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Nicholas Wood

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Raquel Duran; Aikaterini V Angeli; Kailash P Bhatia; Timothy M Cox; Emma Deas; Patrick Deegan; John Hardy; Henry Houlden; derralynn hughes; Paul R Jarman; Andrew J Lees; Patricia Limousin; Atul Mehta; Niccolo E Mencacci; Anthony H Schapira; Maryam Shoai; Nicholas W Wood; Tom Foltynie
The glucocerobrosidase E326K variant predisposes to Parkinson's disease, but does not cause Gaucher's disease.
Una-Marie Sheerin; Tamara Shiner; Sian D Spacey; Maria Stamelou; Enza Maria Valente; Nicholas W Wood; Gavin Charlesworth; Kailash P Bhatia
Migraine with aura as the predominant phenotype in a family with a PRRT2 mutation.
Kira M Holmström; Nephtali Marina; Nicholas W Wood; Artyom Y Baev; Alexander V Gourine; Andrey Y Abramov
Signalling properties of inorganic polyphosphate in the mammalian brain.

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All Publications

2013: Raquel Duran; Aikaterini V Angeli; Kailash P Bhatia; Timothy M Cox; Emma Deas; Patrick Deegan; John Hardy; Henry Houlden; derralynn hughes; Paul R Jarman; Andrew J Lees; Patricia Limousin; Atul Mehta; Niccolo E Mencacci; Anthony H Schapira; Maryam Shoai; Nicholas W Wood; Tom Foltynie
The glucocerobrosidase E326K variant predisposes to Parkinson's disease, but does not cause Gaucher's disease.
Movement disorders : official journal of the Movement Disorder Society 2013;28(2):232-6.
2013: Una-Marie Sheerin; Tamara Shiner; Sian D Spacey; Maria Stamelou; Enza Maria Valente; Nicholas W Wood; Gavin Charlesworth; Kailash P Bhatia
Migraine with aura as the predominant phenotype in a family with a PRRT2 mutation.
Journal of neurology 2013;260(2):656-60.
2013: Kira M Holmström; Nephtali Marina; Nicholas W Wood; Artyom Y Baev; Alexander V Gourine; Andrey Y Abramov
Signalling properties of inorganic polyphosphate in the mammalian brain.
Nature communications 2013;4():1362.
2013: Alison Wood-Kaczmar; Emma Deas; Nicholas W Wood; Andrey Y Abramov
The role of the mitochondrial NCX in the mechanism of neurodegeneration in Parkinson's disease.
Advances in experimental medicine and biology 2013;961():241-9.
2012: Gavin Charlesworth; Kira M Holmström; Vincent Plagnol; Elisavet Preza; Ignacio Rubio-Agusti; Mina Ryten; Susanne A Schneider; Una-Marie Sheerin; Maria Stamelou; Daniah Trabzuni; Andrey Y Abramov; Kailash P Bhatia; Jose Bras; Nicholas W Wood
Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis.
American journal of human genetics 2012;91(6):1041-50.
2012: Maja Kojovic; Rodger Palmer; Ignacio Rubio-Agusti; Anirban Saha; Una-Marie Sheerin; Nicholas W Wood; Jose Bras; Vaneesha Gibbons; John Hardy; Henry Houlden; Kailash P Bhatia
Young-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family.
Movement disorders : official journal of the Movement Disorder Society 2012;27(14):1827-9.
2012: Florian Mittag; Mike A Nalls; Mohamad Saad; Claudia Schulte; Manu Sharma; Javier Simón-Sánchez; Andrew B Singleton; Nicholas W Wood; Andreas Zell; Zoltan Bochdanovits; Alexis Brice; Finja Büchel; Thomas Gasser; J Raphael Gibbs; John Hardy; Dena G Hernandez; Peter Heutink; Andreas Jahn; Margaux Keller; Suzanne Lesage; Maria Martinez
Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunities.
Human mutation 2012;33(12):1708-18.
2012: Alice R Gardiner; Michael Hanna; Kailash P Bhatia; Tim Counihan; Russell C Dale; Dimitri M Kullmann; Manju A Kurian; Andrew Lees; Salmo Raskin; Josemir W. Sander; Anthony H Schapira; Susanne A Schneider; Laura Silveira-Moriyama; Sian D Spacey; Maria Stamelou; Hélio A G Teive; Enza Maria Valente; Gurusidheshwar M Wali; Tom Warner; Nicholas W Wood; Henry Houlden
PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.
Neurology 2012;79(21):2115-21.
2012: Margaux F Keller; Laura L Kilarski; Kari Majamaa; Maria Martinez; Florian Mittag; Huw R Morris; Valentina Moskvina; Michael A Nalls; Nayia Nicolaou; Mohamad Saad; Claudia Schulte; Manu Sharma; Javier Simón-Sánchez; Andrew B Singleton; Hreinn Stefánsson; Nigel Williams; Nicholas W Wood; Pauli Ylikotila; Francesco Bettella; Jose Bras; Alexis Brice; Finja Büchel; Alexandra Durr; Thomas Gasser; J Raphael Gibbs; Rita Guerreiro; John Hardy; Dena G Hernandez; Peter Heutink; Peter Holmans
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease.
Human molecular genetics 2012;21(22):4996-5009.
2012: Matthew E Gegg; John Hardy; Simon J R Heales; Derek Burke; J Mark Cooper; Nicholas W Wood; Anthony H V Schapira
Glucocerebrosidase deficiency in substantia nigra of parkinson disease brains.
Annals of neurology 2012;72(3):455-63.
2012: Georgios Koutsis; Henry Houlden; GEORGIA KARADIMA; A Pandraud; R Paudel; Mary G Sweeney; Nicholas W Wood; Marios Panas
Genetic screening of Greek patients with Huntington’s disease phenocopies identifies an SCA8 expansion.
Journal of neurology 2012;259(9):1874-8.
2012: Georgios Koutsis; Marios Panas; Amelie Pandraud; James M Polke; Nicholas W Wood; GEORGIA KARADIMA; Henry Houlden
Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot-Marie-Tooth disease.
Brain : a journal of neurology 2012;135(Pt 8):e217, 1-6; author reply e218, 1-2.
2012: Georgios Koutsis; Marios Panas; Reema Paudel; Sally Pemble; Mary G Sweeney; Nicholas W Wood; Athina Kladi; Henry Houlden
Analysis of spinocerebellar ataxias due to expanded triplet repeats in Greek patients with cerebellar ataxia.
Journal of the neurological sciences 2012;318(1-2):178-80.
2012: Arianna Tucci; Nicholas W Wood; Gavin Charlesworth; Vincent Plagnol; Una-Marie Sheerin; John Hardy
Study of the genetic variability in a Parkinson's Disease gene: EIF4G1.
Neuroscience letters 2012;518(1):19-22.
2012: Nunilo Cremades; Emma Deas; Christopher M Dobson; Paul Dunne; Andrey Y Abramov; Francesco A Aprile; CARLOS WALTER BERTONCINI; Allen Y Chen; Richard W Clarke; Samuel I A Cohen; Tuomas P J Knowles; Angel Orte; Massimo Sandal; Nicholas W Wood; David Klenerman
Direct observation of the interconversion of normal and toxic forms of α-synuclein.
Cell 2012;149(5):1048-59.
2012: Gavin Charlesworth; Patrick F Chinnery; Sonia Gandhi; Stephen M Gentleman; Rita Guerreiro; John Hardy; Janice L Holton; Andrew J Lees; Huw Morris; Karen Morrison; Tamas Revesz; Una-Marie Sheerin; Nigel Williams; Roger A Barker; Jose M Bras; David J Burn; Nicholas W Wood
Tau acts as an independent genetic risk factor in pathologically proven PD.
Neurobiology of aging 2012;33(4):838.e7-11.
2012: Hélène Plun-Favreau; Nicholas W Wood; Z Yao; V S Burchell; K Cain; Campanella Michelangelo; Emma Deas; V Fedele; Alexander V Gourine; K M Holmström; L Miguel Martins; Nicoleta Moisoi; Andrey Y Abramov
HtrA2 deficiency causes mitochondrial uncoupling through the F₁F₀-ATP synthase and consequent ATP depletion.
Cell death & disease 2012;3():e335.
2012: Sonia Gandhi; Annika Vaarmann; Nicholas W Wood; Zhi Yao; Michael R Duchen; Andrey Y Abramov
Dopamine induced neurodegeneration in a PINK1 model of Parkinson's disease.
PloS one 2012;7(5):e37564.
2012: Paola Giunti; D A Hilton; Henry Houlden; Janel Johnson; Tamas Revesz; Mary B Davis; Christopher Gardner-Thorpe; Paul Worth; Nicholas W Wood
Spinocerebellar ataxia type 11.
Handbook of clinical neurology 2012;103():521-34.
2011: Zhi Yao; Victoria S Burchell; Sonia Gandhi; Hélène Plun-Favreau; Nicholas W Wood; Andrey Y Abramov
Cell metabolism affects selective vulnerability in PINK1-associated Parkinson's disease.
Journal of cell science 2011;124(Pt 24):4194-202.
2011: S Sharma; C Vilariño-Güell; Nicholas W Wood; Rina Bandopadhyay; C Kallis; Ann E Kingsbury; R Kumaran; Tammaryn Lashley; Andrew J Lees; Sean S O'Sullivan; A E M Renton; Tamas Revesz; Janice L Holton
LRRK2 expression in idiopathic and G2019S positive Parkinson's disease subjects: a morphological and quantitative study.
Neuropathology and applied neurobiology 2011;37(7):777-90.
2011: Michael J Devine; Hélène Plun-Favreau; Nicholas W Wood
Parkinson's disease and cancer: two wars, one front.
Nature reviews. Cancer 2011;11(11):812-23.
2011: christos proukakis; Nicholas W Wood; Robyn Labrum; David Moore; Henry Houlden
Detection of novel mutations and review of published data suggests that hereditary spastic paraplegia caused by spastin (SPAST) mutations is found more often in males.
Journal of the neurological sciences 2011;306(1-2):62-5.
2011: Helen Ling; James M Polke; Mary G Sweeney; Andrea Haworth; Catherine A Sandford; Simon J R Heales; Nicholas W Wood; Mary B Davis; Andrew J Lees
An intragenic duplication in guanosine triphosphate cyclohydrolase-1 gene in a dopa-responsive dystonia family.
Movement disorders : official journal of the Movement Disorder Society 2011;26(5):905-9.
2011: Emma Deas; Nicholas W Wood; Hélène Plun-Favreau
Mitophagy and Parkinson's disease: the PINK1-parkin link.
Biochimica et biophysica acta 2011;1813(4):623-33.
2010: Arianna Tucci; Mike A Nalls; Henry Houlden; Tamas Revesz; Andrew Singleton; Nicholas W Wood; John Hardy; Coro Paisan-Ruiz
Genetic variability at the PARK16 locus.
European journal of human genetics : EJHG 2010;18(12):1356-9.
2010: Araceli Alonso-Canovas; Petra Katschnig; Arianna Tucci; Miryam Carecchio; Nicholas W Wood; Mark Edwards; Juan Carlos Martínez Castrillo; Derek Burke; Simon Heales; Kailash P Bhatia
Atypical parkinsonism with apraxia and supranuclear gaze abnormalities in type 1 Gaucher disease. Expanding the spectrum: case report and literature review.
Movement disorders : official journal of the Movement Disorder Society 2010;25(10):1506-9.
2010: Georg Kägi; Christine Klein; Nicholas W Wood; Susanne A Schneider; Peter P Pramstaller; Vera Tadic; Niall Quinn; Bart P C van de Warrenburg; Kailash P Bhatia
Nonmotor symptoms in Parkin gene-related parkinsonism.
Movement disorders : official journal of the Movement Disorder Society 2010;25(9):1279-84.
2010: Sonia Gandhi; Nicholas W Wood
Genome-wide association studies: the key to unlocking neurodegeneration?
Nature neuroscience 2010;13(7):789-94.
2010: Sanjeev Rajakulendran; Tracey D Graves; Robyn W Labrum; Dimitrios Kotzadimitriou; Louise H Eunson; Mary B Davis; Rosalyn Davies; Nicholas W Wood; Dimitri M Kullmann; Michael G Hanna; Stephanie Schorge
Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy.
The Journal of physiology 2010;588(Pt 11):1905-13.
2010: Victoria S Burchell; Sonia Gandhi; Emma Deas; Nicholas W Wood; Andrey Y Abramov; Hélène Plun-Favreau
Targeting mitochondrial dysfunction in neurodegenerative disease: Part II.
Expert opinion on therapeutic targets 2010;14(5):497-511.
2010: Victoria S Burchell; Sonia Gandhi; Emma Deas; Nicholas W Wood; Andrey Y Abramov; Hélène Plun-Favreau
Targeting mitochondrial dysfunction in neurodegenerative disease: Part I.
Expert opinion on therapeutic targets 2010;14(4):369-85.
2010: Nicola Pavese; Robert Y Moore; Christoph Scherfler; Naheed L Khan; Gary Hotton; Niall Quinn; Kailash P Bhatia; Nicholas W Wood; David J Brooks; Andrew J Lees; Paola Piccini
In vivo assessment of brain monoamine systems in parkin gene carriers: a PET study.
Experimental neurology 2010;222(1):120-4.
2010: Hélène Plun-Favreau; Patrick A Lewis; John Hardy; L Miguel Martins; Nicholas W Wood
Cancer and neurodegeneration: between the devil and the deep blue sea.
PLoS genetics 2010;6(12):e1001257.
2009: Nicola Pavese; Naheed L Khan; Christoph Scherfler; Lisa Cohen; David J Brooks; Nicholas W Wood; Kailash P Bhatia; Niall Quinn; Andrew J Lees; Paola Piccini
Nigrostriatal dysfunction in homozygous and heterozygous parkin gene carriers: an 18F-dopa PET progression study.
Movement disorders : official journal of the Movement Disorder Society 2009;24(15):2260-6.
2009: Cristine Alves da Costa; Claire Sunyach; Emilie Giaime; Andrew West; Olga Corti; Alexis Brice; Stephen Safe; Patrick M Abou-Sleiman; Nicholas W Wood; Hitoshi Takahashi; Mathew S Goldberg; Jie Shen; Frédéric Checler
Transcriptional repression of p53 by parkin and impairment by mutations associated with autosomal recessive juvenile Parkinson's disease.
Nature cell biology 2009;11(11):1370-5.
