Author

Sian D. Spacey

Observed names: S. D. Spacey, S.D. Spacey, Sian D Spacey, Sian Spacey, Siân D. Spacey

Institutions: University of British Columbia Hospital, University of British Columbia, Vancouver General Hospital

Observed institutions: University of British Columbia Hospital, The University of Sydney, University of British Columbia, Ollscoil na Gaillimhe – University of Galway, Vancouver Hospital and Health Sciences Centre, The Royal Free Hospital, St. Paul's Hospital, Children's Hospital at Westmead, Vancouver General Hospital, Westmead Hospital, KLE Society Hospital, St. Paul's Hospital, National Hospital for Neurology and Neurosurgery, UCL Queen Square Institute of Neurology, Centre for Heart Lung Innovation, University College London

OpenAlex ID: A5069067442

PRRT2 gene mutations: From paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine

2012 · Alice R. Gardiner, Kailash P. Bhatia, et al. · Neurology · 183

PDF

Neuroimaging Features of Heroin Inhalation Toxicity: “Chasing the Dragon”

2003 · Ciaran F. Keogh, Gordon T. Andrews, et al. · American Journal of Roentgenology · 153

Two Novel CACNA1A Gene Mutations Associated With Episodic Ataxia Type 2 and Interictal Dystonia

2005 · Sian D. Spacey, Luke A. Materek, et al. · Archives of Neurology · 90

Ca V 2.1 P/Q-type calcium channel alternative splicing affects the functional impact of familial hemiplegic migraine mutations: Implications for calcium channelopathies

2009 · Paul J. Adams, Esperanza Garcia, et al. · Channels · 89

Functional implications of a novel EA2 mutation in the P/Q‐type calcium channel

2004 · Sian D. Spacey, Michael E. Hildebrand, et al. · Annals of Neurology · 85

Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: Evidence for a third EKD gene

2002 · Sian D. Spacey, Enza‐Maria Valente, et al. · Movement Disorders · 80

Genetic heterogeneity in paroxysmal nonkinesigenic dyskinesia

2006 · S. D. Spacey, P. J. Adams, et al. · Neurology · 61

Chasing the dragon - characterizing cases of leukoencephalopathy associated with heroin inhalation in British Columbia

2011 · Jane A Buxton, Renee Sebastian, et al. · Harm Reduction Journal · 44

PDF

Pseudomigraine With Lymphocytic Pleocytosis: A Calcium Channelopathy? Clinical Description of 10 Cases and Genetic Analysis of the Familial Hemiplegic Migraine Gene CACNA1A

2003 · Kristine M. Chapman, Blazej I. Szczygielski, et al. · Headache The Journal of Head and Face Pain · 44

The Molecular Basis and Clinical Management of Ataxia Telangiectasia

2000 · Sian D. Spacey, Richard A. Gatti, et al. · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · 41

PDF

Adult Onset Spinocerebellar Ataxia in a Canadian Movement Disorders Clinic

2005 · Scott Kraft, Sarah Furtado, et al. · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · 38

PDF

The paroxysmal dyskinesias

2001 · Nardo Nardocci, Emilio Fernández-Alvarez, et al. · Cambridge University Press eBooks · 27

Ataxia and the Role of Antigliadin Antibodies

2007 · D. Wong, M. Dwinnel, et al. · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · 24

PDF

Fatal Familial Insomnia: The First Account in a Family of Chinese Descent

2004 · Sian D. Spacey, Manuela Pastore, et al. · Archives of Neurology · 23

Malaysian Siblings with Friedreich Ataxia and Chorea: A Novel Deletion in the Frataxin Gene

2004 · Siân D. Spacey, Blazej I. Szczygielski, et al. · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · 22

PDF

A real‐world, observational study of erenumab for migraine prevention in Canadian patients

2022 · Werner J. Becker, Sian Spacey, et al. · Headache The Journal of Head and Face Pain · 20

The genetics of Parkinsonʼs disease

1999 · Siân D. Spacey, Nicholas W. Wood · Current Opinion in Neurology · 20

Migraine with aura as the predominant phenotype in a family with a PRRT2 mutation

2012 · Una-Marie Sheerin, Maria Stamelou, et al. · Journal of Neurology · 16

PDF

Familial Hemiplegic Migraine Presenting as Recurrent Encephalopathy in a Native Indian Family

2005 · Sian D. Spacey, Kaate R. J. Vanmolkot, et al. · Headache The Journal of Head and Face Pain · 16

Radiation induced apoptosis in ataxia telangiectasia homozygote, heterozygote and normal cells

2001 · D.Gwyn Bebb, Pamela J Warrington, et al. · Mutation research. Fundamental and molecular mechanisms of mutagenesis · 15

Episodic Ataxia Type 2

2015 · Sian Spacey · 14

Unilateral Pallidal Deep Brain Stimulation in a Patient with Dystonia Secondary to Episodic Ataxia Type 2

2013 · Anwen M. Harries, Mandeep Sandhu, et al. · Stereotactic and Functional Neurosurgery · 12

Mutation analysis of the sodium/hydrogen exchanger gene (NHE5) in familial paroxysmal kinesigenic dyskinesia

2002 · S. D. Spacey, B. I. Szczygielski, et al. · Journal of Neural Transmission · 12

Familial Paroxysmal Kinesigenic Dyskinesia

2013 · Sian Spacey, Paul J. Adams · University of Washington, Seattle eBooks · 9

Early Clinical Features Differentiate Cerebellar Variant MSA and Sporadic Ataxia

2013 · Alexandra Lloyd-Smith, Patrizio Jacova, et al. · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · 3

PDF

Works count: 42

Citation count: 1,146

H-index: 17

I10-index: 23