.5× 132 0.6× 141 0.8× 49 0.7× 25 478
Jiro Idezuka Japan 10 218 0.8× 133 0.5× 396 1.9× 41 0.2× 87 1.3× 17 557
Stanley D. Johnsen United States 13 102 0.4× 510 2.0× 87 0.4× 45 0.3× 71 1.0× 29 895
Lubov Blumkin Israel 14 161 0.6× 214 0.8× 90 0.4× 101 0.6× 50 0.7× 31 502

Countries citing papers authored by Sian Spacey

Since Specialization
Citations

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

Fields of papers citing papers by Sian Spacey

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sian Spacey

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

All Works

20 of 20 papers shown
1.
Spacey, Sian & Paul J. Adams. (2013). Familial Paroxysmal Kinesigenic Dyskinesia. 6 indexed citations
2.
Spacey, Sian, et al.. (2013). Unilateral Pallidal Deep Brain Stimulation in a Patient with Dystonia Secondary to Episodic Ataxia Type 2. Stereotactic and Functional Neurosurgery. 91(4). 233–235. 9 indexed citations
3.
Schulzer, Michael, et al.. (2013). Early Clinical Features Differentiate Cerebellar Variant MSA and Sporadic Ataxia. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 40(2). 252–254. 2 indexed citations
4.
Gardiner, A., Kailash P. Bhatia, Russell C. Dale, et al.. (2012). Prrt2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine. ARAN (University of Galway Research Repository) (Ollscoil na Gaillimhe – University of Galway). 5 indexed citations
5.
Buxton, Jane A., et al.. (2011). Chasing the dragon - characterizing cases of leukoencephalopathy associated with heroin inhalation in British Columbia. Harm Reduction Journal. 8(1). 3–3. 28 indexed citations
6.
7.
Schulzer, Michael, et al.. (2007). Ataxia and the Role of Antigliadin Antibodies. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 34(2). 193–196. 17 indexed citations
8.
Spacey, Sian, et al.. (2005). Familial Hemiplegic Migraine Presenting as Recurrent Encephalopathy in a Native Indian Family. Headache The Journal of Head and Face Pain. 45(9). 1244–1249. 16 indexed citations
9.
Spacey, Sian, et al.. (2005). Two Novel CACNA1A Gene Mutations Associated With Episodic Ataxia Type 2 and Interictal Dystonia. Archives of Neurology. 62(2). 314–314. 54 indexed citations
10.
Furtado, Sarah, Ranjit Ranawaya, Jillian S. Parboosingh, et al.. (2005). Adult Onset Spinocerebellar Ataxia in a Canadian Movement Disorders Clinic. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 32(4). 450–458. 22 indexed citations
11.
Spacey, Sian, et al.. (2004). Fatal Familial Insomnia. Archives of Neurology. 61(1). 122–122. 16 indexed citations
12.
Spacey, Sian, et al.. (2004). Malaysian Siblings with Friedreich Ataxia and Chorea: A Novel Deletion in the Frataxin Gene. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 31(3). 383–386. 18 indexed citations
13.
Spacey, Sian, et al.. (2004). Functional implications of a novel EA2 mutation in the P/Q‐type calcium channel. Annals of Neurology. 56(2). 213–220. 60 indexed citations
14.
Chapman, Kristine, Cory Toth, Andrew R. Woolfenden, et al.. (2003). Pseudomigraine With Lymphocytic Pleocytosis: A Calcium Channelopathy? Clinical Description of 10 Cases and Genetic Analysis of the Familial Hemiplegic Migraine Gene CACNA1A. Headache The Journal of Head and Face Pain. 43(8). 892–895. 32 indexed citations
15.
Spacey, Sian, et al.. (2002). Mutation analysis of the sodium/hydrogen exchanger gene (NHE5) in familial paroxysmal kinesigenic dyskinesia. Journal of Neural Transmission. 109(9). 1189–1194. 7 indexed citations
16.
Spacey, Sian, Enza Maria Valente, Thomas T. Warner, et al.. (2002). Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: Evidence for a third EKD gene. Movement Disorders. 17(4). 717–725. 40 indexed citations
17.
Bebb, D. Gwyn, Gary de Jong, Zhe Yu, et al.. (2001). Radiation induced apoptosis in ataxia telangiectasia homozygote, heterozygote and normal cells. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 476(1-2). 13–20. 12 indexed citations
18.
Spacey, Sian, R A Gatti, & Gwyn Bebb. (2000). The Molecular Basis and Clinical Management of Ataxia Telangiectasia. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 27(3). 184–191. 23 indexed citations
19.
Spacey, Sian & Nicholas Wood. (1999). The genetics of Parkinsonʼs disease. Current Opinion in Neurology. 12(4). 427–432. 15 indexed citations
20.
Spacey, Sian & Paul J. Adams. (1993). Familial Paroxysmal Kinesigenic Dyskinesia – RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY. 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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