2009: Ravindran Kumaran; Jana Vandrovcova; Connie Luk; Simone Sharma; Adrian Renton; Nicholas W Wood; John Hardy; Andrew J Lees; Rina Bandopadhyay
Differential DJ-1 gene expression in Parkinson's disease.
Neurobiology of disease 2009;36(2):393-400.
2009: Jana Vandrovcova; Alan Pittman; Elke Malzer; Patrick M Abou-Sleiman; Andrew J Lees; Nicholas W Wood; Rohan de Silva
Association of MAPT haplotype-tagging SNPs with sporadic Parkinson's disease.
Neurobiology of aging 2009;30(9):1477-82.
2009: I Trender-Gerhard; Mary G Sweeney; P Schwingenschuh; Pablo Mir; Mark J Edwards; A Gerhard; J M Polke; Michael G Hanna; Mary B Davis; Nicholas W Wood; Kailash P Bhatia
Autosomal-dominant GTPCH1-deficient DRD: clinical characteristics and long-term outcome of 34 patients.
Journal of neurology, neurosurgery, and psychiatry 2009;80(8):839-45.
2009: Juliane Neumann; Jose Bras; Emma Deas; Sean S O'Sullivan; Laura Parkkinen; Robin H Lachmann; Abi Li; Janice Holton; Rita Guerreiro; Reema Paudel; Badmavady Segarane; Andrew Singleton; Andrew J Lees; John Hardy; Henry Houlden; Tamas Revesz; Nicholas W Wood
Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease.
Brain : a journal of neurology 2009;132(Pt 7):1783-94.
2009: P M A Sleiman; Daniel G Healy; M M K Muqit; Y X Yang; M Van Der Brug; Janice L Holton; Tamas Revesz; Niall Quinn; K Bhatia; J K J Diss; Andrew J Lees; Mark Cookson; David S Latchman; Nicholas W Wood
Characterisation of a novel NR4A2 mutation in Parkinson's disease brain.
Neuroscience letters 2009;457(2):75-9.
2009: Daniel G Healy; Susan Bressman; John Dickson; Laura Silveira-Moriyama; Susanne A Schneider; Sean S O Sullivan; Luke Massey; Kailash P Bhatia; Karen Shaw; Kailash P Bhatia; Jamshed Bomanji; Nicholas W Wood; Andrew J Lees
Evidence for pre and postsynaptic nigrostriatal dysfunction in the fragile X tremor-ataxia syndrome.
Movement disorders : official journal of the Movement Disorder Society 2009;24(8):1245-7.
2009: Emma Deas; Helene Plun-Favreau; Nicholas W Wood
PINK1 function in health and disease.
EMBO molecular medicine 2009;1(3):152-65.
2009: A W Michell; M Laura; J Blake; M P Lunn; A Cox; V S Gibbons; M B Davis; Nicholas W Wood; H Manji; H Houlden; N M F Murray; M M Reilly
GJB1 gene mutations in suspected inflammatory demyelinating neuropathies not responding to treatment.
Journal of neurology, neurosurgery, and psychiatry 2009;80(6):699-700.
2009: Jonathan P Roiser; Benedetto de Martino; Geoffrey C Y Tan; Dharshan Kumaran; Ben Seymour; Nicholas W Wood; Raymond J Dolan
A genetically mediated bias in decision making driven by failure of amygdala control.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2009;29(18):5985-91.
2009: Sonja W Scholz; Henry Houlden; Claudia Schulte; Manu Sharma; Abi Li; Daniela Berg; Anna Melchers; Reema Paudel; J Raphael Gibbs; Javier Simon-Sanchez; Coro Paisan-Ruiz; Jose Bras; Jinhui Ding; Honglei Chen; Bryan Joseph Traynor; Sampath Arepalli; Ryan R Zonozi; Tamas Revesz; Janice Holton; Nicholas W Wood; Andrew Lees; Wolfgang H Oertel; Ullrich Wüllner; Stefano Goldwurm; Maria Teresa Pellecchia; Thomas Illig; Olaf Riess; Hubert H Fernandez; Ramon L Rodriguez; Michael S Okun; Werner Poewe; Gregor K Wenning; John Hardy; Andrew Singleton; Francesca Del Sorbo; Susanne Schneider; Kailash P Bhatia; Thomas Gasser
SNCA variants are associated with increased risk for multiple system atrophy.
Annals of neurology 2009;65(5):610-4.
2009: B Segarane; A Li; R Paudel; S Scholz; J Neumann; Andrew J Lees; Tamas Revesz; John Hardy; Christopher J Mathias; Nicholas W Wood; J Holton; Henry Houlden
Glucocerebrosidase mutations in 108 neuropathologically confirmed cases of multiple system atrophy.
Neurology 2009;72(13):1185-6.
2009: Sonia Gandhi; Alison Wood-Kaczmar; Zhi Yao; Helene Plun-Favreau; Emma Deas; Kristina Klupsch; Julian Downward; David S Latchman; Sarah J Tabrizi; Nicholas W Wood; Michael R Duchen; Andrey Y Abramov
PINK1-associated Parkinson's disease is caused by neuronal vulnerability to calcium-induced cell death.
Molecular cell 2009;33(5):627-38.
2009: N Moisoi; K Klupsch; V Fedele; P East; S Sharma; Adrian Renton; H Plun-Favreau; Richard E Edwards; Peter Teismann; Mauro Degli Esposti; A D Morrison; Nicholas W Wood; J Downward; L M Martins
Mitochondrial dysfunction triggered by loss of HtrA2 results in the activation of a brain-specific transcriptional stress response.
Cell death and differentiation 2009;16(3):449-64.
2009: Yan Xiang Yang; Nicholas W Wood; David S Latchman
Molecular basis of Parkinson's disease.
Neuroreport 2009;20(2):150-6.
2009: Ammar Al-Chalabi; Alexandra Dürr; Nicholas W Wood; Michael H Parkinson; Agnes Camuzat; Jean-Sébastien Hulot; Karen E Morrison; Adrian Renton; Sigurd D Sussmuth; Bernhard G Landwehrmeyer; Albert Ludolph; Yves Agid; Alexis Brice; P Nigel Leigh; Gilbert Bensimon
Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy.
PloS one 2009;4(9):e7114.
2009: John M Lynch; S K Tate; P Kinirons; M E Weale; Gianpiero L Cavalleri; Chantal Depondt; Kieran Murphy; D O'Rourke; Colin Doherty; Kevin V Shianna; Nicholas W Wood; Josemir W. Sander; N Delanty; David B Goldstein; Sanjay M Sisodiya
No major role of common SV2A variation for predisposition or levetiracetam response in epilepsy.
Epilepsy research 2009;83(1):44-51.
2009: Coro Paisan-Ruiz; Kailash P Bhatia; Abi Li; Dena Hernandez; Mary Davis; Nicholas W Wood; John Hardy; Henry Houlden; Andrew Singleton; Susanne A Schneider
Characterization of PLA2G6 as a locus for dystonia-parkinsonism.
Annals of neurology 2009;65(1):19-23.
2008: Helene Plun-Favreau; Sonia Gandhi; Alison Wood-Kaczmar; Emma Deas; Zhi Yao; Nicholas W Wood
What have PINK1 and HtrA2 genes told us about the role of mitochondria in Parkinson's disease?
Annals of the New York Academy of Sciences 2008;1147():30-6.
2008: Daniel G Healy; Nicholas W Wood; Anthony H V Schapira
Test for LRRK2 mutations in patients with Parkinson's disease.
Practical neurology 2008;8(6):381-5.
2008: Henry Houlden; M Laura; F Wavrant-De Vrièze; Julian Blake; Nicholas W Wood; Mary M Reilly
Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2.
Neurology 2008;71(21):1660-8.
2008: Heather Mortiboys; Kelly Jean Thomas; Werner J H Koopman; Stefanie Klaffke; Patrick M Abou-Sleiman; Simon Olpin; Nicholas W Wood; Peter H G M Willems; Jan A M Smeitink; Mark Cookson; Oliver Bandmann
Mitochondrial function and morphology are impaired in parkin-mutant fibroblasts.
Annals of neurology 2008;64(5):555-65.
2008: Susanne A Schneider; Penelope Talelli; Binith Cheeran; Naheed L Khan; Nicholas W Wood; John C Rothwell; Kailash P Bhatia
Motor cortical physiology in patients and asymptomatic carriers of parkin gene mutations.
Movement disorders : official journal of the Movement Disorder Society 2008;23(13):1812-9.
2008: Coro Paisan-Ruiz; P Nath; Nicholas W Wood; Andrew Singleton; Henry Houlden
Clinical heterogeneity and genotype-phenotype correlations in hereditary spastic paraplegia because of Spatacsin mutations (SPG11).
European journal of neurology : the official journal of the European Federation of Neurological Societies 2008;15(10):1065-70.
2008: Tammaryn Lashley; Tamas Revesz; Gordon Plant; R Bandopadhyay; Andrew J Lees; Blas Frangione; Nicholas W Wood; Rohan de Silva; Jorge Ghiso; Agueda Rostagno; Janice L Holton
Expression of BRI2 mRNA and protein in normal human brain and familial British dementia: its relevance to the pathogenesis of disease.
Neuropathology and applied neurobiology 2008;34(5):492-505.
2008: Laura Silveira-Moriyama; L C Guedes; Ann E Kingsbury; H Ayling; K Shaw; E R Barbosa; Vincenzo Bonifati; Niall Quinn; Patrick M Abou-Sleiman; Nicholas W Wood; A Petrie; Cristina Sampaio; Joaquim Ferreira; J Holton; Tamas Revesz; Andrew J Lees
Hyposmia in G2019S LRRK2-related parkinsonism: clinical and pathologic data.
Neurology 2008;71(13):1021-6.
2008: Sid Gilman; Gregor Wenning; P A Low; David J Brooks; C J Mathias; John Q Trojanowski; Nicholas W Wood; C Colosimo; A Dürr; C J Fowler; H Kaufmann; T Klockgether; Andrew J Lees; Werner Poewe; Niall Quinn; Tamas Revesz; David Robertson; Paola Sandroni; K Seppi; M Vidailhet
Second consensus statement on the diagnosis of multiple system atrophy.
Neurology 2008;71(9):670-6.
2008: Daniel G Healy; Mario Falchi; Sean S O'Sullivan; Vincenzo Bonifati; Alexandra Durr; Susan Bressman; Alexis Brice; Jan Aasly; Cyrus Zabetian; Stefano Goldwurm; Joaquim Ferreira; Eduardo Tolosa; Denise M Kay; Christine Klein; David R Williams; Connie Marras; Anthony E Lang; Zbigniew K Wszolek; Jose Berciano; Anthony H V Schapira; Timothy Lynch; Kailash P Bhatia; Thomas Gasser; Andrew J Lees; Nicholas W Wood
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study.
Lancet neurology 2008;7(7):583-90.
2008: Tammaryn Lashley; Janice L Holton; Emma Gray; Konrad Kirkham; Sean S O'Sullivan; Arlete Hilbig; Nicholas W Wood; Andrew J Lees; Tamas Revesz
Cortical alpha-synuclein load is associated with amyloid-beta plaque burden in a subset of Parkinson's disease patients.
Acta neuropathologica 2008;115(4):417-25.
2008: Janice L Holton; S A Schneider; T Ganesharajah; S Gandhi; Catherine Strand; P Shashidharan; J Barreto; Nicholas W Wood; Andrew J Lees; K P Bhatia; Tamas Revesz
Neuropathology of primary adult-onset dystonia.
Neurology 2008;70(9):695-9.
2008: Alan Pittman; Rohan de Silva; Andrew J Lees; Nicholas W Wood
Genetics of progressive supranuclear palsy.
Handbook of clinical neurology 2008;89():475-85.
2008: Alison Wood-Kaczmar; Sonia Gandhi; Zhi Yao; Andrey Y Abramov; Andrey S Y Abramov; erik miljan; Gregory Keen; Lee Stanyer; Iain Hargreaves; Kristina Klupsch; Emma Deas; Julian Downward; Louise Mansfield; Parmjit Jat; Joanne Taylor; Simon Heales; Michael R Duchen; David Latchman; Sarah J Tabrizi; Nicholas W Wood
PINK1 is necessary for long term survival and mitochondrial function in human dopaminergic neurons.
PloS one 2008;3(6):e2455.
2008: Janel Johnson; Nicholas W Wood; Paola Giunti; Henry Houlden
Clinical and genetic analysis of spinocerebellar ataxia type 11.
Cerebellum (London, England) 2008;7(2):159-64.
2008: Miratul M K Muqit; A J Larner; Mary G Sweeney; Caroline Sewry; VJ Stinton; Mary B Davis; Daniel G Healy; S J Payne; K Chotai; Nicholas W Wood; R J M Lane
Multiple mitochondrial DNA deletions in monozygotic twins with OPMD.
Journal of neurology, neurosurgery, and psychiatry 2008;79(1):68-71.
2007: Matthew McKenzie; Danae Liolitsa; Natalya Akinshina; Campanella Michelangelo; Sanjay M Sisodiya; Ian Hargreaves; Niranjanan Nirmalananthan; Mary G Sweeney; Patrick M Abou-Sleiman; Nicholas W Wood; Michael G Hanna; Michael R Duchen
Mitochondrial ND5 gene variation associated with encephalomyopathy and mitochondrial ATP consumption.
The Journal of biological chemistry 2007;282(51):36845-52.
2007: Nisha Limaye; N Revencu; N Van Regemorter; M Garzon; M Bonduelle; W Chung; M D Daras; M C Fahey; C Garrett; Y Gillerot; G Gillessen-Kaesbach; A Giménez-Arnau; F Guzzetta; D Battaglia; K Heimdal; Willy Lissens; E Taub; L Van Maldergem; W Van Paesschen; D Wieczorek; Nicholas W Wood; L Boon; M Vikkula
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
Human genetics 2007;122(5):552.
2007: Nisha Limaye; N Revencu; N Van Regemorter; M Garzon; M Bonduelle; W Chung; M D Daras; M C Fahey; C Garrett; Y Gillerot; G Gillessen-Kaesbach; A Giménez-Arnau; F Guzzetta; D Battaglia; K Heimdal; Willy Lissens; E Taub; L Van Maldergem; W Van Paesschen; D Wieczorek; Nicholas W Wood; L Boon; M Vikkula
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
Human genetics 2007;122(5):552.
2007: Nisha Limaye; N Revencu; N Van Regemorter; M Garzon; M Bonduelle; W Chung; M D Daras; M C Fahey; C Garrett; Y Gillerot; G Gillessen-Kaesbach; A Giménez-Arnau; F Guzzetta; D Battaglia; K Heimdal; Willy Lissens; E Taub; L Van Maldergem; W Van Paesschen; D Wieczorek; Nicholas W Wood; L Boon; M Vikkula
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
Human genetics 2007;122(5):551.
