n w wood
n w wood
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Title
Cited by
Cited by
Year
Hereditary early-onset Parkinson's disease caused by mutations in PINK1
EM Valente, PM Abou-Sleiman, V Caputo, MMK Muqit, K Harvey, ...
science 304 (5674), 1158-1160, 2004
35162004
Second consensus statement on the diagnosis of multiple system atrophy
S Gilman, GK Wenning, PA Low, DJ Brooks, CJ Mathias, JQ Trojanowski, ...
Neurology 71 (9), 670-676, 2008
25472008
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
S Sawcer, G Hellenthal, M Pirinen, CCA Spencer, NA Patsopoulos, ...
Nature 476 (7359), 214, 2011
25132011
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
C Paisán-Ruı́z, S Jain, EW Evans, WP Gilks, J Simón, M Van Der Brug, ...
Neuron 44 (4), 595-600, 2004
24112004
Genome-wide association study reveals genetic risk underlying Parkinson's disease
J Simon-Sanchez, C Schulte, JM Bras, M Sharma, JR Gibbs, D Berg, ...
Nature genetics 41 (12), 1308-1312, 2009
18692009
Association between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene
CB Lücking, A Dürr, V Bonifati, J Vaughan, G De Michele, T Gasser, ...
New England Journal of Medicine 342 (21), 1560-1567, 2000
17092000
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ...
Nature genetics 46 (9), 989-993, 2014
15012014
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
DG Healy, M Falchi, SS O'Sullivan, V Bonifati, A Durr, S Bressman, ...
The Lancet Neurology 7 (7), 583-590, 2008
13452008
Analysis of shared heritability in common disorders of the brain
V Anttila, B Bulik-Sullivan, HK Finucane, RK Walters, J Bras, L Duncan, ...
Science 360 (6395), 2018
11252018
Expanding insights of mitochondrial dysfunction in Parkinson's disease
PM Abou-Sleiman, MMK Muqit, NW Wood
Nature Reviews Neuroscience 7 (3), 207-219, 2006
9892006
Genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1
A Strange, F Capon, CCA Spencer, J Knight, ME Weale, MH Allen, ...
Nature genetics 42 (11), 985, 2010
9212010
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion
G David, N Abbas, G Stevanin, A Dürr, G Yvert, G Cancel, C Weber, ...
Nature genetics 17 (1), 65-70, 1997
8801997
A common LRRK2 mutation in idiopathic Parkinson's disease
WP Gilks, PM Abou-Sleiman, S Gandhi, S Jain, A Singleton, AJ Lees, ...
The Lancet 365 (9457), 415-416, 2005
8562005
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility
DM Evans, CCA Spencer, JJ Pointon, Z Su, D Harvey, G Kochan, ...
Nature genetics 43 (8), 761-767, 2011
8292011
Association of Multidrug Resistance in Epilepsy with a Polymorphism in the Drug-Transporter Gene ABCB1
A Siddiqui, R Kerb, ME Weale, U Brinkmann, A Smith, DB Goldstein, ...
New England Journal of Medicine 348 (15), 1442-1448, 2003
8032003
Direct observation of the interconversion of normal and toxic forms of α-synuclein
N Cremades, SIA Cohen, E Deas, AY Abramov, AY Chen, A Orte, ...
Cell 149 (5), 1048-1059, 2012
7202012
PINK1-associated Parkinson's disease is caused by neuronal vulnerability to calcium-induced cell death
S Gandhi, A Wood-Kaczmar, Z Yao, H Plun-Favreau, E Deas, K Klupsch, ...
Molecular cell 33 (5), 627-638, 2009
6752009
A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe
N Abbas, CB Lücking, S Ricard, A Dürr, V Bonifati, G De Michele, ...
Human molecular genetics 8 (4), 567-574, 1999
6571999
Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease
J Neumann, J Bras, E Deas, SS O'Sullivan, L Parkkinen, RH Lachmann, ...
Brain 132 (7), 1783-1794, 2009
6332009
Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36
EM Valente, AR Bentivoglio, PH Dixon, A Ferraris, T Ialongo, M Frontali, ...
The American Journal of Human Genetics 68 (4), 895-900, 2001
5972001
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