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Thomas Warner

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Jeremy C Hobart; Stefan J Cano; Thomas T Warner; Alan J Thompson
What sample sizes for reliability and validity studies in neurology?
Camilla N Clark; Holger Lerche; Yvonne W Weber; Thomas T Warner
Paroxysmal exercise-induced dyskinesia of the hands.
Alessandra Granata; Seong Joo Koo; Volker Haucke; Giampietro Schiavo; Thomas T Warner
CSN complex controls the stability of selected synaptic proteins via a torsinA-dependent process.

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All Publications

2012: Jeremy C Hobart; Stefan J Cano; Thomas T Warner; Alan J Thompson
What sample sizes for reliability and validity studies in neurology?
Journal of neurology 2012;259(12):2681-94.
2012: Camilla N Clark; Holger Lerche; Yvonne W Weber; Thomas T Warner
Paroxysmal exercise-induced dyskinesia of the hands.
Movement disorders : official journal of the Movement Disorder Society 2012;27(12):1579-80.
2011: Alessandra Granata; Seong Joo Koo; Volker Haucke; Giampietro Schiavo; Thomas T Warner
CSN complex controls the stability of selected synaptic proteins via a torsinA-dependent process.
The EMBO journal 2011;30(1):181-93.
2010: A Granata; Thomas T Warner
The role of torsinA in dystonia.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2010;17 Suppl 1():81-7.
2010: Thomas T Warner; Alassandra Granata; Giampietro Schiavo
TorsinA and DYT1 dystonia: a synaptopathy?
Biochemical Society transactions 2010;38(2):452-6.
2009: J Paul Simons; Raya Al-Shawi; Shane Minogue; Mark G Waugh; Claudia Wiedemann; Stylianos Evangelou; Andrzej Loesch; Talvinder S Sihra; Rosalind King; Thomas T Warner; J Justin Hsuan
Loss of phosphatidylinositol 4-kinase 2alpha activity causes late onset degeneration of spinal cord axons.
Proceedings of the National Academy of Sciences of the United States of America 2009;106(28):11535-9.
2009: Alessandra Granata; Giampietro Schiavo; Thomas T Warner
TorsinA and dystonia: from nuclear envelope to synapse.
Journal of neurochemistry 2009;109(6):1596-609.
2009: Jan-Willem Taanman; Mariza Daras; Juliane Albrecht; Charles A Davie; Elizabeth A Mallam; John R Muddle; Mark Weatherall; Thomas T Warner; Anthony H V Schapira; Lionel Ginsberg
Characterization of a novel TYMP splice site mutation associated with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).
Neuromuscular disorders : NMD 2009;19(2):151-4.
2008: Maria K Tsaousidou; Karim Ouahchi; Thomas T Warner; Yi Yang; Michael A Simpson; Nigel G Laing; Phillip A Wilkinson; Ricardo E Madrid; Heema Patel; Faycal Hentati; Michael A Patton; A Hentati; Philippa J Lamont; Teepu Siddique; Andrew H Crosby
Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degeneration.
American journal of human genetics 2008;82(2):510-5.
2008: Stefan J Cano; Thomas T Warner; Alan J Thompson; Kailash P Bhatia; Ray Fitzpatrick; Jeremy C Hobart
The cervical dystonia impact profile (CDIP-58): can a Rasch developed patient reported outcome measure satisfy traditional psychometric criteria?
Health and quality of life outcomes 2008;6():58.
2007: sara salinas; Rafael E Carazo-Salas; christos proukakis; Giampietro Schiavo; Thomas T Warner
Spastin and microtubules: Functions in health and disease.
Journal of neuroscience research 2007;85(12):2778-82.
2007: Anjum Misbahuddin; Mark R Placzek; Graham Lennox; Jan-Willem Taanman; Thomas T Warner
Myoclonus-dystonia syndrome with severe depression is caused by an exon-skipping mutation in the epsilon-sarcoglycan gene.
Movement disorders : official journal of the Movement Disorder Society 2007;22(8):1173-5.
2007: Stefan J Cano; Alan J Thompson; Kailash Bhatia; Ray Fitzpatrick; Thomas T Warner; Jeremy C Hobart
Evidence-based guidelines for using the Short Form 36 in cervical dystonia.