2007: Nisha Limaye; N Revencu; N Van Regemorter; M Garzon; M Bonduelle; W Chung; M D Daras; M C Fahey; C Garrett; Y Gillerot; G Gillessen-Kaesbach; A Giménez-Arnau; F Guzzetta; D Battaglia; K Heimdal; Willy Lissens; E Taub; L Van Maldergem; W Van Paesschen; D Wieczorek; Nicholas W Wood; L Boon; M Vikkula
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
Human genetics 2007;122(5):552.
2007: Nisha Limaye; N Revencu; N Van Regemorter; M Garzon; M Bonduelle; W Chung; M D Daras; M C Fahey; C Garrett; Y Gillerot; G Gillessen-Kaesbach; A Giménez-Arnau; F Guzzetta; D Battaglia; K Heimdal; Willy Lissens; E Taub; L Van Maldergem; W Van Paesschen; D Wieczorek; Nicholas W Wood; L Boon; M Vikkula
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
Human genetics 2007;122(5):551.
2007: Nisha Limaye; N Revencu; N Van Regemorter; M Garzon; M Bonduelle; W Chung; M D Daras; M C Fahey; C Garrett; Y Gillerot; G Gillessen-Kaesbach; A Giménez-Arnau; F Guzzetta; D Battaglia; K Heimdal; Willy Lissens; E Taub; L Van Maldergem; W Van Paesschen; D Wieczorek; Nicholas W Wood; L Boon; M Vikkula
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
Human genetics 2007;122(5):551.
2007: Nisha Limaye; N Revencu; N Van Regemorter; M Garzon; M Bonduelle; W Chung; M D Daras; M C Fahey; C Garrett; Y Gillerot; G Gillessen-Kaesbach; A Giménez-Arnau; F Guzzetta; D Battaglia; K Heimdal; Willy Lissens; E Taub; L Van Maldergem; W Van Paesschen; D Wieczorek; Nicholas W Wood; L Boon; M Vikkula
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
Human genetics 2007;122(5):550.
2007: Nisha Limaye; N Revencu; N Van Regemorter; M Garzon; M Bonduelle; W Chung; M D Daras; M C Fahey; C Garrett; Y Gillerot; G Gillessen-Kaesbach; A Giménez-Arnau; F Guzzetta; D Battaglia; K Heimdal; Willy Lissens; E Taub; L Van Maldergem; W Van Paesschen; D Wieczorek; Nicholas W Wood; L Boon; M Vikkula
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
Human genetics 2007;122(5):550.
2007: Nisha Limaye; N Revencu; N Van Regemorter; M Garzon; M Bonduelle; W Chung; M D Daras; M C Fahey; C Garrett; Y Gillerot; G Gillessen-Kaesbach; A Giménez-Arnau; F Guzzetta; D Battaglia; K Heimdal; Willy Lissens; E Taub; L Van Maldergem; W Van Paesschen; D Wieczorek; Nicholas W Wood; L Boon; M Vikkula
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
Human genetics 2007;122(5):550.
2007: Nisha Limaye; N Revencu; N Van Regemorter; M Garzon; M Bonduelle; W Chung; M D Daras; M C Fahey; C Garrett; Y Gillerot; G Gillessen-Kaesbach; A Giménez-Arnau; F Guzzetta; D Battaglia; K Heimda; Willy Lissens; E Taub; L Van Maldergem; W Van Paesschen; D Wieczorek; Nicholas W Wood; L Boon; M Vikkula
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
Human genetics 2007;122(5):549-50.
2007: Nisha Limaye; N Revencu; N Van Regemorter; M Garzon; M Bonduelle; W Chung; M D Daras; M C Fahey; C Garrett; Y Gillerot; G Gillessen-Kaesbach; A Giménez-Arnau; F Guzzetta; D Battaglia; K Heimda; Willy Lissens; E Taub; L Van Maldergem; W Van Paesschen; D Wieczorek; Nicholas W Wood; L Boon; M Vikkula
Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.
Human genetics 2007;122(5):549.
2007: Henry Houlden; Janel Johnson; Christopher Gardner-Thorpe; Tammaryn Lashley; Dena Hernandez; Paul Worth; Andrew Singleton; David A Hilton; Janice Holton; Tamas Revesz; Mary B Davis; Paola Giunti; Paolo Giunti; Nicholas W Wood
Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11.
Nature genetics 2007;39(12):1434-6.
2007: Gianpiero L Cavalleri; Michael E Weale; Kevin V Shianna; Rinki Singh; John M Lynch; Bronwyn Grinton; Cassandra Szoeke; Kieran Murphy; Peter Kinirons; Deirdre O'Rourke; Dongliang Ge; Chantal Depondt; Kristl G Claeys; Massimo Pandolfo; Curtis Gumbs; Nicole Walley; James McNamara; John C Mulley; Kristen N Linney; Leslie J Sheffield; Rodney A Radtke; Sarah K Tate; Stephanie L Chissoe; Rachel A Gibson; David Hosford; Alice Stanton; Tracey D Graves; Michael G Hanna; Kai Eriksson; Anne-Mari Kantanen; Reetta Kalviainen; Terence J O'Brien; Josemir W. Sander; John S Duncan; Ingrid E Scheffer; Samuel F Berkovic; Nicholas W Wood; Colin Doherty; Norman Delanty; Sanjay M Sisodiya; David B Goldstein
Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study.
Lancet neurology 2007;6(11):970-80.
2007: Hélène Plun-Favreau; Kristina Klupsch; Nicoleta Moisoi; Sonia Gandhi; Svend Kjaer; David Frith; Kirsten Harvey; Emma Deas; Robert Justin Harvey; Neil McDonald; Nicholas W Wood; L Miguel Martins; Julian Downward
The mitochondrial protease HtrA2 is regulated by Parkinson's disease-associated kinase PINK1.
Nature cell biology 2007;9(11):1243-52.
2007: Dalia Kasperaviciute; Mike E Weale; Kevin V Shianna; Gareth T Banks; Claire L Simpson; Valerie K Hansen; Martin R Turner; Christopher Shaw; Ammar Al-Chalabi; Hardev S Pall; Emily F Goodall; Karen E Morrison; Richard W Orrell; Marcus Beck; Sibylle Jablonka; Michael Sendtner; Alice Brockington; Paul Geoffrey Ince; Judith Hartley; Hannah Nixon; Pamela J Shaw; Giampietro Schiavo; Nicholas W Wood; David B Goldstein; Elizabeth M C Fisher
Large-scale pathways-based association study in amyotrophic lateral sclerosis.
Brain : a journal of neurology 2007;130(Pt 9):2292-301.
2007: Bart P C van de Warrenburg; Paola Giunti; Susanne A Schneider; Niall Quinn; Nicholas W Wood; Kailash P Bhatia
The syndrome of (predominantly cervical) dystonia and cerebellar ataxia: new cases indicate a distinct but heterogeneous entity.
Journal of neurology, neurosurgery, and psychiatry 2007;78(7):774-5.
2007: Joyce van de Leemput; Jayanth Chandran; Melanie A Knight; Lynne A Holtzclaw; Sonja Scholz; Mark Cookson; Henry Houlden; Katrina Gwinn-Hardy; Hon-Chung Fung; Xian Lin; Dena Hernandez; Javier Simon-Sanchez; Nicholas W Wood; Paola Giunti; Ian Rafferty; John Hardy; Elsdon Storey; R J McKinlay Gardner; Susan M Forrest; Elizabeth M C Fisher; James T Russell; Huaibin Cai; Andrew Singleton
Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans.
PLoS genetics 2007;3(6):e108.
2007: Erin L Heinzen; Woohyun Yoon; Sarah K Tate; Arjune Sen; Nicholas W Wood; Sanjay M Sisodiya; David B Goldstein
Nova2 interacts with a cis-acting polymorphism to influence the proportions of drug-responsive splice variants of SCN1A.
American journal of human genetics 2007;80(5):876-83.
2007: Gianpiero L Cavalleri; Nicole M Walley; Nicole Soranzo; John Mulley; Colin Doherty; Ashish Kapoor; Chantal Depondt; John M Lynch; Ingrid E Scheffer; Armin Heils; Anne Gehrmann; Peter Kinirons; Sonia Gandhi; Parthasarathy Satishchandra; Nicholas W Wood; Anuranjan Anand; Thomas Sander; Samuel F Berkovic; Norman Delanty; David B Goldstein; Sanjay M Sisodiya
A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy.
Epilepsia 2007;48(4):706-12.
2007: Erin L Heinzen; Woohyun Yoon; Michael E Weale; Arjune Sen; Nicholas W Wood; James R Burke; Kathleen A Welsh-Bohmer; Christine M Hulette; Sanjay M Sisodiya; David B Goldstein
Alternative ion channel splicing in mesial temporal lobe epilepsy and Alzheimer's disease.
Genome biology 2007;8(3):R32.
2006: Patrick M Abou-Sleiman; Michael G Hanna; Nicholas W Wood
Genetic association studies of complex neurological diseases.
Journal of neurology, neurosurgery, and psychiatry 2006;77(12):1302-4.
2006: Susanne A Schneider; Bart P C van de Warrenburg; T D Hughes; M Davis; M Sweeney; Nicholas W Wood; Niall Quinn; Kailash P Bhatia
Phenotypic homogeneity of the Huntington disease-like presentation in a SCA17 family.
Neurology 2006;67(9):1701-3.
2006: A Wood-Kaczmar; Sonia Gandhi; Nicholas W Wood
Understanding the molecular causes of Parkinson's disease.
Trends in molecular medicine 2006;12(11):521-8.
2006: Daniel G Healy; Patrick M Abou-Sleiman; Kourosh R Ahmadi; Sonia Gandhi; Miratul M K Muqit; Kailash P Bhatia; Niall Quinn; Andrew J Lees; Janice L Holton; Tamas Revesz; Nicholas W Wood
NR4A2 genetic variation in sporadic Parkinson's disease: a genewide approach.
Movement disorders : official journal of the Movement Disorder Society 2006;21(11):1960-3.
2006: Ina Schmitt; Ullrich Wüllner; Daniel G Healy; Nicholas W Wood; Heike Kölsch; Reinhard Heun
The ADH1C stop mutation in multiple system atrophy patients and healthy probands in the United Kingdom and Germany.
Movement disorders : official journal of the Movement Disorder Society 2006;21(11):2034.
2006: Patrick M Abou-Sleiman; Miratul M K Muqit; Neil McDonald; Yan Xiang Yang; Sonia Gandhi; Daniel G Healy; Kirsten Harvey; Robert Justin Harvey; Emma Deas; Kailash Bhatia; Niall Quinn; Andrew J Lees; David S Latchman; Nicholas W Wood
A heterozygous effect for PINK1 mutations in Parkinson's disease?
Annals of neurology 2006;60(4):414-9.
2006: Peter Kinirons; Gianpiero L Cavalleri; Amre Shahwan; Nicholas W Wood; David B Goldstein; Sanjay M Sisodiya; Norman Delanty; Colin Doherty
Examining the role of common genetic variation in the gamma2 subunit of the GABA(A) receptor in epilepsy using tagging SNPs.
Epilepsy research 2006;70(2-3):229-38.
2006: Peter Kinirons; Gianpiero L Cavalleri; Rinki Singh; Amre Shahwan; James F Acheson; Nicholas W Wood; David B Goldstein; Sanjay M Sisodiya; Colin Doherty; Norman Delanty
A pharmacogenetic exploration of vigabatrin-induced visual field constriction.
Epilepsy research 2006;70(2-3):144-52.
2006: Miratul M K Muqit; Patrick M Abou-Sleiman; Adrian T Saurin; Kirsten Harvey; Sonia Gandhi; Emma Deas; Simon Eaton; Martin D Payne Smith; Kerrie Venner; Antoni Matilla; Daniel G Healy; William P Gilks; Andrew J Lees; Janice Holton; Tamas Revesz; Peter J Parker; Robert Justin Harvey; Nicholas W Wood; David S Latchman
Altered cleavage and localization of PINK1 to aggresomes in the presence of proteasomal stress.
Journal of neurochemistry 2006;98(1):156-69.
2006: Sonia Gandhi; Miratul M K Muqit; L Stanyer; Daniel G Healy; Patrick M Abou-Sleiman; Iain P Hargreaves; S Heales; Milan Ganguly; L Parsons; Andrew J Lees; D S Latchman; Janice L Holton; Nicholas W Wood; Tamas Revesz
PINK1 protein in normal human brain and Parkinson's disease.
Brain : a journal of neurology 2006;129(Pt 7):1720-31.
2006: Manu Sharma; Jakob C Mueller; Alexander Zimprich; Peter Lichtner; Anne Hofer; Petra Leitner; Sylvia Maass; Daniela Berg; Alexandra Dürr; Vincenzo Bonifati; Giuseppe De Michele; B Oostra; Alexis Brice; Nicholas W Wood; Bertram Muller-Myhsok; Thomas Gasser
The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations.
Journal of medical genetics 2006;43(7):557-62.
2006: Miratul M K Muqit; Sonia Gandhi; Nicholas W Wood
Mitochondria in Parkinson disease: back in fashion with a little help from genetics.
Archives of neurology 2006;63(5):649-54.
2006: Tetsutaro Ozawa; Daniel G Healy; Patrick M Abou-Sleiman; Kourosh R Ahmadi; Niall Quinn; Andrew J Lees; K Shaw; Ullrich Wüllner; J Berciano; J Carsten Moller; Christoph Kamm; Katrin Burk; Keith A Josephs; Paolo Barone; Eduardo Tolosa; David B Goldstein; Gregor Wenning; Felix Geser; Janice L Holton; Thomas Gasser; Tamas Revesz; Nicholas W Wood
The alpha-synuclein gene in multiple system atrophy.
Journal of neurology, neurosurgery, and psychiatry 2006;77(4):464-7.
2006: Daniel G Healy; Patrick M Abou-Sleiman; Juan P Casas; Kourosh R Ahmadi; Timothy Lynch; Sonia Gandhi; Miratul M K Muqit; Thomas Foltynie; Roger A Barker; Kailash P Bhatia; Niall Quinn; Andrew J Lees; J Mark Gibson; Janice L Holton; Tamas Revesz; David B Goldstein; Nicholas W Wood
UCHL-1 is not a Parkinson's disease susceptibility gene.
Annals of neurology 2006;59(4):627-33.
