Henry Houlden
Henry Houlden
Prof Neurology and Neurogenetics
Geverifieerd e-mailadres voor ucl.ac.uk - Homepage
Geciteerd door
Geciteerd door
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
M Hutton, CL Lendon, P Rizzu, M Baker, S Froelich, H Houlden, ...
Nature 393 (6686), 702-705, 1998
A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N–terminus of β–amyloid
M Mullan, F Crawford, K Axelman, H Houlden, L Lilius, B Winblad, ...
Nature genetics 1 (5), 345-347, 1992
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
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
Early-onset Alzheimer's disease caused by mutations at codon 717 of the β-amyloid precursor protein gene
MC Chartier-Harlin, F Crawford, H Houlden, A Warren, D Hughes, ...
Nature 353 (6347), 844-846, 1991
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
The Lancet Neurology 18 (12), 1091-1102, 2019
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
E Majounie, AE Renton, K Mok, EGP Dopper, A Waite, S Rollinson, ...
The Lancet Neurology 11 (4), 323-330, 2012
Association of an extended haplotype in the tau gene with progressive supranuclear palsy
M Baker, I Litvan, H Houlden, J Adamson, D Dickson, J Perez-Tur, ...
Human molecular genetics 8 (4), 711-715, 1999
A common polymorphism in the brain‐derived neurotrophic factor gene (BDNF) modulates human cortical plasticity and the response to rTMS
B Cheeran, P Talelli, F Mori, G Koch, A Suppa, M Edwards, H Houlden, ...
The Journal of physiology 586 (23), 5717-5725, 2008
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
Mapping the human genetic architecture of COVID-19
Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ...
Nature 600 (7889), 472-477, 2021
Characterization of PLA2G6 as a locus for dystonia‐parkinsonism
C Paisan‐Ruiz, KP Bhatia, A Li, D Hernandez, M Davis, NW Wood, ...
Annals of neurology 65 (1), 19-23, 2009
A novel α-synuclein missense mutation in Parkinson disease
C Proukakis, CG Dudzik, T Brier, DS MacKay, JM Cooper, GL Millhauser, ...
Neurology 80 (11), 1062-1064, 2013
Parkinson's disease induced pluripotent stem cells with triplication of the α-synuclein locus
MJ Devine, M Ryten, P Vodicka, AJ Thomson, T Burdon, H Houlden, ...
Nature communications 2 (1), 440, 2011
α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson’s disease and multiple system atrophy?
AP Kiely, YT Asi, E Kara, P Limousin, H Ling, P Lewis, C Proukakis, ...
Acta neuropathologica 125, 753-769, 2013
Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype
H Houlden, M Baker, HR Morris, N MacDonald, S Pickering–Brown, ...
Neurology 56 (12), 1702-1706, 2001
A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1
R Crook, A Verkkoniemi, J Perez-Tur, N Mehta, M Baker, H Houlden, ...
Nature medicine 4 (4), 452-455, 1998
Early onset familial Alzheimer’s disease: mutation frequency in 31 families
JC Janssen, JA Beck, TA Campbell, A Dickinson, NC Fox, RJ Harvey, ...
Neurology 60 (2), 235-239, 2003
Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population
J Beck, M Poulter, D Hensman, JD Rohrer, CJ Mahoney, G Adamson, ...
The American Journal of Human Genetics 92 (3), 345-353, 2013
A locus for familial early–onset Alzhelmer's disease on the long arm of chromosome 14, proximal to the α1–antichymotrypsin gene
M Mullan, H Houlden, M Windelspecht, L Fidani, C Lombardi, P Diaz, ...
Nature genetics 2 (4), 340-342, 1992
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