Movement disorders : official journal of the Movement Disorder Society 2007;22(1):122-6.
2006: Stefan J Cano; Jeremy C Hobart; M Edwards; Ray Fitzpatrick; Kailash Bhatia; Alan J Thompson; Thomas T Warner
CDIP-58 can measure the impact of botulinum toxin treatment in cervical dystonia.
Neurology 2006;67(12):2230-2.
2006: Susie M D Henley; Chris Frost; David G MacManus; Thomas T Warner; Nick C Fox; Sarah J Tabrizi
Increased rate of whole-brain atrophy over 6 months in early Huntington disease.
Neurology 2006;67(4):694-6.
2005: sara salinas; Rafael E Carazo-Salas; christos proukakis; J Mark Cooper; Anne E Weston; Giampietro Schiavo; Thomas T Warner
Human spastin has multiple microtubule-related functions.
Journal of neurochemistry 2005;95(5):1411-20.
2005: Sarah J Tabrizi; Andrew M Blamire; David Manners; Bheeshma Rajagopalan; Peter Styles; Anthony H V Schapira; Thomas T Warner
High-dose creatine therapy for Huntington disease: a 2-year clinical and MRS study.
Neurology 2005;64(9):1655-6.
2005: Johanna A Reed; Phillip A Wilkinson; Heema Patel; Michael A Simpson; Arnaud Chatonnet; Dimitri Robay; Michael A Patton; Andrew H Crosby; Thomas T Warner
A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia.
Neurogenetics 2005;6(2):79-84.
2005: Anjum Misbahuddin; Mark R Placzek; Jan-Willem Taanman; Stephen Gschmeissner; Giampietro Schiavo; J Mark Cooper; Thomas T Warner
Mutant torsinA, which causes early-onset primary torsion dystonia, is redistributed to membranous structures enriched in vesicular monoamine transporter in cultured human SH-SY5Y cells.
Movement disorders : official journal of the Movement Disorder Society 2005;20(4):432-40.
2005: Phillip A Wilkinson; Michael A Simpson; L Bastaki; Heema Patel; Johanna A Reed; Kamini Kalidas; E Samilchuk; R Khan; Thomas T Warner; Andrew H Crosby
A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1-12q14.
Journal of medical genetics 2005;42(1):80-2.
2004: Stefan J Cano; Thomas T Warner; J M Linacre; KP Bhatia; Alan J Thompson; Ray Fitzpatrick; Jeremy C Hobart
Capturing the true burden of dystonia on patients: the Cervical Dystonia Impact Profile (CDIP-58).
Neurology 2004;63(9):1629-33.
2004: Henry Houlden; Rosalind H M King; John R Muddle; Thomas T Warner; Mary M Reilly; Richard W Orrell; Lionel Ginsberg
A novel RAB7 mutation associated with ulcero-mutilating neuropathy.
Annals of neurology 2004;56(4):586-90.
2004: Stefan J Cano; Jeremy C Hobart; Ray Fitzpatrick; Kailash Bhatia; Alan J Thompson; Thomas T Warner
Patient-based outcomes of cervical dystonia: a review of rating scales.
Movement disorders : official journal of the Movement Disorder Society 2004;19(9):1054-9.
2004: Thomas T Warner; Heema Patel; christos proukakis; Johanna A Reed; Laura McKie; Adrian Wills; Michael A Patton; Andrew H Crosby
A clinical, genetic and candidate gene study of Silver syndrome, a complicated form of hereditary spastic paraplegia.
Journal of neurology 2004;251(9):1068-74.
2004: Phillip A Wilkinson; Andrew H Crosby; Christopher Turner; Lloyd J Bradley; Lionel Ginsberg; Nicholas W Wood; Anthony H V Schapira; Thomas T Warner
A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia.
Brain : a journal of neurology 2004;127(Pt 5):973-80.
2004: Christian Windpassinger; Michaela Auer-Grumbach; Joy Irobi; Heema Patel; Erwin Petek; Gerd Hörl; Roland Malli; Johanna A Reed; Ines Dierick; Nathalie Verpoorten; Thomas T Warner; christos proukakis; P Y K Van Den Bergh; Christine Verellen; Lionel Van Maldergem; Luciano Merlini; Peter De Jonghe; Vincent Timmerman; Andrew H Crosby; Klaus Wagner
Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome.