2006: Patrick M Abou-Sleiman; Miratul M K Muqit; Nicholas W Wood
Expanding insights of mitochondrial dysfunction in Parkinson's disease.
Nature reviews. Neuroscience 2006;7(3):207-19.
2006: Michele T M Hu; Christoph Scherfler; Naheed L Khan; Joseph V Hajnal; Andrew J Lees; Niall Quinn; Nicholas W Wood; David J Brooks
Nigral degeneration and striatal dopaminergic dysfunction in idiopathic and Parkin-linked Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2006;21(3):299-305.
2006: Susanne A Schneider; M D Mohire; I Trender-Gerhard; F Asmus; M Sweeney; M Davis; Thomas Gasser; Nicholas W Wood; Kailash P Bhatia
Familial dopa-responsive cervical dystonia.
Neurology 2006;66(4):599-601.
2005: Naheed L Khan; Shushant Jain; John M Lynch; Nicola Pavese; Patrick M Abou-Sleiman; Janice L Holton; Daniel G Healy; William P Gilks; Mary G Sweeney; Milan Ganguly; Vaneesha Gibbons; Sonia Gandhi; Jenny Vaughan; Louise H Eunson; Regina Katzenschlager; Juliet Gayton; Graham Lennox; Tamas Revesz; David Nicholl; Kailash P Bhatia; Niall Quinn; David J Brooks; Andrew J Lees; Mary B Davis; Paola Piccini; Andrew Singleton; Nicholas W Wood
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data.
Brain : a journal of neurology 2005;128(Pt 12):2786-96.
2005: Felix Geser; K Seppi; M Stampfer-Kountchev; M Köllensperger; A Diem; J P Ndayisaba; K Ostergaard; E Dupont; A Cardozo; E Tolosa; M Abele; R Dodel; T Klockgether; Imad Ghorayeb; F Yekhlef; F Tison; C Daniels; F Kopper; Günther Deuschl; M Coelho; J Ferreira; M M Rosa; Cristina Sampaio; M Bozi; A Schrag; J Hooker; H Kim; T Scaravilli; C J Mathias; C Fowler; Nicholas W Wood; Niall Quinn; Håkan Widner; C F Nilsson; O Lindvall; N Schimke; K M Eggert; Wolfgang H Oertel; F del Sorbo; F Carella; A Albanese; M T Pellecchia; P Barone; R Djaldetti; Giuseppe Meco; C Colosimo; A Gonzalez-Mandly; J Berciano; T Gurevich; Nir Giladi; M Galitzky; F Ory; Olivier Rascol; C Kamm; K Buerk; S Maass; T Gasser; Werner Poewe; G K Wenning
The European Multiple System Atrophy-Study Group (EMSA-SG).
Journal of neural transmission (Vienna, Austria : 1996) 2005;112(12):1677-86.
2005: Rina Bandopadhyay; Ann E Kingsbury; Miratul M K Muqit; Kirsten Harvey; Andrew R Reid; Linda Kilford; Simone Engelender; Michael G Schlossmacher; Nicholas W Wood; David S Latchman; Robert Justin Harvey; Andrew J Lees
Synphilin-1 and parkin show overlapping expression patterns in human brain and form aggresomes in response to proteasomal inhibition.
Neurobiology of disease 2005;20(2):401-11.
2005: Alan Pittman; Amanda Myers; Patrick M Abou-Sleiman; Hon-Chung Fung; Mona Kaleem; Lauren Marlowe; Jaime Duckworth; Doris Leung; D Williams; Linda Kilford; N Thomas; Christopher M Morris; dennis dickson; Nicholas W Wood; John Hardy; Andrew J Lees; Rohan de Silva
Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration.
Journal of medical genetics 2005;42(11):837-46.
2005: Sonia Gandhi; Nicholas W Wood
Molecular pathogenesis of Parkinson's disease.
Human molecular genetics 2005;14 Spec No. 2():2749-2755.
2005: Shushant Jain; Nicholas W Wood; Daniel G Healy
Molecular genetic pathways in Parkinson's disease: a review.
Clinical science (London, England : 1979) 2005;109(4):355-64.
2005: Daniel G Healy; Patrick M Abou-Sleiman; Niall Quinn; Kourosh R Ahmadi; Tetsutaro Ozawa; Christoph Kamm; Ullrich Wüllner; Wolfgang H Oertel; Katrin Burk; Erik Dupont; Maria T Pellecchia; Eduardo Tolosa; Thomas Gasser; Janice L Holton; Tamas Revesz; David B Goldstein; Andrew J Lees; Nicholas W Wood
UCHL-1 gene in multiple system atrophy: a haplotype tagging approach.
Movement disorders : official journal of the Movement Disorder Society 2005;20(10):1338-43.
2005: Sonia Gandhi; Nicholas W Wood
Molecular pathogenesis of Parkinson's disease.
Human molecular genetics 2005;14(18):2749-55.
2005: Naheed L Khan; Paola Giunti; Mary G Sweeney; Christoph Scherfler; Michael O Brien; Paola Piccini; Nicholas W Wood; Andrew J Lees
Parkinsonism and nigrostriatal dysfunction are associated with spinocerebellar ataxia type 6 (SCA6).
Movement disorders : official journal of the Movement Disorder Society 2005;20(9):1115-9.
2005: Sonia Gandhi; Patrick M Abou-Sleiman; Daniel G Healy; M Weale; William P Gilks; Kourosh R Ahmadi; David B Goldstein; Nicholas W Wood
Population genetic approaches to neurological disease: Parkinson's disease as an example.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences 2005;360(1460):1573-8.
2005: Michael P H Stumpf; D B Goldstein; Nicholas W Wood
Introduction: genetic variation and human health.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences 2005;360(1460):1539-41.
2005: Christoph Kamm; Daniel G Healy; Niall Quinn; Ullrich Wüllner; J Carsten Moller; L Schols; Felix Geser; Katrin Burk; A D Børglum; Maria T Pellecchia; Eduardo Tolosa; F del Sorbo; C Nilsson; O Bandmann; Manu Sharma; Petra Mayer; M Gasteiger; A Haworth; Tetsutaro Ozawa; Andrew J Lees; J Short; P Giunti; Elke Holinski-Feder; T Illig; H E Wichmann; Gregor Wenning; Nicholas W Wood; Thomas Gasser
The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group.
Brain : a journal of neurology 2005;128(Pt 8):1855-60.
2005: Gianpiero L Cavalleri; John M Lynch; Chantal Depondt; Mari-Wyn Burley; Nicholas W Wood; Sanjay M Sisodiya; David B Goldstein
Failure to replicate previously reported genetic associations with sporadic temporal lobe epilepsy: where to from here?
Brain : a journal of neurology 2005;128(Pt 8):1832-40.
2005: Maria Martinez; Alexis Brice; Jenny R Vaughan; Alexander Zimprich; Monique Breteler; Giuseppe Meco; Alessandro Filla; Matthew J Farrer; Christine Bétard; Andrew Singleton; John Hardy; Giuseppe De Michele; Vincenzo Bonifati; Ben A Oostra; Thomas Gasser; Nicholas W Wood; Alexandra Dürr
Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;136B(1):72-4.
2005: Sanjay M Sisodiya; Nicole Soranzo; Nicholas W Wood; David B Goldstein
Association of genetic loci: replication or not, that is the question.
Neurology 2005;64(11):1989.
2005: Nicholas W Wood; Daniel G Healy; Chantal Depondt; Patrick M Abou-Sleiman
Commentary on "A genome wide linkage disequilibrium screen in Parkinson's disease" by Foltynie et al. in J Neurol (2005) 252:597-602.
Journal of neurology 2005;252(5):603-4.
2005: Sarah K Tate; Chantal Depondt; Sanjay M Sisodiya; Gianpiero L Cavalleri; Stephanie Schorge; Nicole Soranzo; Maria Thom; Arjune Sen; Simon D Shorvon; Josemir W. Sander; Nicholas W Wood; David B Goldstein
Genetic predictors of the maximum doses patients receive during clinical use of the anti-epileptic drugs carbamazepine and phenytoin.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(15):5507-12.
2005: Naheed L Khan; Wagner Horta; Louise H Eunson; Elizabeth Graham; Janel Johnson; Shannon Chang; Mary Davis; Andrew Singleton; Nicholas W Wood; Andrew J Lees
Parkin disease in a Brazilian kindred: Manifesting heterozygotes and clinical follow-up over 10 years.
Movement disorders : official journal of the Movement Disorder Society 2005;20(4):479-84.
2005: Jürgen Prestel; Manu Sharma; Petra Leitner; Alexander Zimprich; Jenny R Vaughan; Alexandra Dürr; Vincenzo Bonifati; Giuseppe De Michele; Hasmet Hanagasi; Matthew J Farrer; Anne Hofer; Friedrich Asmus; Giampiero Volpe; Giuseppe Meco; Alexis Brice; Nicholas W Wood; Bertram Müller-Myhsok; Thomas Gasser
PARK11 is not linked with Parkinson's disease in European families.
European journal of human genetics : EJHG 2005;13(2):193-7.
2005: William P Gilks; Patrick M Abou-Sleiman; Sonia Gandhi; Shushant Jain; Andrew Singleton; Andrew J Lees; Karen Shaw; Kailash P Bhatia; Vincenzo Bonifati; Niall Quinn; John Lynch; Daniel G Healy; Janice L Holton; Tamas Revesz; Nicholas W Wood
A common LRRK2 mutation in idiopathic Parkinson's disease.
Lancet 2005;365(9457):415-6.
2005: Naheed L Khan; Christoph Scherfler; Elizabeth Graham; Kailash P Bhatia; Niall Quinn; Andrew J Lees; David J Brooks; Nicholas W Wood; Paola Piccini
Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation.
Neurology 2005;64(1):134-6.
2005: Kourosh R Ahmadi; Michael E Weale; Zhengyu Y Xue; Nicole Soranzo; David P Yarnall; James D Briley; Yuka Maruyama; Mikiro Kobayashi; Nicholas W Wood; Nigel K Spurr; Daniel K Burns; Allen D Roses; Ann M Saunders; David B Goldstein
A single-nucleotide polymorphism tagging set for human drug metabolism and transport.
Nature genetics 2005;37(1):84-9.
2004: Huw R Morris; John C Steele; Richard Crook; Fabienne Wavrant-De Vrièze; Luisa Onstead-Cardinale; Katrina Gwinn-Hardy; Nicholas W Wood; Matthew J Farrer; Andrew J Lees; Patrick L McGeer; Teepu Siddique; John Hardy; Jordi Perez-Tur
Genome-wide analysis of the parkinsonism-dementia complex of Guam.
Archives of neurology 2004;61(12):1889-97.
2004: Maria Martinez; Alexis Brice; Jenny R Vaughan; Alexander Zimprich; Monique Breteler; Giuseppe Meco; Alessandro Filla; Matthew J Farrer; Christine Bétard; John Hardy; Giuseppe De Michele; Vincenzo Bonifati; Ben A Oostra; Thomas Gasser; Nicholas W Wood; Alexandra Dürr
Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease.
Journal of medical genetics 2004;41(12):900-7.
2004: Tetsutaro Ozawa; Dominic C Paviour; Niall Quinn; Keith A Josephs; Hardev Sangha; Linda Kilford; Daniel G Healy; Nicholas W Wood; Andrew J Lees; Janice L Holton; Tamas Revesz
The spectrum of pathological involvement of the striatonigral and olivopontocerebellar systems in multiple system atrophy: clinicopathological correlations.
Brain : a journal of neurology 2004;127(Pt 12):2657-71.
2004: Coro Paisan-Ruiz; Shushant Jain; E Whitney Evans; William P Gilks; Javier Simón; Marcel van der Brug; Adolfo López de Munain; Silvia Aparicio; Angel Martínez Gil; Naheed Khan; Janel Johnson; Javier Ruiz Martinez; David Nicholl; Itxaso Marti Carrera; Amets Saénz Pena; Rohan de Silva; Andrew J Lees; José Félix Martí-Massó; Jordi Pérez-Tur; Nicholas W Wood; Andrew Singleton
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease.
Neuron 2004;44(4):595-600.
2004: Daniel G Healy; Patrick M Abou-Sleiman; Nicholas W Wood
PINK, PANK, or PARK? A clinicians' guide to familial parkinsonism.
Lancet neurology 2004;3(11):652-62.
2004: Henry Houlden; Mathilde Girard; Charles Cockerell; David Ingram; Nicholas W Wood; Michel Goossens; Rodney W H Walker; Mary M Reilly
Connexin 32 promoter P2 mutations: a mechanism of peripheral nerve dysfunction.
Annals of neurology 2004;56(5):730-4.
2004: C M Everett; Nicholas W Wood
Trinucleotide repeats and neurodegenerative disease.
Brain : a journal of neurology 2004;127(Pt 11):2385-405.
2004: Chantal Depondt; Hannah R Cock; Daniel G Healy; Mari-Wyn Burley; D Weinshenker; Nicholas W Wood; David B Goldstein; Sanjay M Sisodiya
The -1021C->T DBH gene variant is not associated with epilepsy or antiepileptic drug response.
Neurology 2004;63(8):1497-9.
2004: Daniel G Healy; Patrick M Abou-Sleiman; J M Gibson; Owen A Ross; Shushant Jain; S Gandhi; David Gosal; Miratul M K Muqit; Nicholas W Wood; Timothy Lynch
PINK1 (PARK6) associated Parkinson disease in Ireland.
Neurology 2004;63(8):1486-8.
2004: Patrick M Abou-Sleiman; Daniel G Healy; Nicholas W Wood
Causes of Parkinson's disease: genetics of DJ-1.
Cell and tissue research 2004;318(1):185-8.
2004: Patrick M Abou-Sleiman; Daniel G Healy; Nicholas W Wood
Genetic approaches to solving common diseases.
Journal of neurology 2004;251(10):1169-72.
2004: Luci P MacCormac; Miratul M K Muqit; David J Faulkes; Nicholas W Wood; David S Latchman
Reduction in endogenous parkin levels renders glial cells sensitive to both caspase-dependent and caspase-independent cell death.
The European journal of neuroscience 2004;20(8):2038-48.
2004: Daniel G Healy; Patrick M Abou-Sleiman; Nicholas W Wood
Genetic causes of Parkinson's disease: UCHL-1.
Cell and tissue research 2004;318(1):189-94.
2004: Daniel G Healy; Nicholas W Wood
Clinical picture of bilateral vestibular schwannomas, sudden bilateral hearing loss, and aviation.
Neurology 2004;63(5):933.
