受强制性开放获取政策约束的文章 - Javier Simón-Sánchez了解详情
无法在其他位置公开访问的文章：1 篇
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A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish family
HA Hanagasi, A Giri, E Kartal, G Guven, B Bilgiç, AK Hauser, M Emre, ...
Parkinsonism & related disorders 29, 117-120, 2016
强制性开放获取政策： US National Institutes of Health, Fundação para a Ciência e a Tecnologia …
可在其他位置公开访问的文章：55 篇
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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
AE Renton, E Majounie, A Waite, J Simón-Sánchez, S Rollinson, ...
Neuron 72 (2), 257-268, 2011
强制性开放获取政策： US National Institutes of Health, German Research Foundation
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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
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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
强制性开放获取政策： US National Institutes of Health, UK Medical Research Council, Parkinson's …
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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
强制性开放获取政策： US National Institutes of Health, German Research Foundation, Motor Neurone …
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Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
International Parkinson Disease Genomics Consortium
The Lancet 377 (9766), 641-649, 2011
强制性开放获取政策： US National Institutes of Health, Parkinson's UK
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A genome-wide association study identifies protein quantitative trait loci (pQTLs)
D Melzer, JRB Perry, D Hernandez, AM Corsi, K Stevens, I Rafferty, ...
PLoS genetics 4 (5), e1000072, 2008
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Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy
S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ...
The American Journal of Human Genetics 98 (3), 500-513, 2016
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Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
LA Robak, IE Jansen, J Van Rooij, AG Uitterlinden, R Kraaij, J Jankovic, ...
Brain 140 (12), 3191-3203, 2017
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Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease
A Beilina, IN Rudenko, A Kaganovich, L Civiero, H Chau, SK Kalia, ...
Proceedings of the National Academy of Sciences 111 (7), 2626-2631, 2014
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SNCA variants are associated with increased risk for multiple system atrophy
SW Scholz, H Houlden, C Schulte, M Sharma, A Li, D Berg, A Melchers, ...
Annals of Neurology: Official Journal of the American Neurological …, 2009
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Parkinson's disease age at onset genome‐wide association study: defining heritability, genetic loci, and α‐synuclein mechanisms
C Blauwendraat, K Heilbron, CL Vallerga, S Bandres‐Ciga, R Von Coelln, ...
Movement Disorders 34 (6), 866-875, 2019
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Using genome-wide complex trait analysis to quantify ‘missing heritability’in Parkinson's disease
MF Keller, M Saad, J Bras, F Bettella, N Nicolaou, J Simón-Sánchez, ...
Human molecular genetics 21 (22), 4996-5009, 2012
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A two-stage meta-analysis identifies several new loci for Parkinson's disease
International Parkinson's Disease Genomics Consortium (IPDGC), ...
PLoS genetics 7 (6), e1002142, 2011
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Genome-wide association study confirms extant PD risk loci among the Dutch
J Simón-Sánchez, JJ Van Hilten, B Van De Warrenburg, B Post, ...
European journal of human genetics 19 (6), 655-661, 2011
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The chromosome 9 ALS and FTD locus is probably derived from a single founder
K Mok, BJ Traynor, J Schymick, PJ Tienari, H Laaksovirta, T Peuralinna, ...
Neurobiology of aging 33 (1), 209. e3-209. e8, 2012
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Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease
JO Johnson, JR Gibbs, A Megarbane, JA Urtizberea, DG Hernandez, ...
Brain 135 (9), 2875-2882, 2012
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Identification of candidate Parkinson disease genes by integrating genome-wide association study, expression, and epigenetic data sets
DA Kia, D Zhang, S Guelfi, C Manzoni, L Hubbard, RH Reynolds, J Botía, ...
JAMA neurology 78 (4), 464-472, 2021
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NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases
C Blauwendraat, F Faghri, L Pihlstrom, JT Geiger, A Elbaz, S Lesage, ...
Neurobiology of aging 57, 247. e9-247. e13, 2017
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A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease
P Holmans, V Moskvina, L Jones, M Sharma, ...
Human molecular genetics 22 (5), 1039-1049, 2013
强制性开放获取政策： US National Institutes of Health, Parkinson's UK
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