Nature genetics 2004;36(3):271-6.
2004: Anjum Misbahuddin; Mark R Placzek; Thomas T Warner
Focal dystonia is associated with a polymorphism of the dopamine D5 receptor gene.
Advances in neurology 2004;94():143-6.
2003: Phillip A Wilkinson; Paul E Hart; Heema Patel; Thomas T Warner; Andrew H Crosby
SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegia.
Journal of the neurological sciences 2003;216(1):43-5.
2003: Enza Maria Valente; Anjum Misbahuddin; Francesco Brancati; Mark R Placzek; Barbara Garavaglia; Sergio Salvi; Andrea Nemeth; Charles Shaw-Smith; Nardo Nardocci; Anna Rita Bentivoglio; Alfredo Berardelli; Roberto Eleopra; Bruno Dallapiccola; Thomas T Warner
Analysis of the epsilon-sarcoglycan gene in familial and sporadic myoclonus-dystonia: evidence for genetic heterogeneity.
Movement disorders : official journal of the Movement Disorder Society 2003;18(9):1047-51.
2003: Azlina Ahmad-Annuar; Paresh Shah; Majid Hafezparast; Holger Hummerich; Abi S Witherden; Karen E Morrison; Pamela J Shaw; Janine Kirby; Thomas T Warner; Andrew H Crosby; christos proukakis; Philip Wilkinson; Richard W Orrell; Lloyd Bradley; Joanne E Martin; Elizabeth M C Fisher
No association with common Caucasian genotypes in exons 8, 13 and 14 of the human cytoplasmic dynein heavy chain gene (DNCHC1) and familial motor neuron disorders.
Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases 2003;4(3):150-7.
2003: Phillip A Wilkinson; Andrew H Crosby; Christopher Turner; Heema Patel; Nicholas W Wood; Anthony H V Schapira; Thomas T Warner
A clinical and genetic study of SPG5A linked autosomal recessive hereditary spastic paraplegia.
Neurology 2003;61(2):235-8.
2003: Sarah J Tabrizi; Andrew M Blamire; David Manners; Bheeshma Rajagopalan; Peter Styles; Anthony H V Schapira; Thomas T Warner
Creatine therapy for Huntington's disease: clinical and MRS findings in a 1-year pilot study.
Neurology 2003;61(1):141-2.
2003: christos proukakis; Michaela Auer-Grumbach; Klaus Wagner; Phillip A Wilkinson; E Reid; Michael A Patton; Thomas T Warner; Andrew H Crosby
Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in the SPG4 (Spastin) gene.
Human mutation 2003;21(2):170.
2003: Thomas T Warner; Anthony H V Schapira
Genetic and environmental factors in the cause of Parkinson's disease.
Annals of neurology 2003;53 Suppl 3():S16-23; discussion S23-5.
2002: Mark R Placzek; Thomas T Warner
Basic genetics for the clinical neurologist.
Journal of neurology, neurosurgery, and psychiatry 2002;73 Suppl 2():II5-11.
2002: christos proukakis; Paul E Hart; Amy Cornish; Thomas T Warner; Andrew H Crosby
Three novel spastin (SPG4) mutations in families with autosomal dominant hereditary spastic paraplegia.
Journal of the neurological sciences 2002;201(1-2):65-9.
2002: Laura Camfield; Yoav Ben-Shlomo; Thomas T Warner
Impact of cervical dystonia on quality of life.
Movement disorders : official journal of the Movement Disorder Society 2002;17(4):838-41.
2002: Sian D Spacey; Enza Maria Valente; Gurusidheshwar M Wali; Thomas T Warner; Paul R Jarman; Anthony H V Schapira; Peter DIxon; Mary B Davis; Kailash P Bhatia; Nicholas W Wood
Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene.
Movement disorders : official journal of the Movement Disorder Society 2002;17(4):717-25.
2002: Anjum Misbahuddin; Mark R Placzek; K Ray Chaudhuri; Nicholas W Wood; KP Bhatia; Thomas T Warner
A polymorphism in the dopamine receptor DRD5 is associated with blepharospasm.