2004: Olaf Ansorge; Paola Giunti; Andrej Michalik; Christine Van Broeckhoven; Brian Harding; Nicholas W Wood; Francesco Scaravilli
Ataxin-7 aggregation and ubiquitination in infantile SCA7 with 180 CAG repeats.
Annals of neurology 2004;56(3):448-52.
2004: Daniel G Healy; Patrick M Abou-Sleiman; Kourosh R Ahmadi; Miratul M K Muqit; Kailash P Bhatia; Niall Quinn; Andrew J Lees; David S Latchmann; David B Goldstein; Nicholas W Wood
The gene responsible for PARK6 Parkinson's disease, PINK1, does not influence common forms of parkinsonism.
Annals of neurology 2004;56(3):329-35.
2004: Daniel G Healy; Patrick M Abou-Sleiman; Andrew J Lees; Juan P Casas; Niall Quinn; K Bhatia; Aroon D Hingorani; Nicholas W Wood
Tau gene and Parkinson's disease: a case-control study and meta-analysis.
Journal of neurology, neurosurgery, and psychiatry 2004;75(7):962-5.
2004: Nicole Soranzo; Gianpiero L Cavalleri; Michael E Weale; Nicholas W Wood; Chantal Depondt; Richard Marguerie; Sanjay M Sisodiya; David B Goldstein
Identifying candidate causal variants responsible for altered activity of the ABCB1 multidrug resistance gene.
Genome research 2004;14(7):1333-44.
2004: Daniel G Healy; Patrick M Abou-Sleiman; Shushant Jain; Kourosh R Ahmadi; Nicholas W Wood
Assessment of a DJ-1 (PARK7) polymorphism in Finnish PD.
Neurology 2004;62(12):2335.
2004: Alan Pittman; Amanda Myers; Jaime Duckworth; Leslie Bryden; Melissa Hanson; Patrick M Abou-Sleiman; Nicholas W Wood; John Hardy; Andrew J Lees; Rohan de Silva
The structure of the tau haplotype in controls and in progressive supranuclear palsy.
Human molecular genetics 2004;13(12):1267-74.
2004: Jonathan A Beck; Mark Poulter; Tracy A Campbell; James B Uphill; Gary Adamson; Jennian F Geddes; Tamas Revesz; Mary B Davis; Nicholas W Wood; John Collinge; Sarah J Tabrizi
Somatic and germline mosaicism in sporadic early-onset Alzheimer's disease.
Human molecular genetics 2004;13(12):1219-24.
2004: Elide Mantuano; Liana Veneziano; Maria Spadaro; Paola Giunti; serena guida; M G Leggio; L Verriello; Nicholas W Wood; C Jodice; Marina Frontali
Clusters of non-truncating mutations of P/Q type Ca2+ channel subunit Ca(v)2.1 causing episodic ataxia 2.
Journal of medical genetics 2004;41(6):e82.
2004: Christoph Scherfler; Naheed L Khan; Nicola Pavese; Louise H Eunson; Elizabeth Graham; Andrew J Lees; Niall Quinn; Nicholas W Wood; David J Brooks; Paola Piccini
Striatal and cortical pre- and postsynaptic dopaminergic dysfunction in sporadic parkin-linked parkinsonism.
Brain : a journal of neurology 2004;127(Pt 6):1332-42.
2004: Enza Maria Valente; Patrick M Abou-Sleiman; Viviana Caputo; Miratul M K Muqit; Kirsten Harvey; Suzana Gispert; Zeeshan Ali; Domenico Del Turco; Anna Rita Bentivoglio; Daniel G Healy; Alberto Albanese; Robert L Nussbaum; Rafael González-Maldonado; Thomas Deller; Sergio Salvi; Pietro Cortelli; William P Gilks; David S Latchman; Robert Justin Harvey; Bruno Dallapiccola; Georg Auburger; Nicholas W Wood
Hereditary early-onset Parkinson's disease caused by mutations in PINK1.
Science (New York, N.Y.) 2004;304(5674):1158-60.
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: Naheed L Khan; Regina Katzenschlager; H Watt; Kailash P Bhatia; Nicholas W Wood; Niall Quinn; Andrew J Lees
Olfaction differentiates parkin disease from early-onset parkinsonism and Parkinson disease.
Neurology 2004;62(7):1224-6.
2004: Daniel G Healy; Patrick M Abou-Sleiman; Tetsutaro Ozawa; Andrew J Lees; Kailash Bhatia; Kourosh R Ahmadi; Ullrich Wüllner; Jose Berciano; J Carsten Moller; Christoph Kamm; Katrin Burk; Paolo Barone; Eduardo Tolosa; Niall Quinn; David B Goldstein; Nicholas W Wood; Paolo Barrone
A functional polymorphism regulating dopamine beta-hydroxylase influences against Parkinson's disease.
Annals of neurology 2004;55(3):443-6.
2004: Krishna K Sinha; Paul Worth; Dilip K Jha; S Sinha; VJ Stinton; Mary B Davis; Nicholas W Wood; Mary G Sweeney; Kailash P Bhatia
Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.
Journal of neurology, neurosurgery, and psychiatry 2004;75(3):448-52.
2004: Rina Bandopadhyay; Ann E Kingsbury; Mark Cookson; Andrew R Reid; Ian Evans; Andrew D Hope; Alan Pittman; Tammaryn Lashley; Canet Rosa; David W Miller; Chris McLendon; Catherine Strand; Andrew J Leonard; Patrick M Abou-Sleiman; Daniel G Healy; Hiroyashi Ariga; Nicholas W Wood; Rohan de Silva; Tamas Revesz; John Hardy; Andrew J Lees
The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's disease.
Brain : a journal of neurology 2004;127(Pt 2):420-30.
2004: Daniel G Healy; Patrick M Abou-Sleiman; Enza Maria Valente; William P Gilks; K Bhatia; Niall Quinn; Andrew J Lees; Nicholas W Wood
DJ-1 mutations in Parkinson's disease.
Journal of neurology, neurosurgery, and psychiatry 2004;75(1):144-5.
2004: Miratul M K Muqit; Sean Davidson; Martin D Payne Smith; Luci P MacCormac; Soren Kahns; Poul Henning Jensen; Nicholas W Wood; David S Latchman
Parkin is recruited into aggresomes in a stress-specific manner: over-expression of parkin reduces aggresome formation but can be dissociated from parkin's effect on neuronal survival.
Human molecular genetics 2004;13(1):117-35.
2003: Naheed L Khan; Nicholas W Wood; Kailash P Bhatia
Autosomal recessive, DYT2-like primary torsion dystonia: a new family.
Neurology 2003;61(12):1801-3.
2003: David B Goldstein; Kourosh R Ahmadi; Michael E Weale; Nicholas W Wood
Genome scans and candidate gene approaches in the study of common diseases and variable drug responses.
Trends in genetics : TIG 2003;19(11):615-22.
2003: Wilson Marques; Mary G Sweeney; Nicholas W Wood
Thr(118)Met amino acid substitution in the peripheral myelin protein 22 does not influence the clinical phenotype of Charcot-Marie-Tooth disease type 1A due to the 17p11.2-p12 duplication.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas / Sociedade Brasileira de Biofísica ... [et al.] 2003;36(10):1403-7.
2003: Patrick M Abou-Sleiman; Daniel G Healy; Niall Quinn; Andrew J Lees; Nicholas W Wood
The role of pathogenic DJ-1 mutations in Parkinson's disease.
Annals of neurology 2003;54(3):283-6.
2003: Michael E Weale; Chantal Depondt; Stuart J Macdonald; Alice Smith; Poh San Lai; Simon D Shorvon; Nicholas W Wood; David B Goldstein
Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping.
American journal of human genetics 2003;73(3):551-65.
2003: Mark J Edwards; Ying-Zu Huang; Nicholas W Wood; John C Rothwell; Kailash P Bhatia
Different patterns of electrophysiological deficits in manifesting and non-manifesting carriers of the DYT1 gene mutation.
Brain : a journal of neurology 2003;126(Pt 9):2074-80.
2003: Rohan de Silva; Andrew D Hope; Alan Pittman; Michael E Weale; Huw R Morris; Nicholas W Wood; Andrew J Lees
Strong association of the Saitohin gene Q7 variant with progressive supranuclear palsy.
Neurology 2003;61(3):407-9.
2003: Ebba Lohmann; Magali Periquet; Vincenzo Bonifati; Nicholas W Wood; Giuseppe De Michele; Anne-Marie Bonnet; Valérie Fraix; Emmanuel Broussolle; Martin Horstink; Marie Vidailhet; Patrice Verpillat; Thomas Gasser; David Nicholl; Hélio A G Teive; Salmo Raskin; Olivier Rascol; Alain Destée; Merle Ruberg; Francesca Gasparini; Giuseppe Meco; Yves Agid; Alexandra Durr; Alexis Brice
How much phenotypic variation can be attributed to parkin genotype?
Annals of neurology 2003;54(2):176-85.
2003: Ming-Jen Lee; Dennis A Stephenson; Michael J Groves; Mary G Sweeney; Mary B Davis; Shu F An; Henry Houlden; Mustafa A Salih; Vincent Timmerman; Peter de Jonghe; Michaela Auer-Grumbach; Emilio Di Maria; Francesco Scaravilli; Nicholas W Wood; Mary M Reilly
Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene.
Human molecular genetics 2003;12(15):1917-25.
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: H R Morris; Y Osaki; J Holton; Andrew J Lees; Nicholas W Wood; Tamas Revesz; Niall Quinn
Tau exon 10 +16 mutation FTDP-17 presenting clinically as sporadic young onset PSP.
Neurology 2003;61(1):102-4.
2003: Rohan de Silva; Tammaryn Lashley; Graham Gibb; Diane P Hanger; Andrew D Hope; A Reid; Rina Bandopadhyay; Michelle A Utton; Catherine Strand; T Jowett; Naheed Khan; Brian H Anderton; Nicholas W Wood; Janice Holton; Tamas Revesz; Andrew J Lees
Pathological inclusion bodies in tauopathies contain distinct complements of tau with three or four microtubule-binding repeat domains as demonstrated by new specific monoclonal antibodies.
Neuropathology and applied neurobiology 2003;29(3):288-302.
2003: Mark Edwards; Nicholas W Wood; Kailash Bhatia
Unusual phenotypes in DYT1 dystonia: a report of five cases and a review of the literature.
Movement disorders : official journal of the Movement Disorder Society 2003;18(6):706-11.
2003: Naheed L Khan; Elizabeth Graham; Peter Critchley; Anette E Schrag; Nicholas W Wood; Andrew J Lees; Kailash P Bhatia; Niall Quinn
Parkin disease: a phenotypic study of a large case series.
Brain : a journal of neurology 2003;126(Pt 6):1279-92.
2003: Magali Periquet; Morwena Latouche; Ebba Lohmann; Nina Rawal; Giuseppe De Michele; Sylvain Ricard; Hélio A G Teive; Valérie Fraix; Marie Vidailhet; David Nicholl; Paolo Barone; Nicholas W Wood; Salmo Raskin; Jean-François Deleuze; Yves Agid; Alexandra Dürr; Alexis Brice
Parkin mutations are frequent in patients with isolated early-onset parkinsonism.
Brain : a journal of neurology 2003;126(Pt 6):1271-8.
2003: Asra Siddiqui; Reinhold Kerb; Michael E Weale; Ulrich Brinkmann; Alice Smith; David B Goldstein; Nicholas W Wood; Sanjay M Sisodiya
Association of multidrug resistance in epilepsy with a polymorphism in the drug-transporter gene ABCB1.
The New England journal of medicine 2003;348(15):1442-8.
2003: Dirk Sibbing; Iris Trender-Gerhardt; Nicholas W Wood; Wolfgang H Oertel; Kailash P Bhatia; Oliver Bandmann
The promoter region of the Menkes gene ATP7A is not altered in focal or generalized dystonia.
Annals of neurology 2003;53(2):278-9; author reply 279-80.
2003: Mikko Kuoppamäki; Paola Giunti; Niall Quinn; Nicholas W Wood; Kailash P Bhatia
Slowly progressive cerebellar ataxia and cervical dystonia: clinical presentation of a new form of spinocerebellar ataxia?
Movement disorders : official journal of the Movement Disorder Society 2003;18(2):200-6.
2002: Paul R Jarman; Nicholas W Wood
Genetics of movement disorders and ataxia.
Journal of neurology, neurosurgery, and psychiatry 2002;73 Suppl 2():II22-6.
2002: Michael G Hanna; Nicholas W Wood
Running a neurogenetic clinic.
Journal of neurology, neurosurgery, and psychiatry 2002;73 Suppl 2():II2-4.
2002: Naheed L Khan; Enza Maria Valente; Anna Rita Bentivoglio; Nicholas W Wood; Alberto Albanese; David J Brooks; Paola Piccini
Clinical and subclinical dopaminergic dysfunction in PARK6-linked parkinsonism: an 18F-dopa PET study.
Annals of neurology 2002;52(6):849-53.
2002: Henry Houlden; Stephen Smith; Mamede de Carvalho; Julian Blake; Christopher Mathias; Nicholas W Wood; Mary M Reilly
Clinical and genetic characterization of families with triple A (Allgrove) syndrome.
Brain : a journal of neurology 2002;125(Pt 12):2681-90.
2002: C Dobson-Stone; Adrian Danek; L Rampoldi; R J Hardie; R M Chalmers; Nicholas W Wood; S Bohlega; M T Dotti; A Federico; M Shizuka; M Tanaka; M Watanabe; Y Ikeda; M Brin; L G Goldfarb; B I Karp; Saidi Mohiddin; L Fananapazir; A Storch; A E Fryer; P Maddison; I Sibon; P C Trevisol-Bittencourt; Carlos Singer; I R Caballero; J O Aasly; K Schmierer; R Dengler; L-P Hiersemenzel; M Zeviani; V Meiner; A Lossos; S Johnson; F C Mercado; Giuseppe Sorrentino; N Dupré; G A Rouleau; Jens Volkmann; J Arpa; A Lees; G Geraud; S Chouinard; A Németh; Anthony P Monaco
Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis.
European journal of human genetics : EJHG 2002;10(11):773-81.
2002: Friedrich Asmus; Alexander Zimprich; Sophie Tezenas du Montcel; Christian Kabus; Günther Deuschl; Andreas Kupsch; Ulf Ziemann; Mirna Castro; Andrea A Kühn; Tim M Strom; Marie Vidailhet; Kailash P Bhatia; Alexandra Dürr; Nicholas W Wood; Alexis Brice; Thomas Gasser
Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype.
