受强制性开放获取政策约束的文章 - alvarez v.了解详情
无法在其他位置公开访问的文章：11 篇
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SPG7 mutational screening in spastic paraplegia patients supports a dominant effect for some mutations and a pathogenic role for p.A510V
E Sánchez‐Ferrero, E Coto, C Beetz, J Gamez, AI Corao, M Diaz, ...
Clinical genetics 83 (3), 257-262, 2013
强制性开放获取政策： Government of Spain
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Circulating microRNAs in Huntington’s disease: Emerging mediators in metabolic impairment
C Díez-Planelles, P Sánchez-Lozano, MC Crespo, J Gil-Zamorano, ...
Pharmacological research 108, 102-110, 2016
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MiRNA profile in the substantia nigra of Parkinson’s disease and healthy subjects
LF Cardo, E Coto, R Ribacoba, M Menéndez, G Moris, E Suárez, ...
Journal of Molecular Neuroscience 54, 830-836, 2014
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A search for new CYP3A4 variants as determinants of tacrolimus dose requirements in renal-transplanted patients
B Tavira, E Coto, C Diaz-Corte, V Alvarez, C López-Larrea, F Ortega
Pharmacogenetics and Genomics 23 (8), 445-448, 2013
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Do Not Trust the Pedigree: Reduced and Sex‐Dependent Penetrance at a Novel Mutation Hotspot in ATL1 Blurs Autosomal Dominant Inheritance of Spastic …
RE Varga, R Schüle, H Fadel, I Valenzuela, F Speziani, M Gonzalez, ...
Human mutation 34 (6), 860-863, 2013
强制性开放获取政策： US National Institutes of Health, Government of Spain
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HTT gene intermediate alleles in neurodegeneration: evidence for association with Alzheimer's disease
M Menéndez-González, J Clarimón, I Rosas-Allende, M Blázquez, ...
Neurobiology of aging 76, 215. e9-215. e14, 2019
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Non optical semi-conductor next generation sequencing of the main cardiac QT-interval duration genes in pooled DNA samples
J Gómez, JR Reguero, C Morís, V Alvarez, E Coto
Journal of cardiovascular translational research 7, 133-137, 2014
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The G263X MYBPC3 mutation is a common and low-penetrant mutation for hypertrophic cardiomyopathy in the region of Asturias (Northern Spain)
JR Reguero, J Gómez, M Martín, JP Flórez, C Morís, S Iglesias, B Alonso, ...
International journal of cardiology 168 (4), 4555-4556, 2013
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Profile of microRNAs in the plasma of hypertrophic cardiomyopathy patients compared to healthy controls
M Palacín, E Coto, JR Reguero, C Morís, V Alvarez
International journal of cardiology 167 (6), 3075-3076, 2013
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A labor and cost effective next generation sequencing of PKHD1 in autosomal recessive polycystic kidney disease patients
B Tavira, J Gómez, S Málaga, F Santos, J Fernández-Aracama, B Alonso, ...
Gene 561 (1), 165-169, 2015
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Intermediate and Expanded HTT Alleles and the Risk for α‐Synucleinopathies
S Pérez‐Oliveira, I Álvarez, I Rosas, M Menendez‐González, ...
Movement Disorders 37 (9), 1841-1849, 2022
强制性开放获取政策： Banking Foundation "la Caixa", Government of Spain
可在其他位置公开访问的文章：100 篇
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Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease
JC Lambert, CA Ibrahim-Verbaas, D Harold, AC Naj, R Sims, ...
Nature genetics 45 (12), 1452-1458, 2013
强制性开放获取政策： US National Institutes of Health, National Institute of Health and Medical …
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Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease
JC Lambert, S Heath, G Even, D Campion, K Sleegers, M Hiltunen, ...
Nature genetics 41 (10), 1094-1099, 2009
强制性开放获取政策： Research Foundation (Flanders), National Institute of Health and Medical …
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Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
BW Kunkle, B Grenier-Boley, R Sims, JC Bis, V Damotte, AC Naj, ...
Nature genetics 51 (3), 414-430, 2019
强制性开放获取政策： US National Institutes of Health, Motor Neurone Disease Association, UK, UK …
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Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
P Hollingworth, D Harold, R Sims, A Gerrish, JC Lambert, ...
Nature genetics 43 (5), 429-435, 2011
强制性开放获取政策： US National Institutes of Health, Research Foundation (Flanders), National …
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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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New insights into the genetic etiology of Alzheimer’s disease and related dementias
C Bellenguez, F Küçükali, IE Jansen, L Kleineidam, S Moreno-Grau, ...
Nature genetics 54 (4), 412-436, 2022
强制性开放获取政策： US National Institutes of Health, Howard Hughes Medical Institute, National …
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Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
R Sims, SJ Van Der Lee, AC Naj, C Bellenguez, N Badarinarayan, ...
Nature genetics 49 (9), 1373-1384, 2017
强制性开放获取政策： US Department of Defense, US National Institutes of Health, US Department of …
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APOE and Alzheimer disease: a major gene with semi-dominant inheritance
E Genin, D Hannequin, D Wallon, K Sleegers, M Hiltunen, O Combarros, ...
Molecular psychiatry 16 (9), 903-907, 2011
强制性开放获取政策： US National Institutes of Health
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Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores
I De Rojas, S Moreno-Grau, N Tesi, B Grenier-Boley, V Andrade, ...
Nature communications 12 (1), 3417, 2021
强制性开放获取政策： US National Institutes of Health, Banking Foundation "la Caixa", National …
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