Neurology 2002;58(1):124-6.
2001: simon mead; christos proukakis; Nicholas W Wood; Andrew H Crosby; G T Plant; Thomas T Warner
A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilepsy in other affected family members.
Journal of neurology, neurosurgery, and psychiatry 2001;71(6):788-91.
2001: Phillip A Wilkinson; J L Bradley; Thomas T Warner
Friedreich's ataxia presenting as an isolated spastic paraparesis.
Journal of neurology, neurosurgery, and psychiatry 2001;71(5):709.
2001: Anjum Misbahuddin; Thomas T Warner
Dystonia: an update on genetics and treatment.
Current opinion in neurology 2001;14(4):471-5.
2001: Mark R Placzek; Anjum Misbahuddin; K Ray Chaudhuri; Nicholas W Wood; KP Bhatia; Thomas T Warner
Cervical dystonia is associated with a polymorphism in the dopamine (D5) receptor gene.
Journal of neurology, neurosurgery, and psychiatry 2001;71(2):262-4.
2001: Heema Patel; Paul E Hart; Thomas T Warner; R S Houlston; Michael A Patton; Steve Jeffery; Andrew H Crosby
The Silver syndrome variant of hereditary spastic paraplegia maps to chromosome 11q12-q14, with evidence for genetic heterogeneity within this subtype.
American journal of human genetics 2001;69(1):209-15.
2000: Sarah J Tabrizi; Michael Orth; J M Wilkinson; Jan-Willem Taanman; Thomas T Warner; J Mark Cooper; Anthony H V Schapira
Expression of mutant alpha-synuclein causes increased susceptibility to dopamine toxicity.
Human molecular genetics 2000;9(18):2683-9.
2000: Raffaele Lodi; Anthony H V Schapira; David Manners; Peter Styles; Nicholas W Wood; Doris J Taylor; Thomas T Warner
Abnormal in vivo skeletal muscle energy metabolism in Huntington's disease and dentatorubropallidoluysian atrophy.
Annals of neurology 2000;48(1):72-6.
1999: Enza Maria Valente; S Povey; Thomas T Warner; Nicholas W Wood; Mary B Davis
Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations.
Annals of human genetics 1999;63(Pt 1):1-8.
1998: Enza Maria Valente; Thomas T Warner; Paul R Jarman; D Mathen; N A Fletcher; CD Marsden; Kailash P Bhatia; Nicholas W Wood
The role of DYT1 in primary torsion dystonia in Europe.
Brain : a journal of neurology 1998;121 ( Pt 12)():2335-9.
1998: Thomas T Warner; Anthony H V Schapira
The role of the alpha-synuclein gene mutation in patients with sporadic Parkinson's disease in the United Kingdom.
Journal of neurology, neurosurgery, and psychiatry 1998;65(3):378-9.
1998: Paul R Jarman; Thomas T Warner
The dystonias.
Journal of medical genetics 1998;35(4):314-8.
1997: Thomas T Warner; Anthony H V Schapira
Genetic counselling in mitochondrial diseases.
Current opinion in neurology 1997;10(5):408-12.
1995: Thomas T Warner; L D Williams; R W Walker; F Flinter; S A Robb; S E Bundey; M Honavar; AE Harding
A clinical and molecular genetic study of dentatorubropallidoluysian atrophy in four European families.
Annals of neurology 1995;37(4):452-9.
1994: Thomas T Warner; G G Lennox; I Janota; AE Harding
Autosomal-dominant dentatorubropallidoluysian atrophy in the United Kingdom.
Movement disorders : official journal of the Movement Disorder Society 1994;9(3):289-96.
1993: D Conway; P G Bain; Thomas T Warner; Mary B Davis; L J Findley; P D Thompson; CD Marsden; AE Harding
Linkage analysis with chromosome 9 markers in hereditary essential tremor.
Movement disorders : official journal of the Movement Disorder Society 1993;8(3):374-6.
1993: Thomas T Warner; N A Fletcher; Mary B Davis; F Ahmad; D Conway; Annaik Feve; P Rondot; CD Marsden; AE Harding
Linkage analysis in British and French families with idiopathic torsion dystonia.
Brain : a journal of neurology 1993;116 ( Pt 3)():739-44.