Annals of neurology 2002;52(4):489-92.
2002: Naheed L Khan; David J Brooks; Nicola Pavese; Mary G Sweeney; Nicholas W Wood; Andrew J Lees; Paola Piccini
Progression of nigrostriatal dysfunction in a parkin kindred: an [18F]dopa PET and clinical study.
Brain : a journal of neurology 2002;125(Pt 10):2248-56.
2002: Rohan de Silva; John Hardy; Julia Crook; Naheed Khan; Elizabeth A Graham; Christopher M Morris; Nicholas W Wood; Andrew J Lees
The tau locus is not significantly associated with pathologically confirmed sporadic Parkinson's disease.
Neuroscience letters 2002;330(2):201-3.
2002: Enza Maria Valente; Francesco Brancati; Viviana Caputo; E A Graham; Mary B Davis; Alessandro Ferraris; Monique Breteler; Thomas Gasser; Vincenzo Bonifati; Anna Rita Bentivoglio; Giuseppe De Michele; Alexandra Dürr; Pietro Cortelli; Alessandro Filla; Giuseppe Meco; Ben A Oostra; Alexis Brice; Alberto Albanese; Bruno Dallapiccola; Nicholas W Wood
PARK6 is a common cause of familial parkinsonism.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2002;23 Suppl 2():S117-8.
2002: Ming-Jen Lee; Yuan-Chung Huang; Mary G Sweeney; Nicholas W Wood; Mary M Reilly; Ping-Keung Yip
Mutation of the sterol 27-hydroxylase gene ( CYP27A1) in a Taiwanese family with cerebrotendinous xanthomatosis.
Journal of neurology 2002;249(9):1311-2.
2002: Sian D Spacey; Blazej I Szczygielski; John E McRory; Gurusidheshwar M Wali; Nicholas W Wood; Terrance P Snutch
Mutation analysis of the sodium/hydrogen exchanger gene (NHE5) in familial paroxysmal kinesigenic dyskinesia.
Journal of neural transmission (Vienna, Austria : 1996) 2002;109(9):1189-94.
2002: M-J Lee; Isabelle P Nelson; Henry Houlden; Mary G Sweeney; D Hilton-Jones; Julian Blake; Nicholas W Wood; Mary M Reilly
Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth disease.
Journal of neurology, neurosurgery, and psychiatry 2002;73(3):304-6.
2002: Huw R Morris; M Baker; K Yasojima; Henry Houlden; M Nadeem Khan; Nicholas W Wood; John Hardy; Murray Grossman; John Q Trojanowski; Tamas Revesz; Eileen H Bigio; C Bergeron; John C Janssen; Patrick L McGeer; Martin N Rossor; Andrew J Lees; Peter L Lantos; Michael Hutton
Analysis of tau haplotypes in Pick's disease.
Neurology 2002;59(3):443-5.
2002: Majid Hafezparast; Azlina Ahmad-Annuar; Nicholas W Wood; Sarah J Tabrizi; Elizabeth M C Fisher
Mouse models for neurological disease.
Lancet neurology 2002;1(4):215-24.
2002: Andrew West; Magali Periquet; Sarah J Lincoln; Christoph B Lücking; David Nicholl; Vincenzo Bonifati; Nina Rawal; Thomas Gasser; Ebba Lohmann; Jean-François Deleuze; Demetrius M Maraganore; Allan Levey; Nicholas W Wood; Alexandra Dürr; John Hardy; Alexis Brice; Matthew J Farrer
Complex relationship between Parkin mutations and Parkinson disease.
American journal of medical genetics 2002;114(5):584-91.
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: Lucy Kinton; Michael R Johnson; Shelagh J M Smith; Fiona Farrell; John Stevens; James B Rance; Angelica M Claudino; John S Duncan; Mary B Davis; Nicholas W Wood; Josemir W. Sander
Partial epilepsy with pericentral spikes: a new familial epilepsy syndrome with evidence for linkage to chromosome 4p15.
Annals of neurology 2002;51(6):740-9.
2002: Jason D Warren; Catherine J Mummery; Amir S Al-Din; Peter Brown; Nicholas W Wood
Corticobasal degeneration syndrome with basal ganglia calcification: Fahr's disease as a corticobasal look-alike?
Movement disorders : official journal of the Movement Disorder Society 2002;17(3):563-7.
2002: Nin Bajaj; A Waldman; R Orrell; Nicholas W Wood; K P Bhatia
Familial adult onset of Krabbe's disease resembling hereditary spastic paraplegia with normal neuroimaging.
Journal of neurology, neurosurgery, and psychiatry 2002;72(5):635-8.
2002: Huw R Morris; Graham Gibb; Regina Katzenschlager; Nicholas W Wood; Diane P Hanger; Catherine Strand; Tammaryn Lashley; Susan E Daniel; Andrew J Lees; Brian H Anderton; Tamas Revesz
Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy.
Brain : a journal of neurology 2002;125(Pt 5):969-75.
2002: John C Janssen; Elizabeth K Warrington; Huw R Morris; Peter Lantos; J Brown; Tamas Revesz; Nicholas W Wood; M Nadeem Khan; Lisa Cipolotti; Nick C Fox; Martin N Rossor
Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation.
Neurology 2002;58(8):1161-8.
2002: Joanna T Pang; Paola Giunti; Susan Chamberlain; Shu F An; Roberta Vitaliani; Tomaso Scaravilli; Lillian Martinian; Nicholas W Wood; Francesco Scaravilli; Olaf Ansorge
Neuronal intranuclear inclusions in SCA2: a genetic, morphological and immunohistochemical study of two cases.
Brain : a journal of neurology 2002;125(Pt 3):656-63.
2002: Huw R Morris; Regina Katzenschlager; John C Janssen; J M Brown; M Ozansoy; Niall Quinn; Tamas Revesz; Martin N Rossor; Susan E Daniel; Nicholas W Wood; Andrew J Lees
Sequence analysis of tau in familial and sporadic progressive supranuclear palsy.
Journal of neurology, neurosurgery, and psychiatry 2002;72(3):388-90.
2002: Oliver Bandmann; Nicholas W Wood
Dopa-responsive dystonia -- the story so far.
Neuropediatrics 2002;33(1):1-5.
2002: Dominick J H McCabe; Nicholas W Wood; Fergus Ryan; Michael G Hanna; Sean Connolly; David P Moore; Janice Redmond; David Barton; Raymond P Murphy
Intrafamilial phenotypic variability in Friedreich ataxia associated with a G130V mutation in the FRDA gene.
Archives of neurology 2002;59(2):296-300.
2002: CM Gabriel; Norman A Gregson; Nicholas W Wood; Richard AC Hughes
Immunological study of hereditary motor and sensory neuropathy type 1a (HMSN1a).
Journal of neurology, neurosurgery, and psychiatry 2002;72(2):230-5.
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.
2002: David Nicholl; Jenny R Vaughan; Naheed L Khan; Shu-Leong Ho; D E W Aldous; Sarah J Lincoln; Matthew J Farrer; J D Gayton; Mary B Davis; Paola Piccini; Susan E Daniel; Graham Lennox; David J Brooks; AC Williams; Nicholas W Wood
Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic study.
Brain : a journal of neurology 2002;125(Pt 1):44-57.
2002: Enza Maria Valente; Francesco Brancati; Alessandro Ferraris; Elizabeth A Graham; Mary B Davis; Monique Breteler; Thomas Gasser; Vincenzo Bonifati; Anna Rita Bentivoglio; Giuseppe De Michele; Alexandra Dürr; Pietro Cortelli; Dietmar Wassilowsky; Biswadjiet S Harhangi; Nina Rawal; Viviana Caputo; Alessandro Filla; Giuseppe Meco; Ben A Oostra; Alexis Brice; Alberto Albanese; Bruno Dallapiccola; Nicholas W Wood
PARK6-linked parkinsonism occurs in several European families.
Annals of neurology 2002;51(1):14-8.
2001: Jorge Ghiso; Tamas Révész; Janice Holton; Agueda Rostagno; Tammaryn Lashley; Henry Houlden; Graham Gibb; Brian H Anderton; T Bek; Marie Bojsen-Møller; Nicholas W Wood; Ruben Vidal; Hans Braendgaard; Gordon Plant; Blas Frangione
Chromosome 13 dementia syndromes as models of neurodegeneration.
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 2001;8(4):277-84.
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: Jorge Ghiso; Janice Holton; Leticia Miravalle; Miguel Calero; Tammaryn Lashley; Ruben Vidal; Henry Houlden; Nicholas W Wood; Thomas A Neubert; Agueda Rostagno; Gordon Plant; Tamas Revesz; Blas Frangione
Systemic amyloid deposits in familial British dementia.
The Journal of biological chemistry 2001;276(47):43909-14.
2001: Huw R Morris; M Nadeem Khan; John C Janssen; J M Brown; J Perez-Tur; M Baker; M Ozansoy; John Hardy; Michael Hutton; Nicholas W Wood; Andrew J Lees; Tamas Revesz; Peter Lantos; Martin N Rossor
The genetic and pathological classification of familial frontotemporal dementia.
Archives of neurology 2001;58(11):1813-6.
2001: Huw R Morris; S Al-Sarraj; Claudia Schwab; Katrina Gwinn-Hardy; Jordi Perez-Tur; Nicholas W Wood; John Hardy; Andrew J Lees; Patrick L McGeer; Susan E Daniel; John C Steele
A clinical and pathological study of motor neurone disease on Guam.
Brain : a journal of neurology 2001;124(Pt 11):2215-22.
2001: Huw R Morris; Anette Schrag; U Nath; David J Burn; Niall Quinn; Susan E Daniel; Nicholas W Wood; Andrew J Lees
Effect of ApoE and tau on age of onset of progressive supranuclear palsy and multiple system atrophy.
Neuroscience letters 2001;312(2):118-20.
2001: Thomas D Bird; Gail P Jarvik; Nicholas W Wood
Genetic association studies: genes in search of diseases.
Neurology 2001;57(7):1153-4.
2001: Rohan de Silva; Markus Weiler; Huw R Morris; Eden R Martin; Nicholas W Wood; Andrew J Lees
Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy.
Neuroscience letters 2001;311(3):145-8.
2001: T Gasser; M Dichgans; J Finsterer; I Hausmanowa-Petrusewicz; K Jurkat-Rott; Thomas Klopstock; E Leguern; A E Lehesjoki; F Lehmann-Horn; T Lynch; H Morris; Martin N Rossor; O K Steinlein; Nicholas W Wood; J Zaremba; M Zeviani; A Zoharn
EFNS Task Force on Molecular Diagnosis of Neurologic Disorders: guidelines for the molecular diagnosis of inherited neurologic diseases. Second of two parts.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2001;8(5):407-24.
2001: Volney L Sheen; Peter DIxon; JW Fox; Susan E Hong; L Kinton; S M Sisodiya; J S Duncan; F Dubeau; IE Scheffer; Steven C Schachter; Andrew Wilner; R Henchy; P Crino; K Kamuro; F DiMario; M Berg; R Kuzniecky; A J Cole; Edward B Bromfield; M Biber; Donald L Schomer; James W Wheless; K Silver; G H Mochida; SF Berkovic; F Andermann; Eva Andermann; William B Dobyns; Nicholas W Wood; Christopher Walsh
Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females.
Human molecular genetics 2001;10(17):1775-83.
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; T Warner; I Allen; H E Phillimore; J R Silver; Nicholas W Wood; Steve Jeffery; Michael A Patton; Andrew H Crosby
Silver syndrome is not linked to any of the previously established autosomal dominant hereditary spastic paraplegia loci.
American journal of medical genetics 2001;102(1):68-72.
2001: Rina Bandopadhyay; Rohan de Silva; Naheed Khan; Elizabeth Graham; J Vaughan; Simone Engelender; Christopher A Ross; H Morris; C Morris; Nicholas W Wood; Susan E Daniel; Andrew J Lees
No pathogenic mutations in the synphilin-1 gene in Parkinson's disease.
Neuroscience letters 2001;307(2):125-7.
2001: Blas Frangione; Tamas Révész; Ruben Vidal; Janice Holton; Tammaryn Lashley; Henry Houlden; Nicholas W Wood; Agueda Rostagno; Gordon Plant; Jorge Ghiso
Familial cerebral amyloid angiopathy related to stroke and dementia.
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 2001;8 Suppl 1():36-42.
2001: T Gasser; M Dichgans; J Finsterer; I Hausmanowa-Petrusewicz; K Jurkat-Rott; Thomas Klopstock; E LeGuern; A E Lehesjoki; F Lehmann-Horn; T Lynch; H Morris; Martin N Rossor; O K Steinlein; Nicholas W Wood; J Zaremba; M Zeviani; A Zoharn
EFNS Task Force on Molecular Diagnosis of Neurologic Disorders: guidelines for the molecular diagnosis of inherited neurologic diseases. First of two parts.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2001;8(4):299-314.
2001: U Nath; Y Ben-Shlomo; Richard G Thomson; H R Morris; Nicholas W Wood; Andrew J Lees; David J Burn
The prevalence of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) in the UK.
Brain : a journal of neurology 2001;124(Pt 7):1438-49.
2001: Henry Houlden; M Baker; H R Morris; N MacDonald; S Pickering-Brown; Jennifer Adamson; Andrew J Lees; Martin N Rossor; Niall Quinn; A Kertesz; M N Khan; John Hardy; P L Lantos; P St George-Hyslop; David G Munoz; D M A Mann; Anthony E Lang; C Bergeron; Eileen H Bigio; Irene Litvan; K P Bhatia; dennis dickson; Nicholas W Wood; Michael Hutton
Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype.
Neurology 2001;56(12):1702-6.
2001: Luca Rampoldi; Carol Dobson-Stone; JP Rubio; Adrian Danek; R M Chalmers; Nicholas W Wood; C Verellen; X Ferrer; Alessandro Malandrini; G M Fabrizi; R Brown; Jeffery Vance; Margaret Pericak-Vance; G Rudolf; S Carrè; E Alonso; M Manfredi; Andrea H Németh; Anthony P Monaco
A conserved sorting-associated protein is mutant in chorea-acanthocytosis.
Nature genetics 2001;28(2):119-20.
2001: Naheed Khan; Elizabeth Graham; Peter DIxon; C Morris; adrian mander; D Clayton; J Vaughan; Niall Quinn; Andrew J Lees; Susan E Daniel; Nicholas W Wood; Rohan de Silva
Parkinson's disease is not associated with the combined alpha-synuclein/apolipoprotein E susceptibility genotype.
Annals of neurology 2001;49(5):665-8.
2001: Henry Houlden; Rosalind H M King; Nicholas W Wood; PK Thomas; Mary M Reilly
Mutations in the 5' region of the myotubularin-related protein 2 (MTMR2) gene in autosomal recessive hereditary neuropathy with focally folded myelin.
Brain : a journal of neurology 2001;124(Pt 5):907-15.
2001: Henry Houlden; Rosalind H M King; A Hashemi-Nejad; Nicholas W Wood; C J Mathias; M Reilly; PK Thomas
A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V.
Annals of neurology 2001;49(4):521-5.
2001: Enza Maria Valente; Anna Rita Bentivoglio; Peter DIxon; Alessandro Ferraris; Tamara Ialongo; Marina Frontali; Alberto Albanese; Nicholas W Wood
Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36.
American journal of human genetics 2001;68(4):895-900.
2001: Jenny R Vaughan; Mary B Davis; Nicholas W Wood
Genetics of Parkinsonism: a review.
Annals of human genetics 2001;65(Pt 2):111-26.
2001: Enza Maria Valente; Anna Rita Bentivoglio; E Cassetta; Peter DIxon; Mary B Davis; Alessandro Ferraris; Tamara Ialongo; Marina Frontali; Nicholas W Wood; Alberto Albanese
DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13--36.32 in an Italian family with cranial-cervical or upper limb onset.
Annals of neurology 2001;49(3):362-6.
2001: Magali Periquet; C Lücking; J Vaughan; Vincenzo Bonifati; Alexandra Dürr; Giuseppe De Michele; Martin Horstink; Matthew J Farrer; Sergei N Illarioshkin; Pierre Pollak; M Borg; C Brefel-Courbon; Patrice DENEFLE; Giuseppe Meco; Thomas Gasser; Monique Breteler; Nicholas W Wood; Yves Agid; Alexis Brice
Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effects.
American journal of human genetics 2001;68(3):617-26.
2001: W Jeptha Davenport; Adrian M Siegel; Johannes Dichgans; P Drigo; I Mammi; P Pereda; Nicholas W Wood; Guy Rouleau
CCM1 gene mutations in families segregating cerebral cavernous malformations.
Neurology 2001;56(4):540-3.
2001: Paul Worth; Nicholas W Wood
Spinocerebellar ataxia type 12 is rare in the United Kingdom.
Neurology 2001;56(3):419-20.
2001: Enza Maria Valente; Anna Rita Bentivoglio; E Cassetta; Peter DIxon; Mary B Davis; Alessandro Ferraris; Tamara Ialongo; Marina Frontali; Nicholas W Wood; Alberto Albanese
Identification of a novel primary torsion dystonia locus (DYT13) on chromosome 1p36 in an Italian family with cranial-cervical or upper limb onset.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2001;22(1):95-6.
2001: Vincenzo Bonifati; Giuseppe De Michele; Christoph B Lücking; Alexandra Dürr; Edito Fabrizio; G Ambrosio; Nicola Vanacore; Michele De Mari; Roberto Marconi; L Capus; Monique Breteler; Thomas Gasser; Ben A Oostra; Nicholas W Wood; Yves Agid; Alessandro Filla; Giuseppe Meco; Alexis Brice
The parkin gene and its phenotype. Italian PD Genetics Study Group, French PD Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2001;22(1):51-2.
2001: Janice L Holton; Jorge Ghiso; Tammaryn Lashley; Agueda Rostagno; C J Guerin; Graham Gibb; Henry Houlden; H Ayling; Lillian Martinian; Brian H Anderton; Nicholas W Wood; Ruben Vidal; Gordon Plant; Blas Frangione; Tamas Revesz
Regional distribution of amyloid-Bri deposition and its association with neurofibrillary degeneration in familial British dementia.
The American journal of pathology 2001;158(2):515-26.
2001: Claudia Gaspar; Iscia Lopes-Cendes; S Hayes; Jun Goto; K Arvidsson; Adelaide Dias; Isabel Silveira; Patrícia Maciel; Paula Coutinho; M Lima; Y X Zhou; bing-wen soong; Masahiko Watanabe; Paola Giunti; Giovanni Stevanin; Olaf Riess; H Sasaki; M Hsieh; G A Nicholson; E Brunt; J J Higgins; M Lauritzen; Lisbeth Tranebjaerg; V Volpini; Nicholas W Wood; Laura P W Ranum; Shoji Tsuji; Alexis Brice; Jorge Sequeiros; Guy Rouleau
Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype study.
American journal of human genetics 2001;68(2):523-8.
2000: Huw R Morris; Jenny R Vaughan; S R Datta; R Bandopadhyay; H A Rohan De Silva; Anette Schrag; Nigel J Cairns; David J Burn; U Nath; Peter L Lantos; Susan E Daniel; Andrew J Lees; Niall Quinn; Nicholas W Wood
Multiple system atrophy/progressive supranuclear palsy: alpha-Synuclein, synphilin, tau, and APOE.
Neurology 2000;55(12):1918-20.
2000: C J Wilson; Nicholas W Wood; J V Leonard; Robert Surtees; S Rahman
Mitochondrial DNA point mutation T9176C in Leigh syndrome.
Journal of child neurology 2000;15(12):830-3.
2000: Henry Houlden; M Baker; E McGowan; P Lewis; Michael Hutton; Richard Crook; Nicholas W Wood; Samir Kumar-Singh; J Geddes; M Swash; Francesco Scaravilli; Janice L Holton; Tammaryn Lashley; T Tomita; T Hashimoto; Auli Verkkoniemi; Hannu Kalimo; Mirja Somer; Anders Paetau; J J Martin; Christine Van Broeckhoven; todd golde; John Hardy; Matti Haltia; Tamas Revesz
Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-beta concentrations.
Annals of neurology 2000;48(5):806-8.
2000: Enza Maria Valente; Sian D Spacey; Gurusidheshwar M Wali; Kailash P Bhatia; Peter DIxon; Nicholas W Wood; Mary B Davis
A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16.
Brain : a journal of neurology 2000;123 ( Pt 10)():2040-5.
2000: Alexander Münchau; Enza Maria Valente; Mary B Davis; VJ Stinton; Nicholas W Wood; Niall Quinn; Kailash P Bhatia
A Yorkshire family with adult-onset cranio-cervical primary torsion dystonia.
Movement disorders : official journal of the Movement Disorder Society 2000;15(5):954-9.
2000: Paul R Jarman; Kailash P Bhatia; Charles Davie; Simon J R Heales; N Turjanski; S D Taylor-Robinson; CD Marsden; Nicholas W Wood
Paroxysmal dystonic choreoathetosis: clinical features and investigation of pathophysiology in a large family.
Movement disorders : official journal of the Movement Disorder Society 2000;15(4):648-57.
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.
2000: H R de Silva; N L Khan; Nicholas W Wood
The genetics of Parkinson's disease.
Current opinion in genetics & development 2000;10(3):292-8.
2000: Christoph B Lücking; Alexandra Dürr; Vincenzo Bonifati; J Vaughan; Giuseppe De Michele; Thomas Gasser; Biswadjiet S Harhangi; Giuseppe Meco; Patrice DENEFLE; Nicholas W Wood; Yves Agid; Alexis Brice
Association between early-onset Parkinson's disease and mutations in the parkin gene.
The New England journal of medicine 2000;342(21):1560-7.
2000: Alexander Münchau; Enza Maria Valente; G A Shahidi; Louise H Eunson; Michael G Hanna; Niall Quinn; Anthony H V Schapira; Nicholas W Wood; Kailash P Bhatia
A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study.
Journal of neurology, neurosurgery, and psychiatry 2000;68(5):609-14.
2000: Paul Worth; Henry Houlden; Paola Giunti; Mary B Davis; Nicholas W Wood
Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia.
Nature genetics 2000;24(3):214-5.
2000: O Bandmann; Jenny R Vaughan; PA Holmans; CD Marsden; Nicholas W Wood
Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2000;15(1):30-5.
1999: Teeratorn Pulkes; Louise H Eunson; V Patterson; A Siddiqui; Nicholas W Wood; Isabelle P Nelson; JA Morgan-Hughes; Michael G Hanna
The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS.
Annals of neurology 1999;46(6):916-9.
1999: Thomasin C Andrews; RA Weeks; N Turjanski; Roger Gunn; Laura H Watkins; Barbara J Sahakian; John R Hodges; Anne E Rosser; Nicholas W Wood; David J Brooks
Huntington's disease progression. PET and clinical observations.
Brain : a journal of neurology 1999;122 ( Pt 12)():2353-63.
1999: J M Flowers; P N Leigh; A M Davies; Natalia Ninkina; Vladimir L Buchman; J Vaughan; Nicholas W Wood; John F Powell
Mutations in the gene encoding human persyn are not associated with amyotrophic lateral sclerosis or familial Parkinson's disease.
Neuroscience letters 1999;274(1):21-4.
1999: H R Morris; Nicholas W Wood; Andrew J Lees
Progressive supranuclear palsy (Steele-Richardson-Olszewski disease).
Postgraduate medical journal 1999;75(888):579-84.
1999: Amilton A Barreira; W Marques Júnior; Mary G Sweeney; Mary B Davis; L Chimelli; M L Paçó-Larson; Nicholas W Wood
A family with Friedreich ataxia and onion-bulb formations at sural nerve biopsy.
Annals of the New York Academy of Sciences 1999;883():466-8.
1999: R M Chalmers; L Andreae; Nicholas W Wood; R V Durai Raj; adrian casey
Familial hydrocephalus.
Journal of neurology, neurosurgery, and psychiatry 1999;67(3):410-11.
1999: Huw R Morris; Andrew J Lees; Nicholas W Wood
Neurofibrillary tangle parkinsonian disorders--tau pathology and tau genetics.
Movement disorders : official journal of the Movement Disorder Society 1999;14(5):731-6.
1999: Paul R Jarman; N Del Grosso; Enza Maria Valente; Barbara Leube; E Cassetta; Anna Rita Bentivoglio; H M Waddy; Ryan Uitti; Demetrius M Maraganore; Alberto Albanese; Marina Frontali; Georg Auburger; Susan Bressman; Nicholas W Wood; TG Nygaard
Primary torsion dystonia: the search for genes is not over.
Journal of neurology, neurosurgery, and psychiatry 1999;67(3):395-7.
1999: Sian D Spacey; Nicholas W Wood
The genetics of Parkinson's disease.
Current opinion in neurology 1999;12(4):427-32.
1999: Paul Worth; Paola Giunti; Christopher Gardner-Thorpe; Peter DIxon; Mary B Davis; Nicholas W Wood
Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3.
American journal of human genetics 1999;65(2):420-6.
1999: Biswadjiet S Harhangi; Matthew J Farrer; Sarah J Lincoln; Vincenzo Bonifati; Giuseppe Meco; Giuseppe De Michele; Alexis Brice; Alexandra Dürr; M Martinez; Thomas Gasser; Benjamin Bereznai; Jenny R Vaughan; Nicholas W Wood; John Hardy; Ben A Oostra; Monique Breteler
The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease.
Neuroscience letters 1999;270(1):1-4.
1999: Wilson Marques; Michael G Hanna; S R Marques; Mary G Sweeney; PK Thomas; Nicholas W Wood
Phenotypic variation of a new P0 mutation in genetically identical twins.
Journal of neurology 1999;246(7):596-9.
1999: Ana I Rojo; Rosario Sanchez-Pernaute; A Fontán; P G Ruíz; Jérôme Honnorat; T Lynch; S Chin; Isabel Gonzalo; Alberto Rábano; A Martínez; Susan E Daniel; P Pramstaller; H Morris; Nicholas W Wood; Andrew J Lees; C Tabernero; T Nyggard; A C Jackson; A Hanson; Justo G de Yébenes; P Pramsteller
Clinical genetics of familial progressive supranuclear palsy.
Brain : a journal of neurology 1999;122 ( Pt 7)():1233-45.
1999: Wilson Marques; J G Sweeney; Nicholas W Wood; S J Wroe; W Marques
Central nervous system involvement in a novel connexin 32 mutation affecting identical twins.
Journal of neurology, neurosurgery, and psychiatry 1999;66(6):803-4.
1999: Paola Giunti; Giovanni Stevanin; Paul Worth; G David; Alexis Brice; Nicholas W Wood
Molecular and clinical study of 18 families with ADCA type II: evidence for genetic heterogeneity and de novo mutation.
American journal of human genetics 1999;64(6):1594-603.
1999: Sameer M Zuberi; Louise H Eunson; Alexander Spauschus; R De Silva; J Tolmie; Nicholas W Wood; Robert C McWilliam; John B P Stephenson; J P Stephenson; Dimitri M Kullmann; Michael G Hanna
A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy.
Brain : a journal of neurology 1999;122 ( Pt 5)():817-25.
1999: Huw R Morris; John C Janssen; O Bandmann; Susan E Daniel; Martin N Rossor; Andrew J Lees; Nicholas W Wood
The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases.
Journal of neurology, neurosurgery, and psychiatry 1999;66(5):665-7.
1999: Kim M Clark; Robert W Taylor; Margaret A Johnson; Patrick F Chinnery; Zofia M A Chrzanowska-Lightowlers; Richard M Andrews; Isabelle P Nelson; Nicholas W Wood; P J Lamont; Michael G Hanna; Robert N Lightowlers; Douglass M Turnbull
An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy.
American journal of human genetics 1999;64(5):1330-9.
1999: Naheed L Khan; Nicholas W Wood
Prader-Willi and Angelman syndromes: update on genetic mechanisms and diagnostic complexities.
Current opinion in neurology 1999;12(2):149-54.
1999: Perry M Elliott; M G Hanna; S A Ward; P F Chinnery; D M Turnbull; Nicholas W Wood; William J McKenna
Diagnostic utility of metabolic exercise testing in a patient with cardiovascular disease.
Heart (British Cardiac Society) 1999;81(4):441-3.
1999: Nacer Abbas; Christoph B Lücking; Sylvain Ricard; Alexandra Dürr; Vincenzo Bonifati; Giuseppe De Michele; S Bouley; Jenny R Vaughan; Thomas Gasser; Roberto Marconi; Emmanuel Broussolle; C Brefel-Courbon; Biswadjiet S Harhangi; Ben A Oostra; Edito Fabrizio; G A Böhme; Laurent Pradier; Nicholas W Wood; Alessandro Filla; Giuseppe Meco; Patrice DENEFLE; Yves Agid; Alexis Brice
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
Human molecular genetics 1999;8(4):567-74.
1999: Sarah J Lincoln; J Vaughan; Nicholas W Wood; Matt Baker; J Adamson; Katrina Gwinn-Hardy; Timothy Lynch; John Hardy; Matthew J Farrer
Low frequency of pathogenic mutations in the ubiquitin carboxy-terminal hydrolase gene in familial Parkinson's disease.
Neuroreport 1999;10(2):427-9.
1999: H R Morris; J Perez-Tur; John C Janssen; J Brown; Andrew J Lees; Nicholas W Wood; John Hardy; Michael Hutton; Martin N Rossor
Mutation in the tau exon 10 splice site region in familial frontotemporal dementia.
Annals of neurology 1999;45(2):270-1.
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.
1999: O Bandmann; J Vaughan; PA Holmans; CD Marsden; Nicholas W Wood
Toxins, genetics, and Parkinson's disease: the role of N-acetyltransferase 2.
Advances in neurology 1999;80():199-204.
1999: R Robinson; G T McCarthy; O Bandmann; MS Dobbie; Robert Surtees; Nicholas W Wood
GTP cyclohydrolase deficiency; intrafamilial variation in clinical phenotype, including levodopa responsiveness.
Journal of neurology, neurosurgery, and psychiatry 1999;66(1):86-9.
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: Christoph B Lücking; Nacer Abbas; Alexandra Dürr; Vincenzo Bonifati; Anne-Marie Bonnet; T de Broucker; G De Michele; Nicholas W Wood; Yves Agid; Alexis Brice
Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Group.
Lancet 1998;352(9137):1355-6.
1998: O Bandmann; Enza Maria Valente; PA Holmans; Robert Surtees; J H Walters; R A Wevers; CD Marsden; Nicholas W Wood
Dopa-responsive dystonia: a clinical and molecular genetic study.
Annals of neurology 1998;44(4):649-56.
1998: Michael G Hanna; Isabelle P Nelson; JA Morgan-Hughes; Nicholas W Wood
MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity.
Journal of neurology, neurosurgery, and psychiatry 1998;65(4):512-7.
1998: Michael G Hanna; Nicholas W Wood; Dimitri M Kullmann
Ion channels and neurological disease: DNA based diagnosis is now possible, and ion channels may be important in common paroxysmal disorders.
Journal of neurology, neurosurgery, and psychiatry 1998;65(4):427-31.
1998: Giovanni Stevanin; Paola Giunti; G D Belal; Alexandra Dürr; Merle Ruberg; Nicholas W Wood; Alexis Brice
De novo expansion of intermediate alleles in spinocerebellar ataxia 7.
Human molecular genetics 1998;7(11):1809-13.
1998: Nicholas W Wood
Genetic risk factors in Parkinson's disease.
Annals of neurology 1998;44(3 Suppl 1):S58-62.
1998: J Vaughan; Alexandra Durr; JP Tassin; Benjamin Bereznai; Thomas Gasser; Vincenzo Bonifati; Giuseppe De Michele; Edito Fabrizio; Giampiero Volpe; O Bandmann; William G Johnson; Lawrence I Golbe; Monique Breteler; Giuseppe Meco; Yves Agid; Alexis Brice; CD Marsden; Nicholas W Wood
The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's Disease.
Annals of neurology 1998;44(2):270-3.
1998: Michael G Hanna; J Stewart; Anthony H V Schapira; Nicholas W Wood; JA Morgan-Hughes; Nicholas M F Murray
Salbutamol treatment in a patient with hyperkalaemic periodic paralysis due to a mutation in the skeletal muscle sodium channel gene (SCN4A).
Journal of neurology, neurosurgery, and psychiatry 1998;65(2):248-50.
1998: P J Lamont; Robert Surtees; C E Woodward; J V Leonard; Nicholas W Wood; AE Harding
Clinical and laboratory findings in referrals for mitochondrial DNA analysis.
Archives of disease in childhood 1998;79(1):22-7.
1998: Michael G Hanna; Isabelle P Nelson; Shamina Rahman; R J Lane; John M Land; Simon J R Heales; M J Cooper; Anthony H V Schapira; JA Morgan-Hughes; Nicholas W Wood
Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.
American journal of human genetics 1998;63(1):29-36.
1998: Wilson Marques; PK Thomas; Mary G Sweeney; L Carr; Nicholas W Wood
Dejerine-Sottas neuropathy and PMP22 point mutations: a new base pair substitution and a possible "hot spot" on Ser72.
Annals of neurology 1998;43(5):680-3.
1998: Jenny R Vaughan; Matthew J Farrer; Zbigniew K Wszolek; Thomas Gasser; Alexandra Durr; Yves Agid; Vincenzo Bonifati; G DeMichele; Giampiero Volpe; Sarah J Lincoln; Monique Breteler; Giuseppe Meco; Alexis Brice; CD Marsden; John Hardy; Nicholas W Wood
Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD).
Human molecular genetics 1998;7(4):751-3.
1998: Nicholas W Wood
Diagnosing Friedreich's ataxia.
Archives of disease in childhood 1998;78(3):204-7.
1998: Paola Giunti; G Sabbadini; Mary G Sweeney; Mary B Davis; Liana Veneziano; Elide Mantuano; A Federico; Rosaria Plasmati; Marina Frontali; Nicholas W Wood
The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates.
Brain : a journal of neurology 1998;121 ( Pt 3)():459-67.
1998: Michael G Hanna; Mary B Davis; Mary G Sweeney; M Noursadeghi; C J Ellis; P Elliot; Nicholas W Wood; CD Marsden
Generalized chorea in two patients harboring the Friedreich's ataxia gene trinucleotide repeat expansion.
Movement disorders : official journal of the Movement Disorder Society 1998;13(2):339-40.
1998: O Bandmann; CD Marsden; Nicholas W Wood
Genetic aspects of Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 1998;13(2):203-11.
1998: O Bandmann; CD Marsden; Nicholas W Wood
Atypical presentations of dopa-responsive dystonia.
Advances in neurology 1998;78():283-90.
1998: Raju Kapoor; David H Miller; Stephen J Jones; Gordon T Plant; A Brusa; A Gass; C P Hawkins; R Page; Nicholas W Wood; D A S Compston; Ivan Moseley; WI McDonald
Effects of intravenous methylprednisolone on outcome in MRI-based prognostic subgroups in acute optic neuritis.
Neurology 1998;50(1):230-7.
1998: J Lopes; Nicole Ravisé; Antoon Vandenberghe; Francesc Palau; V Ionasescu; M Mayer; Nicolas Lévy; Nicholas W Wood; N Tachi; Pierre Bouche; Philippe Latour; Merle Ruberg; Alexis Brice; Eric LeGuern
Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination.
Human molecular genetics 1998;7(1):141-8.
1997: Paul R Jarman; Mary B Davis; Shirley V Hodgson; CD Marsden; Nicholas W Wood
Paroxysmal dystonic choreoathetosis. Genetic linkage studies in a British family.
Brain : a journal of neurology 1997;120 ( Pt 12)():2125-30.
1997: O Bandmann; Mary G Sweeney; Susan E Daniel; Gregor Wenning; Niall Quinn; CD Marsden; Nicholas W Wood
Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration.
Neurology 1997;49(6):1598-604.
1997: Katie Kompoliti; Eric J Pappert; Christopher G Goetz; B Ford; Nicholas W Wood
Progressive cognitive decline with truncal/limb ataxia and ballistic movements.
Movement disorders : official journal of the Movement Disorder Society 1997;12(6):1075-84.
1997: O Bandmann; J Vaughan; PA Holmans; CD Marsden; Nicholas W Wood
Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease.
Lancet 1997;350(9085):1136-9.
1997: Raffaele Lodi; Doris J Taylor; Sarah J Tabrizi; S Kumar; M Sweeney; Nicholas W Wood; Peter Styles; George K Radda; Anthony H V Schapira
In vivo skeletal muscle mitochondrial function in Leber's hereditary optic neuropathy assessed by 31P magnetic resonance spectroscopy.
Annals of neurology 1997;42(4):573-9.
1997: Paul R Jarman; Nicholas W Wood; M T Davis; P V Davis; Kailash P Bhatia; CD Marsden; Mary B Davis
Hereditary geniospasm: linkage to chromosome 9q13-q21 and evidence for genetic heterogeneity.
American journal of human genetics 1997;61(4):928-33.
1997: J Lopes; Antoon Vandenberghe; Sandrine Tardieu; V Ionasescu; Nicolas Lévy; Nicholas W Wood; N Tachi; Pierre Bouche; Philippe Latour; Alexis Brice; Eric LeGuern
Sex-dependent rearrangements resulting in CMT1A and HNPP.
Nature genetics 1997;17(2):136-7.
1997: Paul R Jarman; O Bandmann; CD Marsden; Nicholas W Wood
GTP cyclohydrolase I mutations in patients with dystonia responsive to anticholinergic drugs.
Journal of neurology, neurosurgery, and psychiatry 1997;63(3):304-8.
1997: G David; Nacer Abbas; Giovanni Stevanin; Alexandra Dürr; Gaël Yvert; G Cancel; C Weber; G Imbert; Frédéric Saudou; E Antoniou; Harry A Drabkin; Robert M Gemmill; Paola Giunti; Ali Benomar; Nicholas W Wood; Merle Ruberg; Yves Agid; Jean-Louis Mandel; Alexis Brice
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion.
Nature genetics 1997;17(1):65-70.
1997: Thomas Gasser; Bertram Müller-Myhsok; Zbigniew K Wszolek; Alexandra Dürr; Jenny R Vaughan; Vincenzo Bonifati; Giuseppe Meco; Benjamin Bereznai; R Oehlmann; Yves Agid; Alexis Brice; Nicholas W Wood
Genetic complexity and Parkinson's disease.
Science (New York, N.Y.) 1997;277(5324):388-9; author reply 389.
1997: Isabelle P Nelson; Michael G Hanna; Nicholas W Wood; AE Harding
Depletion of mitochondrial DNA by ddC in untransformed human cell lines.
Somatic cell and molecular genetics 1997;23(4):287-90.
1997: Violaine Planté-Bordeneuve; D Taussig; F Thomas; Gérard Said; Nicholas W Wood; CD Marsden; A E Harding
Evaluation of four candidate genes encoding proteins of the dopamine pathway in familial and sporadic Parkinson's disease: evidence for association of a DRD2 allele.
Neurology 1997;48(6):1589-93.
1997: P J Lamont; Mary B Davis; Nicholas W Wood
Identification and sizing of the GAA trinucleotide repeat expansion of Friedreich's ataxia in 56 patients. Clinical and genetic correlates.
Brain : a journal of neurology 1997;120 ( Pt 4)():673-80.
1997: R M Chalmers; P Riordan-Eva; Nicholas W Wood
Autosomal recessive inheritance of hereditary motor and sensory neuropathy with optic atrophy.
Journal of neurology, neurosurgery, and psychiatry 1997;62(4):385-7.
1997: O Bandmann; Mary G Sweeney; Susan E Daniel; CD Marsden; Nicholas W Wood
Mitochondrial DNA polymorphisms in pathologically proven Parkinson's disease.
Journal of neurology 1997;244(4):262-5.
1996: G David; Paola Giunti; Nacer Abbas; Philippe Coullin; Giovanni Stevanin; W Horta; Robert M Gemmill; Jean Weissenbach; Nicholas W Wood; S Cunha; Harry A Drabkin; A E Harding; Yves Agid; Alexis Brice
The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus.
American journal of human genetics 1996;59(6):1328-36.
1996: O Bandmann; Susan E Daniel; CD Marsden; Nicholas W Wood; AE Harding
The GTP-cyclohydrolase I gene in atypical parkinsonian patients: a clinico-genetic study.
Journal of the neurological sciences 1996;141(1-2):27-32.
1996: R M Chalmers; Mary B Davis; Mary G Sweeney; Nicholas W Wood; AE Harding
Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy.
American journal of human genetics 1996;59(1):103-8.
1996: O Bandmann; Mary B Davis; CD Marsden; Nicholas W Wood
The human homologue of the weaver mouse gene in familial and sporadic Parkinson's disease.
Neuroscience 1996;72(4):877-9.
1996: O Bandmann; TG Nygaard; Robert Surtees; CD Marsden; Nicholas W Wood; AE Harding
Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneity.
Human molecular genetics 1996;5(3):403-6.
1996: Paul Riordan-Eva; Nicholas W Wood
Mitochondrial disorders in neuro-ophthalmology.
Current opinion in neurology 1996;9(1):1-4.
1995: Nicholas W Wood; Stephen Sawcer; H F Kellar-Wood; PA Holmans; David Clayton; N Robertson; D A S Compston
Susceptibility to multiple sclerosis and the immunoglobulin heavy chain variable region.
Journal of neurology 1995;242(10):677-82.
1995: Nicholas W Wood; Stephen Sawcer; H F Kellar-Wood; PA Holmans; David Clayton; N Robertson; D A S Compston
The T-cell receptor beta locus and susceptibility to multiple sclerosis.
Neurology 1995;45(10):1859-63.
1995: H F Kellar-Wood; Nicholas W Wood; PA Holmans; David Clayton; N Robertson; D A S Compston
Multiple sclerosis and the HLA-D region: linkage and association studies.
Journal of neuroimmunology 1995;58(2):183-90.
1995: D A S Compston; H Kellar Wood; N Robertson; Stephen Sawcer; Nicholas W Wood
Genes and susceptibility to multiple sclerosis.
Acta neurologica Scandinavica. Supplementum 1995;161():43-51.
1994: Nicholas W Wood; PA Holmans; David Clayton; N Robertson; D A S Compston
No linkage or association between multiple sclerosis and the myelin basic protein gene in affected sibling pairs.
Journal of neurology, neurosurgery, and psychiatry 1994;57(10):1191-4.
1994: Neil Scolding; John Zajicek; Nicholas W Wood; D A S Compston
The pathogenesis of demyelinating disease.
Progress in neurobiology 1994;43(2):143-73.
1994: M Eoli; Nicholas W Wood; H F Kellar-Wood; PA Holmans; David Clayton; D A S Compston
No linkage between multiple sclerosis and the T cell receptor alpha chain locus.
Journal of the neurological sciences 1994;124(1):32-7.
1994: C J Mumford; Nicholas W Wood; H Kellar-Wood; J W Thorpe; David H Miller; D A S Compston
The British Isles survey of multiple sclerosis in twins.
Neurology 1994;44(1):11-5.
1992: C J Mumford; M B Fraser; Nicholas W Wood; D A S Compston
Multiple sclerosis in the Cambridge health district of east Anglia.
Journal of neurology, neurosurgery, and psychiatry 1992;55(10):877-82.